| Identification | Back Directory | [Name]
quercetin 3-O-gentobioside | [CAS]
7431-83-6 | [Synonyms]
Quercetin 3-gentiobioside
quercetin 3-O-gentobioside
Quercetin 3-O-gentiobioside
Quercetin 3-O-β-Gentiobioside
6''-O-β-D-Glucopyranosylhyperin
Quercetin 3-O-beta-gentiobioside
3,3',4',5,7-Pentahydroxyflavone 3-gentiobioside
quercetin3-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside
quercetin 3-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside
3-[(6-O-β-D-Glucopyranosyl-β-D-glucopyranosyl)oxy]-3',4',5,7-tetrahydroxyflavone
3-[[6-O-(β-D-Glucopyranosyl)-β-D-glucopyranosyl]oxy]-3',4',5,7-tetrahydroxyflavone
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl 6-O-β-D-glucopyranosyl-β-D-glucopyranoside
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3-[(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-5,7-dihydroxy-
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy]methyl]tetrahydropyran-2-yl]oxy]-4H-chromen-4-one | [Molecular Formula]
C27H30O17 | [MDL Number]
MFCD29904548 | [MOL File]
7431-83-6.mol | [Molecular Weight]
626.52 |
| Chemical Properties | Back Directory | [Melting point ]
205-207℃ (chloroform ) | [Boiling point ]
1033.2±65.0 °C(Predicted) | [density ]
1.89±0.1 g/cm3(Predicted) | [pka]
6.17±0.40(Predicted) |
| Hazard Information | Back Directory | [Uses]
Quercetin 3-O-β-Gentiobioside is a derivative of Quercetin (Q509500), a flavonoid with anticancer activity. It is a mitochondrial ATPase and phosphodiesterase inhibitor. It Inhibits PI3-kinase activity and slightly inhibits PIP kinase activity. Quercetin has antiproliferative effects on cancer cell lines, | [Definition]
ChEBI:Quercetin 3-beta-gentiobioside is a quercetin O-glycoside in which the hydroxy hydrogen at position 3 of quercetin has been replaced by a gentiobiosyl group. It has a role as a Brassica napus metabolite. It is a quercetin O-glycoside, a disaccharide derivative and a tetrahydroxyflavone. It is functionally related to a gentiobiose. |
|
|