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ARS-853 是一种选择性共价KRAS G12C 抑制剂,IC50为 2.5 μM。它通过与 GDP 结合的癌蛋白结合并阻止激活来抑制突变 KRAS 驱动的信号传导。


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ARS-853 是一种选择性共价KRAS G12C 抑制剂,IC50为 2.5 μM。它通过与 GDP 结合的癌蛋白结合并阻止激活来抑制突变 KRAS 驱动的信号传导。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 690 | In stock | |
| 5 mg | ¥ 2,490 | In stock | |
| 10 mg | ¥ 3,770 | In stock | |
| 25 mg | ¥ 5,950 | In stock | |
| 50 mg | ¥ 8,380 | In stock | |
| 100 mg | ¥ 11,300 | In stock | |
| 500 mg | ¥ 22,600 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 2,370 | In stock |
ARS-853 相关产品
| 产品描述 | ARS-853 is an inhibitor of K-RASG12C(IC50 : 2.5 μM), a mutant form of K-RAS that accumulates in the active GTP-bound state in certain cancer cells |
| 靶点活性 | KRas (G12C):2.5 μM |
| 体外活性 | ARS-853降低c-RAF、ERK和Akt的磷酸化水平。ARS-853能够抑制含有K-RASG12C突变的六种肺癌细胞系的增殖,包括H358细胞(IC50 = 2.5 μM),但不抑制含有野生型K-RAS的PC-9细胞的增殖[1]。 |
| 分子量 | 432.94 |
| 分子式 | C22H29ClN4O3 |
| CAS No. | 1629268-00-3 |
| Smiles | CC1(CC1)c1cc(NCC(=O)N2CCN(CC2)C2CN(C2)C(=O)C=C)c(O)cc1Cl |
| 密度 | 1.357 g/cm3 (Predicted) |
| 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: 5.5 mg/mL (12.7 mM), Sonication is recommended. | ||||||||||||||||||||
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