(3R,8S)-Falcarindiol

chemical compound
ChemicalSubstance type_of_chemical_entity Q5431681
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(3R,8S)-Falcarindiol

Summary

(3R,8S)-Falcarindiol is a type of chemical entity[1]. (3R,8S)-Falcarindiol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (13 views/month).[2]

Key Facts

  • (3R,8S)-Falcarindiol's instance of is recorded as type of chemical entity[3].
  • (3R,8S)-Falcarindiol's physically interacts with is recorded as taste receptor type 2[4].
  • (3R,8S)-Falcarindiol's canonical SMILES is recorded as CCCCCCCC=CC(C#CC#CC(C=C)O)O[5].
  • (3R,8S)-Falcarindiol's chemical formula is recorded as C₁₇H₂₄O₂[6].
  • (3R,8S)-Falcarindiol is a type of fatty alcohol[7].
  • (3R,8S)-Falcarindiol's Commons category is recorded as Falcarindiol[8].
  • (3R,8S)-Falcarindiol comprises carbon[9].
  • (3R,8S)-Falcarindiol comprises oxygen[10].
  • (3R,8S)-Falcarindiol comprises hydrogen[11].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Angelica dahurica[12].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Angelica sinensis[13].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Ligusticum porteri[14].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Angelica pubescens[15].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Oplopanax horridus[16].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Glehnia littoralis[17].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Anthriscus nitida[18].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Cicuta virosa[19].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Hansenia weberbaueriana[20].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Dendropanax arboreus[21].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Osmorhiza occidentalis[22].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Q7540[23].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Bunium paucifolium[24].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Oenanthe fistulosa[25].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Laserpitium gallicum[26].
  • (3R,8S)-Falcarindiol's found in taxon is recorded as Ferula linkii[27].

Why It Matters

(3R,8S)-Falcarindiol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (13 views/month).[2]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . The Molecular Receptive Ranges of Human TAS2R Bitter Taste Receptors. wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . The anti-staphylococcal activity of Angelica dahurica (Bai Zhi).. wikidata.org.
  11. [13] . Comparative study of roots ofAngelica sinensis and related umbelliferous drugs by thin layer chromatography, high-performance liquid chromatography, and liquid chromatography - mass spectrometry. wikidata.org.
  12. [14] . Comparative study of roots ofAngelica sinensis and related umbelliferous drugs by thin layer chromatography, high-performance liquid chromatography, and liquid chromatography - mass spectrometry. wikidata.org.
  13. [15] . Comparative study of roots ofAngelica sinensis and related umbelliferous drugs by thin layer chromatography, high-performance liquid chromatography, and liquid chromatography - mass spectrometry. wikidata.org.
  14. [16] . Antimycobacterial Polyynes of Devil's Club (Oplopanax horridus), a North American Native Medicinal Plant. wikidata.org.
  15. [17] . Psoralen and other linear furanocoumarins as phytoalexins in Glehnia littoralis. wikidata.org.
  16. [18] . Grilactone and other Terpenoids from Anthriscus nitida. wikidata.org.
  17. [19] . Polyacetylenes from water hemlock, Cicuta virosa.. wikidata.org.
  18. [20] . 5-Lipoxygenase and cyclooxygenase inhibitory active constituents from Qianghuo (Notopterygium incisum).. wikidata.org.
  19. [21] . Cytotoxic falcarinol oxylipins from Dendropanax arboreus. wikidata.org.
  20. [22] . Native American Medicinal Plants. Falcarindiol and 3-O-Methylfalcarindiol From Osmorhiza occidentalis. wikidata.org.
  21. [23] . Elicitation of diacetylenic compounds in suspension cultured cells of eggplant. wikidata.org.
  22. [24] . A sesquiterpene ketal from Bunium paucifolium. wikidata.org.
  23. [25] . Polyacetylenes from sardinian Oenanthe fistulosa: a molecular clue to risus sardonicus. wikidata.org.
  24. [26] . Sesquiterpene lactones from Laserpitium gallicum. wikidata.org.
  25. [27] . Sesquiterpene esters and sesquiterpene coumarin ethers from Ferula linkii-TF. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). (3R,8S)-Falcarindiol. Retrieved May 3, 2026, from https://4ort.xyz/entity/3r-8s-falcarindiol
MLA “(3R,8S)-Falcarindiol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/3r-8s-falcarindiol.
BibTeX @misc{4ortxyz_3r-8s-falcarindiol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(3R,8S)-Falcarindiol}}, year = {2026}, url = {https://4ort.xyz/entity/3r-8s-falcarindiol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (3R,8S)-Falcarindiol — https://4ort.xyz/entity/3r-8s-falcarindiol (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. 4w ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Has part(s) carbon, oxygen, hydrogen
    Aliases
    Instance of type of chemical entity
    Physically interacts with taste receptor type 2
    + 7 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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