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NVP-TAE226

Chemical Structure : NVP-TAE226

CAS No.: 761437-28-9

NVP-TAE226 (TAE-226;TAE226)

Catalog No.: 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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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

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.

Physicochemical Properties

M.Wt 468.936
Formula C23H25ClN6O3
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
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-

References

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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