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bufotalin

chemical compound
ChemicalSubstance type_of_chemical_entity Q5760807
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bufotalin

Summary

bufotalin is a type of chemical entity[1]. bufotalin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2]

Key Facts

  • bufotalin's instance of is recorded as type of chemical entity[3].
  • bufotalin's chemical structure is recorded as Bufotalin.svg[4].
  • bufotalin's chemical structure is recorded as Strukturformel Bufotalin.svg[5].
  • bufotalin's CAS Registry Number is recorded as 471-95-4[6].
  • bufotalin's canonical SMILES is recorded as CC(=O)OC1CC2(C3CCC4CC(CCC4(C3CCC2(C1C5=COC(=O)C=C5)C)C)O)O[7].
  • bufotalin's InChI is recorded as InChI=1S/C26H36O6/c1-15(27)32-21-13-26(30)20-6-5-17-12-18(28)8-10-24(17,2)19(20)9-11-25(26,3)23(21)16-4-7-22(29)31-14-16/h4,7,14,17-21,23,28,30H,5-6,8-13H2,1-3H3/t17-,18+,19+,20-,21+,23+,24+,25-,26+/m1/s1[8].
  • bufotalin's InChIKey is recorded as VOZHMAYHYHEWBW-NVOOAVKYSA-N[9].
  • bufotalin's chemical formula is recorded as C₂₆H₃₆O₆[10].
  • bufotalin's subclass of is recorded as bufanolide[11].
  • bufotalin's Commons category is recorded as Bufotalin[12].
  • bufotalin's ChEMBL ID is recorded as CHEMBL463064[13].
  • bufotalin's Freebase ID is recorded as /m/05m47g[14].
  • bufotalin's UNII is recorded as EGL9670I6P[15].
  • bufotalin's ChemSpider ID is recorded as 16735710[16].
  • bufotalin's PubChem CID is recorded as 12302120[17].
  • bufotalin's KEGG ID is recorded as C16923[18].
  • bufotalin's ChEBI ID is recorded as 80799[19].
  • bufotalin's found in taxon is recorded as Bufo[20].
  • bufotalin's found in taxon is recorded as Duttaphrynus melanostictus[21].
  • bufotalin's found in taxon is recorded as Bufo bankorensis[22].
  • bufotalin's found in taxon is recorded as Phrynoidis asper[23].
  • bufotalin's found in taxon is recorded as common toad[24].
  • bufotalin's found in taxon is recorded as Asiatic toad[25].
  • bufotalin's isomeric SMILES is recorded as CC(=O)O[C@H]1C[C@@]2([C@@H]3CC[C@@H]4CC@HO)OC@HO)O">[26].
  • bufotalin's LIPID MAPS ID is recorded as LMST01130023[27].

Why It Matters

bufotalin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2] bufotalin has Wikipedia articles in 5 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] ↑ . 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  12. [14] ↑ . Freebase Data Dumps. wikidata.org.
  13. [15] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] ↑ . Q2311683. Retrieved . wikidata.org.
  15. [17] ↑ . PubChem. Retrieved . wikidata.org.
  16. [18] ↑ . ChEBI. Retrieved . wikidata.org.
  17. [19] ↑ . ChEMBL. Retrieved . wikidata.org.
  18. [20] ↑ . Studies on toad venom (2): Examination of the drying processing method. wikidata.org.
  19. [21] ↑ . Chemical Constituents of Vietnamese Toad Venom, Collected From Bufo melanostictus Schneider. Part II. The Bufadienolides. wikidata.org.
  20. [22] ↑ . Occurrence of marinobufotoxin and telocinobufotoxin homologs in the skin of Bufo bankorensis BORBOUR.. wikidata.org.
  21. [23] ↑ . Studies on Steroids CCVIII. Bufadienolides from Bufo asper. wikidata.org.
  22. [24] ↑ . Isolation and characterization of cinobufagin 3-glutaroyl-L-arginine ester from Bufo bufo gargarizans Cantor.. wikidata.org.
  23. [25] ↑ . C23 steroids from the venom of Bufo bufo gargarizans. wikidata.org.
  24. [26] ↑ . PubChem. Retrieved . wikidata.org.
  25. [27] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: 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). bufotalin. Retrieved May 3, 2026, from https://4ort.xyz/entity/bufotalin
MLA “bufotalin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/bufotalin.
BibTeX @misc{4ortxyz_bufotalin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{bufotalin}}, year = {2026}, url = {https://4ort.xyz/entity/bufotalin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): bufotalin — https://4ort.xyz/entity/bufotalin (retrieved 2026-05-03)

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