Pseudobaptigenin

Pseudobaptigenin
Chemical structure of pseudobaptigenin
Pseudobaptigenin molecule
Names
IUPAC name
7-Hydroxy-3′,4′-[methylenebis(oxy)]isoflavone
Systematic IUPAC name
3-(2H-1,3-Benzodioxol-5-yl)-7-hydroxy-4H-1-benzopyran-4-one
Other names
ψ-Baptigenin
Psi-baptigenin
7-Hydroxy-3',4'-methylenedioxyisoflavone
7-Hydroxy-3', 4'-methylenedioxyisoflavone
Identifiers
CAS Number
  • 90-29-9
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:8602 checkY
ChEMBL
  • ChEMBL486176
ChemSpider
  • 4445117
KEGG
  • C10522
PubChem CID
  • 5281805
UNII
  • 78RRL4HLL9
CompTox Dashboard (EPA)
  • DTXSID70237982 Edit this at Wikidata
InChI
  • InChI=1S/C16H10O5/c17-10-2-3-11-14(6-10)19-7-12(16(11)18)9-1-4-13-15(5-9)21-8-20-13/h1-7,17H,8H2
    Key: KNJNBKINYHZUGC-UHFFFAOYSA-N
  • InChI=1/C16H10O5/c17-10-2-3-11-14(6-10)19-7-12(16(11)18)9-1-4-13-15(5-9)21-8-20-13/h1-7,17H,8H2
    Key: KNJNBKINYHZUGC-UHFFFAOYAK
  • C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O
Properties
Chemical formula
 C16H10O5
Molar mass 282.24 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Chemical compound

Pseudobaptigenin is an isoflavone, a type of flavonoid. It can be isolated in Trifolium pratense (red clover).[1]

References

  1. ^ Identification of isoflavones calycosin and pseudobaptigenin in Trifolium pratense. David R. Biggs and Geoffrey A. Lane, Phytochemistry, Volume 17, Issue 9, 1978, Pages 1683-1684
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Isoflavones and their glycosides
IsoflavonesO-methylated isoflavonesGlycosidesPrenylated isoflavones
Pyranoisoflavones
Derivatives
Synthetic


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