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醛氧化酶代谢:药物设计与药物发现挑战的互补方法。

Metabolism by Aldehyde Oxidase: Drug Design and Complementary Approaches to Challenges in Drug Discovery.

机构信息

UCB Celltech , 208 Bath Road , Slough SL13WE , United Kingdom.

UCB BioPharma , Chemin du Foriest 1 , 1420 Braine-l'Alleud , Belgium.

出版信息

J Med Chem. 2019 Dec 26;62(24):10955-10994. doi: 10.1021/acs.jmedchem.9b00875. Epub 2019 Aug 20.

Abstract

Aldehyde oxidase (AO) catalyzes oxidations of azaheterocycles and aldehydes, amide hydrolysis, and diverse reductions. AO substrates are rare among marketed drugs, and many candidates failed due to poor pharmacokinetics, interspecies differences, and adverse effects. As most issues arise from complex and poorly understood AO biology, an effective solution is to stop or decrease AO metabolism. This perspective focuses on rational drug design approaches to modulate AO-mediated metabolism in drug discovery. AO biological aspects are also covered, as they are complementary to chemical design and important when selecting the experimental system for risk assessment. The authors' recommendation is an early consideration of AO-mediated metabolism supported by computational and in vitro experimental methods but not an automatic avoidance of AO structural flags, many of which are versatile and valuable building blocks. Preferably, consideration of AO-mediated metabolism should be part of the multiparametric drug optimization process, with the goal to improve overall drug-like properties.

摘要

醛氧化酶(AO)催化杂环氮原子和醛的氧化、酰胺水解以及多种还原反应。AO 的底物在上市药物中较为罕见,许多候选药物由于药代动力学不佳、种间差异和不良反应而失败。由于大多数问题源于复杂且尚未充分了解的 AO 生物学,因此有效的解决方案是阻止或减少 AO 代谢。本观点重点介绍了在药物发现中调节 AO 介导的代谢的合理药物设计方法。还涵盖了 AO 的生物学方面,因为它们与化学设计相辅相成,在选择用于风险评估的实验系统时非常重要。作者的建议是在计算和体外实验方法的支持下,尽早考虑 AO 介导的代谢,但并非自动避免 AO 结构标记,因为其中许多标记是多功能且有价值的构建块。最好将 AO 介导的代谢考虑纳入多参数药物优化过程中,以提高整体类药性。

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