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  2. Carnitine - Wikipedia

    en.wikipedia.org/wiki/Carnitine

    L-Carnitine, acetyl-l-carnitine, and propionyl-l-carnitine are available in dietary supplement pills or powders, with a daily amount of 0.5 to 1 g considered to be safe. [1] [3] It is also a drug approved by the Food and Drug Administration to treat primary and certain secondary carnitine-deficiency syndromes secondary to inherited diseases. [1 ...

  3. Glycine propionyl-L-carnitine - Wikipedia

    en.wikipedia.org/wiki/Glycine_propionyl-l-carnitine

    Results indicated that power output was up to 15% higher following the glycine propionyl-l-carnitine trials compared to placebo, while post-exercise blood lactic acid was 15-16% lower compared to placebo. These data are in reference to trained men performing repeated cycle sprints.

  4. Acetylcarnitine - Wikipedia

    en.wikipedia.org/wiki/Acetylcarnitine

    Acetyl-L-carnitine, ALCAR or ALC, is an acetylated form of L-carnitine. It is naturally produced by the human body, and it is available as a dietary supplement. Acetylcarnitine is broken down in the blood by plasma esterases to carnitine which is used by the body to transport fatty acids into the mitochondria for breakdown and energy production.

  5. Propionyl-CoA - Wikipedia

    en.wikipedia.org/wiki/Propionyl-CoA

    Propionyl-CoA is a coenzyme A derivative of propionic acid.It is composed of a 24 total carbon chain (without the coenzyme, it is a 3 carbon structure) and its production and metabolic fate depend on which organism it is present in. [1] Several different pathways can lead to its production, such as through the catabolism of specific amino acids or the oxidation of odd-chain fatty acids. [2]

  6. Propionic acidemia - Wikipedia

    en.wikipedia.org/wiki/Propionic_acidemia

    Patients with propionic acidemia should be started as early as possible on a low protein diet. In addition to a protein mixture that is devoid of methionine, threonine, valine, and isoleucine, the patient should also receive L-carnitine treatment and should be given antibiotics 10 days per month in order to remove the intestinal propiogenic ...

  7. Beta oxidation - Wikipedia

    en.wikipedia.org/wiki/Beta_oxidation

    The reaction is stereospecific, forming only the L isomer. Hydroxyl group is positioned suitable for the subsequent oxidation reaction by 3-hydroxyacyl-CoA dehydrogenase to create a β-keto group. enoyl CoA hydratase: L-β-hydroxyacyl CoA Oxidation by NAD +: The third step is the oxidation of L-β-hydroxyacyl CoA by NAD +.

  8. Ketogenesis - Wikipedia

    en.wikipedia.org/wiki/Ketogenesis

    Ketogenesis pathway. The three ketone bodies (acetoacetate, acetone, and beta-hydroxy-butyrate) are marked within orange boxes. Ketogenesis is the biochemical process through which organisms produce ketone bodies by breaking down fatty acids and ketogenic amino acids.

  9. Propionylation - Wikipedia

    en.wikipedia.org/wiki/Propionylation

    Propionylation is a post-translational modification of proteins, in which a propionyl-group is added to a lysine amino acid of a protein. Propionylation participates in crucial biological processes, including metabolic processes and cellular stress response.