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- 详细信息
- 技术资料
- 保存条件:
Powder: -20°C, 3 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1221962-86-2
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥880.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥335.0 |
| 规格: | 5 mg | 产品价格: | ¥773.0 |
| 规格: | 10 mg | 产品价格: | ¥1246.0 |
| 规格: | 25 mg | 产品价格: | ¥2475.0 |
| 规格: | 50 mg | 产品价格: | ¥4475.0 |
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PS210
CAS No. : 1221962-86-2
MCE 国际站:PS210
产品活性:PS210 是一种针对 PDK1 的 PIF 结合口袋的有效且选择性的 PDK1 激活剂。PS210 对其他蛋白激酶 (包括 PDK1 下游信号传导成分,如 S6K,PKB/Akt 或 GSK3) 无活性。在细胞中,PS210 的前药 PS423 可作为 PDK1 的底物选择性抑制剂,抑制 S6K 的磷酸化和活化。
研究领域:PI3K/Akt/mTOR
作用靶点:PDK-1
In Vitro: When PS210 induces a stabilization of PDK1 to the temperature gradien, PS210 stabilized the residue Arg131, located opposite to the helix a-B at the other extreme of the helix a-C. Thus, the residues forming part of the phosphate-binding site appear to be a fixed point that allows for the relative movement of the helices in the process of PDK1 activation.
相关产品:Bioactive Compound Library Plus | Kinase Inhibitor Library | PI3K/Akt/mTOR Compound Library | Anti-Cancer Compound Library | Anti-Aging Compound Library | Reprogramming Compound Library | Oxygen Sensing Compound Library | Glycolysis Compound Library | Cytoskeleton Compound Library | Anti-Pancreatic Cancer Compound Library | Anti-Cancer Metabolism Compound Library | Glucose Metabolism Compound Library | Highly Selective Activators Library | BX795 | GSK2334470 | Polyphyllin I | BX-912 | MP7 | BX517 | OSU-03012 | PS48 | (R)-PS210 | PDK1-IN-RS2 | BX-320 | PS47 | CRTh2 antagonist 3 | LDHA/PDKs-IN-1 | LDHA/PDKs-IN-2 | PDKtide | PKD-IN-1 dihydrochloride | PKM2 activator 6 | PKM2/PDK1-IN-1
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