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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/19797
Title: Vindoline and its Reactions
Authors: INAM-UL-HAQUE
HINA SABA
Issue Date: 20-Dec-2011
Publisher: HEJ Research Institute of Chemistry, University of Karachi, Karachi.
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.
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.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/19797
ISSN: 0253-5106
Appears in Collections:Issue 06

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