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Ginsenoside Rg3

CAT: 0013-GTR19159643-01Size: 200 mgDry Ice: NoHazardous: No
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CAT#:0013-GTR19159643-01Size:200 mg
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Description
Ginsenoside Rg3 is a K 7.1 channel activator, γ2 GABA-A receptor agonist, and a α10 nAChR antagonist found in Panax. It exhibits a wide variety of biological activities, including decreasing expression of pro-inflammatory cytokines, reducing oxidative stress, and inhibiting tubular formation and migration of endothelial progenitor cells. (In Vitro) :Ginsenoside Rg3 plays an important role in its effect on the Na+ channel. Treatment with Ginsenoside Rg3 reversibly inhibits the inward Na+ peak current (INa) with an IC50 of 32.2±4.5 μM, and the inhibition is voltage-dependent. Ginsenoside Rg3 at 100 μM inhibits the hKv1.4 channel currents by an average of 65%.The Ginsenoside Rg3 effect is concentration-dependent and reversible. The IC50 value and Hill coefficient are 32.6±2.2 μM and 1.59±0.13, respectively. Ginsenoside Rg3 shows the significant inhibition of NF-κB activity thereby reduced COX-2 expression. To examine the cytotoxicity of Ginsenoside Rg3 on IL-1β-induced inflamed A549 cells, the cells are firstly treated with IL-1β (10 ng/mL) for 4 h and treated with 100 to 900 ng/mL concentration of Ginsenoside Rg3 for 12 h. Cell viability is analyzed using an MTT assay. There is no observed cytotoxicity of Ginsenoside Rg3 in IL-1β-induced inflamed A549 cells compared to only PBS-treated cells (Con) .To obtain the anti-inflammatory effects of Ginsenoside Rg3 on inflammation induced human lung epithelial cells, A549 cells inflammation is induced by IL-1β (10 ng/mL) and then treated by 5 μM of Dexamethasone (Dex) or 900 nM of Rg3. The NF-κB activation is analyzed by a western blot analysis to evaluate the effect of Ginsenoside Rg3 treatment on A549 cells. Phospho-NF-κB p65/total NF-κB p65 densitometry in the cells treated with Rg3 shows the significant decrease compared to IL-1β-induced inflamed A549 cells. The meaning of reducing the ratio of p-p65/p65 by Rg3 treatment is associated with NF-κB activation. Ginsenoside Rg3 also downregulates the expression of COX-2 effectively. (In Vivo) :Ginsenoside Rg3 ((20S) -Rg3) is an Aβ-lowering Natural Compound. APP/PS1 mice are treated with Ginsenoside Rg3 once a day for 4 weeks by intraperitoneal injection (10 mg/kg/day) . Aβ ELISA analysis of brain tissues reveal that Ginsenoside Rg3 treatment results in a significant reduction of Aβ40 and Aβ42 in the brain.
CAS Number
14197-60-5
Product Name Alternative
Ginsenoside RG3 | VN10040 | VN 10040
Purity
>98% (HPLC)
Solubility
DMSO : ≥ 50 mg/mL; 63.69 mM
Smiles
[C@@H]1 ([C@@H] ([C@H] ([C@@H] ([C@H] (O1) CO) O) O) O) O[C@H]1[C@@H] (O[C@@H] ([C@H] ([C@@H]1O) O) CO) O[C@H]1CC[C@]2 ([C@H] (C1 (C) C) CC[C@]1 ([C@@]3 (CC[C@@H] ([C@H]3[C@@H] (C[C@H]21) O) [C@] (C) (CCC=C (C) C) O) C) C) C
Molecular Formula
C42H72O13
Molecular Weight
785.02
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Other Product Names
2- ((4,5-dihydroxy-2- ((12-hydroxy-17- (2-hydroxy-6-methylhept-5-en-2-yl) -4,4,8,10,14-pentamethylhexadecahydro-1H-cyclopenta[a]phenanthren-3-yl) oxy) -6- (hydroxymethyl) tetrahydro-2H-pyran-3-yl) oxy) -6- (hydroxymethyl) tetrahydro-2H-pyran-3,4,5-triol