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| 1 | INN | Class | Route (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 complex | Targets from DrugCentral | Links | |||
| IRBESARTAN
| IRBESARTAN |
CARDIOVASCULAR | 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 UNIPROT P30556 AGTR1 more at DrugCentral | EMA | |||
