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naringin

chemical compound
ChemicalSubstance type_of_chemical_entity Q418469
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naringin

Summary

naringin is a type of chemical entity[1]. naringin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (55 views/month).[2]

Key Facts

  • naringin's instance of is recorded as type of chemical entity[3].
  • naringin's chemical structure is recorded as Naringin.svg[4].
  • naringin's physically interacts with is recorded as Solute carrier organic anion transporter family member 1A2[5].
  • naringin's CAS Registry Number is recorded as 10236-47-2[6].
  • naringin's EC number is recorded as 233-566-4[7].
  • 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[8].
  • naringin's InChI is recorded as InChI=1S/C27H32O14/c1-10-20(32)22(34)24(36)26(37-10)41-25-23(35)21(33)18(9-28)40-27(25)38-13-6-14(30)19-15(31)8-16(39-17(19)7-13)11-2-4-12(29)5-3-11/h2-7,10,16,18,20-30,32-36H,8-9H2,1H3/t10-,16-,18+,20-,21+,22+,23-,24+,25+,26-,27+/m0/s1[9].
  • naringin's InChIKey is recorded as DFPMSGMNTNDNHN-ZPHOTFPESA-N[10].
  • naringin's chemical formula is recorded as C₂₇H₃₂O₁₄[11].
  • naringin's subclass of is recorded as Naringenin 7-Rhamnoglucoside[12].
  • naringin's Commons category is recorded as Naringin[13].
  • naringin's ChEMBL ID is recorded as CHEMBL451532[14].
  • naringin's Guide to Pharmacology Ligand ID is recorded as 4738[15].
  • naringin's Freebase ID is recorded as /m/082j2w[16].
  • naringin's UNII is recorded as N7TD9J649B[17].
  • naringin's ChemSpider ID is recorded as 390868[18].
  • naringin's PubChem CID is recorded as 442428[19].
  • naringin's KEGG ID is recorded as C09789[20].
  • naringin's ChEBI ID is recorded as 28819[21].
  • naringin's found in taxon is recorded as Coriandrum sativum[22].
  • naringin's found in taxon is recorded as Pyrrosia serpens[23].
  • naringin's found in taxon is recorded as Citrus grandis[24].
  • naringin's found in taxon is recorded as Salvia officinalis[25].
  • naringin's found in taxon is recorded as Vitis vinifera[26].
  • naringin's found in taxon is recorded as Daphniphyllum angustifolium[27].

Why It Matters

naringin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (55 views/month).[2] naringin has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[28] naringin is known by 9 alternative names across languages and contexts.[29]

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] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . ChEMBL. Retrieved . wikidata.org.
  13. [15] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  14. [16] ↑ . Freebase Data Dumps. wikidata.org.
  15. [17] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] ↑ . Q2311683. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . ChEMBL. Retrieved . wikidata.org.
  20. [22] ↑ . Antioxidant activity of methanolic extracts from three coriander (Coriandrum sativum L.) fruit varieties. wikidata.org.
  21. [23] ↑ . Kaempferol 3-O-sophoroside-7-O-α-l-arabinofuranoside, neohesperidosides and other flavonoids from the fern Pyrrosia serpens. wikidata.org.
  22. [24] ↑ . Quantitative survey of narirutin, naringin, hesperidin, and neohesperidin in citrus. wikidata.org.
  23. [25] ↑ . Antioxidant activity and phenolic compounds in selected herbs. wikidata.org.
  24. [26] ↑ . RP-HPLC analysis of phenolic compounds and flavonoids in beverages and plant extracts using a CoulArray detector.. wikidata.org.
  25. [27] ↑ . A new biflavonoid from Daphniphyllum angustifolium Hutch.. 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.
  3. [29] ↑ . 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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