Title : Sex-dependent pharmacokinetics and in vitro reductive metabolism of acetohexamide in Wistar-Imamichi rats.

Pub. Date : 1999 Apr

PMID : 10328570






2 Functional Relationships(s)
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1 The co-administration of sulfamethazine, which is known to be metabolized by a male-specific cytochrome P450 (CYP) isoform (CYP2C11), significantly decreased the CLp of acetohexamide in male Wistar-IM rats. Acetohexamide cytochrome P450, subfamily 2, polypeptide 11 Rattus norvegicus
2 Based on these results, it is reasonable to assume that the sex-dependent pharmacokinetics of acetohexamide observed in Wistar-IM rats is associated with the male-specific hydroxylation catalyzed by CYP2C11. Acetohexamide cytochrome P450, subfamily 2, polypeptide 11 Rattus norvegicus