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D-Phenylalanine is distributed to the various tissues of the body via the systemic circulation. 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.
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
Flavonoids are synthesized by the phenylpropanoid metabolic pathway in which the amino acid phenylalanine is used to produce 4-coumaroyl-CoA. [1] This can be combined with malonyl-CoA to yield the true backbone of flavonoids, a group of compounds called chalcones , which contain two phenyl rings.
L-phenylalanine + pyruvate phenylpyruvate + L-alanine 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.
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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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