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PubMed · 7126424

Polymorphically acetylated aminoglutethimide in humans.

R C Coombes·A B Foster·S J Harland·M Jarman·E C Nice
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Abstract

The urinary excretion during 24 h of aminoglutethimide (AG) its major metabolite (N-acetylAG) and two minor metabolites (N-formylAG and nitroG) were measured in 10 volunteers given AG who had been typed for acetylator phenotype using sulphadimidine. The slow acetylators of sulphadimidine excreted more AG (mean 28% of the administered dose) than did the fast acetylators (12%), but the latter excreted more of the dose as N-acetylAG (8.8%) than did the former (3.9%). NitroG and N-formylAG were minor urinary metabolites of AG in humans. The former was more abundant in the urine of slow acetylators (0.10% of the dose) than in that of fast acetylators (0.047%), whereas the respective proportions of doses excreted as the N-formyl derivative (0.475 and 0.465%) were not significantly different for the two acetylator phenotypes. These results show that AG is among those drugs that are polymorphically acetylated in humans.

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AcetylationAdultAminoglutethimideHumansPhenotypePolymorphism, GeneticSulfamethazineJournal ArticleResearch Support, Non-U.S. Gov't

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R C Coombes, A B Foster, S J Harland, M Jarman, E C Nice. 1982. Polymorphically acetylated aminoglutethimide in humans.. https://doi.org/10.1038/bjc.1982.209

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