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The metabolism of N-hydroxyphentermine by rat liver microsomes.
- 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.
- Subjects :
- Animals
Hemoglobins pharmacology
In Vitro Techniques
Liver enzymology
Male
Microsomes, Liver drug effects
Microsomes, Liver enzymology
Mixed Function Oxygenases metabolism
Phenobarbital pharmacology
Phentermine metabolism
Rats
Subcellular Fractions enzymology
Microsomes, Liver metabolism
Phentermine analogs & derivatives
Subjects
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