Synthesis and SAR of derivatives based on 2-biarylethylimidazole as bombesin receptor subtype-3 (BRS-3) agonists for the treatment of obesity

Bioorg Med Chem Lett. 2010 Apr 1;20(7):2074-7. doi: 10.1016/j.bmcl.2010.02.076. Epub 2010 Feb 21.

Abstract

This Letter describes a series of potent and selective BRS-3 agonists containing a biarylethylimidazole pharmacophore. Extensive SAR studies were carried out with different aryl substitutions. This work led to the identification of a compound 2-{2-[4-(pyridin-2-yl)phenyl]ethyl}-5-(2,2-dimethylbutyl)-1H-imidazole 9 with excellent binding affinity (IC(50)=18 nM, hBRS-3) and functional agonist activity (EC(50)=47 nM, 99% activation). After oral administration, compound 9 had sufficient exposure in diet induced obese mice to demonstrate efficacy in lowering food intake and body weight via BRS-3 activation.

MeSH terms

  • Animals
  • Body Weight / drug effects
  • Eating / drug effects
  • Humans
  • Imidazoles / chemistry*
  • Imidazoles / pharmacokinetics
  • Imidazoles / therapeutic use*
  • Mice
  • Obesity / drug therapy*
  • Rats
  • Receptors, Bombesin / agonists*
  • Receptors, Bombesin / metabolism*
  • Structure-Activity Relationship

Substances

  • 2-(2-(4-(pyridin-2-yl)phenyl)ethyl)-5-(2,2-dimethylbutyl)-1H-imidazole
  • Imidazoles
  • Receptors, Bombesin
  • bombesin receptor subtype 3