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Multi-target kinase-IN-9 是一种具有抗增殖和抗血管生成活性的多靶点酶抑制剂,对肝癌细胞显示显著选择性。其可广泛结合 DNA 聚合酶 β、丙酮酸激酶 (Pyruvate Kinase)M2(PKM2) 等关键酶的活性位点或 ATP 结合区域,破坏 DNA 修复与复制、糖酵解、染色质动态及转录程序,并抑制癌症干细胞自我更新,进而导致基因组不稳定性、溶酶体功能障碍及自噬流中断,诱导肿瘤细胞死亡,抑制肿瘤增殖、侵袭、转移与血管生成,并显著降低异种移植模型中的肿瘤体积,可用于肝癌相关研究。
Multi-target kinase-IN-9 是一种具有抗增殖和抗血管生成活性的多靶点酶抑制剂,对肝癌细胞显示显著选择性。其可广泛结合 DNA 聚合酶 β、丙酮酸激酶 (Pyruvate Kinase)M2(PKM2) 等关键酶的活性位点或 ATP 结合区域,破坏 DNA 修复与复制、糖酵解、染色质动态及转录程序,并抑制癌症干细胞自我更新,进而导致基因组不稳定性、溶酶体功能障碍及自噬流中断,诱导肿瘤细胞死亡,抑制肿瘤增殖、侵袭、转移与血管生成,并显著降低异种移植模型中的肿瘤体积,可用于肝癌相关研究。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 10 mg | 待询 | 待询 | |
| 50 mg | 待询 | 待询 |
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| 产品描述 | Multi-target kinase-IN-9 is a multi-target enzyme inhibitor with antiproliferative and antiangiogenic activity, showing significant selectivity for liver cancer cells. By extensively binding to active sites or ATP-binding regions of several key enzymes, such as DNA polymerase β and pyruvate kinase M2 (PKM2), it disrupts DNA repair and replication, glycolysis, chromatin dynamics, and transcriptional programs, blocking cancer stem cell self-renewal. This compound induces genomic instability, lysosomal dysfunction, and autophagic flux interruption, leading to tumor cell death. It effectively inhibits tumor proliferation, invasion, metastasis, and angiogenesis, significantly reducing tumor volume in xenograft models. Multi-target kinase-IN-9 is applicable in liver cancer research. |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. 实际储存温度请以COA为准 |
对于不同动物的给药剂量换算,您也可以参考 更多