Specifications
A cell-permeable, non-peptide inhibitor of MDM2-p53 interactions (Ki=120nM). Treatment of cancer cells activates p53 and accumulation of p21, p53, and MDM2. The structure mimics three p53 residues involved in binding to MDM2.
Info
| Purity | >97% (TLC, HPLC), NMR (conforms) |
| Quantity | 10 mg |
| Molecular Weight | 340.4 Da |
| Physical State | White solid |
| Solubility | DMSO (25mg/ml) |
| CAS No. | 6964-62-1 |
| Storage | 4°C, (-20°C Long term). The product can be shipped at room temperature. |
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