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Studies on the demethylation,hydroxylation and N-oxidation of imipramine in rat liver
- Source :
- Biochemical Pharmacology. 19:1363-1369
- Publication Year :
- 1970
- Publisher :
- Elsevier BV, 1970.
-
Abstract
- Metabolic pathways responsible for the demethylation, N -oxidation and 2-hydroxylation of imipramine were studied in rat liver in vitro . Isotope-trapping experiments have revealed that imipramine- N -oxide is not involved as an intermediate in the formation of desmethylimipramine from imipramine. The enzyme systems for demethylation and 2-hydroxylation are induced by phenobarbital, but that for N -oxidation is not induced. All available evidence indicates that the demethylation, N -oxidation and 2-hydroxylation reactions may be independent of one another.
- Subjects :
- Male
Imipramine
Chromatography, Paper
Pharmacology
Methylation
Biochemistry
Hydroxylation
chemistry.chemical_compound
Chlorides
Ethylamines
Valerates
medicine
Animals
Magnesium
Demethylation
chemistry.chemical_classification
Carbon Isotopes
Chemistry
Proadifen
Desipramine
Oxides
Amino Alcohols
In vitro
Rats
Metabolic pathway
Metabolism
Enzyme
Liver
Dealkylation
Phenobarbital
Rat liver
Oxidation-Reduction
medicine.drug
Subjects
Details
- ISSN :
- 00062952
- Volume :
- 19
- Database :
- OpenAIRE
- Journal :
- Biochemical Pharmacology
- Accession number :
- edsair.doi.dedup.....efaf0cf5efcb7245c2bd5b076484d206
- Full Text :
- https://doi.org/10.1016/0006-2952(70)90051-1