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紧密接触:水杨醛在赖氨酸靶向共价药物中的应用不断扩大。

A Tight Contact: The Expanding Application of Salicylaldehydes in Lysine-Targeting Covalent Drugs.

机构信息

Dipartimento di Chimica, Università degli Studi di Milano, Via C. Golgi, 19, 20133, Milan, Italy.

出版信息

Chembiochem. 2024 Apr 2;25(7):e202300743. doi: 10.1002/cbic.202300743. Epub 2023 Nov 28.

Abstract

The installation of aldehydes into synthetic protein ligands is an efficient strategy to engage protein lysine residues in remarkably stable imine bonds and augment the compound affinity and selectivity for their biological targets. The high frequency of lysine residues in proteins and the reversibility of the covalent ligand-protein bond support the application of aldehyde-bearing ligands, holding promises for their future use as drugs. This review highlights the increasing exploitation of salicylaldehyde modules in various classes of protein binders, aimed at the reversible-covalent engagement of lysine residues.

摘要

将醛基引入合成蛋白配体中是一种有效的策略,可以使蛋白赖氨酸残基形成非常稳定的亚胺键,并提高化合物对其生物靶标的亲和力和选择性。蛋白中赖氨酸残基的高频率和共价配体-蛋白键的可逆性支持了含醛配体的应用,为其未来作为药物的应用提供了前景。本文综述了水杨醛模块在各种类型的蛋白配体中的应用,旨在实现赖氨酸残基的可逆共价结合。

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