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astilbin

chemical compound
ChemicalSubstance type_of_chemical_entity Q4810880
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astilbin

Summary

astilbin is a type of chemical entity[1]. astilbin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (9 views/month).[2]

Key Facts

  • astilbin's instance of is recorded as type of chemical entity[3].
  • astilbin's CAS Registry Number is recorded as 29838-67-3[4].
  • astilbin's EC number is recorded as 694-695-3[5].
  • astilbin's canonical SMILES is recorded as CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O[6].
  • astilbin's InChI is recorded as InChI=1S/C21H22O11/c1-7-15(26)17(28)18(29)21(30-7)32-20-16(27)14-12(25)5-9(22)6-13(14)31-19(20)8-2-3-10(23)11(24)4-8/h2-7,15,17-26,28-29H,1H3/t7-,15-,17+,18+,19+,20-,21-/m0/s1[7].
  • astilbin's InChIKey is recorded as ZROGCCBNZBKLEL-MPRHSVQHSA-N[8].
  • astilbin's chemical formula is recorded as C₂₁H₂₂O₁₁[9].
  • astilbin's subclass of is recorded as flavanone[10].
  • astilbin's ChEMBL ID is recorded as CHEMBL486017[11].
  • astilbin's Freebase ID is recorded as /m/07k9l6f[12].
  • astilbin's ChemSpider ID is recorded as 106533[13].
  • astilbin's PubChem CID is recorded as 119258[14].
  • astilbin's KEGG ID is recorded as C09803[15].
  • astilbin's ChEBI ID is recorded as 38200[16].
  • astilbin's found in taxon is recorded as Hypericum perforatum[17].
  • astilbin's found in taxon is recorded as Vitis vinifera[18].
  • astilbin's found in taxon is recorded as Stelechocarpus cauliflorus[19].
  • astilbin's found in taxon is recorded as Desmos cochinchinensis[20].
  • astilbin's found in taxon is recorded as Mallotus metcalfianus[21].
  • astilbin's found in taxon is recorded as Petiveria alliacea[22].
  • astilbin's found in taxon is recorded as Andira inermis[23].
  • astilbin's found in taxon is recorded as Astilbe thunbergii[24].
  • astilbin's found in taxon is recorded as Calliandra haematocephala[25].
  • astilbin's found in taxon is recorded as Cratoxylum formosum[26].
  • astilbin's found in taxon is recorded as Drimys granadensis[27].

Why It Matters

astilbin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (9 views/month).[2] astilbin 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] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] ↑ . ECHA Substance Infocard database. Retrieved . 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] ↑ . Q2311683. Retrieved . wikidata.org.
  12. [14] ↑ . PubChem. Retrieved . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . ChEBI. Retrieved . wikidata.org.
  15. [17] ↑ . Phenolic compounds from Hypericum perforatum. wikidata.org.
  16. [18] ↑ . Phenolic composition of grape stems. wikidata.org.
  17. [19] ↑ . Inhibitors of aldose reductase and advanced glycation end-products formation from the leaves of Stelechocarpus cauliflorus R.E. Fr. wikidata.org.
  18. [20] ↑ . Phenolic constituents with inhibitory activity against NFAT transcription from Desmos chinensis. wikidata.org.
  19. [21] ↑ . Polyphenols isolated from antiradical extracts of Mallotus metcalfianus.. wikidata.org.
  20. [22] ↑ . 6-C-formyl and 6-C-hydroxymethyl flavanones from Petiveria alliacea. wikidata.org.
  21. [23] ↑ . Andinermals A-C, antiplasmodial constituents from Andira inermis. wikidata.org.
  22. [24] ↑ . Norepinephrine-Augmenting Lipolytic Effectors from Astilbe thunbergii Rhizomes. wikidata.org.
  23. [25] ↑ . ANTIBACTERIAL CONSTITUENTS OF CALLIANDRA HAEMATOCEPHALA. wikidata.org.
  24. [26] ↑ . Two xanthones from roots of Cratoxylum formosanum. wikidata.org.
  25. [27] ↑ . Flavonoid glycosides from Cassia alata. 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). astilbin. Retrieved May 3, 2026, from https://4ort.xyz/entity/astilbin
MLA “astilbin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/astilbin.
BibTeX @misc{4ortxyz_astilbin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{astilbin}}, year = {2026}, url = {https://4ort.xyz/entity/astilbin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): astilbin — https://4ort.xyz/entity/astilbin (retrieved 2026-05-03)

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