scoparone

chemical compound
ChemicalSubstance type_of_chemical_entity Q15424761
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scoparone

Summary

scoparone is a type of chemical entity[1]. scoparone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 views/month).[2]

Key Facts

  • scoparone's instance of is recorded as type of chemical entity[3].
  • scoparone's chemical structure is recorded as Scoparone.svg[4].
  • scoparone's CAS Registry Number is recorded as 120-08-1[5].
  • scoparone's EC number is recorded as 204-369-0[6].
  • scoparone's canonical SMILES is recorded as COC1=C(C=C2C(=C1)C=CC(=O)O2)OC[7].
  • scoparone's InChI is recorded as InChI=1S/C11H10O4/c1-13-9-5-7-3-4-11(12)15-8(7)6-10(9)14-2/h3-6H,1-2H3[8].
  • scoparone's InChIKey is recorded as GUAFOGOEJLSQBT-UHFFFAOYSA-N[9].
  • scoparone's chemical formula is recorded as C₁₁H₁₀O₄[10].
  • scoparone's subclass of is recorded as biogenic coumarin[11].
  • scoparone's MeSH descriptor ID is recorded as C018145[12].
  • scoparone's ChEMBL ID is recorded as CHEMBL325864[13].
  • scoparone's Freebase ID is recorded as /m/0vzr91j[14].
  • scoparone's UNII is recorded as H5841PDT4Y[15].
  • scoparone's ChemSpider ID is recorded as 8110[16].
  • scoparone's PubChem CID is recorded as 8417[17].
  • scoparone's KEGG ID is recorded as C09311[18].
  • scoparone's ChEBI ID is recorded as 9055[19].
  • scoparone's found in taxon is recorded as Calea ternifolia[20].
  • scoparone's found in taxon is recorded as Artemisia capillaris[21].
  • scoparone's found in taxon is recorded as Pimpinella anisum[22].
  • scoparone's found in taxon is recorded as Apium graveolens[23].
  • scoparone's found in taxon is recorded as Artemisia nova[24].
  • scoparone's found in taxon is recorded as Q161421[25].
  • scoparone's found in taxon is recorded as Artemisia tridentata[26].
  • scoparone's found in taxon is recorded as Achillea biserrata[27].

Why It Matters

scoparone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 views/month).[2] scoparone has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[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] . Medical Subject Headings. Retrieved . wikidata.org.
  11. [13] . ChEMBL. Retrieved . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] . Q2311683. Retrieved . wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . ChEBI. Retrieved . wikidata.org.
  17. [19] . ChEMBL. Retrieved . wikidata.org.
  18. [20] . Anti-Hyperglycemic Activity of Major Compounds from Calea ternifolia.. wikidata.org.
  19. [21] . Determination of Phenolic Compounds inArtemisia capillaris. wikidata.org.
  20. [22] . Identification of eight coumarins occurring with psoralen, xanthotoxin, and bergapten on leaf surfaces. wikidata.org.
  21. [23] . Identification of eight coumarins occurring with psoralen, xanthotoxin, and bergapten on leaf surfaces. wikidata.org.
  22. [24] . High-performance liquid chromatographic analysis of coumarins and flavonoids from section tridentatae of Artemisia. wikidata.org.
  23. [25] . Reverse-phase high pressure liquid chromatographic analysis of hydroxycoumarins in plant extracts. Quantitative determination of hydroxycoumarins inFraxinus ornus. wikidata.org.
  24. [26] . Seasonal variation of coumarin and flavonoid concentrations in persistent leaves of wyoming big sagebrush (Artemisia tridentata ssp. wyomingensis: Asteraceae). wikidata.org.
  25. [27] . Components ofPtarmica bisserata. 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.

📑 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). scoparone. Retrieved May 3, 2026, from https://4ort.xyz/entity/scoparone
MLA “scoparone.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/scoparone.
BibTeX @misc{4ortxyz_scoparone_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{scoparone}}, year = {2026}, url = {https://4ort.xyz/entity/scoparone}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): scoparone — https://4ort.xyz/entity/scoparone (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/scoparone · Last refreshed:

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. 14d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Instance of type of chemical entity
    Found in taxon Calea ternifolia, Artemisia capillaris, Pimpinella anisum +161
    Subclass of biogenic coumarin
    Subject has role antiarrhythmic agent, antihypertensive drug, vasodilator agent +1
    + 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.