MP7 (PDK1 inhibitor) is a phosphoinositide-dependent kinase-1 ( PDK1 ) inhibitor. In Vitro Cell counting of U87MG-derived glioma stem cells (GSCs) confirms that Alisertib and, to a minor extent, MP7 (PDK1 inhibitor) are able to decrease the number of viable cells. When combined together, GSC viability is further reduced with respect to single-treated cells. As observed in U87MG cells, when used at the highest concentrations (i.e., 1.5 μM Alisertib and 2.5 μM MP7), a significant enhancement in the number of dead cells is evidenced. Following 72 h treatment, MP7 alone does not show a significant inhibition of glioblastoma multiforme (GBM) proliferation. MP7 has been shown to have only minimal effects on monolayer cell growth in several cancer cell lines, with IC 50 values in the micromolar range. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid IC50& Target:PDK1
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MP7
CAS number：1001409-50-2 molecular formula：C28H22F2N4O4
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| Chinese alias | - | ||
| English alias | DTXSID90678515 | 1-(3,4-Difluorobenzyl)-2-Oxo-N-{(1r)-2-[(2-Oxo-2,3-Dihydro-1h-Benzimidazol-5-Yl)oxy]-1-Phenylethyl}-1,2-Dihydropyridine-3-Carboxamide | BRD-K09186807-001-01-6 | CHEBI:91373 | HY-14440 | PDK1 inhibitor | BDBM50361645 | NCGC00346947-02 | SC | ||
| CAS number | 1001409-50-2 | molecular formula | C28H22F2N4O4 |
| molecular weight | 516.50 g/mol | Exact mass | ≥99% |
| PSA | 99.800 Ų | logp | 4 |
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