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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 | |||
| PANTOPRAZOLE
| PANTOPRAZOLE |
METABOLISM | ORAL INTRAVENOUS INJECTION | Cmax 6.5 MICROMOLAR Tmax 2.5 HOUR F 77 PERCENT VD 17.3 LITER PPB 98 PERCENT Cl 10.8 LITER / HOUR HT 1 HOUR SOLUBILITY FREELY SOLUBLE IN WATER | POTASSIUM TRANSPORTING ATPASE | POTASSIUM-TRANSPORTING ATPASE INHIBITOR CHEMBL2095173 POTASSIUM-TRANSPORTING ATPASE P20648 POTASSIUM-TRANSPORTING ATPASE ALPHA CHAIN 1 HOMO SAPIENS ENZYME HYDROLASE | EMA | |||
