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α-viniferin

chemical compound
ChemicalSubstance type_of_chemical_entity Q4734921
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α-viniferin

Summary

α-viniferin is a type of chemical entity[1]. α-viniferin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 views/month).[2]

Key Facts

  • α-viniferin's instance of is recorded as type of chemical entity[3].
  • α-viniferin's chemical structure is recorded as Alpha-viniferin.svg[4].
  • α-viniferin's CAS Registry Number is recorded as 62218-13-7[5].
  • α-viniferin's canonical SMILES is recorded as C1=CC(=CC=C1C2C3C4=CC(=CC5=C4C(C(O5)C6=CC=C(C=C6)O)C7=CC(=CC8=C7C(C(O8)C9=CC=C(C=C9)O)C1=CC(=CC(=C31)O2)O)O)O)O[6].
  • α-viniferin's InChI is recorded as InChI=1S/C42H30O9/c43-22-7-1-19(2-8-22)40-37-28-13-25(46)17-32-35(28)39(42(50-32)21-5-11-24(45)12-6-21)30-15-27(48)18-33-36(30)38(29-14-26(47)16-31(49-40)34(29)37)41(51-33)20-3-9-23(44)10-4-20/h1-18,37-48H/t37-,38-,39+,40+,41+,42-/m1/s1[7].
  • α-viniferin's InChIKey is recorded as KUTVNHOAKHJJFL-ZSIJVUTGSA-N[8].
  • α-viniferin's chemical formula is recorded as C₄₂H₃₀O₉[9].
  • α-viniferin's subclass of is recorded as alpha-Viniferin[10].
  • α-viniferin's ChEMBL ID is recorded as CHEMBL443463[11].
  • α-viniferin's Freebase ID is recorded as /m/0807t5n[12].
  • α-viniferin's UNII is recorded as 53XER6FHLX[13].
  • α-viniferin's ChemSpider ID is recorded as 333272[14].
  • α-viniferin's PubChem CID is recorded as 196402[15].
  • α-viniferin's ChEBI ID is recorded as 66359[16].
  • α-viniferin's found in taxon is recorded as Caragana rosea[17].
  • α-viniferin's found in taxon is recorded as Caragana brevifolia[18].
  • α-viniferin's found in taxon is recorded as Caragana stenophylla[19].
  • α-viniferin's found in taxon is recorded as Caragana korshinskii[20].
  • α-viniferin's found in taxon is recorded as Caragana leucophloea[21].
  • α-viniferin's found in taxon is recorded as Caragana sinica[22].
  • α-viniferin's found in taxon is recorded as Dipterocarpus grandiflorus[23].
  • α-viniferin's found in taxon is recorded as Carex humilis[24].
  • α-viniferin's found in taxon is recorded as Iris clarkei[25].
  • α-viniferin's found in taxon is recorded as Shorea hemsleyana[26].
  • α-viniferin's found in taxon is recorded as Sophora davidii[27].

Why It Matters

α-viniferin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 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] ↑ . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . PubChem. 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] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis. wikidata.org.
  16. [18] ↑ . Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis. wikidata.org.
  17. [19] ↑ . Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis. wikidata.org.
  18. [20] ↑ . Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis. wikidata.org.
  19. [21] ↑ . Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis. wikidata.org.
  20. [22] ↑ . Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis. wikidata.org.
  21. [23] ↑ . Two New Resveratrol (=5-[(1E)-2-(4-Hydroxyphenyl)ethenyl]benzene-1,3-diol) Tetramers with a Tetrahydrofuran Ring fromDipterocarpus grandiflorus. wikidata.org.
  22. [24] ↑ . α-Viniferin: A Prostaglandin H2Synthase Inhibitor from Root ofCarex humilis. wikidata.org.
  23. [25] ↑ . Resveratrol-type oligostilbenes from Iris clarkei antagonize 20-hydroxyecdysone action in the Drosophila melanogaster B(II) cell line. wikidata.org.
  24. [26] ↑ . Stilbenoids isolated from stem bark of Shorea hemsleyana. wikidata.org.
  25. [27] ↑ . Stilbene oligomers in roots of Sophora davidii. 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). α-viniferin. Retrieved May 3, 2026, from https://4ort.xyz/entity/viniferin-q4734921
MLA “α-viniferin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/viniferin-q4734921.
BibTeX @misc{4ortxyz_viniferin-q4734921_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{α-viniferin}}, year = {2026}, url = {https://4ort.xyz/entity/viniferin-q4734921}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): α-viniferin — https://4ort.xyz/entity/viniferin-q4734921 (retrieved 2026-05-03)

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