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别名 PHPS-1, PHPS 1
PHPS1 是 Shp2的选择性抑制剂,对 Shp2,Shp2-R362K,Shp1,PTP1B 和 PTP1B-Q 的 Ki 分别为 0.73,5.8,10.7,5.8 和 0.47 μM。

PHPS1 是 Shp2的选择性抑制剂,对 Shp2,Shp2-R362K,Shp1,PTP1B 和 PTP1B-Q 的 Ki 分别为 0.73,5.8,10.7,5.8 和 0.47 μM。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 378 | In Stock | |
| 5 mg | ¥ 892 | In Stock | |
| 10 mg | ¥ 1,380 | In Stock | |
| 25 mg | ¥ 2,730 | In Stock | |
| 50 mg | ¥ 3,850 | In Stock | |
| 100 mg | ¥ 5,390 | In Stock | |
| 200 mg | ¥ 7,470 | In Stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 933 | In Stock |
PHPS1 相关产品
| 产品描述 | PHPS1 is an inhibitor of Shp2. PHPS1 efficiently inhibits activation of Erk1/2 by the leukemia-associated Shp2 mutant, Shp2-E76K, and blocks the anchorage-independent growth of a variety of human tumor cell lines. |
| 靶点活性 | SHP1:10.7 μM(Ki), PTP1B:5.8 μM(Ki), PTP1B Q:0.47 μM(Ki), Shp2 (R362K):5.8 μM(Ki;Shp2-R362K), SHP2:0.73 μM(Ki) |
| 体外活性 | PHPS1 (30 μM; 6 days) inhibits proliferation of human tumor cells[1]. PHPS1 (5-20 μM; 5-360 minutes) inhibits Erk1/2 but not Akt and Stat3 phosphorylation in a dose-dependent manner[1]. |
| 体内活性 | PHPS1 (3 mg/kg; i.p. injection; every day during the last week on the high-fat diet) renders Ldlr-/- mice less susceptible to atherosclerosis development[2]. |
| 别名 | PHPS-1, PHPS 1 |
| 分子量 | 465.44 |
| 分子式 | C21H15N5O6S |
| CAS No. | 314291-83-3 |
| Smiles | OS(=O)(=O)c1ccc(N\N=C2/C(=O)N(N=C2c2ccc(cc2)[N+]([O-])=O)c2ccccc2)cc1 |
| 密度 | 1.54 g/cm3 (Predicted) |
| 颜色 | Orange |
| 物理性状 | Solid |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||
| 溶解度信息 | DMSO: 16.25 mg/mL (34.91 mM), Sonication is recommended. | |||||||||||||||||||||||||
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DMSO
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