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Ellagic acid is a natural antioxidant as well as a potent, ATP-competitive inhibitor of CK2 and SHP2 with IC50 and Ki values of 40 nM and 20 nM, respectively.In addition, Ellagic acid exhibits antiproliferative activity and inhibition of topoisomerase II (Topoisomerase II).
| Cell Experiment | |
|---|---|
| Cell lines | Peripheral blood mononuclear cells (PBMCs) |
| Preparation method | Cells were cultured in a humidified incubator maintained at 37 °C and 5% CO2 atmosphere with or without known concentrations of caffeic acid, ellagic acid and ferulic acid for 18 h. Cell viability was assayed by trypan exclusion method. |
| Concentrations | 100 and 200 μM |
| Incubation time | 18 h |
| Animal Experiment | |
|---|---|
| Animal models | Sprague-Dawley rat |
| Formulation | DMSO |
| Dosages | 75 mg/kg |
| Administration | IP injections |
| Molecular Weight | 302.19 |
| Formula | C14H6O8 |
| CAS Number | 476-66-4 |
| Solubility (25°C) | DMSO |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
[2] Jasmina Djedjibegovic, et al. Ellagic Acid-Derived Urolithins as Modulators of Oxidative Stress
[4] Giuseppe Derosa, et al. Ellagic Acid and Its Role in Chronic Diseases
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| Irinotecan Hydrochloride Trihydrate
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