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alpha-Viniferin

group of stereoisomers with the chemical formula C₄₂H₃₀O₉
ChemicalSubstance group_of_stereoisomers Q105146363
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alpha-Viniferin

Summary

alpha-Viniferin is a group of stereoisomers[1].

Key Facts

  • alpha-Viniferin's instance of is recorded as group of stereoisomers[2].
  • alpha-Viniferin's canonical SMILES is recorded as OC1=CC=C(C=C1)C2OC3=CC(O)=CC4=C3C2C=5C=C(O)C=C6OC(C7=CC=C(O)C=C7)C(C=8C=C(O)C=C9OC(C%10=CC=C(O)C=C%10)C4C98)C65[3].
  • alpha-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[4].
  • alpha-Viniferin's InChIKey is recorded as KUTVNHOAKHJJFL-UHFFFAOYSA-N[5].
  • alpha-Viniferin's chemical formula is recorded as C₄₂H₃₀O₉[6].
  • alpha-Viniferin's subclass of is recorded as chemical compound[7].
  • alpha-Viniferin's PubChem CID is recorded as 375682[8].
  • alpha-Viniferin's found in taxon is recorded as Shorea gibbosa[9].
  • alpha-Viniferin's found in taxon is recorded as Caragana aurantiaca[10].
  • alpha-Viniferin's found in taxon is recorded as Vitis vinifera[11].
  • alpha-Viniferin's found in taxon is recorded as Craibia grandiflora[12].
  • alpha-Viniferin's Human Metabolome Database ID is recorded as HMDB0030603[13].
  • alpha-Viniferin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+678.18898254'}[14].
  • alpha-Viniferin's SureChEMBL ID is recorded as 2721242[15].
  • alpha-Viniferin's UniChem compound ID is recorded as 27198930[16].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . Stilbenoids isolated from stem bark of Shorea hemsleyana. wikidata.org.
  9. [10] ↑ . Oligomeric stilbenes from the root of Caragana stenophylla. wikidata.org.
  10. [11] ↑ . Disease resistance of Vitis spp. and the production of the stress metabolites resveratrol, ε-viniferin, α-viniferin and pterostilbene. wikidata.org.
  11. [12] ↑ . Two New Resveratrol (=5-[(1E)-2-(4-Hydroxyphenyl)ethenyl]benzene-1,3-diol) Tetramers with a Tetrahydrofuran Ring fromDipterocarpus grandiflorus. wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). alpha-Viniferin. Retrieved May 3, 2026, from https://4ort.xyz/entity/alpha-viniferin
MLA “alpha-Viniferin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/alpha-viniferin.
BibTeX @misc{4ortxyz_alpha-viniferin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{alpha-Viniferin}}, year = {2026}, url = {https://4ort.xyz/entity/alpha-viniferin}, note = {Accessed: 2026-05-03}}
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