Phytochemica: A platform to explore phytochemicals of medicinal plants

References for PDM ID: CARS0472


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 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
3 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
4 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
5 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
6 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
7 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
8 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
9 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
10 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
11 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
12 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
13 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
14 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
15 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
16 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
17 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
18 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
19 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
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 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
22 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
23 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
24 Zenk MH, El-Shagi H, Arens H, St?ckigt J, Weiler EW, Deus B. Formation of the Indole Alkaloids Serpentine and Ajmalicine in Cell Suspension Cultures of Catharanthus roseus. In: Barz W, Reinhard E, Zenk MH, editors. Plant Tissue Culture and Its Bio-technological Application. Berlin, Heidelberg: Springer Berlin Heidelberg; 1977. pp. 27–43. doi:10.1007/978-3-642-66646-9_3LINK
25 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
26 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
27 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
28 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
29 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
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 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
32 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
33 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
34 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
35 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
36 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
37 V?zquez-Flota F, Moreno-Valenzuela O, Miranda-Ham ML, Coello-Coello J, Loyola-Vargas VM. Catharanthine and ajmalicine synthesis in Catharanthus roseus hairy root cultures. Plant Cell Tissue Organ Cult. 1994;38: 273–279. doi:10.1007/BF00033887LINK
38 Gupta MM, Singh D V, Tripathi AK, Pandey R, Verma RK, Singh S, et al. Simultaneous determination of vincristine, vinblastine, catharanthine, and vindoline in leaves of catharanthus roseus by high-performance liquid chromatography. J Chromatogr Sci. 2005;43: 450–453. doi:10.1093/chromsci/43.9.450LINK
39 Verma A, Laakso I, Sepp?nen-Laakso T, Huhtikangas A, Riekkola M-L. A simplified procedure for indole alkaloid extraction from Catharanthus roseus combined with a semi-synthetic production process for vinblastine. Molecules. Molecular Diversity Preservation International; 2007;12: 1307–1315. doi:10.3390/12071307LINK
40 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
41 DiCosmo F, Quesnel A, Misawa M, Tallevi SG. Increased synthesis of ajmalicine and catharanthine by cell suspension cultures of Catharanthus roseus in response to fungal culture-filtrates. Appl Biochem Biotechnol. 1987;14: 101–106. doi:10.1007/BF02798428LINK
42 Yu J, Yuan S, Pang H, Zhang X, Jia X, Tang Z, et al. Distribution and accumulation of vindoline, catharanthine and vinblastine in Catharanthus roseus cultivated in China. Zhongguo Zhongyao Zazhi. 2010;35: 3093–3096. doi:10.4268/cjcmm20102301LINK
43 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
44 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
45 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
46 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
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 Wagner H, H?rhammer L. 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
49 Besseau S, Kellner F, Lanoue A, Thamm AMK, Salim V, Schneider B, et al. A pair of tabersonine 16-hydroxylases initiates the synthesis of vindoline in an organ-dependent manner in Catharanthus roseus. Plant Physiol. 2013;163: 1792–1803. doi:10.1104/pp.113.222828LINK
50 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
51 DeLuca V, Balsevich J, Tyler RT, Eilert U, Panchuk BD, Kurz WGW. Biosynthesis of Indole Alkaloids: Developmental Regulation of the Biosynthetic Pathway from Tabersonine to Vindoline in Catharanthus roseus. J Plant Physiol. 1986;125: 147–156. doi:10.1016/S0176-1617(86)80252-8LINK
52 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
53 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
54 Ataei-Azimi A, Hashemloian BD, Ebrahimzadeh H, Majd A. High in vitro production of ant-canceric indole alkaloids from periwinkle Catharanthus roseus tissue culture. African J Biotechnol. 2008;7: 2834–2839.LINK
55 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
56 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
57 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
58 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
59 Wagner H, H?rhammer L. 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
60 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
61 Sathiya S, Karthikeyan B, Jaleel CA, Azooz MM, Iqbal M. Antibiogram of Catharanthus roseus Extracts. Glob J Mol Sci. 2008;3: 1–7.LINK
62 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
63 Eilert U, Nesbitt LR, Constabel F. Laticifers and latex in fruits of periwinkle, Catharanthus roseus. Can J Bot. 1985;63: 1540–1546. doi:10.1139/b85-213LINK
64 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
65 Ali I. Isolation and structural studies on the alkaloids of Catharanths roseus [Internet]. University of Karachi. 1985. p. 144.LINK
66 Qifang P. Metabolomic characteristics of Catharanthus roseus plants in time and space [Internet]. Institute of Biology (IBL), Faculty of Science, Leiden University. 2014. p. 180.LINK
67 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
68 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
69 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
70 Schmelzer GH, Gurib-Fakim A. Plant Resources of Tropical Africa 11(1). Medicinal Plants [Internet]. 1st ed. Schmelzer GH, Gurib-Fakim A, editors. Wageningen, Netherlands: PROTA Foundation; 2008. p. 790. ISBN: 9789057822049.LINK
71 Hirata K, Miyamoto K, Miura Y. Catharanthus roseus L. (Periwinkle): Production of Vindoline and Catharanthine in Multiple Shoot Cultures. In: Bajaj YPS, editor. Medicinal and Aromatic Plants VI. Berlin, Heidelberg: Springer Berlin Heidelberg; 1994. pp. 46–55. doi:10.1007/978-3-642-57970-7_3LINK
72 Gupta MM, Singh D V, Tripathi AK, Pandey R, Verma RK, Singh S, et al. Simultaneous determination of vincristine, vinblastine, catharanthine, and vindoline in leaves of catharanthus roseus by high-performance liquid chromatography. J Chromatogr Sci. 2005;43: 450–453. doi:10.1093/chromsci/43.9.450LINK
73 Yu J, Yuan S, Pang H, Zhang X, Jia X, Tang Z, et al. Distribution and accumulation of vindoline, catharanthine and vinblastine in Catharanthus roseus cultivated in China. Zhongguo Zhongyao Zazhi. 2010;35: 3093–3096. doi:10.4268/cjcmm20102301LINK
74 Wagner H, H?rhammer L. 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
75 Junaid A, Khan SH, Siddiqui ZH, Zohra F, Mehpara M, Bhat MA, et al. Catharanthus roseus (L.) G. Don. An important drug: It’s applications and production. Pharm Glob (International J Compr Pharmacy). 2010;1.LINK
76 De Luca V, Laflamme P. The expanding universe of alkaloid biosynthesis. Curr Opin Pant Biol. 2001;4: 225–233. doi:10.1016/S1369-5266(00)00165-5LINK
77 Campos-Tamayo F, Hern?ndez-Dom?nguez E, V?zquez-Flota F. Vindoline formation in shoot cultures of Catharanthus roseus is synchronously activated with morphogenesis through the last biosynthetic step. Ann Bot. 2008;102: 409–415. doi:10.1093/aob/mcn108LINK
78 Zhong X-Z, Wang G-C, Wang Y, Zhang X-Q, Ye W-C. Monomeric indole alkaloids from the aerial parts of Catharanthus roseus. Acta Pharm Sin. 2010;45: 471–474.LINK
79 Wang Q, Xing S, Pan Q, Yuan F, Zhao J, Tian Y, et al. Development of efficient Catharanthus roseus regeneration and transformation system using agrobacterium tumefaciens and hypocotyls as explants. BMC Botechnology. 2012;12: 34. doi:10.1186/1472-6750-12-34LINK
80 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
81 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
82 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
83 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
84 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
85 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
86 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
87 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
88 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
89 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
90 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
91 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
92 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
93 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
94 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
95 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
96 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
97 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
98 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
99 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
100 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
101 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
102 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
103 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
104 Ferreres F, Pereira DM, Valent?o P, Andrade PB, Seabra RM, Sottomayor M. New phenolic compounds and antioxidant potential of Catharanthus roseus. J Agric Food Chem. American Chemical Society; 2008;56: 9967–9974. doi:10.1021/jf8022723LINK
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501 Richord Talbot Brown. The chemistry of the Vinca alkaloids sitsirikine, catharanthine, and their derivatives. The University of British Columbia. 1964. p. 155.LINK
502 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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504 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
505 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
506 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
507 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
508 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
509 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
510 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
511 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
512 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
513 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
514 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
515 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
516 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
517 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
518 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
519 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
520 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
521 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
522 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
523 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
524 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
525 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
526 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
527 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
528 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
529 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
530 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
531 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
532 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
533 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
534 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
535 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
536 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
537 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
538 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
539 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
540 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
541 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
542 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
543 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
544 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
545 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
546 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
547 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
548 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
549 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
550 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
551 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
552 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
553 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
554 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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767 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
768 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
769 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
770 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
771 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
772 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
773 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
774 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
775 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
776 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
777 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
778 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
779 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
780 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
781 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
782 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
783 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
784 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
785 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
786 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
787 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
788 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
789 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
790 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
791 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
792 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
793 Wagner H, H?rhammer L. 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
794 Zhang W-K, Xu J-K, Tian H-Y, Wang L, Zhang X-Q, Xu-Zhi Xiao PL, et al. Further bisindole alkaloids from Catharanthus roseus and their cytotoxicity. Heterocycles. 2013;87: 627–636. doi:10.3987/COM-12-12659LINK
795 Wang C-H, Wang G-C, Wang Y, Zhang X-Q, Huang X-J, Zhang D-M, et al. Cytotoxic dimeric indole alkaloids from Catharanthus roseus. Fitoterapia. 2012;83: 765–769. doi:10.1016/j.fitote.2012.03.007LINK
796 Wagner H, H?rhammer L. 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
797 Wagner H, H?rhammer L. 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
798 Wagner H, H?rhammer L. 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
799 Wagner H, H?rhammer L. 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
800 Wagner H, H?rhammer L. 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
801 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
802 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
803 Atta-ur-Rahman, Sohail M, Albert K. Structural studies on vindolinine. Zeitschrift Fuer Naturforsch. 1986;41b: 386—392.LINK
804 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
805 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
806 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
807 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
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)85069-6LINK
809 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
810 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
811 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
812 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
813 Wagner H, H?rhammer L. 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
814 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
815 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
816 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
817 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
818 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
819 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
820 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
821 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
822 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
823 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
824 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
825 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
826 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
827 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
828 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
829 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
830 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
831 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
832 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
833 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
834 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
835 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
836 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
837 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
838 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
839 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
840 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
841 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
842 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
843 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
844 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
845 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
846 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
847 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
848 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
849 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
850 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
851 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
852 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
853 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
854 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
855 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
856 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
857 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
858 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK
859 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
860 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
861 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
862 Wagner H, H?rhammer L. 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
863 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
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867 Wagner H, H?rhammer L. Pharmacognosy and Phytochemistry. 1st ed. Wagner H, H?rhammer L, editors. Phytochemistry. Springer-Verlag; 1971. p. 386. doi:10.1016/0031-9422(72)85069-6LINK
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873 Daniel M. Medicinal plants: Chemistry and properties. 1st ed. Oxford & IBH Publishing Company Pvt. Limited; 2005. p. 260.LINK
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887 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
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897 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
898 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
899 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
900 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
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902 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
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1099 Chung IM, Ali M, Chun SC, San KY, Peebles CAM, Ahmad A. New catharanthusopimaranoside A and B from hairy root cultures of Catharanthus roseus. Chem Nat Compd. 2008;44: 458–462. doi:10.1007/s10600-008-9096-xLINK
1100 Chung IM, Ali M, Chun SC, San KY, Peebles CAM, Ahmad A. New catharanthusopimaranoside A and B from hairy root cultures of Catharanthus roseus. Chem Nat Compd. 2008;44: 458–462. doi:10.1007/s10600-008-9096-xLINK
1101 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1102 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1103 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1104 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1105 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1106 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1107 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1108 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
1109 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1110 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1111 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1112 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1113 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1114 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1115 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1116 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1117 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1118 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1119 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1120 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1121 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1122 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1123 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1124 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1125 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1126 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1127 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1128 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1129 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1130 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1131 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1132 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1133 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1134 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1135 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1136 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1137 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1138 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1139 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1140 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1141 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1142 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1143 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1144 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1145 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1146 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1147 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1148 Pandey-Rai S, Mallavarapu GR, Naqvi AA, Yadav A, Rai SK, Srivastava S, et al. Volatile components of leaves and flowers of periwinkle Catharanthus roseus (L.) G. Don from New Delhi. Flavour Fragr J. 2006;21: 427–430. doi:10.1002/ffj.1606LINK
1149 Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline and 20’-epi-vincovaline. J Org Chem. American Chemical Society; 1991;56: 513–528. doi:10.1021/jo00002a008LINK