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Econazole nitrate salt

SIGMA/E4632

Synonym: 1-(2-[(4-Chlorophenyl)methoxy]-2-[2,4-dichlorophenyl]ethyl)-1H-imidazole

CAS Number: 24169-02-6
Empirical Formula (Hill Notation): C18H15Cl3N2O · HNO3
Molecular Weight: 444.70
EC Number: 246-053-5
MDL Number: MFCD00058160
Linear Formula: C18H15Cl3N2O · HNO3
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-E4632-5G 5 g
$0.00
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45-E4632-25G 25 g
$335.00
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45-E4632-100G 100 g
$0.00
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antibiotic activity spectrum fungi
  Gram-positive bacteria
color white to off-white
form powder or crystals
InChI 1S/C18H15Cl3N2O.HNO3/c19-14-3-1-13(2-4-14)11-24-18(10-23-8-7-22-12-23)16-6-5-15(20)9-17(16)21;2-1(3)4/h1-9,12,18H,10-11H2;(H,2,3,4)
InChI key DDXORDQKGIZAME-UHFFFAOYSA-N
mode of action cell membrane | interferes
  cell wall synthesis | interferes
  enzyme | inhibits
Quality Level 200 
SMILES string O[N+]([O-])=O.Clc1ccc(COC(Cn2ccnc2)c3ccc(Cl)cc3Cl)cc1
Application: Econazole is a broad spectrum antimycotic similar to ketoconazole. It has some action against Gram positive bacteria. It is used topically in dermatomycoses as well as orally and parenterally. It is used for studies on processes such as platelet serotonin uptake, prostanoid biosynthesis, EDHF-mediated relaxation, and Ca2+ transport pathways in thymic lymphocytes.
Biochem/physiol Actions: Econazole interacts with 14-α demethylase, a cytochrome P-450 enzyme necessary to convert lanosterol to ergosterol. Inhibition of ergosterol results in increased cellular permeability causing leakage of cellular contents. Econazole may also inhibit endogenous respiration, interact with membrane phospholipids, inhibit the transformation of yeasts to mycelial forms, inhibit purine uptake, and impair triglyceride and phospholipid biosynthesis.
General description: Chemical structure: imidazole
UNSPSC 51102829

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