Chemistry:Quercetin 3,4'-diglucoside

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Quercetin 3,4'-diglucoside
Chemical structure of quercetin 3,4'-diglucoside.
Names
IUPAC name
3,4′-Bis(β-D-glucopyranosyloxy)-3′,5,7-trihydroxyflavone
Systematic IUPAC name
5,7-Dihydroxy-2-(3-hydroxy-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-1-benzopyran-4-one
Other names
Quercetin 3,4’-di-O-β-glucopyranoside
Quercetin-3,4'-O-di-beta-glucopyranoside
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
Properties
C27H30O17
Molar mass 626.4 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Tracking categories (test):

Quercetin 3,4'-diglucoside is a flavonol glycoside found in onions (Allium cepa)[1][2] and in horse chestnut seeds (Aesculus hippocastanum).[3]

References

  1. Williamson, Gary; Plumb, Geoff W.; Uda, Yasushi; Price, Keith R.; Rhodes, Michael J.C. (1996). "Dietary quercetin glycosides: Antioxidant activity and induction of the anticarcinogenic phase II marker enzyme quinone reductase in Hepalclc7 cells". Carcinogenesis 17 (11): 2385–7. doi:10.1093/carcin/17.11.2385. PMID 8968052. 
  2. Olsson, Marie E.; Gustavsson, Karl-Erik; Vågen, Ingunn M. (2010). "Quercetin and Isorhamnetin in Sweet and Red Cultivars of Onion (Allium cepaL.) at Harvest, after Field Curing, Heat Treatment, and Storage". Journal of Agricultural and Food Chemistry 58 (4): 2323–30. doi:10.1021/jf9027014. PMID 20099844. 
  3. Wagner, J. (1961). "Quercetin-3,4′-diglukosid, ein Flavonolglykosid des Roßkastaniensamens". Die Naturwissenschaften 48 (2): 54. doi:10.1007/BF00603428. Bibcode1961NW.....48Q..54W.