| Name | Mogroside III-E |
| Description | Mogroside III-E, a cucurbitane-type compound isolated from Siraitia grosvenorii, exhibits anti-inflammatory activity by attenuating LPS-induced acute lung injury in mice through the regulation of the TLR4/MAPK/NF-κB axis via AMPK activation. Additionally, it demonstrates anti-fibrotic activity by reducing pulmonary fibrosis through Toll-Like receptor 4 pathways. |
| In vitro | MG IIIE elevated the cell viability of HG-induced MPC-5 cells, reduced the concentrations of inflammatory cytokines and decreased the levels of oxidative stress-related markers.?What's more, the apoptosis of podocytes induced by HG was inhibited after MG IIIE intervention, accompanied by the upregulated expression of Bcl-2 and downregulated expression of Bax, cleaved caspase-3 and cleaved caspase-9.?It was also found that MG IIIE could activate the AMPK/SIRT1 signaling, but compound C inhibited this pathway and reversed the inhibitory effects of MG IIIE on inflammation, oxidative stress and apoptosis in HG-stimulated podocytes. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 1 mg/mL (1.04 mM), Sonication is recommended. DMSO : 9.64 mg/mL (10.01 mM), Sonication is recommended.
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| Keywords | TNF-α | TLR | Mogroside III-E | Mogroside IIIE | Mogroside III E | Inhibitor | inhibit | ILReceptor | IL Receptor |
| Inhibitors Related | Kaolin | Undecane | Acetylcysteine | Ethyl palmitate | Gum arabic | Hydroxychloroquine | Benzyl alcohol | 1,8-Cineole | Dodecane | 1,4-Naphthoquinone | Tributyrin | Glucosamine |
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