CHEBI:30653 - homoserine

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ChEBI Name homoserine
Definition An α-amino acid that is glycine substituted at the α-position by a 2-hydroxyethyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C4H9NO3
Net Charge 0
Average Mass 119.11920
Monoisotopic Mass 119.058
InChI InChI=1S/C4H9NO3/c5-3(1-2-6)4(7)8/h3,6H,1-2,5H2,(H,7,8)
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): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
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 homoserine (CHEBI:30653) has role metabolite (CHEBI:25212)
homoserine (CHEBI:30653) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
homoserine (CHEBI:30653) is conjugate acid of homoserinate (CHEBI:62980)
Incoming N-acylhomoserine (CHEBI:55414) has functional parent homoserine (CHEBI:30653)
O-acetylhomoserine (CHEBI:7671) has functional parent homoserine (CHEBI:30653)
D-homoserine (CHEBI:30654) is a homoserine (CHEBI:30653)
L-homoserine (CHEBI:15699) is a homoserine (CHEBI:30653)
homoserinate (CHEBI:62980) is conjugate base of homoserine (CHEBI:30653)
Synonyms Sources
2-amino-4-hydroxybutanoic acid IUPAC
DL-Homoserine ChemIDplus
Registry Numbers Types Sources
1721682 Reaxys Registry Number Reaxys
1721682 Beilstein Registry Number Beilstein
1927-25-9 CAS Registry Number ChemIDplus
498-19-1 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
15753300 PubMed citation Europe PMC
17439666 PubMed citation Europe PMC
Last Modified
26 March 2015