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Econazole nitrate salt_Molecular_structure_CAS_24169-02-6)
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Econazole nitrate salt

Catalog No. E4632 Name Sigma Aldrich
CAS Number 24169-02-6 Website http://www.sigmaaldrich.com
M. F. C18H16Cl3N3O4 Telephone 1-800-521-8956
M. W. 444.69634 Fax
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Storage Chembase ID: 73070

SYNONYMS

IUPAC name
1-{2-[(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazole; nitric acid
IUPAC Traditional name
acid, nitric; econazole
Synonyms
1-(2-[(4-Chlorophenyl)methoxy]-2-[2,4-dichlorophenyl]ethyl)-1H-imidazole

DATABASE IDS

PubChem SID 24894567
MDL Number MFCD00058160
CAS Number 24169-02-6
EC Number 246-053-5

PROPERTIES

GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302-H315-H319
European Hazard Symbols Harmful Harmful (Xn)
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P305 + P351 + P338
Risk Statements 22-36/38
RTECS NI4450000
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
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 lymphocytes1.
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. It Inhibits Ca2+ transport pathways in thymic lymphocytes1.

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