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PDK1-IN-RS2 inhibits the activation of the downstream kinases S6K1 by PDK1. PDK1-IN-RS2 is a mimic of the peptide docking motif (PIFtide) and is a substrate-selective PDK1 inhibitor (Kd: 9 μM).
PDK1-IN-RS2 inhibits the activation of the downstream kinases S6K1 by PDK1. PDK1-IN-RS2 is a mimic of the peptide docking motif (PIFtide) and is a substrate-selective PDK1 inhibitor (Kd: 9 μM).
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
2 mg | ¥ 740 | 5日内发货 | |
5 mg | ¥ 1,230 | 5日内发货 | |
1 mL x 10 mM (in DMSO) | ¥ 1,370 | 5日内发货 |
产品描述 | PDK1-IN-RS2 inhibits the activation of the downstream kinases S6K1 by PDK1. PDK1-IN-RS2 is a mimic of the peptide docking motif (PIFtide) and is a substrate-selective PDK1 inhibitor (Kd: 9 μM). |
靶点活性 | PDK1:(kd)9 μM |
体外活性 | Because the sulfonamide is likely ionized under the crystallization conditions, the sulfonyl group of PDK1-IN-RS2 interacts with Arg131 through a salt bridge. PDK1-IN-RS2 stimulates the catalytic activity of PDK1 toward a peptide substrate by sixfold [1]. |
分子量 | 380.89 |
分子式 | C15H9ClN2O2S3 |
CAS No. | 1643958-89-7 |
密度 | 1.649 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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