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Vitisin A

chemical compound
ChemicalSubstance type_of_chemical_entity Q7937130
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Vitisin A

Summary

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

Key Facts

  • Vitisin A's instance of is recorded as type of chemical entity[3].
  • Vitisin A's chemical structure is recorded as Vitisin A (stilbenoid).png[4].
  • Vitisin A's CAS Registry Number is recorded as 142449-89-6[5].
  • Vitisin A's canonical SMILES is recorded as C1=CC(=CC=C1C2C(C3=CC(=CC4=C3C(C(O4)C5=CC=C(C=C5)O)C6=CC(=CC(=C26)O)O)O)C7=C(C=CC(=C7)C=CC8=CC(=CC9=C8C(C(O9)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O)O[6].
  • Vitisin A's InChI is recorded as InChI=1S/C56H42O12/c57-33-10-4-28(5-11-33)49-51(42-23-40(64)26-47-53(42)54(43-22-39(63)24-45(66)52(43)49)56(68-47)30-8-14-35(59)15-9-30)41-17-27(2-16-44(41)65)1-3-31-18-38(62)25-46-48(31)50(32-19-36(60)21-37(61)20-32)55(67-46)29-6-12-34(58)13-7-29/h1-26,49-51,54-66H/b3-1+/t49-,50+,51+,54+,55-,56-/m1/s1[7].
  • Vitisin A's InChIKey is recorded as XAXVWWYPKOGXSY-DBHYGPPCSA-N[8].
  • Vitisin A's chemical formula is recorded as C₅₆H₄₂O₁₂[9].
  • Vitisin A's subclass of is recorded as biogenic benzofuran[10].
  • Vitisin A's ChEMBL ID is recorded as CHEMBL507409[11].
  • Vitisin A's Freebase ID is recorded as /m/0gk_b4t[12].
  • Vitisin A's UNII is recorded as 832N5294M6[13].
  • Vitisin A's ChemSpider ID is recorded as 17288137[14].
  • Vitisin A's PubChem CID is recorded as 16131430[15].
  • Vitisin A's ChEBI ID is recorded as 189580[16].
  • Vitisin A's found in taxon is recorded as Vitis coignetiae[17].
  • Vitisin A's found in taxon is recorded as Vitis vinifera[18].
  • Vitisin A's found in taxon is recorded as Vitis amurensis[19].
  • Vitisin A's found in taxon is recorded as Vitis davidii[20].
  • Vitisin A's found in taxon is recorded as Vitis flexuosa[21].
  • Vitisin A's found in taxon is recorded as Vitis chunganensis[22].
  • Vitisin A's found in taxon is recorded as Vitis rotundifolia[23].
  • Vitisin A's isomeric SMILES is recorded as C1=CC(=CC=C1[C@@H]2C@HC7=C(C=CC(=C7)/C=C/C8=CC(=CC9=C8C@@HC1=CC(=CC(=C1)O)O)O)O)OC@HC7=C(C=CC(=C7)/C=C/C8=CC(=CC9=C8C@@HC1=CC(=CC(">[24].
  • Vitisin A's KNApSAcK ID is recorded as C00052490[25].
  • Vitisin A's mass is recorded as {'unit': 'Q483261', 'amount': '+906.267627'}[26].
  • Vitisin A's SureChEMBL ID is recorded as 13241392[27].

Why It Matters

Vitisin A ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (1 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. 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Q2311683. Retrieved . wikidata.org.
  13. [15] ↑ . PubChem. Retrieved . wikidata.org.
  14. [16] ↑ . ChEBI release 2022-06-13. wikidata.org.
  15. [17] ↑ . Absolute configurations of some oligostilbenes from Vitis coignetiae and Vitis vinifera ‘Kyohou’. wikidata.org.
  16. [18] ↑ . 3-Hydroxy-3-methylglutaryl-CoA (HMG-CoA) reductase inhibitory effect of Vitis vinifera. wikidata.org.
  17. [19] ↑ . Inhibition of cholinesterase and amyloid-beta aggregation by resveratrol oligomers from Vitis amurensis. wikidata.org.
  18. [20] ↑ . Oligostilbenes from vitis betulifolia. wikidata.org.
  19. [21] ↑ . Flexuosol A, a New Tetrastilbene from Vitis flexuosa. wikidata.org.
  20. [22] ↑ . Chunganenol: an unusual antioxidative resveratrol hexamer from Vitis chunganensis. wikidata.org.
  21. [23] ↑ . Antibacterial Activities of Metabolites from (Muscadine) Roots against Fish Pathogenic Bacteria. wikidata.org.
  22. [24] ↑ . PubChem. Retrieved . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . PubChem. Retrieved . wikidata.org.
  25. [27] ↑ . 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). Vitisin A. Retrieved May 3, 2026, from https://4ort.xyz/entity/vitisin-a
MLA “Vitisin A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vitisin-a.
BibTeX @misc{4ortxyz_vitisin-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Vitisin A}}, year = {2026}, url = {https://4ort.xyz/entity/vitisin-a}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Vitisin A — https://4ort.xyz/entity/vitisin-a (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. 22d ago · KaleemBot bot · 2026-04-30 view diff on Wikidata ↗
    Subclass of → biogenic benzofuran
    Found in taxon → Vitis coignetiae, Vitis vinifera, Vitis amurensis +4
    Mass → {'unit': 'Q483261', 'amount': '+906.267627'}
    Stereoisomer of → r-2-Viniferin, (+)-cis-Vitisin A
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:ویٹیسن اے (اسٹائل بینائڈ)]]"
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