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D-glucopyranuronic acid

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q78172907
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Key Facts

  • Canonical SMILES: C1(C(C(OC(C1O)O)C(=O)O)O)O[1]
  • Chemical formula: C₆H₁₀O₇[2]
  • Subclass of: uronic acid[3]
  • Found in taxon: Ramalina fraxinea[4], Acanthospermum hispidum[5], Astragalus brachycarpus[6], Codonopsis pilosula[7], Medicago lupulina[8], Phycomyces blakesleeanus[9], Suaeda aegyptiaca[10], Symplocos tinctoria[11], Chlamydomonas reinhardtii[12], Streptomyces[13], Siraitia grosvenorii[14], Vachellia tortuosa[15], Caenorhabditis elegans[16]
  • Isomeric SMILES: [C@@H]1(C@@HO)OC@@HO)O">[17]
  • Mass: 194.04265266 dalton[18]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [1] ↑ . wikidata.org.
  2. [2] ↑ . wikidata.org.
  3. [3] ↑ . wikidata.org.
  4. [4] ↑ . Chemical composition of the Ramalina fraxinea (L.) Ach. thallus. wikidata.org.
  5. [5] ↑ . Plant-derived sweetening agents: saccharide and polyol constituents of some sweet-tasting plants. wikidata.org.
  6. [6] ↑ . Phenolic compounds ofAstragalus brachycarpus. I. wikidata.org.
  7. [7] ↑ . Development and application of a capillary electrophoretic method for the composition analysis of a typical heteropolysaccharide from Codonopsis pilosula NANNF.. wikidata.org.
  8. [8] ↑ . Studies on Medicago lupulina saponins. 2. Isolation, chemical characterization and biological activity of saponins from M. lupulina tops. wikidata.org.
  9. [9] ↑ . Acidic metabolites from Phycomyces blakesleeanus. wikidata.org.
  10. [10] ↑ . Chemical Constituents of Salvia aegyptiaca. wikidata.org.
  11. [11] ↑ . Plant-derived sweetening agents: saccharide and polyol constituents of some sweet-tasting plants. wikidata.org.
  12. [12] ↑ . The response of Chlamydomonas reinhardtii to nitrogen deprivation: a systems biology analysis. wikidata.org.
  13. [13] ↑ . Isolation, Characterization and Bioactivities of an Extracellular Polysaccharide Produced from Streptomyces sp. MOE6.. wikidata.org.
  14. [14] ↑ . Plant-derived sweetening agents: saccharide and polyol constituents of some sweet-tasting plants. wikidata.org.
  15. [15] ↑ . The polysaccharide gum from Accia tortuosa. wikidata.org.
  16. [16] ↑ . Metabotyping of the C. elegans sir-2.1 Mutant Using in Vivo Labeling and 13C-Heteronuclear Multidimensional NMR Metabolomics. wikidata.org.
  17. [17] ↑ . wikidata.org.
  18. [18] ↑ . wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). D-glucopyranuronic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/d-glucopyranuronic-acid
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BibTeX @misc{4ortxyz_d-glucopyranuronic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{D-glucopyranuronic acid}}, year = {2026}, url = {https://4ort.xyz/entity/d-glucopyranuronic-acid}, note = {Accessed: 2026-05-03}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 15w ago · Michael D. Turnbull · 2026-06-29 view diff on Wikidata ↗
    Pubchem cid → 94715
    Isomeric smiles → [C@@H]1([C@@H]([C@H](OC([C@@H]1O)O)C(=O)O)O)O
    Inchikey → AEMOLEFTQBMNLQ-AQKNRBDQSA-N
    Massbank accession id → MSBNK-Keio_Univ-KO000814, MSBNK-Keio_Univ-KO000815, MSBNK-Keio_Univ-KO000816 +6
    + 21 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-create:2||1 */ Chemical structure: D-glucopyranuronic acid.svg"
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