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  2. Keto acid - Wikipedia

    en.wikipedia.org/wiki/Keto_acid

    The presence of the keto group at the beta position allows them to easily undergo thermal decarboxylation. [7] Gamma-keto acids, Gamma-ketoacids, or 4-oxoacids have the ketone group at the third carbon from the carboxylic acid. Levulinic acid is an example. Keto acids appear in a wide variety of anabolic pathways in metabolism.

  3. Category:Beta-keto acids - Wikipedia

    en.wikipedia.org/wiki/Category:Beta-keto_acids

    Pages in category "Beta-keto acids" The following 9 pages are in this category, out of 9 total. This list may not reflect recent changes. A. Acetoacetic acid;

  4. Acetoacetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetoacetic_acid

    Acetoacetic acid (IUPAC name: 3-oxobutanoic acid, also known as acetonecarboxylic acid or diacetic acid) is the organic compound with the formula CH 3 COCH 2 COOH. It is the simplest beta- keto acid , and like other members of this class, it is unstable.

  5. Ketone bodies - Wikipedia

    en.wikipedia.org/wiki/Ketone_bodies

    Ketone bodies are water-soluble molecules or compounds that contain the ketone groups produced from fatty acids by the liver (ketogenesis). [1] [2] Ketone bodies are readily transported into tissues outside the liver, where they are converted into acetyl-CoA (acetyl-Coenzyme A) – which then enters the citric acid cycle (Krebs cycle) and is oxidized for energy.

  6. Category:Keto acids - Wikipedia

    en.wikipedia.org/wiki/Category:Keto_acids

    Beta-keto acids (1 C, 9 P) Pages in category "Keto acids" The following 10 pages are in this category, out of 10 total. This list may not reflect recent changes. ...

  7. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    Keto-enol tautomerism. 1 is the keto form; 2 is the enol. Ketones that have at least one alpha-hydrogen, undergo keto-enol tautomerization; the tautomer is an enol. Tautomerization is catalyzed by both acids and bases. Usually, the keto form is more stable than the enol. This equilibrium allows ketones to be prepared via the hydration of alkynes.

  8. Ketogenesis - Wikipedia

    en.wikipedia.org/wiki/Ketogenesis

    Ketogenesis is the biochemical process through which organisms produce ketone bodies by breaking down fatty acids and ketogenic amino acids. [ 1 ] [ 2 ] The process supplies energy to certain organs, particularly the brain , heart and skeletal muscle , under specific scenarios including fasting , caloric restriction , sleep, [ 3 ] or others.

  9. α-Ketoglutaric acid - Wikipedia

    en.wikipedia.org/wiki/Α-Ketoglutaric_acid

    α-Ketoglutaric acid is an organic compound with the formula H 2 CC(O)(CH 2) 2 CO 2 H). A white, nontoxic solid, it is a common dicarboxylic acid. Relevant to its biological roles, it exists in water as its conjugate base α-ketoglutarate. It is also classified as a 2-ketocarboxylic acid. β-Ketoglutaric acid is an isomer. "Ketoglutaric acid ...