Luteone (isoflavone)

For other uses, see Luteone (disambiguation).

Luteone

Chemical structure of luteone
Names
IUPAC name 2′,4′,5,7-Tetrahydroxy-6-(3-methylbut-2-en-1-yl)isoflavone
Systematic IUPAC name 3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-en-1-yl)-4H-1-benzopyran-4-one
Other names Ruizgenin
Identifiers
CAS Number	41743-56-0  Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:27917  N
ChEMBL	ChEMBL549617
ChemSpider	4445109  N
KEGG	C10498
PubChem CID	5281797
UNII	FU3E0232IF  Y
CompTox Dashboard (EPA)	DTXSID00194574
InChI InChI=1S/C20H18O6/c1-10(2)3-5-13-16(23)8-17-18(19(13)24)20(25)14(9-26-17)12-6-4-11(21)7-15(12)22/h3-4,6-9,21-24H,5H2,1-2H3 Key: MMPVAPMCVABQPS-UHFFFAOYSA-N
SMILES CC(=CCC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=C(C=C(C=C3)O)O)O)C
Properties
Chemical formula	C20H18O6
Molar mass	354.358 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N  verify  (what is  YN ?) Infobox references

Luteone is a prenylated isoflavone, a type of flavonoid. It can be found in the pods of Laburnum anagyroides ^[1] and can be synthesized. ^[2]

References

1. Sato H.; Tahara S.; Ingham J. L.; Dziedzic S. Z. (1995). "Isoflavones from pods of Laburnum anagyroides" . Phytochemistry . 39 (3): 673–676. doi:10.1016/0031-9422(95)00029-7.
2. Tsukayama M.; Wada H.; Kishida M.; Nishiuchi M.; Kawamura Y. (2000). "Regioselective Synthesis of Prenylisoflavones. Syntheses of Luteone and Luteone Hydrate" . Chem Lett . 29 (12): 1362–1363. doi:10.1246/cl.2000.1362.