The Identification of Three New Metabolic Products of Phentermine after Liver Microsomal Incubation
- 1 January 1974
- journal article
- research article
- Published by Taylor & Francis in Xenobiotica
- Vol. 4 (8) , 509-519
- https://doi.org/10.3109/00498257409052103
Abstract
1. N-Hydroxyphentermine (II), α, α-dimethyl-α-nitroso-β-phenylethane (III) and α, α-dimethyl-α-nitro-β-phenylethane (IV) were obtained from ethereal or n-pentane extracts after incubation of phentermine (I) with 10 000 g and 140 000 g liver microsomal preparations of various animal species. 2. The metabolites (II and III) produced the metabonate (IV) under aqueous alkaline conditions. 3. The structure, synthesis and physico-chemical and metabolic characteristics of these compounds are reported.Keywords
This publication has 8 references indexed in Scilit:
- N-ethyl-α-methyl-α-(m-trifluoromethylbenzyl)nitron—the major in vitro metabolic product of fenfluramine in guinea-pig liver microsomal fractionsJournal of Pharmacy and Pharmacology, 1973
- The mechanism of oxidation of amphetamine enantiomorphs by liver microsomal preparations from different speciesJournal of Pharmacy and Pharmacology, 1972
- Metabolic oxidation on aliphatic basic nitrogen atoms and their α-carbon atoms—some unifying principlesJournal of Pharmacy and Pharmacology, 1971
- tert-Alkylnitroso compounds. Synthesis and dimerization equilibriumsThe Journal of Organic Chemistry, 1971
- Some physico-chemical properties of amphetamine and related drugsJournal of Pharmacy and Pharmacology, 1969
- Electroörganic Preparations. XVIII. Preparation and Polarographic Determination of some N-Alkylhydroxylamines.Acta Chemica Scandinavica, 1965
- Structure and properties of C-nitroso-compoundsQuarterly Reviews, Chemical Society, 1958
- The Synthesis of Tertiary Nitroparaffins1,2Journal of the American Chemical Society, 1956