Synthesis and evaluation of aryl thioxothiazolidinone inhibitors of ADAMTS-5 (Aggrecanase-2)

Bioorg Med Chem Lett. 2007 Mar 1;17(5):1185-8. doi: 10.1016/j.bmcl.2006.12.027. Epub 2006 Dec 12.

Abstract

5-Benzylidene-2-thioxo-thiazolidin-4-one inhibitors of ADAMTS-5 (Aggrecanase-2) have been prepared via commercially available starting materials. The identified compounds show micromolar ADAMTS-5 potency and demonstrate SAR trends for both the aryl group and thioxothiazolidinone zinc chelator. This series of compounds represents steps toward a metalloprotease inhibitor as a disease-modifying osteoarthritis drug.

MeSH terms

  • ADAM Proteins / antagonists & inhibitors*
  • ADAMTS5 Protein
  • Chelating Agents
  • Enzyme Inhibitors / pharmacology
  • Enzyme Inhibitors / therapeutic use
  • Humans
  • Metalloproteases / antagonists & inhibitors
  • Osteoarthritis / drug therapy
  • Structure-Activity Relationship
  • Thiazolidinediones / chemical synthesis*
  • Thiazolidinediones / pharmacology*
  • Zinc

Substances

  • Chelating Agents
  • Enzyme Inhibitors
  • Thiazolidinediones
  • Metalloproteases
  • ADAM Proteins
  • ADAMTS5 Protein
  • ADAMTS5 protein, human
  • Zinc