naringenin 7-O-beta-D-glucoside

chemical compound
ChemicalSubstance type_of_chemical_entity Q15424791
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naringenin 7-O-beta-D-glucoside

Summary

naringenin 7-O-beta-D-glucoside is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2]

Key Facts

  • naringenin 7-O-beta-D-glucoside's instance of is recorded as type of chemical entity[3].
  • naringenin 7-O-beta-D-glucoside's chemical structure is recorded as Prunin.svg[4].
  • naringenin 7-O-beta-D-glucoside's CAS Registry Number is recorded as 529-55-5[5].
  • naringenin 7-O-beta-D-glucoside's EC number is recorded as 208-464-8[6].
  • naringenin 7-O-beta-D-glucoside's canonical SMILES is recorded as C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O[7].
  • naringenin 7-O-beta-D-glucoside's InChI is recorded as InChI=1S/C21H22O10/c22-8-16-18(26)19(27)20(28)21(31-16)29-11-5-12(24)17-13(25)7-14(30-15(17)6-11)9-1-3-10(23)4-2-9/h1-6,14,16,18-24,26-28H,7-8H2/t14-,16+,18+,19-,20+,21+/m0/s1[8].
  • naringenin 7-O-beta-D-glucoside's InChIKey is recorded as DLIKSSGEMUFQOK-SFTVRKLSSA-N[9].
  • naringenin 7-O-beta-D-glucoside's chemical formula is recorded as C₂₁H₂₂O₁₀[10].
  • naringenin 7-O-beta-D-glucoside's subclass of is recorded as flavanone[11].
  • naringenin 7-O-beta-D-glucoside's Commons category is recorded as Prunin[12].
  • naringenin 7-O-beta-D-glucoside's ChEMBL ID is recorded as CHEMBL469654[13].
  • naringenin 7-O-beta-D-glucoside's Freebase ID is recorded as /m/0wxpkvy[14].
  • naringenin 7-O-beta-D-glucoside's UNII is recorded as LSB8HDX4E5[15].
  • naringenin 7-O-beta-D-glucoside's ChemSpider ID is recorded as 83766[16].
  • naringenin 7-O-beta-D-glucoside's PubChem CID is recorded as 92794[17].
  • naringenin 7-O-beta-D-glucoside's KEGG ID is recorded as C09099[18].
  • naringenin 7-O-beta-D-glucoside's ChEBI ID is recorded as 28327[19].
  • naringenin 7-O-beta-D-glucoside's found in taxon is recorded as Phlomis aurea[20].
  • naringenin 7-O-beta-D-glucoside's found in taxon is recorded as Phlomis floccosa[21].
  • naringenin 7-O-beta-D-glucoside's found in taxon is recorded as Vachellia farnesiana var. farnesiana[22].
  • naringenin 7-O-beta-D-glucoside's found in taxon is recorded as Holarrhena pubescens[23].
  • naringenin 7-O-beta-D-glucoside's found in taxon is recorded as Phyllanthus emblica[24].
  • naringenin 7-O-beta-D-glucoside's found in taxon is recorded as Juniperus communis[25].
  • naringenin 7-O-beta-D-glucoside's found in taxon is recorded as Ipomoea nil[26].
  • naringenin 7-O-beta-D-glucoside's found in taxon is recorded as Cynara scolymus[27].

Why It Matters

naringenin 7-O-beta-D-glucoside ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 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] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . ChEMBL. Retrieved . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . Q2311683. Retrieved . wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . ChEBI. Retrieved . wikidata.org.
  18. [20] . Flavonoids of Phlomis aurea and P. floccosa. wikidata.org.
  19. [21] . Flavonoids of Phlomis aurea and P. floccosa. wikidata.org.
  20. [22] . Chemical composition of Acacia farnesiana (L) Willd fruits and its activity against Mycobacterium tuberculosis and dysentery bacteria. wikidata.org.
  21. [23] . Constituents of the leaves of Holarrhena pubescens. wikidata.org.
  22. [24] . Two new acylated flavanone glycosides from the leaves and branches of Phyllanthus emblica. wikidata.org.
  23. [25] . Neolignan and flavonoid glycosides in Juniperus communis var. depressa. wikidata.org.
  24. [26] . Flavonoids in the acyanic flowers of Pharbitis nil. wikidata.org.
  25. [27] . The flavonoids of Cynara sibthorpiana. 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). naringenin 7-O-beta-D-glucoside. Retrieved May 3, 2026, from https://4ort.xyz/entity/naringenin-7-o-beta-d-glucoside
MLA “naringenin 7-O-beta-D-glucoside.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/naringenin-7-o-beta-d-glucoside.
BibTeX @misc{4ortxyz_naringenin-7-o-beta-d-glucoside_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{naringenin 7-O-beta-D-glucoside}}, year = {2026}, url = {https://4ort.xyz/entity/naringenin-7-o-beta-d-glucoside}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): naringenin 7-O-beta-D-glucoside — https://4ort.xyz/entity/naringenin-7-o-beta-d-glucoside (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. 6w ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Stereoisomer of 4',5-Dihydroxy-7-glucosyloxyflavanone, (R)-5-Hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)chroman-4-one, (2S)-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one
    Subclass of flavanone
    Aliases
    Subclass of
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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