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liriodendrin

chemical compound
ChemicalSubstance type_of_chemical_entity Q72487546
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liriodendrin

Summary

liriodendrin is a type of chemical entity[1]. liriodendrin is known by 3 alternative names across languages and contexts.[2]

Key Facts

  • liriodendrin's instance of is recorded as type of chemical entity[3].
  • liriodendrin's chemical structure is recorded as Liriodendrin structure.svg[4].
  • liriodendrin's CAS Registry Number is recorded as 573-44-4[5].
  • liriodendrin's canonical SMILES is recorded as OCC1OC(OC2=C(OC)C=C(C=C2OC)C3OCC4C(OCC34)C5=CC(OC)=C(OC6OC(CO)C(O)C(O)C6O)C(OC)=C5)C(O)C(O)C1O[6].
  • liriodendrin's InChI is recorded as InChI=1S/C34H46O18/c1-43-17-5-13(6-18(44-2)31(17)51-33-27(41)25(39)23(37)21(9-35)49-33)29-15-11-48-30(16(15)12-47-29)14-7-19(45-3)32(20(8-14)46-4)52-34-28(42)26(40)24(38)22(10-36)50-34/h5-8,15-16,21-30,33-42H,9-12H2,1-4H3/t15-,16-,21+,22+,23+,24+,25-,26-,27+,28+,29+,30+,33-,34-/m0/s1[7].
  • liriodendrin's InChIKey is recorded as FFDULTAFAQRACT-XKBSQSBASA-N[8].
  • liriodendrin's chemical formula is recorded as C₃₄H₄₆O₁₈[9].
  • liriodendrin's subclass of is recorded as 2-[4-[(3aR,6aS)-6-[3,5-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol[10].
  • liriodendrin's subclass of is recorded as eleutheroside D[11].
  • liriodendrin's subclass of is recorded as (2S,3S,5S)-2-[4-[(3S,3aR,6S,6aR)-6-[3,5-dimethoxy-4-[(2R,3S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol[12].
  • liriodendrin's subclass of is recorded as (2R,3S,4R,5R,6S)-2-{4-[4-(3,5-dimethoxy-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2,6-dimethoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol[13].
  • liriodendrin's subclass of is recorded as Liriodendrin[14].
  • liriodendrin's subclass of is recorded as Eleutheroside[15].
  • liriodendrin's subclass of is recorded as (2S,3R,4S,5S,6R)-2-[4-[(6S)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol[16].
  • liriodendrin's Freebase ID is recorded as /m/0y7v3mv[17].
  • liriodendrin's UNII is recorded as J2SJ3W6H9R[18].
  • liriodendrin's PubChem CID is recorded as 21603207[19].
  • liriodendrin's found in taxon is recorded as Daphne feddei[20].
  • liriodendrin's found in taxon is recorded as Plumeria rubra[21].
  • liriodendrin's found in taxon is recorded as Porcelia macrocarpa[22].
  • liriodendrin's found in taxon is recorded as Eleutherococcus senticosus[23].
  • liriodendrin's found in taxon is recorded as Annona cherimola[24].
  • liriodendrin's found in taxon is recorded as Cistanche tubulosa[25].
  • liriodendrin's found in taxon is recorded as Coleogyne ramosissima[26].
  • liriodendrin's found in taxon is recorded as Galium sinaicum[27].

Why It Matters

liriodendrin is known by 3 alternative names across languages and contexts.[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] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. wikidata.org.
  19. [21] ↑ . Cytotoxic constituents of the bark of Plumeria rubra collected in Indonesia. wikidata.org.
  20. [22] ↑ . Separação e identificação de constituintes químicos polares dos galhos de Porcelia Macrocarpa. wikidata.org.
  21. [23] ↑ . Phenolic compounds from stem bark of Acanthopanax senticosus and their pharmacological effect in chronic swimming stressed rats. wikidata.org.
  22. [24] ↑ . Lignans and Kauranes from the Stems ofAnnona cherimola. wikidata.org.
  23. [25] ↑ . The constituents of Cistanche tubulosa (Schrenk) Hook. f. II. Isolation and structures of a new phenylethanoid glycoside and a new neolignan glycoside.. wikidata.org.
  24. [26] ↑ . Flavonoid and benzophenone glycosides from Coleogyne ramosissima. wikidata.org.
  25. [27] ↑ . Lignan bis-glucosides from Galium sinaicum. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata aliases. wikidata.org.

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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). liriodendrin. Retrieved May 3, 2026, from https://4ort.xyz/entity/liriodendrin
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BibTeX @misc{4ortxyz_liriodendrin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{liriodendrin}}, year = {2026}, url = {https://4ort.xyz/entity/liriodendrin}, 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. 16d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Stereoisomer of → (2S,3R,4S,5S,6R)-2-[4-[(3S,3aS,6S,6aS)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol, (-)-syringaresinol O,O'-bis(beta-D-glucoside), (2S,3R,4S,5R,6R)-2-[4-[(3S,3aR,6R,6aS)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol +6
    Subclass of → 2-[4-[(3aR,6aS)-6-[3,5-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol, eleutheroside D, (2S,3S,5S)-2-[4-[(3S,3aR,6S,6aR)-6-[3,5-dimethoxy-4-[(2R,3S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol +4
    Aliases → —
    Subclass of → —
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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