(+)-pinoresinol

chemical compound
ChemicalSubstance type_of_chemical_entity Q3388802
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(+)-pinoresinol

Summary

(+)-pinoresinol is a type of chemical entity[1]. (+)-pinoresinol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (26 views/month).[2]

Key Facts

  • (+)-pinoresinol's instance of is recorded as type of chemical entity[3].
  • (+)-pinoresinol's chemical structure is recorded as Pinoresinol.svg[4].
  • (+)-pinoresinol's CAS Registry Number is recorded as 487-36-5[5].
  • (+)-pinoresinol's canonical SMILES is recorded as OC1=CC=C(C=C1OC)C2OCC3C(OCC23)C4=CC=C(O)C(OC)=C4[6].
  • (+)-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/t13-,14-,19+,20+/m0/s1[7].
  • (+)-pinoresinol's InChIKey is recorded as HGXBRUKMWQGOIE-AFHBHXEDSA-N[8].
  • (+)-pinoresinol's chemical formula is recorded as C₂₀H₂₂O₆[9].
  • (+)-pinoresinol's subclass of is recorded as pinoresinol[10].
  • (+)-pinoresinol's subclass of is recorded as 4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol[11].
  • (+)-pinoresinol's part of is recorded as (+)-pinoresinol metabolic process[12].
  • (+)-pinoresinol's part of is recorded as (+)-pinoresinol catabolic process[13].
  • (+)-pinoresinol's part of is recorded as (+)-pinoresinol biosynthetic process[14].
  • (+)-pinoresinol's part of is recorded as piperitol synthase activity[15].
  • (+)-pinoresinol's Commons category is recorded as Pinoresinol[16].
  • (+)-pinoresinol's has part is recorded as carbon[17].
  • (+)-pinoresinol's has part is recorded as oxygen[18].
  • (+)-pinoresinol's has part is recorded as hydrogen[19].
  • (+)-pinoresinol's ChEMBL ID is recorded as CHEMBL487611[20].
  • (+)-pinoresinol's Freebase ID is recorded as /m/0fqqql0[21].
  • (+)-pinoresinol's UNII is recorded as V4N1UDY811[22].
  • (+)-pinoresinol's PubChem CID is recorded as 73399[23].
  • (+)-pinoresinol's KEGG ID is recorded as C05366[24].
  • (+)-pinoresinol's ChEBI ID is recorded as 40[25].
  • (+)-pinoresinol's found in taxon is recorded as Dendrobium plicatile[26].
  • (+)-pinoresinol's found in taxon is recorded as Forsythia suspensa[27].

Why It Matters

(+)-pinoresinol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (26 views/month).[2] (+)-pinoresinol has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28]

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] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . PubChem. wikidata.org.
  6. [8] . PubChem. wikidata.org.
  7. [9] . PubChem. wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . Gene Ontology release 2019-11-16. wikidata.org.
  11. [13] . Gene Ontology release 2019-11-16. wikidata.org.
  12. [14] . Gene Ontology release 2019-11-16. wikidata.org.
  13. [15] . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . Freebase Data Dumps. wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . 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.
  25. [27] . Phenolic compounds from Forsythia leaves. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . 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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