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5-Dehydroavenasterol

chemical compound
ChemicalSubstance group_of_stereoisomers Q27149247
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5-Dehydroavenasterol

Summary

5-Dehydroavenasterol is a group of stereoisomers[1].

Key Facts

  • 5-Dehydroavenasterol's instance of is recorded as group of stereoisomers[2].
  • 5-Dehydroavenasterol's canonical SMILES is recorded as CC=C(CCC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C)C(C)C[3].
  • 5-Dehydroavenasterol's InChI is recorded as InChI=1S/C29H46O/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/h7,10-11,19-20,23,25-27,30H,8-9,12-18H2,1-6H3/b21-7-/t20-,23+,25?,26?,27?,28+,29-/m1/s1[4].
  • 5-Dehydroavenasterol's InChIKey is recorded as XPRWWANUPMYKMF-UUHDPGOWSA-N[5].
  • 5-Dehydroavenasterol's chemical formula is recorded as C₂₉H₄₆O[6].
  • 5-Dehydroavenasterol's subclass of is recorded as stigmastan-type steroid[7].
  • 5-Dehydroavenasterol's ChemSpider ID is recorded as 30792036[8].
  • 5-Dehydroavenasterol's PubChem CID is recorded as 23724575[9].
  • 5-Dehydroavenasterol's KEGG ID is recorded as C15783[10].
  • 5-Dehydroavenasterol's ChEBI ID is recorded as 80097[11].
  • 5-Dehydroavenasterol's found in taxon is recorded as Vernonia galamensis[12].
  • 5-Dehydroavenasterol's isomeric SMILES is recorded as C/C=C(/CCC@@HC1CCC2[C@@]1(CCC3C2=CC=C4[C@@]3(CCC@@HO)C)C)\C(C)CC@@HC1CCC2[C@@]1(CCC3C2=CC=C4[C@@]3(CCC@@HO)C)C)\C(C)C">[13].
  • 5-Dehydroavenasterol's KNApSAcK ID is recorded as C00007527[14].
  • 5-Dehydroavenasterol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+410.355'}[15].
  • 5-Dehydroavenasterol's SureChEMBL ID is recorded as 13324302[16].
  • 5-Dehydroavenasterol's UniChem compound ID is recorded as 1066352[17].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . Q2311683. Retrieved . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . ChEBI. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . Sterols of seed oils ofVernonia galamensis,Amaranthus cruentus,Amaranthus caudatus,Amaranthus hybridus andAmaranthus hypochondriacus grown in the humid tropics. wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . ChEBI. Retrieved . wikidata.org.
  14. [15] ↑ . PubChem. Retrieved . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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). 5-Dehydroavenasterol. Retrieved May 3, 2026, from https://4ort.xyz/entity/5-dehydroavenasterol
MLA “5-Dehydroavenasterol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/5-dehydroavenasterol.
BibTeX @misc{4ortxyz_5-dehydroavenasterol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{5-Dehydroavenasterol}}, year = {2026}, url = {https://4ort.xyz/entity/5-dehydroavenasterol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 5-Dehydroavenasterol — https://4ort.xyz/entity/5-dehydroavenasterol (retrieved 2026-05-03)

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