Structure-activity relationship (SAR) investigations of substituted imidazole analogs as TRPV1 antagonists

Bioorg Med Chem Lett. 2007 Nov 1;17(21):5825-30. doi: 10.1016/j.bmcl.2007.08.044. Epub 2007 Aug 25.

Abstract

A novel series of 4,5-biarylimidazoles as TRPV1 antagonists were designed based on the previously reported 4,6-disubstituted benzimidazole series. The analogs were evaluated for their ability to block capsaicin- or acid-induced calcium influx in TRPV1-expressing CHO cells. These studies led to the identification of a highly potent and orally bioavailable TRPV1 antagonist, imidazole 33.

MeSH terms

  • Administration, Oral
  • Animals
  • CHO Cells
  • Cricetinae
  • Cricetulus
  • Imidazoles / administration & dosage
  • Imidazoles / chemistry*
  • Imidazoles / pharmacokinetics
  • Imidazoles / pharmacology*
  • Rats
  • Structure-Activity Relationship
  • TRPV Cation Channels / antagonists & inhibitors*

Substances

  • Imidazoles
  • TRPV Cation Channels
  • TRPV1 protein, human