CB2 selective sulfamoyl benzamides: optimization of the amide functionality

Bioorg Med Chem Lett. 2009 Jan 15;19(2):309-13. doi: 10.1016/j.bmcl.2008.11.091. Epub 2008 Nov 27.

Abstract

Previous research within our laboratories identified sulfamoyl benzamides as novel cannabinoid receptor ligands. Optimization of the amide linkage led to the reverse amide 40. The compound exhibited robust antiallodynic activity in a rodent pain model when administered intraperitoneally. Efficacy after oral administration was observed only when ABT, a cytochrome P450 suicide inhibitor, was coadministered.

MeSH terms

  • Animals
  • Benzamides / administration & dosage
  • Benzamides / chemistry
  • Benzamides / pharmacology*
  • Benzamides / therapeutic use
  • Pain / drug therapy
  • Receptor, Cannabinoid, CB2 / drug effects*
  • Rodentia

Substances

  • Benzamides
  • Receptor, Cannabinoid, CB2