genistin

chemical compound
ChemicalSubstance type_of_chemical_entity Q5533221
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genistin

Summary

genistin is a type of chemical entity[1]. genistin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2]

Key Facts

  • genistin's instance of is recorded as type of chemical entity[3].
  • genistin's chemical structure is recorded as Genistin.svg[4].
  • genistin's CAS Registry Number is recorded as 529-59-9[5].
  • genistin's EC number is recorded as 610-921-5[6].
  • genistin's canonical SMILES is recorded as C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O[7].
  • genistin's InChI is recorded as InChI=1S/C21H20O10/c22-7-15-18(26)19(27)20(28)21(31-15)30-11-5-13(24)16-14(6-11)29-8-12(17(16)25)9-1-3-10(23)4-2-9/h1-6,8,15,18-24,26-28H,7H2/t15-,18-,19+,20-,21-/m1/s1[8].
  • genistin's InChIKey is recorded as ZCOLJUOHXJRHDI-CMWLGVBASA-N[9].
  • genistin's chemical formula is recorded as C₂₁H₂₀O₁₀[10].
  • genistin's subclass of is recorded as genistein 7-O-glucoside[11].
  • genistin's ChEMBL ID is recorded as CHEMBL486625[12].
  • genistin's Freebase ID is recorded as /m/07k6w_w[13].
  • genistin's UNII is recorded as 1POG3SCN5T[14].
  • genistin's ChemSpider ID is recorded as 4444736[15].
  • genistin's PubChem CID is recorded as 5281377[16].
  • genistin's KEGG ID is recorded as C09126[17].
  • genistin's ChEBI ID is recorded as 27514[18].
  • genistin's found in taxon is recorded as Adenocarpus complicatus[19].
  • genistin's found in taxon is recorded as Lupinus albus[20].
  • genistin's found in taxon is recorded as Achlys triphylla[21].
  • genistin's found in taxon is recorded as Calycotome villosa[22].
  • genistin's found in taxon is recorded as Chaenomeles sinensis[23].
  • genistin's found in taxon is recorded as Chamaecytisus supinus[24].
  • genistin's found in taxon is recorded as Cicer arietinum[25].
  • genistin's found in taxon is recorded as Eriosema tuberosum[26].
  • genistin's found in taxon is recorded as Ficus septica[27].

Why It Matters

genistin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2] genistin is known by 7 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] . wikidata.org.
  3. [5] . Global Substance Registration System. 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] . ChEMBL. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] . Q2311683. Retrieved . wikidata.org.
  14. [16] . PubChem. Retrieved . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . ChEMBL. Retrieved . wikidata.org.
  17. [19] . Potential Value of Plants as Sources of New Antifertility Agents II *. wikidata.org.
  18. [20] . Detection of isoflavonoids and their glycosides by liquid chromatography/electrospray ionization mass spectrometry in root extracts of lupin (Lupinus albus). wikidata.org.
  19. [21] . Four flavonol glycosides from Achlys triphylla. wikidata.org.
  20. [22] . Flavonoids from Calicotome villosa. wikidata.org.
  21. [23] . Tissue factor inhibitory flavonoids from the fruits of Chaenomeles sinensis. wikidata.org.
  22. [24] . Flavonoids and Alkaloids of Chamaecytisus hirsutus and Chamaecytisus supinus. wikidata.org.
  23. [25] . High-performance liquid chromatography of isoflavones and phytoalexins from Cicer arietinum. wikidata.org.
  24. [26] . Isoflavonoid glycosides from eriosema tuberosum. wikidata.org.
  25. [27] . Phenanthroindolizidine Alkaloids and Their Cytotoxicity from the Leaves of Ficus septica. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). genistin. Retrieved May 3, 2026, from https://4ort.xyz/entity/genistin
MLA “genistin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/genistin.
BibTeX @misc{4ortxyz_genistin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{genistin}}, year = {2026}, url = {https://4ort.xyz/entity/genistin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): genistin — https://4ort.xyz/entity/genistin (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. 19d ago · Shuaib-bot bot · 2026-05-02 view diff on Wikidata ↗
    Instance of
    Stereoisomer of 5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one, 5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one, 5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one +1
    Found in taxon Adenocarpus complicatus, Lupinus albus, Achlys triphylla +52
    Subclass of genistein 7-O-glucoside
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||ur */"
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