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  2. Phenylalanine - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine

    Phenylalanine is a precursor for tyrosine, the monoamine neurotransmitters dopamine, norepinephrine (noradrenaline), and epinephrine (adrenaline), and the biological pigment melanin. It is encoded by the messenger RNA codons UUU and UUC. Phenylalanine is found naturally in the milk of mammals.

  3. Phenylalanine (data page) - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine_(data_page)

    ^a CID 71567 from PubChem (D-phenylalanine) ^a CID 6140 from PubChem (L-phenylalanine) This page was last edited on 12 January 2024, at 23:28 (UTC). Text is ...

  4. α-Methylphenylalanine - Wikipedia

    en.wikipedia.org/wiki/Α-Methylphenylalanine

    α-Methylphenylalanine (α-MePhe or AMPA) is an artificial amino acid and a phenethylamine and amphetamine derivative. [1] It is the α-methylated analogue of phenylalanine, the precursor of the catecholamine neurotransmitters, and the amino acid analogue of amphetamine (α-methylphenethylamine), a psychostimulant and monoamine releasing agent.

  5. Aspartame - Wikipedia

    en.wikipedia.org/wiki/Aspartame

    Aspartame is an artificial non-saccharide sweetener 200 times sweeter than sucrose and is commonly used as a sugar substitute in foods and beverages. [4] It is a methyl ester of the aspartic acid/phenylalanine dipeptide with brand names NutraSweet, Equal, and Canderel. [4]

  6. Phenylacetic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylacetic_acid

    PubChem CID. 999; RTECS number ... 1.0809 g/cm 3: Melting point: 76 to 77 °C (169 to 171 °F; 349 to 350 K) ... Endogenously, it is a catabolite of phenylalanine.

  7. D-Phenylalanine - Wikipedia

    en.wikipedia.org/wiki/D-phenylalanine

    D-Phenylalanine (DPA, D-Phe), sold under the brand names Deprenon, Sabiben, and Sabiden, is an enantiomer of phenylalanine which is described as an antidepressant and is marketed as a prescription drug for medical use in Argentina. [1] [2] The medication has been marketed since at least the 1970s [3] and continued to be available by the 2000s. [1]

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  9. Phenylpyruvic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylpyruvic_acid

    The compound exists in equilibrium with its (E)- and (Z)-enol tautomers.[citation needed] It is a product from the oxidative deamination of phenylalanine.When the activity of the enzyme phenylalanine hydroxylase is reduced, the amino acid phenylalanine accumulates and gets converted into phenylpyruvic acid (phenylpyruvate), which leads to 'Phenylketonuria (PKU)' instead of 'tyrosine' which is ...

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