Heteroarylimino-4-thiazolidinones as inhibitors of cartilage degradation

Bioorg Chem. 2011 Feb;39(1):48-52. doi: 10.1016/j.bioorg.2010.11.002. Epub 2010 Dec 5.

Abstract

2-Benzo[d]thiazolyl- and 2-benzo[d]isothiazolyl-imino-5-benzylidene-4-thiazolidinone derivatives were investigated as potential metalloproteinases (MMPs) inhibitors and evaluated for their antidegenerative activity on human chondrocyte cultures stimulated by IL-1β, using an experimental model that reproduces the mechanisms involved in osteoarthritic (OA) diseases. Cell viability, the amount of glycosaminoglycans (GAGs) and the production of nitric oxide (NO) were measured. The most potent compound, 5-(4-methoxy-benzylidene)-2-(benzo[d]isothiazol-3-ylimino)-thiazolidin-4-one (4b), a MMP-13 inhibitor at nanomolar concentration (IC(50)=0.036 μM), could be considered as a lead compound for the development of novel clinical agents, inhibitors of cartilage degradation, for the treatment of OA.

MeSH terms

  • Cartilage / drug effects*
  • Cartilage / immunology
  • Cartilage / metabolism
  • Cells, Cultured
  • Chondrocytes / drug effects
  • Chondrocytes / immunology
  • Chondrocytes / metabolism
  • Glycosaminoglycans / metabolism
  • Humans
  • Interleukin-1beta / immunology
  • Metalloproteases / antagonists & inhibitors*
  • Metalloproteases / metabolism
  • Nitrogen Oxides / immunology
  • Osteoarthritis / drug therapy*
  • Osteoarthritis / immunology
  • Osteoarthritis / metabolism
  • Thiazolidines / chemistry*
  • Thiazolidines / pharmacology*

Substances

  • Glycosaminoglycans
  • Interleukin-1beta
  • Nitrogen Oxides
  • Thiazolidines
  • Metalloproteases