naringenin

main polyphenol in citrus fruit
ChemicalSubstance type_of_chemical_entity Q418374
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naringenin

Summary

naringenin is a type of chemical entity[1]. naringenin has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • naringenin's instance of is recorded as type of chemical entity[3].
  • naringenin's canonical SMILES is recorded as C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O[4].
  • naringenin's chemical formula is recorded as C₁₅H₁₂O₅[5].
  • naringenin is a type of flavanone[6].
  • naringenin is part of naringenin 7-O-methyltransferase activity[7].
  • naringenin is part of naringenin 2-hydroxylase activity[8].
  • naringenin's Commons category is recorded as Naringenin[9].
  • naringenin's found in taxon is recorded as Ficus nervosa[10].
  • naringenin's found in taxon is recorded as Arabidopsis thaliana[11].
  • naringenin's found in taxon is recorded as Broussonetia papyrifera[12].
  • naringenin's found in taxon is recorded as Chrysothamnus humilis[13].
  • naringenin's found in taxon is recorded as Chrysothamnus viscidiflorus[14].
  • naringenin's found in taxon is recorded as Cochlospermum gillivraei[15].
  • naringenin's found in taxon is recorded as Dalbergia stevensonii[16].
  • naringenin's found in taxon is recorded as Dendrobium densiflorum[17].
  • naringenin's found in taxon is recorded as Equisetum arvense[18].
  • naringenin's found in taxon is recorded as Garcinia multiflora[19].
  • naringenin's found in taxon is recorded as liquorice[20].
  • naringenin's found in taxon is recorded as Gynerium sagittatum[21].
  • naringenin's found in taxon is recorded as Intsia bijuga[22].
  • naringenin's found in taxon is recorded as Lespedeza cyrtobotrya[23].
  • naringenin's found in taxon is recorded as Lupinus subcarnosus[24].
  • naringenin's found in taxon is recorded as Lupinus texensis[25].
  • naringenin's found in taxon is recorded as Maclura tinctoria[26].
  • naringenin's found in taxon is recorded as Millettia brandisiana[27].

Why It Matters

naringenin has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[2] naringenin is known by 18 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] . PubChem. Retrieved . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Gene Ontology release 2020-05-02. wikidata.org.
  6. [8] . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa. wikidata.org.
  9. [11] . The Arabidopsis TDS4 gene encodes leucoanthocyanidin dioxygenase (LDOX) and is essential for proanthocyanidin synthesis and vacuole development.. wikidata.org.
  10. [12] . Aromatase inhibitors from Broussonetia papyrifera. wikidata.org.
  11. [13] . Leaf surface flavonoids of Chrysothamnus. wikidata.org.
  12. [14] . Leaf surface flavonoids of Chrysothamnus. wikidata.org.
  13. [15] . Flavonoids from Cochlospermum gillivraei. wikidata.org.
  14. [16] . Dalbergia species. Part IX. Phytochemical examination of Dalbergia stevensonii standl. wikidata.org.
  15. [17] . Chemical constituents from Dendrobium densiflorum. wikidata.org.
  16. [18] . Phenolic acids of Equisetum arvense. wikidata.org.
  17. [19] . Xanthones and benzophenones from the stems of Garcinia multiflora. wikidata.org.
  18. [20] . Flavonoids of the epigeal part of Glycyrrhiza glabra. wikidata.org.
  19. [21] . Flavonoids and isoflavonoids from Gynerium sagittatum. wikidata.org.
  20. [22] . Polyphenols of Intsia heartwoods. wikidata.org.
  21. [23] . Melanin synthesis inhibitors from Lespedeza cyrtobotrya. wikidata.org.
  22. [24] . Flavonoids of Lupinus texensis and L. subcarnosus. wikidata.org.
  23. [25] . Flavonoids of Lupinus texensis and L. subcarnosus. wikidata.org.
  24. [26] . Antioxidant chalcone glycosides and flavanones from Maclura (Chlorophora) tinctoria. wikidata.org.
  25. [27] . Brandisianins A-F, isoflavonoids isolated from Millettia brandisiana in a screening program for death-receptor expression enhancement activity. 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). naringenin. Retrieved May 3, 2026, from https://4ort.xyz/entity/naringenin
MLA “naringenin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/naringenin.
BibTeX @misc{4ortxyz_naringenin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{naringenin}}, year = {2026}, url = {https://4ort.xyz/entity/naringenin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): naringenin — https://4ort.xyz/entity/naringenin (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. 14d ago · Adamrb12345 · 2026-08-05 view diff on Wikidata ↗
    Described by source
    Found in taxon Ficus nervosa, Arabidopsis thaliana, Broussonetia papyrifera +283
    "/* wbcreateclaim-create:1| */ [[Property:P703]]: [[Q160575]], #quickstatements; #temporary_batch_1785942942558"
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