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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
CILOSTAZOL

CILOSTAZOL


ATC B01AC23

BLOOD
ANTITHROMBOTIC
A QUINOLINONE DERIVATIVE
VASODILATOR AGENTS
PHOSPHODIESTERASE III INHIBITORS

ORAL

Cmax 3.25 MICROMOLAR

Tmax 2 HOUR

PPB 96.5 PERCENT

HT 12 HOUR

SOLUBILITY PRACTICALLY INSOLUBLE IN WATER

PHOSPHODIESTERASE III (PDE)

CAMP-SPECIFIC 3',5'-CYCLIC PHOSPHODIESTERASE 4A P27815 CAMP-SPECIFIC 3',5'-CYCLIC PHOSPHODIESTERASE 4A HOMO SAPIENS ENZYME PHOSPHODIESTERASE PDE_4 PDE_4AEMA

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BindingDB
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