Covalent Warheads Targeting Cysteine Residue: The Promising Approach in Drug Development

被引:62
作者
Huang, Fangjiao [1 ,2 ]
Han, Xiaoli [1 ,2 ]
Xiao, Xiaohui [1 ,2 ]
Zhou, Jinming [1 ,2 ]
机构
[1] Zhejiang Normal Univ, Dept Chem, Minist Educ Adv Catalysis Mat, Key Lab, 688 Yingbin Rd, Jinhua 321004, Zhejiang, Peoples R China
[2] Zhejiang Normal Univ, Coll Chem & Life Sci, Drug Dev & Innovat Ctr, 688 Yingbin Rd, Jinhua 321004, Zhejiang, Peoples R China
关键词
cysteine; covalent warheads; covalent inhibitor; ENOLPYRUVYL TRANSFERASE MURA; IRREVERSIBLE INHIBITORS; RESISTANCE; CANCER; RECEPTOR; DOMAIN; ELECTROPHILE; REACTIVITY; DISCOVERY; DESIGN;
D O I
10.3390/molecules27227728
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cysteine is one of the least abundant amino acids in proteins of many organisms, which plays a crucial role in catalysis, signal transduction, and redox regulation of gene expression. The thiol group of cysteine possesses the ability to perform nucleophilic and redox-active functions that are not feasible for other natural amino acids. Cysteine is the most common covalent amino acid residue and has been shown to react with a variety of warheads, especially Michael receptors. These unique properties have led to widespread interest in this nucleophile, leading to the development of a variety of cysteine-targeting warheads with different chemical compositions. Herein, we summarized the various covalent warheads targeting cysteine residue and their application in drug development.
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页数:18
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