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Ke Chen

Researcher at University of North Carolina at Chapel Hill

Publications -  28
Citations -  1201

Ke Chen is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Polanisia dodecandra & Triterpene. The author has an hindex of 17, co-authored 27 publications receiving 1144 citations.

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Anti-AIDS agents, 10. Acacetin-7-O-beta-D-galactopyranoside, an anti-HIV principle from Chrysanthemum morifolium and a structure-activity correlation with some related flavonoids.

TL;DR: An active anti-HIV principle, acacetin-7-O-beta-D-galactopyranoside, has been isolated from Chrysanthemum morifolium and a known flavone, chrysin, was found to be the most promising compound in this series of flavonoids.
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Anti-AIDS agents-XXVI. Structure-activity correlations of gomisin-G-related anti-HIV lignans from Kadsura interior and of related synthetic analogues

TL;DR: The anti-HIV data indicated that the relative position and types of substituents on the phenolic hydroxy groups of either the natural lignans or the synthetic biphenyl compounds rather than the numbers of bromine(s) on the aromatic rings are of primary importance.
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Two new lignans, interiotherins A and B, as anti-HIV principles from Kadsura interior.

TL;DR: Two new lignans, interiotherins A and B and B, along with two known lignan, angeloylgomisin R and schisantherin D, were isolated from Kadsura interior and their structures and stereochemistries were determined from spectral data.
Journal Article

Recent progress in the development of tubulin inhibitors as antimitotic antitumor agents.

TL;DR: A review of the development of tubulin inhibitors can be found in this article, where the authors describe the recent progress being made in the discovery of novel antimitotic antitumor tubulin inhibitor.
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Antitumor agents. 174. 2',3',4',5,6,7-Substituted 2-phenyl-1,8-naphthyridin-4-ones: their synthesis, cytotoxicity, and inhibition of tubulin polymerization.

TL;DR: A good correlation was found between cytotoxicity and inhibition of tubulin polymerization in the 2-phenyl-1,8-naphthyridin-4-one series and further investigation is underway to determine if substitution at the 3'-position and multisubstitutions in ring C will result in compounds with increased activity.