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首页-小分子抑制剂&激动剂-Tyrosine Kinase-Focal Adhesion Kinase (FAK)-NVP-TAE226
NVP-TAE226

Chemical Structure : NVP-TAE226

CAS No.: 761437-28-9

NVP-TAE226 (TAE-226;TAE226)

货号: PC-43388Not For Human Use, Lab Use Only.

NVP-TAE226 (TAE226) is a potent FAK inhibitor with IC50 of 5.5 nM, also potently inhibits Pyk2 (IC50=5 nM), 10- to 100-fold less potent against IR, IGF-IR, ALK, and c-Met kinases.

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10 mg ¥1380 In stock
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50 mg ¥3580 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

NVP-TAE226 (TAE226) is a potent FAK inhibitor with IC50 of 5.5 nM, also potently inhibits Pyk2 (IC50=5 nM), 10- to 100-fold less potent against IR, IGF-IR, ALK, and c-Met kinases.
TAE226 suppresses the growth and invasion of glioma cells, inhibits extracellular matrix-induced autophosphorylation of FAK Tyr397.
TAE226 also inhibits IGF-I-induced phosphorylation of IGF-IR and activity of its downstream target genes such as MAPK and Akt.
TAE226 significantly increases the survival rate of animals in glioma xenograft model.

物理化学性质&存储条件

分子量 468.936
分子式 C23H25ClN6O3
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

Benzamide, 2-[[5-chloro-2-[[2-methoxy-4-(4-morpholinyl)phenyl]amino]-4-pyrimidinyl]amino]-N-methyl-

参考文献

1. Halder J, et al. Cancer Res. 2007 Nov 15;67(22):10976-83.

2. Liu TJ, et al. Mol Cancer Ther. 2007 Apr;6(4):1357-67.

3. Watanabe N, et al. Clin Cancer Res. 2008 Jul 15;14(14):4631-9.

4. Sakurama K, et al. Mol Cancer Ther. 2009 Jan;8(1):127-34.

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