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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
LEVORPHANOL

LEVORPHANOL

NERVOUS SYSTEM
ANALGESICS
OPIOID
NARCOTICS

INJECTION ORAL

Tmax 1 HOUR

VD 747.5 LITER (65 KILOGRAM)

PPB 40 PERCENT

Cl 61.1 LITER / HOUR (65 KILOGRAM)

HT 13.5 HOUR

SOLUBILITY SOLUBLE IN WATER

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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