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PARP1-IN-27 (Compound 9B),作为PARP1和PARP2的有效抑制剂,在SUM149PT细胞中的IC50分别达到2.53 nM和6.45 nM。此外,PARP1-IN-27对BRCA突变癌细胞系SUM149PT、HCC1937和Capan-1的增殖抑制效果显著,相应的IC50值为0.62、1.91和4.26 μM。该化合物能够加剧DNA双链断裂,促进ROS生成,并在G2/M期阻滞细胞周期,最终在SUM149PT细胞中触发细胞凋亡(apoptosis)。
PARP1-IN-27 (Compound 9B),作为PARP1和PARP2的有效抑制剂,在SUM149PT细胞中的IC50分别达到2.53 nM和6.45 nM。此外,PARP1-IN-27对BRCA突变癌细胞系SUM149PT、HCC1937和Capan-1的增殖抑制效果显著,相应的IC50值为0.62、1.91和4.26 μM。该化合物能够加剧DNA双链断裂,促进ROS生成,并在G2/M期阻滞细胞周期,最终在SUM149PT细胞中触发细胞凋亡(apoptosis)。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 询价 | 期货 | |
50 mg | 询价 | 期货 |
产品描述 | PARP1-IN-27 (Compound 9B) serves as an inhibitor of both PARP1 and PARP2, exhibiting IC 50 values of 2.53 nM and 6.45 nM, respectively, in SUM149PT cells. This compound effectively suppresses the proliferation of BRCA-mutated cancer cell lines such as SUM149PT, HCC1937, and Capan-1, with respective IC 50 values of 0.62, 1.91, and 4.26 μM. Additionally, PARP1-IN-27 exacerbates DNA double-strand breaks, enhances ROS production, causes G2/M phase cell cycle arrest, and triggers apoptosis in SUM149PT cells. |
分子量 | 313.28 |
分子式 | C17H12FNO4 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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