EMBL-EBI | Chemical Biology | ChEBI

Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search

CHEBI:15699 - L-homoserine

Default Structure
ChEBI IDCHEBI:15699
ChEBI NameL-homoserine
Stars
ASCII NameL-homoserine
DefinitionThe L-enantiomer of homoserine.
Secondary ChEBI IDsCHEBI:6246, CHEBI:13123, CHEBI:21330, CHEBI:43131
Last Modified25 February 2020
DownloadsMolfile
FormulaC4H9NO3
Net Charge0
Average Mass119.120
Monoisotopic Mass119.05824
SMILESN[C@@H](CCO)C(=O)O
InChIInChI=1S/C4H9NO3/c5-3(1-2-6)4(7)8/h3,6H,1-2,5H2,(H,7,8)/t3-/m0/s1
InChIKeyUKAUYVFTDYCKQA-VKHMYHEASA-N
Wikipedia
Species of MetaboliteComponentSourceComments
Chlamydomonas reinhardtii (ncbitaxon:3055) - PubMed (25515814)
Escherichia coli (ncbitaxon:562) - PubMed (21988831)
Homo sapiens (ncbitaxon:9606) - DOI (10.1038/nbt.2488)
Saccharomyces cerevisiae (ncbitaxon:4932) - PubMed (24678285) Source: yeast.sf.net
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).
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 Roles:
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.
ChEBI Ontology
Outgoing Relation(s)
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 Relation(s)
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  Source
2-Amino-4-hydroxybutanoic acidHMDB
2-Amino-4-hydroxybutyric acidKEGG COMPOUND
(2S)-2-amino-4-hydroxybutanoic acidIUPAC
HomoserineHMDB
L-HomoserineKEGG COMPOUND
L-HOMOSERINEPDBeChem
Manual XrefsDatabases
C00001366KNApSAcK
C00263KEGG COMPOUND
DB04193DrugBank
HMDB0000719HMDB
HOMO-SERMetaCyc
HomoserineWikipedia
HSEPDBeChem
Registry NumbersSources
Reaxys:1721681Reaxys
CAS:672-15-1ChemIDplus
CAS:672-15-1KEGG COMPOUND
Citations