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cerberin

chemical compound
ChemicalSubstance type_of_chemical_entity Q5063899
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cerberin

Summary

cerberin is a type of chemical entity[1]. cerberin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (51 views/month).[2]

Key Facts

  • cerberin's instance of is recorded as type of chemical entity[3].
  • cerberin's chemical structure is recorded as Cerberin structure.svg[4].
  • cerberin's CAS Registry Number is recorded as 25633-33-4[5].
  • cerberin's canonical SMILES is recorded as CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)OC(=O)C)OC)O[6].
  • cerberin's InChI is recorded as InChI=1S/C32H48O9/c1-17-26(35)27(37-5)28(40-18(2)33)29(39-17)41-21-8-11-30(3)20(15-21)6-7-24-23(30)9-12-31(4)22(10-13-32(24,31)36)19-14-25(34)38-16-19/h14,17,20-24,26-29,35-36H,6-13,15-16H2,1-5H3/t17-,20+,21-,22+,23-,24+,26-,27+,28-,29-,30-,31+,32-/m0/s1[7].
  • cerberin's InChIKey is recorded as UYQMTWMXBKEHJQ-IVHDSYOHSA-N[8].
  • cerberin's chemical formula is recorded as C₃₂H₄₈O₉[9].
  • cerberin's subclass of is recorded as cardanolides[10].
  • cerberin's ChEMBL ID is recorded as CHEMBL554969[11].
  • cerberin's Freebase ID is recorded as /m/0ndhjj8[12].
  • cerberin's UNII is recorded as KW5A155S64[13].
  • cerberin's ChemSpider ID is recorded as 8206634[14].
  • cerberin's PubChem CID is recorded as 10031063[15].
  • cerberin's KEGG ID is recorded as C19984[16].
  • cerberin's ChEBI ID is recorded as 75049[17].
  • cerberin's found in taxon is recorded as Cerbera odollam[18].
  • cerberin's found in taxon is recorded as Cerbera manghas[19].
  • cerberin's found in taxon is recorded as Thevetia ahouai[20].
  • cerberin's found in taxon is recorded as Thevetia[21].
  • cerberin's Reaxys registry number is recorded as 101650[22].
  • cerberin's isomeric SMILES is recorded as C[C@H]1C@@HOC@@HO">[23].
  • cerberin's mass is recorded as {'unit': 'Q483261', 'amount': '+576.33'}[24].
  • cerberin's SureChEMBL ID is recorded as 868106[25].
  • cerberin's DSSTox substance ID is recorded as DTXSID30893922[26].
  • cerberin's stereoisomer of is recorded as [(2S,3S,4R,5S,6S)-5-hydroxy-2-[[(3S,5S,8R,9S,10S,13R,14S,17S)-14-hydroxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]-4-methoxy-6-methyloxan-3-yl] acetate[27].

Why It Matters

cerberin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (51 views/month).[2] cerberin is known by 3 alternative names across languages and contexts.[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] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . ChEMBL. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  12. [14] ↑ . Q2311683. Retrieved . wikidata.org.
  13. [15] ↑ . PubChem. Retrieved . wikidata.org.
  14. [16] ↑ . ChEBI. Retrieved . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . Cytotoxic cardenolide glycoside from the seeds of Cerbera odollam. wikidata.org.
  17. [19] ↑ . New cytotoxic cardenolide glycoside from the seeds of Cerbera manghas. wikidata.org.
  18. [20] ↑ . Cardenolide Glycosides from Thevetia ahouai (LINN.) A.DC.. wikidata.org.
  19. [21] ↑ . The differential cytotoxicity of cardenolides fromThevetia ahouia. wikidata.org.
  20. [22] ↑ . ChEBI. Retrieved . wikidata.org.
  21. [23] ↑ . PubChem. Retrieved . wikidata.org.
  22. [24] ↑ . PubChem. Retrieved . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . 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 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). cerberin. Retrieved May 3, 2026, from https://4ort.xyz/entity/cerberin
MLA “cerberin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cerberin.
BibTeX @misc{4ortxyz_cerberin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cerberin}}, year = {2026}, url = {https://4ort.xyz/entity/cerberin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cerberin — https://4ort.xyz/entity/cerberin (retrieved 2026-05-03)

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