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Exploring of drug leads from diversity-oriented Michael-acceptor library derived from natural products 被引量:1

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摘要 A potential strategy for drug lead identification and in-active natural products re-discovery is elaborated.Starting from fifteen structurally diverse natural products,a focused library featured by Michael acceptors is constructed with IBX mediated oxidation.Biological assay on five tumor cell lines indicates that four Michael acceptors,8a,11a,12a,14a,are with improved cytotoxicity(3-10 folds more potent than the parent compounds),which merit further investigations.Further thiol-sensitive assay of the active hit 8a revealed that it was an irreversible Michael acceptor.The results suggest that the strategy is not only effective and relatively high discovery rate(28%),but also resource saving.
出处 《Natural Products and Bioprospecting》 CAS 2012年第5期210-216,共7页 应用天然产物(英文)
基金 We thanked the National Natural Science Foundation of China(No.90813004,U0932602,20802083 and 973 Program No.2009CB522303 and No.2011CB915503) the State Key Laboratory of Phytochemistry and Plant Resources in West China(P2010-ZZ18)for financial support.
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