RETV804M kinase inhibitor is a selective c-RET (V804M) inhibitor with IC50 value of 20nM.
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产品名称 | c-RET ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Regorafenib |
+++
RET, IC50: 1.5 nM |
98% | |||||||||||||||||
TG101209 |
++
RET, IC50: 17 nM |
FLT3 | 99%+ | ||||||||||||||||
Danusertib |
+
RET, IC50: 31 nM |
99%+ | |||||||||||||||||
AD80 |
++++
RET V804M, IC50: 0.6 nM RET wt, IC50: 1.3 nM |
Src,Raf | 99+% | ||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | RET is a single-pass transmembrane protein with a typical intracellular tyrosine kinase domain. Among the various oncogene drivers in NSCLC (non-small-cell lung cancer), the RET gene is involved in various chromosomal rearrangements, which can be found in 1%–2% of all NSCLC patients[2]. RETV804M kinase inhibitor is a wt-RET-selective inhibitor of RETV804M kinase with an IC50 of 20 nM, which exhibits 3.7 and 110 fold selectivity over wt-RET and KDR, respectively[1]. |
作用机制 | The pyrazolopyrimidine core of RETV804M kinase inhibitor would bind to the hinge region, directing the benzamide towards the catalytic lysine (Lys758) and placing the pyridine in the pocket normally occupied by the ribose moiety of ATP[1]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.90mL 0.58mL 0.29mL |
14.52mL 2.90mL 1.45mL |
29.04mL 5.81mL 2.90mL |
CAS号 | 2414909-94-5 |
分子式 | C19H16N6O |
分子量 | 344.37 |
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 Inert atmosphere,Room Temperature |
溶解度 |
DMSO: 120 mg/mL(348.46 mM),配合低频超声助溶,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 |