panaxynol

neurotoxic compound protecting carrot roots
ChemicalSubstance type_of_chemical_entity Q413192
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panaxynol

Summary

panaxynol is a type of chemical entity[1]. panaxynol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (48 views/month).[2]

Key Facts

  • panaxynol's instance of is recorded as type of chemical entity[3].
  • panaxynol's chemical structure is recorded as Falcarinol Structural Formula V1.svg[4].
  • panaxynol's chemical structure is recorded as Falcarinol.svg[5].
  • panaxynol's CAS Registry Number is recorded as 21852-80-2[6].
  • panaxynol's canonical SMILES is recorded as CCCCCCCC=CCC#CC#CC(C=C)O[7].
  • panaxynol's InChI is recorded as InChI=1S/C17H24O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17(18)4-2/h4,10-11,17-18H,2-3,5-9,12H2,1H3/b11-10-/t17-/m1/s1[8].
  • panaxynol's InChIKey is recorded as UGJAEDFOKNAMQD-QXPKXGMISA-N[9].
  • panaxynol's chemical formula is recorded as C₁₇H₂₄O[10].
  • panaxynol's subclass of is recorded as fatty alcohol[11].
  • panaxynol's subclass of is recorded as acetylenic compound[12].
  • panaxynol's Commons category is recorded as Falcarinol[13].
  • panaxynol's has part is recorded as carbon[14].
  • panaxynol's has part is recorded as oxygen[15].
  • panaxynol's has part is recorded as hydrogen[16].
  • panaxynol's ChEMBL ID is recorded as CHEMBL71260[17].
  • panaxynol's Freebase ID is recorded as /m/05x0b3[18].
  • panaxynol's UNII is recorded as 8P1DJD416I[19].
  • panaxynol's ChemSpider ID is recorded as 4444589[20].
  • panaxynol's PubChem CID is recorded as 5281149[21].
  • panaxynol's KEGG ID is recorded as C08450[22].
  • panaxynol's ChEBI ID is recorded as 66722[23].
  • panaxynol's found in taxon is recorded as Oplopanax horridus[24].
  • panaxynol's found in taxon is recorded as Angelica japonica[25].
  • panaxynol's found in taxon is recorded as Apium graveolens[26].
  • panaxynol's found in taxon is recorded as Bunium paucifolium[27].

Why It Matters

panaxynol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (48 views/month).[2] panaxynol has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] panaxynol 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] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: 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] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . ChEMBL. Retrieved . wikidata.org.
  16. [18] . Freebase Data Dumps. wikidata.org.
  17. [19] . Global Substance Registration System. Retrieved . wikidata.org.
  18. [20] . Q2311683. Retrieved . wikidata.org.
  19. [21] . PubChem. Retrieved . wikidata.org.
  20. [22] . ChEBI. Retrieved . wikidata.org.
  21. [23] . ChEMBL. Retrieved . wikidata.org.
  22. [24] . Antimycobacterial Polyynes of Devil's Club (Oplopanax horridus), a North American Native Medicinal Plant. wikidata.org.
  23. [25] . Novel antiproliferative falcarindiol furanocoumarin ethers from the root of Angelica japonica. wikidata.org.
  24. [26] . Simultaneous HPLC Quantification of Two Dermatotoxins, 5-Methoxypsoralen and Falcarinol, in Healthy Celery. wikidata.org.
  25. [27] . A sesquiterpene ketal from Bunium paucifolium. 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). panaxynol. Retrieved May 3, 2026, from https://4ort.xyz/entity/panaxynol
MLA “panaxynol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/panaxynol.
BibTeX @misc{4ortxyz_panaxynol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{panaxynol}}, year = {2026}, url = {https://4ort.xyz/entity/panaxynol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): panaxynol — https://4ort.xyz/entity/panaxynol (retrieved 2026-05-03)

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