hyperoside

chemical compound
ChemicalSubstance type_of_chemical_entity Q5242815
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hyperoside

Summary

hyperoside is a type of chemical entity[1]. hyperoside ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (14 views/month).[2]

Key Facts

  • hyperoside's instance of is recorded as type of chemical entity[3].
  • hyperoside's CAS Registry Number is recorded as 482-36-0[4].
  • hyperoside's EC number is recorded as 207-580-6[5].
  • hyperoside's canonical SMILES is recorded as C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O[6].
  • hyperoside's InChI is recorded as InChI=1S/C21H20O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-18,21-27,29-30H,6H2/t13-,15+,17+,18-,21+/m1/s1[7].
  • hyperoside's InChIKey is recorded as OVSQVDMCBVZWGM-DTGCRPNFSA-N[8].
  • hyperoside's chemical formula is recorded as C₂₁H₂₂O₁₂[9].
  • hyperoside's subclass of is recorded as hyperin[10].
  • hyperoside's Freebase ID is recorded as /m/07k65t5[11].
  • hyperoside's UNII is recorded as 8O1CR18L82[12].
  • hyperoside's ChemSpider ID is recorded as 4444962[13].
  • hyperoside's PubChem CID is recorded as 5281643[14].
  • hyperoside's KEGG ID is recorded as C10073[15].
  • hyperoside's ChEBI ID is recorded as 67486[16].
  • hyperoside's found in taxon is recorded as Vauquelinia corymbosa[17].
  • hyperoside's found in taxon is recorded as Humulus lupulus[18].
  • hyperoside's found in taxon is recorded as Hypericum perforatum[19].
  • hyperoside's found in taxon is recorded as Ocimum gratissimum[20].
  • hyperoside's found in taxon is recorded as Oenanthe javanica[21].
  • hyperoside's found in taxon is recorded as Euphorbia hyssopifolia[22].
  • hyperoside's found in taxon is recorded as Aguacate[23].
  • hyperoside's found in taxon is recorded as Sanicula graveolens[24].
  • hyperoside's found in taxon is recorded as Apocynum venetum[25].
  • hyperoside's found in taxon is recorded as Lysimachia fortunei[26].
  • hyperoside's found in taxon is recorded as Crataegus oxyacantha L. (1753)[27].

Why It Matters

hyperoside ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (14 views/month).[2] hyperoside has Wikipedia articles in 8 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] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . ChEBI release 2020-09-01. wikidata.org.
  7. [9] . PubChem. wikidata.org.
  8. [10] . 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] . α-Glucosidase Inhibitors from Vauquelinia corymbosa. wikidata.org.
  16. [18] . Quantitative analysis of hop acids, essential oils and flavonoids as a clue to the identification of hop varieties. wikidata.org.
  17. [19] . High performance liquid chromatography/electrospray mass spectrometry of Hypericum perforatum extracts. wikidata.org.
  18. [20] . The application of atmospheric pressure chemical ionisation liquid chromatography-mass spectrometry in the chemotaxonomic study of flavonoids: characterisation of flavonoids from Ocimum gratissimum var. gratissimum. wikidata.org.
  19. [21] . Effects of methanol extract ofOenanthe javanica on the hepatic alcohol-metabolizing enzyme system and its bioactive component. wikidata.org.
  20. [22] . HIV-1 reverse transcriptase inhibitory principles from Chamaesyce hyssopifolia. wikidata.org.
  21. [23] . Flavonol monoglycosides isolated from the antiviral fractions ofPersea americana (Lauraceae) leaf infusion. wikidata.org.
  22. [24] . Free radical scavengers from Mutisia friesiana (Asteraceae) and Sanicula graveolens (Apiaceae).. wikidata.org.
  23. [25] . Inhibitory effects of an aqueous extract of Apocynum venetum leaves and its constituents on Cu(2+)-induced oxidative modification of low density lipoprotein. wikidata.org.
  24. [26] . Flavonol glycosides from Lysimachia barystachys. wikidata.org.
  25. [27] . Inhibition of thromboxane A2 biosynthesis in vitro by the main components of Crataegus oxyacantha (Hawthorn) flower heads. 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). hyperoside. Retrieved May 3, 2026, from https://4ort.xyz/entity/hyperoside
MLA “hyperoside.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hyperoside.
BibTeX @misc{4ortxyz_hyperoside_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hyperoside}}, year = {2026}, url = {https://4ort.xyz/entity/hyperoside}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hyperoside — https://4ort.xyz/entity/hyperoside (retrieved 2026-05-03)

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