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1 INNClassRoute (list)PK parameters= Cmax; Tmax; F: bioavailability; t1/2: half-life; VD: volume of distribution; Cl: clearance; PPB: plasma protein binding;(EQN means that value was calculated using VD=(Cl*t1/2)/0.693)Primary Target and PDB code of Protein-Drug complexTargets from DrugCentral Links
FLUVOXAMINE

FLUVOXAMINE


ATC N06AB08

NERVOUS SYSTEM
ANTIOBSESSIONAL AGENT
ANTIDEPRESSANT
ANTI-ANXIETY AGENTS
SELECTIVE SEROTONIN REUPTAKE INHIBITORS (SSRIS)

ORAL

Cmax 1.71 MICROMOLAR

Tmax 5.5 HOUR

F 53 PERCENT

VD 1625 LITER (65 KILOGRAM)

PPB 80 PERCENT

Cl 72 LITER / HOUR (EQN)

HT 15.6 HOUR

SOLUBILITY SPARINGLY SOLUBLE IN WATER

SEROTONIN TRANSPORTER (SERT)

PDB 6AWP (X-RAY STRUCTURE OF THE TS3 HUMAN SEROTONIN TRANSPORTER COMPLEXED WITH FLUVOXAMINE AT THE CENTRAL SITE)

LIGAND CODE = FVX (link to the list of PDB complexes)

Download experimental 3D coordinates of FVX with added hydrogens

SEROTONIN TRANSPORTER INHIBITOR CHEMBL228 SEROTONIN TRANSPORTER P31645 SODIUM-DEPENDENT SEROTONIN TRANSPORTER HOMO SAPIENS TRANSPORTER ELECTROCHEMICAL SLC SLC06ANSM (in French)

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