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eugeniin

chemical compound
ChemicalSubstance type_of_chemical_entity Q7697608
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eugeniin

Summary

eugeniin is a type of chemical entity[1]. eugeniin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2]

Key Facts

  • eugeniin's instance of is recorded as type of chemical entity[3].
  • eugeniin's chemical structure is recorded as Tellimagrandin II.svg[4].
  • eugeniin's CAS Registry Number is recorded as 58970-75-5[5].
  • eugeniin's canonical SMILES is recorded as C1=C(C=C(C(=C1O)O)O)C(=O)OC2(C3(C(COC(C4=CC(=C(C(=C4C=5C(=CC(=C(C5O)O)O)C(=O)O3)O)O)O)=O)(OC(C2(OC(C6=CC(=C(C(=C6)O)O)O)=O)[H])(OC(C7=CC(=C(C(=C7)O)O)O)=O)[H])[H])[H])[H][6].
  • eugeniin's InChI is recorded as InChI=1S/C41H30O26/c42-15-1-10(2-16(43)26(15)50)36(57)65-34-33-23(9-62-39(60)13-7-21(48)29(53)31(55)24(13)25-14(40(61)64-33)8-22(49)30(54)32(25)56)63-41(67-38(59)12-5-19(46)28(52)20(47)6-12)35(34)66-37(58)11-3-17(44)27(51)18(45)4-11/h1-8,23,33-35,41-56H,9H2/t23-,33-,34+,35-,41+/m1/s1[7].
  • eugeniin's InChIKey is recorded as JCGHAEBIBSEQAD-UUUCSUBKSA-N[8].
  • eugeniin's chemical formula is recorded as C₄₁H₃₀O₂₆[9].
  • eugeniin's subclass of is recorded as CID 11766372[10].
  • eugeniin's ChEMBL ID is recorded as CHEMBL450745[11].
  • eugeniin's Freebase ID is recorded as /m/0bh88zw[12].
  • eugeniin's ChemSpider ID is recorded as 391036[13].
  • eugeniin's PubChem CID is recorded as 442679[14].
  • eugeniin's KEGG ID is recorded as C10224[15].
  • eugeniin's ChEBI ID is recorded as 4916[16].
  • eugeniin's found in taxon is recorded as Quercus acutissima[17].
  • eugeniin's found in taxon is recorded as Quercus phillyraeoides[18].
  • eugeniin's found in taxon is recorded as Mallotus repandus[19].
  • eugeniin's found in taxon is recorded as Euphorbia thymifolia[20].
  • eugeniin's found in taxon is recorded as Quercus aliena[21].
  • eugeniin's found in taxon is recorded as Syzygium aqueum[22].
  • eugeniin's found in taxon is recorded as clove[23].
  • eugeniin's found in taxon is recorded as Cornus[24].
  • eugeniin's found in taxon is recorded as Tellima grandiflora[25].
  • eugeniin's found in taxon is recorded as Geum japonicum[26].
  • eugeniin's found in taxon is recorded as Tamarix nilotica[27].

Why It Matters

eugeniin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2] eugeniin is known by 3 alternative names across languages and contexts.[28]

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] ↑ . ChEBI. Retrieved . wikidata.org.
  4. [6] ↑ . ChEBI. Retrieved . wikidata.org.
  5. [7] ↑ . ChEBI. Retrieved . wikidata.org.
  6. [8] ↑ . ChEBI. 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] ↑ . Q2311683. Retrieved . wikidata.org.
  12. [14] ↑ . PubChem. Retrieved . wikidata.org.
  13. [15] ↑ . ChEBI. Retrieved . wikidata.org.
  14. [16] ↑ . ChEBI. Retrieved . wikidata.org.
  15. [17] ↑ . Tannin production in callus cultures of Quercus acutissima. wikidata.org.
  16. [18] ↑ . Tannins and related compounds. LXXXIII. Isolation and structures of hydrolyzable tannins, phillyraeoidins A-E from Quercus phillyraeoides.. wikidata.org.
  17. [19] ↑ . Tannins and related compounds. LXXXVII. Isolation and characterization of four new hydrolyzable tannins from the leaves of Mallotus repandus.. wikidata.org.
  18. [20] ↑ . Hydrolysable tannins from Euphorbia thymifolia. wikidata.org.
  19. [21] ↑ . Tannins and related compounds. CIX. Isolation of alienanins A and B, novel C,C-linked ellagitannin dimers from Quercus aliena Blume.. wikidata.org.
  20. [22] ↑ . Tannins and Related Compounds. CXIX. Samarangenins A and B, Novel Proanthocyanidins with Doubly Bonded Structures, from Syzygium samarangens and S. aqueum.. wikidata.org.
  21. [23] ↑ . Tannins and Related Compounds. CXXIII. Chromone, Acetophenone and Phenylpropanoid Glycosides and Their Galloyl and /or Hexahydroxydiphenoyl Esters from the Leaves of Syzygium aromaticum MERR. et PERRY.. wikidata.org.
  22. [24] ↑ . Ellagitannin biosynthesis: laccase-catalyzed dimerization of tellimagrandin II to cornusiin E in Tellima grandiflora. wikidata.org.
  23. [25] ↑ . Ellagitannin biosynthesis: laccase-catalyzed dimerization of tellimagrandin II to cornusiin E in Tellima grandiflora. wikidata.org.
  24. [26] ↑ . Effects of tannins from Geum japonicum on the catalytic activity of thrombin and factor Xa of blood coagulation cascade. wikidata.org.
  25. [27] ↑ . Hydrolyzable tannins of tamaricaceous plants. III. Hellinoyl- and macrocyclic-type ellagitannins from Tamarix nilotica. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata aliases. wikidata.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). eugeniin. Retrieved May 3, 2026, from https://4ort.xyz/entity/eugeniin
MLA “eugeniin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/eugeniin.
BibTeX @misc{4ortxyz_eugeniin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{eugeniin}}, year = {2026}, url = {https://4ort.xyz/entity/eugeniin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): eugeniin — https://4ort.xyz/entity/eugeniin (retrieved 2026-05-03)

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