CHEBI:15699 - L-homoserine

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ChEBI Name L-homoserine
ChEBI ID CHEBI:15699
ChEBI ASCII Name L-homoserine
Definition The L-enantiomer of homoserine.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:43131, CHEBI:6246, CHEBI:13123, CHEBI:21330
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Formula C4H9NO3
Net Charge 0
Average Mass 119.11920
Monoisotopic Mass 119.05824
InChI InChI=1S/C4H9NO3/c5-3(1-2-6)4(7)8/h3,6H,1-2,5H2,(H,7,8)/t3-/m0/s1
InChIKey UKAUYVFTDYCKQA-VKHMYHEASA-N
SMILES N[C@@H](CCO)C(O)=O
Metabolite of Species Details
Chlamydomonas reinhardtii (NCBI:txid3055) See: PubMed
Saccharomyces cerevisiae (NCBI:txid4932) Source: yeast.sf.net See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Homo sapiens (NCBI:txid9606) See: DOI
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): 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 ).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
algal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via homoserine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing L-homoserine (CHEBI:15699) has role Escherichia coli metabolite (CHEBI:76971)
L-homoserine (CHEBI:15699) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
L-homoserine (CHEBI:15699) has role algal metabolite (CHEBI:84735)
L-homoserine (CHEBI:15699) has role human metabolite (CHEBI:77746)
L-homoserine (CHEBI:15699) is a homoserine (CHEBI:30653)
L-homoserine (CHEBI:15699) is enantiomer of D-homoserine (CHEBI:30654)
L-homoserine (CHEBI:15699) is tautomer of L-homoserine zwitterion (CHEBI:57476)
Incoming N-(octanoyl)-L-homoserine (CHEBI:74404) has functional parent L-homoserine (CHEBI:15699)
N-heptanoyl-L-homoserine (CHEBI:85607) has functional parent L-homoserine (CHEBI:15699)
O-acetyl-L-homoserine (CHEBI:16288) has functional parent L-homoserine (CHEBI:15699)
L-canaline (CHEBI:41401) has functional parent L-homoserine (CHEBI:15699)
L-canavanine (CHEBI:609827) has functional parent L-homoserine (CHEBI:15699)
isonocardicin A (CHEBI:16483) has functional parent L-homoserine (CHEBI:15699)
isonocardicin C (CHEBI:81022) has functional parent L-homoserine (CHEBI:15699)
D-homoserine (CHEBI:30654) is enantiomer of L-homoserine (CHEBI:15699)
L-homoserine zwitterion (CHEBI:57476) is tautomer of L-homoserine (CHEBI:15699)
IUPAC Name
L-homoserine
Synonyms Sources
(2S)-2-amino-4-hydroxybutanoic acid IUPAC
2-Amino-4-hydroxybutanoic acid HMDB
2-Amino-4-hydroxybutyric acid KEGG COMPOUND
Homoserine HMDB
L-Homoserine KEGG COMPOUND
L-HOMOSERINE PDBeChem
Manual Xrefs Databases
C00001366 KNApSAcK
C00263 KEGG COMPOUND
DB04193 DrugBank
HMDB0000719 HMDB
HOMO-SER MetaCyc
Homoserine Wikipedia
HSE PDBeChem
View more database links
Registry Numbers Types Sources
1721681 Beilstein Registry Number Beilstein
1721681 Reaxys Registry Number Reaxys
672-15-1 CAS Registry Number KEGG COMPOUND
672-15-1 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
22770225 PubMed citation Europe PMC
Last Modified
25 February 2020