ATC Group: D01AE Other antifungals for topical use

The World Health Organization's ATC classification organizes medical drugs based on therapeutic properties, chemical composition, and anatomy. It helps make essential medicines readily available globally and is widely used in the pharmaceutical industry.

Position of D01AE in the ATC hierarchy

Level Code Title
1 D Dermatologicals
2 D01 Antifungals for dermatological use
3 D01A Antifungals for topical use
4 D01AE Other antifungals for topical use

Group D01AE contents

Code Title
D01AE01 Bromochlorosalicylanilide
D01AE02 Methylrosaniline
D01AE03 Tribromometacresol
D01AE04 Undecylenic acid
D01AE05 Polynoxylin
D01AE06 2-(4-chlorphenoxy)-ethanol
D01AE07 Chlorphenesin
D01AE08 Ticlatone
D01AE09 Sulbentine
D01AE10 Ethyl hydroxybenzoate
D01AE11 Haloprogin
D01AE12 Salicylic acid
D01AE13 Selenium sulfide
D01AE14 Ciclopirox
D01AE15 Terbinafine
D01AE16 Amorolfine
D01AE17 Dimazole
D01AE18 Tolnaftate
D01AE19 Tolciclate
D01AE20 Combinations
D01AE21 Flucytosine
D01AE22 Naftifine
D01AE23 Butenafine
D01AE24
D01AE25
D01AE54 Undecylenic acid, combinations

Active ingredients in D01AE

Active Ingredient Description
Amorolfine

Amorolfine is a broad spectrum antimycotic. Amorolfine belongs to a new chemical class, and its fungicidal action is based on an alteration of the fungal cell membrane targeted primarily on sterol biosynthesis. The ergosterol content is reduced, and at the same time unusual sterically nonplanar sterols accumulate.

Butenafine

Butenafine is a benzylamine derivative with a mode of action similar to that of the allylamine class of antifungal drugs. Butenafine HCl is hypothesized to act by inhibiting the epoxidation of squalene, thus blocking the biosynthesis of ergosterol, an essential component of fungal cell membranes. It is indicated for the topical treatment of the dermatologic infection, tinea (pityriasis) versicolor due to M. furfur (formerly P. orbiculare).

Chlorphenesin
Ciclopirox olamine

Ciclopirox is a hydroxypyridone antifungal agent which is active in vitro inhibiting the growth of various fungal species including the yeast Malassezia furfur (formerly known as Pityrosporum ovale or Pityrosporum orbiculare).

Ethyl hydroxybenzoate
Flucytosine

Flucytosine is a fluorinated pyrimidine derivative. It is an antimycotic agent exerting fungistatic and fungicidal activity by interfering with protein and DNA synthesis. Fluorodeoxyuridine interferes with the enzyme thymidylate synthase. Inhibition of thymidylate synthase subsequently causes disruption of DNA synthesis.

Liranaftate
Methylrosaniline
Naftifine

Naftifine is a topical antifungal drug. it is used for the the treatment of interdigital tinea pedis caused by the organisms Trichophyton rubrum, Trichophyton mentagrophytes, and Epidermophyton floccosum.

Salicylic acid

Salicylic acid has bacteriostatic and fungicidal actions, but it is its keratolytic properties which are important for this medicinal product. When applied externally it produces slow and painless destruction of the epithelium.

Selenium sulfide

Selenium sulfide appears to have a cytostatic effect on cells of the epidermis and follicular epithelium, reducing corneocyte production.

Tavaborole

Tavaborole is an oxaborole antifungal indicated for the treatment of onychomycosis of the toenails due to Trichophyton rubrum or Trichophyton mentagrophytes.

Terbinafine

Terbinafine is an allylamine which has a broad spectrum of antifungal activity. Terbinafine acts by inhibition of squalene epoxidase in the fungal cell membrane. At low concentrations terbinafine is fungicidal against dermatophytes, moulds and certain dimorphic fungi. The activity versus yeasts is fungicidal or fungistatic depending on the species.

Tolnaftate
Undecylenic acid

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