Phytochemica: A platform to explore phytochemicals of medicinal plants

References for PDM ID: CARS0398


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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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1349 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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1605 Atta-ur-Rahman, Sohail M, Albert K. Structural studies on vindolinine. Zeitschrift Fuer Naturforsch. 1986;41b: 386—392.LINK
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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
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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
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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
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1740 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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