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hederagenin

chemical compound
ChemicalSubstance type_of_chemical_entity Q5697238
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hederagenin

Summary

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

Key Facts

  • hederagenin's instance of is recorded as type of chemical entity[3].
  • hederagenin's chemical structure is recorded as Hederagenin.svg[4].
  • hederagenin's CAS Registry Number is recorded as 465-99-6[5].
  • hederagenin's EC number is recorded as 207-369-9[6].
  • hederagenin's canonical SMILES is recorded as CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C[7].
  • hederagenin's InChI is recorded as InChI=1S/C30H48O4/c1-25(2)13-15-30(24(33)34)16-14-28(5)19(20(30)17-25)7-8-22-26(3)11-10-23(32)27(4,18-31)21(26)9-12-29(22,28)6/h7,20-23,31-32H,8-18H2,1-6H3,(H,33,34)/t20-,21+,22+,23-,26-,27-,28+,29+,30-/m0/s1[8].
  • hederagenin's InChIKey is recorded as PGOYMURMZNDHNS-MYPRUECHSA-N[9].
  • hederagenin's chemical formula is recorded as C₃₀H₄₈O₄[10].
  • hederagenin's subclass of is recorded as oleanane triterpenoid[11].
  • hederagenin's subclass of is recorded as carboxylic acid[12].
  • hederagenin's ChEMBL ID is recorded as CHEMBL486400[13].
  • hederagenin's Freebase ID is recorded as /m/0bs3yq8[14].
  • hederagenin's UNII is recorded as RQF57J8212[15].
  • hederagenin's ChemSpider ID is recorded as 66038[16].
  • hederagenin's PubChem CID is recorded as 73299[17].
  • hederagenin's ChEBI ID is recorded as 69579[18].
  • hederagenin's found in taxon is recorded as Blighia sapida[19].
  • hederagenin's found in taxon is recorded as Chenopodium quinoa[20].
  • hederagenin's found in taxon is recorded as Nigella sativa[21].
  • hederagenin's found in taxon is recorded as Anisomeles indica[22].
  • hederagenin's found in taxon is recorded as Cephalaria transsylvanica[23].
  • hederagenin's found in taxon is recorded as Drypetes molunduana[24].
  • hederagenin's found in taxon is recorded as Stauntonia hexaphylla[25].
  • hederagenin's found in taxon is recorded as Atractylis carduus[26].
  • hederagenin's found in taxon is recorded as Abrus precatorius[27].

Why It Matters

hederagenin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (6 views/month).[2] hederagenin has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] hederagenin is known by 4 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] ↑ . ChEBI. 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  12. [14] ↑ . 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] ↑ . Ackee poisoning. wikidata.org.
  18. [20] ↑ . Gas chromatography-mass spectrometry of oleanane- and ursane-type triterpenes—application to Chenopodium quinoa triterpenes. wikidata.org.
  19. [21] ↑ . Complete assignments of1H and13C NMR spectra of the pentacyclic triterpene hederagenin fromNigella sativa Linn. wikidata.org.
  20. [22] ↑ . Bioactive cembrane diterpenoids of Anisomeles indica. wikidata.org.
  21. [23] ↑ . Oleanolic acid and hederagenin from the stems of Cephalaria transsylvanica. wikidata.org.
  22. [24] ↑ . Sesquiterpene lactone and friedelane derivative from drypetes molunduana. wikidata.org.
  23. [25] ↑ . A phenolic glycoside and triterpenoids from Stauntonia hexaphylla. wikidata.org.
  24. [26] ↑ . Flavonoid glycosides and triterpenoids from Atractylis flava. wikidata.org.
  25. [27] ↑ . A new sapogenol and other constituents in Abri Semen, the seeds of Abrus precatorius L. I.. 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). hederagenin. Retrieved May 3, 2026, from https://4ort.xyz/entity/hederagenin
MLA “hederagenin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hederagenin.
BibTeX @misc{4ortxyz_hederagenin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hederagenin}}, year = {2026}, url = {https://4ort.xyz/entity/hederagenin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hederagenin — https://4ort.xyz/entity/hederagenin (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 4w ago · KaleemBot bot · 2026-05-01 view diff on Wikidata ↗
    Subclass of → oleanane triterpenoid, carboxylic acid
    Found in taxon → Blighia sapida, Chenopodium quinoa, Nigella sativa +90
    Mass → {'unit': 'Q483261', 'amount': '+472.355'}
    Stereoisomer of → (4aS,6aS,6aS,6bR,8aR,9S,10R,12aS,14bR)-10-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid, (4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid, scutellaric acid +6
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:ہیڈرای جینن]]"
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