CHEBI:32486 - L-phenylalaninate

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ChEBI Name L-phenylalaninate
ChEBI ID CHEBI:32486
ChEBI ASCII Name L-phenylalaninate
Definition An optically active form of phenylalaninate having L-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information eMolecules:538461, ZINC000012494625
Download Molfile XML SDF
Formula C9H10NO2
Net Charge -1
Average Mass 164.18120
Monoisotopic Mass 164.07170
InChI InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/p-1/t8-/m0/s1
InChIKey COLNVLDHVKWLRT-QMMMGPOBSA-M
SMILES N[C@@H](Cc1ccccc1)C([O-])=O
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Roles Classification
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing L-phenylalaninate (CHEBI:32486) has role Escherichia coli metabolite (CHEBI:76971)
L-phenylalaninate (CHEBI:32486) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
L-phenylalaninate (CHEBI:32486) has role plant metabolite (CHEBI:76924)
L-phenylalaninate (CHEBI:32486) is a L-α-amino acid anion (CHEBI:59814)
L-phenylalaninate (CHEBI:32486) is a phenylalaninate (CHEBI:32504)
L-phenylalaninate (CHEBI:32486) is conjugate base of L-phenylalanine (CHEBI:17295)
L-phenylalaninate (CHEBI:32486) is enantiomer of D-phenylalaninate (CHEBI:32494)
Incoming N-acetyl-L-phenylalaninate (CHEBI:57702) has functional parent L-phenylalaninate (CHEBI:32486)
L-phenylalanine (CHEBI:17295) is conjugate acid of L-phenylalaninate (CHEBI:32486)
D-phenylalaninate (CHEBI:32494) is enantiomer of L-phenylalaninate (CHEBI:32486)
IUPAC Name
L-phenylalaninate
Synonyms Sources
(2S)-2-amino-3-phenylpropanoate IUPAC
L-phenylalanine anion JCBN
Registry Numbers Types Sources
329084 Gmelin Registry Number Gmelin
4136718 Reaxys Registry Number Reaxys
Citation Type Source
21956539 PubMed citation Europe PMC
Last Modified
11 November 2014