CHEBI:57441 - 2,3-diketogulonate

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ChEBI Name 2,3-diketogulonate ChEBI ID CHEBI:57441 Definition A dioxo monocarboxylic acid anion that is the conjugate base of 2,3-diketogulonic acid, and the major species at pH 7.3. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information No supplier information found for this compound. Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C6H7O7 Net Charge -1 Average Mass 191.11560 Monoisotopic Mass 191.01918 InChI InChI=1S/C6H8O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h2-3,7-9H,1H2,(H,12,13)/p-1/t2-,3+/m0/s1 InChIKey GJQWCDSAOUMKSE-STHAYSLISA-M SMILES OC[C@H](O)[C@@H](O)C(=O)C(=O)C([O-])=O Metabolite of Species Details Homo sapiens (NCBI:txid9606) See: DOI Roles Classification Biological Role(s): human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing 2,3-diketogulonate (CHEBI:57441) has role human metabolite (CHEBI:77746) 2,3-diketogulonate (CHEBI:57441) is a carbohydrate acid anion (CHEBI:33721) 2,3-diketogulonate (CHEBI:57441) is a dioxo monocarboxylic acid anion (CHEBI:35979) 2,3-diketogulonate (CHEBI:57441) is a hydroxy monocarboxylic acid anion (CHEBI:36059) 2,3-diketogulonate (CHEBI:57441) is conjugate base of 2,3-diketogulonic acid (CHEBI:15622) Incoming 2,3-diketogulonic acid (CHEBI:15622) is conjugate acid of 2,3-diketogulonate (CHEBI:57441) IUPAC Names (4R,5S)-4,5,6-trihydroxy-2,3-dioxohexanoate L-threo-hexo-2,3-diulosonate Synonyms Sources 2,3-diketo-L-gulonate ChEBI 2,3-dioxo-L-gulonate UniProt 2,3-dioxo-L-gulonate(1−) ChEBI 2,3-dioxo-L-gulonic ChEBI Registry Number Type Source 3907464 Beilstein Registry Number Beilstein Citations Types Sources 16698813 PubMed citation Europe PMC 17222174 PubMed citation Europe PMC 9506998 PubMed citation Europe PMC Last Modified 18 October 2017

General Comment 2010-12-14 A vitamin C metabolite. The oxalate formed by spontaneous cleavage between C-2 and C-3 may play a role in kidney stone development.