(+)-pinoresinol

chemical compound
ChemicalSubstance type_of_chemical_entity Q3388802
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(+)-pinoresinol

Summary

(+)-pinoresinol is a type of chemical entity[1]. (+)-pinoresinol has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • (+)-pinoresinol's instance of is recorded as type of chemical entity[3].
  • (+)-pinoresinol's canonical SMILES is recorded as OC1=CC=C(C=C1OC)C2OCC3C(OCC23)C4=CC=C(O)C(OC)=C4[4].
  • (+)-pinoresinol's chemical formula is recorded as C₂₀H₂₂O₆[5].
  • (+)-pinoresinol is a type of pinoresinol[6].
  • (+)-pinoresinol is a type of 4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol[7].
  • (+)-pinoresinol is part of (+)-pinoresinol metabolic process[8].
  • (+)-pinoresinol is part of (+)-pinoresinol catabolic process[9].
  • (+)-pinoresinol is part of (+)-pinoresinol biosynthetic process[10].
  • (+)-pinoresinol is part of piperitol synthase activity[11].
  • (+)-pinoresinol's Commons category is recorded as Pinoresinol[12].
  • (+)-pinoresinol comprises carbon[13].
  • (+)-pinoresinol comprises oxygen[14].
  • (+)-pinoresinol comprises hydrogen[15].
  • (+)-pinoresinol's found in taxon is recorded as Dendrobium plicatile[16].
  • (+)-pinoresinol's found in taxon is recorded as Forsythia suspensa[17].
  • (+)-pinoresinol's found in taxon is recorded as Forsythia koreana[18].
  • (+)-pinoresinol's found in taxon is recorded as Doliocarpus dentatus[19].
  • (+)-pinoresinol's found in taxon is recorded as Balanophora abbreviata[20].
  • (+)-pinoresinol's found in taxon is recorded as Enterococcus faecalis[21].
  • (+)-pinoresinol's found in taxon is recorded as Goniothalamus amuyon[22].
  • (+)-pinoresinol's found in taxon is recorded as Helicteres angustifolia[23].
  • (+)-pinoresinol's found in taxon is recorded as Peperomia leptostachya[24].
  • (+)-pinoresinol's found in taxon is recorded as Saussurea medusa[25].
  • (+)-pinoresinol's found in taxon is recorded as Tarenna attenuata[26].
  • (+)-pinoresinol's found in taxon is recorded as Diplospora dubia[27].

Why It Matters

(+)-pinoresinol has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[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] . PubChem. wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Gene Ontology release 2019-11-16. wikidata.org.
  7. [9] . Gene Ontology release 2019-11-16. wikidata.org.
  8. [10] . Gene Ontology release 2019-11-16. wikidata.org.
  9. [11] . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . Constituents of Ephemerantha fimbriata. Isolation and Structure Elucidation of Two New Phenanthrenes, Fimbriol-A and Fimbriol-B, and a New Dihydrophenanthrene, Ephemeranthol-C.. wikidata.org.
  15. [17] . Phenolic compounds from Forsythia leaves. wikidata.org.
  16. [18] . Phenolic compounds from Forsythia leaves. wikidata.org.
  17. [19] . Isolation of leishmanicidal triterpenes and lignans from the Amazonian liana Doliocarpus dentatus (dilleniaceae). wikidata.org.
  18. [20] . A new lignan from Balanophora abbreviata and inhibition of lipopolysaccharide (LPS)-induced inducible nitric oxide synthase (iNOS) expression. wikidata.org.
  19. [21] . Biotransformation of Pinoresinol Diglucoside to Mammalian Lignans by Human Intestinal Microflora, and Isolation of Enterococcus faecalis Strain PDG-1 Responsible for the Transformation of (+)-Pinoresinol to (+)-Lariciresinol. wikidata.org.
  20. [22] . Cytotoxic Styrylpyrones from Goniothalamus amuyon. wikidata.org.
  21. [23] . Pregnane, coumarin and lupane derivatives and cytotoxic constituents from Helicteres angustifolia. wikidata.org.
  22. [24] . Chemical and cytotoxic constituents from Peperomia sui. wikidata.org.
  23. [25] . Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa. wikidata.org.
  24. [26] . Mixed lignan-neolignans from Tarenna attenuata. wikidata.org.
  25. [27] . Rearranged ent-kauranes from the stems of Tricalysia dubia and their biological activities. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. 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). (+)-pinoresinol. Retrieved May 3, 2026, from https://4ort.xyz/entity/pinoresinol
MLA “(+)-pinoresinol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/pinoresinol.
BibTeX @misc{4ortxyz_pinoresinol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(+)-pinoresinol}}, year = {2026}, url = {https://4ort.xyz/entity/pinoresinol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (+)-pinoresinol — https://4ort.xyz/entity/pinoresinol (retrieved 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. 21d ago · FlocciNivis · 2026-06-25 view diff on Wikidata ↗
    Pdb ligand id GEC
    "/* wbcreateclaim-create:1| */ [[Property:P3636]]: GEC, [[:toollabs:quickstatements/#/batch/259826|batch #259826]]"
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