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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 | |||
| PARICALCITOL
| PARICALCITOL | METABOLISM | INTRAVENOUS ORAL INJECTION | Cmax 4.03 NANOMOLAR F 79 PERCENT VD 34 LITER PPB 99.8 PERCENT Cl 1.49 LITER / HOUR HT 5 HOUR | VITAMIN D3 RECEPTOR | VITAMIN D RECEPTOR AGONIST CHEMBL1977 VITAMIN D RECEPTOR P11473 VITAMIN D3 RECEPTOR HOMO SAPIENS TRANSCRIPTION FACTOR NUCLEAR RECEPTOR NR1 NR1I NR1I1 | EMA | |||
