CHEBI:30031 - succinate(2−)

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ChEBI Name succinate(2−) ChEBI ID CHEBI:30031 ChEBI ASCII Name succinate(2-) Definition A dicarboxylic acid dianion resulting from the removal of a proton from both of the carboxy groups of succinic acid. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:15125, CHEBI:26803, CHEBI:22941 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 C4H4O4 Net Charge -2 Average Mass 116.07216 Monoisotopic Mass 116.01206 InChI InChI=1S/C4H6O4/c5-3(6)1-2-4(7)8/h1-2H2,(H,5,6)(H,7,8)/p-2 InChIKey KDYFGRWQOYBRFD-UHFFFAOYSA-L SMILES [O-]C(=O)CCC([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 succinate(2−) (CHEBI:30031) has role Saccharomyces cerevisiae metabolite (CHEBI:75772) succinate(2−) (CHEBI:30031) has role human metabolite (CHEBI:77746) succinate(2−) (CHEBI:30031) is a C4-dicarboxylate (CHEBI:61336) succinate(2−) (CHEBI:30031) is a dicarboxylic acid dianion (CHEBI:28965) succinate(2−) (CHEBI:30031) is a succinate (CHEBI:26806) succinate(2−) (CHEBI:30031) is conjugate base of succinate(1−) (CHEBI:30779) Incoming (2S)-2-isopropyl-3-oxosuccinate(2−) (CHEBI:17214) has functional parent succinate(2−) (CHEBI:30031) 2-benzylsuccinate(2−) (CHEBI:57621) has functional parent succinate(2−) (CHEBI:30031) 2-isopropylmalate(2−) (CHEBI:28107) has functional parent succinate(2−) (CHEBI:30031) 2-mercaptosuccinate (CHEBI:38712) has functional parent succinate(2−) (CHEBI:30031) 3-(acetamidomethylene)-2-(hydroxymethyl)succinate(2−) (CHEBI:19418) has functional parent succinate(2−) (CHEBI:30031) 3-isopropylmalate(2−) (CHEBI:15592) has functional parent succinate(2−) (CHEBI:30031) trans-2,3-epoxysuccinate(2−) (CHEBI:57558) has functional parent succinate(2−) (CHEBI:30031) bromosuccinate (CHEBI:73706) has functional parent succinate(2−) (CHEBI:30031) itaconate(2−) (CHEBI:17240) has functional parent succinate(2−) (CHEBI:30031) malate(2−) (CHEBI:15595) has functional parent succinate(2−) (CHEBI:30031) oxaloacetate(2−) (CHEBI:16452) has functional parent succinate(2−) (CHEBI:30031) thiomalate(3−) (CHEBI:38715) has functional parent succinate(2−) (CHEBI:30031) sodium succinate (anhydrous) (CHEBI:63675) has part succinate(2−) (CHEBI:30031) succinate(1−) (CHEBI:30779) is conjugate acid of succinate(2−) (CHEBI:30031) IUPAC Name butanedioate Synonyms Sources butanedioic acid, ion(2−) ChemIDplus −OOC‒CH2‒CH2‒COO− ChEBI succinate UniProt Manual Xrefs Databases c0312 UM-BBD SUC MetaCyc View more database links Registry Numbers Types Sources 1863859 Beilstein Registry Number Beilstein 1863859 Reaxys Registry Number Reaxys 240255 Gmelin Registry Number Gmelin 56-14-4 CAS Registry Number ChemIDplus Citation Type Source 17190852 PubMed citation Europe PMC Last Modified 14 September 2021