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fucosterol

chemical compound
ChemicalSubstance type_of_chemical_entity Q15410971
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fucosterol

Summary

fucosterol is a type of chemical entity[1]. fucosterol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2]

Key Facts

  • fucosterol's instance of is recorded as type of chemical entity[3].
  • fucosterol's chemical structure is recorded as Fucosterol.svg[4].
  • fucosterol's CAS Registry Number is recorded as 17605-67-3[5].
  • fucosterol's canonical SMILES is recorded as CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C[6].
  • fucosterol's InChI is recorded as InChI=1S/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h7,10,19-20,23-27,30H,8-9,11-18H2,1-6H3/b21-7+/t20-,23+,24+,25-,26+,27+,28+,29-/m1/s1[7].
  • fucosterol's InChIKey is recorded as OSELKOCHBMDKEJ-JUGJNGJRSA-N[8].
  • fucosterol's chemical formula is recorded as C₂₉H₄₈O[9].
  • fucosterol's subclass of is recorded as Stigmasta-5,24(28)-dien-3-ol, (3beta,24E)-[10].
  • fucosterol's ChEMBL ID is recorded as CHEMBL519971[11].
  • fucosterol's Freebase ID is recorded as /m/0xnbwhx[12].
  • fucosterol's UNII is recorded as 504ZAM710C[13].
  • fucosterol's ChemSpider ID is recorded as 4444705[14].
  • fucosterol's PubChem CID is recorded as 5281328[15].
  • fucosterol's KEGG ID is recorded as C08817[16].
  • fucosterol's ChEBI ID is recorded as 27865[17].
  • fucosterol's found in taxon is recorded as Justicia tranquebariensis[18].
  • fucosterol's found in taxon is recorded as Ulva rigida[19].
  • fucosterol's found in taxon is recorded as Chara australis[20].
  • fucosterol's found in taxon is recorded as Chara buckellii[21].
  • fucosterol's found in taxon is recorded as Nitellopsis obtusa[22].
  • fucosterol's found in taxon is recorded as Lamprothamnium papulosum[23].
  • fucosterol's found in taxon is recorded as Dictyopteris divaricata[24].
  • fucosterol's found in taxon is recorded as Dictyota dichotoma[25].
  • fucosterol's found in taxon is recorded as Sarcophyton crassocaule[26].
  • fucosterol's found in taxon is recorded as Turbinaria conoides[27].

Why It Matters

fucosterol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2] fucosterol is known by 6 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] ↑ . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . Justica tranquebariensis Linn. f.. wikidata.org.
  17. [19] ↑ . Sterols from some black sea ulvaceae. wikidata.org.
  18. [20] ↑ . Sterols of the Charophyceae. wikidata.org.
  19. [21] ↑ . Sterols of the Charophyceae. wikidata.org.
  20. [22] ↑ . Sterols of the Charophyceae. wikidata.org.
  21. [23] ↑ . Sterols of the Charophyceae. wikidata.org.
  22. [24] ↑ . Cadinane sesquiterpenes from the brown alga Dictyopteris divaricata. wikidata.org.
  23. [25] ↑ . Sterols from brazilian marine brown algae. wikidata.org.
  24. [26] ↑ . Novel epoxy steroids from the indian ocean soft coral Sarcophyton crassocaule. wikidata.org.
  25. [27] ↑ . Isolation of 24-Hydroperoxy-24-Vinylcholesterol and Fucosterol from the Brown AlgaTurbinaria Conoides. 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). fucosterol. Retrieved May 3, 2026, from https://4ort.xyz/entity/fucosterol
MLA “fucosterol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/fucosterol.
BibTeX @misc{4ortxyz_fucosterol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{fucosterol}}, year = {2026}, url = {https://4ort.xyz/entity/fucosterol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): fucosterol — https://4ort.xyz/entity/fucosterol (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. 14d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Stereoisomer of → (3S,8S,9R,10R,13S,14S,17S)-10,13-dimethyl-17-[(E,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol, (3S,8R,9R,10R,13R,14R,17R)-10,13-dimethyl-17-[(E,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol, (3S,8S,9S,10R,13R,14S,17R)-17-((R,Z)-5-isopropylhept-5-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol +2
    Subclass of → Stigmasta-5,24(28)-dien-3-ol, (3beta,24E)-
    Aliases → —
    Subclass of → —
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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