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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 the equation t1/2 = VD / Cl * 0.693 was used | Primary Target and PDB code of Protein-Drug complex | Targets from DrugCentral | Links | |||
| CEFDINIR
| CEFDINIR | ANTIINFECTIVES | ORAL | Cmax 7.26 MICROMOLAR VD 22.75 LITER (65 KILOGRAM) PPB 65 PERCENT Cl 60 LITER / HOUR (65 KILOGRAM) HT 1.7 HOUR SOLUBILITY SPARINGLY SOLUBLE IN WATER | PENICILLIN-BINDING PROTEINS (PBPS) | Bacterial penicillin-binding protein UNIPROT P02918 mrcA more at DrugCentral | EMA | |||
