Pseudobaptigenin

Pseudobaptigenin
Names
	IUPAC name 3-(1,3-benzodioxol-5-yl)-7-hydroxychromen-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 ;
ChEMBL	ChEMBL486176;
ChemSpider	4445117;
KEGG	C10522;
PubChem CID	5281805;
UNII	78RRL4HLL9;
CompTox Dashboard (EPA)	DTXSID70237982 ;
	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;
	SMILES 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

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

References

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Isoflavones and their glycosides
Isoflavones	Daidzein Genistein Orobol
O-methylated isoflavones	Biochanin A Calycosin Formononetin Glycitein Irigenin 5-O-methylgenistein Pratensein Prunetin Psi-tectorigenin Retusin Tectorigenin
Glycosides	Daidzin Genistin Iridin Mirificin Ononin Puerarin Sophoricoside Tectoridin
Prenylated isoflavones	Bidwillol A Derrubone Luteone 7-O-Methylluteone Wighteone
Pyranoisoflavones	Alpinumisoflavone Barbigerone Di-O-methylalpinumisoflavone 4'-methyl-alpinumisoflavone
Derivatives	Anagyroidisoflavone A and B Irilone Pseudobaptigenin Rotenoids
Synthetic	Ipriflavone