Benzimidazole-substituted (3-phenoxypropyl)amines as histamine H3 receptor ligands

Bioorg Med Chem Lett. 2008 Sep 15;18(18):5032-6. doi: 10.1016/j.bmcl.2008.08.008. Epub 2008 Aug 7.

Abstract

A series of non-imidazole histamine H(3) receptor antagonists based on the (3-phenoxypropyl)amine motif, which is a common pharmacophore for H(3) antagonists, has been identified. A preliminary SAR study around the amine moiety has identified 8a as a potent H(3) antagonist possessing a good pharmacokinetic profile in the rat.

MeSH terms

  • Amines / chemical synthesis*
  • Amines / chemistry
  • Amines / pharmacology*
  • Animals
  • Benzimidazoles / chemical synthesis*
  • Benzimidazoles / chemistry
  • Benzimidazoles / pharmacology*
  • Combinatorial Chemistry Techniques
  • Molecular Structure
  • Rats
  • Receptors, Histamine H3 / drug effects*
  • Structure-Activity Relationship

Substances

  • Amines
  • Benzimidazoles
  • Receptors, Histamine H3