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genistein

chemical compound
ChemicalSubstance type_of_chemical_entity Q415957
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genistein

Summary

genistein is a type of chemical entity[1]. genistein has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • genistein's instance of is recorded as type of chemical entity[3].
  • genistein's physically interacts with is recorded as cystic fibrosis transmembrane conductance regulator[4].
  • genistein's physically interacts with is recorded as estrogen receptor 2[5].
  • genistein's physically interacts with is recorded as Estrogen related receptor alpha[6].
  • genistein's physically interacts with is recorded as Estrogen related receptor beta[7].
  • genistein's physically interacts with is recorded as Estrogen related receptor gamma[8].
  • genistein's physically interacts with is recorded as Transient receptor potential cation channel subfamily C member 5[9].
  • genistein's physically interacts with is recorded as taste receptor type 2[10].
  • genistein's canonical SMILES is recorded as C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O[11].
  • genistein's chemical formula is recorded as C₁₅H₁₀O₅[12].
  • genistein is a type of isoflavone[13].
  • genistein is part of cellular response to genistein[14].
  • genistein is part of response to genistein[15].
  • genistein is part of soy isoflavones[16].
  • genistein's Commons category is recorded as Genistein[17].
  • genistein comprises carbon[18].
  • genistein's found in taxon is recorded as Vigna radiata[19].
  • genistein's found in taxon is recorded as Trifolium pratense[20].
  • genistein's found in taxon is recorded as liquorice[21].
  • genistein's found in taxon is recorded as Lupinus albus[22].
  • genistein's found in taxon is recorded as Trifolium incarnatum[23].
  • genistein's found in taxon is recorded as Syzygium jambos[24].
  • genistein's found in taxon is recorded as Styphnolobium japonicum[25].
  • genistein's found in taxon is recorded as Ficus nervosa[26].
  • genistein's found in taxon is recorded as Acacia adunca[27].

Why It Matters

genistein has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[2] genistein is known by 15 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] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  4. [6] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  5. [7] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  6. [8] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  7. [9] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  8. [10] ↑ . Bitter Taste Receptor Activation by Flavonoids and Isoflavonoids: Modeled Structural Requirements for Activation of hTAS2R14 and hTAS2R39. wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . PubChem. Retrieved . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Gene Ontology release 2019-11-16. wikidata.org.
  13. [15] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . Antifungal Phytoalexins in Phaseolus aureus Roxb. wikidata.org.
  18. [20] ↑ . Effects of phytoestrogens derived from red clover on atherogenic adhesion molecules in human endothelial cells.. wikidata.org.
  19. [21] ↑ . Blockade of the dioxin pathway by herbal medicine Formula Bupleuri Minor: identification of active entities for suppression of AhR activation.. wikidata.org.
  20. [22] ↑ . Fungitoxic dihydrofuranoisoflavones and related compounds in white lupin, Lupinus albus. wikidata.org.
  21. [23] ↑ . High Performance Liquid Chromatographic Separation of Isoflavones and Structural Elucidation of Isoflavone 7-O-glucoside 6''-malonates from Cicer arietinum. wikidata.org.
  22. [24] ↑ . A general method for the dereplication of flavonoid glycosides utilizing high performance liquid chromatography/mass spectrometric analysis. wikidata.org.
  23. [25] ↑ . Inhibitory effects of isoflavones on lipid peroxidation by reactive oxygen species. wikidata.org.
  24. [26] ↑ . Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa. wikidata.org.
  25. [27] ↑ . A phytochemical survey of the Australian species of Acacia. 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.

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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). genistein. Retrieved May 3, 2026, from https://4ort.xyz/entity/genistein
MLA “genistein.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/genistein.
BibTeX @misc{4ortxyz_genistein_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{genistein}}, year = {2026}, url = {https://4ort.xyz/entity/genistein}, note = {Accessed: 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. 16d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Described at url → —
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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