lariciresinol

chemical compound
ChemicalSubstance type_of_chemical_entity Q6489358
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lariciresinol

Summary

lariciresinol is a type of chemical entity[1]. lariciresinol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (5 views/month).[2]

Key Facts

  • lariciresinol's instance of is recorded as type of chemical entity[3].
  • lariciresinol's chemical structure is recorded as Lariciresinol.svg[4].
  • lariciresinol's CAS Registry Number is recorded as 27003-73-2[5].
  • lariciresinol's EC number is recorded as 694-741-2[6].
  • lariciresinol's canonical SMILES is recorded as COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O[7].
  • lariciresinol's InChI is recorded as InChI=1S/C20H24O6/c1-24-18-8-12(3-5-16(18)22)7-14-11-26-20(15(14)10-21)13-4-6-17(23)19(9-13)25-2/h3-6,8-9,14-15,20-23H,7,10-11H2,1-2H3/t14-,15-,20+/m0/s1[8].
  • lariciresinol's InChIKey is recorded as MHXCIKYXNYCMHY-AUSJPIAWSA-N[9].
  • lariciresinol's chemical formula is recorded as C₂₀H₂₄O₆[10].
  • lariciresinol's subclass of is recorded as 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol[11].
  • lariciresinol's part of is recorded as (+)-lariciresinol metabolic process[12].
  • lariciresinol's part of is recorded as (+)-lariciresinol catabolic process[13].
  • lariciresinol's part of is recorded as (+)-lariciresinol biosynthetic process[14].
  • lariciresinol's ChEMBL ID is recorded as CHEMBL518421[15].
  • lariciresinol's Freebase ID is recorded as /m/0b777fm[16].
  • lariciresinol's UNII is recorded as 73XCE5OZB0[17].
  • lariciresinol's ChemSpider ID is recorded as 294521[18].
  • lariciresinol's PubChem CID is recorded as 332427[19].
  • lariciresinol's KEGG ID is recorded as C10646[20].
  • lariciresinol's ChEBI ID is recorded as 67246[21].
  • lariciresinol's found in taxon is recorded as Taxus wallichiana[22].
  • lariciresinol's found in taxon is recorded as Magnolia denudata[23].
  • lariciresinol's found in taxon is recorded as Hemerocallis fulva[24].
  • lariciresinol's found in taxon is recorded as Daphne feddei[25].
  • lariciresinol's found in taxon is recorded as Arum italicum[26].
  • lariciresinol's found in taxon is recorded as Abies pinsapo[27].

Why It Matters

lariciresinol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (5 views/month).[2] lariciresinol is known by 3 alternative names across languages and contexts.[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] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . 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] . ChEMBL. Retrieved . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] . Q2311683. Retrieved . wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . ChEBI. Retrieved . wikidata.org.
  19. [21] . ChEMBL. Retrieved . wikidata.org.
  20. [22] . Structural and spectroscopic characteristics of two lignans from Taxus baccata L.. wikidata.org.
  21. [23] . Lignan and Neolignan Derivatives from Magnolia denudata.. wikidata.org.
  22. [24] . Lipid peroxidation inhibitory compounds from daylily (Hemerocallis fulva) leaves. wikidata.org.
  23. [25] . Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. wikidata.org.
  24. [26] . Two New Lignan Glucosides from Arum italicum. wikidata.org.
  25. [27] . Lignans from the wood of Abies pinsapo. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata aliases. 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). lariciresinol. Retrieved May 3, 2026, from https://4ort.xyz/entity/lariciresinol
MLA “lariciresinol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/lariciresinol.
BibTeX @misc{4ortxyz_lariciresinol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{lariciresinol}}, year = {2026}, url = {https://4ort.xyz/entity/lariciresinol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): lariciresinol — https://4ort.xyz/entity/lariciresinol (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. 29d ago · KaleemBot bot · 2026-04-30 view diff on Wikidata ↗
    Subclass of 4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol
    Found in taxon Taxus wallichiana, Magnolia denudata, Hemerocallis fulva +110
    Mass {'unit': 'Q483261', 'amount': '+360.157'}
    Part of (+)-lariciresinol metabolic process, (+)-lariciresinol catabolic process, (+)-lariciresinol biosynthetic process
    + 6 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:لاریسی ریسینول]]"
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