RT Journal Article
SR Electronic
T1 Microsomal N-hydroxylation of trans-4'-alkoxy-4-acetamidostilbenes.
JF Drug Metabolism and Disposition
JO Drug Metab Dispos
FD American Society for Pharmacology and Experimental Therapeutics
SP 226
OP 231
VO 6
IS 3
A1 R E Gammans
A1 R D Sehon
A1 M W Anders
A1 P E Hanna
YR 1978
UL http://dmd.aspetjournals.org/content/6/3/226.abstract
AB Hamster liver microsomes catalyze the N-hydroxylation of the 4'-OCH3, 4'-OCH2CH3, 4'-O(CH2)2CH3, and 4'-O(CH2)3CH3 analogs of trans-4-acetamidostilbene. Other metabolites which were identified were the O-deethylation product of the 4'-OCH2CH3 analog as well as the alpha,beta-epoxides of the 4'-OCH2CH3 and 4'-O(CH2)2CH3 compounds and the (omega-1)-hydroxylation product of trans-4'-n-butoxy-4-acetamidostilbene. The kinetics of metabolism of the 4'-O(CH2)3CH3 analog were determined, but the rates of formation of the metabolites of the other members of the series were not linearly related to substrate concentration.