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campesterol

chemical compound
ChemicalSubstance type_of_chemical_entity Q2756479
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campesterol

Summary

campesterol is a type of chemical entity[1]. campesterol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (17 views/month).[2]

Key Facts

  • campesterol's instance of is recorded as type of chemical entity[3].
  • campesterol's chemical structure is recorded as Campesterol.png[4].
  • campesterol's CAS Registry Number is recorded as 474-62-4[5].
  • campesterol's EC number is recorded as 207-484-4[6].
  • campesterol's canonical SMILES is recorded as CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C[7].
  • campesterol'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/h9,18-20,22-26,29H,7-8,10-17H2,1-6H3/t19-,20-,22+,23+,24-,25+,26+,27+,28-/m1/s1[8].
  • campesterol's InChIKey is recorded as SGNBVLSWZMBQTH-PODYLUTMSA-N[9].
  • campesterol's chemical formula is recorded as C₂₈H₄₈O[10].
  • campesterol's subclass of is recorded as 24-α-methylcholesterol[11].
  • campesterol's subclass of is recorded as (3S,10R,13R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol[12].
  • campesterol's subclass of is recorded as (3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol[13].
  • campesterol's Commons category is recorded as Campesterol[14].
  • campesterol's ChEMBL ID is recorded as CHEMBL520535[15].
  • campesterol's Freebase ID is recorded as /m/0b6d7v_[16].
  • campesterol's UNII is recorded as 5L5O665639[17].
  • campesterol's ChemSpider ID is recorded as 151215[18].
  • campesterol's PubChem CID is recorded as 173183[19].
  • campesterol's KEGG ID is recorded as C01789[20].
  • campesterol's ChEBI ID is recorded as 28623[21].
  • campesterol's found in taxon is recorded as Acanthaster planci[22].
  • campesterol's found in taxon is recorded as Vernicia fordii[23].
  • campesterol's found in taxon is recorded as Blutaparon portulacoides[24].
  • campesterol's found in taxon is recorded as Boehmeria holosericea[25].
  • campesterol's found in taxon is recorded as Brassica campestris[26].
  • campesterol's found in taxon is recorded as Brassica rapa[27].

Why It Matters

campesterol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (17 views/month).[2] campesterol has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] campesterol 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] ↑ . 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] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . ChEMBL. Retrieved . wikidata.org.
  14. [16] ↑ . Freebase Data Dumps. wikidata.org.
  15. [17] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] ↑ . Q2311683. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . ChEMBL. Retrieved . wikidata.org.
  20. [22] ↑ . Identification of 23-demethylacanthasterol in an asteroid, Acanthaster planci and its synthesis. wikidata.org.
  21. [23] ↑ . The Toxic Constituent of the Fruits of Aleurites fordii. wikidata.org.
  22. [24] ↑ . A methylenedioxyflavonol from aerial parts of Blutaparon portulacoides. wikidata.org.
  23. [25] ↑ . Flavones and other compounds of Boehmeria tricuspis and B. Holosericea. wikidata.org.
  24. [26] ↑ . Additions and Corrections - Preparation of 22,23-Dihydrostigmasterol and 22,23-Dihydrobrassicasterol. wikidata.org.
  25. [27] ↑ . Additions and Corrections - Preparation of 22,23-Dihydrostigmasterol and 22,23-Dihydrobrassicasterol. 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). campesterol. Retrieved May 3, 2026, from https://4ort.xyz/entity/campesterol
MLA “campesterol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/campesterol.
BibTeX @misc{4ortxyz_campesterol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{campesterol}}, year = {2026}, url = {https://4ort.xyz/entity/campesterol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): campesterol — https://4ort.xyz/entity/campesterol (retrieved 2026-05-03)

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