(E)-AG 99CAS号: 122520-85-8分子式: C10H8N2O3分子量: 204.2描述纯度储存/保存方法别名可溶性/溶解性靶点In vitro(体外研究)参考文献
产品描述 | |
描述 |
AG 99 is a potent inhibitor of EGF receptor tyrosine kinase with IC50 value of 10 μM .AG 99 is a potent and competitive EGFR tyrosine kinase inhibitor against both the substrate polyGAT and ATP . In serum-starved human bladder carcinoma cell line 5637 cells, the 145-kDa protein, which was the β-subunit of c-Met/hepatocyte growth factor (HGF) receptor, was phosphorylated on 1003, 1234 and 1235 tyrosine residues. Also, tyrosine kinases EGFR and Src were activated. While, AG99 or inhibitors of Src (PP2, SU6656) significantly inhibited tyrosine phosphorylation of p145met and induced cell death through activation of caspase-like proteases. These results suggested that serum-independent growth of 5637 cells was involved by the tyrosine phosphorylation of p145met mediated by Src and EGFR.
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纯度 |
≥98%
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储存/保存方法 |
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
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基本信息 | |
别名 |
AG 99
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可溶性/溶解性 |
DMSO : 20 mg/mL
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生物活性 | |
靶点 |
EGFR
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In vitro(体外研究) |
AG99, a potent inhibitor of EGFR, was shown to inhibit the appearance of pp145 to some extent. AG99 promotes cell death of normal and cancer cells via activation of caspase-like proteases in vitro.
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参考文献 | |
参考文献 |
1.Gazit, A.,Yaish, P.,Gilon, C., et al. Tyrphostins I: Synthesis and biological activity of protein tyrosine kinase inhibitors. Journal of Medicinal Chemistry 32(10), 2344-2352 (1989).
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分子结构图