Applications of covalent chemistry in targeted protein degradation

被引:25
作者
Lu, Dong [1 ]
Yu, Xin [1 ]
Lin, Hanfeng [1 ]
Cheng, Ran [1 ]
Monroy, Erika Y. [1 ]
Qi, Xiaoli [1 ]
Wang, Meng C. [2 ,3 ,4 ]
Wang, Jin [1 ,5 ]
机构
[1] Baylor Coll Med, Dept Pharmacol & Chem Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Baylor Coll Med, Huffington Ctr Aging, Houston, TX 77030 USA
[4] Baylor Coll Med, Howard Hughes Med Inst, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
关键词
IDIOSYNCRATIC DRUG-REACTIONS; ANTIBODY-MEDIATED DELIVERY; IRREVERSIBLE INHIBITORS; PROTAC DESIGN; EGF RECEPTOR; CDDO-ME; DISCOVERY; BINDING; MECHANISM; AFFINITY;
D O I
10.1039/d2cs00362g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Proteolysis-targeting chimeras (PROTACs) and targeted covalent inhibitors (TCIs) are currently two exciting strategies in the fields of chemical biology and drug discovery. Extensive research in these two fields has been conducted, and significant progress in these fields has resulted in many clinical candidates, some of which have been approved by FDA. Recently, a novel concept termed covalent PROTACs that combine these two strategies has emerged and gained an increasing interest in the past several years. Herein, we briefly review and highlight the mechanism and advantages of TCIs and PROTACs, respectively, and the recent development of covalent PROTACs using irreversible and reversible covalent chemistry.
引用
收藏
页码:9243 / 9261
页数:19
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