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  2. Phenylalanine - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine

    It appears to cross the blood–brain barrier less efficiently than L-phenylalanine, and so a small amount of an ingested dose of D-phenylalanine is excreted in the urine without penetrating the central nervous system. [24] L-Phenylalanine is an antagonist at α 2 δ Ca 2+ calcium channels with a K i of 980 nM. [25]

  3. Neotame - Wikipedia

    en.wikipedia.org/wiki/Neotame

    The major metabolic pathway leads to N-(3,3-dimethylbutyl)-L-aspartyl - L - phenylalanine with a side product of methanol, and the minor pathway happens when the N-(3,3-dimethylbutyl)-L-aspartyl - L - phenylalanine is oxidized into 3,3-dimethylbutyric acid. The side products for the minor pathway is methanol, aspartic acid and phenylalanine. [12]

  4. L-DOPA - Wikipedia

    en.wikipedia.org/wiki/L-DOPA

    l-DOPA, also known as l-3,4-dihydroxyphenylalanine and used medically as levodopa, is made and used as part of the normal biology of some plants [2] and animals, including humans. Humans, as well as a portion of the other animals that utilize l -DOPA, make it via biosynthesis from the amino acid l -tyrosine .

  5. Hyperphenylalaninemia - Wikipedia

    en.wikipedia.org/wiki/Hyperphenylalaninemia

    Phenylketonuria (PKU)-like symptoms, including more pronounced developmental defects, skin irritation, and vomiting, may appear when phenylalanine levels are near 20 mg/dL (1200 mol/L). [1] Hyperphenylalaninemia is a recessive hereditary metabolic disorder that is caused by the body's failure to convert phenylalanine to tyrosine as a result of ...

  6. Cathinone - Wikipedia

    en.wikipedia.org/wiki/Cathinone

    The synthesis of cathinone in khat begins with L-phenylalanine and the first step is carried out by L-phenylalanine ammonia lyase (PAL), which cleaves off an ammonia group and creates a carbon-carbon double bond, forming cinnamic acid. [18] After this, the molecule can either go through a beta-oxidative pathway or a non-beta-oxidative pathway.

  7. Phenethylamine - Wikipedia

    en.wikipedia.org/wiki/Phenethylamine

    In mammals, phenethylamine is produced from the amino acid L-phenylalanine by the enzyme aromatic L-amino acid decarboxylase via enzymatic decarboxylation. [14] In addition to its presence in mammals, phenethylamine is found in many other organisms and foods, such as chocolate, especially after microbial fermentation.

  8. Lac-Phe - Wikipedia

    en.wikipedia.org/wiki/Lac-Phe

    Lactoylphenylalanine, or Lac-Phe, is a metabolite generated by intense exercise. [1] [2] [3] In mice, high levels of Lac-Phe in the blood cause a decrease of food intake [1] and in humans, its production has been shown to correlate with adipose tissue loss during an endurance exercise intervention. [4]

  9. L-Phenylalanine - Wikipedia

    en.wikipedia.org/?title=L-Phenylalanine&redirect=no

    This page was last edited on 24 July 2006, at 16:57 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may ...

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