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Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site. Activates phosphodiesterase in the absence of Ca2+ and inhibits Ca2+-mediated cytotoxicity and apoptosis (IC50 = 33 μM).
Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site. Activates phosphodiesterase in the absence of Ca2+ and inhibits Ca2+-mediated cytotoxicity and apoptosis (IC50 = 33 μM).
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 1,260 | 期货 | |
5 mg | ¥ 4,930 | 期货 | |
10 mg | ¥ 8,360 | 期货 | |
25 mg | ¥ 14,300 | 期货 | |
50 mg | ¥ 21,600 | 期货 | |
100 mg | ¥ 32,800 | 期货 |
产品描述 | Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site. Activates phosphodiesterase in the absence of Ca2+ and inhibits Ca2+-mediated cytotoxicity and apoptosis (IC50 = 33 μM). |
分子量 | 881.08 |
分子式 | C44H68N10O9 |
CAS No. | 261969-05-5 |
密度 | no data available |
存储 | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
溶解度信息 | H2O: 1 mg/mL |
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