| Size | Price | Stock |
|---|---|---|
| 1mg | $220 | In-stock |
| 5mg | $550 | In-stock |
| 10 mg | Get quote | |
| 50 mg | Get quote | |
| We match the lowest price on market. | ||
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| Cat. No. : | HY-N3841 |
| M.Wt: | 454.47 |
| Formula: | C28H22O6 |
| Purity: | >98 % |
| Solubility: | 10 mM in DMSO |
ε-Viniferin (epsilon-Viniferin), the dimer of Resveratrol and can be isolated from Vitis vinifera, displays a potent inhibitory for all the CYP activities, with Ki values from 0.5-20 μM. ε-Viniferin possesses potent antioxidant, anti-inflammatory, anti-diabetic, and anti-neurodegenerative capacity[1][2][3].
In Vitro:ε-Viniferin (1-15 μM, 24-72 h) inhibits proliferation of HOS, U2OS, and A549 cells[3].
ε-Viniferin (20 μM, 24 h) induces DNA fragmentation and nuclear condensation in HOS, U2OS, A549 cells[3].
ε-Viniferin (10 μM, 1 h) inhibits TGF-β1 induced EMT, invasion and migration, and reverses TGF-β1-induced ROS, MMP2, vimentin, Zeb1, Snail, p-SMAD2, p-SMAD3, and ABCG2 expression in A549 cells[4].
ε-Viniferin (10 μM, 3 min) inhibits fMLP (0.1 μM)-induced superoxide anion production in human neutrophils, as well as fMLP-induced phosphorylation of ERK, Akt, Src or intracellular calcium mobilization[5].
ε-Viniferin (50 nM-10 μM, 48 h) protects cells against Rotenone (HY-B1756)-induced neurotoxicity in SH-SY5Y cells via the SIRT3/FOXO3 pathway[6].
ε-Viniferin (1 μM, 24 h) inhibits Rotenone (HY-B1756)-induced mitochondrial depolarization and oxidative stress in SH-SY5Y cells[6].
In Vivo:ε-Viniferin (5 mg/kg, i.p., 5 days per week for 4 weeks) inhibits tumor growth in A549 cell xenograft nude mice model without hepatic and kidney injury, and inhibits tumor metastasis in A549 cell lung metastasis mouse model[3][4].
ε-Viniferin (0.2% in diet, 4 weeks) prevents diet-induced obesity in mice[7].
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