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1
Use of stable isotopes in studies on the metabolism of amphetamine.
Life Sci. 1978 Jul 24;23(4):283-90. doi: 10.1016/0024-3205(78)90012-7.
2
Hydroxylation of amphetamine to parahydroxyamphetamine by rat liver microsomes.
Biochem Pharmacol. 1974 Nov 15;23(22):3191-7. doi: 10.1016/0006-2952(74)90605-4.
3
Microsomal N-hydroxylation of phenylalkylamines. Identification of N-hydroxylated phenylalkylamines as their trimethylsilyl derivatives by GC-Ms.
Acta Pharm Suec. 1973 Dec;10(6):493-506.
4
In vitro metabolism of amphetamine: an apparent enantiomeric interaction.
Res Commun Chem Pathol Pharmacol. 1976 Nov;15(3):525-40.
5
Activation energies of alpha-C-oxidation and N-oxidation of N-alkyl-substituted amphetamines by rat liver microsomes. Stereochemistry and deuterium isotope effects.
Xenobiotica. 1974 Feb;4(2):121-30. doi: 10.3109/00498257409049351.
6
The identification, properties and analysis of N-hydroxyamphetamine--a metabolite of amphetamine.
J Pharm Pharmacol. 1973 Apr;25(4):329-34.
7
Metabolism of lynestrenol: characterization of 3-hydroxylation using rabbit liver microsomes in vitro.
J Steroid Biochem. 1984 Dec;21(6):777-80. doi: 10.1016/0022-4731(84)90044-x.
8
Aromatic hydroxylation of amphetamine with rat liver microsomes, perfused liver, and isolated hepatocytes.
Biochem Pharmacol. 1978;27(21):2525-9. doi: 10.1016/0006-2952(78)90320-9.
9
The N-hydroxylation of phentermine (2-methyl-1-phenylisopropylamine) by rabbit liver microsomes.
Res Commun Chem Pathol Pharmacol. 1972 Nov;4(3):519-28.
10
On the mechanism of 11-hydroxylation of lauric acid by rat liver microsomes.
Biochem Biophys Res Commun. 1973 Jan 23;50(2):581-7. doi: 10.1016/0006-291x(73)90879-6.
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