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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 | |||
| EPROSARTAN DISCONTINUED
| EPROSARTAN | CARDIOVASCULAR | ORAL | F 13 PERCENT VD 308 LITER PPB 98 PERCENT Cl 48.5 LITER / HOUR HT 20 HOUR SOLUBILITY INSOLUBLE IN WATER | TYPE-1 ANGIOTENSIN II RECEPTOR (AT1) | Type-1 angiotensin II receptor UNIPROT P30556 AGTR1 more at DrugCentral | EMA | |||
