Home › Entities › type_of_chemical_entity › 5-O-Methylgenistein

5-O-Methylgenistein

chemical compound
ChemicalSubstance type_of_chemical_entity Q4639636
Press Enter · cited answer in seconds

5-O-Methylgenistein

Summary

5-O-Methylgenistein is a type of chemical entity[1]. 5-O-Methylgenistein ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2]

Key Facts

  • 5-O-Methylgenistein's instance of is recorded as type of chemical entity[3].
  • 5-O-Methylgenistein's chemical structure is recorded as 5-O-methylgenistein.svg[4].
  • 5-O-Methylgenistein's CAS Registry Number is recorded as 4569-98-6[5].
  • 5-O-Methylgenistein's EC number is recorded as 803-860-2[6].
  • 5-O-Methylgenistein's canonical SMILES is recorded as COC1=C2C(=CC(=C1)O)OC=C(C2=O)C3=CC=C(C=C3)O[7].
  • 5-O-Methylgenistein's InChI is recorded as InChI=1S/C16H12O5/c1-20-13-6-11(18)7-14-15(13)16(19)12(8-21-14)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3[8].
  • 5-O-Methylgenistein's InChIKey is recorded as YSINCDVRUMTOPK-UHFFFAOYSA-N[9].
  • 5-O-Methylgenistein's chemical formula is recorded as C₁₆H₁₂O₅[10].
  • 5-O-Methylgenistein's subclass of is recorded as isoflavone[11].
  • 5-O-Methylgenistein's Commons category is recorded as 5-O-Methylgenistein[12].
  • 5-O-Methylgenistein's ChEMBL ID is recorded as CHEMBL1479463[13].
  • 5-O-Methylgenistein's Freebase ID is recorded as /m/0bbwfhf[14].
  • 5-O-Methylgenistein's UNII is recorded as Q2UG76ML8U[15].
  • 5-O-Methylgenistein's ChemSpider ID is recorded as 4678012[16].
  • 5-O-Methylgenistein's PubChem CID is recorded as 5748551[17].
  • 5-O-Methylgenistein's found in taxon is recorded as Ulex europaeus[18].
  • 5-O-Methylgenistein's found in taxon is recorded as Genista morisii[19].
  • 5-O-Methylgenistein's found in taxon is recorded as Ormosia monosperma[20].
  • 5-O-Methylgenistein's found in taxon is recorded as Laburnum anagyroides[21].
  • 5-O-Methylgenistein's found in taxon is recorded as Cotoneaster simonsii[22].
  • 5-O-Methylgenistein's found in taxon is recorded as Echinospartum horridum[23].
  • 5-O-Methylgenistein's found in taxon is recorded as Genista corsica[24].
  • 5-O-Methylgenistein's found in taxon is recorded as Genista ephedroides[25].
  • 5-O-Methylgenistein's found in taxon is recorded as Lupinus luteus[26].
  • 5-O-Methylgenistein's found in taxon is recorded as Ormosia excelsa[27].

Why It Matters

5-O-Methylgenistein ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2]

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] ↑ . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . ECHA Substance Infocard database. 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . Q2311683. Retrieved . wikidata.org.
  15. [17] ↑ . PubChem. Retrieved . wikidata.org.
  16. [18] ↑ . Isoflavones from root bark of gorse. wikidata.org.
  17. [19] ↑ . Estradiol-antagonistic activity of phenolic compounds from leguminous plants. wikidata.org.
  18. [20] ↑ . Anti-oral microbial activity of isoflavonoids in root bark of Ormosia monosperma. wikidata.org.
  19. [21] ↑ . Isoflavones from pods of laburnum anagyroides. wikidata.org.
  20. [22] ↑ . Flavonols and isoflavones from Cotoneaster simonsii. wikidata.org.
  21. [23] ↑ . 5-O-methylbiochanin a, a new isoflavone from Echinospartum horridum. wikidata.org.
  22. [24] ↑ . A new isoflavone from Genista corsica. wikidata.org.
  23. [25] ↑ . Flavonoids from Genista ephedroides. wikidata.org.
  24. [26] ↑ . New 5-O-Methylisoflavones in the Roots of Yellow Lupin (Lupinus luteusL. cv. Barpine). wikidata.org.
  25. [27] ↑ . 5-O-methylgenistein from Ormosia excelsa. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). 5-O-Methylgenistein. Retrieved May 3, 2026, from https://4ort.xyz/entity/5-o-methylgenistein
MLA “5-O-Methylgenistein.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/5-o-methylgenistein.
BibTeX @misc{4ortxyz_5-o-methylgenistein_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{5-O-Methylgenistein}}, year = {2026}, url = {https://4ort.xyz/entity/5-o-methylgenistein}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 5-O-Methylgenistein — https://4ort.xyz/entity/5-o-methylgenistein (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/5-o-methylgenistein · Last refreshed: