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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 | |||
| MICAFUNGIN
| MICAFUNGIN | ANTIINFECTIVES | INTRAVENOUS INJECTION | Cmax 7.95 MICROMOLAR VD 25.35 LITER (65 KILOGRAM) PPB 99 PERCENT Cl 1.16 LITER / HOUR (65 KILOGRAM) HT 13.4 HOUR SOLUBILITY FREELY SOLUBLE IN WATER | BETA-1,3-GLUCAN SYNTHASE | 1,3-BETA-GLUCAN SYNTHASE INHIBITOR CHEMBL2364673 1,3-BETA-GLUCAN SYNTHASE O13428 BETA-1,3-GLUCAN SYNTHASE CATALYTIC SUBUNIT 1 CANDIDA ENZYME TRANSFERASE | EMA | |||
