glyceollin III

chemical compound
ChemicalSubstance type_of_chemical_entity Q5572524
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glyceollin III

Summary

glyceollin III is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (11 views/month).[2]

Key Facts

  • glyceollin III's instance of is recorded as type of chemical entity[3].
  • glyceollin III's chemical structure is recorded as Glyceollin III.svg[4].
  • glyceollin III's CAS Registry Number is recorded as 61080-23-7[5].
  • glyceollin III's canonical SMILES is recorded as CC(=C)C1CC2=CC3=C(C=C2O1)OCC4(C3OC5=C4C=CC(=C5)O)O[6].
  • glyceollin III's InChI is recorded as InChI=1S/C20H18O5/c1-10(2)15-6-11-5-13-17(8-16(11)24-15)23-9-20(22)14-4-3-12(21)7-18(14)25-19(13)20/h3-5,7-8,15,19,21-22H,1,6,9H2,2H3/t15-,19-,20+/m0/s1[7].
  • glyceollin III's InChIKey is recorded as MIYTVBARXCVVHZ-RYGJVYDSSA-N[8].
  • glyceollin III's chemical formula is recorded as C₂₀H₁₈O₅[9].
  • glyceollin III's subclass of is recorded as 6C-prenylisoflavane[10].
  • glyceollin III's subclass of is recorded as glyceollin[11].
  • glyceollin III's ChEMBL ID is recorded as CHEMBL2229450[12].
  • glyceollin III's Freebase ID is recorded as /m/0gh5zm8[13].
  • glyceollin III's UNII is recorded as 629FG6XLLL[14].
  • glyceollin III's ChemSpider ID is recorded as 10128488[15].
  • glyceollin III's PubChem CID is recorded as 11954193[16].
  • glyceollin III's KEGG ID is recorded as C15511[17].
  • glyceollin III's ChEBI ID is recorded as 52086[18].
  • glyceollin III's found in taxon is recorded as Glycine clandestina[19].
  • glyceollin III's found in taxon is recorded as Glycine latifolia[20].
  • glyceollin III's found in taxon is recorded as Glycine soja[21].
  • glyceollin III's found in taxon is recorded as Glycine tabacina[22].
  • glyceollin III's found in taxon is recorded as Aspergillus sojae[23].
  • glyceollin III's found in taxon is recorded as soybean[24].
  • glyceollin III's Reaxys registry number is recorded as 1268819[25].
  • glyceollin III's isomeric SMILES is recorded as CC(=C)[C@@H]1CC2=CC3=C(C=C2O1)OC[C@@]4([C@H]3OC5=C4C=CC(=C5)O)O[26].
  • glyceollin III's LIPID MAPS ID is recorded as LMPK12070109[27].

Why It Matters

glyceollin III ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (11 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] . Global Substance Registration System. 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] . wikidata.org.
  10. [12] . ChEMBL. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] . Q2311683. Retrieved . wikidata.org.
  14. [16] . PubChem. Retrieved . wikidata.org.
  15. [17] . ChEBI. Retrieved . wikidata.org.
  16. [18] . ChEMBL. Retrieved . wikidata.org.
  17. [19] . Phytoalexin Production as a Chemosystematic Parameter Within the Genus Glycine. wikidata.org.
  18. [20] . Phytoalexin Production as a Chemosystematic Parameter Within the Genus Glycine. wikidata.org.
  19. [21] . Phytoalexin Production as a Chemosystematic Parameter Within the Genus Glycine. wikidata.org.
  20. [22] . Phytoalexin Production as a Chemosystematic Parameter Within the Genus Glycine. wikidata.org.
  21. [23] . Antifungal activity of glyceollins isolated from soybean elicited with Aspergillus sojae. wikidata.org.
  22. [24] . Quantification of glyceollins in non-elicited seedlings of Glycine max by gas chromatography-mass spectrometry. wikidata.org.
  23. [25] . ChEBI. Retrieved . wikidata.org.
  24. [26] . PubChem. Retrieved . wikidata.org.
  25. [27] . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: 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). glyceollin III. Retrieved May 3, 2026, from https://4ort.xyz/entity/glyceollin-iii
MLA “glyceollin III.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/glyceollin-iii.
BibTeX @misc{4ortxyz_glyceollin-iii_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{glyceollin III}}, year = {2026}, url = {https://4ort.xyz/entity/glyceollin-iii}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): glyceollin III — https://4ort.xyz/entity/glyceollin-iii (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/glyceollin-iii · Last refreshed:

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. 4w ago · KaleemBot bot · 2026-05-01 view diff on Wikidata ↗
    Subclass of 6C-prenylisoflavane, glyceollin
    Found in taxon Glycine clandestina, Glycine latifolia, Glycine soja +3
    Mass {'unit': 'Q483261', 'amount': '+338.115'}
    Stereoisomer of glyceollin III, (1S,6R,13S)-6-prop-1-en-2-yl-7,11,20-trioxapentacyclo[11.7.0.02,10.04,8.014,19]icosa-2(10),3,8,14(19),15,17-hexaene-13,17-diol
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:گلائیسی اولن III]]"
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