vicianin

chemical compound
Class type of: Lucuminoside Q6609212

Facts

8 properties
Instance of
type of chemical entity
Subclass of
Lucuminoside
Canonical SMILES
C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(C#N)C3=CC=CC=C3)O)O)O)O)O)O
Chemical formula
C₁₉H₂₅NO₁₀
Isomeric SMILES
C1[C@@H]([C@@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)O[C@@H](C#N)C3=CC=CC=C3)O)O)O)O)O)O
Mass
+427.147846
Stereoisomer of
(R)-vicianin, (2S)-2-phenyl-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyacetonitrile, Epilucumin, lucumin
🏷️ Also known as
en vicianin fa ویسیانین fr Vicianine ja ビシアニン
🔖 Identifiers · 14
CAS Registry Number
155-57-7
ChEBI ID
166510
ChemSpider ID
570879
DSSTOX compound identifier
DTXCID901363749
DSSTox substance ID
DTXSID70935113
Freebase ID
/m/0bwg0b1
KEGG ID
C01870
Microsoft Academic ID (discontinued)
2779267519
PubChem CID
656493
SureChEMBL ID
17387703
Show all 14 identifiers +2
UniChem compound ID
1072360

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🔗 Connections
Found in taxon 3
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Summary

vicianin is a type of chemical entity[1].

Key Facts

  • Canonical SMILES: C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(C#N)C3=CC=CC=C3)O)O)O)O)O)O[2]
  • Chemical formula: C₁₉H₂₅NO₁₀[3]
  • Subclass of: Lucuminoside[4]
  • Found in taxon: Davallia trichomanoides[5], Gerbera jamesonii[6], Vicia sativa[7]
  • Isomeric SMILES: C1C@@HOC@@HO">[8]
  • Mass: 427.147846 dalton[9]
  • Stereoisomer of: (R)-vicianin[10], (2S)-2-phenyl-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyacetonitrile[11], Epilucumin[12], lucumin[13]

References

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

Direct Wikidata claims

  1. [2] ↑ . PubChem. Retrieved . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . Identification of (R)-Vicianin in Davallia trichomanoides Blume. wikidata.org.
  5. [6] ↑ . Cyanogenic glycosides and 4-hydroxycoumarin glycosides from Gerbera jamesonii hybrida.. wikidata.org.
  6. [7] ↑ . Vicianin, prunasin, and beta-cyanoalanine in common vetch seed as sources of urinary thiocyanate in the rat.. wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). vicianin. Retrieved November 8, 2026, from https://4ort.xyz/entity/vicianin
MLA “vicianin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 8 Nov. 2026, https://4ort.xyz/entity/vicianin.
BibTeX @misc{4ortxyz_vicianin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{vicianin}}, year = {2026}, url = {https://4ort.xyz/entity/vicianin}, note = {Accessed: 2026-11-08}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): vicianin — https://4ort.xyz/entity/vicianin (retrieved 2026-11-08)

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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. 26w ago · Marbletan · 2026-05-14 view diff on Wikidata ↗
    Chemical structure → Vicianin 2.svg
    "Created claim: Chemical structure: Vicianin 2.svg"
  2. 27w ago · KaleemBot bot · 2026-05-02 view diff on Wikidata ↗
    Found in taxon → Davallia trichomanoides, Gerbera jamesonii, Vicia sativa
    Instance of → type of chemical entity
    Subclass of → Lucuminoside
    Mass → 427.147846 dalton
    + 1 other property edited (see Wikidata diff for full list)
    "Changed the item: Added ur:ویسیانن"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.