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ChemicalBook--->CAS DataBase List--->166734-06-1

166734-06-1

166734-06-1 Structure

166734-06-1 Structure
IdentificationBack Directory
[Name]

beta-D-Glucopyranoside 3-[(1Z)-2-[4-(beta-D-glucopyranosyloxy)-2-hydroxyphenyl]ethenyl]-5-hydroxyphenyl
[CAS]

166734-06-1
[Synonyms]

cis-Mulberroside A
beta-D-Glucopyranoside 3-[(1Z)-2-[4-(beta-D-glucopyranosyloxy)-2-hydroxyphenyl]ethenyl]-5-hydroxyphenyl
[Molecular Formula]

C26H32O14
[MDL Number]

MFCD17167012
[MOL File]

166734-06-1.mol
[Molecular Weight]

568.524
Chemical PropertiesBack Directory
[Boiling point ]

954.7±65.0 °C(Predicted)
[density ]

1.654
[form ]

Solid
[pka]

9.03±0.40(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

Cis-Mulberroside A is an impurity of Mulberroside A is a stilbenoid found in Morus alba plants. Potential metabolite for Oxyresveratrol (O861920), a natural hydroxystilbene with similar bioactivity to resveratrol. COX-1 inhibitor like resveratrol (R150000), anti-cancer agent.
[in vivo]

Mulberroside A (10, 20, and 40 mg/kg) decreases serum uric acid levels and increases urinary urate excretion and fractional excretion of uric acid in hyperuricemic mice[4].

Animal Model:Male Kun-Ming mice (20±2 g)[4]
Dosage:5, 10, 20, and 40 mg/kg; the dose volume 10 mL/kg body weight
Administration:Orally initiated at 9:00 a.m.
Result:10, 20, and 40 mg/kg significantly increased urinary urate excretion in 24 h, resulting in a remarkable elevation of fractional excretion of uric acid (FEUA), and the highest dose completely reversed FEUA alteration of hyperuricemic mice to normal.
[IC 50]

IL-6; IL-1β
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