%0 Journal Article %A K. B. ALTON %A R. M. GRIMES %A C. SHAW %A J. E. PATRICK %A J. L. MCGUIRE %T BIOTRANSFORMATION OF A 1,5-BENZODIAZEPINE, TRIFLUBAZAM, BY MAN %D 1975 %J Drug Metabolism and Disposition %P 352-360 %V 3 %N 5 %X The biotransformation of triblubazam (ORF 8063; 1-methyl-5-phenyl-7-trifluoromethyl-1H-1,5-benzodiazepin-2,4-[3H,5H]-dione) was studied in man. Seven male subjects received a chronic regimen of orally administered triflubazam for 19 consecutive days and their urine was collected for 29 days. Seven urinary metabolites were isolated by application of Sephadex LH-20 column chromatography and preparative thin-layer chromatography. Six of the purified compounds were subsequently characterized by utilizing thin-layer and gas-liquid chromatography and infrared, nuclear magnetic resonance, and mass spectrometry. The structure of a seventh metabolite was established by the use of an enzymatic assay involving catechol 0-methyltransferase. These compounds included unchanged triflubazam, the N-desmethyl catechol derivative, the 4'-hydroxyphenyl derivative, N-desmethyltriflubazam, the N-desmethyl dihydrodiol derivative, the N-desmethyl-4'-hydroxy compound, and the N-desmethyl-3'-methoxy-4'-hydroxy derivative. Unlike the situation in the metabolism of 1,4-benzodiazepines by man, no C3-hydroxylated derivatives of triflubazam were isolated. The metabolism of triflubazam by man is characterized by extensive N-demethylation, aromatic hydroxylation, aromatic 0-methylation, and dihydrodiol formation. Copyright © 1975 by The American Society for Pharmacology and Experimental Therapeutics %U https://dmd.aspetjournals.org/content/dmd/3/5/352.full.pdf