Zhao Zheng, Bourne Philip E
School of Data Science, University of Virginia, Charlottesville, Virginia, USA.
Department of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, USA.
Med Res Rev. 2025 Mar;45(2):629-653. doi: 10.1002/med.22084. Epub 2024 Sep 17.
Reversible covalent kinase inhibitors (RCKIs) are a class of novel kinase inhibitors attracting increasing attention because they simultaneously show the selectivity of covalent kinase inhibitors yet avoid permanent protein-modification-induced adverse effects. Over the last decade, RCKIs have been reported to target different kinases, including Atypical group of kinases. Currently, three RCKIs are undergoing clinical trials. Here, advances in RCKIs are reviewed to systematically summarize the characteristics of electrophilic groups, chemical scaffolds, nucleophilic residues, and binding modes. In so doing, we integrate key insights into privileged electrophiles, the distribution of nucleophiles, and hence effective design strategies for the development of RCKIs. Finally, we provide a further perspective on future design strategies for RCKIs, including those that target proteins other than kinases.
可逆共价激酶抑制剂(RCKIs)是一类新型激酶抑制剂,因其同时兼具共价激酶抑制剂的选择性,又能避免永久性蛋白质修饰引起的不良反应而备受关注。在过去十年中,已报道RCKIs可作用于不同的激酶,包括非典型激酶组。目前,有三种RCKIs正在进行临床试验。本文对RCKIs的研究进展进行综述,系统总结亲电基团、化学骨架、亲核残基和结合模式的特点。通过这样做,我们整合了对优势亲电试剂、亲核试剂分布的关键见解,以及RCKIs开发的有效设计策略。最后,我们对RCKIs未来的设计策略提供了进一步的展望,包括那些针对激酶以外蛋白质的策略。