Phytochemica: A platform to explore phytochemicals of medicinal plants

References for PDM ID: CARS0459


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 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
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 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
6 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
7 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
8 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
9 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
10 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
11 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
12 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
13 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
14 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
15 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
16 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
17 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
18 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
19 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
20 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
21 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
22 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
23 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
24 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
25 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
26 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
27 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
28 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
29 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
30 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
31 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
32 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
33 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
34 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
35 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
36 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
37 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
38 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
39 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
40 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
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 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
44 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
45 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
46 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
47 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
48 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
49 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
50 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
51 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
52 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
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 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
56 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
57 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
58 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
59 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
60 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
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 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
64 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
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 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
70 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
71 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
72 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
73 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
74 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
75 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
76 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
77 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
78 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
79 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
80 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
81 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
82 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
83 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
84 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
85 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
86 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
87 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
88 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
89 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
90 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
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 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
94 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
95 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
96 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
97 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
98 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
99 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
100 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
101 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
102 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
103 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
104 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
105 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
106 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
107 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
108 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
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238 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
239 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
240 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
241 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
242 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
243 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
244 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
245 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
246 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
247 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
248 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
249 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
250 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
251 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
252 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
253 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
254 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
255 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
256 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
257 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
258 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
259 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
260 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
261 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
262 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
263 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
264 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
265 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
266 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
267 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
268 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
269 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
270 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
271 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
272 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
273 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
274 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
275 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
276 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
277 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
278 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
279 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
280 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
281 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
282 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
283 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
284 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
285 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
286 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
287 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
288 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
289 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
290 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
291 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
292 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
293 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
294 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
295 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
296 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
297 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
298 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
299 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
300 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
301 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
302 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
303 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
304 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
305 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
306 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
307 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
308 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
309 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
310 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
311 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
312 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
313 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
314 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
315 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
316 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
317 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
318 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
319 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
320 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
321 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
322 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
323 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
324 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
325 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
326 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
327 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
328 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
329 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
330 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
331 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
332 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
333 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
334 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
335 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
336 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
337 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
338 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
339 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
340 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
341 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
342 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
343 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
344 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
345 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
346 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
347 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
348 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
349 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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580 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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604 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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606 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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608 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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645 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
646 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
647 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
648 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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651 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
652 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
653 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
654 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
655 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
656 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
657 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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662 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
663 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
664 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
665 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
666 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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670 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
671 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
672 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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675 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
676 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
677 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
678 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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684 O’Connor SE, Maresh JJ. Chemistry and biology of monoterpene indole alkaloid biosynthesis. Nat Prod Rep. The Royal Society of Chemistry; 2006;23: 532–547. doi:10.1039/b512615kLINK
685 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
686 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
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698 O’Connor SE, Maresh JJ. Chemistry and biology of monoterpene indole alkaloid biosynthesis. Nat Prod Rep. The Royal Society of Chemistry; 2006;23: 532–547. doi:10.1039/b512615kLINK
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700 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
701 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
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703 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
704 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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706 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
707 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
708 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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770 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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775 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
776 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
777 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
778 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
779 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
780 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
781 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
782 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
783 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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786 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
787 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
788 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
789 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
790 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
791 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
792 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
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796 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
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799 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
800 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
801 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
802 Pietrosiuk A, Furmanowa M. Preliminary results of indole alkaloids production in different roots of Catharanthus roseus cultured in vitro. Acta Soc Bot Pol. 2001;70: 261–265. doi:10.5586/asbp.2001.033LINK
803 Pietrosiuk A, Furmanowa M. Preliminary results of indole alkaloids production in different roots of Catharanthus roseus cultured in vitro. Acta Soc Bot Pol. 2001;70: 261–265. doi:10.5586/asbp.2001.033LINK
804 Pietrosiuk A, Furmanowa M. Preliminary results of indole alkaloids production in different roots of Catharanthus roseus cultured in vitro. Acta Soc Bot Pol. 2001;70: 261–265. doi:10.5586/asbp.2001.033LINK
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 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
808 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
809 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
810 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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814 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
815 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
816 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
817 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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820 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
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
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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 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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843 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
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846 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
847 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
848 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
849 Guιritte F, Langlois N, Pιtiard V. Mιtabolites secondaires isolιs d’une culture de tissus de Catharanthus roseus. J Nat Prod. American Chemical Society; 1983;46: 144–148. doi:10.1021/np50025a018LINK
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853 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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885 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
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888 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
889 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
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892 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
893 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
894 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
895 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
896 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
897 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
898 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
899 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
900 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
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 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
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 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
906 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
907 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
908 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
909 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
910 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
911 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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913 Aynilian GH, Weiss SG, Cordell GA, Abraham DJ, Crane FA, Farnsworth NR. Catharanthus alkaloids XXIX: Isolation and structure elucidation of vincoline. J Pharm Sci. 1974;63: 536–538. doi:10.1002/jps.2600630409LINK
914 Aynilian GH, Weiss SG, Cordell GA, Abraham DJ, Crane FA, Farnsworth NR. Catharanthus alkaloids XXIX: Isolation and structure elucidation of vincoline. J Pharm Sci. 1974;63: 536–538. doi:10.1002/jps.2600630409LINK
915 Aynilian GH, Weiss SG, Cordell GA, Abraham DJ, Crane FA, Farnsworth NR. Catharanthus alkaloids XXIX: Isolation and structure elucidation of vincoline. J Pharm Sci. 1974;63: 536–538. doi:10.1002/jps.2600630409LINK
916 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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918 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
919 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
920 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
921 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
922 Bashir M, Kaleem S, Fatima T. 16-epi-19-S-vindolinine, an indoline alkaloid from Catharanthus roseus. Phytochemistry. 1983;22: 1021–1023. doi:10.1016/0031-9422(83)85046-8LINK
923 Bashir M, Kaleem S, Fatima T. 16-epi-19-S-vindolinine, an indoline alkaloid from Catharanthus roseus. Phytochemistry. 1983;22: 1021–1023. doi:10.1016/0031-9422(83)85046-8LINK
924 Bashir M, Kaleem S, Fatima T. 16-epi-19-S-vindolinine, an indoline alkaloid from Catharanthus roseus. Phytochemistry. 1983;22: 1021–1023. doi:10.1016/0031-9422(83)85046-8LINK
925 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
926 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
927 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
928 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
929 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
930 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
931 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
932 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
933 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
934 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
935 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
936 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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938 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
939 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
940 Vani SN. Bioreactor design for scaleup of Catharanthus roseus hairy root cultures for production of indole alkaloids [Internet]. Rice University. 1996.LINK
941 Vani SN. Bioreactor design for scaleup of Catharanthus roseus hairy root cultures for production of indole alkaloids [Internet]. Rice University. 1996.LINK
942 Vani SN. Bioreactor design for scaleup of Catharanthus roseus hairy root cultures for production of indole alkaloids [Internet]. Rice University. 1996.LINK
943 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
944 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
945 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
946 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
947 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
948 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
949 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
950 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
951 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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955 Furuya T, Sakamoto K, Iida K, Asada Y, Yoshikawa T, Sakai S, et al. Biotransformation of tabersonine in cell suspension cultures of Catharanthus roseus. Phytochemistry. 1992;31: 3065–8. doi:10.1016/0031-9422(92)83447-7LINK
956 Furuya T, Sakamoto K, Iida K, Asada Y, Yoshikawa T, Sakai S, et al. Biotransformation of tabersonine in cell suspension cultures of Catharanthus roseus. Phytochemistry. 1992;31: 3065–8. doi:10.1016/0031-9422(92)83447-7LINK
957 Furuya T, Sakamoto K, Iida K, Asada Y, Yoshikawa T, Sakai S, et al. Biotransformation of tabersonine in cell suspension cultures of Catharanthus roseus. Phytochemistry. 1992;31: 3065–8. doi:10.1016/0031-9422(92)83447-7LINK
958 Rischer H, Oresic M, Sepp?nen-Laakso T, Katajamaa M, Lammertyn F, Ardiles-Diaz W, et al. Gene-to-metabolite networks for terpenoid indole alkaloid biosynthesis in Catharanthus roseus cells. Proc Natl Acad Sci U S A. 2006;103: 5614–5619. doi:10.1073/pnas.0601027103LINK
959 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
960 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
961 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
962 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
963 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
964 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
965 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
966 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
967 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
968 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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970 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
971 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
972 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
973 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
974 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
975 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
976 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
977 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
978 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
979 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
980 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
981 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
982 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
983 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
984 H SG, M G, H TR. Alkaloids of V. Rosea (Catharanthus roseus). 25. Lochrovine, Perimivine, Vincoline, Lochrovidine, Lochrovicine and Vincolidine. Lloydia. 1964;27: 20–213.LINK
985 Biblioth L. Substances naturelles se fixant sur la tubulinemise en œuvre d’un criblage par spectromιtrie de masse. Universitι Henri Poincarι Nancy 1. 2009. p. 74. ISBN:0070297770.NA
986 Biblioth L. Substances naturelles se fixant sur la tubulinemise en œuvre d’un criblage par spectromιtrie de masse. Universitι Henri Poincarι Nancy 1. 2009. p. 74. ISBN:0070297770.NA
987 Biblioth L. Substances naturelles se fixant sur la tubulinemise en œuvre d’un criblage par spectromιtrie de masse. Universitι Henri Poincarι Nancy 1. 2009. p. 74. ISBN:0070297770.NA
988 Brossi A, Suffness M. The Alkaloids: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.) V37: Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). 37th ed. Elsevier Science; 1990. p. 249.LINK
989 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
990 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
991 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
992 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
993 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
994 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
995 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
996 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
997 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
998 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
999 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
1000 Cordall GA, Weiss SG, Farnsworth NR. Structure elucidation and chemistry of Catharanthus alkaloids. XXX. Isolation and structure elucidation of vincarodine. J Org Chem. American Chemical Society; 1974;39: 431–434. doi:10.1021/jo00918a001LINK
1001 Cordall GA, Weiss SG, Farnsworth NR. Structure elucidation and chemistry of Catharanthus alkaloids. XXX. Isolation and structure elucidation of vincarodine. J Org Chem. American Chemical Society; 1974;39: 431–434. doi:10.1021/jo00918a001LINK
1002 Cordall GA, Weiss SG, Farnsworth NR. Structure elucidation and chemistry of Catharanthus alkaloids. XXX. Isolation and structure elucidation of vincarodine. J Org Chem. American Chemical Society; 1974;39: 431–434. doi:10.1021/jo00918a001LINK
1003 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
1004 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
1005 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
1006 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
1007 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
1008 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
1009 Southon IW, Buckingham J. Dictionary of Alkaloids [Internet]. 2nd ed. CRC Press; 1989. p. 620. ISBN: 9780412249105.LINK
1010 Southon IW, Buckingham J. Dictionary of Alkaloids [Internet]. 2nd ed. CRC Press; 1989. p. 620. ISBN: 9780412249105.LINK
1011 Southon IW, Buckingham J. Dictionary of Alkaloids [Internet]. 2nd ed. CRC Press; 1989. p. 620. ISBN: 9780412249105.LINK
1012 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
1013 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
1014 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
1015 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
1016 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
1017 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
1018 He L, Yang L, Tan R, Zhao S, Hu Z. Enhancement of vindoline production in suspension culture of the Catharanthus roseus cell line C20hi by light and methyl jasmonate elicitation. Anal Sci. 2011;27: 1243–1248. doi:10.2116/analsci.27.1243LINK
1019 He L, Yang L, Tan R, Zhao S, Hu Z. Enhancement of vindoline production in suspension culture of the Catharanthus roseus cell line C20hi by light and methyl jasmonate elicitation. Anal Sci. 2011;27: 1243–1248. doi:10.2116/analsci.27.1243LINK
1020 He L, Yang L, Tan R, Zhao S, Hu Z. Enhancement of vindoline production in suspension culture of the Catharanthus roseus cell line C20hi by light and methyl jasmonate elicitation. Anal Sci. 2011;27: 1243–1248. doi:10.2116/analsci.27.1243LINK
1021 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
1022 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
1023 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
1024 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
1025 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
1026 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
1027 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
1028 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
1029 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
1030 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
1031 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
1032 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
1033 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.?1104/?pp.?125.?1.?189
1034 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.?1104/?pp.?125.?1.?189
1035 Laflamme P, St-Pierre B, De Luca V. Molecular and biochemical analysis of a Madagascar periwinkle root-specific minovincinine-19-hydroxy-O-acetyltransferase. Plant Physiol. 2001;125: 189–198. doi:10.?1104/?pp.?125.?1.?189
1036 St-Pierre B. Multicellular Compartmentation of Catharanthus roseus Alkaloid Biosynthesis Predicts Intercellular Translocation of a Pathway Intermediate. Plant Cell. 1999;11: 887–900. doi:?10.?1105/?tpc.?11.?5.?887LINK
1037 St-Pierre B. Multicellular Compartmentation of Catharanthus roseus Alkaloid Biosynthesis Predicts Intercellular Translocation of a Pathway Intermediate. Plant Cell. 1999;11: 887–900. doi:?10.?1105/?tpc.?11.?5.?887LINK
1038 St-Pierre B. Multicellular Compartmentation of Catharanthus roseus Alkaloid Biosynthesis Predicts Intercellular Translocation of a Pathway Intermediate. Plant Cell. 1999;11: 887–900. doi:?10.?1105/?tpc.?11.?5.?887LINK
1039 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
1040 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
1041 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
1042 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
1043 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
1044 Kutney JP. Studies in plant tissue culture: potential sources of clinically important antitumor agents. Pure Appl Chem. International Union of Pure and Applied Chemistry; 1982;54: 2523–2536. doi:10.1351/pac198254122523LINK
1045 Ali I, Chaudhry MI. Isolation and 13C-NMR Studies on Cathovaline, an Alkaloid from the Leaves of Catharanthus roseus. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1985;51: 447–448. doi:10.1055/s-2007-969546LINK
1046 Ali I, Chaudhry MI. Isolation and 13C-NMR Studies on Cathovaline, an Alkaloid from the Leaves of Catharanthus roseus. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1985;51: 447–448. doi:10.1055/s-2007-969546LINK
1047 Ali I, Chaudhry MI. Isolation and 13C-NMR Studies on Cathovaline, an Alkaloid from the Leaves of Catharanthus roseus. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1985;51: 447–448. doi:10.1055/s-2007-969546LINK
1048 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
1049 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
1050 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
1051 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
1052 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
1053 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
1054 Tiong SH, Looi CY, Hazni H, Arya A, Paydar M, Wong WF, et al. Antidiabetic and antioxidant properties of alkaloids from Catharanthus roseus (L.) G. Don. Molecules. 2013;18: 9770–9784. doi:10.3390/molecules18089770LINK
1055 Tiong SH, Looi CY, Hazni H, Arya A, Paydar M, Wong WF, et al. Antidiabetic and antioxidant properties of alkaloids from Catharanthus roseus (L.) G. Don. Molecules. 2013;18: 9770–9784. doi:10.3390/molecules18089770LINK
1056 Tiong SH, Looi CY, Hazni H, Arya A, Paydar M, Wong WF, et al. Antidiabetic and antioxidant properties of alkaloids from Catharanthus roseus (L.) G. Don. Molecules. 2013;18: 9770–9784. doi:10.3390/molecules18089770LINK
1057 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
1058 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
1059 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
1060 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
1061 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
1062 Kurz WG, Chatson KB, Constabel F, Kutney JP, Choi LS, Kolodziejczyk P, et al. Alkaloid Production in Catharanthus roseus cell cultures VIII. Planta Med. 1981;42: 22–31. doi:10.1055/s-2007-971541LINK
1063 Nagakura N, Ruffer M, Zenk MH. The biosynthesis of monoterpenoid indole alkaloids from strictosidine. J Chem Soc Perkin Trans 1. The Royal Society of Chemistry; 1979;1: 2308–2312. doi:10.1039/P19790002308LINK
1064 Nagakura N, Ruffer M, Zenk MH. The biosynthesis of monoterpenoid indole alkaloids from strictosidine. J Chem Soc Perkin Trans 1. The Royal Society of Chemistry; 1979;1: 2308–2312. doi:10.1039/P19790002308LINK
1065 Nagakura N, Ruffer M, Zenk MH. The biosynthesis of monoterpenoid indole alkaloids from strictosidine. J Chem Soc Perkin Trans 1. The Royal Society of Chemistry; 1979;1: 2308–2312. doi:10.1039/P19790002308LINK
1066 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
1067 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
1068 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
1069 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
1070 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
1071 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
1072 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
1073 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
1074 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
1075 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
1076 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
1077 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
1078 Ouwerkerk PB, Memelink J. A G-box element from the Catharanthus roseus strictosidine synthase (Str) gene promoter confers seed-specific expression in transgenic tobacco plants. Mol Gen Genet. 1999;261: 635–643. doi:10.1007/s004380050006LINK
1079 Ouwerkerk PB, Memelink J. A G-box element from the Catharanthus roseus strictosidine synthase (Str) gene promoter confers seed-specific expression in transgenic tobacco plants. Mol Gen Genet. 1999;261: 635–643. doi:10.1007/s004380050006LINK
1080 Ouwerkerk PB, Memelink J. A G-box element from the Catharanthus roseus strictosidine synthase (Str) gene promoter confers seed-specific expression in transgenic tobacco plants. Mol Gen Genet. 1999;261: 635–643. doi:10.1007/s004380050006LINK
1081 Miettinen K, Dong L, Navrot N, Schneider T, Burlat V, Pollier J, et al. The seco-iridoid pathway from Catharanthus roseus. Nat Commun. Nature Publishing Group; 2014;5: 3606. doi:10.1038/ncomms4606LINK
1082 Miettinen K, Dong L, Navrot N, Schneider T, Burlat V, Pollier J, et al. The seco-iridoid pathway from Catharanthus roseus. Nat Commun. Nature Publishing Group; 2014;5: 3606. doi:10.1038/ncomms4606LINK
1083 Miettinen K, Dong L, Navrot N, Schneider T, Burlat V, Pollier J, et al. The seco-iridoid pathway from Catharanthus roseus. Nat Commun. Nature Publishing Group; 2014;5: 3606. doi:10.1038/ncomms4606LINK
1084 Guirimand G, Guihur A, Ginis O, Poutrain P, Hιricourt F, Oudin A, et al. The subcellular organization of strictosidine biosynthesis in Catharanthus roseus epidermis highlights several trans-tonoplast translocations of intermediate metabolites. FEBS J. 2011;278: 749–763. doi:10.1111/j.1742-4658.2010.07994.xLINK
1085 Guirimand G, Guihur A, Ginis O, Poutrain P, Hιricourt F, Oudin A, et al. The subcellular organization of strictosidine biosynthesis in Catharanthus roseus epidermis highlights several trans-tonoplast translocations of intermediate metabolites. FEBS J. 2011;278: 749–763. doi:10.1111/j.1742-4658.2010.07994.xLINK
1086 Guirimand G, Guihur A, Ginis O, Poutrain P, Hιricourt F, Oudin A, et al. The subcellular organization of strictosidine biosynthesis in Catharanthus roseus epidermis highlights several trans-tonoplast translocations of intermediate metabolites. FEBS J. 2011;278: 749–763. doi:10.1111/j.1742-4658.2010.07994.xLINK
1087 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
1088 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
1089 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
1090 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
1091 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
1092 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
1093 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
1094 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
1095 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
1096 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
1097 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
1098 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
1099 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
1100 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
1101 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
1102 Hannewald P. Study of drug/receptor interaction by mass spectrometry?: development and validation of new tests of molecular screening [Internet]. Paul Verlaine University – Metz. 2008. p. 229.LINK
1103 Hannewald P. Study of drug/receptor interaction by mass spectrometry?: development and validation of new tests of molecular screening [Internet]. Paul Verlaine University – Metz. 2008. p. 229.LINK
1104 Hannewald P. Study of drug/receptor interaction by mass spectrometry?: development and validation of new tests of molecular screening [Internet]. Paul Verlaine University – Metz. 2008. p. 229.LINK
1105 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
1106 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
1107 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
1108 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
1109 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
1110 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
1111 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
1112 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
1113 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
1114 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
1115 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
1116 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
1117 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
1118 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
1119 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
1120 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
1121 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
1122 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
1123 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
1124 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
1125 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
1126 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
1127 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
1128 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
1129 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
1130 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
1131 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
1132 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
1133 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
1134 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
1135 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
1136 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
1137 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
1138 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
1139 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
1140 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
1141 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
1142 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
1143 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
1144 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
1145 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
1146 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
1147 Price NPJ, Firmin JL, Robins RJ, Gray DO. High-performance liquid chromatography of the alkaloid perivine from Catharanthus roseus after derivatisation with dansyl chloride. J Chromatogr A. 1993;653: 161–166. doi:10.1016/0021-9673(93)80406-XLINK
1148 Price NPJ, Firmin JL, Robins RJ, Gray DO. High-performance liquid chromatography of the alkaloid perivine from Catharanthus roseus after derivatisation with dansyl chloride. J Chromatogr A. 1993;653: 161–166. doi:10.1016/0021-9673(93)80406-XLINK
1149 Price NPJ, Firmin JL, Robins RJ, Gray DO. High-performance liquid chromatography of the alkaloid perivine from Catharanthus roseus after derivatisation with dansyl chloride. J Chromatogr A. 1993;653: 161–166. doi:10.1016/0021-9673(93)80406-XLINK
1150 Endo T, Goodbody A, Misawa M. Alkaloid Production in root and shoot cultures of Catharanthus roseus. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1987;53: 479–482. doi:10.1055/s-2006-962777LINK
1151 Endo T, Goodbody A, Misawa M. Alkaloid Production in root and shoot cultures of Catharanthus roseus. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1987;53: 479–482. doi:10.1055/s-2006-962777LINK
1152 Endo T, Goodbody A, Misawa M. Alkaloid Production in root and shoot cultures of Catharanthus roseus. Planta Med. © Georg Thieme Verlag Stuttgart · New York; 1987;53: 479–482. doi:10.1055/s-2006-962777LINK
1153 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
1154 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
1155 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
1156 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
1157 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
1158 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
1159 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
1160 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
1161 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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1163 Brittain HG, Klaus Florey. Profiles of drug substances, excipients and related methodology. Elsevier Science; 1992. p. 695. ISBN: 9780080861166.LINK
1164 Brittain HG, Klaus Florey. Profiles of drug substances, excipients and related methodology. Elsevier Science; 1992. p. 695. ISBN: 9780080861166.LINK
1165 Kuboyama T, Yokoshima S, Tokuyama H, Fukuyama T. Stereocontrolled total synthesis of (+)-vincristine. Proc Natl Acad Sci U S A. 2004;101: 11966–11970. doi:10.1073/pnas.0401323101LINK
1166 Kuboyama T, Yokoshima S, Tokuyama H, Fukuyama T. Stereocontrolled total synthesis of (+)-vincristine. Proc Natl Acad Sci U S A. 2004;101: 11966–11970. doi:10.1073/pnas.0401323101LINK
1167 Kuboyama T, Yokoshima S, Tokuyama H, Fukuyama T. Stereocontrolled total synthesis of (+)-vincristine. Proc Natl Acad Sci U S A. 2004;101: 11966–11970. doi:10.1073/pnas.0401323101LINK
1168 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
1169 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
1170 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
1171 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
1172 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
1173 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
1174 El-Sayed A, Cordell GA. Catharanthus alkaloids. XXXIV. Catharanthamine, a New Antitumor bisindole alkaloid from Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 289–293. doi:10.1021/np50015a009LINK
1175 El-Sayed A, Cordell GA. Catharanthus alkaloids. XXXIV. Catharanthamine, a New Antitumor bisindole alkaloid from Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 289–293. doi:10.1021/np50015a009LINK
1176 El-Sayed A, Cordell GA. Catharanthus alkaloids. XXXIV. Catharanthamine, a New Antitumor bisindole alkaloid from Catharanthus roseus. J Nat Prod. American Chemical Society; 1981;44: 289–293. doi:10.1021/np50015a009LINK
1177 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
1178 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
1179 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
1180 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
1181 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
1182 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
1183 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
1184 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
1185 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
1186 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
1187 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
1188 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
1189 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
1190 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
1191 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
1192 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
1193 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
1194 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
1195 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
1196 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
1197 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
1198 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
1199 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
1200 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
1201 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
1202 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
1203 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
1204 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
1205 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
1206 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
1207 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
1208 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
1209 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
1210 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
1211 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
1212 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
1213 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
1214 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
1215 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
1216 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
1217 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
1218 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
1219 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
1220 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
1221 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
1222 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
1223 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
1224 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
1225 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
1226 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
1227 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
1228 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
1229 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
1230 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
1231 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
1232 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
1233 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
1234 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
1235 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
1236 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
1237 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
1238 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
1239 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
1240 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
1241 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
1242 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
1243 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
1244 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
1245 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
1246 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
1247 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
1248 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
1249 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
1250 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
1251 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
1252 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
1253 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
1254 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
1255 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
1256 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
1257 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
1258 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
1259 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
1260 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
1261 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
1262 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
1263 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
1264 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
1265 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
1266 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
1267 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
1268 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
1269 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
1270 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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1272 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
1273 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
1274 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
1275 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
1276 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
1277 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
1278 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
1279 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
1280 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
1281 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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1285 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
1286 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
1287 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
1288 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
1289 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
1290 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
1291 Rodrigo RGA. The Alkaloids: Chemistry and Physiology V20: Chemistry and Physiology. Elsevier Science; 1982. p. 340. ISBN: 9780080865447.LINK
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1294 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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1296 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
1297 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
1298 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
1299 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
1300 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
1301 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
1302 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
1303 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
1304 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
1305 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
1306 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
1307 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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1351 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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1353 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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1357 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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1366 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
1367 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
1368 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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1371 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
1372 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
1373 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
1374 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
1375 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
1376 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
1377 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
1378 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
1379 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
1380 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
1381 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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1383 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
1384 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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1386 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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1390 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
1391 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
1392 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
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1396 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
1397 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
1398 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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1412 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
1413 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
1414 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
1415 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
1416 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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1426 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
1427 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
1428 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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1432 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
1433 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
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1446 Sander GW. Quantitative analysis of metabolic pathways in Catharanthus roseus hairy roots metabolically engineered for terpenoid indole alkaloid overproduction [Internet]. Iowa State University. 2009. p. 10820.LINK
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1510 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
1511 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
1512 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
1513 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
1514 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
1515 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
1516 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
1517 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
1518 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
1519 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
1520 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
1521 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
1522 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
1523 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
1524 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
1525 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
1526 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
1527 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
1528 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
1529 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
1530 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
1531 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
1532 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
1533 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
1534 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
1535 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
1536 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
1537 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
1538 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
1539 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
1540 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
1541 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
1542 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
1543 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
1544 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
1545 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
1546 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
1547 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
1548 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
1549 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
1550 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
1551 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
1552 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
1553 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
1554 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
1555 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
1556 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
1557 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
1558 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
1559 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
1560 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
1561 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
1562 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
1563 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
1564 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
1565 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
1566 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
1567 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
1568 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
1569 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
1570 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
1571 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
1572 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
1573 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
1574 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
1575 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
1576 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
1577 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
1578 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
1579 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
1580 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
1581 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
1582 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
1583 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
1584 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
1585 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
1586 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
1587 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
1588 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
1589 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
1590 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
1591 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
1592 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
1593 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
1594 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
1595 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
1596 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
1597 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
1598 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
1599 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
1600 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
1601 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
1602 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
1603 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
1604 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
1605 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
1606 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
1607 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
1608 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
1609 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
1610 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
1611 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
1612 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
1613 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
1614 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
1615 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
1616 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
1617 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
1618 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
1619 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
1620 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
1621 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
1622 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
1623 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
1624 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
1625 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
1626 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
1627 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
1628 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
1629 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
1630 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
1631 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
1632 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
1633 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
1634 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
1635 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
1636 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
1637 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
1638 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
1639 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
1640 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
1641 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
1642 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
1643 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
1644 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
1645 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
1646 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
1647 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
1648 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
1649 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
1650 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
1651 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
1652 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
1653 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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1655 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
1656 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
1657 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
1658 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
1659 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
1660 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
1661 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
1662 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
1663 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
1664 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
1665 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
1666 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
1667 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
1668 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
1669 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
1670 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
1671 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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1681 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
1682 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
1683 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
1684 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
1685 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
1686 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
1687 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
1688 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
1689 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
1690 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
1691 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
1692 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
1693 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
1694 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
1695 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
1696 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
1697 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
1698 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
1699 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
1700 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
1701 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
1702 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
1703 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
1704 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
1705 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
1706 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
1707 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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1866 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
1867 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
1868 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
1869 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
1870 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1871 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1872 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1873 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1874 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1875 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1876 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1877 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1878 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1879 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1880 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1881 Chung I-M, Ahmad A, Ali M, Lee O-K, Kim M-Y, Kim J-H, et al. Flavonoid glucosides from the hairy roots of Catharanthus roseus. J Nat Prod. 2009;72: 613–620. doi:10.1021/np800378qLINK
1882 Chung I, Ali M, Yang Y, Peebles C a M, Chun S, Lee S, et al. Identification of new compounds from Catharanthus roseus hairy root cultures. Bull Korean Chem Soc. 2007;28: 1294–1298.LINK
1883 Chung I, Ali M, Yang Y, Peebles C a M, Chun S, Lee S, et al. Identification of new compounds from Catharanthus roseus hairy root cultures. Bull Korean Chem Soc. 2007;28: 1294–1298.LINK
1884 Chung I, Ali M, Yang Y, Peebles C a M, Chun S, Lee S, et al. Identification of new compounds from Catharanthus roseus hairy root cultures. Bull Korean Chem Soc. 2007;28: 1294–1298.LINK
1885 Chung I, Ali M, Yang Y, Peebles C a M, Chun S, Lee S, et al. Identification of new compounds from Catharanthus roseus hairy root cultures. Bull Korean Chem Soc. 2007;28: 1294–1298.LINK
1886 Chung I, Ali M, Yang Y, Peebles C a M, Chun S, Lee S, et al. Identification of new compounds from Catharanthus roseus hairy root cultures. Bull Korean Chem Soc. 2007;28: 1294–1298.LINK
1887 Chung I, Ali M, Yang Y, Peebles C a M, Chun S, Lee S, et al. Identification of new compounds from Catharanthus roseus hairy root cultures. Bull Korean Chem Soc. 2007;28: 1294–1298.LINK
1888 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
1889 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
1890 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
1891 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
1892 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
1893 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
1894 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
1895 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
1896 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
1897 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
1898 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
1899 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
1900 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
1901 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
1902 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
1903 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
1904 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
1905 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
1906 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
1907 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
1908 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
1909 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
1910 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
1911 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
1912 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
1913 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
1914 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
1915 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
1916 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
1917 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
1918 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
1919 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
1920 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
1921 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
1922 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
1923 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
1924 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
1925 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
1926 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
1927 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
1928 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
1929 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
1930 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
1931 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
1932 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
1933 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
1934 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
1935 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
1936 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
1937 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
1938 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
1939 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
1940 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
1941 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
1942 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
1943 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
1944 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
1945 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
1946 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
1947 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
1948 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
1949 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
1950 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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1953 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
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1957 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1958 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1959 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1960 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1961 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1962 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1963 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1964 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1965 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1966 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1967 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1968 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1969 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1970 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1971 Runguphan W, O’Connor SE. Metabolic reprogramming of periwinkle plant culture. Nat Chem Biol. 2009;5: 151–153. doi:10.1038/nchembio.141LINK
1972 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
1973 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
1974 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
1975 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
1976 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
1977 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
1978 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
1979 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
1980 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
1981 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
1982 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
1983 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
1984 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
1985 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
1986 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
1987 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1988 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1989 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1990 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1991 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1992 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1993 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1994 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1995 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1996 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1997 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1998 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
1999 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
2000 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
2001 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
2002 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
2003 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
2004 Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T. 7-O-Methylated anthocyanidin glycosides from Catharanthus roseus. Phytochemistry. 2008;69: 1215–9. doi:10.1016/j.phytochem.2007.11.005LINK
2005 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2006 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2007 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2008 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
2009 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
2010 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
2011 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
2012 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
2013 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
2014 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2015 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2016 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2017 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
2018 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
2019 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
2020 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
2021 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
2022 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
2023 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2024 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2025 Daniel M. Medicinal plants: Chemistry and properties. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2026 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
2027 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
2028 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
2029 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
2030 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
2031 Carew D. Anthocyanidins of Catharanthus roseus callus cultures. Phytochemistry. 1976;15: 442. doi:10.1016/S0031-9422(00)86854-5LINK
2032 Nayak BS, Pinto Pereira LM. Catharanthus roseus flower extract has wound-healing activity in Sprague Dawley rats. BMC Complement Aternative Med. 2006;6: 41. doi:10.1186/1472-6882-6-41LINK
2033 Nayak BS, Pinto Pereira LM. Catharanthus roseus flower extract has wound-healing activity in Sprague Dawley rats. BMC Complement Aternative Med. 2006;6: 41. doi:10.1186/1472-6882-6-41LINK
2034 Nayak BS, Pinto Pereira LM. Catharanthus roseus flower extract has wound-healing activity in Sprague Dawley rats. BMC Complement Aternative Med. 2006;6: 41. doi:10.1186/1472-6882-6-41LINK
2035 Nayak BS, Anderson M, Pinto Pereira LM. Evaluation of wound-healing potential of Catharanthus roseus leaf extract in rats. Fitoterapia. 2007;78: 540–544. doi:10.1016/j.fitote.2007.06.008LINK
2036 Nayak BS, Anderson M, Pinto Pereira LM. Evaluation of wound-healing potential of Catharanthus roseus leaf extract in rats. Fitoterapia. 2007;78: 540–544. doi:10.1016/j.fitote.2007.06.008LINK
2037 Nayak BS, Anderson M, Pinto Pereira LM. Evaluation of wound-healing potential of Catharanthus roseus leaf extract in rats. Fitoterapia. 2007;78: 540–544. doi:10.1016/j.fitote.2007.06.008LINK
2038 Gautam S, Mishra A, Tiwari A. Catharanthus alkaloids and their enhanced production using elicitors: A review. Int J Pharm Technol. 2011;3: 713–724.LINK
2039 Gautam S, Mishra A, Tiwari A. Catharanthus alkaloids and their enhanced production using elicitors: A review. Int J Pharm Technol. 2011;3: 713–724.LINK
2040 Gautam S, Mishra A, Tiwari A. Catharanthus alkaloids and their enhanced production using elicitors: A review. Int J Pharm Technol. 2011;3: 713–724.LINK
2041 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
2042 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
2043 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
2044 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
2045 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
2046 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
2047 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
2048 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
2049 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
2050 Mustafa NR, Kim HK, Choi YH, Erkelens C, Lefeber AWM, Spijksma G, et al. Biosynthesis of salicylic acid in fungus elicited Catharanthus roseus cells. Phytochemistry. 2009;70: 532–539. doi:10.1016/j.phytochem.2009.01.009LINK
2051 Mustafa NR, Kim HK, Choi YH, Erkelens C, Lefeber AWM, Spijksma G, et al. Biosynthesis of salicylic acid in fungus elicited Catharanthus roseus cells. Phytochemistry. 2009;70: 532–539. doi:10.1016/j.phytochem.2009.01.009LINK
2052 Mustafa NR, Kim HK, Choi YH, Erkelens C, Lefeber AWM, Spijksma G, et al. Biosynthesis of salicylic acid in fungus elicited Catharanthus roseus cells. Phytochemistry. 2009;70: 532–539. doi:10.1016/j.phytochem.2009.01.009LINK
2053 Muljono RAB, Scheffer JJC, Verpoorte R. Effect of feeding salicylic acid on 2,3-dihydroxybenzoic acid formation in cultured cells of Catharanthus roseus. Pharm Biol. Informa UK Ltd UK; 2003;41: 284–290. doi:10.1076/phbi.41.4.284.15681LINK
2054 Muljono RAB, Scheffer JJC, Verpoorte R. Effect of feeding salicylic acid on 2,3-dihydroxybenzoic acid formation in cultured cells of Catharanthus roseus. Pharm Biol. Informa UK Ltd UK; 2003;41: 284–290. doi:10.1076/phbi.41.4.284.15681LINK
2055 Muljono RAB, Scheffer JJC, Verpoorte R. Effect of feeding salicylic acid on 2,3-dihydroxybenzoic acid formation in cultured cells of Catharanthus roseus. Pharm Biol. Informa UK Ltd UK; 2003;41: 284–290. doi:10.1076/phbi.41.4.284.15681LINK
2056 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
2057 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
2058 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
2059 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
2060 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
2061 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
2062 Ridaura-Sanz VE. Novel chromium carbonyl complexes of dihydropyridines and their application to the synthesis of dehydrosecodine. University of British Columbia. 1979.LINK
2063 Ridaura-Sanz VE. Novel chromium carbonyl complexes of dihydropyridines and their application to the synthesis of dehydrosecodine. University of British Columbia. 1979.LINK
2064 Ridaura-Sanz VE. Novel chromium carbonyl complexes of dihydropyridines and their application to the synthesis of dehydrosecodine. University of British Columbia. 1979.LINK
2065 Ruszkowska J, Chrobak R, Maurin JK, Czarnocki Z. Vindoline and 16-demethoxyvindoline: two catharanthus-derived alkaloids. Acta Crystallogr. International Union of Crystallography; 2004;60: o377–o380. doi:10.1107/S0108270104004342LINK
2066 Ruszkowska J, Chrobak R, Maurin JK, Czarnocki Z. Vindoline and 16-demethoxyvindoline: two catharanthus-derived alkaloids. Acta Crystallogr. International Union of Crystallography; 2004;60: o377–o380. doi:10.1107/S0108270104004342LINK
2067 Ruszkowska J, Chrobak R, Maurin JK, Czarnocki Z. Vindoline and 16-demethoxyvindoline: two catharanthus-derived alkaloids. Acta Crystallogr. International Union of Crystallography; 2004;60: o377–o380. doi:10.1107/S0108270104004342LINK
2068 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2069 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2070 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2071 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2072 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2073 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2074 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2075 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2076 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2077 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2078 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2079 Ning L-L, Han J, Zhang X-Y, Guo H-Z, Bi K-S, Guo D-A. Biotransformation of triptolide and triptonide by cell suspension cultures of Catharanthus roseus. J Asian Nat Prod Res. Taylor & Francis GroupAbingdon, UK; 2006;6: 93–97. doi:10.1080/1028602031000135567LINK
2080 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
2081 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
2082 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
2083 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
2084 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
2085 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
2086 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
2087 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
2088 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
2089 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
2090 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
2091 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
2092 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
2093 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
2094 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
2095 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
2096 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
2097 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
2098 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2099 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2100 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2101 Hodes ME, Rohn RJ, Bond WH, Yardley J. Clinical trials with leurosine methiodide, an alkaloid from Vinca rosea Linn. Cancer Chemother Reports. 1963;28: 53–55.LINK
2102 Hodes ME, Rohn RJ, Bond WH, Yardley J. Clinical trials with leurosine methiodide, an alkaloid from Vinca rosea Linn. Cancer Chemother Reports. 1963;28: 53–55.LINK
2103 Hodes ME, Rohn RJ, Bond WH, Yardley J. Clinical trials with leurosine methiodide, an alkaloid from Vinca rosea Linn. Cancer Chemother Reports. 1963;28: 53–55.LINK
2104 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2105 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2106 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2107 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2108 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2109 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2110 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2111 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2112 Hardouin C, Doris E, Rousseau B, Mioskowski C. Selective deoxygenation of leurosine: concise access to anhydrovinblastine. J Org Chem. American Chemical Society; 2002;67: 6571–6574. doi:10.1021/jo0202942LINK
2113 Fisch KM. Biosynthesis of natural products by microbial iterative hybrid PKS–NRPS. RSC Adv. The Royal Society of Chemistry; 2013;3: 18228–18247. doi:10.1039/C3RA42661KLINK
2114 Fisch KM. Biosynthesis of natural products by microbial iterative hybrid PKS–NRPS. RSC Adv. The Royal Society of Chemistry; 2013;3: 18228–18247. doi:10.1039/C3RA42661KLINK
2115 Fisch KM. Biosynthesis of natural products by microbial iterative hybrid PKS–NRPS. RSC Adv. The Royal Society of Chemistry; 2013;3: 18228–18247. doi:10.1039/C3RA42661KLINK
2116 Marfori EC, Kajiyama S, Fukusaki E, Kobayashi A. Trichosetin, a novel tetramic acid antibiotic produced in dual culture of Trichoderma harzianum and Catharanthus roseus Callus. Zeitschrift fόr Naturforsch. 2002;57: 465–470.LINK
2117 Marfori EC, Kajiyama S, Fukusaki E, Kobayashi A. Trichosetin, a novel tetramic acid antibiotic produced in dual culture of Trichoderma harzianum and Catharanthus roseus Callus. Zeitschrift fόr Naturforsch. 2002;57: 465–470.LINK
2118 Marfori EC, Kajiyama S, Fukusaki E, Kobayashi A. Trichosetin, a novel tetramic acid antibiotic produced in dual culture of Trichoderma harzianum and Catharanthus roseus Callus. Zeitschrift fόr Naturforsch. 2002;57: 465–470.LINK
2119 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
2120 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
2121 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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2123 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
2124 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
2125 Mustafa NR, Kim HK, Choi YH, Erkelens C, Lefeber AWM, Spijksma G, et al. Biosynthesis of salicylic acid in fungus elicited Catharanthus roseus cells. Phytochemistry. 2009;70: 532–539. doi:10.1016/j.phytochem.2009.01.009LINK
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2127 Mustafa NR, Kim HK, Choi YH, Erkelens C, Lefeber AWM, Spijksma G, et al. Biosynthesis of salicylic acid in fungus elicited Catharanthus roseus cells. Phytochemistry. 2009;70: 532–539. doi:10.1016/j.phytochem.2009.01.009LINK
2128 Muljono RAB, Scheffer JJC, Verpoorte R. Effect of feeding salicylic acid on 2,3-dihydroxybenzoic acid formation in cultured cells of Catharanthus roseus. Pharm Biol. Informa UK Ltd UK; 2003;41: 284–290. doi:10.1076/phbi.41.4.284.15681LINK
2129 Muljono RAB, Scheffer JJC, Verpoorte R. Effect of feeding salicylic acid on 2,3-dihydroxybenzoic acid formation in cultured cells of Catharanthus roseus. Pharm Biol. Informa UK Ltd UK; 2003;41: 284–290. doi:10.1076/phbi.41.4.284.15681LINK
2130 Muljono RAB, Scheffer JJC, Verpoorte R. Effect of feeding salicylic acid on 2,3-dihydroxybenzoic acid formation in cultured cells of Catharanthus roseus. Pharm Biol. Informa UK Ltd UK; 2003;41: 284–290. doi:10.1076/phbi.41.4.284.15681LINK
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2134 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
2135 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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2137 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
2138 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
2139 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
2140 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
2141 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
2142 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
2143 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
2144 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
2145 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
2146 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
2147 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
2148 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
2149 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
2150 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
2151 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
2152 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
2153 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
2154 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
2155 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
2156 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
2157 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
2158 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
2159 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
2160 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
2161 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
2162 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
2163 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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2278 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
2279 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
2280 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
2281 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
2282 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
2283 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
2284 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
2285 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
2286 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
2287 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
2288 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
2289 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
2290 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
2291 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
2292 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
2293 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
2294 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
2295 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
2296 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
2297 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
2298 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
2299 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
2300 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
2301 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
2302 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
2303 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
2304 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
2305 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
2306 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
2307 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
2308 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
2309 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
2310 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
2311 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
2312 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
2313 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
2314 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
2315 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
2316 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
2317 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
2318 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
2319 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
2320 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
2321 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
2322 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
2323 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
2324 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
2325 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
2326 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
2327 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
2328 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
2329 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
2330 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
2331 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
2332 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
2333 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
2334 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
2335 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
2336 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
2337 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
2338 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
2339 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
2340 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
2341 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
2342 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
2343 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
2344 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
2345 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
2346 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
2347 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
2348 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
2349 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
2350 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
2351 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
2352 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
2353 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
2354 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
2355 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
2356 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
2357 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
2358 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
2359 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
2360 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
2361 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
2362 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
2363 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
2364 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
2365 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
2366 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
2367 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
2368 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
2369 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
2370 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
2371 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
2372 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
2373 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
2374 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
2375 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
2376 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
2377 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
2378 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
2379 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
2380 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2381 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2382 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
2383 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
2384 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
2385 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
2386 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
2387 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
2388 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
2389 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
2390 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
2391 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
2392 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
2393 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
2394 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
2395 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
2396 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
2397 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
2398 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
2399 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
2400 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
2401 Ruiz-May E, Galaz-Avalos RM, Loyola-Vargas VM. Differential secretion and accumulation of terpene indole alkaloids in hairy roots of Catharanthus roseus treated with methyl jasmonate. Mol Biotechnol. 2009;41: 278–285. doi:10.1007/s12033-008-9111-2LINK
2402 Ruiz-May E, Galaz-Avalos RM, Loyola-Vargas VM. Differential secretion and accumulation of terpene indole alkaloids in hairy roots of Catharanthus roseus treated with methyl jasmonate. Mol Biotechnol. 2009;41: 278–285. doi:10.1007/s12033-008-9111-2LINK
2403 Ruiz-May E, Galaz-Avalos RM, Loyola-Vargas VM. Differential secretion and accumulation of terpene indole alkaloids in hairy roots of Catharanthus roseus treated with methyl jasmonate. Mol Biotechnol. 2009;41: 278–285. doi:10.1007/s12033-008-9111-2LINK
2404 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
2405 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
2406 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
2407 Atta-ur-Rahman, Sohail M, Albert K. Structural studies on vindolinine. Zeitschrift Fuer Naturforsch. 1986;41b: 386—392.LINK
2408 Atta-ur-Rahman, Sohail M, Albert K. Structural studies on vindolinine. Zeitschrift Fuer Naturforsch. 1986;41b: 386—392.LINK
2409 Atta-ur-Rahman, Sohail M, Albert K. Structural studies on vindolinine. Zeitschrift Fuer Naturforsch. 1986;41b: 386—392.LINK
2410 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
2411 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
2412 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
2413 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
2414 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
2415 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
2416 Bashir M, Kaleem S, Fatima T. 16-epi-19-S-vindolinine, an indoline alkaloid from Catharanthus roseus. Phytochemistry. 1983;22: 1021–1023. doi:10.1016/0031-9422(83)85046-8LINK
2417 Bashir M, Kaleem S, Fatima T. 16-epi-19-S-vindolinine, an indoline alkaloid from Catharanthus roseus. Phytochemistry. 1983;22: 1021–1023. doi:10.1016/0031-9422(83)85046-8LINK
2418 Bashir M, Kaleem S, Fatima T. 16-epi-19-S-vindolinine, an indoline alkaloid from Catharanthus roseus. Phytochemistry. 1983;22: 1021–1023. doi:10.1016/0031-9422(83)85046-8LINK
2419 Zhou H, Tai Y, Sun C, Pan Y. Rapid identification of vinca alkaloids by direct-injection electrospray ionisation tandem mass spectrometry and confirmation by high-performance liquid chromatography-mass spectrometry. Phytochem Anal. 2005;16: 328–333. doi:10.1002/pca.852LINK
2420 Zhou H, Tai Y, Sun C, Pan Y. Rapid identification of vinca alkaloids by direct-injection electrospray ionisation tandem mass spectrometry and confirmation by high-performance liquid chromatography-mass spectrometry. Phytochem Anal. 2005;16: 328–333. doi:10.1002/pca.852LINK
2421 Zhou H, Tai Y, Sun C, Pan Y. Rapid identification of vinca alkaloids by direct-injection electrospray ionisation tandem mass spectrometry and confirmation by high-performance liquid chromatography-mass spectrometry. Phytochem Anal. 2005;16: 328–333. doi:10.1002/pca.852LINK
2422 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
2423 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
2424 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
2425 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
2426 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
2427 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
2428 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
2429 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
2430 Parr AJ, Peerless AC, Hamill JD, Walton NJ, Robins RJ, Rhodes MJ. Alkaloid production by transformed root cultures of Catharanthus roseus. Plant Cell Rep. 1988;7: 309–312. doi:10.1007/BF00269925LINK
2431 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
2432 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
2433 Kutney JP, Brown RT. The structural elucidation of sitsirikine, dihydrositsirikine and isositsirikine?: Three new alkaloids from Vinca rosea linn. Tetrahedron. 1966;22: 321–336. doi:10.1016/0040-4020(66)80133-3LINK
2434 Mukhopadhyay S, El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids XXXVII. 16-Epi-Z-isositsirikine, a monomeric indole alkaloid with antineoplastic activity from Catharanthus roseus and Rhazya stricta. J Nat Prod. 1983;46: 409–413. doi:10.1021/np50027a019LINK
2435 Mukhopadhyay S, El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids XXXVII. 16-Epi-Z-isositsirikine, a monomeric indole alkaloid with antineoplastic activity from Catharanthus roseus and Rhazya stricta. J Nat Prod. 1983;46: 409–413. doi:10.1021/np50027a019LINK
2436 Mukhopadhyay S, El-Sayed A, Handy GA, Cordell GA. Catharanthus alkaloids XXXVII. 16-Epi-Z-isositsirikine, a monomeric indole alkaloid with antineoplastic activity from Catharanthus roseus and Rhazya stricta. J Nat Prod. 1983;46: 409–413. doi:10.1021/np50027a019LINK
2437 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
2438 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
2439 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
2440 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
2441 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
2442 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
2443 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
2444 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
2445 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
2446 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
2447 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
2448 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
2449 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
2450 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
2451 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
2452 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
2453 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
2454 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
2455 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
2456 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
2457 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
2458 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
2459 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
2460 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
2461 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
2462 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
2463 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
2464 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
2465 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
2466 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
2467 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
2468 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
2469 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
2470 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
2471 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
2472 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
2473 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
2474 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
2475 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
2476 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
2477 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
2478 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
2479 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
2480 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
2481 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
2482 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
2483 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
2484 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
2485 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
2486 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
2487 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
2488 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
2489 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
2490 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
2491 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
2492 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
2493 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
2494 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
2495 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
2496 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
2497 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
2498 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
2499 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
2500 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
2501 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
2502 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
2503 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
2504 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
2505 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
2506 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
2507 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
2508 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
2509 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
2510 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
2511 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
2512 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
2513 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
2514 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
2515 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
2516 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
2517 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
2518 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
2519 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
2520 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
2521 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
2522 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
2523 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
2524 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
2525 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
2526 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
2527 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
2528 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
2529 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
2530 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
2531 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
2532 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
2533 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
2534 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
2535 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
2536 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
2537 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
2538 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
2539 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
2540 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
2541 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
2542 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
2543 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
2544 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
2545 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
2546 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
2547 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
2548 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
2549 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
2550 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
2551 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
2552 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
2553 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
2554 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
2555 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
2556 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
2557 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
2558 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
2559 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
2560 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
2561 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
2562 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
2563 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
2564 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
2565 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
2566 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
2567 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
2568 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
2569 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
2570 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
2571 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
2572 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
2573 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
2574 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
2575 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
2576 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
2577 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
2578 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
2579 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
2580 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
2581 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
2582 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
2583 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
2584 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
2585 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
2586 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
2587 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
2588 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
2589 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
2590 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
2591 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
2592 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
2593 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
2594 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
2595 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
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2597 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
2598 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
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2601 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
2602 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2603 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2604 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2605 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
2606 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
2607 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
2608 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2609 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2610 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2611 Zhou J, Xie G, Yan X. Encyclopedia of Traditional Chinese Medicines - Molecular Structures, Pharmacological Activities, Natural Sources and Applications: Vol. 1: Isolated Compounds A-C. Springer Berlin Heidelberg; 2011. p. 557. ISBN: 9783642167355.LINK
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2614 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
2615 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
2616 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
2617 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2618 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2619 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2620 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2621 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2622 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
2623 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2624 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2625 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2626 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2627 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2628 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2629 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
2630 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
2631 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
2632 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2633 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2634 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2635 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2636 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2637 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2638 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
2639 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
2640 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
2641 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
2642 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
2643 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
2644 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
2645 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
2646 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
2647 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
2648 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
2649 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
2650 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
2651 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
2652 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
2653 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
2654 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
2655 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
2656 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
2657 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
2658 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
2659 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
2660 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
2661 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
2662 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2663 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2664 Guo J-X, Kimura T, But PPH, Sung CK. Northeast Asia. World Scientific; 2001. p. 227. ISBN: 9789812810359.NA
2665 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
2666 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
2667 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
2668 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
2669 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
2670 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
2671 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
2672 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
2673 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
2674 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
2675 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
2676 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
2677 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
2678 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
2679 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
2680 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
2681 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
2682 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
2683 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
2684 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
2685 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
2686 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
2687 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
2688 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
2689 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
2690 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
2691 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
2692 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
2693 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
2694 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
2695 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
2696 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
2697 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
2698 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
2699 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
2700 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
2701 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
2702 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
2703 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
2704 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
2705 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
2706 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
2707 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
2708 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
2709 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
2710 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
2711 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
2712 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
2713 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
2714 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
2715 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
2716 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
2717 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
2718 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
2719 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
2720 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
2721 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
2722 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
2723 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
2724 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
2725 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
2726 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
2727 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
2728 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
2729 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
2730 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
2731 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
2732 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
2733 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
2734 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
2735 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
2736 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
2737 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
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2739 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
2740 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
2741 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
2742 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
2743 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2744 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2745 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2746 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2747 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2748 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2749 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2750 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2751 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2752 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2753 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2754 Esser K, Kadereit JW, Luttge U. Progress in Botany. illustrate. Springer; 2000. p. 467. ISBN: 9783540675518.NA
2755 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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2761 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
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2764 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
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2782 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
2783 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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2788 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
2789 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
2790 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
2791 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
2792 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
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2794 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
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2796 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
2797 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
2798 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
2799 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
2800 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
2801 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
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2803 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
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2805 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
2806 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
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2818 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
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2834 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
2835 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
2836 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
2837 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
2838 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
2839 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
2840 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
2841 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
2842 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
2843 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
2844 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
2845 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
2846 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
2847 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
2848 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
2849 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
2850 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
2851 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
2852 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
2853 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
2854 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
2855 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
2856 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
2857 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
2858 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
2859 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
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2864 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
2865 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
2866 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
2867 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
2868 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
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2875 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
2876 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
2877 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
2878 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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2880 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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2889 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
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2898 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
2899 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2900 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2901 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
2902 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
2903 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
2904 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
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2909 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
2910 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
2911 Bajaj YPS. Medicinal and aromatic plants IX. Springer Science & Business Media; 1996. p. 414. ISBN: 9783540605973.LINK
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2914 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
2915 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
2916 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
2917 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
2918 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
2919 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
2920 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
2921 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
2922 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
2923 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
2924 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
2925 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
2926 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
2927 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
2928 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
2929 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
2930 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
2931 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
2932 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
2933 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
2934 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
2935 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
2936 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
2937 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
2938 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
2939 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
2940 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
2941 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
2942 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
2943 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
2944 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
2945 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
2946 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
2947 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
2948 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
2949 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
2950 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
2951 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
2952 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
2953 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
2954 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
2955 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
2956 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
2957 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
2958 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
2959 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
2960 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
2961 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
2962 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
2963 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
2964 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
2965 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
2966 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
2967 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
2968 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
2969 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
2970 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
2971 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
2972 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
2973 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
2974 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
2975 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
2976 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
2977 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
2978 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
2979 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
2980 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
2981 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
2982 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
2983 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
2984 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
2985 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
2986 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
2987 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
2988 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
2989 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
2990 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
2991 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
2992 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
2993 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
2994 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
2995 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
2996 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
2997 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
2998 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
2999 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
3000 Mustafa NR, Verpoorte R. Phenolic compounds in Catharanthus roseus. Phytochem Rev. 2007;6: 243–258. doi:10.1007/s11101-006-9039-8LINK
3001 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
3002 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
3003 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
3004 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
3005 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
3006 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
3007 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
3008 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
3009 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260. ISBN: 9788120416895.LINK
3010 Panneerselvam C, Murugan K, Kovendan K, Kumar PM, Ponarulselvam S, Amerasan D, et al. Larvicidal efficacy of Catharanthus roseus Linn. (Family: Apocynaceae) leaf extract and bacterial insecticide Bacillus thuringiensis against Anopheles stephensi Liston. Asian Pac J Trop Med. 2013;6: 847–53.LINK
3011 Panneerselvam C, Murugan K, Kovendan K, Kumar PM, Ponarulselvam S, Amerasan D, et al. Larvicidal efficacy of Catharanthus roseus Linn. (Family: Apocynaceae) leaf extract and bacterial insecticide Bacillus thuringiensis against Anopheles stephensi Liston. Asian Pac J Trop Med. 2013;6: 847–53.LINK
3012 Panneerselvam C, Murugan K, Kovendan K, Kumar PM, Ponarulselvam S, Amerasan D, et al. Larvicidal efficacy of Catharanthus roseus Linn. (Family: Apocynaceae) leaf extract and bacterial insecticide Bacillus thuringiensis against Anopheles stephensi Liston. Asian Pac J Trop Med. 2013;6: 847–53.LINK
3013 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
3014 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
3015 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
3016 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
3017 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
3018 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
3019 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
3020 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
3021 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
3022 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
3023 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
3024 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
3025 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
3026 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
3027 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
3028 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
3029 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
3030 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
3031 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
3032 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
3033 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
3034 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
3035 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
3036 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
3037 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
3038 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
3039 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
3040 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
3041 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
3042 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
3043 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
3044 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
3045 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
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3050 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
3051 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
3052 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
3053 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
3054 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
3055 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
3056 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
3057 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
3058 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
3059 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
3060 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
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3079 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
3080 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
3081 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
3082 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
3083 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
3084 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
3085 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
3086 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
3087 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
3088 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
3089 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
3090 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
3091 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
3092 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
3093 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
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3098 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
3099 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
3100 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
3101 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
3102 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
3103 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
3104 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
3105 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
3106 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
3107 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
3108 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
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3110 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
3111 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
3112 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
3113 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
3114 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
3115 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
3116 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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3198 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
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3200 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3201 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
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3208 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
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3211 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3212 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3213 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3214 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
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3217 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3218 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3219 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3220 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3221 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3222 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3223 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3224 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3225 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3226 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3227 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
3228 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
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3231 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
3232 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
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3284 Runguphan W, Qu X, O’Connor SE. Integrating carbon-halogen bond formation into medicinal plant metabolism. Nature. Nature Publishing Group; 2010;468: 461–464. doi:10.1038/nature09524LINK
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3301 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
3302 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
3303 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
3304 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
3305 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
3306 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
3307 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
3308 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
3309 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
3310 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
3311 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
3312 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
3313 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
3314 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
3315 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
3316 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
3317 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
3318 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
3319 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
3320 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
3321 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
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3324 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
3325 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
3326 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
3327 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
3328 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
3329 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
3330 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
3331 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
3332 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
3333 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
3334 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
3335 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
3336 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
3337 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
3338 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
3339 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
3340 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
3341 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
3342 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
3343 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
3344 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
3345 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
3346 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
3347 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
3348 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
3349 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
3350 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
3351 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
3352 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
3353 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
3354 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
3355 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
3356 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
3357 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
3358 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
3359 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
3360 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
3361 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
3362 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
3363 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
3364 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
3365 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
3366 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
3367 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
3368 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
3369 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
3370 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
3371 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
3372 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
3373 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
3374 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
3375 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
3376 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
3377 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
3378 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
3379 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
3380 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
3381 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
3382 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
3383 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
3384 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
3385 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
3386 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
3387 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
3388 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
3389 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
3390 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
3391 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
3392 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
3393 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
3394 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
3395 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
3396 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
3397 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
3398 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
3399 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
3400 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
3401 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
3402 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
3403 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
3404 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
3405 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
3406 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
3407 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
3408 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
3409 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
3410 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
3411 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
3412 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
3413 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
3414 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
3415 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
3416 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
3417 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
3418 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
3419 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
3420 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
3421 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
3422 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
3423 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
3424 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
3425 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
3426 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
3427 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
3428 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
3429 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
3430 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
3431 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
3432 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
3433 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
3434 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
3435 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
3436 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
3437 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
3438 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
3439 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
3440 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
3441 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
3442 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
3443 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
3444 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
3445 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
3446 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
3447 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