Vindoline and its Reactions

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DC Field	Value	Language
dc.contributor.author	INAM-UL-HAQUE	-
dc.contributor.author	HINA SABA	-
dc.date.accessioned	2023-10-05T10:04:48Z	-
dc.date.available	2023-10-05T10:04:48Z	-
dc.date.issued	2011-12-20	-
dc.identifier.citation	Qu, Y., Easson, M. L., Froese, J., Simionescu, R., Hudlicky, T., & De Luca, V. (2015). Completion of the seven-step pathway from tabersonine to the anticancer drug precursor vindoline and its assembly in yeast. Proceedings of the National Academy of Sciences, 112(19), 6224-6229.	en_US
dc.identifier.issn	0253-5106	-
dc.identifier.uri	http://142.54.178.187:9060/xmlui/handle/123456789/19797	-
dc.description.abstract	Vindoline is a major alkaloid from the leaves of Vinca roseus Linn. (Catharanthus roseus G. Don) Apocynaceae. Chemically vindoline lacks physiological activity alone but is contained as the pentacyclic moiety in the antineoplastic agents, vinblastine and vincristine. Synthesis, reactions and determination of vindoline by different methods are reviewed from 1976 to 2010.	en_US
dc.description.sponsorship	The chemical society of Pakistan is an approved society from the PSF.	en_US
dc.language.iso	en	en_US
dc.publisher	HEJ Research Institute of Chemistry, University of Karachi, Karachi.	en_US
dc.title	Vindoline and its Reactions	en_US
dc.type	Article	en_US
Appears in Collections:	Issue 06

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