Substance

ID:7

Names and Identifiers
IUPAC Traditional name
L-phenylalanine
IUPAC name
(2S)-2-amino-3-phenylpropanoic acid
Synonyms
L-Phenylalanine(S)-alpha-Amino-beta-phenylpropionic acid
Registration numbers
CAS Number
PubChem CID
PubChem SID
Properties
Physical Property
Hydrophobicity(logP)
-1.4
Solubility
Slight (0.1-1%)
Molecule Details
Drug Groups
approved; nutraceutical
Description
An essential aromatic amino acid that is a precursor of melanin; dopamine; noradrenalin (norepinephrine), and thyroxine. [PubChem]
Indication
L-phenylalanine may be helpful in some with depression. It may also be useful in the treatment of vitiligo. There is some evidence that L-phenylalanine may exacerbate tardive dyskinesia in some schizophrenic patients and in some who have used neuroleptic drugs.
Pharmacology
Used by the brain to produce Norepinephrine, a chemical that transmits signals between nerve cells and the brain; keeps you awake and alert; reduces hunger pains; functions as an antidepressant and helps improve memory.
Toxicity
L-phenylalanine will exacerbate symptoms of phenylketonuria if used by phenylketonurics. L-phenylalanine was reported to exacerbate tardive dyskinesia when used by some with schizophrenia.
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic. L-phenylalanine that is not metabolized in the liver is distributed via the systemic circulation to the various tissues of the body, where it undergoes metabolic reactions similar to those that take place in the liver.
Absorption
Absorbed from the small intestine by a sodium dependent active transport process.
External Links
Molecular Spectra
No Data Available
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References
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