Vescalagin

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q104198109
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Vescalagin

Summary

Vescalagin is a group of stereoisomers[1].

Key Facts

  • Vescalagin's instance of is recorded as group of stereoisomers[2].
  • Vescalagin's physically interacts with is recorded as taste receptor type 2[3].
  • Vescalagin's CAS Registry Number is recorded as 24312-00-3[4].
  • Vescalagin's canonical SMILES is recorded as O=C1OCC2OC(=O)C3=CC(O)=C(O)C(O)=C3C4=C(O)C(O)=C(O)C5=C4C(=O)OC(C6OC(=O)C7=C5C(O)=C(O)C(O)=C7C6O)C2OC(=O)C8=CC(O)=C(O)C(O)=C8C9=C(O)C(O)=C(O)C=C19[5].
  • Vescalagin's InChI is recorded as InChI=1S/C41H26O26/c42-8-1-5-12(24(48)21(8)45)13-6(2-9(43)22(46)25(13)49)39(60)65-34-11(4-63-37(5)58)64-38(59)7-3-10(44)23(47)26(50)14(7)15-18-16(28(52)32(56)27(15)51)17-19-20(30(54)33(57)29(17)53)31(55)35(66-41(19)62)36(34)67-40(18)61/h1-3,11,31,34-36,42-57H,4H2[6].
  • Vescalagin's InChIKey is recorded as UDYKDZHZAKSYCO-UHFFFAOYSA-N[7].
  • Vescalagin's chemical formula is recorded as C₄₁H₂₆O₂₆[8].
  • Vescalagin's subclass of is recorded as chemical compound[9].
  • Vescalagin's PubChem CID is recorded as 168165[10].
  • Vescalagin's found in taxon is recorded as pomegranate[11].
  • Vescalagin's found in taxon is recorded as Castanea mollissima[12].
  • Vescalagin's found in taxon is recorded as Q156137[13].
  • Vescalagin's found in taxon is recorded as Quercus faginea[14].
  • Vescalagin's Human Metabolome Database ID is recorded as HMDB0030602[15].
  • Vescalagin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+934.0712309520007'}[16].
  • Vescalagin's SureChEMBL ID is recorded as 12477174[17].
  • Vescalagin's SureChEMBL ID is recorded as 29370035[18].
  • Vescalagin's DSSTox substance ID is recorded as DTXSID201029283[19].
  • Vescalagin's UniChem compound ID is recorded as 420001[20].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Human Bitter Taste Receptors Are Activated by Different Classes of Polyphenols. wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . Broad spectrum antimutagenic activity of antioxidant active fraction of punica granatum L. peel extracts. wikidata.org.
  11. [12] . Polyphenols isolated from the bark of castanea sativa Mill. chemical structures and auto-association in honour of professor G. H. Neil Towers 75th birthday. wikidata.org.
  12. [13] . Antioxidant and biological properties of bioactive phenolic compounds from Quercus suber L.. wikidata.org.
  13. [14] . Tannins and Related Compounds, 101. Isolation and Structures of C-Glycosyl Hydrolyzable Tannins from Turkish Galls. wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . UniChem. wikidata.org.

Class ancestry

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

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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). Vescalagin. Retrieved May 3, 2026, from https://4ort.xyz/entity/vescalagin
MLA “Vescalagin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vescalagin.
BibTeX @misc{4ortxyz_vescalagin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Vescalagin}}, year = {2026}, url = {https://4ort.xyz/entity/vescalagin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Vescalagin — https://4ort.xyz/entity/vescalagin (retrieved 2026-05-03)

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