capsaicin

chemical compound
ChemicalSubstance type_of_chemical_entity Q273169
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capsaicin

Summary

capsaicin is a type of chemical entity[1]. capsaicin ranks in the top 0.98% of type_of_chemical_entity entities by monthly Wikipedia readership (2,080 views/month, #123 of 12,596).[2]

Key Facts

  • capsaicin's instance of is recorded as type of chemical entity[3].
  • capsaicin's chemical structure is recorded as Capsaicin.svg[4].
  • capsaicin's chemical structure is recorded as Struktur Capsaicin.svg[5].
  • capsaicin's physically interacts with is recorded as cystic fibrosis transmembrane conductance regulator[6].
  • capsaicin's physically interacts with is recorded as Potassium voltage-gated channel, shaker-related subfamily, member 1[7].
  • capsaicin's physically interacts with is recorded as Potassium voltage-gated channel, shaker-related subfamily, member 7[8].
  • capsaicin's physically interacts with is recorded as Potassium voltage gated channel, Shaw-related subfamily, member 1[9].
  • capsaicin's physically interacts with is recorded as Transient receptor potential cation channel subfamily V member 1[10].
  • capsaicin's physically interacts with is recorded as Transient receptor potential cation channel, subfamily V, member 1[11].
  • capsaicin's physically interacts with is recorded as Transient receptor potential cation channel subfamily V member 6[12].
  • capsaicin's GND ID is recorded as 7538173-4[13].
  • capsaicin's CAS Registry Number is recorded as 404-86-4[14].
  • capsaicin's EC number is recorded as 206-969-8[15].
  • capsaicin's canonical SMILES is recorded as CC(C)C=CCCCCC(=O)NCC1=CC(=C(C=C1)O)OC[16].
  • capsaicin's InChI is recorded as InChI=1S/C18H27NO3/c1-14(2)8-6-4-5-7-9-18(21)19-13-15-10-11-16(20)17(12-15)22-3/h6,8,10-12,14,20H,4-5,7,9,13H2,1-3H3,(H,19,21)/b8-6+[17].
  • capsaicin's InChIKey is recorded as YKPUWZUDDOIDPM-SOFGYWHQSA-N[18].
  • capsaicin's Library of Congress authority ID is recorded as sh85020016[19].
  • capsaicin's ATC code is recorded as N01BX04[20].
  • capsaicin's ATC code is recorded as M02AB01[21].
  • capsaicin's ATC code is recorded as M02AB[22].
  • capsaicin's chemical formula is recorded as C₁₈H₂₇NO₃[23].
  • capsaicin's subclass of is recorded as capsaicinoid[24].
  • capsaicin's subclass of is recorded as N-acyl amines[25].
  • capsaicin's part of is recorded as capsicum oleoresin[26].
  • capsaicin's has use is recorded as medication[27].

Why It Matters

capsaicin ranks in the top 0.98% of type_of_chemical_entity entities by monthly Wikipedia readership (2,080 views/month, #123 of 12,596).[2] capsaicin has Wikipedia articles in 29 language editions, a strong signal of global cultural recognition.[28] capsaicin is known by 26 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  5. [7] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  6. [8] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  7. [9] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  8. [10] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  9. [11] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  10. [12] . Calcium selective channel TRPV6: Structure, function, and implications in health and disease. wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  13. [15] . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] . PubChem. Retrieved . wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . PubChem. Retrieved . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . LIPID MAPS. wikidata.org.
  24. [26] . drugbank.ca. Retrieved . drugbank.ca. Provenance: wikidata.org.
  25. [27] . 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). capsaicin. Retrieved May 3, 2026, from https://4ort.xyz/entity/capsaicin
MLA “capsaicin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/capsaicin.
BibTeX @misc{4ortxyz_capsaicin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{capsaicin}}, year = {2026}, url = {https://4ort.xyz/entity/capsaicin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): capsaicin — https://4ort.xyz/entity/capsaicin (retrieved 2026-05-03)

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