esculin

chemical compound
ChemicalSubstance type_of_chemical_entity Q376432
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esculin

Summary

esculin is a type of chemical entity[1]. esculin has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • esculin's instance of is recorded as type of chemical entity[3].
  • esculin's physically interacts with is recorded as taste receptor type 2[4].
  • esculin's canonical SMILES is recorded as C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O[5].
  • esculin's chemical formula is recorded as C₁₅H₁₆O₉[6].
  • esculin is a type of biogenic coumarin[7].
  • esculin's found in taxon is recorded as Fraxinus excelsior[8].
  • esculin's found in taxon is recorded as Actinidia chinensis[9].
  • esculin's found in taxon is recorded as Actinidia chinensis var. hispida[10].
  • esculin's found in taxon is recorded as Aesculus hippocastanum[11].
  • esculin's found in taxon is recorded as Afraegle paniculata[12].
  • esculin's found in taxon is recorded as Althaea armeniaca[13].
  • esculin's found in taxon is recorded as Althaea officinalis[14].
  • esculin's found in taxon is recorded as Artemisia absinthium[15].
  • esculin's found in taxon is recorded as Artemisia jacutica[16].
  • esculin's found in taxon is recorded as Artemisia nova[17].
  • esculin's found in taxon is recorded as Artemisia siversiana[18].
  • esculin's found in taxon is recorded as Artemisia tridentata[19].
  • esculin's found in taxon is recorded as Artemisia vulgaris[20].
  • esculin's found in taxon is recorded as Cichorium intybus[21].
  • esculin's found in taxon is recorded as Cynara cornigera[22].
  • esculin's found in taxon is recorded as Daphne gnidioides[23].
  • esculin's found in taxon is recorded as Ficus septica[24].
  • esculin's found in taxon is recorded as Fraxinus floribunda[25].
  • esculin's found in taxon is recorded as Fraxinus insularis[26].
  • esculin's found in taxon is recorded as Fraxinus japonica[27].

Why It Matters

esculin has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2] esculin is known by 14 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] . The human TAS2R16 receptor mediates bitter taste in response to beta-glucopyranosides. wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Secoiridoids and hydroxycoumarins in Bulgarian Fraxinus species. wikidata.org.
  7. [9] . Fraxin and esculin: two coumarins specific to Actinidia chinensis and A. deliciosa (kiwifruit). wikidata.org.
  8. [10] . Fraxin and esculin: two coumarins specific to Actinidia chinensis and A. deliciosa (kiwifruit). wikidata.org.
  9. [11] . Aesculus hippocastanum L.. wikidata.org.
  10. [12] . The mutagenicities of seven coumarin derivatives and a furan derivative (nimbolide) isolated from three medicinal plants. wikidata.org.
  11. [13] . Coumarins of Althaea officinalis and A. armenica. wikidata.org.
  12. [14] . Coumarins of Althaea officinalis and A. armenica. wikidata.org.
  13. [15] . Coumarins of wormwoods of the Frigidae series. wikidata.org.
  14. [16] . Coumarins of wormwoods of the Frigidae series. wikidata.org.
  15. [17] . High-performance liquid chromatographic analysis of coumarins and flavonoids from section tridentatae of Artemisia. wikidata.org.
  16. [18] . Coumarins of wormwoods of the Frigidae series. wikidata.org.
  17. [19] . Seasonal variation of coumarin and flavonoid concentrations in persistent leaves of wyoming big sagebrush (Artemisia tridentata ssp. wyomingensis: Asteraceae). wikidata.org.
  18. [20] . Coumarins of Artemesia vulgaris. wikidata.org.
  19. [21] . The role of sesquiterpene lactones and phenolics in the chemical defence of the chicory plant. wikidata.org.
  20. [22] . Polyphenolic constituents from the leaves of two Cynara species growing in Greece. wikidata.org.
  21. [23] . Coumarins and flavonoids from Daphne gnidioides. wikidata.org.
  22. [24] . Phenanthroindolizidine Alkaloids and Their Cytotoxicity from the Leaves of Ficus septica. wikidata.org.
  23. [25] . Coumarins from Fraxinus floribunda leaves. wikidata.org.
  24. [26] . Isolation of Oleayunnanoside from Fraxinus insularis and Revision of Its Structure to Insularoside-6'''-O-.BETA.-D-glucoside.. wikidata.org.
  25. [27] . Isolation and identification of anti-platelet aggregation principles from the bark of Fraxinus japonica BLUME. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.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). esculin. Retrieved May 3, 2026, from https://4ort.xyz/entity/esculin
MLA “esculin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/esculin.
BibTeX @misc{4ortxyz_esculin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{esculin}}, year = {2026}, url = {https://4ort.xyz/entity/esculin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): esculin — https://4ort.xyz/entity/esculin (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. 13d ago · FlocciNivis · 2026-06-25 view diff on Wikidata ↗
    Pdb ligand id 7OU
    "/* wbcreateclaim-create:1| */ [[Property:P3636]]: 7OU, [[:toollabs:quickstatements/#/batch/259826|batch #259826]]"
  2. 20d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of 7-hydroxy-6-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one, 6-(alpha-D-Glucopyranosyloxy)-7-hydroxycoumarin
    Instance of type of chemical entity
    Has characteristic bitterness
    Subclass of
    + 6 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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