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resiniferatoxin

chemical compound
ChemicalSubstance type_of_chemical_entity Q3277888
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resiniferatoxin

Summary

resiniferatoxin is a type of chemical entity[1]. resiniferatoxin ranks in the top 4% of type_of_chemical_entity entities by monthly Wikipedia readership (205 views/month).[2]

Key Facts

  • resiniferatoxin's instance of is recorded as type of chemical entity[3].
  • resiniferatoxin's chemical structure is recorded as Resiniferatoxin.svg[4].
  • resiniferatoxin's CAS Registry Number is recorded as 57444-62-9[5].
  • resiniferatoxin's canonical SMILES is recorded as O=C(OCC1=CC2C3OC4(OC3(C(=C)C)CC(C)C2(O4)C5C=C(C(=O)C5(O)C1)C)CC=6C=CC=CC6)CC7=CC=C(O)C(OC)=C7[6].
  • resiniferatoxin's InChI is recorded as InChI=1S/C37H40O9/c1-21(2)35-17-23(4)37-27(33(35)44-36(45-35,46-37)19-24-9-7-6-8-10-24)14-26(18-34(41)30(37)13-22(3)32(34)40)20-43-31(39)16-25-11-12-28(38)29(15-25)42-5/h6-15,23,27,30,33,38,41H,1,16-20H2,2-5H3/t23-,27+,30-,33-,34-,35-,36-,37-/m1/s1[7].
  • resiniferatoxin's InChIKey is recorded as DSDNAKHZNJAGHN-MXTYGGKSSA-N[8].
  • resiniferatoxin's chemical formula is recorded as C₃₇H₄₀O₉[9].
  • resiniferatoxin's subclass of is recorded as (+/-)-resiniferatoxin[10].
  • resiniferatoxin's subclass of is recorded as CID 5148108[11].
  • resiniferatoxin's subclass of is recorded as [(1R,2R,6R,11R,13S,15S,17R)-13-benzyl-6-hydroxy-4,17-dimethyl-5-oxo-15-prop-1-en-2-yl-12,14,18-trioxapentacyclo[11.4.1.01,10.02,6.011,15]octadeca-3,8-dien-8-yl]methyl 2-(4-hydroxy-3-methoxyphenyl)acetate[12].
  • resiniferatoxin's Commons category is recorded as Resiniferatoxin[13].
  • resiniferatoxin's has part is recorded as carbon[14].
  • resiniferatoxin's has part is recorded as oxygen[15].
  • resiniferatoxin's has part is recorded as hydrogen[16].
  • resiniferatoxin's ChEMBL ID is recorded as CHEMBL17976[17].
  • resiniferatoxin's Guide to Pharmacology Ligand ID is recorded as 2491[18].
  • resiniferatoxin's Guide to Pharmacology Ligand ID is recorded as 4091[19].
  • resiniferatoxin's Freebase ID is recorded as /m/09zgjt[20].
  • resiniferatoxin's UNII is recorded as A5O6P1UL4I[21].
  • resiniferatoxin's RTECS number is recorded as CY1633700[22].
  • resiniferatoxin's ChemSpider ID is recorded as 4642871[23].
  • resiniferatoxin's PubChem CID is recorded as 5702546[24].
  • resiniferatoxin's ChEBI ID is recorded as 8809[25].
  • resiniferatoxin's found in taxon is recorded as Euphorbia resinifera[26].
  • resiniferatoxin's found in taxon is recorded as Euphorbia unispina[27].

Why It Matters

resiniferatoxin ranks in the top 4% of type_of_chemical_entity entities by monthly Wikipedia readership (205 views/month).[2] resiniferatoxin has Wikipedia articles in 19 language editions, a strong signal of global cultural recognition.[28] resiniferatoxin is known by 6 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] ↑ . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . ChEBI release 2020-09-01. wikidata.org.
  7. [9] ↑ . PubChem. wikidata.org.
  8. [10] ↑ . 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] ↑ . wikidata.org.
  16. [18] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  17. [19] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  18. [20] ↑ . Freebase Data Dumps. wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . Bisnorsesquiterpenoids from Euphorbia resinifera Berg. and an Expeditious Procedure to Obtain Resiniferatoxin from Its Fresh Latex. wikidata.org.
  25. [27] ↑ . Structure-activity relations of polyfunctional diterpenes of the daphnane type. I. Revised structure for resiniferatoxin and structure-activity relations of resiniferonol and some of its esters. 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). resiniferatoxin. Retrieved May 3, 2026, from https://4ort.xyz/entity/resiniferatoxin
MLA “resiniferatoxin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/resiniferatoxin.
BibTeX @misc{4ortxyz_resiniferatoxin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{resiniferatoxin}}, year = {2026}, url = {https://4ort.xyz/entity/resiniferatoxin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): resiniferatoxin — https://4ort.xyz/entity/resiniferatoxin (retrieved 2026-05-03)

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