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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 | |||
| CHLORPROTHIXENE DISCONTINUED
| CHLORPROTHIXENE | NERVOUS SYSTEM | ORAL INJECTION | Cmax 1.36 MICROMOLAR Tmax 4 HOUR F 17 PERCENT (PMID10525070) VD 1035 LITER Cl 52 LITER / HOUR HT 25.8 HOUR | D(2) DOPAMINE 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 | |||
