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Revision as of 00:12, 21 June 2020 editFswitzer4 (talk | contribs)Extended confirmed users10,572 editsm Added FDA UNII← Previous edit Revision as of 02:39, 6 June 2021 edit undoLegionMammal978 (talk | contribs)Extended confirmed users7,894 edits correct IUPAC nameNext edit →
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| ImageSize1 = 220 | ImageSize1 = 220
| ImageAlt1 = Orborol molecule | ImageAlt1 = Orborol molecule
| IUPACName = 3-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one | IUPACName = 3′,4′,5,7-Tetrahydroxyisoflavone
| PIN = 3-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4''H''-1-benzopyran-4-one
| OtherNames = Isoluteolin<br>Santol<br>5,7,3',4'-Tetrahydroxyisoflavone<br>3',4',5,7-Tetrahydroxyisoflavone | OtherNames = Isoluteolin<br>Santol<br>5,7,3',4'-Tetrahydroxyisoflavone
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}} | CASNo_Ref = {{cascite|correct|??}}

Revision as of 02:39, 6 June 2021

Orobol
Orborol molecule
Names
IUPAC name 3′,4′,5,7-Tetrahydroxyisoflavone
Preferred IUPAC name 3-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one
Other names Isoluteolin
Santol
5,7,3',4'-Tetrahydroxyisoflavone
Identifiers
CAS Number
3D model (JSmol)
Beilstein Reference 292790
ChEBI
ChemSpider
MeSH D011794
PubChem CID
UNII
CompTox Dashboard (EPA)
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/h1-6,16-19HKey: IOYHCQBYQJQBSK-UHFFFAOYSA-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/h1-6,16-19HKey: 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 , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

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.

References

  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". Archived from the original on 2009-07-19. Retrieved 2009-09-15.
Isoflavones and their glycosides
Isoflavones
O-methylated isoflavones
Glycosides
Prenylated isoflavones
Pyranoisoflavones
Derivatives
Synthetic
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