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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 | |||
| FENOLDOPAM
| FENOLDOPAM | CARDIOVASCULAR | INJECTION | HT 0.083 HOUR SOLUBILITY SPARINGLY SOLUBLE IN WATER | D1 DOPAMINE RECEPTOR | DOPAMINE D1 RECEPTOR AGONIST CHEMBL2056 DOPAMINE D1 RECEPTOR P21728 D(1A) DOPAMINE RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL MONOAMINE RECEPTOR DOPAMINE RECEPTOR | EMA | |||
