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KN-62 是一种选择性的、可逆的钙调蛋白依赖性蛋白激酶 II (CaMK-II) 抑制剂,直接与 CaMK-II 酶的钙调蛋白结合位点结合,对大鼠脑 CaMK-II 的IC50值为 0.9 μM。它是非竞争性的P2X7受体拮抗剂,IC50约为 15 nM。
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KN-62 是一种选择性的、可逆的钙调蛋白依赖性蛋白激酶 II (CaMK-II) 抑制剂,直接与 CaMK-II 酶的钙调蛋白结合位点结合,对大鼠脑 CaMK-II 的IC50值为 0.9 μM。它是非竞争性的P2X7受体拮抗剂,IC50约为 15 nM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 285 | 现货 | |
2 mg | ¥ 397 | 现货 | |
5 mg | ¥ 663 | 现货 | |
10 mg | ¥ 1,080 | 现货 | |
25 mg | ¥ 2,290 | 现货 | |
50 mg | ¥ 3,430 | 现货 | |
100 mg | ¥ 4,890 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 795 | 现货 |
产品描述 | KN-62 is a potent and specific Ca2+/calmodulin-dependent protein kinase II (CaMKII) inhibitor with Ki of 0.9 μM. |
靶点活性 | CaMK II:0.9 μM(Ki), CaMK V:0.8 μM(Ki) |
体外活性 | KN-62作用于成年大鼠,降低其脑中癫痫诱导的脑源性神经生长因子mRNA的表达水平. |
体内活性 | KN-62抑制K562细胞的增殖,并阻断细胞周期进程。10 μM KN-62作用于大鼠胰岛细胞,抑制卡巴胆碱和钾刺激的胰岛素分泌。KN-62抑制PC12 D细胞中A23187诱导的Ca2+/CaM激酶磷酸化作用。 |
激酶实验 | Kinase assay: Total kinase activity of CaMKII, determined in a standard 2 min assay (100 μL), contained 35 mM HEPES, 10 mM MgCl2, 1 mM CaCl2, 10 μg of chicken gizzard myosin 20-kD light chain, 0.1 μM calmodulin, and 10 μM [γ-33]ATP at 30 °C. The kinase reaction is halted by adding 1 mL of 10% trichloroacetic acid. |
细胞实验 | For cell growth analysis, K562 cells are plated in a 3-cm dish with 5 mL of culture medium containing various concentration of KN-62. After two days in these condition cell numbers are counted. (Only for Reference) |
分子量 | 721.84 |
分子式 | C38H35N5O6S2 |
CAS No. | 127191-97-3 |
Smiles | O=C([C@H](Cc1ccc(OS(=O)(=O)c2cccc3cnccc23)cc1)NCS(=O)(=O)c1cccc2cnccc12)N1CCN(CC1)c1ccccc1 |
密度 | 1.388 g/cm3 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 72.2 mg/mL (100 mM) | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
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