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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. Epoxiconazole - Wikipedia

    en.wikipedia.org/wiki/Epoxiconazole

    Epoxiconazole is a fungicide active ingredient from the class of azoles developed to protect crops. In particular, the substance inhibits the metabolism of fungi cells infesting useful plants, and thereby prevents the growth of the mycelia (fungal cells).

  4. 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 ...

  5. Oxazole - Wikipedia

    en.wikipedia.org/wiki/Oxazole

    Oxazole is the parent compound for a vast class of heterocyclic aromatic organic compounds.These are azoles with an oxygen and a nitrogen separated by one carbon. [4] Oxazoles are aromatic compounds but less so than the thiazoles.

  6. Tiabendazole - Wikipedia

    en.wikipedia.org/wiki/Tiabendazole

    Tiabendazole is also used as a food additive, [2] [3] a preservative with E number E233 (INS number 233). For example, it is applied to bananas to ensure freshness, and is a common ingredient in the waxes applied to the skins of citrus fruits. It is not approved as a food additive in the EU, [4] Australia and New Zealand. [5]

  7. Category:Azoles - Wikipedia

    en.wikipedia.org/wiki/Category:Azoles

    Thiadiazoles (1 C, 40 P) Thiazoles (5 C, 126 P) ... Azole This page was last edited on 16 July 2021, at 16:48 (UTC). Text is available under the Creative ...

  8. Fungistatics - Wikipedia

    en.wikipedia.org/wiki/Fungistatics

    Itraconazole has a broader spectrum of activity than fluconazole (but not as broad as voriconazole or posaconazole). In particular, it is active against Aspergillus, which fluconazole is not. The mechanism of action of itraconazole is the same as the other azole antifungals: it inhibits the fungal-mediated synthesis of ergosterol.

  9. Pyrazole - Wikipedia

    en.wikipedia.org/wiki/Pyrazole

    3-(Difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid is used in the manufacture of six commercial fungicides which are inhibitors of succinate dehydrogenase. [ 20 ] [ 21 ] Pyrazole is an inhibitor of the alcohol dehydrogenase enzyme, and, as such, is used as an adjuvant with ethanol, to induce alcohol dependency in experimental laboratory ...