Thiazolidine-diones. Biochemical and biological activity of a novel class of tyrosine protein kinase inhibitors

J Biol Chem. 1990 Dec 25;265(36):22255-61.

Abstract

Various derivatives of thiazolidine-diones have been identified as tyrosine protein kinase inhibitors. The epidermal growth factor (EGF) receptor kinase and c-src kinase were inhibited in vitro with IC50 values in the range of 1-7 microM. The v-abl tyrosine protein kinase was not inhibited by thiazolidine-diones. Inhibition was found to be specific for tyrosine protein kinases. Inhibition of serine/threonine protein kinases was not observed. The active derivatives were shown to inhibit EGF-induced receptor autophosphorylation, either in vitro or in intact cells, and were also found to inhibit growth of the EGF-dependent BALB/MK and A431 cell lines (IC50 1-3 microM). Growth of the interleukin-3-dependent myeloid cell line FDC-P1 was inhibited with equal efficiency. Thus, in these cell lines, members of the c-src kinase family are also potential targets for inhibition by the compounds.

MeSH terms

  • Animals
  • Cell Division / drug effects
  • Cell Line
  • ErbB Receptors / drug effects
  • ErbB Receptors / metabolism
  • Humans
  • Indicators and Reagents
  • Kinetics
  • Protein Kinase Inhibitors
  • Protein-Tyrosine Kinases / antagonists & inhibitors*
  • Structure-Activity Relationship
  • Substrate Specificity
  • Thiazoles / chemical synthesis
  • Thiazoles / pharmacology*

Substances

  • Indicators and Reagents
  • Protein Kinase Inhibitors
  • Thiazoles
  • ErbB Receptors
  • Protein-Tyrosine Kinases