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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
HYDROMORPHONE (is an active metabolite)

HYDROMORPHONE


ATC N02AA03
ATC N02AG04
ATC N02AA53

NERVOUS SYSTEM
ANALGESIC
NARCOTICS

INJECTION ORAL

Cmax 20 NANOMOLAR

Tmax 0.73 HOUR

VD 302.9 LITER

PPB 13 PERCENT

Cl 117.6 LITER / HOUR

HT 2.3 HOUR

SOLUBILITY FREELY 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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