chrysophanol

chemical compound
ChemicalSubstance type_of_chemical_entity Q3604508
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chrysophanol

Summary

chrysophanol is a type of chemical entity[1]. chrysophanol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2]

Key Facts

  • chrysophanol's instance of is recorded as type of chemical entity[3].
  • chrysophanol's chemical structure is recorded as Chrysophanol Structure.svg[4].
  • chrysophanol's CAS Registry Number is recorded as 481-74-3[5].
  • chrysophanol's EC number is recorded as 207-572-2[6].
  • chrysophanol's canonical SMILES is recorded as CC1=CC(=C2C(=C1)C(=O)C3=C(C2=O)C(=CC=C3)O)O[7].
  • chrysophanol's InChI is recorded as InChI=1S/C15H10O4/c1-7-5-9-13(11(17)6-7)15(19)12-8(14(9)18)3-2-4-10(12)16/h2-6,16-17H,1H3[8].
  • chrysophanol's InChIKey is recorded as LQGUBLBATBMXHT-UHFFFAOYSA-N[9].
  • chrysophanol's chemical formula is recorded as C₁₅H₁₀O₄[10].
  • chrysophanol's subclass of is recorded as anthraquinones[11].
  • chrysophanol's subclass of is recorded as aromatic polyketide[12].
  • chrysophanol's Commons category is recorded as Chrysophanol[13].
  • chrysophanol's MeSH descriptor ID is recorded as C027113[14].
  • chrysophanol's ChEMBL ID is recorded as CHEMBL41092[15].
  • chrysophanol's Freebase ID is recorded as /m/0wxzb86[16].
  • chrysophanol's UNII is recorded as N1ST8V8RR2[17].
  • chrysophanol's ChemSpider ID is recorded as 9793[18].
  • chrysophanol's PubChem CID is recorded as 10208[19].
  • chrysophanol's KEGG ID is recorded as C10315[20].
  • chrysophanol's ChEBI ID is recorded as 3687[21].
  • chrysophanol's found in taxon is recorded as Rhamnus prinoides[22].
  • chrysophanol's found in taxon is recorded as Vismia latifolia[23].
  • chrysophanol's found in taxon is recorded as Rumex alpinus[24].
  • chrysophanol's found in taxon is recorded as Rheum undulatum[25].
  • chrysophanol's found in taxon is recorded as Rheum franzenbachii[26].
  • chrysophanol's found in taxon is recorded as Rheum hotaoense[27].

Why It Matters

chrysophanol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2] chrysophanol is known by 8 alternative names across languages and contexts.[28]

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] . Global Substance Registration System. 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] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Medical Subject Headings. Retrieved . wikidata.org.
  13. [15] . ChEMBL. Retrieved . wikidata.org.
  14. [16] . 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] . ChEBI. Retrieved . wikidata.org.
  19. [21] . ChEMBL. Retrieved . wikidata.org.
  20. [22] . Electrospray liquid chromatography-mass spectrometry of the leaf extract of Rhamnus prinoides. wikidata.org.
  21. [23] . Total assignment of 1H and 13C NMR spectra of a prenylated oxanthrone fromVismia latifolia. wikidata.org.
  22. [24] . 13C NMR spectral analysis of anthraquinone derivatives from Rumex alpinus. wikidata.org.
  23. [25] . Ethnopharmacologic study of Chinese rhubarb. wikidata.org.
  24. [26] . Ethnopharmacologic study of Chinese rhubarb. wikidata.org.
  25. [27] . Ethnopharmacologic study of Chinese rhubarb. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . 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). chrysophanol. Retrieved May 3, 2026, from https://4ort.xyz/entity/chrysophanol
MLA “chrysophanol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/chrysophanol.
BibTeX @misc{4ortxyz_chrysophanol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{chrysophanol}}, year = {2026}, url = {https://4ort.xyz/entity/chrysophanol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): chrysophanol — https://4ort.xyz/entity/chrysophanol (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. 16d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Instance of type of chemical entity
    Found in taxon Rhamnus prinoides, Vismia latifolia, Rumex alpinus +251
    Mass {'unit': 'Q483261', 'amount': '+254.058'}
    Subclass of
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.