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1 INNClassRoute (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 complexTargets from DrugCentral Links
CEFDINIR

CEFDINIR


ATC J01DD15

ANTIINFECTIVES
ANTIBIOTIC
ANTIBACTERIAL
CEPHALOSPORINS
INHIBITION OF CELL WALL SYNTHESIS

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 INHIBITOR CHEMBL2354204 BACTERIAL PENICILLIN-BINDING PROTEIN P02918 PENICILLIN-BINDING PROTEIN 1A BACTERIA ENZYME PROTEASE SERINE UNCLASSIFIEDANSM (in French)

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