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homovanillyl alcohol

chemical compound
ChemicalSubstance type_of_chemical_entity Q5891855
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homovanillyl alcohol

Summary

homovanillyl alcohol is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2]

Key Facts

  • homovanillyl alcohol's instance of is recorded as type of chemical entity[3].
  • homovanillyl alcohol's chemical structure is recorded as Homovanillyl alcohol.png[4].
  • homovanillyl alcohol's CAS Registry Number is recorded as 2380-78-1[5].
  • homovanillyl alcohol's EC number is recorded as 219-175-1[6].
  • homovanillyl alcohol's canonical SMILES is recorded as COC1=C(C=CC(=C1)CCO)O[7].
  • homovanillyl alcohol's InChI is recorded as InChI=1S/C9H12O3/c1-12-9-6-7(4-5-10)2-3-8(9)11/h2-3,6,10-11H,4-5H2,1H3[8].
  • homovanillyl alcohol's InChIKey is recorded as XHUBSJRBOQIZNI-UHFFFAOYSA-N[9].
  • homovanillyl alcohol's chemical formula is recorded as C₉H₁₂O₃[10].
  • homovanillyl alcohol's subclass of is recorded as chemical compound[11].
  • homovanillyl alcohol's MeSH descriptor ID is recorded as D015098[12].
  • homovanillyl alcohol's Freebase ID is recorded as /m/05zy8gj[13].
  • homovanillyl alcohol's UNII is recorded as 9A7EE8MS6A[14].
  • homovanillyl alcohol's ChemSpider ID is recorded as 16039[15].
  • homovanillyl alcohol's PubChem CID is recorded as 16928[16].
  • homovanillyl alcohol's MeSH tree code is recorded as D02.455.426.559.389.657.166.500[17].
  • homovanillyl alcohol's ChEBI ID is recorded as 173769[18].
  • homovanillyl alcohol's found in taxon is recorded as Urtica dioica[19].
  • homovanillyl alcohol's found in taxon is recorded as Bongardia chrysogonum[20].
  • homovanillyl alcohol's found in taxon is recorded as Aconitum baicalense[21].
  • homovanillyl alcohol's found in taxon is recorded as Fraxinus japonica[22].
  • homovanillyl alcohol's found in taxon is recorded as Nicotiana tabacum[23].
  • homovanillyl alcohol's found in taxon is recorded as Cyclopia intermedia[24].
  • homovanillyl alcohol's found in taxon is recorded as Saussurea medusa[25].
  • homovanillyl alcohol's found in taxon is recorded as ginger[26].
  • homovanillyl alcohol's found in taxon is recorded as Olea europaea[27].

Why It Matters

homovanillyl alcohol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2] It 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] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] ↑ . Q2311683. Retrieved . wikidata.org.
  14. [16] ↑ . PubChem. Retrieved . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . ChEBI release 2022-06-13. wikidata.org.
  17. [19] ↑ . Phenolic compounds from roots of Urtica dioica. wikidata.org.
  18. [20] ↑ . An Investigation of Bongardia chrysogonum. wikidata.org.
  19. [21] ↑ . Two phenolic compounds fromAconitum baicalense. wikidata.org.
  20. [22] ↑ . Anti-platelet aggregation principles from the bark of Fraxinus japonica Blume. wikidata.org.
  21. [23] ↑ . Two new acidic constituents of flue-cured Virginia tobacco. wikidata.org.
  22. [24] ↑ . Polyphenols from Honeybush tea (Cyclopia intermedia).. wikidata.org.
  23. [25] ↑ . Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa. wikidata.org.
  24. [26] ↑ . Inhibitory effects of Zingiber officinale Roscoe derived components on aldose reductase activity in vitro and in vivo. wikidata.org.
  25. [27] ↑ . Absorption and metabolism of olive oil secoiridoids in the small intestine. 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). homovanillyl alcohol. Retrieved May 3, 2026, from https://4ort.xyz/entity/homovanillyl-alcohol
MLA “homovanillyl alcohol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/homovanillyl-alcohol.
BibTeX @misc{4ortxyz_homovanillyl-alcohol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{homovanillyl alcohol}}, year = {2026}, url = {https://4ort.xyz/entity/homovanillyl-alcohol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): homovanillyl alcohol — https://4ort.xyz/entity/homovanillyl-alcohol (retrieved 2026-05-03)

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