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> Main
CHEBI:46837 - dipicolinic acid
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ChEBI Name
dipicolinic acid
ChEBI ID
CHEBI:46837
Definition
A pyridinedicarboxylic acid carrying two carboxy groups at positions 2 and 6.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:36171, CHEBI:44858
Supplier Information
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Formula
C7H5NO4
Net Charge
0
Average Mass
167.11890
Monoisotopic Mass
167.02186
InChI
InChI=1S/C7H5NO4/c9-6(10)4-2-1-3-5(8-4)7(11)12/h1-3H,(H,9,10)(H,11,12)
InChIKey
WJJMNDUMQPNECX-UHFFFAOYSA-N
SMILES
OC(=O)c1cccc(n1)C(O)=O
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):
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
dipicolinic acid (
CHEBI:46837
)
has role
bacterial metabolite (
CHEBI:76969
)
dipicolinic acid (
CHEBI:46837
)
is a
pyridinedicarboxylic acid (
CHEBI:36112
)
dipicolinic acid (
CHEBI:46837
)
is conjugate acid of
dipicolinate(1−) (
CHEBI:46835
)
Incoming
(2
S
,4
S
)-4-hydroxy-2,3,4,5-tetrahydrodipicolinic acid (
CHEBI:67205
)
has functional parent
dipicolinic acid (
CHEBI:46837
)
2,3,4,5-tetrahydrodipicolinic acid (
CHEBI:32976
)
has functional parent
dipicolinic acid (
CHEBI:46837
)
3-(2-deoxy-5-
O
-phosphonoribofuranosyl)pyridine-2,6-dicarboxylic acid (
CHEBI:42018
)
has functional parent
dipicolinic acid (
CHEBI:46837
)
dihydrodipicolinic acid (
CHEBI:23741
)
has functional parent
dipicolinic acid (
CHEBI:46837
)
dipicolinate(1−) (
CHEBI:46835
)
is conjugate base of
dipicolinic acid (
CHEBI:46837
)
IUPAC Name
pyridine-2,6-dicarboxylic acid
Synonyms
Sources
2,6-dicarboxypyridine
NIST Chemistry WebBook
2,6-Dipicolinic acid
ChemIDplus
2,6-pyridinedicarboxylic acid
NIST Chemistry WebBook
Dipicolinic acid
ChemIDplus
PYRIDINE-2,6-DICARBOXYLIC ACID
PDBeChem
Manual Xrefs
Databases
DB04267
DrugBank
Dipicolinic_acid
Wikipedia
HMDB0033161
HMDB
PDC
PDBeChem
US5298478
Patent
View more database links
Registry Numbers
Types
Sources
131629
Beilstein Registry Number
Beilstein
131629
Reaxys Registry Number
Reaxys
499-83-2
CAS Registry Number
NIST Chemistry WebBook
499-83-2
CAS Registry Number
ChemIDplus
50798
Gmelin Registry Number
Gmelin
Citations
Types
Sources
23396907
PubMed citation
Europe PMC
24123749
PubMed citation
Europe PMC
Last Modified
04 March 2014