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echinacoside

chemical compound
ChemicalSubstance type_of_chemical_entity Q475631
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echinacoside

Summary

echinacoside is a type of chemical entity[1]. echinacoside ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (21 views/month).[2]

Key Facts

  • echinacoside's instance of is recorded as type of chemical entity[3].
  • echinacoside's chemical structure is recorded as Echinacoside.svg[4].
  • echinacoside's CAS Registry Number is recorded as 82854-37-3[5].
  • echinacoside's EC number is recorded as 617-397-7[6].
  • echinacoside's canonical SMILES is recorded as O=C(OC1C(OC(OCCC2=CC=C(O)C(O)=C2)C(O)C1OC3OC(C)C(O)C(O)C3O)COC4OC(CO)C(O)C(O)C4O)C=CC5=CC=C(O)C(O)=C5[7].
  • echinacoside's InChI is recorded as InChI=1S/C35H46O20/c1-14-24(42)26(44)29(47)35(51-14)55-32-30(48)34(49-9-8-16-3-6-18(38)20(40)11-16)53-22(13-50-33-28(46)27(45)25(43)21(12-36)52-33)31(32)54-23(41)7-4-15-2-5-17(37)19(39)10-15/h2-7,10-11,14,21-22,24-40,42-48H,8-9,12-13H2,1H3/b7-4+/t14-,21+,22+,24-,25+,26+,27-,28+,29+,30+,31+,32+,33+,34+,35-/m0/s1[8].
  • echinacoside's InChIKey is recorded as FSBUXLDOLNLABB-ISAKITKMSA-N[9].
  • echinacoside's chemical formula is recorded as C₃₅H₄₆O₂₀[10].
  • echinacoside's subclass of is recorded as [6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate[11].
  • echinacoside's ChEMBL ID is recorded as CHEMBL393090[12].
  • echinacoside's Freebase ID is recorded as /m/0g5rd_4[13].
  • echinacoside's UNII is recorded as I04O1DT48T[14].
  • echinacoside's ChemSpider ID is recorded as 4445084[15].
  • echinacoside's PubChem CID is recorded as 5281771[16].
  • echinacoside's ChEBI ID is recorded as 4745[17].
  • echinacoside's found in taxon is recorded as Echinacea pallida[18].
  • echinacoside's found in taxon is recorded as Buddleja globosa[19].
  • echinacoside's found in taxon is recorded as Buddleja officinalis[20].
  • echinacoside's found in taxon is recorded as Buddleja yunnanensis[21].
  • echinacoside's found in taxon is recorded as Cistanche deserticola[22].
  • echinacoside's found in taxon is recorded as Cistanche mongolica[23].
  • echinacoside's found in taxon is recorded as Cistanche salsa[24].
  • echinacoside's found in taxon is recorded as Echinacea angustifolia[25].
  • echinacoside's found in taxon is recorded as Echinacea atrorubens[26].
  • echinacoside's found in taxon is recorded as Echinacea paradoxa[27].

Why It Matters

echinacoside ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (21 views/month).[2] echinacoside has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[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] ↑ . wikidata.org.
  4. [6] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . PubChem. wikidata.org.
  7. [9] ↑ . PubChem. wikidata.org.
  8. [10] ↑ . PubChem. wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . ChEBI release 2019-10-02. wikidata.org.
  16. [18] ↑ . Caffeoyl conjugates from Echinacea species: Structures and biological activity. wikidata.org.
  17. [19] ↑ . Effects of Buddleja globosa leaf and its constituents relevant to wound healing. wikidata.org.
  18. [20] ↑ . Phenylethanoid glycosides from Osmanthus asiaticus. wikidata.org.
  19. [21] ↑ . Novel and known constituents from Buddleja species and their activity against leukocyte eicosanoid generation. wikidata.org.
  20. [22] ↑ . Inhibition of nitric oxide by phenylethanoids in activated macrophages. wikidata.org.
  21. [23] ↑ . New phenylethanoid glycosides from Cistanche tubulosa (SCHRENK) HOOOK. f. I.. wikidata.org.
  22. [24] ↑ . Echinacoside rescues the SHSY5Y neuronal cells from TNFalpha-induced apoptosis. wikidata.org.
  23. [25] ↑ . Field desorption mass spectrometry, fast atom bombardment mass spectrometry and fast atom bombardment tandem mass spectrometry of echinacoside, the main caffeoyl-glycoside fromEchinacea angustifolia roots (Asteraceae). wikidata.org.
  24. [26] ↑ . Phytochemical variation in echinacea from roots and flowerheads of wild and cultivated populations. wikidata.org.
  25. [27] ↑ . Analysis of alkamides and caffeic acid derivatives from Echinacea simulata and E. paradoxa roots. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. 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). echinacoside. Retrieved May 3, 2026, from https://4ort.xyz/entity/echinacoside
MLA “echinacoside.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/echinacoside.
BibTeX @misc{4ortxyz_echinacoside_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{echinacoside}}, year = {2026}, url = {https://4ort.xyz/entity/echinacoside}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): echinacoside — https://4ort.xyz/entity/echinacoside (retrieved 2026-05-03)

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