naringin

chemical compound
ChemicalSubstance type_of_chemical_entity Q418469
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naringin

Summary

naringin is a type of chemical entity[1]. naringin has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • naringin's instance of is recorded as type of chemical entity[3].
  • naringin's physically interacts with is recorded as Solute carrier organic anion transporter family member 1A2[4].
  • naringin's canonical SMILES is recorded as CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O[5].
  • naringin's chemical formula is recorded as C₂₇H₃₂O₁₄[6].
  • naringin is a type of Naringenin 7-Rhamnoglucoside[7].
  • naringin's Commons category is recorded as Naringin[8].
  • naringin's found in taxon is recorded as Coriandrum sativum[9].
  • naringin's found in taxon is recorded as Pyrrosia serpens[10].
  • naringin's found in taxon is recorded as Citrus grandis[11].
  • naringin's found in taxon is recorded as Salvia officinalis[12].
  • naringin's found in taxon is recorded as Vitis vinifera[13].
  • naringin's found in taxon is recorded as Daphniphyllum angustifolium[14].
  • naringin's found in taxon is recorded as Daphniphyllum himalayense[15].
  • naringin's found in taxon is recorded as Euphorbia condylocarpa[16].
  • naringin's found in taxon is recorded as Holarrhena pubescens[17].
  • naringin's found in taxon is recorded as Onopordum illyricum[18].
  • naringin's found in taxon is recorded as Podocarpus fasciculus[19].
  • naringin's found in taxon is recorded as Citrus medica[20].
  • naringin's found in taxon is recorded as Citrus sudachi[21].
  • naringin's found in taxon is recorded as Leptosphaeria maculans[22].
  • naringin's found in taxon is recorded as Ailanthus integrifolia[23].
  • naringin's found in taxon is recorded as Cicer arietinum[24].
  • naringin's found in taxon is recorded as Citrus latipes[25].
  • naringin's found in taxon is recorded as Hyuganatsu[26].
  • naringin's found in taxon is recorded as Citrus unshiu[27].

Why It Matters

naringin has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2] naringin is known by 9 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . Antioxidant activity of methanolic extracts from three coriander (Coriandrum sativum L.) fruit varieties. wikidata.org.
  8. [10] . Kaempferol 3-O-sophoroside-7-O-α-l-arabinofuranoside, neohesperidosides and other flavonoids from the fern Pyrrosia serpens. wikidata.org.
  9. [11] . Quantitative survey of narirutin, naringin, hesperidin, and neohesperidin in citrus. wikidata.org.
  10. [12] . Antioxidant activity and phenolic compounds in selected herbs. wikidata.org.
  11. [13] . RP-HPLC analysis of phenolic compounds and flavonoids in beverages and plant extracts using a CoulArray detector.. wikidata.org.
  12. [14] . A new biflavonoid from Daphniphyllum angustifolium Hutch.. wikidata.org.
  13. [15] . A new biflavonoid from Daphniphyllum angustifolium Hutch.. wikidata.org.
  14. [16] . Optimal extraction method of phenolics from the root of Euphorbia condylocarpa. wikidata.org.
  15. [17] . Constituents of the leaves of Holarrhena pubescens. wikidata.org.
  16. [18] . New metabolites from onopordum illyricum. wikidata.org.
  17. [19] . Cytotoxic constituents from Podocarpus fasciculus. wikidata.org.
  18. [20] . Chemical constituents from the peels of Citrus sudachi. wikidata.org.
  19. [21] . Chemical constituents from the peels of Citrus sudachi. wikidata.org.
  20. [22] . Sterol composition of mycelia of the plant pathogenic ascomycete Leptosphaeria maculans. wikidata.org.
  21. [23] . Studies on the constituents of Ailanthus integrifolia. wikidata.org.
  22. [24] . Accumulation of Phenolic Compounds and Phytoalexins in Sliced and Elicitor-Treated Cotyledons of Cicer arietinum L.. wikidata.org.
  23. [25] . Limonoid and flavonoid composition in varieties of Papeda and Papedocitrus. wikidata.org.
  24. [26] . Phenolic composition of various tissues of rutaceae species. wikidata.org.
  25. [27] . Chemical composition of the juice of the fruit ofCitrus unshiu. 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). naringin. Retrieved May 3, 2026, from https://4ort.xyz/entity/naringin
MLA “naringin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/naringin.
BibTeX @misc{4ortxyz_naringin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{naringin}}, year = {2026}, url = {https://4ort.xyz/entity/naringin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): naringin — https://4ort.xyz/entity/naringin (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. 9d ago · FlocciNivis · 2026-06-25 view diff on Wikidata ↗
    Pdb ligand id ZWN
    "/* wbcreateclaim-create:1| */ [[Property:P3636]]: ZWN, [[:toollabs:quickstatements/#/batch/259826|batch #259826]]"
  2. 16d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of (2S)-7-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one, (2S)-7-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-2-oxanyl]oxy]-2-oxanyl]oxy]-5-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one, (2R)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside +1
    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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