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STAT3/HDAC-IN-2(化合物18)为STAT3与HDAC的双重抑制剂,通过促进细胞自噬及细胞凋亡发挥作用。该化合物是以天然产物异丙醇内酯 (IAL) 为基础制成的两亲性羟肟酸杂化物,并表现为纳米级抗癌剂。在水中,STAT3/HDAC-IN-2 能自组装成纳米颗粒,相较于游离态,其在肿瘤组织中的积累量和细胞摄取率更高,从而展现出更强大的抗癌效能。
STAT3/HDAC-IN-2(化合物18)为STAT3与HDAC的双重抑制剂,通过促进细胞自噬及细胞凋亡发挥作用。该化合物是以天然产物异丙醇内酯 (IAL) 为基础制成的两亲性羟肟酸杂化物,并表现为纳米级抗癌剂。在水中,STAT3/HDAC-IN-2 能自组装成纳米颗粒,相较于游离态,其在肿瘤组织中的积累量和细胞摄取率更高,从而展现出更强大的抗癌效能。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 待询 | 期货 | |
50 mg | 待询 | 期货 |
产品描述 | STAT3/HDAC-IN-2 (compound 18), a dual inhibitor of STAT3 and HDAC, promotes autophagy and apoptosis. This compound features an amphiphilic hydroxamic acid hybrid structure, derived from the natural product isopropanol lactone (IAL), and functions as a nanoscale anticancer agent. It has the ability to self-assemble into nanoparticles in aqueous environments, leading to enhanced tumor tissue accumulation, increased cellular uptake, and improved anticancer efficacy compared to its free state. |
分子量 | 508.56 |
分子式 | C28H32N2O7 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice./Shipping at ambient temperature. |
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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