Medicinal Chemistry Research Group, Research Centre for Natural Sciences, Budapest, Hungary.
Expert Opin Drug Discov. 2022 Apr;17(4):413-422. doi: 10.1080/17460441.2022.2034783. Epub 2022 Feb 6.
Covalent drugs have been used for more than hundred years, but gathered larger interest in the last two decades. There are currently over a 100 different electrophilic warheads used in covalent ligands, and there are several considerations tailoring their reactivity against the target of interest, which is still a challenging task.
This review aims to give an overview of electrophilic warheads used for protein labeling in chemical biology and medicinal chemistry. The warheads are discussed by targeted residues, mechanism and selectivity, and analyzed through three different datasets including our collection of warheads, the CovPDB database, and the FDA approved covalent drugs. Moreover, the authors summarize general practices that facilitate the selection of the appropriate warhead for the target of interest.
In spite of the numerous electrophilic warheads, only a fraction of them is used in current drug discovery projects. Recent studies identified new tractable residues by applying a wider array of warhead chemistries. However, versatile, selective warheads are not available for all targetable amino acids, hence discovery of new warheads for these residues is needed. Broadening the toolbox of the warheads could result in novel inhibitors even for challenging targets developing with significant therapeutic potential.
共价药物已经使用了一百多年,但在过去二十年中引起了更大的兴趣。目前,在共价配体中使用了超过 100 种不同的亲电弹头,并且有几种考虑因素可以针对感兴趣的靶标调整它们的反应性,这仍然是一项具有挑战性的任务。
本文旨在概述用于化学生物学和药物化学中蛋白质标记的亲电弹头。这些弹头按靶向残基、机制和选择性进行讨论,并通过三个不同的数据集进行分析,包括我们的弹头集合、CovPDB 数据库和 FDA 批准的共价药物。此外,作者总结了促进为感兴趣的靶标选择合适弹头的一般实践。
尽管有许多亲电弹头,但目前只有其中一小部分用于当前的药物发现项目。最近的研究通过应用更广泛的弹头化学方法鉴定了新的可处理残基。然而,并非所有可靶向氨基酸都有多功能、选择性的弹头,因此需要为这些残基发现新的弹头。拓宽弹头工具箱可能会导致即使对于具有重要治疗潜力的挑战性靶标也能开发出新型抑制剂。