pinoresinol

group of stereoisomers with the chemical formula C₂₀H₂₂O₆
ChemicalSubstance group_of_stereoisomers Q104167841
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pinoresinol

Summary

pinoresinol is a group of stereoisomers[1].

Key Facts

  • pinoresinol's instance of is recorded as group of stereoisomers[2].
  • pinoresinol's canonical SMILES is recorded as OC1=CC=C(C=C1OC)C2OCC3C(OCC23)C4=CC=C(O)C(OC)=C4[3].
  • pinoresinol's InChI is recorded as InChI=1S/C20H22O6/c1-23-17-7-11(3-5-15(17)21)19-13-9-26-20(14(13)10-25-19)12-4-6-16(22)18(8-12)24-2/h3-8,13-14,19-22H,9-10H2,1-2H3[4].
  • pinoresinol's InChIKey is recorded as HGXBRUKMWQGOIE-UHFFFAOYSA-N[5].
  • pinoresinol's chemical formula is recorded as C₂₀H₂₂O₆[6].
  • pinoresinol's subclass of is recorded as chemical compound[7].
  • pinoresinol's PubChem CID is recorded as 234817[8].
  • pinoresinol's found in taxon is recorded as Zanthoxylum kellermanii[9].
  • pinoresinol's found in taxon is recorded as Forsythia koreana[10].
  • pinoresinol's found in taxon is recorded as Arnica mollis[11].
  • pinoresinol's found in taxon is recorded as Zanthoxylum ailanthoides[12].
  • pinoresinol's found in taxon is recorded as Helicteres hirsuta[13].
  • pinoresinol's found in taxon is recorded as Forsythia viridissima[14].
  • pinoresinol's found in taxon is recorded as Harrisonia perforata[15].
  • pinoresinol's found in taxon is recorded as Pinus sylvestris[16].
  • pinoresinol's found in taxon is recorded as Saussurea pulchella[17].
  • pinoresinol's found in taxon is recorded as Penstemon gentianoides[18].
  • pinoresinol's found in taxon is recorded as Balanophora harlandii[19].
  • pinoresinol's found in taxon is recorded as Passiflora morifolia[20].
  • pinoresinol's found in taxon is recorded as Q158783[21].
  • pinoresinol's found in taxon is recorded as Uncaria rhynchophylla[22].
  • pinoresinol's found in taxon is recorded as Thuja plicata[23].
  • pinoresinol's found in taxon is recorded as Daphne pseudomezereum[24].
  • pinoresinol's found in taxon is recorded as Daphne oleoides[25].
  • pinoresinol's found in taxon is recorded as Daphne genkwa[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] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . PubChem. Retrieved . wikidata.org.
  8. [9] . New indolopyridoquinazoline, benzo[c]phenanthridines and cytotoxic constituents from Zanthoxylum integrifoliolum. wikidata.org.
  9. [10] . Simultaneous determination of 12 major constituents in Forsythia suspensa by high performance liquid chromatography--DAD method. wikidata.org.
  10. [11] . Lignans from Arnica species. wikidata.org.
  11. [12] . New indolopyridoquinazoline, benzo[c]phenanthridines and cytotoxic constituents from Zanthoxylum integrifoliolum. wikidata.org.
  12. [13] . Cytotoxic lignans from the stems of Helicteres hirsuta collected in Indonesia. wikidata.org.
  13. [14] . Simultaneous determination of 12 major constituents in Forsythia suspensa by high performance liquid chromatography--DAD method. wikidata.org.
  14. [15] . Chemical constituents from fruits of Harrisonia perforata. wikidata.org.
  15. [16] . Phenolic extractives from the bark of Pinus sylvestris L. and their effects on inflammatory mediators nitric oxide and prostaglandin E2.. wikidata.org.
  16. [17] . Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa. wikidata.org.
  17. [18] . Neue iridoidglykoside der gattung penstemon. wikidata.org.
  18. [19] . A new lignan from Balanophora abbreviata and inhibition of lipopolysaccharide (LPS)-induced inducible nitric oxide synthase (iNOS) expression. wikidata.org.
  19. [20] . Cyanogenesis in Passifloraceae. wikidata.org.
  20. [21] . New sesquiterpene lactones from Liriodendron tulipifera. wikidata.org.
  21. [22] . New indole alkaloids from the bark of Nauclea orientalis. wikidata.org.
  22. [23] . Recombinant pinoresinol-lariciresinol reductases from western red cedar (Thuja plicata) catalyze opposite enantiospecific conversions. wikidata.org.
  23. [24] . Inhaltsstoffe von Daphne tangutica. wikidata.org.
  24. [25] . Inhaltsstoffe von Daphne tangutica. wikidata.org.
  25. [26] . Inhaltsstoffe von Daphne tangutica. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). pinoresinol. Retrieved May 3, 2026, from https://4ort.xyz/entity/pinoresinol-q104167841
MLA “pinoresinol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/pinoresinol-q104167841.
BibTeX @misc{4ortxyz_pinoresinol-q104167841_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{pinoresinol}}, year = {2026}, url = {https://4ort.xyz/entity/pinoresinol-q104167841}, note = {Accessed: 2026-05-03}}
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