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> Main
CHEBI:16452 - oxaloacetate(2−)
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ChEBI Name
oxaloacetate(2−)
ChEBI ID
CHEBI:16452
ChEBI ASCII Name
oxaloacetate(2-)
Definition
A C4-dicarboxylate resuting from deprotonation of both carboxy groups of oxaloacetic acid.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:14703, CHEBI:29049, CHEBI:12820, CHEBI:24958, CHEBI:25731
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Formula
C4H2O5
Net Charge
-2
Average Mass
130.05568
Monoisotopic Mass
129.99132
InChI
InChI=1S/C4H4O5/c5-2(4(8)9)1-3(6)7/h1H2,(H,6,7)(H,8,9)/p-2
InChIKey
KHPXUQMNIQBQEV-UHFFFAOYSA-L
SMILES
[O-]C(=O)CC(=O)C([O-])=O
Metabolite of Species
Details
Saccharomyces cerevisiae
(NCBI:txid4932)
Source: yeast.sf.net See:
PubMed
Homo sapiens
(NCBI:txid9606)
See:
DOI
Roles Classification
Biological Role
(s):
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
oxaloacetate(2−) (
CHEBI:16452
)
has functional parent
succinate(2−) (
CHEBI:30031
)
oxaloacetate(2−) (
CHEBI:16452
)
has role
Saccharomyces cerevisiae
metabolite (
CHEBI:75772
)
oxaloacetate(2−) (
CHEBI:16452
)
has role
human metabolite (
CHEBI:77746
)
oxaloacetate(2−) (
CHEBI:16452
)
is a
C4-dicarboxylate (
CHEBI:61336
)
oxaloacetate(2−) (
CHEBI:16452
)
is a
oxo dicarboxylic acid dianion (
CHEBI:133294
)
oxaloacetate(2−) (
CHEBI:16452
)
is conjugate base of
oxaloacetic acid (
CHEBI:30744
)
Incoming
oxaloacetic acid (
CHEBI:30744
)
is conjugate acid of
oxaloacetate(2−) (
CHEBI:16452
)
IUPAC Name
2-oxobutanedioate
Synonyms
Sources
oxalacetate
ChEBI
oxaloacetate
UniProt
oxaloacetate
ChEBI
oxaloacetate dianion
ChEBI
oxobutanedioate
ChemIDplus
oxobutanedioic acid, ion(2−)
ChemIDplus
oxosuccinate
ChEBI
Manual Xrefs
Databases
C00036
KEGG COMPOUND
OXALACETIC_ACID
MetaCyc
View more database links
Registry Numbers
Types
Sources
1242579
Gmelin Registry Number
Gmelin
149-63-3
CAS Registry Number
ChemIDplus
3605372
Reaxys Registry Number
Reaxys
Citations
Types
Sources
19793063
PubMed citation
Europe PMC
21098488
PubMed citation
Europe PMC
21175886
PubMed citation
Europe PMC
21178163
PubMed citation
Europe PMC
21185899
PubMed citation
Europe PMC
21434608
PubMed citation
Europe PMC
21495723
PubMed citation
Europe PMC
21745184
PubMed citation
Europe PMC
Last Modified
21 January 2016