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CaCCinh-A01 是钙激活氯离子通道和TMEM16A 抑制剂,IC50值分别为 10 和 2.1 μM。
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CaCCinh-A01 是钙激活氯离子通道和TMEM16A 抑制剂,IC50值分别为 10 和 2.1 μM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 221 | 现货 | |
5 mg | ¥ 493 | 现货 | |
10 mg | ¥ 798 | 现货 | |
25 mg | ¥ 1,730 | 现货 | |
50 mg | ¥ 2,890 | 期货 | |
100 mg | ¥ 4,270 | 期货 | |
1 mL x 10 mM (in DMSO) | ¥ 537 | 现货 |
产品描述 | CaCCinh-A01 is an inhibitor of the calcium-activated chloride channel (CaCC, 10 μM) and TMEM16A (IC50: 2.1 μM). |
靶点活性 | TMEM16A:2.1 μM, CaCC:10 μM |
体外活性 | 单宁酸(100 μM)和CaCCinh-A01(30 μM)有效抑制ATP刺激后的CaCC电流[1]。CaCCinh-A01以不同浓度(0.1/1/10 μM)分别降低钙依赖性氯流(38±14%、66±10%、91±1%)。在10 μM和30 μM CaCCinh-A01作用下,ATP诱导的短路电流分别降低38±7%和78±3%。 |
细胞实验 | Each well of a 96-well plate is washed three times with PBS (200 μL/wash), leaving 50 μL of PBS. Test compounds (including CaCCinh-A01) (0.5 μL) are added to each well at 25 μM final concentration. After 10 min, 96-well plates are transferred to a plate reader for fluorescence assay. Each well is assayed individually for TMEM16A-mediated I- influx by recording fluorescence continuously (400 ms/point) for 2 s (baseline), then 50 μL of a 140 mM I-solution containing 200 μM ATP is added. |
分子量 | 347.43 |
分子式 | C18H21NO4S |
CAS No. | 407587-33-1 |
Smiles | CC(C)(C)C1CCc2c(C1)sc(NC(=O)c1ccco1)c2C(O)=O |
密度 | 1.305 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: 55 mg/mL (158.31 mM) | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
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