| | ||||||||||
| 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 | |||
| ODEVIXIBAT
| ODEVIXIBAT | METABOLISM | ORAL | Cmax 0.9 NANOMOLAR Tmax 3 HOUR PPB 99 PERCENT HT 2.3 HOUR SOLUBILITY INCREASES IN WATER WITH PH | ILEAL BILE ACID TRANSPORTER | More at DrugCentral | EMA | |||
