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Afuresertib hydrochloride 是一个口服有效的,ATP 竞争性的选择性泛Akt 抑制剂,作用于Akt1、Akt2和Akt3,Ki 值分别为 0.08、2和 2.6 nM。
Afuresertib hydrochloride 是一个口服有效的,ATP 竞争性的选择性泛Akt 抑制剂,作用于Akt1、Akt2和Akt3,Ki 值分别为 0.08、2和 2.6 nM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 382 | 现货 | |
2 mg | ¥ 553 | 现货 | |
5 mg | ¥ 745 | 现货 | |
10 mg | ¥ 1,090 | 现货 | |
25 mg | ¥ 1,980 | 现货 | |
50 mg | ¥ 3,230 | 现货 | |
100 mg | ¥ 4,790 | 现货 | |
200 mg | ¥ 6,680 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 758 | 现货 |
产品描述 | Afuresertib hydrochloride is an inhibitor of Akt kinase (Kis of 0.08/2/2.6 nM for Akt1/Akt2/Akt3 respectively) |
靶点活性 | Akt3:2.6 nM(Ki), Akt2:2 nM(Ki), Akt1:0.08 nM(Ki) |
体外活性 | Afuresertib诱导的p21表达通过促进FOXO活性从而促使G1期阻滞。此外,afuresertib显著增强了顺铂诱导的细胞毒性。Afuresertib调节了与成纤维细胞核心血清反应相关的E2F1和MYC的表达。这表明afuresertib是治疗MPM[1]患者的有效抗癌化合物。 |
细胞实验 | Cell confluence proliferation assay was performed using Incucyte ZOOM Live‐Cell Imaging System.?Briefly, ACC‐MESO‐4 and MSTO‐211H cells were seeded in 12‐well plates (cell density, 1 × 104 cells/well) and were incubated for 24 h at 37°C.?Then, the cells were incubated with 0, 2, 5, or 10 μmol/L afuresertib.?During treatment, cell growth was monitored by recording phase images using the IncuCyte ZOOM Live‐Cell Imaging System (magnification, ×100)[1]. |
分子量 | 463.8 |
分子式 | C18H18Cl3FN4OS |
CAS No. | 1047645-82-8 |
Smiles | Cl.Cn1ncc(Cl)c1-c1cc(sc1Cl)C(=O)N[C@H](CN)Cc1cccc(F)c1 |
密度 | no data available |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 100 mg/mL (215.62 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
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