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sitogluside

chemical compound
ChemicalSubstance type_of_chemical_entity Q15410900
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sitogluside

Summary

sitogluside is a type of chemical entity[1]. sitogluside ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (9 views/month).[2]

Key Facts

  • sitogluside's instance of is recorded as type of chemical entity[3].
  • sitogluside's chemical structure is recorded as Eleutheroside A.svg[4].
  • sitogluside's CAS Registry Number is recorded as 474-58-8[5].
  • sitogluside's canonical SMILES is recorded as CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C[6].
  • sitogluside's InChI is recorded as InChI=1S/C35H60O6/c1-7-22(20(2)3)9-8-21(4)26-12-13-27-25-11-10-23-18-24(14-16-34(23,5)28(25)15-17-35(26,27)6)40-33-32(39)31(38)30(37)29(19-36)41-33/h10,20-22,24-33,36-39H,7-9,11-19H2,1-6H3/t21-,22-,24+,25+,26-,27+,28+,29-,30-,31+,32-,33-,34+,35-/m1/s1[7].
  • sitogluside's InChIKey is recorded as NPJICTMALKLTFW-OFUAXYCQSA-N[8].
  • sitogluside's chemical formula is recorded as C₃₅H₆₀O₆[9].
  • sitogluside's subclass of is recorded as eleutheroside[10].
  • sitogluside's subclass of is recorded as (2R,3R,4S,5S,6R)-2-[[(8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol[11].
  • sitogluside's subclass of is recorded as Sitosteryl glucoside[12].
  • sitogluside's part of is recorded as beta-sitosterol UDP-glucosyltransferase activity[13].
  • sitogluside's ChEMBL ID is recorded as CHEMBL506678[14].
  • sitogluside's Freebase ID is recorded as /m/0yp0gx2[15].
  • sitogluside's UNII is recorded as U45VN859W3[16].
  • sitogluside's ChemSpider ID is recorded as 4674825[17].
  • sitogluside's PubChem CID is recorded as 5742590[18].
  • sitogluside's KEGG ID is recorded as D05848[19].
  • sitogluside's ChEBI ID is recorded as 67554[20].
  • sitogluside's found in taxon is recorded as Cynomorium songaricum[21].
  • sitogluside's found in taxon is recorded as Solanum crispum[22].
  • sitogluside's found in taxon is recorded as Croton urucurana[23].
  • sitogluside's found in taxon is recorded as Verbena officinalis[24].
  • sitogluside's found in taxon is recorded as Catha edulis[25].
  • sitogluside's found in taxon is recorded as Mimosa tenuiflora[26].
  • sitogluside's found in taxon is recorded as Panax ginseng[27].

Why It Matters

sitogluside ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (9 views/month).[2] sitogluside is known by 12 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] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: 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] ↑ . wikidata.org.
  11. [13] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  12. [14] ↑ . ChEMBL. Retrieved . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] ↑ . Q2311683. Retrieved . wikidata.org.
  16. [18] ↑ . PubChem. Retrieved . wikidata.org.
  17. [19] ↑ . ChEBI. Retrieved . wikidata.org.
  18. [20] ↑ . ChEMBL. Retrieved . wikidata.org.
  19. [21] ↑ . Inhibitory effects of ursolic acid derivatives from Cynomorium songaricum, and related triterpenes on human immunodeficiency viral protease. wikidata.org.
  20. [22] ↑ . Antipyretic, hypothermic and antiinflammatory activities and metabolites fromSolanum ligustrinum Lood.. wikidata.org.
  21. [23] ↑ . Analgesic compounds ofCroton urucurana Baillon. Pharmaco-chemical criteria used in their isolation. wikidata.org.
  22. [24] ↑ . Antiinflammatory activity and chemical composition of extracts of Verbena officinalis. wikidata.org.
  23. [25] ↑ . Steroidal alkaloids. wikidata.org.
  24. [26] ↑ . Pharmacognosy of Mimosa tenuiflora (Willd.) Poiret. wikidata.org.
  25. [27] ↑ . Chemical Studies on Crude Drug Precession. I. On the Constituents of Ginseng Radix Rubra (1). 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). sitogluside. Retrieved May 3, 2026, from https://4ort.xyz/entity/sitogluside
MLA “sitogluside.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/sitogluside.
BibTeX @misc{4ortxyz_sitogluside_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{sitogluside}}, year = {2026}, url = {https://4ort.xyz/entity/sitogluside}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): sitogluside — https://4ort.xyz/entity/sitogluside (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. 14d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Stereoisomer of → Glucoclionasterol, (2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol, (2R,3R,4S,5S,6R)-2-[[(3R,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol +15
    Subclass of → eleutheroside, (2R,3R,4S,5S,6R)-2-[[(8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol, Sitosteryl glucoside
    Drugbank id → DB21240
    Part of → beta-sitosterol UDP-glucosyltransferase activity
    + 7 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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