(+)-taxifolin

chemical compound
ChemicalSubstance type_of_chemical_entity Q412191
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(+)-taxifolin

Summary

(+)-taxifolin is a type of chemical entity[1]. (+)-taxifolin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (26 views/month).[2]

Key Facts

  • (+)-taxifolin's instance of is recorded as type of chemical entity[3].
  • (+)-taxifolin's chemical structure is recorded as (+)-Taxifolin.svg[4].
  • (+)-taxifolin's chemical structure is recorded as Taxifolin structure.svg[5].
  • (+)-taxifolin's CAS Registry Number is recorded as 480-18-2[6].
  • (+)-taxifolin's EC number is recorded as 207-543-4[7].
  • (+)-taxifolin's canonical SMILES is recorded as O=C1C=2C(O)=CC(O)=CC2OC(C3=CC=C(O)C(O)=C3)C1O[8].
  • (+)-taxifolin's InChI is recorded as InChI=1S/C15H12O7/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,14-19,21H/t14-,15+/m0/s1[9].
  • (+)-taxifolin's InChIKey is recorded as CXQWRCVTCMQVQX-LSDHHAIUSA-N[10].
  • (+)-taxifolin's chemical formula is recorded as C₁₅H₁₂O₇[11].
  • (+)-taxifolin's subclass of is recorded as 2,3-dihydroquercetin[12].
  • (+)-taxifolin's subclass of is recorded as (2r)-2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydro-4h-chromen-4-one[13].
  • (+)-taxifolin's part of is recorded as (+)-taxifolin 5'-hydroxylase activity[14].
  • (+)-taxifolin's Commons category is recorded as Taxifolin[15].
  • (+)-taxifolin's MeSH descriptor ID is recorded as C003377[16].
  • (+)-taxifolin's has part is recorded as carbon[17].
  • (+)-taxifolin's ChEMBL ID is recorded as CHEMBL66[18].
  • (+)-taxifolin's Freebase ID is recorded as /m/07k4f_8[19].
  • (+)-taxifolin's UNII is recorded as 9SOB9E3987[20].
  • (+)-taxifolin's UNII is recorded as EAS93SC1VS[21].
  • (+)-taxifolin's ChemSpider ID is recorded as 458[22].
  • (+)-taxifolin's PubChem CID is recorded as 439533[23].
  • (+)-taxifolin's KEGG ID is recorded as C01617[24].
  • (+)-taxifolin's ChEBI ID is recorded as 17948[25].
  • (+)-taxifolin's found in taxon is recorded as Picea abies[26].
  • (+)-taxifolin's found in taxon is recorded as Larix gmelinii[27].

Why It Matters

(+)-taxifolin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (26 views/month).[2] (+)-taxifolin has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[28] (+)-taxifolin 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] . wikidata.org.
  4. [6] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . PubChem. wikidata.org.
  8. [10] . PubChem. wikidata.org.
  9. [11] . PubChem. wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . Medical Subject Headings. Retrieved . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . Freebase Data Dumps. wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . Characterisation of Phenolic Constituents from Juvenile and Mature Needles of Norway Spruce by Means of High Performance Liquid Chromatography-Mass Spectrometry. wikidata.org.
  25. [27] . Antioxidant Activity of a Dihydroquercetin Isolated fromLarix gmelinii (Rupr.) Rupr. Wood. 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). (+)-taxifolin. Retrieved May 3, 2026, from https://4ort.xyz/entity/taxifolin
MLA “(+)-taxifolin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/taxifolin.
BibTeX @misc{4ortxyz_taxifolin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(+)-taxifolin}}, year = {2026}, url = {https://4ort.xyz/entity/taxifolin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (+)-taxifolin — https://4ort.xyz/entity/taxifolin (retrieved 2026-05-03)

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