ε-viniferin

chemical compound
ChemicalSubstance type_of_chemical_entity Q5383943
Press Enter · cited answer in seconds

ε-viniferin

Summary

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

Key Facts

  • ε-viniferin's instance of is recorded as type of chemical entity[3].
  • ε-viniferin's chemical structure is recorded as Epsilon-viniferin.svg[4].
  • ε-viniferin's CAS Registry Number is recorded as 62218-08-0[5].
  • ε-viniferin's canonical SMILES is recorded as C1=CC(=CC=C1C=CC2=CC(=CC3=C2C(C(O3)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O)O[6].
  • ε-viniferin's InChI is recorded as InChI=1S/C28H22O6/c29-20-7-2-16(3-8-20)1-4-18-11-24(33)15-25-26(18)27(19-12-22(31)14-23(32)13-19)28(34-25)17-5-9-21(30)10-6-17/h1-15,27-33H/b4-1+/t27-,28+/m1/s1[7].
  • ε-viniferin's InChIKey is recorded as FQWLMRXWKZGLFI-YVYUXZJTSA-N[8].
  • ε-viniferin's chemical formula is recorded as C₂₈H₂₂O₆[9].
  • ε-viniferin's subclass of is recorded as biogenic benzofuran[10].
  • ε-viniferin's Commons category is recorded as Epsilon-Viniferin[11].
  • ε-viniferin's ChEMBL ID is recorded as CHEMBL1224875[12].
  • ε-viniferin's Freebase ID is recorded as /m/080hghk[13].
  • ε-viniferin's UNII is recorded as 0K8Z2K6Y7O[14].
  • ε-viniferin's ChemSpider ID is recorded as 4445043[15].
  • ε-viniferin's PubChem CID is recorded as 5281728[16].
  • ε-viniferin's KEGG ID is recorded as C10289[17].
  • ε-viniferin's ChEBI ID is recorded as 10556[18].
  • ε-viniferin's found in taxon is recorded as Carex kobomugi[19].
  • ε-viniferin's found in taxon is recorded as Dipterocarpus grandiflorus[20].
  • ε-viniferin's found in taxon is recorded as Upuna borneensis[21].
  • ε-viniferin's found in taxon is recorded as Vitis vinifera[22].
  • ε-viniferin's found in taxon is recorded as Gnetum parvifolium[23].
  • ε-viniferin's found in taxon is recorded as Rheum coreanum[24].
  • ε-viniferin's found in taxon is recorded as Sophora leachiana[25].
  • ε-viniferin's found in taxon is recorded as Sophora alopecuroides[26].
  • ε-viniferin's found in taxon is recorded as Vitis coignetiae[27].

Why It Matters

ε-viniferin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (6 views/month).[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] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . ChEMBL. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] . Q2311683. Retrieved . wikidata.org.
  14. [16] . PubChem. Retrieved . wikidata.org.
  15. [17] . ChEBI. Retrieved . wikidata.org.
  16. [18] . ChEMBL. Retrieved . wikidata.org.
  17. [19] . Oligostilbenes from Carex kobomugi. wikidata.org.
  18. [20] . Two New Resveratrol (=5-[(1E)-2-(4-Hydroxyphenyl)ethenyl]benzene-1,3-diol) Tetramers with a Tetrahydrofuran Ring fromDipterocarpus grandiflorus. wikidata.org.
  19. [21] . Resveratrol derivatives from Upuna borneensis. wikidata.org.
  20. [22] . 3-Hydroxy-3-methylglutaryl-CoA (HMG-CoA) reductase inhibitory effect of Vitis vinifera. wikidata.org.
  21. [23] . A dimeric stilbene from Gnetum parvifolium. wikidata.org.
  22. [24] . Inhibition of human low density lipoprotein and high density lipoprotein oxidation by oligostilbenes from rhubarb. wikidata.org.
  23. [25] . A flavonostilbene and two stilbene oligomers in roots of Sophora leachiana. wikidata.org.
  24. [26] . Six flavonostilbenes and a flavanone in roots of Sophora alopecuroides. wikidata.org.
  25. [27] . Vitisin A and cis-vitisin A, strongly hepatotoxic plant oligostilbenes from Vitis coignetiae (Vitaceae). wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). ε-viniferin. Retrieved May 3, 2026, from https://4ort.xyz/entity/viniferin
MLA “ε-viniferin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/viniferin.
BibTeX @misc{4ortxyz_viniferin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{ε-viniferin}}, year = {2026}, url = {https://4ort.xyz/entity/viniferin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): ε-viniferin — https://4ort.xyz/entity/viniferin (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/viniferin · Last refreshed:

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 · KaleemBot bot · 2026-04-30 view diff on Wikidata ↗
    Subclass of biogenic benzofuran
    Found in taxon Carex kobomugi, Dipterocarpus grandiflorus, Upuna borneensis +34
    Mass {'unit': 'Q483261', 'amount': '+454.141638'}
    Stereoisomer of (2R,3S)-cis-epsilon-viniferin, (+)-ε-viniferin, (Z)-ε-viniferin +5
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:ایپسیلون-وینیفرین]]"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.