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Flavanomarein

🥰Excellent
Catalog No. TN1644Cas No. 577-38-8

Flavanomarein demonstrates potent antioxidative property, including free radical scavenging activity, inhibition of lipid peroxidation, as well as lipid-lowering effects in human HepG2 hepatocellular carcinoma cells treated with free fatty acids (FFAs).

Flavanomarein

Flavanomarein

🥰Excellent
Purity: 98.63%
Catalog No. TN1644Cas No. 577-38-8
Flavanomarein demonstrates potent antioxidative property, including free radical scavenging activity, inhibition of lipid peroxidation, as well as lipid-lowering effects in human HepG2 hepatocellular carcinoma cells treated with free fatty acids (FFAs).
Pack SizePriceAvailabilityQuantity
1 mg$40In Stock
5 mg$64In Stock
10 mg$106In Stock
25 mg$176In Stock
1 mL x 10 mM (in DMSO)$82In Stock
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Purity:98.63%
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Product Introduction

Bioactivity
Description
Flavanomarein demonstrates potent antioxidative property, including free radical scavenging activity, inhibition of lipid peroxidation, as well as lipid-lowering effects in human HepG2 hepatocellular carcinoma cells treated with free fatty acids (FFAs).
In vitro
The present study aimed to identify the active compounds of Coreopsis tinctoria and to investigate the molecular mechanisms underlying its effects on lipid dysregulation by measuring lipid levels, reactive oxygen species, lipid peroxidation and fatty acid synthesis. The present results demonstrated that snow chrysanthemum aqueous extracts significantly reduced serum lipid levels and oxidative stress in vivo. The main compounds that were isolated were identified as Flavanomarein (compound 1) and eriodictyol 7-O-β-D glucopyranoside (compound 2). Compounds 1 and 2 demonstrated potent antioxidative properties, including free radical scavenging activity, inhibition of lipid peroxidation, as well as lipid-lowering effects in human HepG2 hepatocellular carcinoma cells treated with free fatty acids (FFAs). Compound 2 was revealed to suppress the elevation of triglyceride levels and inhibit lipid peroxidation following FFA treatment. In addition, it was demonstrated to significantly reduce intracellular levels of reactive oxygen species and improve the mitochondrial membrane potential and adenosine triphosphate levels, thus protecting mitochondrial function in FFA-treated HepG2 cells. Furthermore, compound 2 markedly suppressed the protein expression levels of disulfide-isomerase A3 precursor and fatty acid synthase, thus suppressing FFA-induced lipogenesis in HepG2 cells[1]
Chemical Properties
Molecular Weight450.39
FormulaC21H22O11
Cas No.577-38-8
SmilesOC[C@H]1O[C@@H](Oc2ccc3C(=O)C[C@H](Oc3c2O)c2ccc(O)c(O)c2)[C@H](O)[C@@H](O)[C@@H]1O
Relative Density.1.665g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 60 mg/mL (133.22 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.2203 mL11.1015 mL22.2030 mL111.0149 mL
5 mM0.4441 mL2.2203 mL4.4406 mL22.2030 mL
10 mM0.2220 mL1.1101 mL2.2203 mL11.1015 mL
20 mM0.1110 mL0.5551 mL1.1101 mL5.5507 mL
50 mM0.0444 mL0.2220 mL0.4441 mL2.2203 mL
100 mM0.0222 mL0.1110 mL0.2220 mL1.1101 mL

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