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比尤延宁类化合物库的设计、合成与生物评价。

Design, synthesis, and biological evaluation of a biyouyanagin compound library.

机构信息

Department of Chemistry, Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

Proc Natl Acad Sci U S A. 2011 Apr 26;108(17):6715-20. doi: 10.1073/pnas.1015258108. Epub 2011 Jan 18.

Abstract

Modern drug discovery efforts rely, to a large extent, on lead compounds from two classes of small organic molecules; namely, natural products (i.e., secondary metabolites) and designed compounds (i.e., synthetic molecules). In this article, we demonstrate how these two domains of lead compounds can be merged through total synthesis and molecular design of analogs patterned after the targeted natural products, whose promising biological properties provide the motivation. Specifically, the present study targeted the naturally occurring biyouyanagins A and B and their analogs through modular chemical synthesis and led to the discovery of small organic molecules possessing anti-HIV and anti-arenavirus properties.

摘要

现代药物发现工作在很大程度上依赖于两类小分子的先导化合物

天然产物(即次生代谢产物)和设计化合物(即合成分子)。本文通过对目标天然产物进行全合成和类似物的分子设计,展示了如何将这两个先导化合物领域结合起来,这些天然产物具有有前景的生物特性,为研究提供了动力。具体来说,本研究通过模块化化学合成针对天然存在的比优岩藻素 A 和 B 及其类似物,并发现了具有抗 HIV 和抗沙粒病毒特性的小分子有机化合物。

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