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  2. Phenylalanine - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine

    The biological functions of D-amino acids remain unclear, although D-phenylalanine has pharmacological activity at niacin receptor 2. [17] DL-Phenylalanine (DLPA) is marketed as a nutritional supplement for its purported analgesic and antidepressant activities, which have been supported by clinical trials.

  3. Phenethylamine - Wikipedia

    en.wikipedia.org/wiki/Phenethylamine

    In the brain, phenethylamine regulates monoamine neurotransmission by binding to trace amine-associated receptor 1 (TAAR1) and inhibiting vesicular monoamine transporter 2 (VMAT2) in monoamine neurons. [1] [11] [12] To a lesser extent, it also acts as a neurotransmitter in the human central nervous system. [13]

  4. Neurotransmitter - Wikipedia

    en.wikipedia.org/wiki/Neurotransmitter

    For example, the precursor of serotonin is the amino acid tryptophan. ... Dopamine has a number of important functions in the brain. ... L-phenylalanine and L ...

  5. Catecholamine - Wikipedia

    en.wikipedia.org/wiki/Catecholamine

    The amino acids phenylalanine and tyrosine are precursors for catecholamines. Both amino acids are found in high concentrations in blood plasma and the brain. In mammals, tyrosine can be formed from dietary phenylalanine by the enzyme phenylalanine hydroxylase, found in large amounts in the liver.

  6. Monoamine neurotransmitter - Wikipedia

    en.wikipedia.org/wiki/Monoamine_neurotransmitter

    Examples are dopamine, norepinephrine and serotonin. All monoamines are derived from aromatic amino acids like phenylalanine, tyrosine, and tryptophan by the action of aromatic amino acid decarboxylase enzymes. They are deactivated in the body by the enzymes known as monoamine oxidases which clip off the amine group.

  7. 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.

  8. Neurochemistry - Wikipedia

    en.wikipedia.org/wiki/Neurochemistry

    For example, in Parkinson's Disease, there is an imbalance in the brain's level of dopamine. Medications include neurochemicals that are used to alter brain function and treat disorders of the brain. A typical neurochemist might study how the chemical components of the brain interact, neural plasticity, neural development, physical changes in ...

  9. Phenylketonuria - Wikipedia

    en.wikipedia.org/wiki/Phenylketonuria

    Tyrosine, which is normally derived from phenylalanine and which is necessary for normal brain function, is usually supplemented. Consumption of the protein substitute formulas can actually reduce phenylalanine levels, probably because it stops the process of protein catabolism from releasing Phe stored in the muscles and other tissues into the ...