Ligands of the histamine H3-receptor: new potent antagonists of the 2-thioimidazole type

Farmaco. 1997 May;52(5):295-302.

Abstract

An overview of H3-receptor ligands is presented, with particular attention to antagonists. The protein binding of the classical H3-receptor antagonist thioperamide and its effect on in vivo distribution are discussed. A series of H3-receptor antagonists characterised by the presence of an imidazole ring, a spacer (ethylthio-, ethylamino-, propylthio- or propylamino-chain), a second heterocycle nucleus and a lipophilic group is described. Their H3-receptor antagonist potency has been measured on electrically stimulated guinea-pig intestine, and their affinity for central H3-receptor has been determined by competitive inhibition of [3H]N alpha-methylhistamine binding to rat cortex. Biphasic inhibition curves have been observed in some cases. Compounds endowed with interesting activity belong mostly to the class of 2-[[2-[4(5)-imidazolyl]ethyl]thio]imidazole, having a phenyl or a cyclohexyl group.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Guinea Pigs
  • Histamine Antagonists / chemical synthesis
  • Histamine Antagonists / pharmacology*
  • Imidazoles / chemical synthesis
  • Imidazoles / pharmacology*
  • Ligands
  • Rats
  • Receptors, Histamine H3 / drug effects*
  • Structure-Activity Relationship

Substances

  • Histamine Antagonists
  • Imidazoles
  • Ligands
  • Receptors, Histamine H3