lupinisoflavone A

group of stereoisomers with the chemical formula C₂₀H₁₆O₆
ChemicalSubstance group_of_stereoisomers Q104384990
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lupinisoflavone A

Summary

lupinisoflavone An is a group of stereoisomers[1].

Key Facts

  • lupinisoflavone A's instance of is recorded as group of stereoisomers[2].
  • lupinisoflavone A's CAS Registry Number is recorded as 93373-45-6[3].
  • lupinisoflavone A's canonical SMILES is recorded as O=C1C(=COC=2C=C3OC(C(=C)C)CC3=C(O)C12)C=4C=CC(O)=CC4O[4].
  • lupinisoflavone A's InChI is recorded as InChI=1S/C20H16O6/c1-9(2)15-6-12-16(26-15)7-17-18(19(12)23)20(24)13(8-25-17)11-4-3-10(21)5-14(11)22/h3-5,7-8,15,21-23H,1,6H2,2H3[5].
  • lupinisoflavone A's InChIKey is recorded as DOGAHANJPKBCGB-UHFFFAOYSA-N[6].
  • lupinisoflavone A's chemical formula is recorded as C₂₀H₁₆O₆[7].
  • lupinisoflavone A's subclass of is recorded as 6C-prenylisoflavone[8].
  • lupinisoflavone A's PubChem CID is recorded as 5319901[9].
  • lupinisoflavone A's ChEBI ID is recorded as 175503[10].
  • lupinisoflavone A's found in taxon is recorded as Morus insignis[11].
  • lupinisoflavone A's found in taxon is recorded as Lupinus texensis[12].
  • lupinisoflavone A's found in taxon is recorded as Cajanus[13].
  • lupinisoflavone A's found in taxon is recorded as Lupinus albus[14].
  • lupinisoflavone A's found in taxon is recorded as Lupinus luteus[15].
  • lupinisoflavone A's Human Metabolome Database ID is recorded as HMDB0038127[16].
  • lupinisoflavone A's LIPID MAPS ID is recorded as LMPK12050278[17].
  • lupinisoflavone A's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+352.094688232'}[18].
  • lupinisoflavone A's SureChEMBL ID is recorded as 29934592[19].
  • lupinisoflavone A's DSSTox substance ID is recorded as DTXSID201314808[20].
  • lupinisoflavone A's UniChem compound ID is recorded as 248591[21].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Chemical Abstracts Service. Retrieved . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . PubChem. Retrieved . wikidata.org.
  9. [10] . ChEBI release 2022-06-13. wikidata.org.
  10. [11] . Components of the Root Bark of Morus insignis Bur. 2. Structures of Four New Isoprenylated Xanthones, Morusignins E, F, G. and H. wikidata.org.
  11. [12] . Flavonoids from Lupinus texensis and their free radical scavenging activity. wikidata.org.
  12. [13] . Two isoprenylated isoflavone phytoalexins from Cajanus cajan. wikidata.org.
  13. [14] . Application of gas chromatography-mass spectrometry to the identification of isoflavonoids in lupine root extracts. wikidata.org.
  14. [15] . Prenylated flavonoids in the roots of yellow lupin. wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . wikidata.org.
  20. [21] . UniChem. wikidata.org.

Class ancestry

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

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APA 4ort.xyz Knowledge Graph. (2026). lupinisoflavone A. Retrieved May 3, 2026, from https://4ort.xyz/entity/lupinisoflavone-a
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BibTeX @misc{4ortxyz_lupinisoflavone-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{lupinisoflavone A}}, year = {2026}, url = {https://4ort.xyz/entity/lupinisoflavone-a}, note = {Accessed: 2026-05-03}}
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