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RET-IN-22

更新时间:2024-01-26 22:44:45

RET-IN-22结构式
RET-IN-22结构式
品牌特惠专场
常用名 RET-IN-22 英文名 RET-IN-22
CAS号 2918281-79-3 分子量 584.59
密度 N/A 沸点 N/A
分子式 C29H31F3N6O4 熔点 N/A
MSDS N/A 闪点 N/A

 RET-IN-22用途


RET-IN-22(化合物17b)是一种强效、选择性和口服活性的RET抑制剂,野生型RET和RET-V804M的IC50分别为20.9nM和18.3nM。RET-IN-22对大多数激酶显示出高度选择性,尤其是对EGFR和VEGFR2。RET-IN-22具有抗癌作用[1]。

 RET-IN-22名称

英文名 RET-IN-22

 RET-IN-22生物活性

描述 RET-IN-22(化合物17b)是一种强效、选择性和口服活性的RET抑制剂,野生型RET和RET-V804M的IC50分别为20.9nM和18.3nM。RET-IN-22对大多数激酶显示出高度选择性,尤其是对EGFR和VEGFR2。RET-IN-22具有抗癌作用[1]。
相关类别
靶点实验

IC50: 20.9 nM (wild-type RET) and 18.3 nM (RET-V804M)[1]

参考文献

[1]. Kaifu Wu, et al. Discovery of 3,5-diaryl-1H-pyrazol-based ureas as potent RET inhibitors. Eur J Med Chem. 2023 May 5;251:115237.  

 RET-IN-22物理化学性质

分子式 C29H31F3N6O4
分子量 584.59

 RET-IN-22靶点实验

查看更多实验

实验名称:Inhibition of RET signalling pathway in mouse BaF3 cells harboring CCDC6-RET-G810C mu...
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase receptor Ret
External Id:CHEMBL5349061
实验名称:AUC (0 to infinity) in Sprague-Dawley rat at 5 mg/kg, iv
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5349062
实验名称:Inhibition of RET signalling pathway in mouse BaF3 cells harboring CCDC6-RET-G810C mu...
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase receptor Ret
External Id:CHEMBL5349059
实验名称:Inhibition of RET signalling pathway in mouse BaF3 cells harboring CCDC6-RET-G810C mu...
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase receptor Ret
External Id:CHEMBL5349060
实验名称:Inhibition of RET signalling pathway in mouse BaF3 cells harboring CCDC6-RET assessed...
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase receptor Ret
External Id:CHEMBL5349057
实验名称:Inhibition of RET signalling pathway in mouse BaF3 cells harboring CCDC6-RET-V804M mu...
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase receptor Ret
External Id:CHEMBL5349058
实验名称:Inhibition of RET signalling pathway in mouse BaF3 cells harboring CCDC6-RET-V804M mu...
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase receptor Ret
External Id:CHEMBL5349055
实验名称:Inhibition of RET signalling pathway in mouse BaF3 cells harboring CCDC6-RET-G810C mu...
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase receptor Ret
External Id:CHEMBL5349056
实验名称:Inhibition of RET signalling pathway in mouse BaF3 cells harboring CCDC6-RET assessed...
来源:ChEMBL
靶标:Proto-oncogene tyrosine-protein kinase receptor Ret
External Id:CHEMBL5349054
实验名称:Antiproliferative activity against mouse BaF3 cells incubated for 72 hrs by CCK8 assa...
来源:ChEMBL
靶标:BaF3
External Id:CHEMBL5349045
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