Targeted Covalent Inhibitors for Drug Design

被引:358
|
作者
Baillie, Thomas A. [1 ]
机构
[1] Univ Washington, Dept Med Chem, Sch Pharm, Box 357610, Seattle, WA 98195 USA
关键词
covalent drugs; drug design; electrophiles; inhibitors; protein modifications; GROWTH-FACTOR RECEPTOR; IRREVERSIBLE KINASE INHIBITORS; PROTEIN-TYROSINE KINASES; INDUCED LIVER-INJURY; MASS-SPECTROMETRY; METABOLIC-ACTIVATION; CHEMICAL TOXICOLOGY; ENZYME-INHIBITORS; CELLULAR-ACTIVITY; ORAL MEDICATIONS;
D O I
10.1002/anie.201601091
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In contrast to the traditional mechanism of drug action that relies on the reversible, noncovalent interaction of a ligand with its biological target, a targeted covalent inhibitor (TCI) is designed such that the initial, reversible association is followed by the formation of a covalent bond between an electrophile on the ligand and a nucleophilic center in the protein. Although this approach offers a variety of potential benefits (high potency and extended duration of action), concerns over the possible toxicological consequences of protein haptenization have hindered the development of the TCI concept. Recently, approaches to mitigate the risk of serious adverse reactions to this new class of agent have emerged, thus stimulating interest in the field and leading to authorization of the first cadre of TCIs to be marketed. The covalent inhibitor approach is rapidly gaining acceptance as a valuable tool in drug discovery, and is poised to make a major impact on the design of enzyme inhibitors and receptor modulators.
引用
收藏
页码:13408 / 13421
页数:14
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