Cheminformatic Tools and Databases for Pharmacology

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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
IRBESARTAN

IRBESARTAN


ATC C09CA04
ATC C09DB05
ATC C09DA04
ATC C09DX07

CARDIOVASCULAR
ANGIOTENSIN II RECEPTOR ANTAGONIST
ANTIHYPERTENSIVE AGENTS

ORAL

Tmax 1.75 HOUR

F 70 PERCENT

VD 73 LITER

PPB 90 PERCENT

Cl 9.9 LITER / HOUR

HT 13 HOUR

SOLUBILITY PRACTICALLY INSOLUBLE IN WATER

TYPE-1 ANGIOTENSIN II RECEPTOR

TYPE-1 ANGIOTENSIN II RECEPTOR ANTAGONIST CHEMBL227 TYPE-1 ANGIOTENSIN II RECEPTOR P30556 TYPE-1 ANGIOTENSIN II RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 PEPTIDE SHORT PEPTIDE ANGIOTENSIN RECEPTORANSM (in French)

Dailymed
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SIDER side effects

Chemical Probes Portal

ChEMBL
BindingDB
DrugBank



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