Synthesis and biological evaluation of imidazole-based small molecule antagonists of the melanocortin 4 receptor (MC4-R)

Bioorg Med Chem Lett. 2004 Jul 16;14(14):3721-5. doi: 10.1016/j.bmcl.2004.05.003.

Abstract

A novel series of imidazole-based small molecule antagonists of the melanocortin 4 receptor (MC4-R) is reported. Members of this series have been identified, which exhibit sub-micromolar binding affinity for the MC4-R, functional potency <100nM, and good oral exposure in rat. Antagonists of the MC4-R are potentially useful in the therapeutic treatment of involuntary weight loss due to advanced age or disease (e.g. cancer or AIDS), an area of large, unmet medical need.

MeSH terms

  • Animals
  • Binding Sites
  • Body Weight / drug effects*
  • Body Weight / physiology
  • Cells, Cultured
  • Imidazoles / chemical synthesis*
  • Imidazoles / pharmacology
  • Rats
  • Receptor, Melanocortin, Type 4 / antagonists & inhibitors*
  • Receptor, Melanocortin, Type 4 / metabolism
  • Structure-Activity Relationship

Substances

  • Imidazoles
  • Receptor, Melanocortin, Type 4
  • imidazole