Quercetagetin

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 Edit this at Wikidata
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).
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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. ^ d'Agostino, Mario; Simone, Francesco De; Piacente, Sonia; Pizza, Cosimo; Senatore, Felice (May 1997). "Quercetagetin 6-O-β-d-glucopyranoside from Tagetes mandonii". Phytochemistry. 45 (1): 201–202. Bibcode:1997PChem..45..201D. doi:10.1016/S0031-9422(96)00727-3.