ampelopsin

chemical compound
ChemicalSubstance type_of_chemical_entity Q422305
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ampelopsin

Summary

ampelopsin is a type of chemical entity[1]. ampelopsin ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (78 views/month).[2]

Key Facts

  • ampelopsin's instance of is recorded as type of chemical entity[3].
  • ampelopsin's chemical structure is recorded as Ampelopsin.svg[4].
  • ampelopsin's CAS Registry Number is recorded as 27200-12-0[5].
  • ampelopsin's canonical SMILES is recorded as O=C1C=2C(O)=CC(O)=CC2OC(C3=CC(O)=C(O)C(O)=C3)C1O[6].
  • ampelopsin's InChI is recorded as InChI=1S/C15H12O8/c16-6-3-7(17)11-10(4-6)23-15(14(22)13(11)21)5-1-8(18)12(20)9(19)2-5/h1-4,14-20,22H/t14-,15+/m0/s1[7].
  • ampelopsin's InChIKey is recorded as KJXSIXMJHKAJOD-LSDHHAIUSA-N[8].
  • ampelopsin's chemical formula is recorded as C₁₅H₁₂O₈[9].
  • ampelopsin's subclass of is recorded as dihydromyricetin (unspecified stereochemistry)[10].
  • ampelopsin's part of is recorded as (+)-taxifolin 5'-hydroxylase activity[11].
  • ampelopsin's Commons category is recorded as Ampelopsin[12].
  • ampelopsin's Freebase ID is recorded as /m/07kc0z4[13].
  • ampelopsin's UNII is recorded as KD8QND6427[14].
  • ampelopsin's ChemSpider ID is recorded as 16735660[15].
  • ampelopsin's PubChem CID is recorded as 161557[16].
  • ampelopsin's KEGG ID is recorded as C02906[17].
  • ampelopsin's ChEBI ID is recorded as 28429[18].
  • ampelopsin's found in taxon is recorded as Pimenta dioica[19].
  • ampelopsin's found in taxon is recorded as Berberis duclouxiana[20].
  • ampelopsin's found in taxon is recorded as Brassica carinata[21].
  • ampelopsin's found in taxon is recorded as Intsia bijuga[22].
  • ampelopsin's found in taxon is recorded as Manilkara zapota[23].
  • ampelopsin's found in taxon is recorded as Rhododendron[24].
  • ampelopsin's found in taxon is recorded as Xanthoceras sorbifolia[25].
  • ampelopsin's found in taxon is recorded as Burkea africana[26].
  • ampelopsin's found in taxon is recorded as Catharanthus roseus[27].

Why It Matters

ampelopsin ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (78 views/month).[2] ampelopsin has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] ampelopsin is known by 3 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . PubChem. wikidata.org.
  6. [8] . PubChem. wikidata.org.
  7. [9] . PubChem. wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Freebase Data Dumps. wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . Phenolic glycosides from berries of Pimenta dioica. wikidata.org.
  18. [20] . Constituents of Mahonia siamensis. wikidata.org.
  19. [21] . Pigmentation in the developing seed coat and seedling leaves of Brassica carinata is controlled at the dihydroflavonol reductase locus. wikidata.org.
  20. [22] . Polyphenols of Intsia heartwoods. wikidata.org.
  21. [23] . Bioactive novel polyphenols from the fruit of Manilkara zapota (Sapodilla).. wikidata.org.
  22. [24] . Leaf survey of flavonoids and simple phenols in the genus Rhododendron. wikidata.org.
  23. [25] . Inhibitory effects on HIV-1 protease of constituents from the wood of Xanthoceras sorbifolia. wikidata.org.
  24. [26] . Oligomeric flavanoids. Part 2. The first profisetinidins with dihydroflavonol constituent units. wikidata.org.
  25. [27] . A flavonol O-methyltransferase from Catharanthus roseus performing two sequential methylations. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . Wikidata aliases. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). ampelopsin. Retrieved May 3, 2026, from https://4ort.xyz/entity/ampelopsin
MLA “ampelopsin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/ampelopsin.
BibTeX @misc{4ortxyz_ampelopsin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{ampelopsin}}, year = {2026}, url = {https://4ort.xyz/entity/ampelopsin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): ampelopsin — https://4ort.xyz/entity/ampelopsin (retrieved 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. 21d ago · KaleemBot bot · 2026-04-30 view diff on Wikidata ↗
    Described at url
    "/* wbeditentity-update-languages-and-other-short:0||ur */"
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