daidzin

group of stereoisomers with the chemical formula C₂₁H₂₀O₉
ChemicalSubstance group_of_stereoisomers Q105147884
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daidzin

Summary

daidzin is a group of stereoisomers[1].

Key Facts

  • daidzin's instance of is recorded as group of stereoisomers[2].
  • daidzin's canonical SMILES is recorded as O=C1C(=COC2=CC(OC3OC(CO)C(O)C(O)C3O)=CC=C12)C=4C=CC(O)=CC4[3].
  • daidzin's InChI is recorded as InChI=1S/C21H20O9/c22-8-16-18(25)19(26)20(27)21(30-16)29-12-5-6-13-15(7-12)28-9-14(17(13)24)10-1-3-11(23)4-2-10/h1-7,9,16,18-23,25-27H,8H2[4].
  • daidzin's InChIKey is recorded as KYQZWONCHDNPDP-UHFFFAOYSA-N[5].
  • daidzin's chemical formula is recorded as C₂₁H₂₀O₉[6].
  • daidzin's subclass of is recorded as isoflavone[7].
  • daidzin's PubChem CID is recorded as 4183640[8].
  • daidzin's found in taxon is recorded as Pueraria tuberosa[9].
  • daidzin's found in taxon is recorded as Baptisia arachnifera[10].
  • daidzin's found in taxon is recorded as Baptisia cinerea[11].
  • daidzin's found in taxon is recorded as Baptisia lanceolata[12].
  • daidzin's found in taxon is recorded as Baptisia megacarpa[13].
  • daidzin's found in taxon is recorded as Baptisia simplicifolia[14].
  • daidzin's found in taxon is recorded as Baptisia calycosa[15].
  • daidzin's found in taxon is recorded as Baptisia perfoliata[16].
  • daidzin's found in taxon is recorded as Baptisia lecontei[17].
  • daidzin's found in taxon is recorded as Baptisia bracteata[18].
  • daidzin's found in taxon is recorded as Baptisia nuttalliana[19].
  • daidzin's found in taxon is recorded as soybean[20].
  • daidzin's found in taxon is recorded as Thermopsis fabacea[21].
  • daidzin's found in taxon is recorded as Pueraria montana var. thomsonii[22].
  • daidzin's found in taxon is recorded as Pueraria montana var. lobata[23].
  • daidzin's Human Metabolome Database ID is recorded as HMDB0247842[24].
  • daidzin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+416.11073222'}[25].
  • daidzin's SureChEMBL ID is recorded as 3423674[26].

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] . A Chemical Investigation of Pueraria mirifica Roots. wikidata.org.
  9. [10] . The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae). wikidata.org.
  10. [11] . The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae). wikidata.org.
  11. [12] . The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae). wikidata.org.
  12. [13] . The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae). wikidata.org.
  13. [14] . The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae). wikidata.org.
  14. [15] . The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae). wikidata.org.
  15. [16] . The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae). wikidata.org.
  16. [17] . Distribution of flavonoids in the genus baptisia (leguminosae). wikidata.org.
  17. [18] . The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae). wikidata.org.
  18. [19] . The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae). wikidata.org.
  19. [20] . Malonyl Isoflavone Glycosides in Soybean Seeds (Glycine maxMerrill). wikidata.org.
  20. [21] . Isoflavonoids in the roots of Thermopsis fabacea D.C. (Leguminosae).. wikidata.org.
  21. [22] . Neurocytoprotective effects of the bioactive constituents of Pueraria thomsonii in 6-hydroxydopamine (6-OHDA)-treated nerve growth factor (NGF)-differentiated PC12 cells. wikidata.org.
  22. [23] . Isolation of two new C-glucofuranosyl isoflavones from Pueraria lobata (Wild.) Ohwi with HPLC-MS guiding analysis. wikidata.org.
  23. [24] . wikidata.org.
  24. [25] . wikidata.org.
  25. [26] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. 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). daidzin. Retrieved May 3, 2026, from https://4ort.xyz/entity/daidzin-q105147884
MLA “daidzin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/daidzin-q105147884.
BibTeX @misc{4ortxyz_daidzin-q105147884_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{daidzin}}, year = {2026}, url = {https://4ort.xyz/entity/daidzin-q105147884}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): daidzin — https://4ort.xyz/entity/daidzin-q105147884 (retrieved 2026-05-03)

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