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- 详细信息
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 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:
1180676-32-7
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥848.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥269.0 |
| 规格: | 5 mg | 产品价格: | ¥600.0 |
| 规格: | 10 mg | 产品价格: | ¥800.0 |
| 规格: | 25 mg | 产品价格: | ¥1500.0 |
| 规格: | 50 mg | 产品价格: | ¥2200.0 |
| 规格: | 100 mg | 产品价格: | ¥3400.0 |
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PS48
CAS No. : 1180676-32-7
MCE 国际站:PS48
产品活性:PS48 是 一种 PDK1 激活剂,AC50 为 8 μM。
研究领域:PI3K/Akt/mTOR
作用靶点:PDK-1
In Vitro: PS48 activates full length PDK1 (His-PDK1- FL) and PDK1 50-359[Tyr288Gly;Gln292Ala] (His-PDK1 dm) with AC50s (the concentrations required to reach 50% of the maximal activation) of 7.95±0.2 and 10.0±2.0 μM, respectively. PS48 binds to PDK150–359 with a 1:1 stoichiometry and a binding affinity in the micromolar range (Kd=10.3 μM). PDK1 activator, PS48, has the ability to reverse the cell proliferation inhibition role of triptolide (TP) in vitro. The inhibition role of TP in cell number is significantly reversed by PS48. TP significantly increases the cell proportion in G0-G1 phase and decreases the cell proportion in G2-M and S phase. However, the effect of TP on cell cycle distribution is all reversed by PS48. In addition, suppression of PDK1/Akt/mTOR pathway by TP in high glucose (HG)-treated human renal mesangial cells (HRMCs) is also reversed by PS48, as well as the expression of Ki-67 and proliferating cell nuclear antigen (PCNA).
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