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1816331-66-4

中文名称 1816331-66-4
CAS 1816331-66-4
分子式 C30H31FN6O4
分子量 558.6
MOL 文件 1816331-66-4.mol
更新日期 2024/05/28 12:00:31
1816331-66-4 结构式 1816331-66-4 结构式

基本信息

中文别名
异柠檬酸脱氢酶1(IDH1)突变体抑制剂(GSK864)
英文别名
GSK864
GSK864 >=98% (HPLC)
1H-Pyrazolo[4,3-c]pyridine-3,7-dicarboxamide, 1-[(4-fluorophenyl)methyl]-4,5,6,7-tetrahydro-N3-(4-methoxy-3,5-dimethylphenyl)-7-methyl-5-(1H-pyrrol-2-ylcarbonyl)-, (7S)-

物理化学性质

储存条件2-8°C
形态粉末
颜色白色至米色
旋光性 (optical activity)[α]/D -66 to -76°, c = 0.5 in methanol
1816331-66-4价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-195401816331-66-4
GSK864
1816331-66-42mg850元
2024/04/30HY-195401816331-66-4
GSK864
1816331-66-45mg2000元
2024/04/30HY-195401816331-66-4
GSK864
1816331-66-410mM * 1mLin DMSO2458元

常见问题列表

生物活性
GSK864是异柠檬酸脱氢酶1 (IDH1) 突变体抑制剂; 抑制IDH1突变体R132C,R132H和R132G的IC50值分别为8.8,15.2和16.6 nM。
靶点

IC50: 8.8 nM (IDH1 mutants R132C), 15.2 nM (IDH1 mutants R132H), 16.6 nM (IDH1 mutants R132G)

体外研究

GSK864 inhibits 2-HG production in R132C IDH1 mutant HT1080 fibrosarcoma cells with an EC 50 of 320 nM by LCMS/MS analysis.

体内研究

Following intraperitoneal (IP) administration in CD-1 mice, significant concentrations of GSK864 are maintained in peripheral blood samples of mice for up to 24 hours. Analysis of BM cells for expression of markers of early differentiation reveals slightly increased numbers of huCD45 + CD38 + cells in R132C or R132H IDH1 mutant engrafted mice treated with GSK864.

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