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eriocitrin

chemical compound
Class type of: flavanone Q13567664

Facts

8 properties
Instance of
type of chemical entity
Subclass of
flavanone
Canonical SMILES
CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O
Chemical formula
C₂₇H₃₂O₁₅
Found in taxon
Satureja montana, citron, Citrus sudachi, Citrus grandis, Citrus hystrix, Citrus jambhiri, Citrus latipes, Citrus longispina, Citrus macrophylla, Citrus shunkokan, Citrus sulcata, Citrus unshiu, Lycopus europaeus, Mentha piperita, Mentha piperita piperita, Citrus wilsonii, Cyclopia falcata, Cyclopia subternata, Salvia, Citrus × paradisi, Foeniculum vulgare, pomelo, Citrus reticulata, Citrus × deliciosa, kumquat, Salvia officinalis, Citrus japonica
Isomeric SMILES
C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC3=CC(=C4C(=O)C[C@H](OC4=C3)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O
Mass
+596.174
Stereoisomer of
(2R)-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one
🏷️ Also known as
en eriocitrin en Eriodictioside fr Ériocitrine it eriocitrina ja エリオシトリン ru Эриоцитрин

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🔗 Connections
Found in taxon 19
Foeniculum vulgare, Citrus reticulata, pomelo, Citrus × paradisi, citron, Salvia, Salvia officinalis, kumquat +11 more
Subclass of 1
flavanone
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Summary

eriocitrin is a type of chemical entity[1]. eriocitrin is a type of flavanone[2].

Key Facts

  • Canonical SMILES: CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O[3]
  • Chemical formula: C₂₇H₃₂O₁₅[4]
  • Found in taxon: Satureja montana[5], Citrus medica[6], Citrus sudachi[7], Citrus grandis[8], Citrus hystrix[9], Citrus jambhiri[10], Citrus latipes[11], Citrus longispina[12], Citrus macrophylla[13], Citrus shunkokan[14], Citrus sulcata[15], Citrus unshiu[16], Lycopus europaeus[17], Mentha piperita[18]
  • Isomeric SMILES: C[C@H]1C@@HOC@@HO">[19]
  • Mass: 596.174 dalton[20]
  • Stereoisomer of: (2R)-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one[21]

References

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

Direct Wikidata claims

  1. [3] ↑ . PubChem. Retrieved . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [2] ↑ . wikidata.org.
  4. [5] ↑ . Secondary Metabolites from Satureja Species. New Triterpenoid from Satureja acinos. wikidata.org.
  5. [6] ↑ . Chemical constituents from the peels of Citrus sudachi. wikidata.org.
  6. [7] ↑ . Chemical constituents from the peels of Citrus sudachi. wikidata.org.
  7. [8] ↑ . Phenolic composition of various tissues of rutaceae species. wikidata.org.
  8. [9] ↑ . Limonoid and flavonoid composition in varieties of Papeda and Papedocitrus. wikidata.org.
  9. [10] ↑ . Phenolic composition of various tissues of rutaceae species. wikidata.org.
  10. [11] ↑ . Limonoid and flavonoid composition in varieties of Papeda and Papedocitrus. wikidata.org.
  11. [12] ↑ . Phenolic composition of various tissues of rutaceae species. wikidata.org.
  12. [13] ↑ . Limonoid and flavonoid composition in varieties of Papeda and Papedocitrus. wikidata.org.
  13. [14] ↑ . Phenolic composition of various tissues of rutaceae species. wikidata.org.
  14. [15] ↑ . Phenolic composition of various tissues of rutaceae species. wikidata.org.
  15. [16] ↑ . High-performance liquid chromatographic determination of naturally occurring flavonoids in Citrus with a photodiode-array detector. wikidata.org.
  16. [17] ↑ . Flavonoid glycosides from Lycopus europaeus. wikidata.org.
  17. [18] ↑ . Analysis and Distribution of Flavonoid Glycosides and Rosmarinic Acid in 40 Mentha x piperita Clones. wikidata.org.
  18. [19] ↑ . PubChem. Retrieved . wikidata.org.
  19. [20] ↑ . PubChem. Retrieved . wikidata.org.
  20. [21] ↑ . 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). eriocitrin. Retrieved November 8, 2026, from https://4ort.xyz/entity/eriocitrin
MLA “eriocitrin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 8 Nov. 2026, https://4ort.xyz/entity/eriocitrin.
BibTeX @misc{4ortxyz_eriocitrin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{eriocitrin}}, year = {2026}, url = {https://4ort.xyz/entity/eriocitrin}, note = {Accessed: 2026-11-08}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): eriocitrin — https://4ort.xyz/entity/eriocitrin (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. 20w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of → (2R)-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3
    Instance of → type of chemical entity
    Found in taxon → Satureja montana, citron, Citrus sudachi +1
    Subclass of → flavanone
    + 1 other property edited (see Wikidata diff for full list)
    "Changed [tr] labels, descriptions or aliases: QuickStatements 3.0 batch #37300"
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