PD184161

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Chemical Structure| 212631-67-9 同义名 : -
CAS号 : 212631-67-9
货号 : A685594
分子式 : C17H13BrClF2IN2O2
纯度 : 99%+
分子量 : 557.56
MDL号 : MFCD16038897
存储条件:

Pure form Keep in dark place, sealed in dry, 2-8°C

In solvent -20°C:3-6个月-80°C:12个月

溶解度 : -
动物实验配方:
生物活性
描述 PD184161 is an orally active MEK inhibitor. It inhibits MEK activity in a time- and concentration-dependent manner with an IC50 ranging from 10 to 100 nM. PD184161 suppresses cell proliferation and induces apoptosis. It also produces antidepressant-like behaviors[1][2]. PD184161 inhibits cell proliferation and induces apoptosis in a time- and concentration-dependent manner within the concentration range of 1-20 μM, over time periods of 24, 48, or 72 hours. PD184161 (0.1 and 1.0 μM; 1 hour) inhibits the phosphorylation of ERK1,2[1].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

1.79mL

0.36mL

0.18mL

8.97mL

1.79mL

0.90mL

17.94mL

3.59mL

1.79mL

参考文献

[1]Deng M, Qin Y, et al. Combination of celecoxib and PD184161 exerts synergistic inhibitory effects on gallbladder cancer cell proliferation. Oncol Lett. 2017 May;13(5):3850-3858.

[2]Gladbach A, van Eersel J, et al. ERK inhibition with PD184161 mitigates brain damage in a mouse model of stroke. J Neural Transm (Vienna). 2014 May;121(5):543-7.