Phytochemica: A platform to explore phytochemicals of medicinal plants

References for PDM ID: CARS0447


S.No. Reference Link
1 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
2 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
3 Verma, A.K. LU, Singh, R.R. LU, Singh, S. LU. Improved alkaloid content in callus culture of Catharanthus roseus. Bot Serbica. 2012;36: 123–130.LINK
4 Verma, A.K. LU, Singh, R.R. LU, Singh, S. LU. Improved alkaloid content in callus culture of Catharanthus roseus. Bot Serbica. 2012;36: 123–130.LINK
5 Ten Hoopen HJG, van Gulik WM, Schlatmann JE, Moreno PRH, Vinke JL, Heijnen JJ, et al. Ajmalicine production by cell cultures of Catharanthus roseus: from shake flask to bioreactor. Plant Cell Tissue Organ Cult. 1994;38: 85–91. doi:10.1007/BF00033865LINK
6 Ten Hoopen HJG, van Gulik WM, Schlatmann JE, Moreno PRH, Vinke JL, Heijnen JJ, et al. Ajmalicine production by cell cultures of Catharanthus roseus: from shake flask to bioreactor. Plant Cell Tissue Organ Cult. 1994;38: 85–91. doi:10.1007/BF00033865LINK
7 Almagro L, L?pez Perez AJ, Pedre?o MA. New method to enhance ajmalicine production in Catharanthus roseus cell cultures based on the use of cyclodextrins. Biotechnol Lett. 2011;33: 381–385. doi:10.1007/s10529-010-0430-6LINK
8 Almagro L, L?pez Perez AJ, Pedre?o MA. New method to enhance ajmalicine production in Catharanthus roseus cell cultures based on the use of cyclodextrins. Biotechnol Lett. 2011;33: 381–385. doi:10.1007/s10529-010-0430-6LINK
9 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
10 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
11 Rijhwani SK, Shanks J V. Effect of elicitor dosage and exposure time on biosynthesis of indole alkaloids by Catharanthus roseus hairy root cultures. Biotechnol Prog. 1998;14: 442–449. doi:10.1021/bp980029vLINK
12 Rijhwani SK, Shanks J V. Effect of elicitor dosage and exposure time on biosynthesis of indole alkaloids by Catharanthus roseus hairy root cultures. Biotechnol Prog. 1998;14: 442–449. doi:10.1021/bp980029vLINK
13 Bhadra R, Shanks J V. Transient studies of nutrient uptake, growth, and indole alkaloid accumulation in heterotrophic cultures of hairy roots of Catharanthus roseus. Biotechnol Bioeng. 1997;55: 527–534. doi:10.1002/(SICI)1097-0290(19970805)55:3<527::AID-BIT9>3.0.CO;2-ELINK
14 Bhadra R, Shanks J V. Transient studies of nutrient uptake, growth, and indole alkaloid accumulation in heterotrophic cultures of hairy roots of Catharanthus roseus. Biotechnol Bioeng. 1997;55: 527–534. doi:10.1002/(SICI)1097-0290(19970805)55:3<527::AID-BIT9>3.0.CO;2-ELINK
15 Islas I, Loyola-Vargas VM, de Lourdes Miranda-Ham M. Tryptophan decarboxylase activity in transformed roots fromCatharanthus roseus and its relationship to tryptamine, ajmalicine, and catharanthine accumulation during the culture cycle. Vitr Cell Dev Biol. 1994;30: 81–83. doi:10.1007/BF02632125LINK
16 Islas I, Loyola-Vargas VM, de Lourdes Miranda-Ham M. Tryptophan decarboxylase activity in transformed roots fromCatharanthus roseus and its relationship to tryptamine, ajmalicine, and catharanthine accumulation during the culture cycle. Vitr Cell Dev Biol. 1994;30: 81–83. doi:10.1007/BF02632125LINK
17 Satdive RK, Fulzele DP, Eapen S. Studies on production of ajmalicine in shake flasks by multiple shoot cultures of Catharanthus roseus. Biotechnol Prog. 2003;19: 1071–1075. doi:10.1021/bp020138gLINK
18 Satdive RK, Fulzele DP, Eapen S. Studies on production of ajmalicine in shake flasks by multiple shoot cultures of Catharanthus roseus. Biotechnol Prog. 2003;19: 1071–1075. doi:10.1021/bp020138gLINK
19 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
20 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
21 Jaleel CA, Gopi R, Manivannan P, Sankar B, Kishorekumar A, Panneerselvam R. Antioxidant potentials and ajmalicine accumulation in Catharanthus roseus after treatment with giberellic acid. Colloids Surfaces B Biointerfaces. 2007;60: 195–200. doi:10.1016/j.colsurfb.2007.06.009LINK
22 Jaleel CA, Gopi R, Manivannan P, Sankar B, Kishorekumar A, Panneerselvam R. Antioxidant potentials and ajmalicine accumulation in Catharanthus roseus after treatment with giberellic acid. Colloids Surfaces B Biointerfaces. 2007;60: 195–200. doi:10.1016/j.colsurfb.2007.06.009LINK
23 Zenk MH, El-Shagi H, Arens H, St?ckigt J, Weiler EW, Deus B. Formation of the Indole Alkaloids Serpentine and Ajmalicine in Cell Suspension Cultures of Catharanthus roseus. In: Barz W, Reinhard E, Zenk MH, editors. Plant Tissue Culture and Its Bio-technological Application. Berlin, Heidelberg: Springer Berlin Heidelberg; 1977. pp. 27–43. doi:10.1007/978-3-642-66646-9_3LINK
24 Zenk MH, El-Shagi H, Arens H, St?ckigt J, Weiler EW, Deus B. Formation of the Indole Alkaloids Serpentine and Ajmalicine in Cell Suspension Cultures of Catharanthus roseus. In: Barz W, Reinhard E, Zenk MH, editors. Plant Tissue Culture and Its Bio-technological Application. Berlin, Heidelberg: Springer Berlin Heidelberg; 1977. pp. 27–43. doi:10.1007/978-3-642-66646-9_3LINK
25 Behzadifar M, Chehrazi M, Aboutalebi A. Effect of salt stress by using unconventional water on some morphological characters and ajmalicine alkaloid amount in the roots of Catharanthus roseus Cvs. Rosea and Alba. Ann Biol Res. 2013;4: 229.LINK
26 Behzadifar M, Chehrazi M, Aboutalebi A. Effect of salt stress by using unconventional water on some morphological characters and ajmalicine alkaloid amount in the roots of Catharanthus roseus Cvs. Rosea and Alba. Ann Biol Res. 2013;4: 229.LINK
27 El-Sayed M, Verpoorte R. Growth, metabolic profiling and enzymes activities of Catharanthus roseus seedlings treated with plant growth regulators. Plant Growth Regul. 2004;44: 53–58. doi:10.1007/s10725-004-2604-5LINK
28 El-Sayed M, Verpoorte R. Growth, metabolic profiling and enzymes activities of Catharanthus roseus seedlings treated with plant growth regulators. Plant Growth Regul. 2004;44: 53–58. doi:10.1007/s10725-004-2604-5LINK
29 Lourdes Miranda-Ham M de, Islas-Flores I, V?zquez-Flota AF. Accumulation of monoterpenoid indole alkaloids in periwinkle seedlings (Catharanthus roseus) as a model for the study of plant-environment interactions. Biochem Mol Biol Educ. 2007;35: 206–210. doi:10.1002/bambed.60LINK
30 Lourdes Miranda-Ham M de, Islas-Flores I, V?zquez-Flota AF. Accumulation of monoterpenoid indole alkaloids in periwinkle seedlings (Catharanthus roseus) as a model for the study of plant-environment interactions. Biochem Mol Biol Educ. 2007;35: 206–210. doi:10.1002/bambed.60LINK
31 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
32 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
33 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
34 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
35 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
36 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
37 Rijhwani SK, Shanks J V. Effect of elicitor dosage and exposure time on biosynthesis of indole alkaloids by Catharanthus roseus hairy root cultures. Biotechnol Prog. 1998;14: 442–449. doi:10.1021/bp980029vLINK
38 Rijhwani SK, Shanks J V. Effect of elicitor dosage and exposure time on biosynthesis of indole alkaloids by Catharanthus roseus hairy root cultures. Biotechnol Prog. 1998;14: 442–449. doi:10.1021/bp980029vLINK
39 Bhadra R, Shanks J V. Transient studies of nutrient uptake, growth, and indole alkaloid accumulation in heterotrophic cultures of hairy roots of Catharanthus roseus. Biotechnol Bioeng. 1997;55: 527–534. doi:10.1002/(SICI)1097-0290(19970805)55:3<527::AID-BIT9>3.0.CO;2-ELINK
40 Bhadra R, Shanks J V. Transient studies of nutrient uptake, growth, and indole alkaloid accumulation in heterotrophic cultures of hairy roots of Catharanthus roseus. Biotechnol Bioeng. 1997;55: 527–534. doi:10.1002/(SICI)1097-0290(19970805)55:3<527::AID-BIT9>3.0.CO;2-ELINK
41 El-Sayed M, Verpoorte R. Growth, metabolic profiling and enzymes activities of Catharanthus roseus seedlings treated with plant growth regulators. Plant Growth Regul. 2004;44: 53–58. doi:10.1007/s10725-004-2604-5LINK
42 El-Sayed M, Verpoorte R. Growth, metabolic profiling and enzymes activities of Catharanthus roseus seedlings treated with plant growth regulators. Plant Growth Regul. 2004;44: 53–58. doi:10.1007/s10725-004-2604-5LINK
43 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
44 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
45 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
46 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
47 Zenk MH, El-Shagi H, Arens H, St?ckigt J, Weiler EW, Deus B. Formation of the Indole Alkaloids Serpentine and Ajmalicine in Cell Suspension Cultures of Catharanthus roseus. In: Barz W, Reinhard E, Zenk MH, editors. Plant Tissue Culture and Its Bio-technological Application. Berlin, Heidelberg: Springer Berlin Heidelberg; 1977. pp. 27–43. doi:10.1007/978-3-642-66646-9_3LINK
48 Zenk MH, El-Shagi H, Arens H, St?ckigt J, Weiler EW, Deus B. Formation of the Indole Alkaloids Serpentine and Ajmalicine in Cell Suspension Cultures of Catharanthus roseus. In: Barz W, Reinhard E, Zenk MH, editors. Plant Tissue Culture and Its Bio-technological Application. Berlin, Heidelberg: Springer Berlin Heidelberg; 1977. pp. 27–43. doi:10.1007/978-3-642-66646-9_3LINK
49 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
50 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
51 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
52 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
53 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
54 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
55 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
56 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
57 Islas I, Loyola-Vargas VM, de Lourdes Miranda-Ham M. Tryptophan decarboxylase activity in transformed roots fromCatharanthus roseus and its relationship to tryptamine, ajmalicine, and catharanthine accumulation during the culture cycle. Vitr Cell Dev Biol. 1994;30: 81–83. doi:10.1007/BF02632125LINK
58 Islas I, Loyola-Vargas VM, de Lourdes Miranda-Ham M. Tryptophan decarboxylase activity in transformed roots fromCatharanthus roseus and its relationship to tryptamine, ajmalicine, and catharanthine accumulation during the culture cycle. Vitr Cell Dev Biol. 1994;30: 81–83. doi:10.1007/BF02632125LINK
59 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
60 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
61 El-Sayed M, Verpoorte R. Growth, metabolic profiling and enzymes activities of Catharanthus roseus seedlings treated with plant growth regulators. Plant Growth Regul. 2004;44: 53–58. doi:10.1007/s10725-004-2604-5LINK
62 El-Sayed M, Verpoorte R. Growth, metabolic profiling and enzymes activities of Catharanthus roseus seedlings treated with plant growth regulators. Plant Growth Regul. 2004;44: 53–58. doi:10.1007/s10725-004-2604-5LINK
63 Lourdes Miranda-Ham M de, Islas-Flores I, V?zquez-Flota AF. Accumulation of monoterpenoid indole alkaloids in periwinkle seedlings (Catharanthus roseus) as a model for the study of plant-environment interactions. Biochem Mol Biol Educ. 2007;35: 206–210. doi:10.1002/bambed.60LINK
64 Lourdes Miranda-Ham M de, Islas-Flores I, V?zquez-Flota AF. Accumulation of monoterpenoid indole alkaloids in periwinkle seedlings (Catharanthus roseus) as a model for the study of plant-environment interactions. Biochem Mol Biol Educ. 2007;35: 206–210. doi:10.1002/bambed.60LINK
65 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
66 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
67 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
68 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
69 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
70 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
71 Hirata K, Miyamoto K, Miura Y. Catharanthus roseus L. (Periwinkle): Production of Vindoline and Catharanthine in Multiple Shoot Cultures. In: Bajaj YPS, editor. Medicinal and Aromatic Plants VI. Berlin, Heidelberg: Springer Berlin Heidelberg; 1994. pp. 46–55. doi:10.1007/978-3-642-57970-7_3LINK
72 Hirata K, Miyamoto K, Miura Y. Catharanthus roseus L. (Periwinkle): Production of Vindoline and Catharanthine in Multiple Shoot Cultures. In: Bajaj YPS, editor. Medicinal and Aromatic Plants VI. Berlin, Heidelberg: Springer Berlin Heidelberg; 1994. pp. 46–55. doi:10.1007/978-3-642-57970-7_3LINK
73 V?zquez-Flota F, Moreno-Valenzuela O, Miranda-Ham ML, Coello-Coello J, Loyola-Vargas VM. Catharanthine and ajmalicine synthesis in Catharanthus roseus hairy root cultures. Plant Cell Tissue Organ Cult. 1994;38: 273–279. doi:10.1007/BF00033887LINK
74 V?zquez-Flota F, Moreno-Valenzuela O, Miranda-Ham ML, Coello-Coello J, Loyola-Vargas VM. Catharanthine and ajmalicine synthesis in Catharanthus roseus hairy root cultures. Plant Cell Tissue Organ Cult. 1994;38: 273–279. doi:10.1007/BF00033887LINK
75 Gupta MM, Singh D V, Tripathi AK, Pandey R, Verma RK, Singh S, et al. Simultaneous determination of vincristine, vinblastine, catharanthine, and vindoline in leaves of catharanthus roseus by high-performance liquid chromatography. J Chromatogr Sci. 2005;43: 450–453. doi:10.1093/chromsci/43.9.450LINK
76 Gupta MM, Singh D V, Tripathi AK, Pandey R, Verma RK, Singh S, et al. Simultaneous determination of vincristine, vinblastine, catharanthine, and vindoline in leaves of catharanthus roseus by high-performance liquid chromatography. J Chromatogr Sci. 2005;43: 450–453. doi:10.1093/chromsci/43.9.450LINK
77 Verma A, Laakso I, Sepp?nen-Laakso T, Huhtikangas A, Riekkola M-L. A simplified procedure for indole alkaloid extraction from Catharanthus roseus combined with a semi-synthetic production process for vinblastine. Molecules. Molecular Diversity Preservation International; 2007;12: 1307–1315. doi:10.3390/12071307LINK
78 Verma A, Laakso I, Sepp?nen-Laakso T, Huhtikangas A, Riekkola M-L. A simplified procedure for indole alkaloid extraction from Catharanthus roseus combined with a semi-synthetic production process for vinblastine. Molecules. Molecular Diversity Preservation International; 2007;12: 1307–1315. doi:10.3390/12071307LINK
79 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
80 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
81 DiCosmo F, Quesnel A, Misawa M, Tallevi SG. Increased synthesis of ajmalicine and catharanthine by cell suspension cultures of Catharanthus roseus in response to fungal culture-filtrates. Appl Biochem Biotechnol. 1987;14: 101–106. doi:10.1007/BF02798428LINK
82 DiCosmo F, Quesnel A, Misawa M, Tallevi SG. Increased synthesis of ajmalicine and catharanthine by cell suspension cultures of Catharanthus roseus in response to fungal culture-filtrates. Appl Biochem Biotechnol. 1987;14: 101–106. doi:10.1007/BF02798428LINK
83 Yu J, Yuan S, Pang H, Zhang X, Jia X, Tang Z, et al. Distribution and accumulation of vindoline, catharanthine and vinblastine in Catharanthus roseus cultivated in China. Zhongguo Zhongyao Zazhi. 2010;35: 3093–3096. doi:10.4268/cjcmm20102301LINK
84 Yu J, Yuan S, Pang H, Zhang X, Jia X, Tang Z, et al. Distribution and accumulation of vindoline, catharanthine and vinblastine in Catharanthus roseus cultivated in China. Zhongguo Zhongyao Zazhi. 2010;35: 3093–3096. doi:10.4268/cjcmm20102301LINK
85 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
86 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
87 Rijhwani SK, Shanks J V. Effect of elicitor dosage and exposure time on biosynthesis of indole alkaloids by Catharanthus roseus hairy root cultures. Biotechnol Prog. 1998;14: 442–449. doi:10.1021/bp980029vLINK
88 Rijhwani SK, Shanks J V. Effect of elicitor dosage and exposure time on biosynthesis of indole alkaloids by Catharanthus roseus hairy root cultures. Biotechnol Prog. 1998;14: 442–449. doi:10.1021/bp980029vLINK
89 Bhadra R, Shanks J V. Transient studies of nutrient uptake, growth, and indole alkaloid accumulation in heterotrophic cultures of hairy roots of Catharanthus roseus. Biotechnol Bioeng. 1997;55: 527–534. doi:10.1002/(SICI)1097-0290(19970805)55:3<527::AID-BIT9>3.0.CO;2-ELINK
90 Bhadra R, Shanks J V. Transient studies of nutrient uptake, growth, and indole alkaloid accumulation in heterotrophic cultures of hairy roots of Catharanthus roseus. Biotechnol Bioeng. 1997;55: 527–534. doi:10.1002/(SICI)1097-0290(19970805)55:3<527::AID-BIT9>3.0.CO;2-ELINK
91 El-Sayed M, Verpoorte R. Growth, metabolic profiling and enzymes activities of Catharanthus roseus seedlings treated with plant growth regulators. Plant Growth Regul. 2004;44: 53–58. doi:10.1007/s10725-004-2604-5LINK
92 El-Sayed M, Verpoorte R. Growth, metabolic profiling and enzymes activities of Catharanthus roseus seedlings treated with plant growth regulators. Plant Growth Regul. 2004;44: 53–58. doi:10.1007/s10725-004-2604-5LINK
93 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
94 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
95 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
96 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
97 Besseau S, Kellner F, Lanoue A, Thamm AMK, Salim V, Schneider B, et al. A pair of tabersonine 16-hydroxylases initiates the synthesis of vindoline in an organ-dependent manner in Catharanthus roseus. Plant Physiol. 2013;163: 1792–1803. doi:10.1104/pp.113.222828LINK
98 Besseau S, Kellner F, Lanoue A, Thamm AMK, Salim V, Schneider B, et al. A pair of tabersonine 16-hydroxylases initiates the synthesis of vindoline in an organ-dependent manner in Catharanthus roseus. Plant Physiol. 2013;163: 1792–1803. doi:10.1104/pp.113.222828LINK
99 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
100 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
101 DeLuca V, Balsevich J, Tyler RT, Eilert U, Panchuk BD, Kurz WGW. Biosynthesis of Indole Alkaloids: Developmental Regulation of the Biosynthetic Pathway from Tabersonine to Vindoline in Catharanthus roseus. J Plant Physiol. 1986;125: 147–156. doi:10.1016/S0176-1617(86)80252-8LINK
102 DeLuca V, Balsevich J, Tyler RT, Eilert U, Panchuk BD, Kurz WGW. Biosynthesis of Indole Alkaloids: Developmental Regulation of the Biosynthetic Pathway from Tabersonine to Vindoline in Catharanthus roseus. J Plant Physiol. 1986;125: 147–156. doi:10.1016/S0176-1617(86)80252-8LINK
103 El-Sayed M, Choi YH, Frιdιrich M, Roytrakul S, Verpoorte R. Alkaloid accumulation in Catharanthus roseus cell suspension cultures fed with stemmadenine. Biotechnol Lett. 2004;26: 793–798. doi:10.1023/B:BILE.0000025879.53632.f2LINK
104 El-Sayed M, Choi YH, Frιdιrich M, Roytrakul S, Verpoorte R. Alkaloid accumulation in Catharanthus roseus cell suspension cultures fed with stemmadenine. Biotechnol Lett. 2004;26: 793–798. doi:10.1023/B:BILE.0000025879.53632.f2LINK
105 Furuya T, Sakamoto K, Iida K, Asada Y, Yoshikawa T, Sakai S, et al. Biotransformation of tabersonine in cell suspension cultures of Catharanthus roseus. Phytochemistry. 1992;31: 3065–8. doi:10.1016/0031-9422(92)83447-7LINK
106 Furuya T, Sakamoto K, Iida K, Asada Y, Yoshikawa T, Sakai S, et al. Biotransformation of tabersonine in cell suspension cultures of Catharanthus roseus. Phytochemistry. 1992;31: 3065–8. doi:10.1016/0031-9422(92)83447-7LINK
107 Ataei-Azimi A, Hashemloian BD, Ebrahimzadeh H, Majd A. High in vitro production of ant-canceric indole alkaloids from periwinkle Catharanthus roseus tissue culture. African J Biotechnol. 2008;7: 2834–2839.LINK
108 Ataei-Azimi A, Hashemloian BD, Ebrahimzadeh H, Majd A. High in vitro production of ant-canceric indole alkaloids from periwinkle Catharanthus roseus tissue culture. African J Biotechnol. 2008;7: 2834–2839.LINK
109 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
110 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
111 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
112 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
113 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
114 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
115 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
116 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
117 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
118 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
119 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
120 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
121 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
122 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
123 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
124 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
125 Eilert U, Nesbitt LR, Constabel F. Laticifers and latex in fruits of periwinkle, Catharanthus roseus. Can J Bot. 1985;63: 1540–1546. doi:10.1139/b85-213LINK
126 Eilert U, Nesbitt LR, Constabel F. Laticifers and latex in fruits of periwinkle, Catharanthus roseus. Can J Bot. 1985;63: 1540–1546. doi:10.1139/b85-213LINK
127 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
128 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
129 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
130 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
131 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
132 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
133 El-Sayed M, Verpoorte R. Growth, metabolic profiling and enzymes activities of Catharanthus roseus seedlings treated with plant growth regulators. Plant Growth Regul. 2004;44: 53–58. doi:10.1007/s10725-004-2604-5LINK
134 El-Sayed M, Verpoorte R. Growth, metabolic profiling and enzymes activities of Catharanthus roseus seedlings treated with plant growth regulators. Plant Growth Regul. 2004;44: 53–58. doi:10.1007/s10725-004-2604-5LINK
135 Lourdes Miranda-Ham M de, Islas-Flores I, V?zquez-Flota AF. Accumulation of monoterpenoid indole alkaloids in periwinkle seedlings (Catharanthus roseus) as a model for the study of plant-environment interactions. Biochem Mol Biol Educ. 2007;35: 206–210. doi:10.1002/bambed.60LINK
136 Lourdes Miranda-Ham M de, Islas-Flores I, V?zquez-Flota AF. Accumulation of monoterpenoid indole alkaloids in periwinkle seedlings (Catharanthus roseus) as a model for the study of plant-environment interactions. Biochem Mol Biol Educ. 2007;35: 206–210. doi:10.1002/bambed.60LINK
137 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
138 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
139 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
140 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
141 Hirata K, Miyamoto K, Miura Y. Catharanthus roseus L. (Periwinkle): Production of Vindoline and Catharanthine in Multiple Shoot Cultures. In: Bajaj YPS, editor. Medicinal and Aromatic Plants VI. Berlin, Heidelberg: Springer Berlin Heidelberg; 1994. pp. 46–55. doi:10.1007/978-3-642-57970-7_3LINK
142 Hirata K, Miyamoto K, Miura Y. Catharanthus roseus L. (Periwinkle): Production of Vindoline and Catharanthine in Multiple Shoot Cultures. In: Bajaj YPS, editor. Medicinal and Aromatic Plants VI. Berlin, Heidelberg: Springer Berlin Heidelberg; 1994. pp. 46–55. doi:10.1007/978-3-642-57970-7_3LINK
143 Gupta MM, Singh D V, Tripathi AK, Pandey R, Verma RK, Singh S, et al. Simultaneous determination of vincristine, vinblastine, catharanthine, and vindoline in leaves of catharanthus roseus by high-performance liquid chromatography. J Chromatogr Sci. 2005;43: 450–453. doi:10.1093/chromsci/43.9.450LINK
144 Gupta MM, Singh D V, Tripathi AK, Pandey R, Verma RK, Singh S, et al. Simultaneous determination of vincristine, vinblastine, catharanthine, and vindoline in leaves of catharanthus roseus by high-performance liquid chromatography. J Chromatogr Sci. 2005;43: 450–453. doi:10.1093/chromsci/43.9.450LINK
145 Yu J, Yuan S, Pang H, Zhang X, Jia X, Tang Z, et al. Distribution and accumulation of vindoline, catharanthine and vinblastine in Catharanthus roseus cultivated in China. Zhongguo Zhongyao Zazhi. 2010;35: 3093–3096. doi:10.4268/cjcmm20102301LINK
146 Yu J, Yuan S, Pang H, Zhang X, Jia X, Tang Z, et al. Distribution and accumulation of vindoline, catharanthine and vinblastine in Catharanthus roseus cultivated in China. Zhongguo Zhongyao Zazhi. 2010;35: 3093–3096. doi:10.4268/cjcmm20102301LINK
147 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
148 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
149 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
150 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
151 De Luca V, Laflamme P. The expanding universe of alkaloid biosynthesis. Curr Opin Pant Biol. 2001;4: 225–233. doi:10.1016/S1369-5266(00)00165-5LINK
152 De Luca V, Laflamme P. The expanding universe of alkaloid biosynthesis. Curr Opin Pant Biol. 2001;4: 225–233. doi:10.1016/S1369-5266(00)00165-5LINK
153 Campos-Tamayo F, Hern?ndez-Dom?nguez E, V?zquez-Flota F. Vindoline formation in shoot cultures of Catharanthus roseus is synchronously activated with morphogenesis through the last biosynthetic step. Ann Bot. 2008;102: 409–415. doi:10.1093/aob/mcn108LINK
154 Campos-Tamayo F, Hern?ndez-Dom?nguez E, V?zquez-Flota F. Vindoline formation in shoot cultures of Catharanthus roseus is synchronously activated with morphogenesis through the last biosynthetic step. Ann Bot. 2008;102: 409–415. doi:10.1093/aob/mcn108LINK
155 Zhong X-Z, Wang G-C, Wang Y, Zhang X-Q, Ye W-C. Monomeric indole alkaloids from the aerial parts of Catharanthus roseus. Acta Pharm Sin. 2010;45: 471–474.LINK
156 Zhong X-Z, Wang G-C, Wang Y, Zhang X-Q, Ye W-C. Monomeric indole alkaloids from the aerial parts of Catharanthus roseus. Acta Pharm Sin. 2010;45: 471–474.LINK
157 Wang Q, Xing S, Pan Q, Yuan F, Zhao J, Tian Y, et al. Development of efficient Catharanthus roseus regeneration and transformation system using agrobacterium tumefaciens and hypocotyls as explants. BMC Botechnology. 2012;12: 34. doi:10.1186/1472-6750-12-34LINK
158 Wang Q, Xing S, Pan Q, Yuan F, Zhao J, Tian Y, et al. Development of efficient Catharanthus roseus regeneration and transformation system using agrobacterium tumefaciens and hypocotyls as explants. BMC Botechnology. 2012;12: 34. doi:10.1186/1472-6750-12-34LINK
159 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
160 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
161 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
162 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
163 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
164 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
165 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
166 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
167 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
168 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
169 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
170 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
171 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
172 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
173 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
174 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
175 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
176 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
177 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
178 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
179 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
180 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
181 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
182 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
183 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
184 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
185 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
186 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
187 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
188 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
189 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
190 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
191 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
192 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
193 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
194 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
195 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
196 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
197 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
198 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
199 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
200 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
201 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
202 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
203 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
204 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
205 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
206 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
207 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
208 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
209 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
210 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
211 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
212 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
213 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
214 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
215 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
216 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
217 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
218 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
219 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
220 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
221 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
222 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
223 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
224 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
225 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
226 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
227 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
228 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
229 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
230 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
231 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
232 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
233 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
234 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
235 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
236 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
237 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
238 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
239 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
240 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
241 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
242 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
243 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
244 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
245 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
246 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
247 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
248 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
249 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
250 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
251 Verma, A.K. LU, Singh, R.R. LU, Singh, S. LU. Improved alkaloid content in callus culture of Catharanthus roseus. Bot Serbica. 2012;36: 123–130.LINK
252 Verma, A.K. LU, Singh, R.R. LU, Singh, S. LU. Improved alkaloid content in callus culture of Catharanthus roseus. Bot Serbica. 2012;36: 123–130.LINK
253 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
254 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
255 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
256 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
257 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
258 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
259 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
260 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
261 Hirata K, Miyamoto K, Miura Y. Catharanthus roseus L. (Periwinkle): Production of Vindoline and Catharanthine in Multiple Shoot Cultures. In: Bajaj YPS, editor. Medicinal and Aromatic Plants VI. Berlin, Heidelberg: Springer Berlin Heidelberg; 1994. pp. 46–55. doi:10.1007/978-3-642-57970-7_3LINK
262 Hirata K, Miyamoto K, Miura Y. Catharanthus roseus L. (Periwinkle): Production of Vindoline and Catharanthine in Multiple Shoot Cultures. In: Bajaj YPS, editor. Medicinal and Aromatic Plants VI. Berlin, Heidelberg: Springer Berlin Heidelberg; 1994. pp. 46–55. doi:10.1007/978-3-642-57970-7_3LINK
263 Gupta MM, Singh D V, Tripathi AK, Pandey R, Verma RK, Singh S, et al. Simultaneous determination of vincristine, vinblastine, catharanthine, and vindoline in leaves of catharanthus roseus by high-performance liquid chromatography. J Chromatogr Sci. 2005;43: 450–453. doi:10.1093/chromsci/43.9.450LINK
264 Gupta MM, Singh D V, Tripathi AK, Pandey R, Verma RK, Singh S, et al. Simultaneous determination of vincristine, vinblastine, catharanthine, and vindoline in leaves of catharanthus roseus by high-performance liquid chromatography. J Chromatogr Sci. 2005;43: 450–453. doi:10.1093/chromsci/43.9.450LINK
265 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
266 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
267 Yu J, Yuan S, Pang H, Zhang X, Jia X, Tang Z, et al. Distribution and accumulation of vindoline, catharanthine and vinblastine in Catharanthus roseus cultivated in China. Zhongguo Zhongyao Zazhi. 2010;35: 3093–3096. doi:10.4268/cjcmm20102301LINK
268 Yu J, Yuan S, Pang H, Zhang X, Jia X, Tang Z, et al. Distribution and accumulation of vindoline, catharanthine and vinblastine in Catharanthus roseus cultivated in China. Zhongguo Zhongyao Zazhi. 2010;35: 3093–3096. doi:10.4268/cjcmm20102301LINK
269 Ataei-Azimi A, Hashemloian BD, Ebrahimzadeh H, Majd A. High in vitro production of ant-canceric indole alkaloids from periwinkle Catharanthus roseus tissue culture. African J Biotechnol. 2008;7: 2834–2839.LINK
270 Ataei-Azimi A, Hashemloian BD, Ebrahimzadeh H, Majd A. High in vitro production of ant-canceric indole alkaloids from periwinkle Catharanthus roseus tissue culture. African J Biotechnol. 2008;7: 2834–2839.LINK
271 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
272 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
273 Guo Z-G, Liu Y, Gong M-Z, Chen W, Li W-Y. Regulation of vinblastine biosynthesis in cell suspension cultures of catharanthus roseus. Plant Cell Tissue Organ Cult. 2012;112: 43–54. doi:10.1007/s11240-012-0213-yLINK
274 Guo Z-G, Liu Y, Gong M-Z, Chen W, Li W-Y. Regulation of vinblastine biosynthesis in cell suspension cultures of catharanthus roseus. Plant Cell Tissue Organ Cult. 2012;112: 43–54. doi:10.1007/s11240-012-0213-yLINK
275 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
276 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
277 Verma, A.K. LU, Singh, R.R. LU, Singh, S. LU. Improved alkaloid content in callus culture of Catharanthus roseus. Bot Serbica. 2012;36: 123–130.LINK
278 Verma, A.K. LU, Singh, R.R. LU, Singh, S. LU. Improved alkaloid content in callus culture of Catharanthus roseus. Bot Serbica. 2012;36: 123–130.LINK
279 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
280 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
281 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
282 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
283 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
284 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
285 Gupta MM, Singh D V, Tripathi AK, Pandey R, Verma RK, Singh S, et al. Simultaneous determination of vincristine, vinblastine, catharanthine, and vindoline in leaves of catharanthus roseus by high-performance liquid chromatography. J Chromatogr Sci. 2005;43: 450–453. doi:10.1093/chromsci/43.9.450LINK
286 Gupta MM, Singh D V, Tripathi AK, Pandey R, Verma RK, Singh S, et al. Simultaneous determination of vincristine, vinblastine, catharanthine, and vindoline in leaves of catharanthus roseus by high-performance liquid chromatography. J Chromatogr Sci. 2005;43: 450–453. doi:10.1093/chromsci/43.9.450LINK
287 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
288 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
289 Ataei-Azimi A, Hashemloian BD, Ebrahimzadeh H, Majd A. High in vitro production of ant-canceric indole alkaloids from periwinkle Catharanthus roseus tissue culture. African J Biotechnol. 2008;7: 2834–2839.LINK
290 Ataei-Azimi A, Hashemloian BD, Ebrahimzadeh H, Majd A. High in vitro production of ant-canceric indole alkaloids from periwinkle Catharanthus roseus tissue culture. African J Biotechnol. 2008;7: 2834–2839.LINK
291 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
292 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
293 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
294 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
295 Ryu DDY, Furusaki S. Advances in plant biotechnology. Elsevier Science; 2012. p. 390.LINK
296 Ryu DDY, Furusaki S. Advances in plant biotechnology. Elsevier Science; 2012. p. 390.LINK
297 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
298 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
299 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
300 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
301 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
302 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
303 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
304 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
305 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
306 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
307 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
308 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
309 Vani SN. Bioreactor design for scaleup of Catharanthus roseus hairy root cultures for production of indole alkaloids [Internet]. Rice University. 1996.LINK
310 Vani SN. Bioreactor design for scaleup of Catharanthus roseus hairy root cultures for production of indole alkaloids [Internet]. Rice University. 1996.LINK
311 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
312 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
313 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
314 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
315 Buckingham J. Dictionary of Natural Products. illustrate. Taylor & Francis; 1993. p. 8584. ISBN: 9780412466205.NA
316 Buckingham J. Dictionary of Natural Products. illustrate. Taylor & Francis; 1993. p. 8584. ISBN: 9780412466205.NA
317 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
318 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
319 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
320 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
321 Buckingham J. Dictionary of Natural Products. illustrate. Taylor & Francis; 1993. p. 8584. ISBN: 9780412466205.NA
322 Buckingham J. Dictionary of Natural Products. illustrate. Taylor & Francis; 1993. p. 8584. ISBN: 9780412466205.NA
323 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
324 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
325 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
326 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
327 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
328 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
329 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
330 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
331 Scott AI, Mizukami H, Hirata T, Lee S-L. Formation of catharanthine, akuammicine and vindoline in Catharanthus roseus suspension cells. Phytochemistry. 1980;19: 488–489. doi:10.1016/0031-9422(80)83216-XLINK
332 Scott AI, Mizukami H, Hirata T, Lee S-L. Formation of catharanthine, akuammicine and vindoline in Catharanthus roseus suspension cells. Phytochemistry. 1980;19: 488–489. doi:10.1016/0031-9422(80)83216-XLINK
333 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
334 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
335 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
336 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
337 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
338 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
339 Consolacion Y. Ragasa, Vic Marie L. Inte, Rideout JA. An antimicrobial alkaloid from Catharanthus roseus. Manila J Sci. 1998;1: 19–27.LINK
340 Consolacion Y. Ragasa, Vic Marie L. Inte, Rideout JA. An antimicrobial alkaloid from Catharanthus roseus. Manila J Sci. 1998;1: 19–27.LINK
341 Mukhopadhyay S, Cordell GA. Catharanthus Alkaloids. XXXVI. Isolation of Vincaleukoblastine (VLB) and Periformyline From Catharanthus trichophyllus and Pericyclivine From Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 335–339. doi:10.1021/np50015a017LINK
342 Mukhopadhyay S, Cordell GA. Catharanthus Alkaloids. XXXVI. Isolation of Vincaleukoblastine (VLB) and Periformyline From Catharanthus trichophyllus and Pericyclivine From Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 335–339. doi:10.1021/np50015a017LINK
343 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
344 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
345 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
346 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
347 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
348 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
349 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
350 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
351 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
352 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
353 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
354 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
355 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
356 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
357 Fatima J, Albert K. Isolation and structure of rosicine from Catharanthus roseus. Tetrahedron Lett. 1984;25: 6051–6054. doi:10.1016/S0040-4039(01)81759-7LINK
358 Fatima J, Albert K. Isolation and structure of rosicine from Catharanthus roseus. Tetrahedron Lett. 1984;25: 6051–6054. doi:10.1016/S0040-4039(01)81759-7LINK
359 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
360 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
361 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
362 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
363 Herbert RB. Biosynthesis. Herbert RB, editor. Royal Society of Chemistry; 1983. p. 232.NA
364 Herbert RB. Biosynthesis. Herbert RB, editor. Royal Society of Chemistry; 1983. p. 232.NA
365 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
366 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
367 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
368 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
369 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
370 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
371 Consolacion Y. Ragasa, Vic Marie L. Inte, Rideout JA. An antimicrobial alkaloid from Catharanthus roseus. Manila J Sci. 1998;1: 19–27.LINK
372 Consolacion Y. Ragasa, Vic Marie L. Inte, Rideout JA. An antimicrobial alkaloid from Catharanthus roseus. Manila J Sci. 1998;1: 19–27.LINK
373 Patil PJ, Ghosh JS. Antimicrobial activity of Catharanthus roseus – A detailed study. Br J Pharmacol Toxicol. 2010;1: 40–44.LINK
374 Patil PJ, Ghosh JS. Antimicrobial activity of Catharanthus roseus – A detailed study. Br J Pharmacol Toxicol. 2010;1: 40–44.LINK
375 Price NPJ, Firmin JL, Robins RJ, Gray DO. High-performance liquid chromatography of the alkaloid perivine from Catharanthus roseus after derivatisation with dansyl chloride. J Chromatogr A. 1993;653: 161–166. doi:10.1016/0021-9673(93)80406-XLINK
376 Price NPJ, Firmin JL, Robins RJ, Gray DO. High-performance liquid chromatography of the alkaloid perivine from Catharanthus roseus after derivatisation with dansyl chloride. J Chromatogr A. 1993;653: 161–166. doi:10.1016/0021-9673(93)80406-XLINK
377 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
378 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
379 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
380 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
381 Herbert RB. Biosynthesis. Herbert RB, editor. Royal Society of Chemistry; 1983. p. 232.NA
382 Herbert RB. Biosynthesis. Herbert RB, editor. Royal Society of Chemistry; 1983. p. 232.NA
383 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
384 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
385 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
386 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
387 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
388 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
389 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
390 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
391 Herbert RB. Biosynthesis. illustrate. Herbert RB, editor. Royal Society of Chemistry; 1983. p. 232.NA
392 Herbert RB. Biosynthesis. illustrate. Herbert RB, editor. Royal Society of Chemistry; 1983. p. 232.NA
393 Nagakura N, Ruffer M, Zenk MH. The biosynthesis of monoterpenoid indole alkaloids from strictosidine. J Chem Soc Perkin Trans 1. The Royal Society of Chemistry; 1979;1: 2308–2312. doi:10.1039/P19790002308LINK
394 Nagakura N, Ruffer M, Zenk MH. The biosynthesis of monoterpenoid indole alkaloids from strictosidine. J Chem Soc Perkin Trans 1. The Royal Society of Chemistry; 1979;1: 2308–2312. doi:10.1039/P19790002308LINK
395 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
396 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
397 Peraza-S?nchez SR, Gamboa-angulo MM, Erosa-L?pez C, Ram?rez-Erosa I, Escalante-erosa F, Pe?a-Rodr?guez LM, et al. Production of 19(s)-epimisiline by hairy root cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 2006;11: 217–224. doi:10.1080/10575639808044950LINK
398 Peraza-S?nchez SR, Gamboa-angulo MM, Erosa-L?pez C, Ram?rez-Erosa I, Escalante-erosa F, Pe?a-Rodr?guez LM, et al. Production of 19(s)-epimisiline by hairy root cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 2006;11: 217–224. doi:10.1080/10575639808044950LINK
399 Kohl W, Witte B, Sheldrick WS, H?fle G. Indole alkaloids from Catharanthus roseus tissue cultures IV1: 16R-19,20-E-isositsirikin, 16R-19,20-Z-isositsirikin and 21-hydroxycyclolochnerin. Planta Med. © Georg Thieme Verlag Stuttgart • New York; 1984;50: 242–244. doi:10.1055/s-2007-969688LINK
400 Kohl W, Witte B, Sheldrick WS, H?fle G. Indole alkaloids from Catharanthus roseus tissue cultures IV1: 16R-19,20-E-isositsirikin, 16R-19,20-Z-isositsirikin and 21-hydroxycyclolochnerin. Planta Med. © Georg Thieme Verlag Stuttgart • New York; 1984;50: 242–244. doi:10.1055/s-2007-969688LINK
401 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
402 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
403 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
404 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
405 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
406 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
407 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
408 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
409 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
410 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
411 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
412 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
413 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
414 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
415 Kumari K, Gupta S. Antifungal properties of leaf extract of Catharanthus roseus l ( g.) Don. Am J Phytomedicine Clin Ther. 2013;1: 698–705.LINK
416 Kumari K, Gupta S. Antifungal properties of leaf extract of Catharanthus roseus l ( g.) Don. Am J Phytomedicine Clin Ther. 2013;1: 698–705.LINK
417 Kumari K, Gupta S. Phytopotential of Catharanthus roseus L .( G .) Don . Var . “ Rosea ” And “ Alba .” Int J Res Pure Appl Microbiol. 2013;3: 77–82.LINK
418 Kumari K, Gupta S. Phytopotential of Catharanthus roseus L .( G .) Don . Var . “ Rosea ” And “ Alba .” Int J Res Pure Appl Microbiol. 2013;3: 77–82.LINK
419 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
420 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
421 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
422 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
423 Stockigt J, Husson HP, Kan-Fan C, Zenk MH. Cathenamine, a central intermediate in the cell free biosynthesis of ajmalicine and related indole alkaloids. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1977; 164–166. doi:10.1039/C39770000164LINK
424 Stockigt J, Husson HP, Kan-Fan C, Zenk MH. Cathenamine, a central intermediate in the cell free biosynthesis of ajmalicine and related indole alkaloids. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1977; 164–166. doi:10.1039/C39770000164LINK
425 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
426 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
427 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
428 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
429 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
430 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
431 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
432 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
433 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
434 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
435 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
436 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
437 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
438 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
439 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
440 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
441 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
442 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
443 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
444 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
445 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
446 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
447 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
448 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
449 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
450 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
451 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
452 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
453 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
454 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
455 O’Connor SE, Maresh JJ. Chemistry and biology of monoterpene indole alkaloid biosynthesis. Nat Prod Rep. The Royal Society of Chemistry; 2006;23: 532–547. doi:10.1039/b512615kLINK
456 O’Connor SE, Maresh JJ. Chemistry and biology of monoterpene indole alkaloid biosynthesis. Nat Prod Rep. The Royal Society of Chemistry; 2006;23: 532–547. doi:10.1039/b512615kLINK
457 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
458 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
459 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
460 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
461 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
462 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
463 Fatima J, Albert K. Isolation and structure of rosicine from Catharanthus roseus. Tetrahedron Lett. 1984;25: 6051–6054. doi:10.1016/S0040-4039(01)81759-7LINK
464 Fatima J, Albert K. Isolation and structure of rosicine from Catharanthus roseus. Tetrahedron Lett. 1984;25: 6051–6054. doi:10.1016/S0040-4039(01)81759-7LINK
465 O’Connor SE, Maresh JJ. Chemistry and biology of monoterpene indole alkaloid biosynthesis. Nat Prod Rep. The Royal Society of Chemistry; 2006;23: 532–547. doi:10.1039/b512615kLINK
466 O’Connor SE, Maresh JJ. Chemistry and biology of monoterpene indole alkaloid biosynthesis. Nat Prod Rep. The Royal Society of Chemistry; 2006;23: 532–547. doi:10.1039/b512615kLINK
467 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
468 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
469 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
470 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
471 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
472 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
473 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
474 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
475 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
476 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
477 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
478 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
479 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
480 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
481 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
482 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
483 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
484 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
485 Eilert U, Nesbitt LR, Constabel F. Laticifers and latex in fruits of periwinkle, Catharanthus roseus. Can J Bot. 1985;63: 1540–1546. doi:10.1139/b85-213LINK
486 Eilert U, Nesbitt LR, Constabel F. Laticifers and latex in fruits of periwinkle, Catharanthus roseus. Can J Bot. 1985;63: 1540–1546. doi:10.1139/b85-213LINK
487 De Luca V, Laflamme P. The expanding universe of alkaloid biosynthesis. Curr Opin Pant Biol. 2001;4: 225–233. doi:10.1016/S1369-5266(00)00165-5LINK
488 De Luca V, Laflamme P. The expanding universe of alkaloid biosynthesis. Curr Opin Pant Biol. 2001;4: 225–233. doi:10.1016/S1369-5266(00)00165-5LINK
489 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
490 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
491 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
492 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
493 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
494 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
495 Buckingham J. Dictionary of Natural Products. illustrate. Taylor & Francis; 1993. p. 8584. ISBN: 9780412466205.NA
496 Buckingham J. Dictionary of Natural Products. illustrate. Taylor & Francis; 1993. p. 8584. ISBN: 9780412466205.NA
497 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
498 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
499 Bashir M. Isolation of New Alkaloids from Catharanthus roseus. Planta Med. © Hippokrates Verlag Stuttgart; 1983;49: 124–125. doi:10.1055/s-2007-969829LINK
500 Bashir M. Isolation of New Alkaloids from Catharanthus roseus. Planta Med. © Hippokrates Verlag Stuttgart; 1983;49: 124–125. doi:10.1055/s-2007-969829LINK
501 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
502 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
503 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
504 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
505 Rajwar S, Khatri P, Patel R, Dwivedi S, Dwivedi A. An overview on potent herbal anticancer drugs. Int J Res Pharm Chem. 2011;1: 202–210.LINK
506 Rajwar S, Khatri P, Patel R, Dwivedi S, Dwivedi A. An overview on potent herbal anticancer drugs. Int J Res Pharm Chem. 2011;1: 202–210.LINK
507 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
508 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
509 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
510 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
511 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
512 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
513 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
514 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
515 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
516 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
517 Magnotta M, Murata J, Chen J, De Luca V. Expression of deacetylvindoline-4-O-acetyltransferase in Catharanthus roseus hairy roots. Phytochemistry. 2007;68: 1922–1931. doi:10.1016/j.phytochem.2007.04.037LINK
518 Magnotta M, Murata J, Chen J, De Luca V. Expression of deacetylvindoline-4-O-acetyltransferase in Catharanthus roseus hairy roots. Phytochemistry. 2007;68: 1922–1931. doi:10.1016/j.phytochem.2007.04.037LINK
519 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
520 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
521 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
522 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
523 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
524 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
525 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
526 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
527 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
528 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
529 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
530 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
531 Fatima J, Albert K. Isolation and structure of rosicine from Catharanthus roseus. Tetrahedron Lett. 1984;25: 6051–6054. doi:10.1016/S0040-4039(01)81759-7LINK
532 Fatima J, Albert K. Isolation and structure of rosicine from Catharanthus roseus. Tetrahedron Lett. 1984;25: 6051–6054. doi:10.1016/S0040-4039(01)81759-7LINK
533 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
534 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
535 Pietrosiuk A, Furmanowa M. Preliminary results of indole alkaloids production in different roots of Catharanthus roseus cultured in vitro. Acta Soc Bot Pol. 2001;70: 261–265. doi:10.5586/asbp.2001.033LINK
536 Pietrosiuk A, Furmanowa M. Preliminary results of indole alkaloids production in different roots of Catharanthus roseus cultured in vitro. Acta Soc Bot Pol. 2001;70: 261–265. doi:10.5586/asbp.2001.033LINK
537 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
538 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
539 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
540 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
541 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
542 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
543 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
544 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
545 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
546 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
547 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
548 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
549 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
550 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
551 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
552 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
553 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
554 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
555 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
556 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
557 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
558 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
559 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
560 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
561 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
562 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
563 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
564 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
565 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
566 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
567 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
568 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
569 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
570 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
571 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
572 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
573 Peraza-S?nchez SR, Gamboa-angulo MM, Erosa-L?pez C, Ram?rez-Erosa I, Escalante-erosa F, Pe?a-Rodr?guez LM, et al. Production of 19(s)-epimisiline by hairy root cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 2006;11: 217–224. doi:10.1080/10575639808044950LINK
574 Peraza-S?nchez SR, Gamboa-angulo MM, Erosa-L?pez C, Ram?rez-Erosa I, Escalante-erosa F, Pe?a-Rodr?guez LM, et al. Production of 19(s)-epimisiline by hairy root cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 2006;11: 217–224. doi:10.1080/10575639808044950LINK
575 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
576 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
577 Rijhwani SK, Shanks J V. Effect of elicitor dosage and exposure time on biosynthesis of indole alkaloids by Catharanthus roseus hairy root cultures. Biotechnol Prog. 1998;14: 442–449. doi:10.1021/bp980029vLINK
578 Rijhwani SK, Shanks J V. Effect of elicitor dosage and exposure time on biosynthesis of indole alkaloids by Catharanthus roseus hairy root cultures. Biotechnol Prog. 1998;14: 442–449. doi:10.1021/bp980029vLINK
579 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
580 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
581 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
582 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
583 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
584 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
585 Zhong X-Z, Wang G-C, Wang Y, Zhang X-Q, Ye W-C. Monomeric indole alkaloids from the aerial parts of Catharanthus roseus. Acta Pharm Sin. 2010;45: 471–474.LINK
586 Zhong X-Z, Wang G-C, Wang Y, Zhang X-Q, Ye W-C. Monomeric indole alkaloids from the aerial parts of Catharanthus roseus. Acta Pharm Sin. 2010;45: 471–474.LINK
587 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
588 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
589 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
590 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
591 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
592 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
593 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
594 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
595 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
596 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
597 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
598 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
599 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
600 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
601 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
602 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
603 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
604 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
605 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
606 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
607 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
608 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
609 Aynilian GH, Weiss SG, Cordell GA, Abraham DJ, Crane FA, Farnsworth NR. Catharanthus alkaloids XXIX: Isolation and structure elucidation of vincoline. J Pharm Sci. 1974;63: 536–538. doi:10.1002/jps.2600630409LINK
610 Aynilian GH, Weiss SG, Cordell GA, Abraham DJ, Crane FA, Farnsworth NR. Catharanthus alkaloids XXIX: Isolation and structure elucidation of vincoline. J Pharm Sci. 1974;63: 536–538. doi:10.1002/jps.2600630409LINK
611 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
612 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
613 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
614 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
615 Bashir M, Kaleem S, Fatima T. 16-epi-19-S-vindolinine, an indoline alkaloid from Catharanthus roseus. Phytochemistry. 1983;22: 1021–1023. doi:10.1016/0031-9422(83)85046-8LINK
616 Bashir M, Kaleem S, Fatima T. 16-epi-19-S-vindolinine, an indoline alkaloid from Catharanthus roseus. Phytochemistry. 1983;22: 1021–1023. doi:10.1016/0031-9422(83)85046-8LINK
617 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
618 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
619 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
620 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
621 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
622 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
623 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
624 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
625 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
626 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
627 Vani SN. Bioreactor design for scaleup of Catharanthus roseus hairy root cultures for production of indole alkaloids [Internet]. Rice University. 1996.LINK
628 Vani SN. Bioreactor design for scaleup of Catharanthus roseus hairy root cultures for production of indole alkaloids [Internet]. Rice University. 1996.LINK
629 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
630 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
631 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
632 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
633 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
634 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
635 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
636 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
637 Furuya T, Sakamoto K, Iida K, Asada Y, Yoshikawa T, Sakai S, et al. Biotransformation of tabersonine in cell suspension cultures of Catharanthus roseus. Phytochemistry. 1992;31: 3065–8. doi:10.1016/0031-9422(92)83447-7LINK
638 Furuya T, Sakamoto K, Iida K, Asada Y, Yoshikawa T, Sakai S, et al. Biotransformation of tabersonine in cell suspension cultures of Catharanthus roseus. Phytochemistry. 1992;31: 3065–8. doi:10.1016/0031-9422(92)83447-7LINK
639 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
640 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
641 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
642 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
643 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
644 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
645 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
646 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
647 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
648 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
649 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
650 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
651 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
652 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
653 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
654 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
655 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
656 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
657 Biblioth L. Substances naturelles se fixant sur la tubulinemise en œuvre d’un criblage par spectromιtrie de masse. Universitι Henri Poincarι Nancy 1. 2009. p. 74. ISBN:0070297770.NA
658 Biblioth L. Substances naturelles se fixant sur la tubulinemise en œuvre d’un criblage par spectromιtrie de masse. Universitι Henri Poincarι Nancy 1. 2009. p. 74. ISBN:0070297770.NA
659 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
660 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
661 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
662 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
663 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
664 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
665 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
666 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
667 Cordall GA, Weiss SG, Farnsworth NR. Structure elucidation and chemistry of Catharanthus alkaloids. XXX. Isolation and structure elucidation of vincarodine. J Org Chem. American Chemical Society; 1974;39: 431–434. doi:10.1021/jo00918a001LINK
668 Cordall GA, Weiss SG, Farnsworth NR. Structure elucidation and chemistry of Catharanthus alkaloids. XXX. Isolation and structure elucidation of vincarodine. J Org Chem. American Chemical Society; 1974;39: 431–434. doi:10.1021/jo00918a001LINK
669 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
670 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
671 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
672 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
673 Southon IW, Buckingham J. Dictionary of Alkaloids [Internet]. 2nd ed. CRC Press; 1989. p. 620. ISBN: 9780412249105.LINK
674 Southon IW, Buckingham J. Dictionary of Alkaloids [Internet]. 2nd ed. CRC Press; 1989. p. 620. ISBN: 9780412249105.LINK
675 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
676 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
677 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
678 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
679 He L, Yang L, Tan R, Zhao S, Hu Z. Enhancement of vindoline production in suspension culture of the Catharanthus roseus cell line C20hi by light and methyl jasmonate elicitation. Anal Sci. 2011;27: 1243–1248. doi:10.2116/analsci.27.1243LINK
680 He L, Yang L, Tan R, Zhao S, Hu Z. Enhancement of vindoline production in suspension culture of the Catharanthus roseus cell line C20hi by light and methyl jasmonate elicitation. Anal Sci. 2011;27: 1243–1248. doi:10.2116/analsci.27.1243LINK
681 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
682 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
683 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
684 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
685 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
686 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
687 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
688 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
689 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.?1104/?pp.?125.?1.?189
690 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.?1104/?pp.?125.?1.?189
691 St-Pierre B. Multicellular Compartmentation of Catharanthus roseus Alkaloid Biosynthesis Predicts Intercellular Translocation of a Pathway Intermediate. Plant Cell. 1999;11: 887–900. doi:?10.?1105/?tpc.?11.?5.?887LINK
692 St-Pierre B. Multicellular Compartmentation of Catharanthus roseus Alkaloid Biosynthesis Predicts Intercellular Translocation of a Pathway Intermediate. Plant Cell. 1999;11: 887–900. doi:?10.?1105/?tpc.?11.?5.?887LINK
693 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
694 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
695 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
696 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
697 Ali I, Chaudhry MI. Isolation and 13C-NMR Studies on Cathovaline, an Alkaloid from the Leaves of Catharanthus roseus. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1985;51: 447–448. doi:10.1055/s-2007-969546LINK
698 Ali I, Chaudhry MI. Isolation and 13C-NMR Studies on Cathovaline, an Alkaloid from the Leaves of Catharanthus roseus. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1985;51: 447–448. doi:10.1055/s-2007-969546LINK
699 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
700 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
701 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
702 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
703 Tiong SH, Looi CY, Hazni H, Arya A, Paydar M, Wong WF, et al. Antidiabetic and antioxidant properties of alkaloids from Catharanthus roseus (L.) G. Don. Molecules. 2013;18: 9770–9784. doi:10.3390/molecules18089770LINK
704 Tiong SH, Looi CY, Hazni H, Arya A, Paydar M, Wong WF, et al. Antidiabetic and antioxidant properties of alkaloids from Catharanthus roseus (L.) G. Don. Molecules. 2013;18: 9770–9784. doi:10.3390/molecules18089770LINK
705 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
706 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
707 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
708 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
709 Nagakura N, Ruffer M, Zenk MH. The biosynthesis of monoterpenoid indole alkaloids from strictosidine. J Chem Soc Perkin Trans 1. The Royal Society of Chemistry; 1979;1: 2308–2312. doi:10.1039/P19790002308LINK
710 Nagakura N, Ruffer M, Zenk MH. The biosynthesis of monoterpenoid indole alkaloids from strictosidine. J Chem Soc Perkin Trans 1. The Royal Society of Chemistry; 1979;1: 2308–2312. doi:10.1039/P19790002308LINK
711 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
712 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
713 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
714 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
715 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
716 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
717 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
718 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
719 Ouwerkerk PB, Memelink J. A G-box element from the Catharanthus roseus strictosidine synthase (Str) gene promoter confers seed-specific expression in transgenic tobacco plants. Mol Gen Genet. 1999;261: 635–643. doi:10.1007/s004380050006LINK
720 Ouwerkerk PB, Memelink J. A G-box element from the Catharanthus roseus strictosidine synthase (Str) gene promoter confers seed-specific expression in transgenic tobacco plants. Mol Gen Genet. 1999;261: 635–643. doi:10.1007/s004380050006LINK
721 Miettinen K, Dong L, Navrot N, Schneider T, Burlat V, Pollier J, et al. The seco-iridoid pathway from Catharanthus roseus. Nat Commun. Nature Publishing Group; 2014;5: 3606. doi:10.1038/ncomms4606LINK
722 Miettinen K, Dong L, Navrot N, Schneider T, Burlat V, Pollier J, et al. The seco-iridoid pathway from Catharanthus roseus. Nat Commun. Nature Publishing Group; 2014;5: 3606. doi:10.1038/ncomms4606LINK
723 Guirimand G, Guihur A, Ginis O, Poutrain P, Hιricourt F, Oudin A, et al. The subcellular organization of strictosidine biosynthesis in Catharanthus roseus epidermis highlights several trans-tonoplast translocations of intermediate metabolites. FEBS J. 2011;278: 749–763. doi:10.1111/j.1742-4658.2010.07994.xLINK
724 Guirimand G, Guihur A, Ginis O, Poutrain P, Hιricourt F, Oudin A, et al. The subcellular organization of strictosidine biosynthesis in Catharanthus roseus epidermis highlights several trans-tonoplast translocations of intermediate metabolites. FEBS J. 2011;278: 749–763. doi:10.1111/j.1742-4658.2010.07994.xLINK
725 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
726 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
727 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
728 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
729 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
730 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
731 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
732 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
733 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
734 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
735 Hannewald P. Study of drug/receptor interaction by mass spectrometry?: development and validation of new tests of molecular screening [Internet]. Paul Verlaine University – Metz. 2008. p. 229.LINK
736 Hannewald P. Study of drug/receptor interaction by mass spectrometry?: development and validation of new tests of molecular screening [Internet]. Paul Verlaine University – Metz. 2008. p. 229.LINK
737 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
738 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
739 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
740 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
741 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
742 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
743 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
744 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
745 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
746 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
747 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
748 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
749 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
750 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
751 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
752 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
753 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
754 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
755 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
756 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
757 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
758 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
759 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
760 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
761 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
762 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
763 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
764 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
765 Price NPJ, Firmin JL, Robins RJ, Gray DO. High-performance liquid chromatography of the alkaloid perivine from Catharanthus roseus after derivatisation with dansyl chloride. J Chromatogr A. 1993;653: 161–166. doi:10.1016/0021-9673(93)80406-XLINK
766 Price NPJ, Firmin JL, Robins RJ, Gray DO. High-performance liquid chromatography of the alkaloid perivine from Catharanthus roseus after derivatisation with dansyl chloride. J Chromatogr A. 1993;653: 161–166. doi:10.1016/0021-9673(93)80406-XLINK
767 Endo T, Goodbody A, Misawa M. Alkaloid Production in root and shoot cultures of Catharanthus roseus. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1987;53: 479–482. doi:10.1055/s-2006-962777LINK
768 Endo T, Goodbody A, Misawa M. Alkaloid Production in root and shoot cultures of Catharanthus roseus. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1987;53: 479–482. doi:10.1055/s-2006-962777LINK
769 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
770 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
771 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
772 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
773 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
774 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
775 Brittain HG, Klaus Florey. Profiles of drug substances, excipients and related methodology. Elsevier Science; 1992. p. 695. ISBN: 9780080861166.LINK
776 Brittain HG, Klaus Florey. Profiles of drug substances, excipients and related methodology. Elsevier Science; 1992. p. 695. ISBN: 9780080861166.LINK
777 Kuboyama T, Yokoshima S, Tokuyama H, Fukuyama T. Stereocontrolled total synthesis of (+)-vincristine. Proc Natl Acad Sci U S A. 2004;101: 11966–11970. doi:10.1073/pnas.0401323101LINK
778 Kuboyama T, Yokoshima S, Tokuyama H, Fukuyama T. Stereocontrolled total synthesis of (+)-vincristine. Proc Natl Acad Sci U S A. 2004;101: 11966–11970. doi:10.1073/pnas.0401323101LINK
779 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
780 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
781 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
782 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
783 El-Sayed A, Cordell GA. Catharanthus alkaloids. XXXIV. Catharanthamine, a New Antitumor bisindole alkaloid from Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 289–293. doi:10.1021/np50015a009LINK
784 El-Sayed A, Cordell GA. Catharanthus alkaloids. XXXIV. Catharanthamine, a New Antitumor bisindole alkaloid from Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 289–293. doi:10.1021/np50015a009LINK
785 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
786 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
787 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
788 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
789 Hirata K, Miyamoto K, Miura Y. Catharanthus roseus L. (Periwinkle): Production of Vindoline and Catharanthine in Multiple Shoot Cultures. In: Bajaj YPS, editor. Medicinal and Aromatic Plants VI. Berlin, Heidelberg: Springer Berlin Heidelberg; 1994. pp. 46–55. doi:10.1007/978-3-642-57970-7_3LINK
790 Hirata K, Miyamoto K, Miura Y. Catharanthus roseus L. (Periwinkle): Production of Vindoline and Catharanthine in Multiple Shoot Cultures. In: Bajaj YPS, editor. Medicinal and Aromatic Plants VI. Berlin, Heidelberg: Springer Berlin Heidelberg; 1994. pp. 46–55. doi:10.1007/978-3-642-57970-7_3LINK
791 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
792 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
793 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
794 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
795 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
796 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
797 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
798 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
799 El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids, XXXVIII. Confirming structural evidence and antineoplastic activity of the bisindole alkaloids leurosine-N’ b -oxide (pleurosine), roseadine, and vindolicine from Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 517–527. doi:10.1021/np50028a016LINK
800 El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids, XXXVIII. Confirming structural evidence and antineoplastic activity of the bisindole alkaloids leurosine-N’ b -oxide (pleurosine), roseadine, and vindolicine from Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 517–527. doi:10.1021/np50028a016LINK
801 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
802 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
803 Svoboda GH, Barnes AJ. Alkaloids of Vinca rosea linn. (Catharanthus roseus G. Don). XXIV. vinaspine, vincathicine, rovidine, desacetyl VLB, and vinaphamine. J Pharm Sci. 1964;53: 1227–1231.LINK
804 Svoboda GH, Barnes AJ. Alkaloids of Vinca rosea linn. (Catharanthus roseus G. Don). XXIV. vinaspine, vincathicine, rovidine, desacetyl VLB, and vinaphamine. J Pharm Sci. 1964;53: 1227–1231.LINK
805 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
806 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
807 El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids, XXXVIII. Confirming structural evidence and antineoplastic activity of the bisindole alkaloids leurosine-N’ b -oxide (pleurosine), roseadine, and vindolicine from Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 517–527. doi:10.1021/np50028a016LINK
808 El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids, XXXVIII. Confirming structural evidence and antineoplastic activity of the bisindole alkaloids leurosine-N’ b -oxide (pleurosine), roseadine, and vindolicine from Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 517–527. doi:10.1021/np50028a016LINK
809 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
810 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
811 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
812 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
813 Sutarno H, Rudjiman. Catharanthus roseus (L.) G. Don. In: Padua; LS de, Bunyapraphatsara; N, Lemmens RHMJ, editors. Plant Resources of South-East Asia No 12(1): Medicinal and poisonous plants 1. Leiden, The Netherlands: Backhuys Publisher; 1999. pp. 185–190.LINK
814 Sutarno H, Rudjiman. Catharanthus roseus (L.) G. Don. In: Padua; LS de, Bunyapraphatsara; N, Lemmens RHMJ, editors. Plant Resources of South-East Asia No 12(1): Medicinal and poisonous plants 1. Leiden, The Netherlands: Backhuys Publisher; 1999. pp. 185–190.LINK
815 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
816 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
817 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
818 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
819 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
820 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
821 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
822 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
823 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
824 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
825 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
826 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
827 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
828 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
829 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
830 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
831 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
832 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
833 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
834 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
835 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
836 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
837 El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids, XXXVIII. Confirming structural evidence and antineoplastic activity of the bisindole alkaloids leurosine-N’ b -oxide (pleurosine), roseadine, and vindolicine from Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 517–527. doi:10.1021/np50028a016LINK
838 El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids, XXXVIII. Confirming structural evidence and antineoplastic activity of the bisindole alkaloids leurosine-N’ b -oxide (pleurosine), roseadine, and vindolicine from Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 517–527. doi:10.1021/np50028a016LINK
839 Tafur S, Jones WE, Dorman DE, Logsdon EE, Svoboda GH. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don) XXXVI: Isolation and characterization of new dimeric alkaloids. J Pharm Sci. 1975;64: 1953–1957. doi:10.1002/jps.2600641209LINK
840 Tafur S, Jones WE, Dorman DE, Logsdon EE, Svoboda GH. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don) XXXVI: Isolation and characterization of new dimeric alkaloids. J Pharm Sci. 1975;64: 1953–1957. doi:10.1002/jps.2600641209LINK
841 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
842 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
843 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
844 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
845 Mukhopadhyay S, Cordell GA. Catharanthus alkaloids. XXXV. Isolation of leurosidine N’b-oxide from Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 611–613. doi:10.1021/np50017a021LINK
846 Mukhopadhyay S, Cordell GA. Catharanthus alkaloids. XXXV. Isolation of leurosidine N’b-oxide from Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 611–613. doi:10.1021/np50017a021LINK
847 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
848 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
849 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
850 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
851 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
852 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
853 Svoboda GH, Gorman M, Barnes AJ, Oliver AT. Alkaloids of Vinca rosea Linn. (Catharanthus roseus G. Don.). XII Preparation and characterization of trace alkaloids. J Pharm Sci. 1962;51: 518–523. doi:10.1002/jps.2600510605LINK
854 Svoboda GH, Gorman M, Barnes AJ, Oliver AT. Alkaloids of Vinca rosea Linn. (Catharanthus roseus G. Don.). XII Preparation and characterization of trace alkaloids. J Pharm Sci. 1962;51: 518–523. doi:10.1002/jps.2600510605LINK
855 Consolacion Y. Ragasa, Vic Marie L. Inte, Rideout JA. An antimicrobial alkaloid from Catharanthus roseus. Manila J Sci. 1998;1: 19–27.LINK
856 Consolacion Y. Ragasa, Vic Marie L. Inte, Rideout JA. An antimicrobial alkaloid from Catharanthus roseus. Manila J Sci. 1998;1: 19–27.LINK
857 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
858 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
859 Svoboda GH, Gorman M, Barnes AJ, Oliver AT. Alkaloids of Vinca rosea Linn. (Catharanthus roseus G. Don.). XII Preparation and characterization of trace alkaloids. J Pharm Sci. 1962;51: 518–523. doi:10.1002/jps.2600510605LINK
860 Svoboda GH, Gorman M, Barnes AJ, Oliver AT. Alkaloids of Vinca rosea Linn. (Catharanthus roseus G. Don.). XII Preparation and characterization of trace alkaloids. J Pharm Sci. 1962;51: 518–523. doi:10.1002/jps.2600510605LINK
861 Rodrigo RGA. The Alkaloids: Chemistry and Physiology V20: Chemistry and Physiology. Elsevier Science; 1982. p. 340. ISBN: 9780080865447.LINK
862 Rodrigo RGA. The Alkaloids: Chemistry and Physiology V20: Chemistry and Physiology. Elsevier Science; 1982. p. 340. ISBN: 9780080865447.LINK
863 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
864 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
865 Mukhopadhyay S, Cordell GA. Catharanthus alkaloids. XXXV. Isolation of leurosidine N’b-oxide from Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 611–613. doi:10.1021/np50017a021LINK
866 Mukhopadhyay S, Cordell GA. Catharanthus alkaloids. XXXV. Isolation of leurosidine N’b-oxide from Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 611–613. doi:10.1021/np50017a021LINK
867 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
868 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
869 El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids, XXXVIII. Confirming structural evidence and antineoplastic activity of the bisindole alkaloids leurosine-N’ b -oxide (pleurosine), roseadine, and vindolicine from Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 517–527. doi:10.1021/np50028a016LINK
870 El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids, XXXVIII. Confirming structural evidence and antineoplastic activity of the bisindole alkaloids leurosine-N’ b -oxide (pleurosine), roseadine, and vindolicine from Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 517–527. doi:10.1021/np50028a016LINK
871 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
872 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
873 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
874 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
875 Street HE. Plant Tissue and Cell Culture [Internet]. University of California Press; 1973. p. 503. ISBN: 9780520024113.LINK
876 Street HE. Plant Tissue and Cell Culture [Internet]. University of California Press; 1973. p. 503. ISBN: 9780520024113.LINK
877 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
878 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
879 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
880 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
881 Buckingham J. Dictionary of Natural Products. illustrate. Taylor & Francis; 1993. p. 8584. ISBN: 9780412466205.NA
882 Buckingham J. Dictionary of Natural Products. illustrate. Taylor & Francis; 1993. p. 8584. ISBN: 9780412466205.NA
883 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
884 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
885 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
886 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
887 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
888 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
889 Cambie R, Brewis A. Anti-fertility plants of the pacific. Csiro Publishing; 1997. p. 192. ISBN: 9780643102330.LINK
890 Cambie R, Brewis A. Anti-fertility plants of the pacific. Csiro Publishing; 1997. p. 192. ISBN: 9780643102330.LINK
891 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
892 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
893 Southon IW, Buckingham J. Dictionary of Alkaloids. 2nd ed. CRC Press; 1989. p. 620. ISBN: 9780412249105.LINK
894 Southon IW, Buckingham J. Dictionary of Alkaloids. 2nd ed. CRC Press; 1989. p. 620. ISBN: 9780412249105.LINK
895 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
896 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
897 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
898 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
899 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
900 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
901 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
902 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
903 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
904 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
905 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
906 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
907 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
908 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
909 Moreno PRH, van der Heijden R, Verpoorte R. Cell and tissue cultures of Catharanthus roseus: A literature survey. Plant Cell Tissue Organ Cult. 1995;42: 1–25. doi:10.1007/BF00037677LINK
910 Moreno PRH, van der Heijden R, Verpoorte R. Cell and tissue cultures of Catharanthus roseus: A literature survey. Plant Cell Tissue Organ Cult. 1995;42: 1–25. doi:10.1007/BF00037677LINK
911 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
912 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
913 Svoboda GH, Barnes AJ. Alkaloids of Vinca rosea linn. (Catharanthus roseus G. Don). XXIV. vinaspine, vincathicine, rovidine, desacetyl VLB, and vinaphamine. J Pharm Sci. 1964;53: 1227–1231.LINK
914 Svoboda GH, Barnes AJ. Alkaloids of Vinca rosea linn. (Catharanthus roseus G. Don). XXIV. vinaspine, vincathicine, rovidine, desacetyl VLB, and vinaphamine. J Pharm Sci. 1964;53: 1227–1231.LINK
915 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
916 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
917 Svoboda GH, Barnes AJ. Alkaloids of Vinca rosea linn. (Catharanthus roseus G. Don). XXIV. vinaspine, vincathicine, rovidine, desacetyl VLB, and vinaphamine. J Pharm Sci. 1964;53: 1227–1231.LINK
918 Svoboda GH, Barnes AJ. Alkaloids of Vinca rosea linn. (Catharanthus roseus G. Don). XXIV. vinaspine, vincathicine, rovidine, desacetyl VLB, and vinaphamine. J Pharm Sci. 1964;53: 1227–1231.LINK
919 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
920 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
921 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
922 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
923 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
924 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
925 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
926 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
927 Islas I, Loyola-Vargas VM, de Lourdes Miranda-Ham M. Tryptophan decarboxylase activity in transformed roots fromCatharanthus roseus and its relationship to tryptamine, ajmalicine, and catharanthine accumulation during the culture cycle. Vitr Cell Dev Biol. 1994;30: 81–83. doi:10.1007/BF02632125LINK
928 Islas I, Loyola-Vargas VM, de Lourdes Miranda-Ham M. Tryptophan decarboxylase activity in transformed roots fromCatharanthus roseus and its relationship to tryptamine, ajmalicine, and catharanthine accumulation during the culture cycle. Vitr Cell Dev Biol. 1994;30: 81–83. doi:10.1007/BF02632125LINK
929 Lourdes Miranda-Ham M de, Islas-Flores I, V?zquez-Flota AF. Accumulation of monoterpenoid indole alkaloids in periwinkle seedlings (Catharanthus roseus) as a model for the study of plant-environment interactions. Biochem Mol Biol Educ. 2007;35: 206–210. doi:10.1002/bambed.60LINK
930 Lourdes Miranda-Ham M de, Islas-Flores I, V?zquez-Flota AF. Accumulation of monoterpenoid indole alkaloids in periwinkle seedlings (Catharanthus roseus) as a model for the study of plant-environment interactions. Biochem Mol Biol Educ. 2007;35: 206–210. doi:10.1002/bambed.60LINK
931 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
932 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
933 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
934 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
935 Whitmer S, Canel C, Hallard D, Gonηalves C, Verpoorte R. Influence of precursor availability on alkaloid accumulation by transgenic cell line of Catharanthus roseus. Plant Physiol. 1998;116: 853–857.LINK
936 Whitmer S, Canel C, Hallard D, Gonηalves C, Verpoorte R. Influence of precursor availability on alkaloid accumulation by transgenic cell line of Catharanthus roseus. Plant Physiol. 1998;116: 853–857.LINK
937 McCoy EA. Substrate analogs to investigate alkaloid biosynthesis in Catharanthus roseus. Massachusetts Institute of Technology. 2009. p. 396.LINK
938 McCoy EA. Substrate analogs to investigate alkaloid biosynthesis in Catharanthus roseus. Massachusetts Institute of Technology. 2009. p. 396.LINK
939 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
940 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
941 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
942 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
943 Whitmer S, Canel C, Hallard D, Gonηalves C, Verpoorte R. Influence of precursor availability on alkaloid accumulation by transgenic cell line of Catharanthus roseus. Plant Physiol. 1998;116: 853–857.LINK
944 Whitmer S, Canel C, Hallard D, Gonηalves C, Verpoorte R. Influence of precursor availability on alkaloid accumulation by transgenic cell line of Catharanthus roseus. Plant Physiol. 1998;116: 853–857.LINK
945 Peebles CAM, Hong S-B, Gibson SI, Shanks J V, San K-Y. Effects of terpenoid precursor feeding on Catharanthus roseus hairy roots over-expressing the alpha or the alpha and beta subunits of anthranilate synthase. Biotechnol Bioeng. 2006;93: 534–540. doi:10.1002/bit.20739LINK
946 Peebles CAM, Hong S-B, Gibson SI, Shanks J V, San K-Y. Effects of terpenoid precursor feeding on Catharanthus roseus hairy roots over-expressing the alpha or the alpha and beta subunits of anthranilate synthase. Biotechnol Bioeng. 2006;93: 534–540. doi:10.1002/bit.20739LINK
947 Srivastava NK, Srivastava AK. Allocation of different 14C substrates into primary metabolites in relation to total alkaloid accumulation into Catharanthus roseus plants. Journal of Medicinal Plants Research. Academic Journals; 2011. pp. 4747–4753.LINK
948 Srivastava NK, Srivastava AK. Allocation of different 14C substrates into primary metabolites in relation to total alkaloid accumulation into Catharanthus roseus plants. Journal of Medicinal Plants Research. Academic Journals; 2011. pp. 4747–4753.LINK
949 Murata J, Roepke J, Gordon H, De Luca V. The leaf epidermome of Catharanthus roseus reveals its biochemical specialization. Plant Cell. 2008;20: 524–542. doi:10.1105/tpc.107.056630LINK
950 Murata J, Roepke J, Gordon H, De Luca V. The leaf epidermome of Catharanthus roseus reveals its biochemical specialization. Plant Cell. 2008;20: 524–542. doi:10.1105/tpc.107.056630LINK
951 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
952 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
953 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
954 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
955 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
956 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
957 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
958 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
959 Murata J, Roepke J, Gordon H, De Luca V. The leaf epidermome of Catharanthus roseus reveals its biochemical specialization. Plant Cell. 2008;20: 524–542. doi:10.1105/tpc.107.056630LINK
960 Murata J, Roepke J, Gordon H, De Luca V. The leaf epidermome of Catharanthus roseus reveals its biochemical specialization. Plant Cell. 2008;20: 524–542. doi:10.1105/tpc.107.056630LINK
961 Contin A, Heijden R van der, Verpoorte R. Effects of alkaloid precursor feeding and elicitation on the accumulation of secologanin in a Catharanthus roseus cell suspension culture. Plant Cell Tissue Organ Cult. Kluwer Academic Publishers; 1999;56: 111–119. doi:10.1023/A:1006257125191LINK
962 Contin A, Heijden R van der, Verpoorte R. Effects of alkaloid precursor feeding and elicitation on the accumulation of secologanin in a Catharanthus roseus cell suspension culture. Plant Cell Tissue Organ Cult. Kluwer Academic Publishers; 1999;56: 111–119. doi:10.1023/A:1006257125191LINK
963 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
964 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
965 Irmler S, Schr?der G, St-Pierre B, Crouch NP, Hotze M, Schmidt J, et al. Indole alkaloid biosynthesis in Catharanthus roseus: new enzyme activities and identification of cytochrome P450 CYP72A1 as secologanin synthase. Plant J. 2008;24: 797–804. doi:10.1111/j.1365-313X.2000.00922.xLINK
966 Irmler S, Schr?der G, St-Pierre B, Crouch NP, Hotze M, Schmidt J, et al. Indole alkaloid biosynthesis in Catharanthus roseus: new enzyme activities and identification of cytochrome P450 CYP72A1 as secologanin synthase. Plant J. 2008;24: 797–804. doi:10.1111/j.1365-313X.2000.00922.xLINK
967 Yamamoto H, Katano N, Ooi A, Inoue K. Transformation of loganin and 7-deoxyloganin into secologanin by Lonicera japonica cell suspension cultures. Phytochemistry. 1999;50: 417–422. doi:10.1016/S0031-9422(98)00613-XLINK
968 Yamamoto H, Katano N, Ooi A, Inoue K. Transformation of loganin and 7-deoxyloganin into secologanin by Lonicera japonica cell suspension cultures. Phytochemistry. 1999;50: 417–422. doi:10.1016/S0031-9422(98)00613-XLINK
969 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
970 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
971 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
972 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
973 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
974 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-68LINK
975 El-Sayed M, Choi YH, Frιdιrich M, Roytrakul S, Verpoorte R. Alkaloid accumulation in Catharanthus roseus cell suspension cultures fed with stemmadenine. Biotechnol Lett. 2004;26: 793–798. doi:10.1023/B:BILE.0000025879.53632.f2LINK
976 El-Sayed M, Choi YH, Frιdιrich M, Roytrakul S, Verpoorte R. Alkaloid accumulation in Catharanthus roseus cell suspension cultures fed with stemmadenine. Biotechnol Lett. 2004;26: 793–798. doi:10.1023/B:BILE.0000025879.53632.f2LINK
977 Magnotta M. Metabolic, biochemical and molecular profiling of Catharanthus roseus flower cultivars and transformed hairy roots for monoterpenoid indole alkaloid accumulation. Brock University. 2007. p. 235.LINK
978 Magnotta M. Metabolic, biochemical and molecular profiling of Catharanthus roseus flower cultivars and transformed hairy roots for monoterpenoid indole alkaloid accumulation. Brock University. 2007. p. 235.LINK
979 Rai V, Tandon PK, Khatoon S. Effect of chromium on antioxidant potential of Catharanthus roseus varieties and production of their anticancer alkaloids: vincristine and vinblastine. Biomed Res Int. 2014;2014: 10. doi:10.1155/2014/934182LINK
980 Rai V, Tandon PK, Khatoon S. Effect of chromium on antioxidant potential of Catharanthus roseus varieties and production of their anticancer alkaloids: vincristine and vinblastine. Biomed Res Int. 2014;2014: 10. doi:10.1155/2014/934182LINK
981 Choi YH, Tapias EC, Kim HK, Lefeber AWM, Erkelens C, Verhoeven JTJ, et al. Metabolic discrimination of Catharanthus roseus leaves infected by phytoplasma using 1H-NMR spectroscopy and multivariate data analysis. Plant Physiol. 2004;135: 2398–2410. doi:10.1104/pp.104.041012LINK
982 Choi YH, Tapias EC, Kim HK, Lefeber AWM, Erkelens C, Verhoeven JTJ, et al. Metabolic discrimination of Catharanthus roseus leaves infected by phytoplasma using 1H-NMR spectroscopy and multivariate data analysis. Plant Physiol. 2004;135: 2398–2410. doi:10.1104/pp.104.041012LINK
983 Rijhwani SK, Shanks J V. Effect of elicitor dosage and exposure time on biosynthesis of indole alkaloids by Catharanthus roseus hairy root cultures. Biotechnol Prog. 1998;14: 442–449. doi:10.1021/bp980029vLINK
984 Rijhwani SK, Shanks J V. Effect of elicitor dosage and exposure time on biosynthesis of indole alkaloids by Catharanthus roseus hairy root cultures. Biotechnol Prog. 1998;14: 442–449. doi:10.1021/bp980029vLINK
985 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
986 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
987 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249. ISBN: 978-0124695375.LINK
988 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249. ISBN: 978-0124695375.LINK
989 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
990 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
991 Furuya T, Sakamoto K, Iida K, Asada Y, Yoshikawa T, Sakai S, et al. Biotransformation of tabersonine in cell suspension cultures of Catharanthus roseus. Phytochemistry. 1992;31: 3065–8. doi:10.1016/0031-9422(92)83447-7LINK
992 Furuya T, Sakamoto K, Iida K, Asada Y, Yoshikawa T, Sakai S, et al. Biotransformation of tabersonine in cell suspension cultures of Catharanthus roseus. Phytochemistry. 1992;31: 3065–8. doi:10.1016/0031-9422(92)83447-7LINK
993 Zhong X-Z, Wang G-C, Wang Y, Zhang X-Q, Ye W-C. Monomeric indole alkaloids from the aerial parts of Catharanthus roseus. Acta Pharm Sin. 2010;45: 471–474.LINK
994 Zhong X-Z, Wang G-C, Wang Y, Zhang X-Q, Ye W-C. Monomeric indole alkaloids from the aerial parts of Catharanthus roseus. Acta Pharm Sin. 2010;45: 471–474.LINK
995 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
996 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
997 Peraza-S?nchez SR, Gamboa-angulo MM, Erosa-L?pez C, Ram?rez-Erosa I, Escalante-erosa F, Pe?a-Rodr?guez LM, et al. Production of 19(s)-epimisiline by hairy root cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 2006;11: 217–224. doi:10.1080/10575639808044950LINK
998 Peraza-S?nchez SR, Gamboa-angulo MM, Erosa-L?pez C, Ram?rez-Erosa I, Escalante-erosa F, Pe?a-Rodr?guez LM, et al. Production of 19(s)-epimisiline by hairy root cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 2006;11: 217–224. doi:10.1080/10575639808044950LINK
999 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
1000 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
1001 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
1002 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
1003 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
1004 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
1005 Fatima J, Albert K. Isolation and structure of rosicine from Catharanthus roseus. Tetrahedron Lett. 1984;25: 6051–6054. doi:10.1016/S0040-4039(01)81759-7LINK
1006 Fatima J, Albert K. Isolation and structure of rosicine from Catharanthus roseus. Tetrahedron Lett. 1984;25: 6051–6054. doi:10.1016/S0040-4039(01)81759-7LINK
1007 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1008 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1009 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1010 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1011 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1012 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1013 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1014 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1015 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1016 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1017 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1018 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1019 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1020 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1021 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1022 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1023 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1024 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1025 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1026 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1027 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1028 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1029 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1030 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1031 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1032 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1033 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1034 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1035 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1036 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1037 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1038 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1039 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1040 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1041 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1042 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1043 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1044 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1045 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1046 Pereira DM, Faria J, Gaspar L, Ferreres F, Valent?o P, Sottomayor M, et al. Exploiting Catharanthus roseus roots: Source of antioxidants. Food Chem. 2010;121: 56–61. doi:10.1016/j.foodchem.2009.12.002LINK
1047 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1048 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1049 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1050 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1051 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1052 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1053 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1054 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1055 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1056 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1057 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1058 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1059 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1060 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1061 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1062 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1063 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1064 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1065 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1066 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1067 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1068 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1069 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1070 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1071 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1072 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1073 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1074 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1075 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1076 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1077 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1078 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1079 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1080 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1081 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1082 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1083 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1084 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1085 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1086 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1087 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1088 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1089 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1090 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1091 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1092 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1093 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1094 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1095 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1096 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1097 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1098 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1099 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1100 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1101 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1102 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1103 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1104 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1105 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1106 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1107 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1108 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1109 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1110 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1111 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1112 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1113 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1114 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1115 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1116 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1117 Lourdes Miranda-Ham M de, Islas-Flores I, V?zquez-Flota AF. Accumulation of monoterpenoid indole alkaloids in periwinkle seedlings (Catharanthus roseus) as a model for the study of plant-environment interactions. Biochem Mol Biol Educ. 2007;35: 206–210. doi:10.1002/bambed.60LINK
1118 Lourdes Miranda-Ham M de, Islas-Flores I, V?zquez-Flota AF. Accumulation of monoterpenoid indole alkaloids in periwinkle seedlings (Catharanthus roseus) as a model for the study of plant-environment interactions. Biochem Mol Biol Educ. 2007;35: 206–210. doi:10.1002/bambed.60LINK
1119 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
1120 Tikhomiroff C, Jolicoeur M. Screening of Catharanthus roseus secondary metabolites by high-performance liquid chromatography. J Chromatogr A. 2002;955: 87–93. doi:10.1016/S0021-9673(02)00204-2LINK
1121 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1122 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1123 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1124 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1125 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1126 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1127 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1128 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1129 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1130 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1131 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1132 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1133 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1134 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1135 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1136 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1137 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1138 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1139 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1140 Pereira DM, Ferreres F, Oliveira J, Valent?o P, Andrade PB, Sottomayor M. Targeted metabolite analysis of Catharanthus roseus and its biological potential. Food Chem Toxicol. 2009;47: 1349–1354. doi:10.1016/j.fct.2009.03.012LINK
1141 Mukhopadhyay S, Cordell GA. Catharanthus alkaloids. XXXV. Isolation of leurosidine N’b-oxide from Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 611–613. doi:10.1021/np50017a021LINK
1142 Mukhopadhyay S, Cordell GA. Catharanthus alkaloids. XXXV. Isolation of leurosidine N’b-oxide from Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 611–613. doi:10.1021/np50017a021LINK
1143 Karpinski S. Methods for altering the level of phytochemals in plant cells by applying wave lengths of light from 400 nm to 700 nm and apparatus therefore. WO2004103060 A1, 2004.LINK
1144 Karpinski S. Methods for altering the level of phytochemals in plant cells by applying wave lengths of light from 400 nm to 700 nm and apparatus therefore. WO2004103060 A1, 2004.LINK
1145 Huang L, Li J, Ye H, Li C, Wang H, Liu B, et al. Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus. Planta. 2012;236: 1571–1581. doi:10.1007/s00425-012-1712-0LINK
1146 Huang L, Li J, Ye H, Li C, Wang H, Liu B, et al. Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus. Planta. 2012;236: 1571–1581. doi:10.1007/s00425-012-1712-0LINK
1147 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1148 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1149 Huang L, Li J, Ye H, Li C, Wang H, Liu B, et al. Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus. Planta. 2012;236: 1571–1581. doi:10.1007/s00425-012-1712-0LINK
1150 Huang L, Li J, Ye H, Li C, Wang H, Liu B, et al. Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus. Planta. 2012;236: 1571–1581. doi:10.1007/s00425-012-1712-0LINK
1151 Huang L, Li J, Ye H, Li C, Wang H, Liu B, et al. Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus. Planta. 2012;236: 1571–1581. doi:10.1007/s00425-012-1712-0LINK
1152 Huang L, Li J, Ye H, Li C, Wang H, Liu B, et al. Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus. Planta. 2012;236: 1571–1581. doi:10.1007/s00425-012-1712-0LINK
1153 Zhong X-Z, Wang G-C, Wang Y, Zhang X-Q, Ye W-C. Monomeric indole alkaloids from the aerial parts of Catharanthus roseus. Acta Pharm Sin. 2010;45: 471–474.LINK
1154 Zhong X-Z, Wang G-C, Wang Y, Zhang X-Q, Ye W-C. Monomeric indole alkaloids from the aerial parts of Catharanthus roseus. Acta Pharm Sin. 2010;45: 471–474.LINK
1155 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
1156 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
1157 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
1158 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
1159 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1160 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1161 Zhong X-Z, Wang G-C, Wang Y, Zhang X-Q, Ye W-C. Monomeric indole alkaloids from the aerial parts of Catharanthus roseus. Acta Pharm Sin. 2010;45: 471–474.LINK
1162 Zhong X-Z, Wang G-C, Wang Y, Zhang X-Q, Ye W-C. Monomeric indole alkaloids from the aerial parts of Catharanthus roseus. Acta Pharm Sin. 2010;45: 471–474.LINK
1163 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
1164 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
1165 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1166 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1167 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1168 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1169 Svoboda GH, Gorman M, Neuss N, Barnes AJ. Alkaloids of Vinca rosea Linn. (Catharanthus roseus G. Don.) VIII. Preparation and characterization of new minor alkaloids. J Pharm Sci. 1961;50: 409–413. doi:10.1002/jps.2600500508LINK
1170 Svoboda GH, Gorman M, Neuss N, Barnes AJ. Alkaloids of Vinca rosea Linn. (Catharanthus roseus G. Don.) VIII. Preparation and characterization of new minor alkaloids. J Pharm Sci. 1961;50: 409–413. doi:10.1002/jps.2600500508LINK
1171 Chung I-M, Ali M, Chun S-C, Lee S-J, San K-Y, Christie AMP, et al. New Sesquiterpene Glycosides from Culture Hairy Roots ofCatharanthus roseus. Chinese J Chem. 2007;25: 1695–1699. doi:10.1002/cjoc.200790313LINK
1172 Chung I-M, Ali M, Chun S-C, Lee S-J, San K-Y, Christie AMP, et al. New Sesquiterpene Glycosides from Culture Hairy Roots ofCatharanthus roseus. Chinese J Chem. 2007;25: 1695–1699. doi:10.1002/cjoc.200790313LINK
1173 Chung I-M, Ali M, Chun S-C, Lee S-J, San K-Y, Christie AMP, et al. New Sesquiterpene Glycosides from Culture Hairy Roots ofCatharanthus roseus. Chinese J Chem. 2007;25: 1695–1699. doi:10.1002/cjoc.200790313LINK
1174 Chung I-M, Ali M, Chun S-C, Lee S-J, San K-Y, Christie AMP, et al. New Sesquiterpene Glycosides from Culture Hairy Roots ofCatharanthus roseus. Chinese J Chem. 2007;25: 1695–1699. doi:10.1002/cjoc.200790313LINK
1175 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
1176 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
1177 Glenn WS, Nims E, O’Connor SE. Reengineering a tryptophan halogenase to preferentially chlorinate a direct alkaloid precursor. J Am Chem Soc. 2011;133: 19346–19349. doi:10.1021/ja2089348LINK
1178 Glenn WS, Nims E, O’Connor SE. Reengineering a tryptophan halogenase to preferentially chlorinate a direct alkaloid precursor. J Am Chem Soc. 2011;133: 19346–19349. doi:10.1021/ja2089348LINK
1179 Glenn WS, Nims E, O’Connor SE. Reengineering a tryptophan halogenase to preferentially chlorinate a direct alkaloid precursor. J Am Chem Soc. 2011;133: 19346–19349. doi:10.1021/ja2089348LINK
1180 Glenn WS, Nims E, O’Connor SE. Reengineering a tryptophan halogenase to preferentially chlorinate a direct alkaloid precursor. J Am Chem Soc. 2011;133: 19346–19349. doi:10.1021/ja2089348LINK
1181 Lee H-Y, Yerkes N, O’Connor SE. Aza-tryptamine substrates in monoterpene indole alkaloid biosynthesis. Chem Biol. 2009;16: 1225–1229. doi:10.1016/j.chembiol.2009.11.016LINK
1182 Lee H-Y, Yerkes N, O’Connor SE. Aza-tryptamine substrates in monoterpene indole alkaloid biosynthesis. Chem Biol. 2009;16: 1225–1229. doi:10.1016/j.chembiol.2009.11.016LINK
1183 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
1184 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
1185 Glenn WS, Nims E, O’Connor SE. Reengineering a tryptophan halogenase to preferentially chlorinate a direct alkaloid precursor. J Am Chem Soc. 2011;133: 19346–19349. doi:10.1021/ja2089348LINK
1186 Glenn WS, Nims E, O’Connor SE. Reengineering a tryptophan halogenase to preferentially chlorinate a direct alkaloid precursor. J Am Chem Soc. 2011;133: 19346–19349. doi:10.1021/ja2089348LINK
1187 Lee H-Y, Yerkes N, O’Connor SE. Aza-tryptamine substrates in monoterpene indole alkaloid biosynthesis. Chem Biol. 2009;16: 1225–1229. doi:10.1016/j.chembiol.2009.11.016LINK
1188 Lee H-Y, Yerkes N, O’Connor SE. Aza-tryptamine substrates in monoterpene indole alkaloid biosynthesis. Chem Biol. 2009;16: 1225–1229. doi:10.1016/j.chembiol.2009.11.016LINK
1189 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
1190 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
1191 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
1192 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
1193 Atta-ur-Rahman. Bioactive Natural Products (Part G). Elsevier; 2002. p. 1364. ISBN: 9780080542065.LINK
1194 Atta-ur-Rahman. Bioactive Natural Products (Part G). Elsevier; 2002. p. 1364. ISBN: 9780080542065.LINK
1195 Atta-ur-Rahman. Bioactive Natural Products (Part G). Elsevier; 2002. p. 1364. ISBN: 9780080542065.LINK
1196 Atta-ur-Rahman. Bioactive Natural Products (Part G). Elsevier; 2002. p. 1364. ISBN: 9780080542065.LINK
1197 Gonzalez-Cid M. Comparison of the aneugenic effect of vinorelbine and vincristine in cultured human lymphocytes. Mutagenesis. 1999;14: 63–66. doi:10.1093/mutage/14.1.63LINK
1198 Gonzalez-Cid M. Comparison of the aneugenic effect of vinorelbine and vincristine in cultured human lymphocytes. Mutagenesis. 1999;14: 63–66. doi:10.1093/mutage/14.1.63LINK
1199 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
1200 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
1201 Nagakura N, Ruffer M, Zenk MH. The biosynthesis of monoterpenoid indole alkaloids from strictosidine. J Chem Soc Perkin Trans 1. The Royal Society of Chemistry; 1979;1: 2308–2312. doi:10.1039/P19790002308LINK
1202 Nagakura N, Ruffer M, Zenk MH. The biosynthesis of monoterpenoid indole alkaloids from strictosidine. J Chem Soc Perkin Trans 1. The Royal Society of Chemistry; 1979;1: 2308–2312. doi:10.1039/P19790002308LINK
1203 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
1204 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
1205 Proestos C, Chorianopoulos N, Nychas G-JE, Komaitis M. RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity. J Agric Food Chem. American Chemical Society; 2005;53: 1190–1195. doi:10.1021/jf040083tLINK
1206 Proestos C, Chorianopoulos N, Nychas G-JE, Komaitis M. RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity. J Agric Food Chem. American Chemical Society; 2005;53: 1190–1195. doi:10.1021/jf040083tLINK
1207 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
1208 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
1209 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
1210 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
1211 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1212 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1213 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
1214 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
1215 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
1216 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
1217 Wang L, Zhang Y, He H-P, Zhang Q, Li S-F, Hao X-J. Three new terpenoid indole alkaloids from Catharanthus roseus. Planta Med. 2011;77: 754–758. doi:10.1055/s-0030-1250569LINK
1218 Wang L, Zhang Y, He H-P, Zhang Q, Li S-F, Hao X-J. Three new terpenoid indole alkaloids from Catharanthus roseus. Planta Med. 2011;77: 754–758. doi:10.1055/s-0030-1250569LINK
1219 Wang L, Zhang Y, He H-P, Zhang Q, Li S-F, Hao X-J. Three new terpenoid indole alkaloids from Catharanthus roseus. Planta Med. 2011;77: 754–758. doi:10.1055/s-0030-1250569LINK
1220 Wang L, Zhang Y, He H-P, Zhang Q, Li S-F, Hao X-J. Three new terpenoid indole alkaloids from Catharanthus roseus. Planta Med. 2011;77: 754–758. doi:10.1055/s-0030-1250569LINK
1221 Wang L, Zhang Y, He H-P, Zhang Q, Li S-F, Hao X-J. Three new terpenoid indole alkaloids from Catharanthus roseus. Planta Med. 2011;77: 754–758. doi:10.1055/s-0030-1250569LINK
1222 Wang L, Zhang Y, He H-P, Zhang Q, Li S-F, Hao X-J. Three new terpenoid indole alkaloids from Catharanthus roseus. Planta Med. 2011;77: 754–758. doi:10.1055/s-0030-1250569LINK
1223 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
1224 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
1225 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
1226 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
1227 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
1228 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
1229 Wang L, Zhang Y, He H-P, Zhang Q, Li S-F, Hao X-J. Three new terpenoid indole alkaloids from Catharanthus roseus. Planta Med. 2011;77: 754–758. doi:10.1055/s-0030-1250569LINK
1230 Wang L, Zhang Y, He H-P, Zhang Q, Li S-F, Hao X-J. Three new terpenoid indole alkaloids from Catharanthus roseus. Planta Med. 2011;77: 754–758. doi:10.1055/s-0030-1250569LINK
1231 Islam MA, Akhtar MA, Islam MR, Hossain MS, Alam MK, Wahed MII, et al. Antidiabetic and hypolipidemic effects of different fractions of Catharanthus roseus (Linn.) on normal and streptozotocin-induced diabetic rats. J Sci Res. 2009;1: 334–344.LINK
1232 Islam MA, Akhtar MA, Islam MR, Hossain MS, Alam MK, Wahed MII, et al. Antidiabetic and hypolipidemic effects of different fractions of Catharanthus roseus (Linn.) on normal and streptozotocin-induced diabetic rats. J Sci Res. 2009;1: 334–344.LINK
1233 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1234 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1235 Chung I, Park H, Ali M, San KY, Peebles CAM, Hong S, et al. A New Chemical Constituent from the Hairy Root Cultures of Catharanthus roseus. Bull Korean Chem Soc. 2007;28: 229–234. doi:10.5012/bkcs.2007.28.2.229LINK
1236 Chung I, Park H, Ali M, San KY, Peebles CAM, Hong S, et al. A New Chemical Constituent from the Hairy Root Cultures of Catharanthus roseus. Bull Korean Chem Soc. 2007;28: 229–234. doi:10.5012/bkcs.2007.28.2.229LINK
1237 yora-Talavera T, Chappell J, Lozoya-Gloria E, Loyola-Vargas VM. Overexpression in Catharanthus roseus hairy roots of a truncated hamster 3-hydroxy-3-methylglutaryl-CoA reductase gene. Appl Biochem Biotechnol. 2002;97: 135–146. doi:10.1385/ABAB:97:2:135LINK
1238 yora-Talavera T, Chappell J, Lozoya-Gloria E, Loyola-Vargas VM. Overexpression in Catharanthus roseus hairy roots of a truncated hamster 3-hydroxy-3-methylglutaryl-CoA reductase gene. Appl Biochem Biotechnol. 2002;97: 135–146. doi:10.1385/ABAB:97:2:135LINK
1239 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
1240 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
1241 Chung I, Park H, Ali M, San KY, Peebles CAM, Hong S, et al. A New Chemical Constituent from the Hairy Root Cultures of Catharanthus roseus. Bull Korean Chem Soc. 2007;28: 229–234. doi:10.5012/bkcs.2007.28.2.229LINK
1242 Chung I, Park H, Ali M, San KY, Peebles CAM, Hong S, et al. A New Chemical Constituent from the Hairy Root Cultures of Catharanthus roseus. Bull Korean Chem Soc. 2007;28: 229–234. doi:10.5012/bkcs.2007.28.2.229LINK
1243 Chung I, Park H, Ali M, San KY, Peebles CAM, Hong S, et al. A New Chemical Constituent from the Hairy Root Cultures of Catharanthus roseus. Bull Korean Chem Soc. 2007;28: 229–234. doi:10.5012/bkcs.2007.28.2.229LINK
1244 Chung I, Park H, Ali M, San KY, Peebles CAM, Hong S, et al. A New Chemical Constituent from the Hairy Root Cultures of Catharanthus roseus. Bull Korean Chem Soc. 2007;28: 229–234. doi:10.5012/bkcs.2007.28.2.229LINK
1245 Chung I, Park H, Ali M, San KY, Peebles CAM, Hong S, et al. A New Chemical Constituent from the Hairy Root Cultures of Catharanthus roseus. Bull Korean Chem Soc. 2007;28: 229–234. doi:10.5012/bkcs.2007.28.2.229LINK
1246 Chung I, Park H, Ali M, San KY, Peebles CAM, Hong S, et al. A New Chemical Constituent from the Hairy Root Cultures of Catharanthus roseus. Bull Korean Chem Soc. 2007;28: 229–234. doi:10.5012/bkcs.2007.28.2.229LINK
1247 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1248 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1249 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1250 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1251 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1252 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1253 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1254 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1255 Chung I, Ali M, Yang Y, Peebles C a M, Chun S, Lee S, et al. Identification of new compounds from Catharanthus roseus hairy root cultures. Bull Korean Chem Soc. 2007;28: 1294–1298.LINK
1256 Chung I, Ali M, Yang Y, Peebles C a M, Chun S, Lee S, et al. Identification of new compounds from Catharanthus roseus hairy root cultures. Bull Korean Chem Soc. 2007;28: 1294–1298.LINK
1257 Chung I, Ali M, Yang Y, Peebles C a M, Chun S, Lee S, et al. Identification of new compounds from Catharanthus roseus hairy root cultures. Bull Korean Chem Soc. 2007;28: 1294–1298.LINK
1258 Chung I, Ali M, Yang Y, Peebles C a M, Chun S, Lee S, et al. Identification of new compounds from Catharanthus roseus hairy root cultures. Bull Korean Chem Soc. 2007;28: 1294–1298.LINK
1259 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1260 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1261 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1262 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1263 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1264 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1265 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1266 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1267 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1268 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1269 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1270 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1271 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1272 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1273 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1274 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1275 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1276 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1277 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1278 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1279 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1280 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1281 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1282 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1283 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1284 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1285 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1286 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1287 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1288 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1289 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1290 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1291 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1292 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1293 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1294 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1295 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1296 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1297 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1298 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1299 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1300 De Pinho PG, Gonηalves RF, Valent?o P, Pereira DM, Seabra RM, Andrade PB, et al. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry. J Pharm Bomedical Anal. 2009;49: 674–685. doi:10.1016/j.jpba.2008.12.032LINK
1301 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
1302 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
1303 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1304 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1305 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1306 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1307 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1308 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1309 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1310 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1311 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1312 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1313 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1314 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1315 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
1316 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
1317 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
1318 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
1319 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
1320 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
1321 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
1322 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
1323 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
1324 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
1325 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1326 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1327 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1328 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1329 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1330 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1331 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1332 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1333 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1334 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1335 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1336 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1337 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1338 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1339 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1340 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1341 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
1342 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
1343 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1344 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1345 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1346 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1347 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
1348 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
1349 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1350 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1351 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1352 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1353 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
1354 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
1355 Nayak BS, Pinto Pereira LM. Catharanthus roseus flower extract has wound-healing activity in Sprague Dawley rats. BMC Complement Aternative Med. 2006;6: 41. doi:10.1186/1472-6882-6-41LINK
1356 Nayak BS, Pinto Pereira LM. Catharanthus roseus flower extract has wound-healing activity in Sprague Dawley rats. BMC Complement Aternative Med. 2006;6: 41. doi:10.1186/1472-6882-6-41LINK
1357 Nayak BS, Anderson M, Pinto Pereira LM. Evaluation of wound-healing potential of Catharanthus roseus leaf extract in rats. Fitoterapia. 2007;78: 540–544. doi:10.1016/j.fitote.2007.06.008LINK
1358 Nayak BS, Anderson M, Pinto Pereira LM. Evaluation of wound-healing potential of Catharanthus roseus leaf extract in rats. Fitoterapia. 2007;78: 540–544. doi:10.1016/j.fitote.2007.06.008LINK
1359 Gautam S, Mishra A, Tiwari A. Catharanthus alkaloids and their enhanced production using elicitors: A review. Int J Pharm Technol. 2011;3: 713–724.LINK
1360 Gautam S, Mishra A, Tiwari A. Catharanthus alkaloids and their enhanced production using elicitors: A review. Int J Pharm Technol. 2011;3: 713–724.LINK
1361 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1362 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1363 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1364 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1365 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1366 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1367 Mustafa NR, Kim HK, Choi YH, Erkelens C, Lefeber AWM, Spijksma G, et al. Biosynthesis of salicylic acid in fungus elicited Catharanthus roseus cells. Phytochemistry. 2009;70: 532–539. doi:10.1016/j.phytochem.2009.01.009LINK
1368 Mustafa NR, Kim HK, Choi YH, Erkelens C, Lefeber AWM, Spijksma G, et al. Biosynthesis of salicylic acid in fungus elicited Catharanthus roseus cells. Phytochemistry. 2009;70: 532–539. doi:10.1016/j.phytochem.2009.01.009LINK
1369 Muljono RAB, Scheffer JJC, Verpoorte R. Effect of feeding salicylic acid on 2,3-dihydroxybenzoic acid formation in cultured cells of Catharanthus roseus. Pharm Biol. Informa UK Ltd UK; 2003;41: 284–290. doi:10.1076/phbi.41.4.284.15681LINK
1370 Muljono RAB, Scheffer JJC, Verpoorte R. Effect of feeding salicylic acid on 2,3-dihydroxybenzoic acid formation in cultured cells of Catharanthus roseus. Pharm Biol. Informa UK Ltd UK; 2003;41: 284–290. doi:10.1076/phbi.41.4.284.15681LINK
1371 El-Sayed M, Choi YH, Frιdιrich M, Roytrakul S, Verpoorte R. Alkaloid accumulation in Catharanthus roseus cell suspension cultures fed with stemmadenine. Biotechnol Lett. 2004;26: 793–798. doi:10.1023/B:BILE.0000025879.53632.f2LINK
1372 El-Sayed M, Choi YH, Frιdιrich M, Roytrakul S, Verpoorte R. Alkaloid accumulation in Catharanthus roseus cell suspension cultures fed with stemmadenine. Biotechnol Lett. 2004;26: 793–798. doi:10.1023/B:BILE.0000025879.53632.f2LINK
1373 El-Sayed M, Choi YH, Frιdιrich M, Roytrakul S, Verpoorte R. Alkaloid accumulation in Catharanthus roseus cell suspension cultures fed with stemmadenine. Biotechnol Lett. 2004;26: 793–798. doi:10.1023/B:BILE.0000025879.53632.f2LINK
1374 El-Sayed M, Choi YH, Frιdιrich M, Roytrakul S, Verpoorte R. Alkaloid accumulation in Catharanthus roseus cell suspension cultures fed with stemmadenine. Biotechnol Lett. 2004;26: 793–798. doi:10.1023/B:BILE.0000025879.53632.f2LINK
1375 Ridaura-Sanz VE. Novel chromium carbonyl complexes of dihydropyridines and their application to the synthesis of dehydrosecodine. University of British Columbia. 1979.LINK
1376 Ridaura-Sanz VE. Novel chromium carbonyl complexes of dihydropyridines and their application to the synthesis of dehydrosecodine. University of British Columbia. 1979.LINK
1377 Ruszkowska J, Chrobak R, Maurin JK, Czarnocki Z. Vindoline and 16-demethoxyvindoline: two catharanthus-derived alkaloids. Acta Crystallogr. International Union of Crystallography; 2004;60: o377–o380. doi:10.1107/S0108270104004342LINK
1378 Ruszkowska J, Chrobak R, Maurin JK, Czarnocki Z. Vindoline and 16-demethoxyvindoline: two catharanthus-derived alkaloids. Acta Crystallogr. International Union of Crystallography; 2004;60: o377–o380. doi:10.1107/S0108270104004342LINK
1379 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
1380 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
1381 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
1382 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
1383 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
1384 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
1385 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
1386 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
1387 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1388 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1389 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1390 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1391 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1392 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1393 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1394 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1395 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1396 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1397 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1398 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
1399 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
1400 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
1401 Hodes ME, Rohn RJ, Bond WH, Yardley J. Clinical trials with leurosine methiodide, an alkaloid from Vinca rosea Linn. Cancer Chemother Reports. 1963;28: 53–55.LINK
1402 Hodes ME, Rohn RJ, Bond WH, Yardley J. Clinical trials with leurosine methiodide, an alkaloid from Vinca rosea Linn. Cancer Chemother Reports. 1963;28: 53–55.LINK
1403 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
1404 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
1405 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
1406 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
1407 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
1408 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
1409 Fisch KM. Biosynthesis of natural products by microbial iterative hybrid PKS–NRPS. RSC Adv. The Royal Society of Chemistry; 2013;3: 18228–18247. doi:10.1039/C3RA42661KLINK
1410 Fisch KM. Biosynthesis of natural products by microbial iterative hybrid PKS–NRPS. RSC Adv. The Royal Society of Chemistry; 2013;3: 18228–18247. doi:10.1039/C3RA42661KLINK
1411 Marfori EC, Kajiyama S, Fukusaki E, Kobayashi A. Trichosetin, a novel tetramic acid antibiotic produced in dual culture of Trichoderma harzianum and Catharanthus roseus Callus. Zeitschrift fόr Naturforsch. 2002;57: 465–470.LINK
1412 Marfori EC, Kajiyama S, Fukusaki E, Kobayashi A. Trichosetin, a novel tetramic acid antibiotic produced in dual culture of Trichoderma harzianum and Catharanthus roseus Callus. Zeitschrift fόr Naturforsch. 2002;57: 465–470.LINK
1413 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1414 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1415 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1416 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1417 Mustafa NR, Kim HK, Choi YH, Erkelens C, Lefeber AWM, Spijksma G, et al. Biosynthesis of salicylic acid in fungus elicited Catharanthus roseus cells. Phytochemistry. 2009;70: 532–539. doi:10.1016/j.phytochem.2009.01.009LINK
1418 Mustafa NR, Kim HK, Choi YH, Erkelens C, Lefeber AWM, Spijksma G, et al. Biosynthesis of salicylic acid in fungus elicited Catharanthus roseus cells. Phytochemistry. 2009;70: 532–539. doi:10.1016/j.phytochem.2009.01.009LINK
1419 Muljono RAB, Scheffer JJC, Verpoorte R. Effect of feeding salicylic acid on 2,3-dihydroxybenzoic acid formation in cultured cells of Catharanthus roseus. Pharm Biol. Informa UK Ltd UK; 2003;41: 284–290. doi:10.1076/phbi.41.4.284.15681LINK
1420 Muljono RAB, Scheffer JJC, Verpoorte R. Effect of feeding salicylic acid on 2,3-dihydroxybenzoic acid formation in cultured cells of Catharanthus roseus. Pharm Biol. Informa UK Ltd UK; 2003;41: 284–290. doi:10.1076/phbi.41.4.284.15681LINK
1421 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1422 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1423 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1424 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1425 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1426 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1427 Magnotta M, Murata J, Chen J, De Luca V. Expression of deacetylvindoline-4-O-acetyltransferase in Catharanthus roseus hairy roots. Phytochemistry. 2007;68: 1922–1931. doi:10.1016/j.phytochem.2007.04.037LINK
1428 Magnotta M, Murata J, Chen J, De Luca V. Expression of deacetylvindoline-4-O-acetyltransferase in Catharanthus roseus hairy roots. Phytochemistry. 2007;68: 1922–1931. doi:10.1016/j.phytochem.2007.04.037LINK
1429 Giddings L-A, Liscombe DK, Hamilton JP, Childs KL, DellaPenna D, Buell CR, et al. A stereoselective hydroxylation step of alkaloid biosynthesis by a unique cytochrome P450 in Catharanthus roseus. J Biol Chem. 2011;286: 16751–7. doi:10.1074/jbc.M111.225383LINK
1430 Giddings L-A, Liscombe DK, Hamilton JP, Childs KL, DellaPenna D, Buell CR, et al. A stereoselective hydroxylation step of alkaloid biosynthesis by a unique cytochrome P450 in Catharanthus roseus. J Biol Chem. 2011;286: 16751–7. doi:10.1074/jbc.M111.225383LINK
1431 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1432 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1433 Giddings L-A, Liscombe DK, Hamilton JP, Childs KL, DellaPenna D, Buell CR, et al. A stereoselective hydroxylation step of alkaloid biosynthesis by a unique cytochrome P450 in Catharanthus roseus. J Biol Chem. 2011;286: 16751–7. doi:10.1074/jbc.M111.225383LINK
1434 Giddings L-A, Liscombe DK, Hamilton JP, Childs KL, DellaPenna D, Buell CR, et al. A stereoselective hydroxylation step of alkaloid biosynthesis by a unique cytochrome P450 in Catharanthus roseus. J Biol Chem. 2011;286: 16751–7. doi:10.1074/jbc.M111.225383LINK
1435 Balsevich J, DeLuca V, Kurz WGW. Altered alkaloid pattern in dark grown seedlings of Catharanthus roseus. The isolation and characterization of 4-desacetoxyvindoline: A novel indole alkaloid and proposed precursor of vindoline. Heterocycles. 1986;24: 2415–2421. doi:10.3987/R-1986-09-2415LINK
1436 Balsevich J, DeLuca V, Kurz WGW. Altered alkaloid pattern in dark grown seedlings of Catharanthus roseus. The isolation and characterization of 4-desacetoxyvindoline: A novel indole alkaloid and proposed precursor of vindoline. Heterocycles. 1986;24: 2415–2421. doi:10.3987/R-1986-09-2415LINK
1437 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
1438 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
1439 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
1440 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
1441 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
1442 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
1443 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1444 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1445 Giddings L-A, Liscombe DK, Hamilton JP, Childs KL, DellaPenna D, Buell CR, et al. A stereoselective hydroxylation step of alkaloid biosynthesis by a unique cytochrome P450 in Catharanthus roseus. J Biol Chem. 2011;286: 16751–7. doi:10.1074/jbc.M111.225383LINK
1446 Giddings L-A, Liscombe DK, Hamilton JP, Childs KL, DellaPenna D, Buell CR, et al. A stereoselective hydroxylation step of alkaloid biosynthesis by a unique cytochrome P450 in Catharanthus roseus. J Biol Chem. 2011;286: 16751–7. doi:10.1074/jbc.M111.225383LINK
1447 Balsevich J, DeLuca V, Kurz WGW. Altered alkaloid pattern in dark grown seedlings of Catharanthus roseus. The isolation and characterization of 4-desacetoxyvindoline: A novel indole alkaloid and proposed precursor of vindoline. Heterocycles. 1986;24: 2415–2421. doi:10.3987/R-1986-09-2415LINK
1448 Balsevich J, DeLuca V, Kurz WGW. Altered alkaloid pattern in dark grown seedlings of Catharanthus roseus. The isolation and characterization of 4-desacetoxyvindoline: A novel indole alkaloid and proposed precursor of vindoline. Heterocycles. 1986;24: 2415–2421. doi:10.3987/R-1986-09-2415LINK
1449 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
1450 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
1451 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
1452 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
1453 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1454 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1455 Balsevich J, DeLuca V, Kurz WGW. Altered alkaloid pattern in dark grown seedlings of Catharanthus roseus. The isolation and characterization of 4-desacetoxyvindoline: A novel indole alkaloid and proposed precursor of vindoline. Heterocycles. 1986;24: 2415–2421. doi:10.3987/R-1986-09-2415LINK
1456 Balsevich J, DeLuca V, Kurz WGW. Altered alkaloid pattern in dark grown seedlings of Catharanthus roseus. The isolation and characterization of 4-desacetoxyvindoline: A novel indole alkaloid and proposed precursor of vindoline. Heterocycles. 1986;24: 2415–2421. doi:10.3987/R-1986-09-2415LINK
1457 Liscombe DK, O’Connor SE. A virus-induced gene silencing approach to understanding alkaloid metabolism in Catharanthus roseus. Phytochemistry. 2011;72: 1969–1977. doi:10.1016/j.phytochem.2011.07.001LINK
1458 Liscombe DK, O’Connor SE. A virus-induced gene silencing approach to understanding alkaloid metabolism in Catharanthus roseus. Phytochemistry. 2011;72: 1969–1977. doi:10.1016/j.phytochem.2011.07.001LINK
1459 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1460 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1461 Balsevich J, DeLuca V, Kurz WGW. Altered alkaloid pattern in dark grown seedlings of Catharanthus roseus. The isolation and characterization of 4-desacetoxyvindoline: A novel indole alkaloid and proposed precursor of vindoline. Heterocycles. 1986;24: 2415–2421. doi:10.3987/R-1986-09-2415LINK
1462 Balsevich J, DeLuca V, Kurz WGW. Altered alkaloid pattern in dark grown seedlings of Catharanthus roseus. The isolation and characterization of 4-desacetoxyvindoline: A novel indole alkaloid and proposed precursor of vindoline. Heterocycles. 1986;24: 2415–2421. doi:10.3987/R-1986-09-2415LINK
1463 Hisiger S, Jolicoeur M. Analysis of Catharanthus roseus alkaloids by HPLC. Phytochem Rev. 2007;6: 207–234. doi:10.1007/s11101-006-9036-yLINK
1464 Hisiger S, Jolicoeur M. Analysis of Catharanthus roseus alkaloids by HPLC. Phytochem Rev. 2007;6: 207–234. doi:10.1007/s11101-006-9036-yLINK
1465 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1466 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1467 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1468 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.1104/pp.125.1.189LINK
1469 Fujioka S, Noguchi T, Sekimoto M, Takatsuto S, Yoshida S. 28-Norcastasterone is biosynthesized from castasterone. Phytochemistry. 2000;55: 97–101. doi:10.1016/S0031-9422(00)00261-2LINK
1470 Fujioka S, Noguchi T, Sekimoto M, Takatsuto S, Yoshida S. 28-Norcastasterone is biosynthesized from castasterone. Phytochemistry. 2000;55: 97–101. doi:10.1016/S0031-9422(00)00261-2LINK
1471 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
1472 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
1473 Fujioka S, Noguchi T, Sekimoto M, Takatsuto S, Yoshida S. 28-Norcastasterone is biosynthesized from castasterone. Phytochemistry. 2000;55: 97–101. doi:10.1016/S0031-9422(00)00261-2LINK
1474 Fujioka S, Noguchi T, Sekimoto M, Takatsuto S, Yoshida S. 28-Norcastasterone is biosynthesized from castasterone. Phytochemistry. 2000;55: 97–101. doi:10.1016/S0031-9422(00)00261-2LINK
1475 Jordan MA, Himes RH, Wilson L. Comparison of the effects of vinblastine, vincristine, vindesine, and vinepidine on microtubule dynamics and cell proliferation in vitro. Cancer Res. 1985;45: 2741–2747.LINK
1476 Jordan MA, Himes RH, Wilson L. Comparison of the effects of vinblastine, vincristine, vindesine, and vinepidine on microtubule dynamics and cell proliferation in vitro. Cancer Res. 1985;45: 2741–2747.LINK
1477 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
1478 Saxton JE. Recent progress in the chemistry of indole alkaloids and mould metabolites. Nat Prod Rep. The Royal Society of Chemistry; 1985;2: 49. doi:10.1039/NP9850200049LINK
1479 Kohl W, Witte B, Sheldrick WS, H?fle G. Indole alkaloids from Catharanthus roseus tissue cultures IV1: 16R-19,20-E-isositsirikin, 16R-19,20-Z-isositsirikin and 21-hydroxycyclolochnerin. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1984;50: 242–244. doi:10.1055/s-2007-969688LINK
1480 Kohl W, Witte B, Sheldrick WS, H?fle G. Indole alkaloids from Catharanthus roseus tissue cultures IV1: 16R-19,20-E-isositsirikin, 16R-19,20-Z-isositsirikin and 21-hydroxycyclolochnerin. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1984;50: 242–244. doi:10.1055/s-2007-969688LINK
1481 Kohl W, Witte B, Sheldrick WS, H?fle G. Indole alkaloids from Catharanthus roseus tissue cultures IV1: 16R-19,20-E-isositsirikin, 16R-19,20-Z-isositsirikin and 21-hydroxycyclolochnerin. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1984;50: 242–244. doi:10.1055/s-2007-969688LINK
1482 Kohl W, Witte B, Sheldrick WS, H?fle G. Indole alkaloids from Catharanthus roseus tissue cultures IV1: 16R-19,20-E-isositsirikin, 16R-19,20-Z-isositsirikin and 21-hydroxycyclolochnerin. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1984;50: 242–244. doi:10.1055/s-2007-969688LINK
1483 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
1484 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
1485 Gautam S, Mishra A, Tiwari A. Catharanthus alkaloids and their enhanced production using elicitors: A review. Int J Pharm Technol. 2011;3: 713–724.LINK
1486 Gautam S, Mishra A, Tiwari A. Catharanthus alkaloids and their enhanced production using elicitors: A review. Int J Pharm Technol. 2011;3: 713–724.LINK
1487 Atta-ur-Rahman, Ali I, Bashir M. Gomaline-a new indolenine alkaloid from Catharanthus roseus. Heterocycles. 1984;22: 85–86. doi:10.3987/R-1984-01-0085LINK
1488 Atta-ur-Rahman, Ali I, Bashir M. Gomaline-a new indolenine alkaloid from Catharanthus roseus. Heterocycles. 1984;22: 85–86. doi:10.3987/R-1984-01-0085LINK
1489 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus. University of Karachi. 1985. p. 144.LINK
1490 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus. University of Karachi. 1985. p. 144.LINK
1491 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
1492 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
1493 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
1494 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
1495 El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids XXXIII. 21’-oxo-leurosine from Catharanthus roseus (apocynaceae). J Nat Prod. American Chemical Society; 1980;43: 157–161. doi:10.1021/np50007a016LINK
1496 El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids XXXIII. 21’-oxo-leurosine from Catharanthus roseus (apocynaceae). J Nat Prod. American Chemical Society; 1980;43: 157–161. doi:10.1021/np50007a016LINK
1497 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
1498 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
1499 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
1500 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
1501 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
1502 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
1503 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
1504 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
1505 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
1506 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
1507 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
1508 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
1509 NM RH, C DP. Fungal activity of various alkaloids isolated from Catharanthus roseus G. Don. Rev Cubana Med Trop. 1977;29: 147–152.LINK
1510 NM RH, C DP. Fungal activity of various alkaloids isolated from Catharanthus roseus G. Don. Rev Cubana Med Trop. 1977;29: 147–152.LINK
1511 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1512 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1513 NM RH, C DP. Fungal activity of various alkaloids isolated from Catharanthus roseus G. Don. Rev Cubana Med Trop. 1977;29: 147–152.LINK
1514 NM RH, C DP. Fungal activity of various alkaloids isolated from Catharanthus roseus G. Don. Rev Cubana Med Trop. 1977;29: 147–152.LINK
1515 Conrad RA, Cullinan GJ, Gerzon K, Poore GA. Structure-activity relationships of dimeric Catharanthus alkaloids. 2. Experimental antitumor activities of N-substituted deacetylvinblastine amide (vindesine) sulfates. J Med Chem. American Chemical Society; 1979;22: 391–400. doi:10.1021/jm00190a008LINK
1516 Conrad RA, Cullinan GJ, Gerzon K, Poore GA. Structure-activity relationships of dimeric Catharanthus alkaloids. 2. Experimental antitumor activities of N-substituted deacetylvinblastine amide (vindesine) sulfates. J Med Chem. American Chemical Society; 1979;22: 391–400. doi:10.1021/jm00190a008LINK
1517 Conrad RA, Cullinan GJ, Gerzon K, Poore GA. Structure-activity relationships of dimeric Catharanthus alkaloids. 2. Experimental antitumor activities of N-substituted deacetylvinblastine amide (vindesine) sulfates. J Med Chem. American Chemical Society; 1979;22: 391–400. doi:10.1021/jm00190a008LINK
1518 Conrad RA, Cullinan GJ, Gerzon K, Poore GA. Structure-activity relationships of dimeric Catharanthus alkaloids. 2. Experimental antitumor activities of N-substituted deacetylvinblastine amide (vindesine) sulfates. J Med Chem. American Chemical Society; 1979;22: 391–400. doi:10.1021/jm00190a008LINK
1519 Conrad RA, Cullinan GJ, Gerzon K, Poore GA. Structure-activity relationships of dimeric Catharanthus alkaloids. 2. Experimental antitumor activities of N-substituted deacetylvinblastine amide (vindesine) sulfates. J Med Chem. American Chemical Society; 1979;22: 391–400. doi:10.1021/jm00190a008LINK
1520 Conrad RA, Cullinan GJ, Gerzon K, Poore GA. Structure-activity relationships of dimeric Catharanthus alkaloids. 2. Experimental antitumor activities of N-substituted deacetylvinblastine amide (vindesine) sulfates. J Med Chem. American Chemical Society; 1979;22: 391–400. doi:10.1021/jm00190a008LINK
1521 Hussey RL, Newlon WM. High-performance liquid chromatographic and TLC determinations of desacetylvinblastine amide (vindesine) and its monosulfate salt. J Pharm Sci. 1978;67: 1319–1320. doi:10.1002/jps.2600670934LINK
1522 Hussey RL, Newlon WM. High-performance liquid chromatographic and TLC determinations of desacetylvinblastine amide (vindesine) and its monosulfate salt. J Pharm Sci. 1978;67: 1319–1320. doi:10.1002/jps.2600670934LINK
1523 Hussey RL, Newlon WM. High-performance liquid chromatographic and TLC determinations of desacetylvinblastine amide (vindesine) and its monosulfate salt. J Pharm Sci. 1978;67: 1319–1320. doi:10.1002/jps.2600670934LINK
1524 Hussey RL, Newlon WM. High-performance liquid chromatographic and TLC determinations of desacetylvinblastine amide (vindesine) and its monosulfate salt. J Pharm Sci. 1978;67: 1319–1320. doi:10.1002/jps.2600670934LINK
1525 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1526 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1527 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1528 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1529 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1530 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1531 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1532 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1533 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1534 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1535 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1536 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1537 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1538 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1539 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1540 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1541 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1542 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1543 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1544 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1545 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1546 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1547 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1548 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1549 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1550 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1551 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1552 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1553 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1554 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1555 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1556 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1557 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1558 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1559 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1560 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1561 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1562 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1563 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1564 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1565 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1566 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1567 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1568 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1569 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1570 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1571 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1572 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1573 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1574 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1575 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1576 Miller JC, Gutowski GE, Poore GA, Boder GB. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don). 38. 4’-dehydrated derivatives. J Med Chem. 1977;20: 409–413. doi:10.1021/jm00213a019LINK
1577 Rojas Hern?ndez NM, Cuellar Cuellar A. Microbiological analysis of vindolinina (an alkaloid isolated from Catharanthus roseus) and some of its structural changes. Rev Cubana Med Trop. 1976;28: 45–51.LINK
1578 Rojas Hern?ndez NM, Cuellar Cuellar A. Microbiological analysis of vindolinina (an alkaloid isolated from Catharanthus roseus) and some of its structural changes. Rev Cubana Med Trop. 1976;28: 45–51.LINK
1579 Tafur S, Jones WE, Dorman DE, Logsdon EE, Svoboda GH. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don) XXXVI: Isolation and characterization of new dimeric alkaloids. J Pharm Sci. 1975;64: 1953–1957. doi:10.1002/jps.2600641209LINK
1580 Tafur S, Jones WE, Dorman DE, Logsdon EE, Svoboda GH. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don) XXXVI: Isolation and characterization of new dimeric alkaloids. J Pharm Sci. 1975;64: 1953–1957. doi:10.1002/jps.2600641209LINK
1581 Tafur S, Jones WE, Dorman DE, Logsdon EE, Svoboda GH. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don) XXXVI: Isolation and characterization of new dimeric alkaloids. J Pharm Sci. 1975;64: 1953–1957. doi:10.1002/jps.2600641209LINK
1582 Tafur S, Jones WE, Dorman DE, Logsdon EE, Svoboda GH. Alkaloids of Vinca rosea L. (Catharanthus roseus G. Don) XXXVI: Isolation and characterization of new dimeric alkaloids. J Pharm Sci. 1975;64: 1953–1957. doi:10.1002/jps.2600641209LINK
1583 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
1584 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
1585 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1586 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1587 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
1588 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
1589 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
1590 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
1591 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1592 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1593 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1594 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1595 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1596 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1597 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1598 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1599 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1600 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1601 Ruiz-May E, Galaz-Avalos RM, Loyola-Vargas VM. Differential secretion and accumulation of terpene indole alkaloids in hairy roots of Catharanthus roseus treated with methyl jasmonate. Mol Biotechnol. 2009;41: 278–285. doi:10.1007/s12033-008-9111-2LINK
1602 Ruiz-May E, Galaz-Avalos RM, Loyola-Vargas VM. Differential secretion and accumulation of terpene indole alkaloids in hairy roots of Catharanthus roseus treated with methyl jasmonate. Mol Biotechnol. 2009;41: 278–285. doi:10.1007/s12033-008-9111-2LINK
1603 Ebrahimzadeh H, Noori-Dafoi AA-AM-R. The distribution of inole alkaloids in different organs of Catharanthus roseus G. Don. (Vinca rosea L). DARU Journal of Pharmaceutical Sciences. 1996. pp. 11–24.LINK
1604 Ebrahimzadeh H, Noori-Dafoi AA-AM-R. The distribution of inole alkaloids in different organs of Catharanthus roseus G. Don. (Vinca rosea L). DARU Journal of Pharmaceutical Sciences. 1996. pp. 11–24.LINK
1605 Atta-ur-Rahman, Sohail M, Albert K. Structural studies on vindolinine. Zeitschrift Fuer Naturforsch. 1986;41b: 386—392.LINK
1606 Atta-ur-Rahman, Sohail M, Albert K. Structural studies on vindolinine. Zeitschrift Fuer Naturforsch. 1986;41b: 386—392.LINK
1607 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1608 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1609 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1610 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1611 Bashir M, Kaleem S, Fatima T. 16-epi-19-S-vindolinine, an indoline alkaloid from Catharanthus roseus. Phytochemistry. 1983;22: 1021–1023. doi:10.1016/0031-9422(83)85046-8LINK
1612 Bashir M, Kaleem S, Fatima T. 16-epi-19-S-vindolinine, an indoline alkaloid from Catharanthus roseus. Phytochemistry. 1983;22: 1021–1023. doi:10.1016/0031-9422(83)85046-8LINK
1613 Zhou H, Tai Y, Sun C, Pan Y. Rapid identification of vinca alkaloids by direct-injection electrospray ionisation tandem mass spectrometry and confirmation by high-performance liquid chromatography-mass spectrometry. Phytochem Anal. 2005;16: 328–333. doi:10.1002/pca.852LINK
1614 Zhou H, Tai Y, Sun C, Pan Y. Rapid identification of vinca alkaloids by direct-injection electrospray ionisation tandem mass spectrometry and confirmation by high-performance liquid chromatography-mass spectrometry. Phytochem Anal. 2005;16: 328–333. doi:10.1002/pca.852LINK
1615 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1616 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1617 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
1618 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
1619 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
1620 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
1621 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
1622 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
1623 Mukhopadhyay S, El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids XXXVII. 16-Epi-Z-isositsirikine, a monomeric indole alkaloid with antineoplastic activity from Catharanthus roseus and Rhazya stricta. J Nat Prod. 1983;46: 409–413. doi:10.1021/np50027a019LINK
1624 Mukhopadhyay S, El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids XXXVII. 16-Epi-Z-isositsirikine, a monomeric indole alkaloid with antineoplastic activity from Catharanthus roseus and Rhazya stricta. J Nat Prod. 1983;46: 409–413. doi:10.1021/np50027a019LINK
1625 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1626 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1627 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
1628 Ali I, Bashir M. Isolation of Rhazimol from the Leaves of Catharanthus roseus. J Nat Prod. American Chemical Society; 1984;47: 389–389. doi:10.1021/np50032a032LINK
1629 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
1630 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
1631 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1632 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1633 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1634 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1635 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1636 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1637 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1638 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1639 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1640 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1641 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1642 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1643 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1644 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1645 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1646 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1647 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1648 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1649 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1650 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1651 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1652 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1653 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1654 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1655 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1656 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1657 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1658 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1659 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1660 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1661 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1662 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1663 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1664 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1665 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1666 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1667 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1668 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1669 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1670 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1671 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1672 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1673 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1674 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1675 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1676 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1677 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1678 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1679 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1680 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1681 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1682 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1683 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1684 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1685 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1686 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1687 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1688 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1689 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1690 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1691 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1692 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1693 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1694 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1695 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1696 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1697 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1698 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1699 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1700 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1701 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1702 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1703 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1704 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1705 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1706 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1707 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1708 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1709 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1710 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1711 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1712 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1713 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1714 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1715 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1716 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1717 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
1718 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
1719 Rueffer M, Kan-Fan C, Husson H-P, Stockigt J, Zenk MH. 4,21-Dehydrogeissoschizine, an intermediate in heteroyohimbine alkaloid biosynthesis. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1979; 1016–1018. doi:10.1039/C39790001016LINK
1720 Rueffer M, Kan-Fan C, Husson H-P, Stockigt J, Zenk MH. 4,21-Dehydrogeissoschizine, an intermediate in heteroyohimbine alkaloid biosynthesis. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1979; 1016–1018. doi:10.1039/C39790001016LINK
1721 Rueffer M, Kan-Fan C, Husson H-P, Stockigt J, Zenk MH. 4,21-Dehydrogeissoschizine, an intermediate in heteroyohimbine alkaloid biosynthesis. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1979; 1016–1018. doi:10.1039/C39790001016LINK
1722 Rueffer M, Kan-Fan C, Husson H-P, Stockigt J, Zenk MH. 4,21-Dehydrogeissoschizine, an intermediate in heteroyohimbine alkaloid biosynthesis. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1979; 1016–1018. doi:10.1039/C39790001016LINK
1723 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1724 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1725 Rueffer M, Kan-Fan C, Husson H-P, Stockigt J, Zenk MH. 4,21-Dehydrogeissoschizine, an intermediate in heteroyohimbine alkaloid biosynthesis. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1979; 1016–1018. doi:10.1039/C39790001016LINK
1726 Rueffer M, Kan-Fan C, Husson H-P, Stockigt J, Zenk MH. 4,21-Dehydrogeissoschizine, an intermediate in heteroyohimbine alkaloid biosynthesis. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1979; 1016–1018. doi:10.1039/C39790001016LINK
1727 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
1728 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
1729 Lakshmi V, Agarwal SK, Mahdi AA, Mishra V, Pandey HP, Palit G. Vincamine and vindoline from Catharanthus roseus linn. protects the gastric mucosa of gastric ulcer in rats. Pharmacologia. 2013;4: 243–248. doi:10.5567/pharmacologia.2013.243.248LINK
1730 Lakshmi V, Agarwal SK, Mahdi AA, Mishra V, Pandey HP, Palit G. Vincamine and vindoline from Catharanthus roseus linn. protects the gastric mucosa of gastric ulcer in rats. Pharmacologia. 2013;4: 243–248. doi:10.5567/pharmacologia.2013.243.248LINK
1731 Sohajda T, Varga E, Iv?nyi R, Fejos I, Szente L, Nosz?l B, et al. Separation of vinca alkaloid enantiomers by capillary electrophoresis applying cyclodextrin derivatives and characterization of cyclodextrin complexes by nuclear magnetic resonance spectroscopy. J Pharm Biomed Anal. 2010;53: 1258–1266. doi:10.1016/j.jpba.2010.07.032LINK
1732 Sohajda T, Varga E, Iv?nyi R, Fejos I, Szente L, Nosz?l B, et al. Separation of vinca alkaloid enantiomers by capillary electrophoresis applying cyclodextrin derivatives and characterization of cyclodextrin complexes by nuclear magnetic resonance spectroscopy. J Pharm Biomed Anal. 2010;53: 1258–1266. doi:10.1016/j.jpba.2010.07.032LINK
1733 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1734 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
1735 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1736 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1737 Huang L, Li J, Ye H, Li C, Wang H, Liu B, et al. Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus. Planta. 2012;236: 1571–1581. doi:10.1007/s00425-012-1712-0LINK
1738 Huang L, Li J, Ye H, Li C, Wang H, Liu B, et al. Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus. Planta. 2012;236: 1571–1581. doi:10.1007/s00425-012-1712-0LINK
1739 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1740 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1741 Zhou J, Xie G, Yan X. Encyclopedia of Traditional Chinese Medicines - Molecular Structures, Pharmacological Activities, Natural Sources and Applications: Vol. 1: Isolated Compounds A-C. Springer Berlin Heidelberg; 2011. p. 557. ISBN: 9783642167355.LINK
1742 Zhou J, Xie G, Yan X. Encyclopedia of Traditional Chinese Medicines - Molecular Structures, Pharmacological Activities, Natural Sources and Applications: Vol. 1: Isolated Compounds A-C. Springer Berlin Heidelberg; 2011. p. 557. ISBN: 9783642167355.LINK
1743 Kuppusamy C, Murugan K, Arul N, Yasodha P. Larvicidal and insect growth regulator effect of ?-amyrin acetate from Catharanthus Roseus Linn against the malaria vector Anopheles Stephensi Liston (Diptera: Culicidae). Entomol Res. 2009;39: 78–83. doi:10.1111/j.1748-5967.2009.00196.xLINK
1744 Kuppusamy C, Murugan K, Arul N, Yasodha P. Larvicidal and insect growth regulator effect of ?-amyrin acetate from Catharanthus Roseus Linn against the malaria vector Anopheles Stephensi Liston (Diptera: Culicidae). Entomol Res. 2009;39: 78–83. doi:10.1111/j.1748-5967.2009.00196.xLINK
1745 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1746 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1747 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1748 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1749 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
1750 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
1751 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
1752 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
1753 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1754 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1755 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
1756 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
1757 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
1758 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
1759 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1760 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1761 Yuana, Dignum MJW, Verpoorte R. Glucosylation of exogenous vanillin by plant cell cultures. Plant Cell Tissue Organ Cult. 2002;69: 177–182. doi:10.1023/A:1015224425075LINK
1762 Yuana, Dignum MJW, Verpoorte R. Glucosylation of exogenous vanillin by plant cell cultures. Plant Cell Tissue Organ Cult. 2002;69: 177–182. doi:10.1023/A:1015224425075LINK
1763 Murata J, Roepke J, Gordon H, De Luca V. The leaf epidermome of Catharanthus roseus reveals its biochemical specialization. Plant Cell. 2008;20: 524–542. doi:10.?1105/?tpc.?107.?056630LINK
1764 Murata J, Roepke J, Gordon H, De Luca V. The leaf epidermome of Catharanthus roseus reveals its biochemical specialization. Plant Cell. 2008;20: 524–542. doi:10.?1105/?tpc.?107.?056630LINK
1765 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1766 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1767 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
1768 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
1769 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1770 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1771 Murata J, Roepke J, Gordon H, De Luca V. The leaf epidermome of Catharanthus roseus reveals its biochemical specialization. Plant Cell. 2008;20: 524–542. doi:10.?1105/?tpc.?107.?056630LINK
1772 Murata J, Roepke J, Gordon H, De Luca V. The leaf epidermome of Catharanthus roseus reveals its biochemical specialization. Plant Cell. 2008;20: 524–542. doi:10.?1105/?tpc.?107.?056630LINK
1773 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1774 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1775 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
1776 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
1777 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1778 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1779 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1780 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1781 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1782 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1783 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1784 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1785 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1786 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1787 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1788 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1789 Stockigt J, Husson HP, Kan-Fan C, Zenk MH. Cathenamine, a central intermediate in the cell free biosynthesis of ajmalicine and related indole alkaloids. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1977; 164–166. doi:10.1039/C39770000164LINK
1790 Stockigt J, Husson HP, Kan-Fan C, Zenk MH. Cathenamine, a central intermediate in the cell free biosynthesis of ajmalicine and related indole alkaloids. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1977; 164–166. doi:10.1039/C39770000164LINK
1791 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1792 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1793 Yuana, Dignum MJW, Verpoorte R. Glucosylation of exogenous vanillin by plant cell cultures. Plant Cell Tissue Organ Cult. 2002;69: 177–182. doi:10.1023/A:1015224425075LINK
1794 Yuana, Dignum MJW, Verpoorte R. Glucosylation of exogenous vanillin by plant cell cultures. Plant Cell Tissue Organ Cult. 2002;69: 177–182. doi:10.1023/A:1015224425075LINK
1795 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1796 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1797 Yuana, Dignum MJW, Verpoorte R. Glucosylation of exogenous vanillin by plant cell cultures. Plant Cell Tissue Organ Cult. 2002;69: 177–182. doi:10.1023/A:1015224425075LINK
1798 Yuana, Dignum MJW, Verpoorte R. Glucosylation of exogenous vanillin by plant cell cultures. Plant Cell Tissue Organ Cult. 2002;69: 177–182. doi:10.1023/A:1015224425075LINK
1799 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1800 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1801 Yuana, Dignum MJW, Verpoorte R. Glucosylation of exogenous vanillin by plant cell cultures. Plant Cell Tissue Organ Cult. 2002;69: 177–182. doi:10.1023/A:1015224425075LINK
1802 Yuana, Dignum MJW, Verpoorte R. Glucosylation of exogenous vanillin by plant cell cultures. Plant Cell Tissue Organ Cult. 2002;69: 177–182. doi:10.1023/A:1015224425075LINK
1803 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1804 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1805 Yuana, Dignum MJW, Verpoorte R. Glucosylation of exogenous vanillin by plant cell cultures. Plant Cell Tissue Organ Cult. 2002;69: 177–182. doi:10.1023/A:1015224425075LINK
1806 Yuana, Dignum MJW, Verpoorte R. Glucosylation of exogenous vanillin by plant cell cultures. Plant Cell Tissue Organ Cult. 2002;69: 177–182. doi:10.1023/A:1015224425075LINK
1807 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1808 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Ye W-C. Three new monomeric indole alkaloids from the roots of Catharanthus roseus. J Asian Nat Prod Res. 2012;14: 249–255. doi:10.1080/10286020.2011.649728LINK
1809 Proestos C, Chorianopoulos N, Nychas G-JE, Komaitis M. RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity. J Agric Food Chem. American Chemical Society; 2005;53: 1190–1195. doi:10.1021/jf040083tLINK
1810 Proestos C, Chorianopoulos N, Nychas G-JE, Komaitis M. RP-HPLC analysis of the phenolic compounds of plant extracts. investigation of their antioxidant capacity and antimicrobial activity. J Agric Food Chem. American Chemical Society; 2005;53: 1190–1195. doi:10.1021/jf040083tLINK
1811 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1812 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1813 Yamane S, Shimoda K, Watanabe K, Hirata T. Purification and characterization of gentisic acid glucosyltransferase from the cultured cells of Catharanthus roseus. J Mol Catal B Enzym. 2002;17: 59–63. doi:10.1016/S1381-1177(02)00005-XLINK
1814 Yamane S, Shimoda K, Watanabe K, Hirata T. Purification and characterization of gentisic acid glucosyltransferase from the cultured cells of Catharanthus roseus. J Mol Catal B Enzym. 2002;17: 59–63. doi:10.1016/S1381-1177(02)00005-XLINK
1815 Shimoda K, Kubota N, Sano T, Hirakawa H, Hirata T. A novel hydroxylase from Catharanthus roseus participating in the hydroxylation of 2-hydroxybenzoic acid. J Biosci Bioeng. 2004;98: 67–70. doi:10.1016/S1389-1723(04)70244-3LINK
1816 Shimoda K, Kubota N, Sano T, Hirakawa H, Hirata T. A novel hydroxylase from Catharanthus roseus participating in the hydroxylation of 2-hydroxybenzoic acid. J Biosci Bioeng. 2004;98: 67–70. doi:10.1016/S1389-1723(04)70244-3LINK
1817 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1818 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1819 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1820 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1821 Yamane S, Shimoda K, Watanabe K, Hirata T. Purification and characterization of gentisic acid glucosyltransferase from the cultured cells of Catharanthus roseus. J Mol Catal B Enzym. 2002;17: 59–63. doi:10.1016/S1381-1177(02)00005-XLINK
1822 Yamane S, Shimoda K, Watanabe K, Hirata T. Purification and characterization of gentisic acid glucosyltransferase from the cultured cells of Catharanthus roseus. J Mol Catal B Enzym. 2002;17: 59–63. doi:10.1016/S1381-1177(02)00005-XLINK
1823 Shimoda K, Kubota N, Sano T, Hirakawa H, Hirata T. A novel hydroxylase from Catharanthus roseus participating in the hydroxylation of 2-hydroxybenzoic acid. J Biosci Bioeng. 2004;98: 67–70. doi:10.1016/S1389-1723(04)70244-3LINK
1824 Shimoda K, Kubota N, Sano T, Hirakawa H, Hirata T. A novel hydroxylase from Catharanthus roseus participating in the hydroxylation of 2-hydroxybenzoic acid. J Biosci Bioeng. 2004;98: 67–70. doi:10.1016/S1389-1723(04)70244-3LINK
1825 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
1826 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
1827 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1828 Mustafa NR. Retrobiosynthetic study of salicylic acid in Catharanthus roseus cell suspension cultures. Department of Pharmacognosy, Section Metabolomics, Institute of Biology, Faculty of Science, Leiden University. 2007. p. 128.LINK
1829 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
1830 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
1831 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
1832 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
1833 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
1834 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
1835 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
1836 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
1837 Fujimoto Y, Sato N, Iwai K, Hamada H, Yamada J, Morisaki M. Stereochemistry of the reduction of 24-methyldesmosterol to campesterol and dihydrobrassicasterol in higher plants. Chem Commun. The Royal Society of Chemistry; 1997; 681–682. doi:10.1039/A700492CLINK
1838 Fujimoto Y, Sato N, Iwai K, Hamada H, Yamada J, Morisaki M. Stereochemistry of the reduction of 24-methyldesmosterol to campesterol and dihydrobrassicasterol in higher plants. Chem Commun. The Royal Society of Chemistry; 1997; 681–682. doi:10.1039/A700492CLINK
1839 Fujimoto Y, Sato N, Iwai K, Hamada H, Yamada J, Morisaki M. Stereochemistry of the reduction of 24-methyldesmosterol to campesterol and dihydrobrassicasterol in higher plants. Chem Commun. The Royal Society of Chemistry; 1997; 681–682. doi:10.1039/A700492CLINK
1840 Fujimoto Y, Sato N, Iwai K, Hamada H, Yamada J, Morisaki M. Stereochemistry of the reduction of 24-methyldesmosterol to campesterol and dihydrobrassicasterol in higher plants. Chem Commun. The Royal Society of Chemistry; 1997; 681–682. doi:10.1039/A700492CLINK
1841 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1842 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
1843 Fahn W, Kaiser V, Schόbel H, St?ckigt J, Danieli B. Catharanthus roseus enzyme mediated synthesis of 3-hydroxyvoafrine A and B-A simple route to the voafrines. Phytochemistry. 1990;29: 127–133. doi:10.1016/0031-9422(90)89025-5LINK
1844 Fahn W, Kaiser V, Schόbel H, St?ckigt J, Danieli B. Catharanthus roseus enzyme mediated synthesis of 3-hydroxyvoafrine A and B-A simple route to the voafrines. Phytochemistry. 1990;29: 127–133. doi:10.1016/0031-9422(90)89025-5LINK
1845 Fahn W, Kaiser V, Schόbel H, St?ckigt J, Danieli B. Catharanthus roseus enzyme mediated synthesis of 3-hydroxyvoafrine A and B-A simple route to the voafrines. Phytochemistry. 1990;29: 127–133. doi:10.1016/0031-9422(90)89025-5LINK
1846 Fahn W, Kaiser V, Schόbel H, St?ckigt J, Danieli B. Catharanthus roseus enzyme mediated synthesis of 3-hydroxyvoafrine A and B-A simple route to the voafrines. Phytochemistry. 1990;29: 127–133. doi:10.1016/0031-9422(90)89025-5LINK
1847 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1848 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
1849 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1850 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
1851 yora-Talavera T, Chappell J, Lozoya-Gloria E, Loyola-Vargas VM. Overexpression in Catharanthus roseus hairy roots of a truncated hamster 3-hydroxy-3-methylglutaryl-CoA reductase gene. Appl Biochem Biotechnol. 2002;97: 135–146. doi:10.1385/ABAB:97:2:135LINK
1852 yora-Talavera T, Chappell J, Lozoya-Gloria E, Loyola-Vargas VM. Overexpression in Catharanthus roseus hairy roots of a truncated hamster 3-hydroxy-3-methylglutaryl-CoA reductase gene. Appl Biochem Biotechnol. 2002;97: 135–146. doi:10.1385/ABAB:97:2:135LINK
1853 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
1854 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
1855 Fujimoto Y, Sato N, Iwai K, Hamada H, Yamada J, Morisaki M. Stereochemistry of the reduction of 24-methyldesmosterol to campesterol and dihydrobrassicasterol in higher plants. Chem Commun. The Royal Society of Chemistry; 1997; 681–682. doi:10.1039/A700492CLINK
1856 Fujimoto Y, Sato N, Iwai K, Hamada H, Yamada J, Morisaki M. Stereochemistry of the reduction of 24-methyldesmosterol to campesterol and dihydrobrassicasterol in higher plants. Chem Commun. The Royal Society of Chemistry; 1997; 681–682. doi:10.1039/A700492CLINK
1857 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1858 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1859 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1860 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1861 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1862 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1863 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1864 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1865 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1866 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1867 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
1868 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
1869 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1870 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1871 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1872 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1873 Fujioka S, Noguchi T, Sekimoto M, Takatsuto S, Yoshida S. 28-Norcastasterone is biosynthesized from castasterone. Phytochemistry. 2000;55: 97–101. doi:10.1016/S0031-9422(00)00261-2LINK
1874 Fujioka S, Noguchi T, Sekimoto M, Takatsuto S, Yoshida S. 28-Norcastasterone is biosynthesized from castasterone. Phytochemistry. 2000;55: 97–101. doi:10.1016/S0031-9422(00)00261-2LINK
1875 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1876 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
1877 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1878 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1879 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1880 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1881 Riedel B, Morr M, Wu W-I, Carman GM, Wissing JB. Metabolism of diacylglycerol pyrophosphate by suspension cultured Catharanthus roseus cells. Plant Sci. 1997;128: 1–10. doi:10.1016/S0168-9452(97)00120-9LINK
1882 Riedel B, Morr M, Wu W-I, Carman GM, Wissing JB. Metabolism of diacylglycerol pyrophosphate by suspension cultured Catharanthus roseus cells. Plant Sci. 1997;128: 1–10. doi:10.1016/S0168-9452(97)00120-9LINK
1883 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1884 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1885 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1886 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1887 Meijer AH, Pennings EJM, Waal A De, Verpoorte R. Purification of Cytochrome P-450-Dependent Geraniol-10-Hydroxylase from a Cell Suspension Culture of Catharanthus Roseus. In: Nijkamp HJJ, Van Der Plas LHW, Van Aartrijk J, editors. Progress in Plant Cellular and Molecular Biology. Dordrecht: Springer Netherlands; 1990. pp. 769–774. doi:10.1007/978-94-009-2103-0
1888 Meijer AH, Pennings EJM, Waal A De, Verpoorte R. Purification of Cytochrome P-450-Dependent Geraniol-10-Hydroxylase from a Cell Suspension Culture of Catharanthus Roseus. In: Nijkamp HJJ, Van Der Plas LHW, Van Aartrijk J, editors. Progress in Plant Cellular and Molecular Biology. Dordrecht: Springer Netherlands; 1990. pp. 769–774. doi:10.1007/978-94-009-2103-0
1889 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1890 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1891 Meijer AH, Pennings EJM, Waal A De, Verpoorte R. Purification of Cytochrome P-450-Dependent Geraniol-10-Hydroxylase from a Cell Suspension Culture of Catharanthus Roseus. In: Nijkamp HJJ, Van Der Plas LHW, Van Aartrijk J, editors. Progress in Plant Cellular and Molecular Biology. Dordrecht: Springer Netherlands; 1990. pp. 769–774. doi:10.1007/978-94-009-2103-0
1892 Meijer AH, Pennings EJM, Waal A De, Verpoorte R. Purification of Cytochrome P-450-Dependent Geraniol-10-Hydroxylase from a Cell Suspension Culture of Catharanthus Roseus. In: Nijkamp HJJ, Van Der Plas LHW, Van Aartrijk J, editors. Progress in Plant Cellular and Molecular Biology. Dordrecht: Springer Netherlands; 1990. pp. 769–774. doi:10.1007/978-94-009-2103-0
1893 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1894 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1895 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1896 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1897 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1898 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1899 Fujimoto Y, Sato N, Sekiyama Y, Ito M, Suzuki T, Hamada H, et al. Metabolic origin of c-26 and c-27 of isofucosterol in tissue cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 1998;11: 207–210. doi:10.1080/10575639808044948LINK
1900 Fujimoto Y, Sato N, Sekiyama Y, Ito M, Suzuki T, Hamada H, et al. Metabolic origin of c-26 and c-27 of isofucosterol in tissue cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 1998;11: 207–210. doi:10.1080/10575639808044948LINK
1901 Fujimoto Y, Sato N, Sekiyama Y, Ito M, Suzuki T, Hamada H, et al. Metabolic origin of c-26 and c-27 of isofucosterol in tissue cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 1998;11: 207–210. doi:10.1080/10575639808044948LINK
1902 Fujimoto Y, Sato N, Sekiyama Y, Ito M, Suzuki T, Hamada H, et al. Metabolic origin of c-26 and c-27 of isofucosterol in tissue cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 1998;11: 207–210. doi:10.1080/10575639808044948LINK
1903 Fujimoto Y, Sato N, Sekiyama Y, Ito M, Suzuki T, Hamada H, et al. Metabolic origin of c-26 and c-27 of isofucosterol in tissue cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 1998;11: 207–210. doi:10.1080/10575639808044948LINK
1904 Fujimoto Y, Sato N, Sekiyama Y, Ito M, Suzuki T, Hamada H, et al. Metabolic origin of c-26 and c-27 of isofucosterol in tissue cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 1998;11: 207–210. doi:10.1080/10575639808044948LINK
1905 Fujimoto Y, Sato N, Sekiyama Y, Ito M, Suzuki T, Hamada H, et al. Metabolic origin of c-26 and c-27 of isofucosterol in tissue cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 1998;11: 207–210. doi:10.1080/10575639808044948LINK
1906 Fujimoto Y, Sato N, Sekiyama Y, Ito M, Suzuki T, Hamada H, et al. Metabolic origin of c-26 and c-27 of isofucosterol in tissue cultures of Catharanthus roseus. Nat Prod Lett. Taylor & Francis Group; 1998;11: 207–210. doi:10.1080/10575639808044948LINK
1907 Obtrandon-OBat TRAdisional iNDONesia.LINK
1908 Obtrandon-OBat TRAdisional iNDONesia.LINK
1909 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1910 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1911 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1912 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1913 Duke JA. Handbook of Phytochemical Constituents of GRAS Herbs and Other Economic Plants: Herbal Reference Library. Taylor & Francis; 2000. p. 654. ISBN: 9780849338656.LINK
1914 Duke JA. Handbook of Phytochemical Constituents of GRAS Herbs and Other Economic Plants: Herbal Reference Library. Taylor & Francis; 2000. p. 654. ISBN: 9780849338656.LINK
1915 Duke JA. Handbook of Phytochemical Constituents of GRAS Herbs and Other Economic Plants: Herbal Reference Library. Taylor & Francis; 2000. p. 654. ISBN: 9780849338656.LINK
1916 Duke JA. Handbook of Phytochemical Constituents of GRAS Herbs and Other Economic Plants: Herbal Reference Library. Taylor & Francis; 2000. p. 654. ISBN: 9780849338656.LINK
1917 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1918 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1919 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1920 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1921 Moreno PR, van der Heijden R, Verpoorte R. Effect of terpenoid precursor feeding and elicitation on formation of indole alkaloids in cell suspension cultures of Catharanthus roseus. Plant Cell Rep. 1993;12: 702–705. doi:10.1007/BF00233423LINK
1922 Moreno PR, van der Heijden R, Verpoorte R. Effect of terpenoid precursor feeding and elicitation on formation of indole alkaloids in cell suspension cultures of Catharanthus roseus. Plant Cell Rep. 1993;12: 702–705. doi:10.1007/BF00233423LINK
1923 Maccarthy JJ, Stumpf PK. Fatty-acid composition and biosynthesis in cell suspension cultures of Glycine max (L.) Merr., Catharanthus roseus G. Don and Nicotiana tabacum L. Planta. 1980;147: 384–388. doi:10.1007/BF00380177LINK
1924 Maccarthy JJ, Stumpf PK. Fatty-acid composition and biosynthesis in cell suspension cultures of Glycine max (L.) Merr., Catharanthus roseus G. Don and Nicotiana tabacum L. Planta. 1980;147: 384–388. doi:10.1007/BF00380177LINK
1925 Hamada H, Fuchikami Y, Ikematsu Y, Hirata T, Williams HJ, Scott AI. Hydroxylation of piperitone by cell suspension cultures of Catharanthus roseus. Phytochemistry. 1994;37: 1037–1038. doi:10.1016/S0031-9422(00)89524-2LINK
1926 Hamada H, Fuchikami Y, Ikematsu Y, Hirata T, Williams HJ, Scott AI. Hydroxylation of piperitone by cell suspension cultures of Catharanthus roseus. Phytochemistry. 1994;37: 1037–1038. doi:10.1016/S0031-9422(00)89524-2LINK
1927 Kumar S, Varman P, Kumari B. Identification of differentially expressed proteins in response to Pb stress in Catharanthus roseus. African J Environ Sci Technol. Academic Journals; 2011;5: 689–699.LINK
1928 Kumar S, Varman P, Kumari B. Identification of differentially expressed proteins in response to Pb stress in Catharanthus roseus. African J Environ Sci Technol. Academic Journals; 2011;5: 689–699.LINK
1929 India OTA of. The Journal of the Oil Technologists’ Association of India. Colour Publications Limited; 1986.NA
1930 India OTA of. The Journal of the Oil Technologists’ Association of India. Colour Publications Limited; 1986.NA
1931 Murata J, Roepke J, Gordon H, De Luca V. The leaf epidermome of Catharanthus roseus reveals its biochemical specialization. Plant Cell. 2008;20: 524–542. doi:10.?1105/?tpc.?107.?056630LINK
1932 Murata J, Roepke J, Gordon H, De Luca V. The leaf epidermome of Catharanthus roseus reveals its biochemical specialization. Plant Cell. 2008;20: 524–542. doi:10.?1105/?tpc.?107.?056630LINK
1933 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1934 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
1935 Guarnaccia R, Botta L, Coscia CJ. Biosynthesis of acidic iridoid monoterpene glucosides in Vinca Rosea. J Am Chem Soc. American Chemical Society; 1974;96: 7079–7084. doi:10.1021/ja00829a041LINK
1936 Guarnaccia R, Botta L, Coscia CJ. Biosynthesis of acidic iridoid monoterpene glucosides in Vinca Rosea. J Am Chem Soc. American Chemical Society; 1974;96: 7079–7084. doi:10.1021/ja00829a041LINK
1937 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
1938 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
1939 yora-Talavera T, Chappell J, Lozoya-Gloria E, Loyola-Vargas VM. Overexpression in Catharanthus roseus hairy roots of a truncated hamster 3-hydroxy-3-methylglutaryl-CoA reductase gene. Appl Biochem Biotechnol. 2002;97: 135–146. doi:10.1385/ABAB:97:2:135LINK
1940 yora-Talavera T, Chappell J, Lozoya-Gloria E, Loyola-Vargas VM. Overexpression in Catharanthus roseus hairy roots of a truncated hamster 3-hydroxy-3-methylglutaryl-CoA reductase gene. Appl Biochem Biotechnol. 2002;97: 135–146. doi:10.1385/ABAB:97:2:135LINK
1941 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
1942 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
1943 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1944 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1945 Scott IM, Horgan R, McGaw BA. Zeatin-9-glucoside, a major endogenous cytokinin of Vinca rosea L. crown gall tissue. Planta. 1980;149: 472–475. doi:10.1007/BF00385750LINK
1946 Scott IM, Horgan R, McGaw BA. Zeatin-9-glucoside, a major endogenous cytokinin of Vinca rosea L. crown gall tissue. Planta. 1980;149: 472–475. doi:10.1007/BF00385750LINK
1947 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1948 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1949 Scott IM, Horgan R, McGaw BA. Zeatin-9-glucoside, a major endogenous cytokinin of Vinca rosea L. crown gall tissue. Planta. 1980;149: 472–475. doi:10.1007/BF00385750LINK
1950 Scott IM, Horgan R, McGaw BA. Zeatin-9-glucoside, a major endogenous cytokinin of Vinca rosea L. crown gall tissue. Planta. 1980;149: 472–475. doi:10.1007/BF00385750LINK
1951 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1952 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1953 Scott IM, Horgan R, McGaw BA. Zeatin-9-glucoside, a major endogenous cytokinin of Vinca rosea L. crown gall tissue. Planta. 1980;149: 472–475. doi:10.1007/BF00385750LINK
1954 Scott IM, Horgan R, McGaw BA. Zeatin-9-glucoside, a major endogenous cytokinin of Vinca rosea L. crown gall tissue. Planta. 1980;149: 472–475. doi:10.1007/BF00385750LINK
1955 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1956 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1957 Scott IM, Horgan R, McGaw BA. Zeatin-9-glucoside, a major endogenous cytokinin of Vinca rosea L. crown gall tissue. Planta. 1980;149: 472–475. doi:10.1007/BF00385750LINK
1958 Scott IM, Horgan R, McGaw BA. Zeatin-9-glucoside, a major endogenous cytokinin of Vinca rosea L. crown gall tissue. Planta. 1980;149: 472–475. doi:10.1007/BF00385750LINK
1959 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1960 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1961 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1962 Stuchbury T, Palni LM, Horgan R, Wareing PF. The biosynthesis of cytokinins in crown-gall tissue of Vinca rosea. Planta. 1979;147: 97–102. doi:10.1007/BF00389507LINK
1963 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1964 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1965 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1966 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1967 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1968 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1969 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1970 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1971 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1972 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1973 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1974 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1975 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1976 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
1977 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1978 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
1979 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1980 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1981 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1982 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
1983 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1984 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1985 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1986 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1987 Maccarthy JJ, Stumpf PK. Fatty-acid composition and biosynthesis in cell suspension cultures of Glycine max (L.) Merr., Catharanthus roseus G. Don and Nicotiana tabacum L. Planta. 1980;147: 384–388. doi:10.1007/BF00380177LINK
1988 Maccarthy JJ, Stumpf PK. Fatty-acid composition and biosynthesis in cell suspension cultures of Glycine max (L.) Merr., Catharanthus roseus G. Don and Nicotiana tabacum L. Planta. 1980;147: 384–388. doi:10.1007/BF00380177LINK
1989 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1990 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1991 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1992 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1993 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1994 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1995 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1996 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1997 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1998 Satyan RS, Malarvannan S, Eganathan P, Rajalakshmi S, Parida A. Growth inhibitory activity of fatty acid methyl esters in the whole seed oil of madagascar periwinkle (Apocyanaceae) against Helicoverpa armigera (Lepidoptera: Noctuidae). J Econ Entomol. 2009;102: 1197–1202.LINK
1999 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
2000 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
2001 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2002 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2003 Huang L, Li J, Ye H, Li C, Wang H, Liu B, et al. Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus. Planta. 2012;236: 1571–1581. doi:10.1007/s00425-012-1712-0LINK
2004 Huang L, Li J, Ye H, Li C, Wang H, Liu B, et al. Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus. Planta. 2012;236: 1571–1581. doi:10.1007/s00425-012-1712-0LINK
2005 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2006 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2007 Panneerselvam C, Murugan K, Kovendan K, Kumar PM, Ponarulselvam S, Amerasan D, et al. Larvicidal efficacy of Catharanthus roseus Linn. (Family: Apocynaceae) leaf extract and bacterial insecticide Bacillus thuringiensis against Anopheles stephensi Liston. Asian Pac J Trop Med. 2013;6: 847–53.LINK
2008 Panneerselvam C, Murugan K, Kovendan K, Kumar PM, Ponarulselvam S, Amerasan D, et al. Larvicidal efficacy of Catharanthus roseus Linn. (Family: Apocynaceae) leaf extract and bacterial insecticide Bacillus thuringiensis against Anopheles stephensi Liston. Asian Pac J Trop Med. 2013;6: 847–53.LINK
2009 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
2010 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
2011 Jaleel CA, Wang G, Ahmad P, Ikram-ul-Haq. Changes in the photosynthetic characteristics of Catharanthus roseus L. as a result of exogenous growth regulators. Plant Omi J. 2009;2: 169–174.LINK
2012 Jaleel CA, Wang G, Ahmad P, Ikram-ul-Haq. Changes in the photosynthetic characteristics of Catharanthus roseus L. as a result of exogenous growth regulators. Plant Omi J. 2009;2: 169–174.LINK
2013 Jaleel CA, Wang G, Ahmad P, Ikram-ul-Haq. Changes in the photosynthetic characteristics of Catharanthus roseus L. as a result of exogenous growth regulators. Plant Omi J. 2009;2: 169–174.LINK
2014 Jaleel CA, Wang G, Ahmad P, Ikram-ul-Haq. Changes in the photosynthetic characteristics of Catharanthus roseus L. as a result of exogenous growth regulators. Plant Omi J. 2009;2: 169–174.LINK
2015 Jaleel CA, Wang G, Ahmad P, Ikram-ul-Haq. Changes in the photosynthetic characteristics of Catharanthus roseus L. as a result of exogenous growth regulators. Plant Omi J. 2009;2: 169–174.LINK
2016 Jaleel CA, Wang G, Ahmad P, Ikram-ul-Haq. Changes in the photosynthetic characteristics of Catharanthus roseus L. as a result of exogenous growth regulators. Plant Omi J. 2009;2: 169–174.LINK
2017 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2018 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2019 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2020 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2021 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2022 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2023 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2024 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2025 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2026 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2027 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2028 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2029 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2030 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2031 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2032 Jossang A, Fodor P, Bodo B. A New Structural Class of Bisindole Alkaloids from the Seeds of Catharanthus roseus: Vingramine and Methylvingramine. J Org Chem. American Chemical Society; 1998;63: 7162–7167. doi:10.1021/jo972333tLINK
2033 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
2034 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
2035 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
2036 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
2037 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
2038 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
2039 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
2040 Zhao J, Zhu W-H, Hu Q, Guo Y-Q. Compact callus cluster suspension cultures of Catharanthus roseus with enhanced indole alkaloid biosynthesis. Vitr Cell Dev Biol. 2001;37: 68–72. doi:10.1007/s11627-001-0013-2LINK
2041 Verma A, Laakso I, Sepp?nen-Laakso T, Huhtikangas A, Riekkola M-L. A simplified procedure for indole alkaloid extraction from Catharanthus roseus combined with a semi-synthetic production process for vinblastine. Molecules. Molecular Diversity Preservation International; 2007;12: 1307–1315. doi:10.3390/12071307LINK
2042 Verma A, Laakso I, Sepp?nen-Laakso T, Huhtikangas A, Riekkola M-L. A simplified procedure for indole alkaloid extraction from Catharanthus roseus combined with a semi-synthetic production process for vinblastine. Molecules. Molecular Diversity Preservation International; 2007;12: 1307–1315. doi:10.3390/12071307LINK
2043 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
2044 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
2045 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
2046 Herz W, Falk H, Kirby GW. Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna; 1999. p. 168. ISBN: 9783211833117.NA
2047 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2048 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2049 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
2050 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
2051 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
2052 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
2053 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2054 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2055 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
2056 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
2057 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
2058 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
2059 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2060 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2061 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
2062 Pan Q, Wang Q, Yuan F, Xing S, Zhao J, Choi YH, et al. Overexpression of ORCA3 and G10H in Catharanthus roseus plants regulated alkaloid biosynthesis and metabolism revealed by NMR-metabolomics. PLoS One. 2012;7: e43038. doi:10.1371/journal.pone.0043038LINK
2063 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
2064 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
2065 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
2066 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
2067 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
2068 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
2069 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
2070 Ferreres F, Figueiredo R, Bettencourt S, Carqueijeiro I, Oliveira J, Gil-Izquierdo A, et al. Identification of phenolic compounds in isolated vacuoles of the medicinal plant Catharanthus roseus and their interaction with vacuolar class III peroxidase: an H2O2 affair. J Exp Bot. 2011;62: 2841–2854. doi:10.1093/jxb/erq458LINK
2071 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
2072 Vega-?vila E, Cano-Velasco JL, Alarc?n-Aguilar FJ, Fajardo Ort?z MDC, Almanza-Pιrez JC, Rom?n-Ramos R. Hypoglycemic activity of aqueous extracts from catharanthus roseus. Evidence-based Complement Altern Med. 2012;2012. doi:10.1155/2012/934258LINK
2073 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2074 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2075 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2076 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2077 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2078 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2079 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2080 Pan Q, Dai Y, Nuringtyas TR, Mustafa NR, Schulte AE, Verpoorte R, et al. Investigation of the chemomarkers correlated with flower colour in different organs of Catharanthus roseus using NMR-based metabolomics. Phytochem Anal. 2013;25: 66–74. doi:10.1002/pca.2464LINK
2081 Liscombe DK, O’Connor SE. A virus-induced gene silencing approach to understanding alkaloid metabolism in Catharanthus roseus. Phytochemistry. 2011;72: 1969–1977. doi:10.1016/j.phytochem.2011.07.001LINK
2082 Liscombe DK, O’Connor SE. A virus-induced gene silencing approach to understanding alkaloid metabolism in Catharanthus roseus. Phytochemistry. 2011;72: 1969–1977. doi:10.1016/j.phytochem.2011.07.001LINK
2083 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
2084 Liscombe DK, Usera AR, O’Connor SE. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis. Proc Natl Acad Sci U S A. 2010;107: 18793–18798. doi:10.1073/pnas.1009003107LINK
2085 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
2086 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
2087 Stockigt J, Husson HP, Kan-Fan C, Zenk MH. Cathenamine, a central intermediate in the cell free biosynthesis of ajmalicine and related indole alkaloids. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1977; 164–166. doi:10.1039/C39770000164LINK
2088 Stockigt J, Husson HP, Kan-Fan C, Zenk MH. Cathenamine, a central intermediate in the cell free biosynthesis of ajmalicine and related indole alkaloids. J Chem Soc Chem Commun. The Royal Society of Chemistry; 1977; 164–166. doi:10.1039/C39770000164LINK
2089 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
2090 Kutney JP, Choi LSL, Kolodziejczyk P, Sleigh SK, Stuart KL, Worth BR, et al. Alkaloid production in Catharanthus roseus cell cultures: Isolation and characterization of alkaloids from one cell line. Phytochemistry. 1980;19: 2589–2595. doi:10.1016/S0031-9422(00)83924-2LINK
2091 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
2092 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
2093 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2094 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2095 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
2096 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
2097 Chunsheng X. Compound balson pear capsules for curing diabetes, and prepn. method thereof [Internet]. CN1056980 C, 2000.LINK
2098 Chunsheng X. Compound balson pear capsules for curing diabetes, and prepn. method thereof [Internet]. CN1056980 C, 2000.LINK
2099 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2100 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2101 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2102 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2103 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2104 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2105 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2106 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2107 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2108 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2109 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2110 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2111 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2112 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2113 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2114 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2115 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2116 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2117 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2118 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2119 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2120 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
2121 Mitsuhashi N, Ohnishi M, Sekiguchi Y, Kwon Y-U, Chang Y-T, Chung S-K, et al. Phytic acid synthesis and vacuolar accumulation in suspension-cultured cells of Catharanthus roseus induced by high concentration of inorganic phosphate and cations. Plant Physiol. 2005;138: 1607–1614. doi:?10.?1104/?pp.?105.?060269LINK
2122 Mitsuhashi N, Ohnishi M, Sekiguchi Y, Kwon Y-U, Chang Y-T, Chung S-K, et al. Phytic acid synthesis and vacuolar accumulation in suspension-cultured cells of Catharanthus roseus induced by high concentration of inorganic phosphate and cations. Plant Physiol. 2005;138: 1607–1614. doi:?10.?1104/?pp.?105.?060269LINK
2123 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
2124 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
2125 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xiao X-Z, et al. Two new vinblastine-type N-oxide alkaloids from Catharanthus roseus. Nat Prod Res. 2013;27: 1911–1916. doi:10.1080/14786419.2013.790029LINK
2126 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xiao X-Z, et al. Two new vinblastine-type N-oxide alkaloids from Catharanthus roseus. Nat Prod Res. 2013;27: 1911–1916. doi:10.1080/14786419.2013.790029LINK
2127 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xiao X-Z, et al. Two new vinblastine-type N-oxide alkaloids from Catharanthus roseus. Nat Prod Res. 2013;27: 1911–1916. doi:10.1080/14786419.2013.790029LINK
2128 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xiao X-Z, et al. Two new vinblastine-type N-oxide alkaloids from Catharanthus roseus. Nat Prod Res. 2013;27: 1911–1916. doi:10.1080/14786419.2013.790029LINK
2129 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2130 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2131 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2132 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2133 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2134 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2135 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
2136 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
2137 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
2138 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
2139 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
2140 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
2141 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2142 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2143 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
2144 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
2145 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2146 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2147 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2148 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2149 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2150 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2151 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2152 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2153 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
2154 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
2155 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
2156 Yang S-O, Kim S-H, Kim Y, Kim H-S, Chun Y-J, Choi H-K. Metabolic discrimination of Catharanthus roseus calli according to their relative locations using (1)H-NMR and principal component analysis. Biosci Botechnology, Biochem. 2009;73: 2032–2036. doi:10.1271/bbb.90240LINK
2157 Fulda S. Betulinic acid for cancer treatment and prevention. Int J Mol Sci. 2008;9: 1096–1107. doi:10.3390/ijms9061096LINK
2158 Fulda S. Betulinic acid for cancer treatment and prevention. Int J Mol Sci. 2008;9: 1096–1107. doi:10.3390/ijms9061096LINK
2159 Fulda S. Betulinic acid for cancer treatment and prevention. Int J Mol Sci. 2008;9: 1096–1107. doi:10.3390/ijms9061096LINK
2160 Fulda S. Betulinic acid for cancer treatment and prevention. Int J Mol Sci. 2008;9: 1096–1107. doi:10.3390/ijms9061096LINK
2161 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
2162 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
2163 Fulda S. Betulinic acid for cancer treatment and prevention. Int J Mol Sci. 2008;9: 1096–1107. doi:10.3390/ijms9061096LINK
2164 Fulda S. Betulinic acid for cancer treatment and prevention. Int J Mol Sci. 2008;9: 1096–1107. doi:10.3390/ijms9061096LINK
2165 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
2166 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
2167 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
2168 Mujib A, Ilah A, Aslam J, Fatima S, Siddiqui ZH, Maqsood M. Catharanthus roseus alkaloids: application of biotechnology for improving yield. Plant Growth Regul. 2012;68: 111–127. doi:10.1007/s10725-012-9704-4LINK
2169 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
2170 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
2171 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
2172 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
2173 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
2174 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
2175 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
2176 Katsuragi H, Shimoda K, Yamamoto R, Ishihara K, Hamada H. Glycosylation of capsaicin derivatives and phenylpropanoid derivatives using cultured plant cells. Biochem Insights. 2011; doi:10.4137/bci.s6682LINK
2177 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2178 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2179 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2180 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2181 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2182 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2183 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2184 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2185 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2186 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2187 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2188 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2189 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2190 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
2191 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
2192 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
2193 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
2194 Piovan A, Filippini R, Favretto D. Characterization of the anthocyanins of Catharanthus roseus (L.) G. Don in vivo and in vitro by electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom. 1998;12: 361–367. doi:10.1002/,28SICI,291097-0231,2819980415,2912,3A7,3C361,3A,3AAID-RCM162,3E3.0.CO,3B2-ULINK
2195 Hanssen HW. Studies related to the synthesis and biosynthesis of indole alkaloids [Internet]. University of British Columbia. 1978.LINK
2196 Hanssen HW. Studies related to the synthesis and biosynthesis of indole alkaloids [Internet]. University of British Columbia. 1978.LINK
2197 Chung IM, Ali M, Chun SC, San KY, Peebles CAM, Ahmad A. New catharanthusopimaranoside A and B from hairy root cultures of Catharanthus roseus. Chem Nat Compd. 2008;44: 458–462. doi:10.1007/s10600-008-9096-xLINK
2198 Chung IM, Ali M, Chun SC, San KY, Peebles CAM, Ahmad A. New catharanthusopimaranoside A and B from hairy root cultures of Catharanthus roseus. Chem Nat Compd. 2008;44: 458–462. doi:10.1007/s10600-008-9096-xLINK
2199 Chung IM, Ali M, Chun SC, San KY, Peebles CAM, Ahmad A. New catharanthusopimaranoside A and B from hairy root cultures of Catharanthus roseus. Chem Nat Compd. 2008;44: 458–462. doi:10.1007/s10600-008-9096-xLINK
2200 Chung IM, Ali M, Chun SC, San KY, Peebles CAM, Ahmad A. New catharanthusopimaranoside A and B from hairy root cultures of Catharanthus roseus. Chem Nat Compd. 2008;44: 458–462. doi:10.1007/s10600-008-9096-xLINK
2201 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2202 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2203 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2204 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2205 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2206 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2207 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2208 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2209 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2210 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2211 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2212 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2213 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2214 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2215 Liu H, Zheng K, Lu X, Wang X, Hong R. Study on the total synthesis of velbanamine: Chemoselective dioxygenation of alkenes with PIFA via a stop-and-flow strategy. Beilstein J Org Chem. 2013;9: 983–990. doi:10.3762/bjoc.9.113LINK
2216 Liu H, Zheng K, Lu X, Wang X, Hong R. Study on the total synthesis of velbanamine: Chemoselective dioxygenation of alkenes with PIFA via a stop-and-flow strategy. Beilstein J Org Chem. 2013;9: 983–990. doi:10.3762/bjoc.9.113LINK
2217 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2218 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2219 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2220 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2221 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2222 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2223 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2224 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2225 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2226 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2227 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2228 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2229 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2230 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2231 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2232 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2233 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2234 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2235 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2236 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2237 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2238 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2239 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2240 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2241 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2242 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2243 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2244 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2245 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2246 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2247 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2248 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2249 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2250 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2251 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2252 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2253 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2254 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2255 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2256 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2257 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2258 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2259 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2260 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2261 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2262 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2263 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2264 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2265 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2266 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2267 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2268 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2269 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2270 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2271 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2272 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2273 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2274 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2275 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2276 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2277 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2278 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2279 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2280 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2281 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2282 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2283 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2284 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2285 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2286 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2287 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2288 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2289 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2290 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2291 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2292 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2293 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2294 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2295 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2296 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
2297 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
2298 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK