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AKT-IN-1 (AZD-26) 是一种变构的 AKT 抑制剂,其 IC50=1.042 μM。
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AKT-IN-1 (AZD-26) 是一种变构的 AKT 抑制剂,其 IC50=1.042 μM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 947 | 现货 | |
2 mg | ¥ 1,320 | 现货 | |
5 mg | ¥ 1,980 | 现货 | |
10 mg | ¥ 3,730 | 现货 | |
25 mg | ¥ 5,960 | 现货 | |
50 mg | ¥ 7,880 | 现货 | |
100 mg | ¥ 10,800 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 1,580 | 现货 |
产品描述 | AKT-IN-1 (AZD-26) is an allosteric AKT inhibitor (IC50: 1.04 μM). |
靶点活性 | Akt (allosteric):1.04 μM |
体外活性 | AZD-26 is able to potently inhibit phosphorylation of AKT in cells at both Thr308 (IC50: 0.422 μM) and Ser473 (IC50: 0.322 μM). AZD-26 inhibits the phosphorylation of ribosomal protein S6, a downstream effector of the PI3K-AKT pathway. AZD-26 potently inhibits the phosphorylation of PRAS40 [1]. |
体内活性 | The effects of AZD-26 in vivo are characterized by measuring the pharmacodynamic activity of AZD-26 in a BT474c breast adenocarcinoma xenograft model. Following acute doses of 100 and 200 mg/kg, AZD-26 potently inhibits the phosphorylation of its downstream substrate GSK3β as well as the phosphorylation of AKT (Ser473), with a potency consistent with its pharmacokinetic profile. The in vivo activity of AZD-26 is further characterized by measuring the effects on the growth of tumour cell xenografts. Continuous (daily) oral dosing of AZD-26 (100 and 200 mg/kg) to nude mice bearing BT474c breast adenocarcinoma xenografts results in inhibition of tumour growth in a dose-dependent manner. When dosed at 200 mg/kg daily, AZD-26 causes significant tumour growth inhibition[1]. |
别名 | AZD-26, AZD26, AZD 26, 6-[4-(1-氨基环丁基)苯基]-5-苯基-3-吡啶甲酰胺 |
分子量 | 343.42 |
分子式 | C22H21N3O |
CAS No. | 1357158-81-6 |
Smiles | NC(=O)c1cnc(-c2ccc(cc2)C2(N)CCC2)c(c1)-c1ccccc1 |
密度 | 1.210 g/cm3 (Predicted) |
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: 11 mg/mL (32.03 mM), Sonication is recommended. | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
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