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 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search 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