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Geraniin is a TNF-α releasing inhibitor with an IC50 of 43 μM, it has numerous activities including anticancer, anti-inflammatory, and anti-hyperglycemic activities. Geraniin significantly decreases the viability of OVCAR3 and SKOV3 cells in a concentration-dependent fashion. The IC50 value for Geraniin treatment is 34.5±2.8 μM in OVCAR3 cells and 23.6±1.9 μM in SKOV3 cells.
In vivo, oral administration of Geraniin to rats (50 mg/kg/d or 100 mg/kg/d) inhibit the elevation of serum total cholesterol, lipid peroxide, free fatty acid, triglyceride, glutamic oxaloacetic transaminase and glutamic pyruvic transaminase induced by treatment with peroxidized oil.
Molecular Weight | 952.64 |
Formula | C41H28O27 |
CAS Number | 60976-49-0 |
Solubility (25°C) | DMSO ≥ 90 mg/mL |
Storage | 2-8°C, protect from light, dry, sealed |
[5] Erika Moreno, et al. Geraniin is a diuretic by inhibiting the Na +-K +-2Cl - cotransporter NKCC2
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