CHEBI:16288 - O-acetyl-L-homoserine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name O-acetyl-L-homoserine
ChEBI ID CHEBI:16288
ChEBI ASCII Name O-acetyl-L-homoserine
Definition The O-acetyl derivative of L-homoserine.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:7667, CHEBI:12709, CHEBI:12684, CHEBI:21937
Supplier Information
Download Molfile XML SDF
Formula C6H11NO4
Net Charge 0
Average Mass 161.15588
Monoisotopic Mass 161.06881
InChI InChI=1S/C6H11NO4/c1-4(8)11-3-2-5(7)6(9)10/h5H,2-3,7H2,1H3,(H,9,10)/t5-/m0/s1
InChIKey FCXZBWSIAGGPCB-YFKPBYRVSA-N
SMILES CC(=O)OCC[C@H](N)C(O)=O
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) Source: yeast.sf.net 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): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing O-acetyl-L-homoserine (CHEBI:16288) has functional parent L-homoserine (CHEBI:15699)
O-acetyl-L-homoserine (CHEBI:16288) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
O-acetyl-L-homoserine (CHEBI:16288) is a O-acetylhomoserine (CHEBI:7671)
O-acetyl-L-homoserine (CHEBI:16288) is a acetyl-amino acid (CHEBI:22195)
O-acetyl-L-homoserine (CHEBI:16288) is enantiomer of O-acetyl-D-homoserine (CHEBI:37034)
O-acetyl-L-homoserine (CHEBI:16288) is tautomer of O-acetyl-L-homoserine zwitterion (CHEBI:57716)
Incoming O-acetyl-D-homoserine (CHEBI:37034) is enantiomer of O-acetyl-L-homoserine (CHEBI:16288)
O-acetyl-L-homoserine zwitterion (CHEBI:57716) is tautomer of O-acetyl-L-homoserine (CHEBI:16288)
IUPAC Name
(2S)-4-(acetyloxy)-2-aminobutanoic acid
Synonyms Sources
O-Acetyl-L-homoserine KEGG COMPOUND
O-Acetylhomoserine KEGG COMPOUND
Manual Xrefs Databases
C00019570 KNApSAcK
C01077 KEGG COMPOUND
CPD-667 MetaCyc
View more database links
Registry Numbers Types Sources
1724342 Beilstein Registry Number Beilstein
7540-67-2 CAS Registry Number KEGG COMPOUND
Citations Waiting for Citations Types Sources
11566369 PubMed citation Europe PMC
16233482 PubMed citation Europe PMC
2517474 PubMed citation Europe PMC
35287716 PubMed citation Europe PMC
Last Modified
14 May 2024