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抗菌药物化学——我们能设计出什么?

Antibacterial medicinal chemistry - what can we design for?

作者信息

Parkes Alastair L

机构信息

Discovery Chemistry, Evotec (UK) Ltd , Abingdon, UK.

出版信息

Expert Opin Drug Discov. 2020 Sep;15(9):1005-1013. doi: 10.1080/17460441.2020.1767065. Epub 2020 May 26.

Abstract

INTRODUCTION

The need for new antibacterial agents continues to grow, but success in development of antibiotics in recent years has been limited. To improve the chances that new compounds will progress into clinical trials and beyond, it is vital that we consider as early as possible in the process the various challenges that discoverers and developers of new antibiotics will face.

AREAS COVERED

The author looks at the factors that affect medicinal chemistry aimed at providing successful antibacterial agents. Target selection, target inhibition, accumulation in bacteria, and pharmacokinetics are all discussed, with a particular emphasis on how our current understanding should impact design and optimization strategies.

EXPERT OPINION

From the perspective of a medicinal chemist, the primary question when considering the various aspects of antibacterial drug discovery should be 'what can I design for?' It is important to be aware of the limitations of our understanding, and also the constraints and challenges that arise due to the diversity of the bacteria we try to address. Progress is needed to simplify approval pathways and to increase return on investment for the next generations of clinically useful agents to succeed.

摘要

引言

对抗菌新药的需求持续增长,但近年来抗生素研发的成功率有限。为提高新化合物进入临床试验及后续阶段的几率,在研发过程中尽早考虑新抗生素的发现者和开发者将面临的各种挑战至关重要。

涵盖领域

作者探讨了影响旨在研发成功抗菌药物的药物化学的因素。讨论了靶点选择、靶点抑制、在细菌中的蓄积以及药代动力学等方面,特别强调了我们目前的认识应如何影响设计和优化策略。

专家观点

从药物化学家的角度来看,在考虑抗菌药物发现的各个方面时,首要问题应该是“我能设计什么?” 重要的是要意识到我们认识的局限性,以及由于我们试图应对的细菌多样性而产生的限制和挑战。需要取得进展以简化审批途径,并提高下一代临床有用药物成功的投资回报率。

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