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类药性:天然产物库设计的指导原则。

Drug-like properties: guiding principles for the design of natural product libraries.

机构信息

Eskitis Institute, Griffith University, Brisbane, QLD 4111, Australia.

出版信息

J Nat Prod. 2012 Jan 27;75(1):72-81. doi: 10.1021/np200687v. Epub 2011 Dec 28.

Abstract

While natural products or their derivatives and mimics have contributed around 50% of current drugs, there has been no approach allowing front-loading of chemical space compliant with lead- and drug-like properties. The importance of physicochemical properties of molecules in the development of orally bioavailable drugs has been recognized. Classical natural product drug discovery has only been able to undertake this analysis retrospectively after compounds are isolated and structures elucidated. The present approach addresses front-loading of both extracts and subsequent fractions with desired physicochemical properties prior to screening for drug discovery. The physicochemical profiles of natural products active against two neglected disease targets, malaria and African trypanosomiasis, are presented based on this strategy. This approach can ensure timely development of natural product leads at a hitherto unachievable rate.

摘要

虽然天然产物或其衍生物和类似物已经为当前 50%的药物做出了贡献,但目前还没有一种方法可以预先筛选符合先导药物和药物特性的化学空间。人们已经认识到分子的物理化学性质在开发口服生物利用药物中的重要性。经典的天然产物药物发现方法在化合物被分离和结构阐明后才能进行这种分析。本方法旨在在筛选药物发现之前,对提取物和后续馏分进行所需物理化学性质的预先筛选。根据这一策略,提出了针对两种被忽视疾病靶点(疟疾和非洲锥虫病)的天然产物的物理化学特征。这种方法可以确保以以前无法实现的速度及时开发天然产物先导物。

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