Structure-activity relationships of histamine H1-receptor agonists

Mini Rev Med Chem. 2004 Nov;4(9):935-40. doi: 10.2174/1389557043403198.

Abstract

Significant progress in the development of potent and selective histamine H1-receptor agonists has been achieved since 1990. Optimisation of the class of 2-phenylhistamines has furnished 2-[3-(trifluoromethyl)phenyl]histamine and its Nalpha-methyl derivative. The discovery of histaprodifen (2-[2-(3,3-diphenylpropyl)-1H-imidazol-4-yl]ethanamine) and the novel lead compound suprahistaprodifen (Nalpha-2-[(1H-imidazol-4-yl)ethyl]histaprodifen) represents additional milestones in the H1-receptor agonist field.

Publication types

  • Review

MeSH terms

  • Animals
  • Histamine / analogs & derivatives*
  • Histamine / chemistry
  • Histamine / pharmacology
  • Histamine Agonists / chemistry*
  • Histamine Agonists / pharmacology*
  • Humans
  • Imidazoles / chemistry
  • Methylhistamines / chemistry
  • Methylhistamines / pharmacology
  • Structure-Activity Relationship

Substances

  • Histamine Agonists
  • Imidazoles
  • Methylhistamines
  • histaprodifen
  • methylhistaprodifen
  • imidazole
  • Histamine