Development of a selective and potent radioactive ligand for histamine H(3) receptors: A compound potentially useful for receptor occupancy studies

Bioorg Med Chem Lett. 2009 Aug 1;19(15):4075-8. doi: 10.1016/j.bmcl.2009.06.025. Epub 2009 Jun 13.

Abstract

Radioligands are powerful tools for examining the pharmacological profiles of chemical leads and thus facilitate drug discovery. In this study, we identified and characterized 3-([1,1,1-(3)H]methyl)-2-(4-{[3-(1-pyrrolidinyl)propyl]oxy} phenyl)-4(3H)-quinazolinone ([(3)H]1) as a potent and selective radioligand for histamine H(3) receptors. Radioligand [(3)H]1 exhibited appreciable specific signal in brain slices prepared from wild-type mice but not from histamine H(3) receptor-deficient mice, demonstrating the specificity and utility of [(3)H]1 as a selective histamine H(3) receptor radioligand for ex-vivo receptor occupancy assays.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B / chemistry
  • Animals
  • Brain / drug effects
  • Chemistry, Pharmaceutical / methods*
  • Drug Design
  • Humans
  • Kinetics
  • Ligands
  • Mice
  • Models, Chemical
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, G-Protein-Coupled / chemistry
  • Receptors, Histamine H3 / chemistry*
  • Receptors, Histamine H3 / metabolism
  • Structure-Activity Relationship

Substances

  • ATP Binding Cassette Transporter, Subfamily B
  • Ligands
  • Receptors, G-Protein-Coupled
  • Receptors, Histamine H3