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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 | |||
| CLOFAZIMINE DISCONTINUED
| CLOFAZIMINE | ANTIINFECTIVES | ORAL | Cmax 2.1 MICROMOLAR (300 MILLIGRAM) Tmax 10 HOUR F 53 PERCENT HT 1680 HOUR SOLUBILITY INSOLUBLE IN WATER | DNA | DNA INHIBITOR CHEMBL2366041 DNA MYCOBACTERIUM LEPRAE | EMA | |||
