Identification of metabolites of a substance P (neurokinin 1 receptor) antagonist in rat hepatocytes and rat plasma

Drug Metab Dispos. 2002 Aug;30(8):937-43. doi: 10.1124/dmd.30.8.937.

Abstract

[3R,5R,6S]-3-(2-cyclopropyloxy-5-trifluoromethoxyphenyl)-6-phenyl-1-oxa-7-azaspiro[4.5]decane is a substance P (Neurokinin 1 receptor) antagonist. Substance P antagonists are proven in concept to have excellent potential for the treatment of major depression, and they allow superior and sustained protection from acute and delayed chemotherapy-induced emesis. The metabolism of this compound was investigated in rat hepatocytes, and circulating rat plasma metabolites were identified following oral and intravenous dosing. The turnover in rat hepatocytes within 4 h was about 30%, and the major metabolites were identified as two nitrones and a lactam associated with the piperidine ring. Although these metabolites were also observed in rat plasma, the major circulating metabolite was a keto acid following oxidative de-amination of the piperidine ring. Liquid chromatography/tandem mass spectrometry and nuclear magnetic resonance were used to confirm the structure of the latter metabolite. A mechanism leading to the formation of the keto acid metabolite has been suggested, and most intermediates were observed in rat plasma.

MeSH terms

  • Administration, Oral
  • Animals
  • Aza Compounds / blood*
  • Aza Compounds / metabolism*
  • Aza Compounds / pharmacology
  • Chromatography, Liquid
  • Hepatocytes / metabolism*
  • In Vitro Techniques
  • Injections, Intravenous
  • Keto Acids / blood
  • Magnetic Resonance Spectroscopy
  • Male
  • Microsomes, Liver / metabolism
  • Neurokinin-1 Receptor Antagonists*
  • Rats
  • Rats, Sprague-Dawley
  • Spiro Compounds / blood*
  • Spiro Compounds / metabolism*
  • Spiro Compounds / pharmacology
  • Substance P / antagonists & inhibitors*

Substances

  • 3-(2-cyclopropyloxy-5-trifluoromethoxyphenyl)-6-phenyl-1-oxa-7-azaspiro(4.5)decane
  • Aza Compounds
  • Keto Acids
  • Neurokinin-1 Receptor Antagonists
  • Spiro Compounds
  • Substance P