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ChEBI
> Main
CHEBI:24109 - fructosyllysine
Main
ChEBI Ontology
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ChEBI Name
fructosyllysine
ChEBI ID
CHEBI:24109
Definition
A glyco-amino acid consisting of a
D
-fructosyl residue attached to the ε-amino group of
L
-lysine.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Molfile
XML
SDF
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Molfile
Formula
C12H24N2O7
Net Charge
0
Average Mass
308.32820
Monoisotopic Mass
308.15835
InChI
InChI=1S/C12H24N2O7/c13-
7(12(20)
21)
3-
1-
2-
4-
14-
5-
8(16)
10(18)
11(19)
9(17)
6-
15/h7,9-
11,14-
15,17-
19H,1-
6,13H2,(H,20,21)
/t7-
,9+,10+,11+/m0/s1
InChIKey
BFSYFTQDGRDJNV-AYHFEMFVSA-N
SMILES
N[C@@H](CCCCNCC(=O)[C@@H](O)[C@H](O)[C@H](O)CO)C(O)=O
Metabolite of Species
Details
Escherichia coli
(NCBI:txid562)
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):
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in
Escherichia coli
.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
fructosyllysine (
CHEBI:24109
)
has role
Escherichia coli
metabolite (
CHEBI:76971
)
fructosyllysine (
CHEBI:24109
)
is a
fructosamine (
CHEBI:24103
)
fructosyllysine (
CHEBI:24109
)
is a
glyco-amino acid (
CHEBI:35258
)
fructosyllysine (
CHEBI:24109
)
is conjugate acid of
fructosyllysinate (
CHEBI:63523
)
fructosyllysine (
CHEBI:24109
)
is conjugate base of
fructosyllysine(1+) (
CHEBI:61393
)
Incoming
fructosyllysine(1+) (
CHEBI:61393
)
is conjugate acid of
fructosyllysine (
CHEBI:24109
)
fructosyllysinate (
CHEBI:63523
)
is conjugate base of
fructosyllysine (
CHEBI:24109
)
IUPAC Name
N
6
-(1-deoxy-
D
-fructos-1-yl)-
L
-lysine
Synonyms
Sources
1-{[(5
S
)-5-amino-5-carboxypentyl]amino}-1-deoxy-
D
-fructose
IUPAC
epsilon-Fructoselysine
ChemIDplus
ε-fructosyl-
L
-lysine
ChEBI
Fructose lysine
ChemIDplus
Fructosyl-lysine
ChemIDplus
Manual Xref
Database
C16488
KEGG COMPOUND
View more database links
Registry Numbers
Types
Sources
21291-40-7
CAS Registry Number
ChemIDplus
2420179
Reaxys Registry Number
Reaxys
2420179
Beilstein Registry Number
Beilstein
Citations
Types
Sources
14641079
PubMed citation
Europe PMC
15080644
PubMed citation
Europe PMC
1556177
PubMed citation
Europe PMC
23609106
PubMed citation
Europe PMC
25538281
PubMed citation
Europe PMC
7718622
PubMed citation
Europe PMC
IND80109283
Agricola citation
Europe PMC
Last Modified
23 August 2017