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quercitrin

chemical compound
ChemicalSubstance type_of_chemical_entity Q1649777
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quercitrin

Summary

quercitrin is a type of chemical entity[1]. quercitrin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (23 views/month).[2]

Key Facts

  • quercitrin's instance of is recorded as type of chemical entity[3].
  • quercitrin's chemical structure is recorded as Quercitrin.png[4].
  • quercitrin's CAS Registry Number is recorded as 522-12-3[5].
  • quercitrin's EC number is recorded as 208-322-5[6].
  • quercitrin's canonical SMILES is recorded as CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O[7].
  • quercitrin's InChI is recorded as InChI=1S/C21H20O11/c1-7-15(26)17(28)18(29)21(30-7)32-20-16(27)14-12(25)5-9(22)6-13(14)31-19(20)8-2-3-10(23)11(24)4-8/h2-7,15,17-18,21-26,28-29H,1H3/t7-,15-,17+,18+,21-/m0/s1[8].
  • quercitrin's InChIKey is recorded as OXGUCUVFOIWWQJ-HQBVPOQASA-N[9].
  • quercitrin's chemical formula is recorded as C₂₁H₂₀O₁₁[10].
  • quercitrin's subclass of is recorded as flavone[11].
  • quercitrin's part of is recorded as quercitrin binding[12].
  • quercitrin's ChEMBL ID is recorded as CHEMBL82242[13].
  • quercitrin's PDB structure ID is recorded as 4GUE[14].
  • quercitrin's PDB structure ID is recorded as 5A4W[15].
  • quercitrin's Freebase ID is recorded as /m/03nm1p4[16].
  • quercitrin's UNII is recorded as 2Y8906LC5P[17].
  • quercitrin's ChemSpider ID is recorded as 4444112[18].
  • quercitrin's PubChem CID is recorded as 5280459[19].
  • quercitrin's KEGG ID is recorded as C01750[20].
  • quercitrin's ChEBI ID is recorded as 17558[21].
  • quercitrin's found in taxon is recorded as Vauquelinia corymbosa[22].
  • quercitrin's found in taxon is recorded as Euxylophora paraensis[23].
  • quercitrin's found in taxon is recorded as Humulus lupulus[24].
  • quercitrin's found in taxon is recorded as Hypericum perforatum[25].
  • quercitrin's found in taxon is recorded as Aguacate[26].
  • quercitrin's found in taxon is recorded as Sanicula graveolens[27].

Why It Matters

quercitrin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (23 views/month).[2] quercitrin has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] quercitrin is known by 13 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] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . Gene Ontology release 2019-11-16. wikidata.org.
  11. [13] ↑ . ChEMBL. Retrieved . wikidata.org.
  12. [14] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  13. [15] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  14. [16] ↑ . Freebase Data Dumps. wikidata.org.
  15. [17] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] ↑ . Q2311683. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . ChEBI. Retrieved . wikidata.org.
  20. [22] ↑ . α-Glucosidase Inhibitors from Vauquelinia corymbosa. wikidata.org.
  21. [23] ↑ . Fitoquímica e quimiossistemática de Euxylophora paraensis (Rutaceae). wikidata.org.
  22. [24] ↑ . Quantitative analysis of hop acids, essential oils and flavonoids as a clue to the identification of hop varieties. wikidata.org.
  23. [25] ↑ . High performance liquid chromatography/electrospray mass spectrometry of Hypericum perforatum extracts. wikidata.org.
  24. [26] ↑ . Flavonol monoglycosides isolated from the antiviral fractions ofPersea americana (Lauraceae) leaf infusion. wikidata.org.
  25. [27] ↑ . Free radical scavengers from Mutisia friesiana (Asteraceae) and Sanicula graveolens (Apiaceae).. 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). quercitrin. Retrieved May 3, 2026, from https://4ort.xyz/entity/quercitrin
MLA “quercitrin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/quercitrin.
BibTeX @misc{4ortxyz_quercitrin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{quercitrin}}, year = {2026}, url = {https://4ort.xyz/entity/quercitrin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): quercitrin — https://4ort.xyz/entity/quercitrin (retrieved 2026-05-03)

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