Puneet Varma (Editor)

Econazole

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AHFS/Drugs.com
  
Monograph

CAS Number
  
27220-47-9

IUPHAR/BPS
  
2446

CAS ID
  
27220-47-9

MedlinePlus
  
a684049

PubChem CID
  
3198

Molar mass
  
381.683 g/mol

Econazole Econazole Nitrate 1 Cream 15gm Tube McGuff Medical Products

ATC code
  
D01AC03 (WHO) G01AF05 (WHO)

Econazole (commonly used as the nitrate salt) is an antifungal medication of the imidazole class. It is used as a cream under the brand names Spectazole (United States), Ecostatin (Canada), Pevaryl (Western Europe), and Pevisone (the latter consisting of the combination econazole/triamcinolone) 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. In Asia, it is sold under the brand name Endix-G (by Dongkwang, Korea), while in Thailand, it is sold as Ecosone by Qualimed. In Taiwan, it is sold as Vivicome Cream, manufactured by Yong Chang Pharmaceuticals. In Egypt, it is sold as a foam spray by ATM. In Bangladesh, it is sold under the brand name Ecoderm by Rephco Pharmaceuticals Ltd. The combination of econazole nitrate with triamcinolone acetonide is also available under the brand name Ecoderm-TA. Econazole nitrate exhibits strong anti-feeding properties against the keratin-digesting common clothes moth Tineola bisselliella.

Contents

Econazole ECONAZOLE NITRATE CREAM 1

Adverse effects

Econazole Econazole Wikipedia

About 3% of patients treated with econazole nitrate cream reported side effects. The most common symptoms were burning, itching, erythema, and one outbreak of a pruritic rash.

Synthesis

Econazole Econazole Nitrate Cream 1

Imidazoles devoid of the nitro group no longer have any antiprotozoal activity, however, such drugs are effective antifungal agents.

Econazole econazole topical Uses Side Effects Interactions Pictures

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.

Econazole Econazole Nitrate Cream 1



Econazole ECONAZOLE NITRATE CREAM 1

References

Econazole Wikipedia