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Alpana S. Joshi

Researcher at University of Mississippi

Publications -  10
Citations -  210

Alpana S. Joshi is an academic researcher from University of Mississippi. The author has contributed to research in topics: Taxus & Absolute configuration. The author has an hindex of 6, co-authored 7 publications receiving 203 citations.

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Fatty Acid Synthase Inhibitors from Plants: Isolation, Structure Elucidation, and SAR Studies

TL;DR: Three'-Formylgenistein and ellagic acid 4-O-alpha-l-rhamnopyranoside were the most potent compounds against FAS, with IC(50) values of 2.3 and 7.5 microg/mL, respectively.
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Absolute configuration, conformation, and chiral properties of flavanone-(3→8″)-flavone biflavonoids from Rheedia acuminata

TL;DR: In this paper, the absolute configurations of three flavanone-(3→8″)-flavone type biflavonoids, (+)-morelloflavone (1), (+)-volkensiflavone-7-sulfate (2 ), isolated from Rheedia acuminata, were confirmed by circular dichroism as 2 R,3 S, hence clarifying the literature confusion of 2 S,3 R absolute configuration for (+-morelloftlavone.
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Diurnal and Seasonal Effects on the Taxane Content of the Clippings of CertainTaxus Cultivars

TL;DR: The best time to harvest Taxus clippings for the production of taxanes (especially 1 and 6) is approximately one month from the beginning of new growth (flush). The date of harvest could vary depending on the geographic location and weather conditions.
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Concentrations of taxol and related taxanes in the needles of different Taxus cultivars

TL;DR: The taxane content of the needles of 57 cultivars obtained from five major nurseries in the United States is presented in this article, and the results of these analyses showed that the total “useful” taxanes varied between 0.0232-0.113%, with 1 and 6 being the most abundant taxanes.
Journal ArticleDOI

Absolute Configuration, Conformation, and Chiral Properties of Flavanone‐(3→8′′)‐Flavone Biflavonoids from Rheedia acuminata.

TL;DR: In this paper, the absolute configurations of three flavanone-(3→8″)-flavone type biflavonoids, (+)-morelloflavone (1), (+)-volkensiflavone-7-sulfate (2 ), isolated from Rheedia acuminata, were confirmed by circular dichroism as 2 R,3 S, hence clarifying the literature confusion of 2 S,3 R absolute configuration for (+-morelloftlavone.