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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 | |||
| MILTEFOSINE
| MILTEFOSINE | ANTIPARASITIC | ORAL | Cmax 162.2 MICROMOLAR Tmax 7 HOUR PPB 98 PERCENT HT 153.6 HOUR SOLUBILITY FREELY SOLUBLE IN WATER | MEMBRANE | RAC-alpha serine/threonine-protein kinase P31749 (AKT1_HUMAN) | EMA | |||
