γ-ergostenol

chemical compound
ChemicalSubstance type_of_chemical_entity Q15410967
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γ-ergostenol

Summary

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

Key Facts

  • γ-ergostenol's instance of is recorded as type of chemical entity[3].
  • γ-ergostenol's chemical structure is recorded as Fungisterol.svg[4].
  • γ-ergostenol's CAS Registry Number is recorded as 516-78-9[5].
  • γ-ergostenol's EC number is recorded as 208-225-8[6].
  • γ-ergostenol's canonical SMILES is recorded as CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C[7].
  • γ-ergostenol's InChI is recorded as InChI=1S/C28H48O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h10,18-22,24-26,29H,7-9,11-17H2,1-6H3/t19-,20+,21-,22-,24+,25-,26-,27-,28+/m0/s1[8].
  • γ-ergostenol's InChIKey is recorded as PUGBZUWUTZUUCP-ZRKHGVCBSA-N[9].
  • γ-ergostenol's chemical formula is recorded as C₂₈H₄₈O[10].
  • γ-ergostenol's subclass of is recorded as Ergost-7-en-3-ol[11].
  • γ-ergostenol's subclass of is recorded as cholesta4,22-dien-3-one[12].
  • γ-ergostenol's UNII is recorded as XM6JVX97IY[13].
  • γ-ergostenol's ChemSpider ID is recorded as 4446739[14].
  • γ-ergostenol's PubChem CID is recorded as 5283646[15].
  • γ-ergostenol's ChEBI ID is recorded as 69432[16].
  • γ-ergostenol's found in taxon is recorded as Acanthaster planci[17].
  • γ-ergostenol's found in taxon is recorded as Baccharoides anthelmintica[18].
  • γ-ergostenol's found in taxon is recorded as Ganoderma[19].
  • γ-ergostenol's found in taxon is recorded as Carthamus tinctorius[20].
  • γ-ergostenol's found in taxon is recorded as Pisolithus arhizus[21].
  • γ-ergostenol's found in taxon is recorded as Pisolithus tinctorius[22].
  • γ-ergostenol's found in taxon is recorded as Roseofomes[23].
  • γ-ergostenol's found in taxon is recorded as Saccharomyces cerevisiae[24].
  • γ-ergostenol's found in taxon is recorded as Fuligo septica[25].
  • γ-ergostenol's found in taxon is recorded as Axinella cannabina[26].
  • γ-ergostenol's found in taxon is recorded as Candida lipolytica[27].

Why It Matters

γ-ergostenol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (1 views/month).[2] γ-ergostenol is known by 4 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] . Global Substance Registration System. 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] . 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] . Identification of 23-demethylacanthasterol in an asteroid, Acanthaster planci and its synthesis. wikidata.org.
  16. [18] . 4α-methylvernosterol and other sterols from Vernonia anthelmintica seeds. wikidata.org.
  17. [19] . New lanostanoids from the fungus Ganoderma concinna.. wikidata.org.
  18. [20] . Carthami flos extract and its component, stigmasterol, inhibit tumour promotion in mouse skin two-stage carcinogenesis. wikidata.org.
  19. [21] . Triterpenoids of the fungus Pisolithus tinctorius*. wikidata.org.
  20. [22] . Triterpenoids of the fungus Pisolithus tinctorius*. wikidata.org.
  21. [23] . Roseolide a, a novel dimeric drimane sesquiterpenoid from the basidiomycete Roseoformes subflexibilis. wikidata.org.
  22. [24] . Episterol and fungisterol from mutant strains of the yeast Saccharomyces cerevisiae. wikidata.org.
  23. [25] . Ueber Paracholesterin aus Aethalium septicum. wikidata.org.
  24. [26] . Minor and trace sterols in marine invertebrates. Part 35. Isolation and structure elucidation of seventy-four sterols from the sponge Axinella cannabina. wikidata.org.
  25. [27] . Sterols from Candida lipolytica yeast grown on n-alkanes. 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). γ-ergostenol. Retrieved May 3, 2026, from https://4ort.xyz/entity/ergostenol
MLA “γ-ergostenol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/ergostenol.
BibTeX @misc{4ortxyz_ergostenol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{γ-ergostenol}}, year = {2026}, url = {https://4ort.xyz/entity/ergostenol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): γ-ergostenol — https://4ort.xyz/entity/ergostenol (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. 15d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Stereoisomer of (3S,5R,9R,10S,13R,14R,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol, Ergost-7-en-3β-ol, Campest-7-en-3beta-ol +2
    Subclass of Ergost-7-en-3-ol, cholesta4,22-dien-3-one
    Aliases
    Subclass of
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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