| Size | Price | Stock |
|---|---|---|
| 1mg | $130 | In-stock |
| 5mg | $320 | In-stock |
| 10mg | $520 | In-stock |
| 25mg | $990 | In-stock |
| 50 mg | Get quote | |
| 100 mg | Get quote | |
| We match the lowest price on market. | ||
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| Cat. No. : | HY-N3847 |
| M.Wt: | 450.39 |
| Formula: | C21H22O11 |
| Purity: | >98 % |
| Solubility: | DMSO : 100 mg/mL (ultrasonic) |
Eriodictyol-7-O-glucoside (Eriodictyol 7-O-β-D-glucoside), a flavonoid, is an Nrf2 activator. Eriodictyol-7-O-glucoside exhibits significant scavenging effects on both hydroxyl radicals and superoxide anions, with IC50 values of 0.28 mM and 0.30 mM, respectively. Eriodictyol-7-O-glucoside increases the nuclear localization of Nrf2 and induces the expression of the Nrf2/ARE-dependent genes. Eriodictyol-7-O-glucoside provides protection against oxygen and glucose deprivation (OGD)-induced oxidative insult. Eriodictyol-7-O-glucoside demonstrates neuroprotective efficacy in a rat model of focal cerebral ischemia (MCAO). Eriodictyol-7-O-glucoside can be used for the study of stroke[1][2][3].
IC50 & Target:Nrf2[1]
In Vitro:Eriodictyol-7-O-glucoside (7.5-60 μM, 16 h) induces ARE-dependent luciferase activity in a dose-dependent manner in MDA-MB-231-ARE-Luc cells[1].
Eriodictyol-7-O-glucoside (0-80 μM, 0-24 h) increases Nrf2 protein level in a time-dependent and dose-dependent manner, while Keap1 level remains relatively unaffected in MDA-MB-231 cells and primary cultured astrocytes[1][[2].
Eriodictyol-7-O-glucoside (0-160 μM, 24 h) does not affect Nrf2 mRNA level but induces mRNA of HO-1, NQO1 and GCLC dose-dependently in MDA-MB-231 cells[1].
Eriodictyol-7-O-glucoside (0-80 μM, 24 h) increases Nrf2 protein level and the protein levels of HO-1, NQO1, and cGCS in a dose-dependent manner in HRMC cells[1].
Eriodictyol-7-O-glucoside (80 μM, 0-4 h) increases Nrf2 protein levels in nucleus with time and decreases Nrf2 levels in cytoplasm gradually in HRMC cells[1].
Eriodictyol-7-O-glucoside (0-80 μM, 24 h) shows a dose-dependent increase in intracellular glutathione levels in HRMC cells and primary cultured astrocytes[1][2].
Eriodictyol-7-O-glucoside (80 μM) cotreatment with Cisplatin (HY-17394) significantly improves cell survival in HRMC cells[1].
Eriodictyol-7-O-glucoside (20-80 μM, pretreatment for 2 h) reduces oxygen and glucose deprivation (OGD)-induced cell death, intracellular ROS levels, and cleaved caspase-3 expression in primary cultured astrocytes[2].
In Vivo:Eriodictyol-7-O-glucoside (30 mg/kg, i.p., once daily, 5 days) demonstrates neuroprotective efficacy in a rat model of focal cerebral ischemia (MCAO)[2].
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