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genistein 7-O-glucoside

group of stereoisomers with the chemical formula C₂₁H₂₀O₁₀
ChemicalSubstance group_of_stereoisomers Q105371330
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genistein 7-O-glucoside

Summary

genistein 7-O-glucoside is a group of stereoisomers[1].

Key Facts

  • genistein 7-O-glucoside's instance of is recorded as group of stereoisomers[2].
  • genistein 7-O-glucoside's canonical SMILES is recorded as O=C1C(=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC(O)=C12)C=4C=CC(O)=CC4[3].
  • genistein 7-O-glucoside'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[4].
  • genistein 7-O-glucoside's InChIKey is recorded as ZCOLJUOHXJRHDI-VVWFOWEGSA-N[5].
  • genistein 7-O-glucoside's chemical formula is recorded as C₂₁H₂₀O₁₀[6].
  • genistein 7-O-glucoside's subclass of is recorded as isoflavone[7].
  • genistein 7-O-glucoside's PubChem CID is recorded as 44257273[8].
  • genistein 7-O-glucoside's found in taxon is recorded as Adenocarpus artemisiifolius[9].
  • genistein 7-O-glucoside's found in taxon is recorded as Adenocarpus decorticans[10].
  • genistein 7-O-glucoside's isomeric SMILES is recorded as O=c1c(-c2ccc(O)cc2)coc2cc(O[C@@H]3OC(CO)C@@HC@HC3O)cc(O)c12C@@HC@HC3O)cc(O)c12">[11].
  • genistein 7-O-glucoside's LIPID MAPS ID is recorded as LMPK12050166[12].
  • genistein 7-O-glucoside's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+432.10564684'}[13].
  • genistein 7-O-glucoside's SureChEMBL ID is recorded as 241743[14].
  • genistein 7-O-glucoside's UniChem compound ID is recorded as 62677936[15].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . Flavonoids as chemosystematic markers for the genus Adenocarpus. wikidata.org.
  9. [10] ↑ . Flavonoids as chemosystematic markers for the genus Adenocarpus. wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). genistein 7-O-glucoside. Retrieved May 3, 2026, from https://4ort.xyz/entity/genistein-7-o-glucoside
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BibTeX @misc{4ortxyz_genistein-7-o-glucoside_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{genistein 7-O-glucoside}}, year = {2026}, url = {https://4ort.xyz/entity/genistein-7-o-glucoside}, note = {Accessed: 2026-05-03}}
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