Tetrazole-biarylpyrazole derivatives as cannabinoid CB1 receptor antagonists

Bioorg Med Chem Lett. 2008 Apr 1;18(7):2385-9. doi: 10.1016/j.bmcl.2008.02.061. Epub 2008 Feb 29.

Abstract

Cannabinoid CB1 receptors have been the focus of extensive studies since the first clinical results of rimonabant (SR141716) for the treatment of obesity and related metabolic disorders were reported in 2001. To further evaluate the properties of CB receptors, we have designed a new series of tetrazole-biarylpyrazoles. The various analogues were efficiently prepared and bio-assayed for binding to cannabinoid CB1 receptor. Six of the new compounds which displayed high in vitro CB1 binding affinities were assayed for binding to CB2 receptor. Noticeably, cyclopentyl-tetrazole (9a) demonstrated good binding affinity and selectivity for CB1 receptor (IC(50)=11.6nM and CB2/CB1=366).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Obesity Agents / chemical synthesis
  • Anti-Obesity Agents / pharmacology*
  • Binding, Competitive
  • Bridged Bicyclo Compounds, Heterocyclic / chemical synthesis
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacokinetics*
  • Ligands
  • Models, Chemical
  • Pyrazoles / chemical synthesis
  • Pyrazoles / pharmacology*
  • Receptor, Cannabinoid, CB1 / antagonists & inhibitors*
  • Receptor, Cannabinoid, CB1 / metabolism
  • Structure-Activity Relationship
  • Tetrazoles / chemical synthesis
  • Tetrazoles / pharmacology*

Substances

  • Anti-Obesity Agents
  • Bridged Bicyclo Compounds, Heterocyclic
  • Ligands
  • Pyrazoles
  • Receptor, Cannabinoid, CB1
  • Tetrazoles