The major fluvoxamine metabolite in urine is formed by CYP2D6.
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In Silico and Intuitive Predictions of CYP46A1 Inhibition by Marketed Drugs with Subsequent Enzyme Crystallization in Complex with FluvoxamineAntidepressant drugs in the elderly--role of the cytochrome P450 2D6.Genetic polymorphisms of cytochrome P450 enzymes and the effect on interindividual, pharmacokinetic variability in extensive metabolizers.Development of a Physiologically Based Pharmacokinetic/Pharmacodynamic Model to Predict the Impact of Genetic Polymorphisms on the Pharmacokinetics and Pharmacodynamics Represented by Receptor/Transporter Occupancy of Central Nervous System Drugs.Pharmacokinetics and distribution of fluvoxamine to the brain in rats under oxidative stress.Simultaneous Determination of Fluvoxamine and Its Metabolites in Human Liver Microsomes by High‐Performance Liquid Chromatography with Solid‐Phase Extraction
P2860
The major fluvoxamine metabolite in urine is formed by CYP2D6.
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The major fluvoxamine metabolite in urine is formed by CYP2D6.
@en
The major fluvoxamine metabolite in urine is formed by CYP2D6.
@nl
type
label
The major fluvoxamine metabolite in urine is formed by CYP2D6.
@en
The major fluvoxamine metabolite in urine is formed by CYP2D6.
@nl
prefLabel
The major fluvoxamine metabolite in urine is formed by CYP2D6.
@en
The major fluvoxamine metabolite in urine is formed by CYP2D6.
@nl
P2093
P356
P1476
The major fluvoxamine metabolite in urine is formed by CYP2D6.
@en
P2093
Axelsson S
Dahlqvist R
Norström A
P2888
P304
P356
10.1007/S002280100373
P577
2001-11-01T00:00:00Z