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http://142.54.178.187:9060/xmlui/handle/123456789/19797Full metadata record
| 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 | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| ViewByVolume.aspx?v=173&i=VOLUME%2033,%20NO6,%20DEC%202011.htm | 149 B | HTML | View/Open |
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