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fecosterol

chemical compound
ChemicalSubstance type_of_chemical_entity Q15410975
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Summary

fecosterol is a type of chemical entity[1]. fecosterol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (4 views/month).[2]

Key Facts

  • fecosterol's instance of is recorded as type of chemical entity[3].
  • fecosterol's canonical SMILES is recorded as CC(C)C(=C)CCC(C)C1CCC2C1(CCC3=C2CCC4C3(CCC(C4)O)C)C[4].
  • fecosterol's chemical formula is recorded as C₂₈H₄₆O[5].
  • fecosterol is a type of ergostane steroid[6].
  • fecosterol is part of sterol 24-C-methyltransferase activity[7].
  • fecosterol's found in taxon is recorded as Eutypa lata[8].
  • fecosterol's found in taxon is recorded as Candida albicans[9].
  • fecosterol's found in taxon is recorded as Candida utilis[10].
  • fecosterol's found in taxon is recorded as Cyberlindnera jadinii[11].
  • fecosterol's found in taxon is recorded as Neurospora crassa[12].
  • fecosterol's found in taxon is recorded as Candida glabrata[13].
  • fecosterol's found in taxon is recorded as Torulopsis glabrata[14].
  • fecosterol's found in taxon is recorded as Leptosphaeria maculans[15].
  • fecosterol's found in taxon is recorded as Rubus fruticosus[16].
  • fecosterol's found in taxon is recorded as Rubus plicatus[17].
  • fecosterol's found in taxon is recorded as Saccharomyces cerevisiae[18].
  • fecosterol's found in taxon is recorded as maize[19].
  • fecosterol's found in taxon is recorded as Phycomyces blakesleeanus[20].
  • fecosterol's found in taxon is recorded as Rubus cochinchinensis[21].
  • fecosterol's isomeric SMILES is recorded as CC@H[C@H]1CC[C@@H]2[C@@]1(CCC3=C2CC[C@@H]4[C@@]3(CCC@@HO)C)CC@H[C@H]1CC[C@@H]2[C@@]1(CCC3=C2CC[C@@H]4[C@@]3(CCC@@HO)C)C">[22].
  • fecosterol's mass is recorded as {'unit': 'dalton', 'amount': '+398.354866'}[23].

Why It Matters

fecosterol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (4 views/month).[2]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [5] ↑ . PubChem. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  6. [8] ↑ . Sterol composition of the woody plant pathogenic fungus Eutypa lata. wikidata.org.
  7. [9] ↑ . Purification, characterization and inhibition of sterol C24-methyltransferase from Candida albicans.. wikidata.org.
  8. [10] ↑ . Purification, characterization and inhibition of sterol C24-methyltransferase from Candida albicans.. wikidata.org.
  9. [11] ↑ . Purification, characterization and inhibition of sterol C24-methyltransferase from Candida albicans.. wikidata.org.
  10. [12] ↑ . Detection of the ergosterol and episterol isomers lichesterol and fecosterol in nystatin-resistant mutants of Neurospora crassa. wikidata.org.
  11. [13] ↑ . Purification, characterization and inhibition of sterol C24-methyltransferase from Candida albicans.. wikidata.org.
  12. [14] ↑ . Purification, characterization and inhibition of sterol C24-methyltransferase from Candida albicans.. wikidata.org.
  13. [15] ↑ . Sterol composition of mycelia of the plant pathogenic ascomycete Leptosphaeria maculans. wikidata.org.
  14. [16] ↑ . Comparative study of the inhibition of sterol biosynthesis in Rubus fruticosus suspension cultures and zea mays seedlings by N-(1,5,9-trimethyldecyl)-4α,10-dimethyl-8-aza-trans-decal-3β-ol and derivatives. wikidata.org.
  15. [17] ↑ . Comparative study of the inhibition of sterol biosynthesis in Rubus fruticosus suspension cultures and zea mays seedlings by N-(1,5,9-trimethyldecyl)-4α,10-dimethyl-8-aza-trans-decal-3β-ol and derivatives. wikidata.org.
  16. [18] ↑ . Biosynthesis of terpenes and steroids. Part X. The sterols of some yeast mutants doubly defective in ergosterol biosynthesis. wikidata.org.
  17. [19] ↑ . Comparative study of the inhibition of sterol biosynthesis in Rubus fruticosus suspension cultures and zea mays seedlings by N-(1,5,9-trimethyldecyl)-4α,10-dimethyl-8-aza-trans-decal-3β-ol and derivatives. wikidata.org.
  18. [20] ↑ . Phycomysterols and other sterols from the fungus Phycomyces blakesleeanus. wikidata.org.
  19. [21] ↑ . Comparative study of the inhibition of sterol biosynthesis in Rubus fruticosus suspension cultures and zea mays seedlings by N-(1,5,9-trimethyldecyl)-4α,10-dimethyl-8-aza-trans-decal-3β-ol and derivatives. wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). fecosterol. Retrieved October 13, 2026, from https://4ort.xyz/entity/fecosterol
MLA “fecosterol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 13 Oct. 2026, https://4ort.xyz/entity/fecosterol.
BibTeX @misc{4ortxyz_fecosterol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{fecosterol}}, year = {2026}, url = {https://4ort.xyz/entity/fecosterol}, note = {Accessed: 2026-10-13}}
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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. 23w ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Subclass of → ergostane steroid
    Part of → sterol 24-C-methyltransferase activity
    Aliases → —
    Subclass of → —
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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