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Quercetin 3-(6″-caffeoylsophoroside)

Quercetin 3-(6″-caffeoylsophoroside) Basic information
Product Name:Quercetin 3-(6″-caffeoylsophoroside)
Synonyms:Quercetin 3-(6″-caffeoylsophoroside);Butanediamide, N1-[1-(2,3-dimethoxyphenyl)-2-[(1,1-dimethylethyl)amino]-2-oxoethyl]-N1-(3-ethoxypropyl)-N4-(5-methyl-3-isoxazolyl)-
CAS:1032595-77-9
MF:C27H40N4O7
MW:532.63
EINECS:
Product Categories:
Mol File:1032595-77-9.mol
Quercetin 3-(6″-caffeoylsophoroside) Structure
Quercetin 3-(6″-caffeoylsophoroside) Chemical Properties
Boiling point 769.683±60.00 °C(Press: 760.00 Torr)(predicted)
density 1.169±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
pka12.703±0.70(predicted)
Safety Information
MSDS Information
Quercetin 3-(6″-caffeoylsophoroside) Usage And Synthesis
UsesQuercetin 3-(6″-caffeoylsophoroside) is an orally active α-amylase inhibitor, with an IC50 of 73.66 μg/mL. Quercetin 3-(6″-caffeoylsophoroside) presents in thehydro-methanolic extract of Cardamine hirsuta Linn. Quercetin 3-(6″-caffeoylsophoroside) shows the antidiabetic activities by oxidative stress reduction and α-amylase inhibition. Quercetin 3-(6″-caffeoylsophoroside) can be used for diabetes mellitus research[1].
in vivo

Quercetin 3-(6″-caffeoylsophoroside) (50, 100, 500, 1000, and 2000 mg/kg, p.o.) shows safety in acute oral toxicity of SD rats and can be used in anti-diabetic research[1].
Quercetin 3-(6″-caffeoylsophoroside) (125, 250, 500 mg/kg, p.o.) improves type 2 diabetes mellitus of SD rats by oxidative stress reduction and α-amylase inhibition[1].

Animal Model:FED HFD (45% fat) for 30 days to induce type 2 diabetes mellitus in SD rats[1]
Dosage:125, 250, 500 mg/kg
Administration:Oral gavage (p.o.)
Result:Significantly decreased the blood glucose level, improved biochemical parameters as well as oxidative stress by reduction of lipid peroxidation, and increased high-density lipoproteins with dose of 500mg/kg.
Enhanced activities of glutathione-s-transferase, glutathione, superoxide dismutase.
Restored cellular architecture in the histopathological examination.
Animal Model:Acute oral toxicity in 8-week male SD rats[1]
Dosage:50, 100, 500, 1000, and 2000 mg/kg
Administration:Oral gavage (p.o.)
Result:Safe for use in anti-diabetic research.
References[1] Malik A, et.al. In Vitro, In Silico, and In Vivo Studies of Cardamine hirsute Linn as a Potential Antidiabetic Agent in a Rat Model. ACS Omega. 2023 Jun 12;8(25):22623-22636. DOI:10.1021/acsomega.3c01034
Quercetin 3-(6″-caffeoylsophoroside) Preparation Products And Raw materials
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