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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:16855 -
D
-lysine
Main
ChEBI Ontology
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ChEBI Name
D
-lysine
ChEBI ID
CHEBI:16855
ChEBI ASCII Name
D-lysine
Definition
The
D
-enantiomer of the α-amino acid lysine.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:42062, CHEBI:4203, CHEBI:12994, CHEBI:21046
Supplier Information
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Molfile
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Formula
C6H14N2O2
Net Charge
0
Average Mass
146.18764
Monoisotopic Mass
146.10553
InChI
InChI=1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10)/t5-/m1/s1
InChIKey
KDXKERNSBIXSRK-RXMQYKEDSA-N
SMILES
NCCCC[C@@H](N)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):
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
Daphnia magna metabolite
A
Daphnia
metabolite produced by the species
Daphnia magna
.
(via
lysine
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-lysine (
CHEBI:16855
)
has role
bacterial metabolite (
CHEBI:76969
)
D
-lysine (
CHEBI:16855
)
has role
fungal metabolite (
CHEBI:76946
)
D
-lysine (
CHEBI:16855
)
is a
D
-α-amino acid (
CHEBI:16733
)
D
-lysine (
CHEBI:16855
)
is a
lysine (
CHEBI:25094
)
D
-lysine (
CHEBI:16855
)
is conjugate acid of
D
-lysinate (
CHEBI:32556
)
D
-lysine (
CHEBI:16855
)
is conjugate base of
D
-lysinium(1+) (
CHEBI:32557
)
D
-lysine (
CHEBI:16855
)
is enantiomer of
L
-lysine (
CHEBI:18019
)
Incoming
D
-lysine hydrochloride (
CHEBI:53558
)
has part
D
-lysine (
CHEBI:16855
)
D
-lysinium(1+) (
CHEBI:32557
)
is conjugate acid of
D
-lysine (
CHEBI:16855
)
D
-lysinate (
CHEBI:32556
)
is conjugate base of
D
-lysine (
CHEBI:16855
)
L
-lysine (
CHEBI:18019
)
is enantiomer of
D
-lysine (
CHEBI:16855
)
N
2
-
D
-lysino group (
CHEBI:32561
)
is substituent group from
D
-lysine (
CHEBI:16855
)
N
6
-
D
-lysino group (
CHEBI:32562
)
is substituent group from
D
-lysine (
CHEBI:16855
)
D
-lysine residue (
CHEBI:29968
)
is substituent group from
D
-lysine (
CHEBI:16855
)
D
-lysyl group (
CHEBI:32559
)
is substituent group from
D
-lysine (
CHEBI:16855
)
IUPAC Names
(2
R
)-2,6-diaminohexanoic acid
D
-lysine
Synonyms
Sources
(
R
)-2,6-diaminohexanoic acid
ChEBI
D-2,6-Diaminohexanoic acid
KEGG COMPOUND
D
-Lysin
ChEBI
D-Lysine
KEGG COMPOUND
D-LYSINE
PDBeChem
DLY
PDBeChem
Manual Xrefs
Databases
C00739
KEGG COMPOUND
CPD-219
MetaCyc
DB03252
DrugBank
DLY
PDBeChem
HMDB0003405
HMDB
View more database links
Registry Numbers
Types
Sources
1722530
Reaxys Registry Number
Reaxys
1926332
Gmelin Registry Number
Gmelin
923-27-3
CAS Registry Number
KEGG COMPOUND
923-27-3
CAS Registry Number
ChemIDplus
Citations
Types
Sources
10571145
PubMed citation
Europe PMC
10930630
PubMed citation
Europe PMC
125972
PubMed citation
Europe PMC
15561717
PubMed citation
Europe PMC
15914930
PubMed citation
Europe PMC
16595662
PubMed citation
Europe PMC
17259313
PubMed citation
Europe PMC
22569959
PubMed citation
Europe PMC
23023754
PubMed citation
Europe PMC
23090865
PubMed citation
Europe PMC
2435906
PubMed citation
Europe PMC
2493343
PubMed citation
Europe PMC
2503300
PubMed citation
Europe PMC
2510957
PubMed citation
Europe PMC
4359655
PubMed citation
Europe PMC
4391118
PubMed citation
Europe PMC
4710063
PubMed citation
Europe PMC
5128165
PubMed citation
Europe PMC
6448848
PubMed citation
Europe PMC
7563967
PubMed citation
Europe PMC
77880
PubMed citation
Europe PMC
8063049
PubMed citation
Europe PMC
8234494
PubMed citation
Europe PMC
8405749
PubMed citation
Europe PMC
9163947
PubMed citation
Europe PMC
9430472
PubMed citation
Europe PMC
Last Modified
23 October 2015