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新药是如何发现的?

How were new medicines discovered?

机构信息

Roche Palo Alto, 3431 Hillview Avenue, Palo Alto, California 94304, USA.

出版信息

Nat Rev Drug Discov. 2011 Jun 24;10(7):507-19. doi: 10.1038/nrd3480.

Abstract

Preclinical strategies that are used to identify potential drug candidates include target-based screening, phenotypic screening, modification of natural substances and biologic-based approaches. To investigate whether some strategies have been more successful than others in the discovery of new drugs, we analysed the discovery strategies and the molecular mechanism of action (MMOA) for new molecular entities and new biologics that were approved by the US Food and Drug Administration between 1999 and 2008. Out of the 259 agents that were approved, 75 were first-in-class drugs with new MMOAs, and out of these, 50 (67%) were small molecules and 25 (33%) were biologics. The results also show that the contribution of phenotypic screening to the discovery of first-in-class small-molecule drugs exceeded that of target-based approaches - with 28 and 17 of these drugs coming from the two approaches, respectively - in an era in which the major focus was on target-based approaches. We postulate that a target-centric approach for first-in-class drugs, without consideration of an optimal MMOA, may contribute to the current high attrition rates and low productivity in pharmaceutical research and development.

摘要

用于鉴定潜在药物候选物的临床前策略包括基于靶标的筛选、表型筛选、天然物质的修饰和基于生物学的方法。为了研究在新药发现中,某些策略是否比其他策略更成功,我们分析了 1999 年至 2008 年期间美国食品和药物管理局批准的新分子实体和新生物制剂的发现策略和作用机制(MMOA)。在批准的 259 种药物中,有 75 种是具有新 MMOA 的同类首创药物,其中 50 种(67%)是小分子药物,25 种(33%)是生物制剂。结果还表明,在以靶标为基础的方法为主导的时代,表型筛选对同类首创小分子药物的发现的贡献超过了基于靶标的方法——这两种方法分别有 28 种和 17 种药物来自这两种方法。我们推测,对于同类首创药物的以靶标为中心的方法,如果不考虑最佳 MMOA,可能会导致目前制药研发中高淘汰率和低生产力的现状。

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