campestanol

chemical compound
ChemicalSubstance type_of_chemical_entity Q15410858
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campestanol

Summary

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

Key Facts

  • campestanol's instance of is recorded as type of chemical entity[3].
  • campestanol's chemical structure is recorded as Campestanol.svg[4].
  • campestanol's CAS Registry Number is recorded as 474-60-2[5].
  • campestanol's canonical SMILES is recorded as CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C[6].
  • campestanol's InChI is recorded as InChI=1S/C28H50O/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/h18-26,29H,7-17H2,1-6H3/t19-,20-,21+,22+,23+,24-,25+,26+,27+,28-/m1/s1[7].
  • campestanol's InChIKey is recorded as ARYTXMNEANMLMU-ATEDBJNTSA-N[8].
  • campestanol's chemical formula is recorded as C₂₈H₅₀O[9].
  • campestanol's subclass of is recorded as ergostane steroid[10].
  • campestanol's Commons category is recorded as Campestanol[11].
  • campestanol's Freebase ID is recorded as /m/02kcmj_[12].
  • campestanol's UNII is recorded as 5J08LF99N1[13].
  • campestanol's ChemSpider ID is recorded as 106639[14].
  • campestanol's PubChem CID is recorded as 119394[15].
  • campestanol's KEGG ID is recorded as C15787[16].
  • campestanol's ChEBI ID is recorded as 36799[17].
  • campestanol's found in taxon is recorded as Oryza sativa[18].
  • campestanol's found in taxon is recorded as Ornithopus sativus[19].
  • campestanol's found in taxon is recorded as Arabidopsis thaliana[20].
  • campestanol's found in taxon is recorded as Setaria italica[21].
  • campestanol's found in taxon is recorded as Costus spiralis[22].
  • campestanol's found in taxon is recorded as Nigella sativa[23].
  • campestanol's found in taxon is recorded as Nicotiana tabacum[24].
  • campestanol's found in taxon is recorded as Salvia jaminiana[25].
  • campestanol's found in taxon is recorded as Aloe rubroviolacea[26].
  • campestanol's found in taxon is recorded as Avena sativa[27].

Why It Matters

campestanol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (1 views/month).[2] campestanol is known by 10 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] . 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] . Rice Bran and Rice Bran Oil. wikidata.org.
  17. [19] . 6-Deoxo-28-norcastasterone and 6-deoxo-24-epicastasterone —two new brassinosteroids from Ornithopus sativus. wikidata.org.
  18. [20] . Sterols and phytyl esters of Arabidopsis thaliana under normal and chilling temperatures. wikidata.org.
  19. [21] . Identification of Trace Sterols in the Seeds of Foxtail Millet (Setaria italicaBeauv.). wikidata.org.
  20. [22] . Diosgenin und Sterine ausCostus spiralis. wikidata.org.
  21. [23] . The sterols of Nigella sativa seed oil. wikidata.org.
  22. [24] . Chemical composition of tobacco seeds (Nicotiana tabacum L.). wikidata.org.
  23. [25] . Components and antibacterial activity of the roots of Salvia jaminiana. wikidata.org.
  24. [26] . Constituents of Aloe rubroviolacea. wikidata.org.
  25. [27] . Sterols in seeds and leaves of oats (Avena sativa L.).. 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). campestanol. Retrieved May 3, 2026, from https://4ort.xyz/entity/campestanol
MLA “campestanol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/campestanol.
BibTeX @misc{4ortxyz_campestanol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{campestanol}}, year = {2026}, url = {https://4ort.xyz/entity/campestanol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): campestanol — https://4ort.xyz/entity/campestanol (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 ↗
    Subject has role primary metabolite
    Stereoisomer of 5beta-Campestanol, (3S,5S,8S,9S,10R,13R,14S,17S)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol, (3S,5S,8R,9R,10S,13R,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol +2
    Subclass of ergostane steroid
    Human metabolome database id HMDB0000534
    + 6 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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