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首页-小分子抑制剂&激动剂-Ras-Raf-MAPK-ERK Pathway-MEK (MAP2K)-PD184161
PD184161

Chemical Structure : PD184161

CAS No.: 212631-67-9

PD184161 (PD 184161;PD-184161)

货号: PC-60589Not For Human Use, Lab Use Only.

PD184161 is a potent, orally-active MEK1/2 inhibitor with IC50 of 10-100 nM.

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5 mg ¥980 In stock
10 mg ¥1580 In stock
25 mg ¥2780 In stock
50 mg ¥4680 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

PD184161 is a potent, orally-active MEK1/2 inhibitor with IC50 of 10-100 nM.
PD184161 inhibits HCC cell proliferation and induced apoptosis at concentrations of > or = 1.0 uM, significantly suppresses tumor engraftment and initial growth in tumor xenografts.
PD184161 also blocks AngII-driven HIF-1α protein in vascular smooth muscle cells, increases HIF-1α binding to von Hippel-Lindau tumor suppressor protein, blocks mitochondrial ROS production and cellular ATP levels.

物理化学性质&存储条件

分子量 557.6
分子式 C17H13BrClF2IN2O2
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

5-bromo-2-[(2-chloro-4-iodophenyl)amino]-N-(cyclopropylmethoxy)-3,4-difluoro-benzamide

参考文献

1. Klein PJ, et al. Neoplasia. 2006 Jan;8(1):1-8.

2. Yip-Schneider MT, et al. J Pharmacol Exp Ther. 2009 Jun;329(3):1063-70.

3. Mazharian A, et al. Exp Hematol. 2009 Oct;37(10):1238-1249.e5.

4. Jalouli M, et al. Mol Pharmacol. 2017 Nov;92(5):510-518.

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