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ChEBI
> Main
CHEBI:35704 -
N
2
-acetyl-
L
-lysine
Main
ChEBI Ontology
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ChEBI Name
N
2
-acetyl-
L
-lysine
ChEBI ID
CHEBI:35704
ChEBI ASCII Name
N(2)-acetyl-L-lysine
Definition
An acetyl-
L
-lysine where the acetyl group is located at the
N
2
-posiiton.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:21813, CHEBI:31888
Supplier Information
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Molfile
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Formula
C8H16N2O3
Net Charge
0
Average Mass
188.22432
Monoisotopic Mass
188.11609
InChI
InChI=1S/C8H16N2O3/c1-6(11)10-7(8(12)13)4-2-3-5-9/h7H,2-5,9H2,1H3,(H,10,11)(H,12,13)/t7-/m0/s1
InChIKey
VEYYWZRYIYDQJM-ZETCQYMHSA-N
SMILES
CC(=O)N[C@@H](CCCCN)C(O)=O
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
See:
MetaboLights Study
Mus musculus
(NCBI:txid10090)
See:
MetaboLights Study
Mus musculus
(NCBI:txid10090)
See:
DOI
Mus musculus
(NCBI:txid10090)
See:
MetaboLights Study
Homo sapiens
(NCBI:txid9606)
See:
PubMed
Roles Classification
Chemical Role
(s):
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
N
2
-acetyl-
L
-lysine (
CHEBI:35704
)
has role
human metabolite (
CHEBI:77746
)
N
2
-acetyl-
L
-lysine (
CHEBI:35704
)
is a
acetyl-L-lysine (
CHEBI:22193
)
N
2
-acetyl-
L
-lysine (
CHEBI:35704
)
is tautomer of
N
2
-acetyl-
L
-lysine zwitterion (
CHEBI:61512
)
Incoming
N
2
-acetyl-
L
-lysine zwitterion (
CHEBI:61512
)
is tautomer of
N
2
-acetyl-
L
-lysine (
CHEBI:35704
)
IUPAC Name
N
2
-acetyl-
L
-lysine
Synonyms
Sources
(2
S
)-2-(acetylamino)-6-aminohexanoic acid
IUPAC
N
(α)-acetyllysine
ChemIDplus
N
-acetyl-
L
-lysine
ChEBI
N
-α-acetyl-
L
-lysine
ChemIDplus
N2-Acetyl-L-lysine
KEGG COMPOUND
N
α
-acetyl-
L
-lysine
JCBN
Manual Xrefs
Databases
C12989
KEGG COMPOUND
HMDB0000446
HMDB
View more database links
Registry Numbers
Types
Sources
1726281
Beilstein Registry Number
Beilstein
1726281
Reaxys Registry Number
Reaxys
1946-82-3
CAS Registry Number
ChemIDplus
747423
Gmelin Registry Number
Gmelin
Citations
Types
Sources
12212910
PubMed citation
Europe PMC
15131313
PubMed citation
Europe PMC
16274666
PubMed citation
Europe PMC
26800898
PubMed citation
Europe PMC
2897459
PubMed citation
Europe PMC
Last Modified
04 April 2016