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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 | |||
| CISAPRIDE DISCONTINUED
| CISAPRIDE | METABOLISM | ORAL | Tmax 1.25 HOUR F 37.5 PERCENT VD 180 LITER PPB 98 PERCENT Cl 6 LITER / HOUR HT 4 HOUR SOLUBILITY PRACTICALLY INSOLUBLE IN WATER | 5-HYDROXYTRYPTAMINE 4 RECEPTOR | SEROTONIN 4 (5-HT4) RECEPTOR AGONIST CHEMBL1875 SEROTONIN 4 (5-HT4) RECEPTOR Q13639 5-HYDROXYTRYPTAMINE RECEPTOR 4 HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL MONOAMINE RECEPTOR SEROTONIN RECEPTOR | EMA | |||
