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SIAIS039是一款针对c-ros致癌基因1(ROS1)的口服活性PROTAC,它在HCC78细胞、Ba/F3细胞(表达CD74-ROS1融合)以及Ba/F3细胞(表达SDC4-ROS1融合)中展现出的DC50分别为154.46 nM、126.47 nM、143.69 nM.该化合物能够抑制ROS1阳性细胞的增殖、诱导细胞周期停滞和细胞凋亡,并有效抑制克隆形成.在动物体内试验中,SIAIS039也显示出了对ROS1驱动型肿瘤生长的明显抑制效果.SIAIS039的组成包括ALK抑制剂Brigatinib、连接子EM-12以及VHL E3泛素连接酶配体(Red: Brigatinib; Blue: VHL ligand; Black: linker).
SIAIS039是一款针对c-ros致癌基因1(ROS1)的口服活性PROTAC,它在HCC78细胞、Ba/F3细胞(表达CD74-ROS1融合)以及Ba/F3细胞(表达SDC4-ROS1融合)中展现出的DC50分别为154.46 nM、126.47 nM、143.69 nM.该化合物能够抑制ROS1阳性细胞的增殖、诱导细胞周期停滞和细胞凋亡,并有效抑制克隆形成.在动物体内试验中,SIAIS039也显示出了对ROS1驱动型肿瘤生长的明显抑制效果.SIAIS039的组成包括ALK抑制剂Brigatinib、连接子EM-12以及VHL E3泛素连接酶配体(Red: Brigatinib; Blue: VHL ligand; Black: linker).
规格 | 价格 | 库存 | 数量 |
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10 mg | 询价 | 期货 | |
50 mg | 询价 | 期货 |
产品描述 | SIAIS039 is an orally active PROTAC specifically targeting c-ros oncogene 1 (ROS1), demonstrating DC50 values of 154.46 nM, 126.47 nM, and 143.69 nM in HCC78 cells, Ba/F3 cells expressing CD74-ROS1 fusion, and Ba/F3 cells expressing SDC4-ROS1 fusion, respectively. This compound inhibits proliferation, induces cell cycle arrest, and triggers apoptosis in ROS1-positive cells, while also inhibiting colony formation. In vivo, SIAIS039 exhibits potent anti-tumoral activity against ROS1-driven tumor growth. The composition of SIAIS039 includes the ALK inhibitor Brigatinib, linker EM-12, and VHL E3 ubiquitin ligase ligand (Red:Brigatinib; Blue: VHL ligand; Black: linker). |
分子量 | 878.4 |
分子式 | C46H53ClN9O5P |
CAS No. | 2570251-69-1 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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