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> Main
CHEBI:23673 - 2,6-diaminopimelic acid
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ChEBI Name
2,6-diaminopimelic acid
ChEBI ID
CHEBI:23673
Definition
The amino dicarboxylic acid that is heptanedioic acid with amino substituents at C-2 and C-6.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C7H14N2O4
Net Charge
0
Average Mass
190.19714
Monoisotopic Mass
190.09536
InChI
InChI=1S/C7H14N2O4/c8-4(6(10)11)2-1-3-5(9)7(12)13/h4-5H,1-3,8-9H2,(H,10,11)(H,12,13)
InChIKey
GMKMEZVLHJARHF-UHFFFAOYSA-N
SMILES
NC(CCCC(N)C(O)=O)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
2,6-diaminopimelic acid (
CHEBI:23673
)
has functional parent
pimelic acid (
CHEBI:30531
)
2,6-diaminopimelic acid (
CHEBI:23673
)
has role
Escherichia coli
metabolite (
CHEBI:76971
)
2,6-diaminopimelic acid (
CHEBI:23673
)
is a
amino dicarboxylic acid (
CHEBI:36164
)
2,6-diaminopimelic acid (
CHEBI:23673
)
is a
dicarboxylic fatty acid (
CHEBI:189840
)
2,6-diaminopimelic acid (
CHEBI:23673
)
is conjugate acid of
2,6-diaminopimelate(2−) (
CHEBI:23671
)
Incoming
meso
-2,6-diaminopimelic acid (
CHEBI:16488
)
is a
2,6-diaminopimelic acid (
CHEBI:23673
)
D
D
-2,6-diaminopimelic acid (
CHEBI:144636
)
is a
2,6-diaminopimelic acid (
CHEBI:23673
)
L
L
-2,6-diaminopimelic acid (
CHEBI:16026
)
is a
2,6-diaminopimelic acid (
CHEBI:23673
)
2,6-diaminopimelate(2−) (
CHEBI:23671
)
is conjugate base of
2,6-diaminopimelic acid (
CHEBI:23673
)
IUPAC Name
2,6-diaminoheptanedioic acid
Synonyms
Sources
α,ε-diaminopimelic acid
ChEBI
Diaminopimelic acid
ChemIDplus
Dpm
ChEBI
Manual Xref
Database
DB03590
DrugBank
View more database links
Registry Numbers
Types
Sources
1787719
Reaxys Registry Number
Reaxys
583-93-7
CAS Registry Number
ChemIDplus
Citations
Types
Sources
10930630
PubMed citation
Europe PMC
13984704
PubMed citation
Europe PMC
23913026
PubMed citation
Europe PMC
Last Modified
18 April 2024