Orobol

Orobol
Names


IUPAC name 3-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one
Other names Isoluteolin Santol 5,7,3',4'-Tetrahydroxyisoflavone 3',4',5,7-Tetrahydroxyisoflavone
Identifiers
CAS Number	480-23-9^Y
Beilstein Reference	292790
ChEBI	CHEBI:69437^N
ChemSpider	4445113^N
Jmol interactive 3D	Image
MeSH	D011794
PubChem	5281801
InChI InChI=1S/C15H10O6/c16-8-4-12(19)14-13(5-8)21-6-9(15(14)20)7-1-2-10(17)11(18)3-7/h1-6,16-19H^N Key: IOYHCQBYQJQBSK-UHFFFAOYSA-N^N InChI=1/C15H10O6/c16-8-4-12(19)14-13(5-8)21-6-9(15(14)20)7-1-2-10(17)11(18)3-7/h1-6,16-19H Key: IOYHCQBYQJQBSK-UHFFFAOYAR
SMILES C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O
Properties
Chemical formula	C₁₅H₁₀O₆
Molar mass	286.23 g/mol
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

Orobol is one of several known isoflavones. It can be isolated from Aspergillus niger or Streptomyces neyagawaensis. It is a potent inhibitor of Phosphoinositide 3-kinase.^[1]^[2]

References

↑ Orobol on curehunter.com
↑ Isoflavonoids, genistein, psi-tectorigenin, and orobol, increase cytoplasmic free calcium in isolated rat hepatocytes. Tomonaga, T : Mine, T : Kojima, I : Taira, M : Hayashi, H : Isono, K, 1992

Isoflavones and their glycosides

Isoflavones	Daidzein Genistein Irilone Orobol Pseudobaptigenin Anagyroidisoflavone A and B

O-methylated isoflavones	Biochanin A Calycosin Formononetin Glycitein Irigenin 5-O-methylgenistein Pratensein Prunetin Psi-tectorigenin Retusin Tectorigenin

Glycosides	Daidzin Genistin Iridin Ononin Puerarin Sophoricoside Tectoridin

Prenylated isoflavones	Bidwillol A Derrubone Luteone 7-O-Methylluteone Wighteone

Pyranoisoflavones	Alpinumisoflavone Barbigerone Di-O-methylalpinumisoflavone 4'-methyl-alpinumisoflavone

Misc	Rotenoids

Synthetic	Ipriflavone

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