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  2. Pyrogallol - Wikipedia

    en.wikipedia.org/wiki/Pyrogallol

    Pyrogallol is an organic compound with the formula C 6 H 3 (OH) 3. It is a water-soluble, white solid although samples are typically brownish because of its sensitivity toward oxygen. [ 3 ] It is one of three isomers of benzenetriols .

  3. Phloroglucinol - Wikipedia

    en.wikipedia.org/wiki/Phloroglucinol

    Phloroglucinol is an organic compound with the formula C 6 H 3 (OH) 3. It is a colorless solid. It is used in the synthesis of pharmaceuticals and explosives. Phloroglucinol is one of three isomeric benzenetriols. The other two isomers are hydroxyquinol (1,2,4-benzenetriol) and pyrogallol (1,2,3-benzenetriol).

  4. Trihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Trihydroxybenzenes

    The trihydroxybenzenes (or benzenetriols) are organic compounds with the formula C 6 H 3 (OH) 3. Also classified as polyphenols, they feature three hydroxyl groups substituted onto a benzene ring. They are white solids with modest solubility in water.

  5. Polyol pathway - Wikipedia

    en.wikipedia.org/wiki/Polyol_pathway

    The polyol pathway is a two-step process that converts glucose to fructose. [1] In this pathway glucose is reduced to sorbitol, which is subsequently oxidized to fructose. It is also called the sorbitol-aldose reductase pathway. The pathway is implicated in diabetic complications, especially in microvascular damage to the retina, [2] kidney, [3 ...

  6. 1,2,3,5-Tetrahydroxybenzene - Wikipedia

    en.wikipedia.org/wiki/1,2,3,5-Tetrahydroxybenzene

    It is a metabolite in the degradation of 3,4,5-trihydroxybenzoate (gallic acid) by Eubacterium oxidoreducens. [1] The enzyme pyrogallol hydroxytransferase uses 1,2,3,5-tetrahydroxybenzene and 1,2,3-trihydroxybenzene , whereas its two products are 1,3,5-trihydroxybenzene (phloroglucinol) and 1,2,3,5-tetrahydroxybenzene. [2]

  7. Benzonitrile - Wikipedia

    en.wikipedia.org/wiki/Benzonitrile

    Benzonitrile is a useful solvent and a versatile precursor to many derivatives. It reacts with amines to afford N-substituted benzamides after hydrolysis. [3] It is a precursor to diphenylmethanimine via reaction with phenylmagnesium bromide followed by methanolysis.

  8. Ketone bodies - Wikipedia

    en.wikipedia.org/wiki/Ketone_bodies

    In the event of low glucose concentration in the blood, most other tissues have alternative fuel sources besides ketone bodies and glucose (such as fatty acids), but studies have indicated that the brain has an obligatory requirement for some glucose. [13] After strict fasting for 3 days, the brain gets 25% of its energy from ketone bodies. [14]

  9. Glycosyltransferase - Wikipedia

    en.wikipedia.org/wiki/Glycosyltransferase

    Most glycosyltransferase enzymes form one of two folds: GT-A or GT-B. Glycosyltransferases (GTFs, Gtfs) are enzymes that establish natural glycosidic linkages.They catalyze the transfer of saccharide moieties from an activated nucleotide sugar (also known as the "glycosyl donor") to a nucleophilic glycosyl acceptor molecule, the nucleophile of which can be oxygen- carbon-, nitrogen-, or sulfur ...