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同义名 : | ARRY-614 |
CAS号 : | 945614-12-0 | |
货号 : | A189540 | |
分子式 : | C31H33FN6O3 | |
纯度 : | 99%+ | |
分子量 : | 556.63 | |
MDL号 : | MFCD28502055 | |
存储条件: |
Pure form Sealed in dry, 2-8°C In solvent -20°C:3-6个月-80°C:12个月 |
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溶解度 : | - | |
动物实验配方: |
生物活性 | |||
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描述 | Acute myeloid leukemia and myelodysplastic syndromes are incurable hematologic neoplasms in which the angiopoietin-1/Tie-2 pathway is over-activated. Pexmetinib is a small molecular, orally bioavailable inhibitor of the angiopoietin-1 receptor Tie-2 and the pro-inflammatory kinase p38 MAPK. The IC50 values of pexmetinib against Tie-2, p38 MAPK α and β were 1, 35, and 36 nM, respectively. Pexmetinib also inhibited phospho-Tie-2 and phospho-p38 in HEK-Tie2 cells with IC50 values of 16 and 1 nM, respectively. It was predicted that the plasma concentrations of pexmetinib to achieve 50% inhibition for phospho-Tie-2 and phospho-p38 in human blood samples were 2282 and 172 nM, respectively. In TNF-α-treated leukemic KG1 cells, pexmetinib at 10 nM completely abrogated TNF-α-induced activation of p38 MAPK, MAPKAPK2 and EIF4E. In primary CD34+ stem cells, pexmetinib at 0.1 μM significantly reversed the myelosuppressive effects induced by TNF-α[3]. Mechanism: Pexmetinib is a type 2 kinase inhibitor that binds both Tie-2 and p38 MAPK in the “DFG-out” conformation[3]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.80mL 0.36mL 0.18mL |
8.98mL 1.80mL 0.90mL |
17.97mL 3.59mL 1.80mL |
参考文献 |
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