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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
LEVOMETHADYL ACETATE DISCONTINUED

LEVOMETHADYL ACETATE


ATC N07BC03

NERVOUS SYSTEM
ANALGESIC
OPIOID AGONIST
NARCOTICS
USAGE IN OPIATE ADDICTION

ORAL

VD 1300 LITER (65 KILOGRAM)

Cl 14.3 LITER / HOUR (65 KILOGRAM)

HT 62 HOUR

SOLUBILITY > 15 MILLIGRAM / MILLILITER

MU-TYPE OPIOID RECEPTOR

MU OPIOID RECEPTOR AGONIST CHEMBL233 MU OPIOID RECEPTOR P35372 MU-TYPE OPIOID RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 PEPTIDE SHORT PEPTIDE OPIOID RECEPTORANSM (in French)

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