CHEBI:30653 - homoserine

ChEBI IDCHEBI:30653
ChEBI Namehomoserine
Stars
DefinitionAn α-amino acid that is glycine substituted at the α-position by a 2-hydroxyethyl group.
Last Modified26 March 2015
SubmitterKirill Degtyarenko
DownloadsMolfile
FormulaC4H9NO3
Net Charge0
Average Mass119.120
Monoisotopic Mass119.05824
SMILESNC(CCO)C(=O)O
InChIInChI=1S/C4H9NO3/c5-3(1-2-6)4(7)8/h3,6H,1-2,5H2,(H,7,8)
InChIKeyUKAUYVFTDYCKQA-UHFFFAOYSA-N
Roles Classification
Chemical Roles:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
ChEBI Ontology
Outgoing Relation(s)
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 Relation(s)
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)
IUPAC Name 
homoserine
Synonyms  Source
2-amino-4-hydroxybutanoic acidIUPAC
HseIUPAC
DL-HomoserineChemIDplus
Registry NumbersSources
Reaxys:1721682Reaxys
CAS:498-19-1ChemIDplus
CAS:1927-25-9ChemIDplus
Citations