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  2. Antifungal - Wikipedia

    en.wikipedia.org/wiki/Antifungal

    Currently there is no regulation on the use of similar antifungal classes in agriculture and the clinic. [1] [38] [39] The emergence of Candida auris as a potential human pathogen that sometimes exhibits multi-class antifungal drug resistance is concerning and has been associated with several outbreaks globally. The WHO has released a priority ...

  3. ATC code D01 - Wikipedia

    en.wikipedia.org/wiki/ATC_code_D01

    ATC code D01 Antifungals for dermatological use is a therapeutic subgroup of the Anatomical Therapeutic Chemical Classification System, a system of alphanumeric codes developed by the World Health Organization (WHO) for the classification of drugs and other medical products. [1] [2] [3] Subgroup D01 is part of the anatomical group D ...

  4. Category:Antifungals - Wikipedia

    en.wikipedia.org/wiki/Category:Antifungals

    Pages in category "Antifungals" The following 99 pages are in this category, out of 99 total. This list may not reflect recent changes. ...

  5. Topical antifungal - Wikipedia

    en.wikipedia.org/wiki/Topical_antifungal

    The general mechanism of action for topical antifungal drugs is the disruption of the cell membrane. The unique components found in fungal cell membranes are usually the drug targets of antifungal drugs, in particular ergosterol. It is a sterol, which is important in maintaining proper membrane fluidity and normal functions of the cell membrane.

  6. Fluconazole - Wikipedia

    en.wikipedia.org/wiki/Fluconazole

    Antifungal resistance to drugs in the azole class tends to occur gradually over the course of prolonged drug therapy, resulting in clinical failure in immunocompromised patients (e.g., patients with advanced HIV receiving treatment for thrush or esophageal Candida infection).

  7. Echinocandin - Wikipedia

    en.wikipedia.org/wiki/Echinocandin

    Echinocandin B. Echinocandins are a class of antifungal drugs [1] that inhibit the synthesis of β-glucan in the fungal cell wall via noncompetitive inhibition of the enzyme 1,3-β glucan synthase.