| | ||||||||||
| 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 | |||
| CHOLECALCIFEROL (has an active metabolite)
| CHOLECALCIFEROL |
METABOLISM | INTRAVENOUS ORAL | Cmax 10.4 NANOMOLAR Tmax 10.6 HOUR HT 14 HOUR SOLUBILITY PRACTICALLY INSOLUBLE IN WATER | VITAMIN D3-25-HYDROXYLASE (25-OHASE) | Vitamin D3 receptor UNIPROT P11473 VDR more at DrugCentral | EMA | |||
