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VEGFR-2-IN-51 (compound 19) 作为一种口服活性的双靶点抑制剂,针对VEGFR-2 (IC50=15.33 μM) 和tubulin (IC50=0.76 μM) 显示出了抗肿瘤活性.该化合物通过降低线粒体膜电位并提高活性氧 (ROS) 的水平来诱导肿瘤细胞的凋亡 (apoptosis).它还通过阻断VEGFR-2/PI3K/AKT信号通路实现抗血管生成的效果.此外,VEGFR-2-IN-51 在对抗胃癌细胞系MGC-803时表现出极佳的抗增殖活性,其IC50值仅为0.005 μM.
VEGFR-2-IN-51 (compound 19) 作为一种口服活性的双靶点抑制剂,针对VEGFR-2 (IC50=15.33 μM) 和tubulin (IC50=0.76 μM) 显示出了抗肿瘤活性.该化合物通过降低线粒体膜电位并提高活性氧 (ROS) 的水平来诱导肿瘤细胞的凋亡 (apoptosis).它还通过阻断VEGFR-2/PI3K/AKT信号通路实现抗血管生成的效果.此外,VEGFR-2-IN-51 在对抗胃癌细胞系MGC-803时表现出极佳的抗增殖活性,其IC50值仅为0.005 μM.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 询价 | 期货 | |
50 mg | 询价 | 期货 |
产品描述 | VEGFR-2-IN-51 (compound 19) is an orally active dual-target inhibitor of VEGFR-2 (IC50=15.33 μM) and tubulin (IC50=0.76 μM) that exhibits antitumor activity. This compound induces apoptosis in tumor cells by reducing mitochondrial membrane potential and increasing levels of reactive oxygen species (ROS). Additionally, VEGFR-2-IN-51 suppresses angiogenesis through inhibition of the VEGFR-2/PI3K/AKT signaling pathway. Moreover, it demonstrates significant antiproliferative effects on the gastric cancer cell line MGC-803 (IC50=0.005 μM). |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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