Advances in reversible covalent kinase inhibitors

IF 10.9 1区 医学 Q1 CHEMISTRY, MEDICINAL
Zheng Zhao, Philip E. Bourne
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引用次数: 0

Abstract

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.

Abstract Image

可逆共价激酶抑制剂的研究进展
可逆共价激酶抑制剂(RCKIs)是一类新型激酶抑制剂,因其同时具有共价激酶抑制剂的选择性和避免永久性蛋白质修饰引起的不良反应而日益受到关注。据报道,过去十年中,RCKIs 针对不同的激酶,包括非典型激酶。目前,有三种 RCKIs 正在进行临床试验。在此,我们回顾了 RCKIs 的研究进展,系统地总结了亲电基团、化学支架、亲核残基和结合模式的特点。在此过程中,我们整合了关于亲电体特权、亲核体分布的重要见解,从而为 RCKIs 的开发提供了有效的设计策略。最后,我们进一步展望了 RCKIs 的未来设计策略,包括那些以激酶以外的蛋白质为靶点的 RCKIs。
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来源期刊
CiteScore
29.30
自引率
0.00%
发文量
52
审稿时长
2 months
期刊介绍: Medicinal Research Reviews is dedicated to publishing timely and critical reviews, as well as opinion-based articles, covering a broad spectrum of topics related to medicinal research. These contributions are authored by individuals who have made significant advancements in the field. Encompassing a wide range of subjects, suitable topics include, but are not limited to, the underlying pathophysiology of crucial diseases and disease vectors, therapeutic approaches for diverse medical conditions, properties of molecular targets for therapeutic agents, innovative methodologies facilitating therapy discovery, genomics and proteomics, structure-activity correlations of drug series, development of new imaging and diagnostic tools, drug metabolism, drug delivery, and comprehensive examinations of the chemical, pharmacological, pharmacokinetic, pharmacodynamic, and clinical characteristics of significant drugs.
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