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Bioactivation of the narcotic drug codeine in human liver is mediated by the polymorphic monooxygenase catalyzing debrisoquine 4-hydroxylation (cytochrome P-450 dbl/bufI)

Data up to Jan 2025

Published1988
Citations210
References16

Total Citations Per Year

Abstract

References (16)

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Statistical methods

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High-performance liquid chromatographic assays for bufuralol 1′-hydroxylase, debrisoquine 4-hydroxylase, and dextromethorphan O-demethylase in microsomes and purified cytochrome P-450 isozymes of human liver

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1985 • 197 citations

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1983 • 123 citations

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1986 • 113 citations

Debrisoquine/sparteine-type polymorphism of drug oxidation. Purification and characterization of two functionally different human liver cytochrome P-450 isozymes involved in impaired hydroxylation of the prototype substrate bufuralol.

1986 • 112 citations

Evidence for an enzymatic defect in the 4‐hydroxylation of debrisoquine by human liver.

1981 • 93 citations

Inhibition of desmethylimipramine 2-hydroxylation by drugs in human liver microsomes

1985 • 91 citations

Characterization of a common genetic defect of cytochrome P-450 function (debrisoquine-sparteine type polymorphism) — Increased michaelis constant (km) and loss of stereoselectivity of bufuralol 1′-hydroxylation in poor metabolizers

1984 • 66 citations

Enzymatic basis of the debrisoquine/sparteine-type genetic polymorphism of drug oxidation

1987 • 63 citations

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Bioactivation of the narcotic drug codeine in human liver is mediated by the polymorphic… (1988) – Biochemical and Biophysical Research Communications | Metascience Observatory Explorer