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
Supplier Information
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Formula C4H2O5
Net Charge -2
Average Mass 130.05568
Monoisotopic Mass 129.990
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:4932) Source: yeast.sf.net See: PubMed
Homo sapiens (NCBI:9606) 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
Database Links 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 Beilstein Registry Number Beilstein
3605372 Reaxys Registry Number Reaxys
Citations Waiting for 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