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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
VALSARTAN

VALSARTAN


ATC C09CA03
ATC C09DX02
ATC C09DB01
ATC C09DA03
ATC C09DX01
ATC C09DB08
ATC C09DX04
ATC C09DX05
ATC C10BX10

CARDIOVASCULAR
ANTIHYPERTENSIVE
ANGIOTENSIN II ANTAGONIST

ORAL

Tmax 3 HOUR

F 25 PERCENT

VD 17 LITER

PPB 95 PERCENT

Cl 2 LITER / HOUR

HT 6 HOUR

SOLUBILITY SLIGHTLY SOLUBLE IN WATER

TYPE-1 ANGIOTENSIN II RECEPTOR

TYPE-1 ANGIOTENSIN II RECEPTOR ANTAGONIST CHEMBL227 ANGIOTENSIN II RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 PEPTIDE SHORT PEPTIDE ANGIOTENSIN RECEPTORANSM (in French)

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ChEMBL
BindingDB
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