Econazole: Difference between revisions
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{{Chem infobox | |||
|align=right | |||
|image=[[Image:Econazole.jpg|center|thumb|200px]] | |||
|width=200px | |||
|molname=econazole | |||
|synonyms= | |||
|molformula= C<sub>18</sub>H<sub>15</sub>Cl<sub>3</sub>N<sub>2</sub>O | |||
|molmass= 381.6835 | |||
|uses=antifungal drug | |||
|properties=azole compound | |||
|hazards=see drug interactions | |||
|iupac= <small><nowiki>1-[2-[(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl]imidazole</nowiki></small> | |||
|casnumber=27220-47-9 | |||
}} | |||
::''see also [[azole]]/catalog for similar drug compounds'' | |||
'''Econazole''' is a broad-spectrum [[azole]]-based [[antifungal drug]] with limited activity against [[Gram-positive bacteria]]. It is administered topically, orally and intravenously. It is similar to the related azole-based drugs [[fluconazole]], [[clotrimazole]], [[ketoconazole]] and [[intraconazole]], among others. It is used for topical treatment of tinea species, including [[tinea pedis]], [[tineas cruris]], [[tinea versicolor]] and [[tinea corporis]], the Trichophyton species [[Trichophyton rubrum]], [[Trichophyton mentagrophytes]], and [[Trichophyton tonsurans]]. Addition infections treatable with econazole include the Microsporum species [[Microsporum canis]], [[Microsporum audouini]],and [[Microsporum gypseum]], and [[Epidermophyton floccosum]] and cutaneous [[candidiasis]]. | |||
== Mechanism of action == | |||
Like other azole-based antifungal agents, econazole increases cell permeability by interacting with 14-α demethylase, a cytochrome P-450 enzyme necessary in the conversion of [[lanosterol]] to [[ergosterol]], a necessary component of cell membranes. "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/or phospholipid biosynthesis."<ref>{{DrugBank}}</ref> | |||
== Brand names == | |||
* Econazole Nitrate® | |||
* Ecostatin® | |||
* Ecostatin Vaginal Ovules® | |||
* Ecostatin cream® | |||
* Gyno-Pevaryl® | |||
* Gyno-Pevaryl 150® | |||
* Ifenec® | |||
* Palavale® | |||
* Pevaryl® | |||
* Spectazole® | |||
* Spectazole cream® | |||
== References - external links == | |||
* {{DailyMed}} | |||
* {{MedMaster}} | |||
* <references/> |
Revision as of 10:51, 10 May 2008
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econazole | |||||||
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Uses: | antifungal drug | ||||||
Properties: | azole compound | ||||||
Hazards: | see drug interactions | ||||||
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- see also azole/catalog for similar drug compounds
Econazole is a broad-spectrum azole-based antifungal drug with limited activity against Gram-positive bacteria. It is administered topically, orally and intravenously. It is similar to the related azole-based drugs fluconazole, clotrimazole, ketoconazole and intraconazole, among others. It is used for topical treatment of tinea species, including tinea pedis, tineas cruris, tinea versicolor and tinea corporis, the Trichophyton species Trichophyton rubrum, Trichophyton mentagrophytes, and Trichophyton tonsurans. Addition infections treatable with econazole include the Microsporum species Microsporum canis, Microsporum audouini,and Microsporum gypseum, and Epidermophyton floccosum and cutaneous candidiasis.
Mechanism of action
Like other azole-based antifungal agents, econazole increases cell permeability by interacting with 14-α demethylase, a cytochrome P-450 enzyme necessary in the conversion of lanosterol to ergosterol, a necessary component of cell membranes. "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/or phospholipid biosynthesis."[1]
Brand names
- Econazole Nitrate®
- Ecostatin®
- Ecostatin Vaginal Ovules®
- Ecostatin cream®
- Gyno-Pevaryl®
- Gyno-Pevaryl 150®
- Ifenec®
- Palavale®
- Pevaryl®
- Spectazole®
- Spectazole cream®
References - external links
- Econazole - FDA approved drug information (drug label) from DailyMed (U.S. National Library of Medicine).
- Template:MedMaster