Biophysical and catalytic properties of the phenobarbital p-hydroxylase—a cytochrome P-450 dependent mixed function oxidase
Author:
Publisher
Informa UK Limited
Subject
Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/00498258809041691
Reference11 articles.
1. Cooper D. Y., Schleyer H., Thomas J. H., Vars H. M., Rosenthal O. Cytochromes P-450 and b5. Structure and Function, D. Y. Cooper, O. Rosenthal, R. Snyder, C. M. Witmer. Plenum Press, New York 1975; 81–102
2. Steroid Formation by Adrenal Tissue from Hypertensives1
3. LXXIII.—Oxidation of tartaric acid in presence of iron
4. Comparative kinetic studies of the dealkylation reaction and steroid hydroxylations in various oxygen and carbon monoxide:oxygen atmospheres
5. A kinetic study comparing the light-reversal properties of carbon monoxide inhibition of ethylmorphine, benzphetamine, and 7-ethoxycoumarin dealkylation with those of hydroxylation of 17-hydroxyprogesterone and testosterone
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2. Urinary metabolites of phenobarbitone, primidone, and theirN-methyl andN-ethyl derivatives in humans;Xenobiotica;1992-01
3. Use of Bile Fistulas to Solve Problems of Drug Metabolism;Drug Metabolism Reviews;1989-01
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