Potent and selective thiophene urea-templated inhibitors of S6K

Bioorg Med Chem Lett. 2011 Jan 15;21(2):849-52. doi: 10.1016/j.bmcl.2010.11.069. Epub 2010 Nov 21.

Abstract

S6K1 (p70 S6 kinase-1) is thought to play a critical role in the development of obesity and insulin resistance, thus making it an attractive target in developing medicines for the treatment of these disorders. We describe a novel thiophene urea class of S6K inhibitors. The lead matter for the development of these inhibitors came from mining the literature for reports of weak off-target S6K activity. These optimized inhibitors exhibit good potency and excellent selectivity for S6K over a panel of 43 kinases.

MeSH terms

  • Humans
  • Microsomes, Liver / metabolism
  • Protein Kinase Inhibitors / chemistry*
  • Protein Kinase Inhibitors / metabolism
  • Protein Kinase Inhibitors / pharmacology*
  • Ribosomal Protein S6 Kinases, 70-kDa / antagonists & inhibitors*
  • Ribosomal Protein S6 Kinases, 70-kDa / metabolism
  • Structure-Activity Relationship
  • Thiophenes / chemistry*
  • Thiophenes / metabolism
  • Thiophenes / pharmacology*
  • Urea / chemistry
  • Urea / metabolism
  • Urea / pharmacology

Substances

  • Protein Kinase Inhibitors
  • Thiophenes
  • Urea
  • Ribosomal Protein S6 Kinases, 70-kDa