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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 | |||
| ZIPRASIDONE
| ZIPRASIDONE | NERVOUS SYSTEM | ORAL INTRAMUSCULAR | Tmax 7 HOUR F 60 PERCENT VD 97.5 LITER (65 KILOGRAM) PPB 99 PERCENT Cl 29.2 LITER / HOUR (65 KILOGRAM) HT 7 HOUR | ALPHA 1 ADRENERGIC RECEPTOR 5-HYDROXYTRYPTAMINE 1A RECEPTOR D(2) DOPAMINE RECEPTOR 5-HYDROXYTRYPTAMINE 2A RECEPTOR 5-HYDROXYTRYPTAMINE 2C RECEPTOR D(3) DOPAMINE RECEPTOR 5-HYDROXYTRYPTAMINE 1D RECEPTOR | DOPAMINE D2 RECEPTOR ANTAGONIST CHEMBL217 DOPAMINE D2 RECEPTOR P14416 D(2) DOPAMINE RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL MONOAMINE RECEPTOR DOPAMINE RECEPTOR | EMA | |||
