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CID 2011756 是一种具有抗肿瘤活性的ATP 竞争性广谱PKD 抑制剂,对 PKD1 的IC50值为 3.2 µM,在细胞中对 PKD2 和 PKD3 的IC50值分别为 0.6 和 0.7 µM。
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CID 2011756 是一种具有抗肿瘤活性的ATP 竞争性广谱PKD 抑制剂,对 PKD1 的IC50值为 3.2 µM,在细胞中对 PKD2 和 PKD3 的IC50值分别为 0.6 和 0.7 µM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 185 | 现货 | |
5 mg | ¥ 413 | 现货 | |
10 mg | ¥ 619 | 现货 | |
25 mg | ¥ 1,070 | 现货 | |
50 mg | ¥ 1,650 | 现货 | |
100 mg | ¥ 2,480 | 现货 | |
200 mg | ¥ 3,660 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 433 | 现货 |
产品描述 | CID 2011756 is an ATP-competitive and specific PKD1 inhibitor. |
靶点活性 | PKD1:3.2 μM, PKD3:0.7 μM, PKD2:0.6 μM |
激酶实验 | Ub-PLA2 assay: Recombinant enzymes in 20 mM Tris-HCl, pH 8.0, 2 mM CaCl2 and 2 mM β-mercaptoethanol (DUB assay buffer) are preincubated with single doses or dose ranges of PR-619 or P22077 for 30 minutes in a 96 well plate before the addition of Ub-PLA2 and NBD C6-HPC. The liberation of a fluorescent product within the linear range of the assay is monitored at room temperature using a fluorescence plate reader. Vehicle (2%(v/v) DMSO) and 10 mM N-ethylmaleimide are included as controls. Where ≥60% inhibition is observed, EC50 values are determined using a sigmoidal dose response equation. |
别名 | CID-2011756, CID2011756 |
分子量 | 396.87 |
分子式 | C22H21ClN2O3 |
CAS No. | 638156-11-3 |
Smiles | Clc1cccc(c1)-c1ccc(o1)C(=O)Nc1ccc(CN2CCOCC2)cc1 |
密度 | 1.297 g/cm3 (Predicted) |
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: 15 mg/mL (37.8 mM), Sonication is recommended. | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
DMSO
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