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N-deacetylated BMS-202 是 PD-1/PD-L1 相互作用的抑制剂,具有潜在的抗癌活性,可用于研究癌症。
N-deacetylated BMS-202 是 PD-1/PD-L1 相互作用的抑制剂,具有潜在的抗癌活性,可用于研究癌症。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
2 mg | ¥ 553 | In stock | |
5 mg | 待询 | 5日内发货 |
N-deacetylated BMS-202 相关产品
产品描述 | N-deacetylated BMS-202 is an inhibitor of PD-1/PD-L1 interactions and has potential anticancer activity for cancer research. |
体外活性 | N-deacetylated BMS-202 inhibits PD-1/PD-Ll interaction, and may augment therapeutic immune response to a number of histologically distinct tumors. Blockade of the PD-1/PD-Ll ligation using antibodies to PD-Ll has been shown to restore and augment T cell activation in many systems[1]. |
分子量 | 377.48 |
分子式 | C23H27N3O2 |
CAS No. | 2310135-18-1 |
Smiles | N=1C(OCC2=CC=CC(C=3C=CC=CC3)=C2C)=CC=C(C1OC)CNCCN |
密度 | 1.127 g/cm3 (Predicted) |
存储 | store at low temperature | Pure form: -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: 30 mg/mL (79.47 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||
DMSO
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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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