Molecular Identity
L-Phenylalanine
(2S)-2-amino-3-phenylpropanoic acid
PubChem CID: 6140
L-phenylalanine is the L-enantiomer of phenylalanine. It has a role as a micronutrient, a nutraceutical, an EC 3.1.3.1 (alkaline phosphatase) inhibitor, a mouse metabolite, a Saccharomyces cerevisiae metabolite, a plant metabolite, a human xenobiotic metabolite, an Escherichia coli metabolite and an algal metabolite. It is a L-alpha-amino acid, a phenylalanine, an erythrose 4-phosphate/phosphoenolpyruvate family amino acid and a proteinogenic amino acid. It is a conjugate base of a L-phenylalaninium. It is a conjugate acid of a L-phenylalaninate. It is an enantiomer of a D-phenylalanine. It is a tautomer of a L-phenylalanine zwitterion.
2D Structure
Properties
C9H11NO2
Molecular Formula
165.19
Molecular Weight
g/mol
165.0790
Exact Mass
Da
-1.5
XLogP
Drug-like (Lipinski: < 5)
63.3
TPSA
Good oral absorption (< 140 A²)
2
H-Bond Donors
3
H-Bond Acceptors
153
Complexity
SMILES
Canonical SMILES
SMILES: C1=CC=C(C=C1)CC(C(=O)O)NIsomeric SMILES
SMILES: C1=CC=C(C=C1)C[C@@H](C(=O)O)NSynonyms(20)
L-phenylalaninephenylalanine63-91-2(S)-2-Amino-3-phenylpropanoic acid(2S)-2-amino-3-phenylpropanoic acid3-Phenyl-L-alanine(S)-Phenylalanine(L)-Phenylalanine3-Phenylalaninebeta-Phenyl-L-alanine(S)-2-Amino-3-phenylpropionic acidAntibiotic FN 1636L-Alanine, phenyl-Alanine, 3-phenyl-fenilalanina
Data from PubChem (NCBI)
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Drug Network
Trials and conditions connected to L-Phenylalanine
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