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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]
The following other wikis use this file: Usage on ar.wikipedia.org فينيل بروبانويد; Usage on arz.wikipedia.org فينيل ألانين
The following other wikis use this file: Usage on ar.wikipedia.org فينيل ألانين; طلائع أحادية الأمين; Usage on bs.wikipedia.org
A biochemical diagram showing the class of flavonoids and their source in nature through various inter-related plant species. Flavanoids can possess chiral carbons. Methods of analysis should take this element into account [ 2 ] especially regarding bioactivity or enzyme stereospecificity .
Thus, the two substrates of this enzyme are L-phenylalanine and pyruvate, whereas its two products are phenylpyruvate and L-alanine. This enzyme belongs to the family of transferases, specifically the transaminases, which transfer nitrogenous groups. The systematic name of this enzyme class is L-phenylalanine:pyruvate aminotransferase.
The shikimate pathway (shikimic acid pathway) is a seven-step metabolic pathway used by bacteria, archaea, fungi, algae, some protozoans, and plants for the biosynthesis of folates and aromatic amino acids (tryptophan, phenylalanine, and tyrosine). This pathway is not found in mammals.
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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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