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F-1 是 ALK 和 ROS1 的双重抑制剂,抑制 ALK 的磷酸化及下游通路,可作用于对 ALKWT (IC50:2.1 nM),ROS1WT (IC50:2.3 nM),ALKL1196M (IC50:1.3 nM) 和 ALKG1202R (IC50:3.9 nM)。
F-1 是 ALK 和 ROS1 的双重抑制剂,抑制 ALK 的磷酸化及下游通路,可作用于对 ALKWT (IC50:2.1 nM),ROS1WT (IC50:2.3 nM),ALKL1196M (IC50:1.3 nM) 和 ALKG1202R (IC50:3.9 nM)。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 550 | 现货 | |
5 mg | ¥ 1,430 | 现货 | |
10 mg | ¥ 1,980 | 现货 | |
25 mg | ¥ 3,330 | 现货 | |
50 mg | ¥ 4,720 | 现货 | |
100 mg | ¥ 6,360 | 现货 | |
200 mg | ¥ 8,570 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 1,750 | 现货 |
产品描述 | F-1 is IC50s of 2.1 nM, 2.3 nM, 1.3 nM and 3.9 nM for ALKWT, ROS1WT, ALKL1196M and ALKG1202R, respectively. F-1 is a potent ALK and ROS1 dual inhibitor, suppresses phospho-ALK and its relative downstream signaling pathways. |
靶点活性 | ROS1 (WT):2.3 nM, ALK (WT):2.1 nM, ALK (G1202R):3.9 nM, ALK (L1196M):1.3 nM |
分子量 | 519.02 |
分子式 | C22H27ClN8O3S |
CAS No. | 2244775-31-1 |
Smiles | COc1nc(ccc1Nc1ncc(Cl)c(Nc2ccccc2NS(C)(=O)=O)n1)N1CCN(C)CC1 |
密度 | no data available |
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: 100 mg/mL (192.67 mM) | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
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