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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:42024 -
N
6
-dansyl-
L
-lysine
Main
ChEBI Ontology
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ChEBI Name
N
6
-dansyl-
L
-lysine
ChEBI ID
CHEBI:42024
ChEBI ASCII Name
N(6)-dansyl-L-lysine
Definition
An
L
-lysine derivative with a dansyl group at the
N
6
-position.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Molfile
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Molfile
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Molfile
Formula
C18H25N3O4S
Net Charge
0
Average Mass
379.476
Monoisotopic Mass
379.15658
InChI
InChI=1S/C18H25N3O4S/c1-
21(2)
16-
10-
5-
8-
14-
13(16)
7-
6-
11-
17(14)
26(24,25)
20-
12-
4-
3-
9-
15(19)
18(22)
23/h5-
8,10-
11,15,20H,3-
4,9,12,19H2,1-
2H3,(H,22,23)
/t15-
/m0/s1
InChIKey
VQPRNSWQIAHPMS-HNNXBMFYSA-N
SMILES
N(CCCC[C@@H](C(O)=O)N)S(C1=CC=CC2=C1C=CC=C2N(C)C)(=O)=O
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):
epitope
The biological role played by a material entity when bound by a receptor of the adaptive immune system. Specific site on an antigen to which an antibody binds.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
N
6
-dansyl-
L
-lysine (
CHEBI:42024
)
has role
epitope (
CHEBI:53000
)
N
6
-dansyl-
L
-lysine (
CHEBI:42024
)
is a
L
-lysine derivative (
CHEBI:25095
)
N
6
-dansyl-
L
-lysine (
CHEBI:42024
)
is a
non-proteinogenic
L
-α-amino acid (
CHEBI:83822
)
N
6
-dansyl-
L
-lysine (
CHEBI:42024
)
is a
sulfonamide (
CHEBI:35358
)
IUPAC Name
N
6
-
[5-
(dimethylamino)naphthalene-
1-
sulfonyl]-
L
-
lysine
Synonyms
Sources
Dansyllysine
ChemIDplus
Dns-lysine
ChemIDplus
N(epsilon)-Dansyl-L-lysine
ChemIDplus
N
6
-{[5-(dimethylamino)-1-naphthyl]sulfonyl}-
L
-lysine
IUPAC
Manual Xrefs
Databases
1WZ1
PDB
DB04676
DrugBank
DNS
PDBeChem
View more database links
Registry Numbers
Types
Sources
1101-84-4
CAS Registry Number
ChemIDplus
2786589
Beilstein Registry Number
Beilstein
2786589
Reaxys Registry Number
Reaxys
Citations
Types
Sources
16019026
PubMed citation
Europe PMC
6200599
PubMed citation
Europe PMC
9523993
PubMed citation
Europe PMC
Last Modified
28 December 2016