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saringosterol

chemical compound
ChemicalSubstance group_of_stereoisomers Q15426985
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saringosterol

Summary

saringosterol is a group of stereoisomers[1]. saringosterol draws 4 Wikipedia views per month (group_of_stereoisomers category, ranking #216 of 1,063).[2]

Key Facts

  • saringosterol's instance of is recorded as group of stereoisomers[3].
  • saringosterol's chemical structure is recorded as Saringosterol.svg[4].
  • saringosterol's CAS Registry Number is recorded as 6901-60-6[5].
  • saringosterol's canonical SMILES is recorded as CC(C)C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)(C=C)O[6].
  • saringosterol's InChI is recorded as InChI=1S/C29H48O2/c1-7-29(31,19(2)3)17-12-20(4)24-10-11-25-23-9-8-21-18-22(30)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-8,19-20,22-26,30-31H,1,9-18H2,2-6H3/t20-,22+,23+,24-,25+,26+,27+,28-,29?/m1/s1[7].
  • saringosterol's InChIKey is recorded as OPGVEUGCNGNPSX-SVSQYMGHSA-N[8].
  • saringosterol's chemical formula is recorded as C₂₉H₄₈O₂[9].
  • saringosterol's subclass of is recorded as (10R,13R)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol[10].
  • saringosterol's subclass of is recorded as (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol[11].
  • saringosterol's ChEMBL ID is recorded as CHEMBL252366[12].
  • saringosterol's Freebase ID is recorded as /m/0xphyjt[13].
  • saringosterol's ChemSpider ID is recorded as 24682471[14].
  • saringosterol's PubChem CID is recorded as 14161394[15].
  • saringosterol's found in taxon is recorded as Durvillaea potatorum[16].
  • saringosterol's found in taxon is recorded as Tydemania expeditionis[17].
  • saringosterol's found in taxon is recorded as hijiki[18].
  • saringosterol's found in taxon is recorded as Sargassum[19].
  • saringosterol's found in taxon is recorded as Strychnos spinosa[20].
  • saringosterol's isomeric SMILES is recorded as CC@H[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CCC@@HO)C)CC@H[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CCC@@HO)C)C">[21].
  • saringosterol's LIPID MAPS ID is recorded as LMST01040167[22].
  • saringosterol's mass is recorded as {'unit': 'Q483261', 'amount': '+428.365431'}[23].
  • saringosterol's SureChEMBL ID is recorded as 23567091[24].
  • saringosterol's DSSTox substance ID is recorded as DTXSID001045582[25].
  • saringosterol's Microsoft Academic ID is recorded as 2779770202[26].
  • saringosterol's UniChem compound ID is recorded as 199031[27].

Why It Matters

saringosterol draws 4 Wikipedia views per month (group_of_stereoisomers category, ranking #216 of 1,063).[2]

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] ↑ . 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Q2311683. Retrieved . wikidata.org.
  13. [15] ↑ . PubChem. Retrieved . wikidata.org.
  14. [16] ↑ . Lipids from the bull kelp Durvillaea potatorum. wikidata.org.
  15. [17] ↑ . Steroids with inhibitory activity against the prostate cancer cells and chemical diversity of marine alga Tydemania expeditionis. wikidata.org.
  16. [18] ↑ . 24(S)-Saringosterol from edible marine seaweed Sargassum fusiforme is a novel selective LXRβ agonist.. wikidata.org.
  17. [19] ↑ . Antioxidant, cytotoxic, antitumor, and protective DNA damage metabolites from the red sea brown alga Sargassum sp. wikidata.org.
  18. [20] ↑ . Antitrypanosomal activity of triterpenoids and sterols from the leaves of Strychnos spinosa and related compounds. wikidata.org.
  19. [21] ↑ . PubChem. Retrieved . wikidata.org.
  20. [22] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  21. [23] ↑ . PubChem. Retrieved . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). saringosterol. Retrieved May 3, 2026, from https://4ort.xyz/entity/saringosterol
MLA “saringosterol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/saringosterol.
BibTeX @misc{4ortxyz_saringosterol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{saringosterol}}, year = {2026}, url = {https://4ort.xyz/entity/saringosterol}, note = {Accessed: 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 ↗
    Subclass of → (10R,13R)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol, (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
    Aliases → —
    Subclass of → —
    Instance of → group of stereoisomers
    + 3 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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