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[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate

group of stereoisomers with the chemical formula C₁₃H₁₆O₁₀
ChemicalSubstance group_of_stereoisomers Q104393260
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[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate

Summary

[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate is a group of stereoisomers[1].

Key Facts

  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's instance of is recorded as group of stereoisomers[2].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's canonical SMILES is recorded as O=C(OC1OC(CO)C(O)C(O)C1O)C2=CC(O)=C(O)C(O)=C2[3].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's InChI is recorded as InChI=1S/C13H16O10/c14-3-7-9(18)10(19)11(20)13(22-7)23-12(21)4-1-5(15)8(17)6(16)2-4/h1-2,7,9-11,13-20H,3H2[4].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's InChIKey is recorded as GDVRUDXLQBVIKP-UHFFFAOYSA-N[5].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's chemical formula is recorded as C₁₃H₁₆O₁₀[6].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's subclass of is recorded as chemical compound[7].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's PubChem CID is recorded as 4628122[8].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's ChEBI ID is recorded as 190910[9].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's found in taxon is recorded as Prunus domestica[10].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's found in taxon is recorded as Lotus japonicus[11].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's found in taxon is recorded as Phyllanthus emblica[12].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's found in taxon is recorded as Arbutus unedo[13].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's found in taxon is recorded as Eucalyptus viminalis[14].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's found in taxon is recorded as Mallotus japonicus[15].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's found in taxon is recorded as Mallotus repandus[16].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's found in taxon is recorded as Falconeria insignis[17].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's found in taxon is recorded as Rhynchosia volubilis[18].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's found in taxon is recorded as Pelargonium reniforme[19].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's found in taxon is recorded as Quercus salicina[20].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's Human Metabolome Database ID is recorded as HMDB0038728[21].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+332.074346712'}[22].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's SureChEMBL ID is recorded as 22504483[23].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's SureChEMBL ID is recorded as 1315483[24].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's MassBank accession ID is recorded as MSBNK-RIKEN-PR309053[25].
  • [3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate's UniChem compound ID is recorded as 24776376[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . ChEBI release 2022-06-13. wikidata.org.
  9. [10] ↑ . LC/MS/MS characterization of phenolic constituents in dried plums. wikidata.org.
  10. [11] ↑ . Gallic acid esters of bergenin and norbergenin from Mallotus japonicus. wikidata.org.
  11. [12] ↑ . Novel norsesquiterpenoids from the roots of Phyllanthus emblica. wikidata.org.
  12. [13] ↑ . Phenolics of Arbutus unedo L. (Ericaceae) fruits: identification of anthocyanins and gallic acid derivatives.. wikidata.org.
  13. [14] ↑ . Polyphenols from Eucalyptus consideniana and Eucalyptus viminalis. wikidata.org.
  14. [15] ↑ . Gallic acid esters of bergenin and norbergenin from Mallotus japonicus. wikidata.org.
  15. [16] ↑ . Tannins and related compounds. LXXXVII. Isolation and characterization of four new hydrolyzable tannins from the leaves of Mallotus repandus.. wikidata.org.
  16. [17] ↑ . Diterpene esters and phenolic compounds from Sapium insigne (ROYLE) BENTH. ex HOOK. fil.. wikidata.org.
  17. [18] ↑ . Antiproliferative constituents in the plant 8. Seeds of Rhynchosia volubilis.. wikidata.org.
  18. [19] ↑ . Pelargoniins, new ellagitannins from Pelargonium reniforme. wikidata.org.
  19. [20] ↑ . Studies on the Constituents of Quercus spp. : I. On the Constituents of Quercus stenophylla MAKINO. (1). wikidata.org.
  20. [21] ↑ . wikidata.org.
  21. [22] ↑ . wikidata.org.
  22. [23] ↑ . wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  25. [26] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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