Orobol

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Orobol
220px
Orborol molecule
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
480-23-9 YesY
292790
ChEBI CHEBI:69437 N
ChemSpider 4445113 N
Jmol 3D model Interactive image
MeSH D011794
PubChem 5281801
  • 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
  • C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O
Properties
C15H10O6
Molar mass 286.23 g/mol
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
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

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  1. Orobol on curehunter.com
  2. 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