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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
LEVOPROPOXYPHENE DISCONTINUED

LEVOPROPOXYPHENE


ATC N02AC04
ATC N02AC54
ATC N02AC74

NERVOUS SYSTEM
ANTITUSSIVE
OPIOID AGONIST
ANALGESIC

ORAL

Cmax 0.21 MICROMOLAR (65 MILLIGRAM)

Tmax 2.25 HOUR

VD 780 LITER (65 KILOGRAM)

PPB 80 PERCENT

Cl 58.5 LITER / HOUR (65 KILOGRAM)

HT 9 HOUR

SOLUBILITY FREELY SOLUBLE IN WATER

SODIUM CHANNEL
HERG
OPIOID RECEPTOR

Unknown - more at DrugCentralANSM (in French)

Dailymed
Drugs.com

SIDER side effects

Chemical Probes Portal

ChEMBL
BindingDB
DrugBank



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