CHEBI:43103 - L-homophenylalanine

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ChEBI Name L-homophenylalanine
ChEBI ID CHEBI:43103
ChEBI ASCII Name L-homophenylalanine
Definition A non-proteinogenic L-α-amino acid that is an analogue of L-phenylalanine having a 2-phenylethyl rather than a benzyl side-chain.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C10H13NO2
Net Charge 0
Average Mass 179.21570
Monoisotopic Mass 179.09463
InChI InChI=1S/C10H13NO2/c11-9(10(12)13)7-6-8-4-2-1-3-5-8/h1-5,9H,6-7,11H2,(H,12,13)/t9-/m0/s1
InChIKey JTTHKOPSMAVJFE-VIFPVBQESA-N
SMILES N[C@@H](CCc1ccccc1)C(O)=O
Metabolite of Species Details
Nostoc punctiforme (NCBI:txid63737) of strain PCC 73102 See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-alpha-amino acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing L-homophenylalanine (CHEBI:43103) has role bacterial metabolite (CHEBI:76969)
L-homophenylalanine (CHEBI:43103) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
IUPAC Name
(2S)-2-amino-4-phenylbutanoic acid
Synonyms Sources
homophenylalanine ChEBI
L-HPA ChEBI
L-hph MetaCyc
Manual Xrefs Databases
AU2010269286 Patent
C17235 KEGG COMPOUND
CPD-15322 MetaCyc
HPE PDBeChem
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Registry Numbers Types Sources
3201289 Reaxys Registry Number Reaxys
943-73-7 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
23354699 PubMed citation Europe PMC
23893309 PubMed citation Europe PMC
24053171 PubMed citation Europe PMC
24993356 PubMed citation Europe PMC
Last Modified
11 June 2015