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
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Formula C9H10NO2
Net Charge -1
Average Mass 164.18120
Monoisotopic Mass 164.071
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
4136718 Beilstein Registry Number Beilstein
Citation Waiting for Citations Type Source
21956539 PubMed citation Europe PMC
Last Modified
11 November 2014