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2. Tyrosine - Wikipedia

   en.wikipedia.org/wiki/Tyrosine

   In addition to the common amino acid L-tyrosine, which is the para isomer (para-tyr, p-tyr or 4-hydroxyphenylalanine), there are two additional regioisomers, namely meta-tyrosine (also known as 3-hydroxyphenylalanine, L-m-tyrosine, and m-tyr) and ortho-tyrosine (o-tyr or 2-hydroxyphenylalanine), that occur in nature.

3. Catecholamine - Wikipedia

   en.wikipedia.org/wiki/Catecholamine

   In humans, catecholamines (shown in yellow) are derived from the amino acid L-phenylalanine. L-Phenylalanine is converted into L-tyrosine by an aromatic amino acid hydroxylase (AAAH) enzyme (phenylalanine 4-hydroxylase), with molecular oxygen (O 2) and tetrahydrobiopterin as cofactors. L-Tyrosine is converted into L-DOPA by another AAAH enzyme ...

4. Phenylalanine - Wikipedia

   en.wikipedia.org/wiki/Phenylalanine

   The mechanism of DL-phenylalanine's supposed antidepressant activity may also be accounted for in part by the precursor role of L-phenylalanine in the synthesis of the neurotransmitters norepinephrine and dopamine, though clinical trials have not found an antidepressant effect from L-phenylalanine alone. [18]

5. Biopterin-dependent aromatic amino acid hydroxylase - Wikipedia

   en.wikipedia.org/wiki/Biopterin-dependent...

   These enzymes primarily hydroxylate the amino acids L-phenylalanine, L-tyrosine, and L-tryptophan, respectively. The AAAH enzymes are functionally and structurally related proteins which act as rate-limiting catalysts for important metabolic pathways. [1]

6. Monoamine precursor - Wikipedia

   en.wikipedia.org/wiki/Monoamine_precursor

   [1] [2] The amino acids L-tryptophan and L-5-hydroxytryptophan (5-HTP; oxitriptan) are precursors of serotonin and melatonin, while the amino acids L-phenylalanine, L-tyrosine, and L-DOPA (levodopa) are precursors of dopamine, epinephrine (adrenaline), and norepinephrine (noradrenaline).

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   Learn how to download and install or uninstall the Desktop Gold software and if your computer meets the system requirements.

8. Phenylpropanoids metabolism - Wikipedia

   en.wikipedia.org/wiki/Phenylpropanoids_metabolism

   In plants, all phenylpropanoids are derived from the amino acids phenylalanine and tyrosine. Phenylalanine ammonia-lyase (PAL, a.k.a. phenylalanine/tyrosine ammonia-lyase) is an enzyme that transforms L-phenylalanine and tyrosine into trans-cinnamic acid and p-coumaric acid, respectively.

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