engeletin (unspec. stereochem.)

group of stereoisomers with the chemical formula C₂₁H₂₂O₁₀
ChemicalSubstance group_of_stereoisomers Q105291517
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engeletin (unspec. stereochem.)

Summary

engeletin (unspec. stereochem.) is a group of stereoisomers[1].

Key Facts

  • engeletin (unspec. stereochem.)'s instance of is recorded as group of stereoisomers[2].
  • engeletin (unspec. stereochem.)'s canonical SMILES is recorded as O=C1C=2C(O)=CC(O)=CC2OC(C3=CC=C(O)C=C3)C1OC4OC(C)C(O)C(O)C4O[3].
  • engeletin (unspec. stereochem.)'s InChI is recorded as InChI=1S/C21H22O10/c1-8-15(25)17(27)18(28)21(29-8)31-20-16(26)14-12(24)6-11(23)7-13(14)30-19(20)9-2-4-10(22)5-3-9/h2-8,15,17-25,27-28H,1H3[4].
  • engeletin (unspec. stereochem.)'s InChIKey is recorded as VQUPQWGKORWZII-UHFFFAOYSA-N[5].
  • engeletin (unspec. stereochem.)'s chemical formula is recorded as C₂₁H₂₂O₁₀[6].
  • engeletin (unspec. stereochem.)'s subclass of is recorded as flavanone[7].
  • engeletin (unspec. stereochem.)'s PubChem CID is recorded as 12309470[8].
  • engeletin (unspec. stereochem.)'s found in taxon is recorded as Smilax glabra[9].
  • engeletin (unspec. stereochem.)'s found in taxon is recorded as Smilax china[10].
  • engeletin (unspec. stereochem.)'s found in taxon is recorded as Peltophorum dasyrachis[11].
  • engeletin (unspec. stereochem.)'s found in taxon is recorded as Engelhardia roxburghiana[12].
  • engeletin (unspec. stereochem.)'s found in taxon is recorded as Eucalyptus maidenii[13].
  • engeletin (unspec. stereochem.)'s Human Metabolome Database ID is recorded as HMDB0303603[14].
  • engeletin (unspec. stereochem.)'s mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+434.121296904'}[15].
  • engeletin (unspec. stereochem.)'s SureChEMBL ID is recorded as 13360568[16].
  • engeletin (unspec. stereochem.)'s UniChem compound ID is recorded as 29161620[17].
  • engeletin (unspec. stereochem.)'s Probes And Drugs ID is recorded as PD056219[18].

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] . Maltol glucosides from the tuber of Smilax bockii. wikidata.org.
  9. [10] . Maltol glucosides from the tuber of Smilax bockii. wikidata.org.
  10. [11] . Tyrosinase inhibitory constituents from the bark of Peltophorum dasyrachis (yellow batai). wikidata.org.
  11. [12] . Studies on the Constituents of the Bark of Engelhardtia formosana Hay. IV. wikidata.org.
  12. [13] . Phenolic compounds from the branches of Eucalyptus maideni. wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . UniChem. wikidata.org.
  17. [18] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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BibTeX @misc{4ortxyz_engeletin-unspec-stereochem-_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{engeletin (unspec. stereochem.)}}, year = {2026}, url = {https://4ort.xyz/entity/engeletin-unspec-stereochem-}, note = {Accessed: 2026-05-03}}
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