5-Arylidene-2,4-thiazolidinediones as inhibitors of protein tyrosine phosphatases

Bioorg Med Chem. 2007 Aug 1;15(15):5137-49. doi: 10.1016/j.bmc.2007.05.027. Epub 2007 May 17.

Abstract

4-(5-Arylidene-2,4-dioxothiazolidin-3-yl)methylbenzoic acids (2) were synthesized and evaluated in vitro as inhibitors of PTP1B and LMW-PTP, two protein tyrosine phosphatases (PTPs) which act as negative regulators of the metabolic and mitotic signalling of insulin. The synthesis of compounds 2 represents an example of utilizing phosphotyrosine-mimetics to identify effective low molecular weight nonphosphorus inhibitors of PTPs. Several thiazolidinediones 2 exhibited PTP1B inhibitory activity in the low micromolar range with moderate selectivity for human PTP1B and IF1 isoform of human LMW-PTP compared with other related PTPs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Models, Molecular
  • Molecular Structure
  • Protein Tyrosine Phosphatases / antagonists & inhibitors*
  • Structure-Activity Relationship
  • Substrate Specificity
  • Thiazolidinediones / chemistry*
  • Thiazolidinediones / pharmacology*

Substances

  • Thiazolidinediones
  • Protein Tyrosine Phosphatases