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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 | |||
| MAVORIXAFOR
| MAVORIXAFOR | BLOOD | ORAL | Cmax 9.45 MICROMOLAR Tmax 2.8 HOUR VD 768 LITER PPB 93 PERCENT Cl 62 LITER / HOUR HT 82 HOUR SOLUBILITY SLIGHTLY SOLUBLE IN PH 7.5 AQUEOUS BUFFER | CXC CHEMOKINE RECEPTOR 4 (CXCR4) | - more at DrugCentral | EMA | |||
