Xenobiotica · 1981 · 11 citations · 10 references
MedicineMedicinal ChemistryPharmacologyBiochemical PharmacologyDrug MetabolismMass Spectrometric AnalysisDrug DispositionMetabolite IdentificationAntihypertensive TreatmentDrug Metabolite ProfilingIsotope DilutionIsotope Dilution AnalysisIsotope Dilution Mass SpectrometryMetabolite PharmacokineticsStable Isotope Dilution Analysis
1. Tripamide (N-(4-aza-endo-tricyclo[5.2.1.0(2,6)]decan-4-yl)-4-chloro-3-sulphamoyl [carbonyl-14C]benzamide) was metabolized in rat to yield five metabolites which were separated by chromatography, and characterized by mass spectrometry and reverse isotope dilution analysis. 2. The five metabolites were identified as follows; N-(3(or 5)-hydroxy-4-aza-endo-tricyclo[5.2.1.0(2,6)]decan-4-yl)-4-chloro-3-sulphamoylbenzamide (3-hydroxy-tripamide); N-8(or 9)-hydroxy-4-aza-endo-tricyclo[5.2.1.0(2,6)]decan-4-yl)-4-chloro-3-sulphamoylbenzamide (8-hydroxy-tripamide); 4-chloro-3-sulphamoylbenzamide; 4-chloro-3-sulphamoylbenzoic acid; and 4-chloro-3-sulphamoylbenzoic acid-(N'-acetyl)hydrazide. 3. Tripamide was metabolized rapidly and the major metabolite was 4-chloro-3-sulphamoylbenzoic acid in rat blood. 4. After intravenous injection, the excretion rate of the hydroxylated tripamide into bile was about 2-3 times faster than that into urine.
10
John T. Groves, Gary A. McClusky, Ronald E. White et al. · Biochemical and Biophysical Research Communications · 1978 · 538 citations · Full text