Econazole

{{Short description|Antifungal medication}}

{{Use dmy dates|date=January 2020}}

{{Drugbox

| Watchedfields = changed

| verifiedrevid = 461092342

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| chirality = Racemic mixture

| image = Econazole.svg

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| tradename = Spectazole, Ecostatin, others

| Drugs.com = {{drugs.com|monograph|econazole-nitrate}}

| MedlinePlus = a684049

| licence_CA =

| licence_EU =

| DailyMedID = Econazole

| licence_US =

| pregnancy_AU = A

| pregnancy_AU_comment = {{cite web | title=Econazole topical Use During Pregnancy | website=Drugs.com | date=3 September 2018 | url=https://www.drugs.com/pregnancy/econazole-topical.html | access-date=31 January 2020}}

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| routes_of_administration = Topical

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| ATC_prefix = D01

| ATC_suffix = AC03

| ATC_supplemental = {{ATC|G01|AF05}}

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| legal_US = Rx-only

| legal_US_comment = {{cite web | title=Spectazole (econazole nitrate 1%) Cream | work = DailyMed | publisher = U.S. National Library of Medicine | date=30 September 2013 | url=https://dailymed.nlm.nih.gov/dailymed/archives/fdaDrugInfo.cfm?archiveid=121775 | access-date=31 July 2021}}

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| CAS_number_Ref = {{cascite|correct|??}}

| CAS_number = 27220-47-9

| CAS_supplemental =

| PubChem = 3198

| IUPHAR_ligand = 2446

| DrugBank_Ref = {{drugbankcite|correct|drugbank}}

| DrugBank = DB01127

| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

| ChemSpiderID = 3086

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = 6Z1Y2V4A7M

| KEGG_Ref = {{keggcite|correct|kegg}}

| KEGG = D03936

| ChEBI_Ref = {{ebicite|correct|EBI}}

| ChEBI = 4754

| ChEMBL_Ref = {{ebicite|correct|EBI}}

| ChEMBL = 808

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| IUPAC_name = (RS)-1-{2-[(4-Chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazole

| C=18 | H=15 | Cl=3 | N=2 | O=1

| SMILES = Clc1ccc(c(Cl)c1)C(OCc2ccc(Cl)cc2)Cn3ccnc3

| StdInChI_Ref = {{stdinchicite|correct|chemspider}}

| StdInChI = 1S/C18H15Cl3N2O/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/h1-9,12,18H,10-11H2

| StdInChI_comment =

| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}

| StdInChIKey = LEZWWPYKPKIXLL-UHFFFAOYSA-N

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Econazole is an antifungal medication of the imidazole class.{{cite journal | vauthors = Thienpont D, Van Cutsem J, Van Nueten JM, Niemegeers CJ, Marsboom R | title = Bilogical and toxicological properties of econazole, a broad-spectrum antimycotic | journal = Arzneimittel-Forschung | volume = 25 | issue = 2 | pages = 224–230 | date = February 1975 | pmid = 1173036 }}

It was patented in 1968, and approved for medical use in 1974.{{cite book | vauthors = Fischer J, Ganellin CR |title=Analogue-based Drug Discovery |date=2006 |publisher=John Wiley & Sons |isbn=9783527607495 |page=502 |url=https://books.google.com/books?id=FjKfqkaKkAAC&pg=PA502 }}

Medical uses

Econazole is used as a cream to treat skin infections such as athlete's foot, tinea, pityriasis versicolor, ringworm, and jock itch. It is also sold in Canada under the brand name Ecostatin as vaginal ovules to treat vaginal thrush.{{cn|date=December 2022}}

Econazole nitrate exhibits strong anti-feeding properties against the keratin-digesting common clothes moth Tineola bisselliella.{{cite journal | vauthors = Sunderland MR, Cruickshank RH, Leighs SJ | s2cid = 135799368 | date = 2014 | title = The efficacy of antifungal azole and antiprotozoal compounds in protection of wool from keratin-digesting insect larvae | journal = Textile Research Journal | volume = 84 | issue = 9 | pages = 924–931 | doi = 10.1177/0040517513515312 }}

Adverse effects

About 3% of patients treated with econazole nitrate cream reported side effects. The most common symptoms were burning, itching, redness (erythema), and one outbreak of a pruritic rash.{{cite web | title = Econazole nitrate cream | url = https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3acc5e03-0339-4b23-945d-641746e81923 | work = Daily Med | publisher = U.S. National Library of Medicine }}

Synthesis

Imidazoles devoid of the nitro group no longer have any antiprotozoal activity, however, such drugs are effective antifungal agents.{{cn|date=December 2022}}

File:Econazole synthesis.svg).]]

Alkylation of imidazole (2) with bromoketone (1) prepared from o,p-dichloroacetophenone affords the displacement product (3). Reduction of the ketone with sodium borohydride gives the corresponding alcohol (4). Alkylation of the alkoxide from that alcohol with p-chlorobenzyl chloride leads to econazole (5); alkylation with o,p-dichlorobenzyl chloride gives miconazole.

Society and culture

= Brand names =

It is sold under the brand names Spectrazole (United States) and Ecostatin (Canada), among others. It is a component of Pevisone, Ecoderm-TA{{cite web | url = http://www.rephco-bd.com/index.php?option=com_content&view=article&id=22&Itemid=48 | title = Product descriptions: Ecoderm Cream | archive-url = https://web.archive.org/web/20110831013612/http://www.rephco-bd.com/index.php?option=com_content&view=article&id=22&Itemid=48 | archive-date = 2011-08-31 | publisher = REPHCO Pharmaceuticals Limited | location = Bangladesh | access-date = 1 June 2012 }} and ECOSONE (econazole/triamcinolone).

References

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