Peptidomimetic Competitive Inhibitors of Protein Tyrosine Phosphatases

被引:7
|
作者
Shen, Kui [1 ]
Qi, Lixin [1 ]
Stiff, Lynn [1 ]
机构
[1] No Illinois Univ, Dept Chem & Biochem, De Kalb, IL 60115 USA
关键词
Peptidomimetic competitive inhibitor; protein tyrosine phosphatase inhibitor; phosphotyrosine analog; phosphopeptide substrate; activity-based probe; substrate trapping mutant; DIFLUOROMETHYLENESULFONIC ACID GROUP; CONTAINING PHOSPHOTYROSYL MIMETICS; REVERSIBLE COVALENT INHIBITORS; STRUCTURE-BASED DESIGN; SUBSTRATE-SPECIFICITY; INSULIN-RECEPTOR; 1B INHIBITORS; ENANTIOSELECTIVE SYNTHESIS; PEPTIDYL ALDEHYDES; POTENT INHIBITION;
D O I
10.2174/138161210793292537
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This review discusses the development of the active site-directed protein tyrosine phosphatase (PTP) inhibitors based on peptides and some closely related nonpeptidic scaffolds. A straightforward approach is to substitute various nonhydrolyzable analogs for the phosphotyrosine (pTyr) of optimal or physiological phosphopeptide substrates of PTPs. The advances in small molecule peptidic PTP inhibitors and their nonpeptidic derivatives have been greatly aided by X-ray crystallographic and NMR spectrometric studies. Given the importance of PTPs in disease-associated signal transduction and the continuing progress in PTP drug discovery, some clinically useful PTP inhibitors may emerge in the near future.
引用
收藏
页码:3101 / 3117
页数:17
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