formononetin

chemical compound
ChemicalSubstance type_of_chemical_entity Q408859
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formononetin

Summary

formononetin is a type of chemical entity[1]. formononetin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (17 views/month).[2]

Key Facts

  • formononetin's instance of is recorded as type of chemical entity[3].
  • formononetin's chemical structure is recorded as Formononetin.svg[4].
  • formononetin's CAS Registry Number is recorded as 485-72-3[5].
  • formononetin's EC number is recorded as 207-623-9[6].
  • formononetin's canonical SMILES is recorded as COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O[7].
  • formononetin's InChI is recorded as InChI=1S/C16H12O4/c1-19-12-5-2-10(3-6-12)14-9-20-15-8-11(17)4-7-13(15)16(14)18/h2-9,17H,1H3[8].
  • formononetin's InChIKey is recorded as HKQYGTCOTHHOMP-UHFFFAOYSA-N[9].
  • formononetin's chemical formula is recorded as C₁₆H₁₂O₄[10].
  • formononetin's subclass of is recorded as isoflavone[11].
  • formononetin's Commons category is recorded as Formononetin[12].
  • formononetin's MeSH descriptor ID is recorded as C007768[13].
  • formononetin's ChEMBL ID is recorded as CHEMBL242341[14].
  • formononetin's Freebase ID is recorded as /m/07khpvn[15].
  • formononetin's UNII is recorded as 295DQC67BJ[16].
  • formononetin's ChemSpider ID is recorded as 4444070[17].
  • formononetin's PubChem CID is recorded as 5280378[18].
  • formononetin's KEGG ID is recorded as C00858[19].
  • formononetin's ChEBI ID is recorded as 18088[20].
  • formononetin's found in taxon is recorded as Syzygium jambos[21].
  • formononetin's found in taxon is recorded as Astragalus membranaceus[22].
  • formononetin's found in taxon is recorded as Sophora flavescens[23].
  • formononetin's found in taxon is recorded as Trifolium pratense[24].
  • formononetin's found in taxon is recorded as Cicer arietinum[25].
  • formononetin's found in taxon is recorded as Cicer mogoltavicum[26].
  • formononetin's found in taxon is recorded as Trifolium incarnatum[27].

Why It Matters

formononetin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (17 views/month).[2] formononetin has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] formononetin is known by 10 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] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . Global Substance Registration System. 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] . Medical Subject Headings. Retrieved . wikidata.org.
  12. [14] . ChEMBL. Retrieved . wikidata.org.
  13. [15] . Freebase Data Dumps. wikidata.org.
  14. [16] . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] . Q2311683. Retrieved . wikidata.org.
  16. [18] . PubChem. Retrieved . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . ChEBI. Retrieved . wikidata.org.
  19. [21] . A general method for the dereplication of flavonoid glycosides utilizing high performance liquid chromatography/mass spectrometric analysis. wikidata.org.
  20. [22] . Antioxidative components isolated from the roots ofAstragalus membranaceusBunge (Astragali Radix). wikidata.org.
  21. [23] . In vitro antitumour activity of flavonoids from Sophora flavescens. wikidata.org.
  22. [24] . Effects of phytoestrogens derived from red clover on atherogenic adhesion molecules in human endothelial cells.. wikidata.org.
  23. [25] . Potential Value of Plants as Sources of New Antifertility Agents II *. wikidata.org.
  24. [26] . Isoflavonoids ofCiver mogoltavicum. wikidata.org.
  25. [27] . High Performance Liquid Chromatographic Separation of Isoflavones and Structural Elucidation of Isoflavone 7-O-glucoside 6''-malonates from Cicer arietinum. 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). formononetin. Retrieved May 3, 2026, from https://4ort.xyz/entity/formononetin
MLA “formononetin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/formononetin.
BibTeX @misc{4ortxyz_formononetin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{formononetin}}, year = {2026}, url = {https://4ort.xyz/entity/formononetin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): formononetin — https://4ort.xyz/entity/formononetin (retrieved 2026-05-03)

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