Quercetagetin
Chemical structure of quercetagetin
Ball-and-stick model of the quercetagetin molecule
Names
IUPAC name
3,3′,4′,5,6,7-Hexahydroxyflavone
Systematic IUPAC name
2-(3,4-Dihydroxyphenyl)-3,5,6,7-tetrahydroxy-4H-1-benzopyran-4-one
Other names
6-Hydroxyquercetin
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.001.794
UNII
  • InChI=1S/C15H10O8/c16-6-2-1-5(3-7(6)17)15-14(22)13(21)10-9(23-15)4-8(18)11(19)12(10)20/h1-4,16-20,22H ☒N
    Key: ZVOLCUVKHLEPEV-UHFFFAOYSA-N ☒N
  • InChI=1/C15H10O8/c16-6-2-1-5(3-7(6)17)15-14(22)13(21)10-9(23-15)4-8(18)11(19)12(10)20/h1-4,16-20,22H
    Key: ZVOLCUVKHLEPEV-UHFFFAOYAZ
  • C1=CC(=C(C=C1C2=C(C(=O)C3=C(C(=C(C=C3O2)O)O)O)O)O)O
Properties
C15H10O8
Molar mass 318.23 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 checkY☒N ?)
Infobox references

Quercetagetin is a flavonol, a type of flavonoid. It can be found in the genus Eriocaulon.[1]

Glycosides

Quercetagetin-6-O-β-D-glucopyranoside from Tagetes mandonii.[2]

References

  1. ↑ Quercetagetin and patuletin in Eriocaulon. E. C. Bate-Smith and J. B. Harborne, Phytochemistry, Volume 8, Issue 6, June 1969, pp. 1035-1037, doi:10.1016/S0031-9422(00)86351-7
  2. ↑ Quercetagetin-6-O-β-D-glucopyranoside from Tagetes mandonii. Mario D'Agostino, Francesco De Simone, Sonia Piacente, Cosimo Pizza and Felice Senatore, Phytochemistry, Volume 45, Issue 1, May 1997, Pages 201-202


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.