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. Author manuscript; available in PMC: 2011 Jan 1.
Published in final edited form as: J Liq Chromatogr Relat Technol. 2010 Jan 1;33(16):1502–1515. doi: 10.1080/10826076.2010.489000

Fig. 3.

Fig. 3

Chemical structures of ten flavonols from Flos Gossypii isolated by HSCCC

No. compound R1 R2 R3 R4 R5
I Kaempferol-3-O-β-D-(6″-O-p-coumaroyl)-glucoside (6″-p-coumaroyl) –Glu H H OH OH
II 8-methoxyl-kaempferol-7-O-β-D-rhamnoside H Rha OMe H H
III Astragalin Glu H H H H
IV 4′-methoxyl-quercetin-7-O-β-D-glucoside H Glu H OH OMe
V Quercetin-3′-O-β-D-glucoside H H H OGlu H
VI -- -- -- -- -- --
VII Hyperoside Gal H H OH H
VIII Quercetin-3-O-β-D-glucoside Glu H H OH H
IX Quercetin-7-O-β-D-glucoside H Glu H OH H
X Quercetin H H H OH H