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描述 | CH7057288 is a potent and selective TRK inhibitor. In an intracranial implantation model simulating brain metastases, CH7057288 induced intracranial tumour regression and greatly improved event-free survival. CH7057288 can be used as a therapeutic agent for TRK fusion-positive cancers. The TRK receptor tyrosine kinase is expressed in a variety of cancer types, including lung and colorectal cancers, in the form of fusion proteins encoded by various fusion genes[1]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.76mL 0.35mL 0.18mL |
8.78mL 1.76mL 0.88mL |
17.55mL 3.51mL 1.76mL |
CAS号 | 2095616-82-1 |
分子式 | C32H31N3O5S |
分子量 | 569.671 |
别名 | |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,2-8°C |
溶解度 |
DMSO: 35 mg/mL(61.44 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |