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The metabolism of N-hydroxyphentermine by rat liver microsomes.

Authors :
Sum CY
Cho AK
Source :
Drug metabolism and disposition: the biological fate of chemicals [Drug Metab Dispos] 1979 Mar-Apr; Vol. 7 (2), pp. 65-9.
Publication Year :
1979

Abstract

N-Hydroxyphentermine is oxidized to 2-methyl-2-nitro-1-phenylpropane by rat liver microsome preparations. This oxidation accounts for differences noted in levels of N-hydroxyphentermine formed from phentermine in washed and unwashed microsome preparations. The reaction is inhibited by hemoglobin and catalase, whose presence in unwashed microsomes could terminate the N-oxidation of phentermine at the hydroxylamine level. The hydroxylamine-nitro-oxidation appears to be dependent on cytochrome P-450, as the reaction was induced by phenobarbital pretreatment and inhibited by carbon monoxide and 2,4-dichloro-6-phenylphenoxyethylamine.

Details

Language :
English
ISSN :
0090-9556
Volume :
7
Issue :
2
Database :
MEDLINE
Journal :
Drug metabolism and disposition: the biological fate of chemicals
Publication Type :
Academic Journal
Accession number :
38075