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Current Pharmaceutical Design

Editor-in-Chief

ISSN (Print): 1381-6128
ISSN (Online): 1873-4286

Peptidomimetic Competitive Inhibitors of Protein Tyrosine Phosphatases

Author(s): Kui Shen, Lixin Qi and Lynn Stiff

Volume 16, Issue 28, 2010

Page: [3101 - 3117] Pages: 17

DOI: 10.2174/138161210793292537

Price: $65

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Abstract

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.

Keywords: Peptidomimetic competitive inhibitor, protein tyrosine phosphatase inhibitor, phosphotyrosine analog, phosphopeptide substrate, activity-based probe, substrate trapping mutant


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