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ChEBI
> Main
CHEBI:16288 -
O
-acetyl-
L
-homoserine
Main
ChEBI Ontology
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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
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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 (Br
o
nsted acid).
(via
organic amino compound
)
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted 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
(2
S
)-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
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