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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
MEPERIDINE

MEPERIDINE


ATC N02AB02

NERVOUS SYSTEM
ADJUVANTS IN ANESTHESIA
ANALGESICS
OPIOID
NARCOTICS
OPIATE AGONISTS
ANTICHOLINERGIC

ORAL INJECTION

Cmax 1.38 MICROMOLAR (PMID2729638)

VD 149.5 LITER (65 KILOGRAM)

PPB 58 PERCENT

Cl 19.1 LITER / HOUR (65 KILOGRAM)

HT 7.9 HOUR

SOLUBILITY READILY 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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