| | ||||||||||
| 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 | |||
| CANDESARTAN CILEXETIL (has an active metabolite)
| CANDESARTAN CILEXETIL |
CARDIOVASCULAR | ORAL | SOLUBILITY PRACTICALLY INSOLUBLE IN WATER | ANGIOTENSIN II RECEPTOR AT1 | TYPE-1 ANGIOTENSIN II RECEPTOR ANTAGONIST CHEMBL227 ANGIOTENSIN II RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 PEPTIDE SHORT PEPTIDE ANGIOTENSIN RECEPTOR | EMA | |||
