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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
OXYMORPHONE

OXYMORPHONE


ATC N02AA11

NERVOUS SYSTEM
ANALGESIC
ADJUVANTS, ANESTHESIA
NARCOTICS
OPIATE AGONISTS

INJECTION RECTAL ORAL

Cmax 14.8 NANOMOLAR

Tmax 0.12 HOUR

F 10 PERCENT

VD 200.2 LITER (65 KILOGRAM)

PPB 11 PERCENT

Cl 30.8 LITER / HOUR (EQN)

HT 4.5 HOUR

SOLUBILITY FREELY SOLUBLE IN WATER

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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