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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
NALBUPHINE

NALBUPHINE


ATC N02AF02

NERVOUS SYSTEM
NARCOTIC
ANALGESIC
KAPPA OPIOID RECEPTOR AGONIST
PARTIAL MU OPIOID RECEPTOR ANTAGONIST

INJECTION

Tmax 0.041 HOUR

VD 299 LITER (65 KILOGRAM)

PPB 50 PERCENT

Cl 85.8 LITER / HOUR (65 KILOGRAM)

HT 5 HOUR

SOLUBILITY 35.5 MILLIGRAM / MILLILITER IN WATER (25 DEGREE CELCIUS)

DELTA-TYPE OPIOID RECEPTOR
KAPPA-TYPE OPIOID RECEPTOR
MU-TYPE OPIOID RECEPTOR

OPIOID RECEPTORS MU/KAPPA/DELTA AGONIST CHEMBL2095181 OPIOID RECEPTORS MU/KAPPA/DELTA P35372 MU-TYPE OPIOID RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 PEPTIDE SHORT PEPTIDE OPIOID RECEPTORANSM (in French)

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