Emerging and Re-Emerging Warheads for Targeted Covalent Inhibitors: Applications in Medicinal Chemistry and Chemical Biology

被引:472
|
作者
Gehringer, Matthias [1 ]
Laufer, Stefan A. [1 ]
机构
[1] Eberhard Karls Univ Tubingen, Dept Pharmaceut Med Chem, Morgenstelle 8, D-72076 Tubingen, Germany
关键词
GROWTH-FACTOR RECEPTOR; SELECTIVE IRREVERSIBLE INHIBITORS; PROTEIN-TYROSINE PHOSPHATASES; ENOLPYRUVYL TRANSFERASE MURA; MECHANISM-BASED INHIBITION; SMALL-MOLECULE PROBE; THIOL-ENE REACTION; KINASE INHIBITORS; ACTIVE-SITE; CYSTEINE PROTEASES;
D O I
10.1021/acs.jmedchem.8b01153
中图分类号
R914 [药物化学];
学科分类号
100701 ;
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 alpha,beta-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 alpha,beta-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.
引用
收藏
页码:5673 / 5724
页数:52
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