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药物发现中的结构警报设计。

Designing around Structural Alerts in Drug Discovery.

机构信息

Medicine Design, Pfizer Worldwide Research, Development and Medical, 1 Portland Street, Cambridge, Massachusetts 02139, United States.

出版信息

J Med Chem. 2020 Jun 25;63(12):6276-6302. doi: 10.1021/acs.jmedchem.9b00917. Epub 2019 Sep 17.

Abstract

Cumulative research over several decades has implicated the involvement of reactive metabolites in many idiosyncratic adverse drug reactions (IADRs). Consequently, "avoidance" strategies have been inserted into drug discovery paradigms, which include the exclusion of structural alerts and possible termination of reactive metabolite-positive compounds. Several noteworthy examples where reactive metabolite-related liabilities have been resolved through structure-metabolism studies are presented herein. Considerable progress has also been made in addressing the limitations of the avoidance strategy and further refining the process of managing reactive metabolite issues in drug development. These efforts primarily stemmed from the observation that numerous drugs, which contain structural alerts and/or form reactive metabolites, are devoid of ADRs. The Perspective also dwells into an analysis of the structural alert/reactive metabolite concept with a discussion of risk mitigation tactics to support the progression of reactive metabolite-positive drug candidates.

摘要

几十年来的累积研究表明,许多药物不良反应(IADRs)与反应性代谢物有关。因此,“避免”策略已被纳入药物发现范例中,其中包括排除结构警示和可能终止具有反应性代谢物的化合物。本文介绍了一些通过结构代谢研究解决与反应性代谢物相关的局限性的显著例子。在解决避免策略的局限性并进一步完善药物开发中管理反应性代谢物问题的过程方面也取得了相当大的进展。这些努力主要源于以下观察结果:许多含有结构警示和/或形成反应性代谢物的药物没有不良反应。该观点还深入分析了结构警示/反应性代谢物的概念,并讨论了降低风险的策略,以支持具有反应性代谢物的候选药物的进展。

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