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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
SERTACONAZOLE

SERTACONAZOLE


ATC D01AC14
ATC G01AF19

IMIDAZOLE
ANTIFUNGAL
TREATMENT OF INTERDIGITAL TINEA PEDIS
DERMATOLOGICALS
BY INHIBITING THE CYTOCHROME P450-DEPENDENT SYNTHESIS OF ERGOSTEROL, KEY COMPONENT OF THE CELL MEMBRANE OF FUNGI

TOPICAL

Cmax BELOW THE LIMIT OF QUANTITATION (2.5 NANOGRAM / MILLILITER)

SOLUBILITY PRACTICALLY INSOLUBLE IN WATER

CYTOCHROME P450

PDB 1TQN (HUMAN MICROSOMAL P450 3A4)

CYTOCHROME P450 51 INHIBITOR CHEMBL1780 CYTOCHROME P450 51 P10613 LANOSTEROL 14-ALPHA DEMETHYLASE CANDIDA ALBICANS (STRAIN SC5314 / ATCC MYA-2876) (YEAST) ENZYME CYTOCHROME P450 CYP_51 CYP_51A CYP_51A1EMA

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