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ChemicalBook--->CAS DataBase List--->53209-27-1

53209-27-1

53209-27-1 Structure

53209-27-1 Structure
IdentificationBack Directory
[Name]

2'-O-GALLOYLHYPERIN
[CAS]

53209-27-1
[Synonyms]

Q-100605
FT-0689359
-O-GALLOYLHYPERIN
2''-galloylhyperin
3 -O-GALLOYLHYPERIN
2'-O-GALLOYLHYPERIN
Quercetin 3-β-galactoside-2''-gallate
Quercetin 3-b-galactoside-2'-O-gallate
Quercetin 3-beta-galactoside-2''-gallate
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[[2-O-(3,4,5-trihydroxybenzoyl)-β-D-galactopyranosyl]oxy]-
[6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-2,3-dihydroxy-4-(hydroxymethyl)cyclohexyl] 3,5-dihydroxy-4-methoxybenzoate
[(2S,3R,4S,5R,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate
[Molecular Formula]

C28H24O16
[MDL Number]

MFCD07781428
[MOL File]

53209-27-1.mol
[Molecular Weight]

616.48
Chemical PropertiesBack Directory
[Boiling point ]

1106.9±65.0 °C(Predicted)
[density ]

1.94±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 30 mg/ml; Ethanol:PBS (pH 7.2) (1:3): 0.25 mg/ml
[form ]

A crystalline solid
[pka]

6.17±0.40(Predicted)
[color ]

Light yellow to yellow
Safety DataBack Directory
[HS Code ]

29389090
Hazard InformationBack Directory
[Uses]

2"-O-Galloylhyperin, an active compound isolated from Pyrola incarnate Fisch., possesses anti-oxidative and anti-inflammatory activities. 2"-O-Galloylhyperin has hepatoprotective effect against oxidative stress-induced liver damage[1][2].
[Definition]

ChEBI: 2''-galloylhyperin is a member of flavonoids and a glycoside.
[References]

[1] Wang P, et al. 2'-O-Galloylhyperin Isolated From Pyrola incarnata Fisch. Attenuates LPS-Induced Inflammatory Response by Activation of SIRT1/Nrf2 and Inhibition of the NF-κB Pathways in Vitro and Vivo. Front Pharmacol. 2018 Jun 27;9:679. DOI:10.3389/fphar.2018.00679
[2] Wang P, et al. Hepatoprotective effect of 2'-O-galloylhyperin against oxidative stress-induced liver damage through induction of Nrf2/ARE-mediated antioxidant pathway. Food Chem Toxicol. 2017 Apr;102:129-142. DOI:10.1016/j.fct.2017.02.016
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