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  2. Oxadiazole - Wikipedia

    en.wikipedia.org/wiki/Oxadiazole

    1,2,4-Oxadiazole, 1,2,5-oxadiazole, and 1,3,4-oxadiazole are all known and appear in a variety of pharmaceutical drugs including raltegravir, butalamine, fasiplon, oxolamine, and pleconaril. The 1,2,3-isomer is unstable and ring-opens to form the diazo ketone tautomer ; [ 2 ] however, it does exist within the unusual sydnone motif.

  3. Antifungal - Wikipedia

    en.wikipedia.org/wiki/Antifungal

    For example, the azole antifungals such as ketoconazole or itraconazole can be both substrates and inhibitors of the P-glycoprotein, which (among other functions) excretes toxins and drugs into the intestines. [34] Azole antifungals are also both substrates and inhibitors of the cytochrome P450 family CYP3A4, [34] causing increased ...

  4. Fluconazole - Wikipedia

    en.wikipedia.org/wiki/Fluconazole

    Development of resistance to one azole in this way will confer resistance to all drugs in the class. Another resistance mechanism employed by both C. albicans and C. glabrata is increasing the rate of efflux of the azole drug from the cell, by both ATP-binding cassette and major facilitator superfamily transporters.

  5. Topical antifungal - Wikipedia

    en.wikipedia.org/wiki/Topical_antifungal

    Most antifungal drugs induce fungal cell death by destroying the cell wall of the fungus. These drugs inhibit the production of ergosterol, which is a fundamental component of the fungal cell membrane and wall. Antifungal drugs are generally classified according to their chemical structures and their corresponding mechanism of actions.

  6. Azole - Wikipedia

    en.wikipedia.org/wiki/Azole

    One, and only one, lone pair of electrons from each heteroatom in the ring is part of the aromatic bonding in an azole. Names of azoles maintain the prefix upon reduction (e.g., pyrazoline, pyrazolidine). The numbering of ring atoms in azoles starts with the heteroatom that is not part of a double bond, and then proceeds towards the other ...

  7. Ketoconazole - Wikipedia

    en.wikipedia.org/wiki/Ketoconazole

    When administered orally, ketoconazole is best absorbed at highly acidic levels, so antacids or other causes of decreased stomach acid levels will lower the drug's absorption. Absorption can be increased by taking it with an acidic beverage, such as cola . [ 56 ]

  8. FDA bans red dye No. 3 from food, drinks and ingested drugs ...

    www.aol.com/fda-bans-red-dye-no-150632670.html

    The US Food and Drug Administration has banned the use of red dye No. 3 in food, beverages and ingested drugs, more than 30 years after scientists discovered links to cancer in animals, the agency ...

  9. Mebendazole - Wikipedia

    en.wikipedia.org/wiki/Mebendazole

    Mebendazole is a highly effective, broad-spectrum antihelmintic indicated for the treatment of nematode infestations, including roundworm, hookworm, whipworm, threadworm (pinworm), and the intestinal form of trichinosis prior to its spread into the tissues beyond the digestive tract.