共价键
化学
化学生物学
半胱氨酸
反应性(心理学)
弹头
生物化学
氨基酸
氨基酸残基
共价结合
组合化学
有机化学
肽序列
酶
航空航天工程
替代医学
病理
工程类
基因
医学
作者
Matthias Gehringer,Stefan Laufer
标识
DOI:10.1021/acs.jmedchem.8b01153
摘要
Targeted covalent inhibitors (TCIs) are designed to bind poorly conserved amino acids by means of reactive groups, the so-called warheads. Currently, targeting noncatalytic cysteine residues with acrylamides and other α,β-unsaturated carbonyl compounds is the predominant strategy in TCI development. The recent ascent of covalent drugs has stimulated considerable efforts to characterize alternative warheads for the covalent-reversible and irreversible engagement of noncatalytic cysteine residues as well as other amino acids. This Perspective article provides an overview of warheads-beyond α,β-unsaturated amides-recently used in the design of targeted covalent ligands. Promising reactive groups that have not yet demonstrated their utility in TCI development are also highlighted. Special emphasis is placed on the discussion of reactivity and of case studies illustrating applications in medicinal chemistry and chemical biology.
科研通智能强力驱动
Strongly Powered by AbleSci AI