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cholest-5-en-3-ol

chemical compound
ChemicalSubstance group_of_stereoisomers Q106040869
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cholest-5-en-3-ol

Summary

cholest-5-en-3-ol is a group of stereoisomers[1].

Key Facts

  • cholest-5-en-3-ol's instance of is recorded as group of stereoisomers[2].
  • cholest-5-en-3-ol's canonical SMILES is recorded as CC(C)CCCC(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C[3].
  • cholest-5-en-3-ol's InChI is recorded as InChI=1S/C27H46O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h9,18-19,21-25,28H,6-8,10-17H2,1-5H3/t19-,21?,22+,23-,24+,25+,26+,27-/m1/s1[4].
  • cholest-5-en-3-ol's InChIKey is recorded as HVYWMOMLDIMFJA-FNOPAARDSA-N[5].
  • cholest-5-en-3-ol's chemical formula is recorded as C₂₇H₄₆O[6].
  • cholest-5-en-3-ol's subclass of is recorded as (8xi,9xi,10xi,14xi,17xi,20xi)-Cholest-5-en-3-ol[7].
  • cholest-5-en-3-ol's PubChem CID is recorded as 11025495[8].
  • cholest-5-en-3-ol's KEGG ID is recorded as C00187[9].
  • cholest-5-en-3-ol's ChEBI ID is recorded as 138486[10].
  • cholest-5-en-3-ol's found in taxon is recorded as Caenorhabditis elegans[11].
  • cholest-5-en-3-ol's isomeric SMILES is recorded as [H][C@@]12CCC@H[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2CC(O)CC[C@]12CC@H[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2CC(O)CC[C@]12C">[12].
  • cholest-5-en-3-ol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+386.35486609199995'}[13].
  • cholest-5-en-3-ol's SureChEMBL ID is recorded as 2157[14].
  • cholest-5-en-3-ol's DSSTox substance ID is recorded as DTXSID40859019[15].
  • cholest-5-en-3-ol's UniChem compound ID is recorded as 1174384[16].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . ChEBI release 2021-03-01. wikidata.org.
  4. [5] ↑ . ChEBI release 2021-03-01. wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . ChEBI release 2021-03-01. wikidata.org.
  8. [9] ↑ . Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism. wikidata.org.
  9. [10] ↑ . ChEBI release 2021-03-01. wikidata.org.
  10. [11] ↑ . Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . 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). cholest-5-en-3-ol. Retrieved May 3, 2026, from https://4ort.xyz/entity/cholest-5-en-3-ol
MLA “cholest-5-en-3-ol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cholest-5-en-3-ol.
BibTeX @misc{4ortxyz_cholest-5-en-3-ol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cholest-5-en-3-ol}}, year = {2026}, url = {https://4ort.xyz/entity/cholest-5-en-3-ol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cholest-5-en-3-ol — https://4ort.xyz/entity/cholest-5-en-3-ol (retrieved 2026-05-03)

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