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Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
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货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1613724-42-7
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10 mM * 1 mL/1 mg/5 mg/10 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥880.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥363.0 |
| 规格: | 5 mg | 产品价格: | ¥800.0 |
| 规格: | 10 mg | 产品价格: | ¥1200.0 |
| 规格: | 50 mg | 产品价格: | ¥3600.0 |
| 规格: | 100 mg | 产品价格: | ¥4850.0 |
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HTH-01-015
CAS No. : 1613724-42-7
MCE 国际站:HTH-01-015
产品活性:HTH-01-015 是一种选择性 NUAK1/ARK5 抑制剂 (IC50 为 100 nM)。HTH-01-015 抑制 NUAK1 的效力比抑制 NUAK2 高 100 倍以上 (IC50>10 μM)。
研究领域:Epigenetics | PI3K/Akt/mTOR
作用靶点:AMPK
In Vitro: HTH-01-015 is a specific NUAK1 inhibitor. The related NUAK1 and NUAK2 are members of the AMPK (AMP-activated protein kinase) family of protein kinases that are activated by the LKB1 (liver kinase B1) tumor suppressor kinase. HTH-01-015 inhibits NUAK1 with an IC50 of 100 nM, but does not significantly inhibit NUAK2 (IC50 of >10 μM).? In all cell lines tested, HTH-01-015 inhibits the phosphorylation of the only well-characterized substrate, MYPT1 (myosin phosphate-targeting subunit 1) that is phosphorylated by NUAK1 at Ser445. In U2OS cells, HTH-01-015 suppresses proliferation and phosphorylation of MYPT1 to the same extent as shRNA-mediated NUAK1 knockdown. In mouse embryonic fibroblasts (MEFs), treatment with 10 μM HTH-01-015 suppresses proliferation and phosphorylation of MYPT1 to the same extent as NUAK1-knockout. To test whether NUAK1 inhibition impaired the ability of the invasive U2OS cells to enter a matrix, 3D Matrigel Transwell invasion assays demonstrate that 10 μM HTH-01-015 markedly inhibits the invasiveness of U2OS cells in this assay.
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