Discovery of small molecule antagonists of TRPV1

Bioorg Med Chem Lett. 2004 Jul 16;14(14):3631-4. doi: 10.1016/j.bmcl.2004.05.028.

Abstract

Small molecule antagonists of the vanilloid receptor 1 (TRPV1, also known as VR1) are disclosed. Ureas such as 5 (SB-452533) were used to explore the structure activity relationship with several potent analogues identified. Pharmacological studies using electrophysiological and FLIPR Ca(2+) based assays showed compound 5 was an antagonist versus capsaicin, noxious heat and acid mediated activation of TRPV1. Study of a quaternary salt of 5 supports a mode of action in which compounds from this series cause inhibition via an extracellularly accessible binding site on the TRPV1 receptor.

MeSH terms

  • Aminobiphenyl Compounds / pharmacology*
  • Animals
  • Binding Sites
  • Calcium / analysis
  • Calcium / metabolism
  • Capsaicin / analogs & derivatives
  • Capsaicin / pharmacology
  • Cell Line
  • Electrophysiology
  • Fluorescence
  • Hot Temperature
  • Humans
  • Hydrogen-Ion Concentration
  • Image Enhancement
  • Patch-Clamp Techniques
  • Rats
  • Receptors, Drug / antagonists & inhibitors*
  • Receptors, Drug / chemistry
  • Structure-Activity Relationship
  • TRPV Cation Channels

Substances

  • Aminobiphenyl Compounds
  • Receptors, Drug
  • TRPV Cation Channels
  • TRPV1 receptor
  • Capsaicin
  • Calcium