- 全部删除
- 您的购物车当前为空
SH514是一种特异性的IRF4抑制剂,IC 50=2.63 μM,结合到IRF4的DNA结合域(IRF4-DBD),从而阻断IRF4的转录活性,抑制IRF4下游基因CCNC、CANX、E2F5、CMYC、HK2、Blimp1,抑制MM细胞周期相关蛋白CDC2、Cyclin B1、Cyclin D1、Cyclin E1、CMYC的表达,可用于研究多发性骨髓瘤和恶性血液病。
SH514是一种特异性的IRF4抑制剂,IC 50=2.63 μM,结合到IRF4的DNA结合域(IRF4-DBD),从而阻断IRF4的转录活性,抑制IRF4下游基因CCNC、CANX、E2F5、CMYC、HK2、Blimp1,抑制MM细胞周期相关蛋白CDC2、Cyclin B1、Cyclin D1、Cyclin E1、CMYC的表达,可用于研究多发性骨髓瘤和恶性血液病。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 10,600 | In stock |
SH514 相关产品
产品描述 | SH514 is a specific IRF4 inhibitor with an IC₅₀ of 2.63 µM, binding to the DNA-binding domain (IRF4-DBD) of IRF4 to block its transcriptional activity and inhibit the expression of downstream genes such as CCNC, CANX, E2F5, CMYC, HK2, and Blimp1, and inhibits the expression of MM cell cycle-related proteins CDC2, Cyclin B1, Cyclin D1, Cyclin E1, and CMYC, making it useful for studying multiple myeloma and malignant haematological diseases. |
别名 | SH 514 |
分子量 | 514.66 |
分子式 | C32H38N2O4 |
Smiles | C[C@@H]([C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C(=O)C=C4[C@@]3(C=C(C(=O)C4(C)C)C#N)C)C)C(=O)NC5=CC=C(C=C5)OC |
存储 | keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 80.00 mg/mL (155.44 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
|
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。
评论内容