CNX-2006
目录号: A13755
EGFR 抑制剂
CNX-2006 是一种强效的、选择性的 EGFR 抑制剂,在具有激活性 EGFR 突变的细胞以及携带 T790M 突变的细胞中表现出优异的体外活性。CNX-2006 是 CO-1686 的原型,目前正在针对 EGFR 突变型肺癌的治疗进行第一阶段临床试验。
Discription | CNX-2006 is a potent, mutant-selective EGFR inhibitor with excellent in vitro activity in cells with activating EGFR mutations, as well as in cells harbouring the T790M mutation. CNX-2006 is the prototype for CO-1686, which is currently in a Phase I clinical trial for the treatment of EGFR-mutant lung cancer. | ||
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Targets |
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目录号 | A13755 |
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分子式 | C26H27F4N7O2 |
分子量 | 545.53 |
CAS号 | 1375465-09-0 |
SMILES | COC1=C(C=CC(=C1)NC2CN(C2)CCF)NC3=NC=C(C(=N3)NC4=CC(=CC=C4)NC(=O)C=C)C(F)(F)F |
其他名称 | CNX2006, CNX 2006 |
储存条件 | Store lyophilized at -20ºC, keep desiccated. |
In vitro | DMSO | 90 mg/mL (164.97 mM) | |
Water | Insoluble | ||
Ethanol | 26 mg/mL (47.65 mM) | ||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
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0.1 mM | 18.33 mL | 91.65 mL | 183.31 mL |
0.5 mM | 3.67 mL | 18.33 mL | 36.66 mL |
1 mM | 1.83 mL | 9.17 mL | 18.33 mL |
5 mM | 0.37 mL | 1.83 mL | 3.67 mL |
Calculate the dilution required to prepare a stock solution. This equation is commonly abbreviated as: C1V1 = C2V2