| | ||||||||||
| 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 the equation t1/2 = VD / Cl * 0.693 was used | Primary Target and PDB code of Protein-Drug complex | Targets from DrugCentral | Links | |||
| ZONGERTINIB
| ZONGERTINIB | ANTINEOPLASTIC | ORAL | Cmax 3 MICROMOLAR Tmax 2 HOUR F 76 PERCENT VD 118 LITER PPB 99 PERCENT Cl 6.9 LITER / HOUR HT 12 HOUR SOLUBILITY PRACTICALLY INSOLUBLE AT PH 6.8 | EPIDERMAL GROWTH FACTOR RECEPTOR 2 (HER2) | - more at DrugCentral | EMA | |||
