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EGFR-IN-11 是 EGFR-酪氨酸激酶的选择性抑制剂,可诱导细胞凋亡。 EGFR-IN-11 抑制三重突变体 EGFRL858R/T790M/C797S,IC50 为 18 nM,并在 G0/G1 时阻止细胞周期。
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EGFR-IN-11 是 EGFR-酪氨酸激酶的选择性抑制剂,可诱导细胞凋亡。 EGFR-IN-11 抑制三重突变体 EGFRL858R/T790M/C797S,IC50 为 18 nM,并在 G0/G1 时阻止细胞周期。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 472 | 现货 | |
5 mg | ¥ 1,150 | 现货 | |
10 mg | ¥ 1,690 | 现货 | |
25 mg | ¥ 2,690 | 现货 | |
50 mg | ¥ 3,550 | 现货 | |
100 mg | ¥ 4,890 | 现货 | |
200 mg | ¥ 6,590 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 1,470 | 现货 |
产品描述 | EGFR-IN-11 is a selective inhibitor of EGFR-tyrosine kinase and induces cell apoptosis. EGFR-IN-11 inhibits triple mutant EGFRL858R/T790M/C797S with an IC50 of 18 nM and arrests cell cycle at G0/G1. |
靶点活性 | EGFR (L858R/T790M/C797S):18 nM |
体外活性 | EGFR-IN-11 (0.1 nM-10 µM) 对HCC827、H1975和A549细胞表现出抗增殖作用,IC50分别为0.88 nM、0.20 µM和2.91 μM。在浓度依赖性的条件下,EGFR-IN-11 (10nM-10 µM) 在HCC827、H1975和A549细胞中抑制了EGFR的磷酸化[1]。 |
分子量 | 573.71 |
分子式 | C29H35N9O2S |
CAS No. | 2463200-44-2 |
Smiles | CN1CCN(CC1)c1ccc(Nc2ncc3nc(Nc4ccccc4)n([C@@H]4CCN(C4)S(=O)(=O)C4CC4)c3n2)cc1 |
密度 | 1.48 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 112.5 mg/mL (196.1 mM ), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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