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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
DINOPROST DISCONTINUED

DINOPROST


ATC G02AD01
ATC G02AD02

GENITO
PROSTAGLANDIN
OXYTOCIC
PROSTAGLANDIN E2 (PGE2)

INJECTION

Cmax 1.2 NANOMOLAR

Tmax 0.6 HOUR

SOLUBILITY IN WATER 1.3 MILLIGRAM / MILLILITER

PROSTAGLANDIN E2 RECEPTOR EP2

PROSTANOID FP RECEPTOR AGONIST CHEMBL1987 PROSTANOID FP RECEPTOR P43088 PROSTAGLANDIN F2-ALPHA RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL LIPID-LIKE LIGAND RECEPTOR PROSTANOID RECEPTORANSM (in French)

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