avenasterol

chemical compound
ChemicalSubstance type_of_chemical_entity Q76422902
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avenasterol

Summary

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

Key Facts

  • avenasterol's instance of is recorded as type of chemical entity[3].
  • avenasterol's chemical structure is recorded as Structure of (3β,5α,24Z)-Stigmasta-7,24(28)-dien-3-ol (23290-26-8).svg[4].
  • avenasterol's CAS Registry Number is recorded as 23290-26-8[5].
  • avenasterol's canonical SMILES is recorded as OC1CCC2(C)C3C(=CCC2C1)C4CCC(C(C)CCC(=CC)C(C)C)C4(C)CC3[6].
  • avenasterol'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/h7,11,19-20,22-23,25-27,30H,8-10,12-18H2,1-6H3/b21-7-/t20-,22+,23+,25-,26+,27+,28+,29-/m1/s1[7].
  • avenasterol's InChIKey is recorded as MCWVPSBQQXUCTB-OQTIOYDCSA-N[8].
  • avenasterol's chemical formula is recorded as C₂₉H₄₈O[9].
  • avenasterol's subclass of is recorded as (24E/Z)-avenasterol[10].
  • avenasterol's UNII is recorded as I0WYR6393O[11].
  • avenasterol's PubChem CID is recorded as 12795736[12].
  • avenasterol's KEGG ID is recorded as C15782[13].
  • avenasterol's ChEBI ID is recorded as 166888[14].
  • avenasterol's found in taxon is recorded as Amaranthus cruentus[15].
  • avenasterol's found in taxon is recorded as Eryngium foetidum[16].
  • avenasterol's found in taxon is recorded as Campanula medium[17].
  • avenasterol's found in taxon is recorded as Amaranthus caudatus[18].
  • avenasterol's found in taxon is recorded as Amaranthus hybridus[19].
  • avenasterol's found in taxon is recorded as Amaranthus hypochondriacus[20].
  • avenasterol's found in taxon is recorded as Amelanchier canadensis[21].
  • avenasterol's found in taxon is recorded as Avena sativa[22].
  • avenasterol's found in taxon is recorded as Bryonia dioica[23].
  • avenasterol's found in taxon is recorded as Canavalia ensiformis[24].
  • avenasterol's found in taxon is recorded as Carthamus tinctorius[25].
  • avenasterol's found in taxon is recorded as Euonymus japonicus[26].
  • avenasterol's found in taxon is recorded as common sunflower[27].

Why It Matters

avenasterol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (4 views/month).[2] avenasterol is known by 3 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] . Chemical Abstracts Service. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . ChEBI. Retrieved . wikidata.org.
  12. [14] . ChEBI release 2021-03-01. wikidata.org.
  13. [15] . Sterols of seed oils ofVernonia galamensis,Amaranthus cruentus,Amaranthus caudatus,Amaranthus hybridus andAmaranthus hypochondriacus grown in the humid tropics. wikidata.org.
  14. [16] . Topical antiinflammatory activity of phytosterols isolated from Eryngium foetidum on chronic and acute inflammation models. wikidata.org.
  15. [17] . Bioactive Compounds and Antiradical Potential of Campanula medium Lipids. wikidata.org.
  16. [18] . Sterols of seed oils ofVernonia galamensis,Amaranthus cruentus,Amaranthus caudatus,Amaranthus hybridus andAmaranthus hypochondriacus grown in the humid tropics. wikidata.org.
  17. [19] . Sterols of seed oils ofVernonia galamensis,Amaranthus cruentus,Amaranthus caudatus,Amaranthus hybridus andAmaranthus hypochondriacus grown in the humid tropics. wikidata.org.
  18. [20] . Sterols of seed oils ofVernonia galamensis,Amaranthus cruentus,Amaranthus caudatus,Amaranthus hybridus andAmaranthus hypochondriacus grown in the humid tropics. wikidata.org.
  19. [21] . Lipid composition of Evonimus japonicus L., Piracanttia coccinea L. and Amelanchier cannadensis L. seed oils. wikidata.org.
  20. [22] . Sterols in seeds and leaves of oats (Avena sativa L.).. wikidata.org.
  21. [23] . (24R)- and (24S)-24-hydoxy-24-vinyllathosterols and other sterols from the aerial part of Bryonia dioica. wikidata.org.
  22. [24] . Canavalia ensiformis neutral lipids, a rich source of lupeol. wikidata.org.
  23. [25] . Carthami flos extract and its component, stigmasterol, inhibit tumour promotion in mouse skin two-stage carcinogenesis. wikidata.org.
  24. [26] . Lipid composition of Evonimus japonicus L., Piracanttia coccinea L. and Amelanchier cannadensis L. seed oils. wikidata.org.
  25. [27] . Determination of sterol and triterpene alcohol acetates in natural products by reversed-phase liquid chromatography and gas chromatography—mass spectrometry. 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). avenasterol. Retrieved May 3, 2026, from https://4ort.xyz/entity/avenasterol
MLA “avenasterol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/avenasterol.
BibTeX @misc{4ortxyz_avenasterol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{avenasterol}}, year = {2026}, url = {https://4ort.xyz/entity/avenasterol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): avenasterol — https://4ort.xyz/entity/avenasterol (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)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol, (3S,5S,9R,10S,13R,14R,17R)-17-((R,E)-5-Isopropylhept-5-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol, (3S,5R,9S,10S,13R,14S,17S)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
    Subclass of (24E/Z)-avenasterol
    Aliases
    Subclass of
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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