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天然产物药物发现:ISP-1 和海兔素 B 的成功优化。

Natural product drug discovery: the successful optimization of ISP-1 and halichondrin B.

机构信息

Novartis Institute for Tropical Diseases, 10 Biopolis Road, Chromos, Singapore 138670, Singapore.

出版信息

Curr Opin Chem Biol. 2011 Aug;15(4):523-8. doi: 10.1016/j.cbpa.2011.05.019. Epub 2011 Jun 22.

Abstract

The concept that natural products provide excellent leads for drug discovery, ultimately producing viable drugs, is a widely accepted view. Natural products embody inherent structural complexity and biological activity which often leads to new targets, pathways, or modes of action. The challenge lies in identifying quality natural product scaffolds that can ultimately result in a drug. Two recently approved drugs originating from unlikely natural product leads, ISP-1 and halichondrin B, were examples of such high quality scaffolds. In initial testing, both compounds displayed excellent in vitro potency, but more importantly were amenable to chemical optimization. This combination of unique biological activity plus the generation of structural activity relationships (SAR) may be early indicators of a high quality natural product scaffold worthy of additional studies.

摘要

天然产物是药物发现的优秀先导化合物,最终能产生可行的药物,这一概念已被广泛接受。天然产物具有内在的结构复杂性和生物活性,这往往能带来新的靶点、途径或作用模式。挑战在于识别高质量的天然产物骨架,最终能开发成药物。最近批准的两种药物 ISP-1 和卤虫内酯 B 就是来自不太可能的天然产物先导物的例子,它们是高质量骨架的代表。在初步测试中,这两种化合物都表现出优异的体外活性,但更重要的是,它们可以进行化学优化。这种独特的生物活性加上结构活性关系(SAR)的产生,可能是高质量天然产物骨架值得进一步研究的早期指标。

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