Antinociceptive activity of furan-containing congeners of improgan and ranitidine

Bioorg Med Chem Lett. 2007 Oct 15;17(20):5715-9. doi: 10.1016/j.bmcl.2007.07.060. Epub 2007 Aug 19.

Abstract

Furan-containing congeners of the histamine H(2) receptor antagonist ranitidine were synthesized and tested for improgan-like antinociceptive activity. The most potent ligand of the series, VUF5498, is the most potent improgan-like agent described to date (ED(50)=25 nmol, icv). This compound is approximately equal in potency with morphine. These non-imidazole, improgan-like pain relievers further define the structural requirements for analgesics of this class and are important tools for ongoing mechanism-based studies.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cimetidine / analogs & derivatives*
  • Cimetidine / chemistry
  • Cimetidine / pharmacology
  • Furans / chemistry*
  • Male
  • Molecular Structure
  • Nociceptors / metabolism*
  • Ranitidine / chemistry*
  • Ranitidine / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Structure-Activity Relationship

Substances

  • Furans
  • SKF 92374
  • Cimetidine
  • Ranitidine
  • furan