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syringaresinol

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q27121534
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syringaresinol

Summary

syringaresinol is a group of stereoisomers[1].

Key Facts

  • syringaresinol's instance of is recorded as group of stereoisomers[2].
  • syringaresinol's chemical structure is recorded as Syringaresinol.svg[3].
  • syringaresinol's canonical SMILES is recorded as COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC[4].
  • syringaresinol's InChI is recorded as InChI=1S/C22H26O8/c1-25-15-5-11(6-16(26-2)19(15)23)21-13-9-30-22(14(13)10-29-21)12-7-17(27-3)20(24)18(8-12)28-4/h5-8,13-14,21-24H,9-10H2,1-4H3[5].
  • syringaresinol's InChIKey is recorded as KOWMJRJXZMEZLD-UHFFFAOYSA-N[6].
  • syringaresinol's chemical formula is recorded as C₂₂H₂₆O₈[7].
  • syringaresinol's subclass of is recorded as lignan[8].
  • syringaresinol's ChemSpider ID is recorded as 90423[9].
  • syringaresinol's PubChem CID is recorded as 100067[10].
  • syringaresinol's ChEBI ID is recorded as 49211[11].
  • syringaresinol's found in taxon is recorded as Ficus septica[12].
  • syringaresinol's found in taxon is recorded as Aspidosperma marcgravianum[13].
  • syringaresinol's found in taxon is recorded as Eleutherococcus sessiliflorus[14].
  • syringaresinol's found in taxon is recorded as Syringa vulgaris[15].
  • syringaresinol's found in taxon is recorded as Chrysanthemum indicum[16].
  • syringaresinol's found in taxon is recorded as Actinidia chinensis[17].
  • syringaresinol's found in taxon is recorded as Asparagus officinalis[18].
  • syringaresinol's found in taxon is recorded as Avena sativa[19].
  • syringaresinol's found in taxon is recorded as Cucumis sativus[20].
  • syringaresinol's found in taxon is recorded as Fagopyrum esculentum[21].
  • syringaresinol's found in taxon is recorded as Fragaria[22].
  • syringaresinol's found in taxon is recorded as Hordeum vulgare[23].
  • syringaresinol's found in taxon is recorded as Linum usitatissimum[24].
  • syringaresinol's found in taxon is recorded as Raphanus sativus var. sativus[25].
  • syringaresinol's found in taxon is recorded as Ribes nigrum[26].

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] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . Q2311683. Retrieved . wikidata.org.
  9. [10] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . Non-Alkaloidal Constituents from the Stem ofFicus Septica. wikidata.org.
  12. [13] ↑ . Alkaloid studies—LVIII: The alkaloids of six Aspidosperma species. wikidata.org.
  13. [14] ↑ . Enantioselective induction of SIRT1 gene by syringaresinol from Panax ginseng berry and Acanthopanax senticosus Harms stem. wikidata.org.
  14. [15] ↑ . Syringaresinol induces mitochondrial biogenesis through activation of PPARβ pathway in skeletal muscle cells. wikidata.org.
  15. [16] ↑ . Chemical constituents from flowers of Chrysanthemum indicum. wikidata.org.
  16. [17] ↑ . Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry. wikidata.org.
  17. [18] ↑ . Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry. wikidata.org.
  18. [19] ↑ . Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry. wikidata.org.
  19. [20] ↑ . Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry. wikidata.org.
  20. [21] ↑ . Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry. wikidata.org.
  21. [22] ↑ . Content, composition, and stereochemical characterisation of lignans in berries and seeds. wikidata.org.
  22. [23] ↑ . Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry. wikidata.org.
  23. [24] ↑ . Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry. wikidata.org.
  24. [25] ↑ . Quantification of lignans in food using isotope dilution gas chromatography/mass spectrometry. wikidata.org.
  25. [26] ↑ . Content, composition, and stereochemical characterisation of lignans in berries and seeds. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). syringaresinol. Retrieved May 3, 2026, from https://4ort.xyz/entity/syringaresinol
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BibTeX @misc{4ortxyz_syringaresinol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{syringaresinol}}, year = {2026}, url = {https://4ort.xyz/entity/syringaresinol}, note = {Accessed: 2026-05-03}}
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