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

被引:9
作者
Hop, CECA
Wang, YF
Kumar, S
Elipe, MVS
Raab, CE
Dean, DC
Poon, GK
Keohane, CA
Strauss, J
Chiu, SHL
Curtis, N
Elliott, J
Gerhard, U
Locker, K
Morrison, D
Mortishire-Smith, R
Thomas, S
Watt, AP
Evans, DC
机构
[1] Merck Res Labs, Dept Drug Metab, Rahway, NJ USA
[2] Merck Sharp & Dohme Ltd, Neurosci Res Ctr, Dept Med Chem, Harlow CM20 2QR, Essex, England
关键词
D O I
10.1124/dmd.30.8.937
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
[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.
引用
收藏
页码:937 / 943
页数:7
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