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AZ 14145845是一种高效且高度选择性的双Mer/Axl激酶抑制剂,其pIC50值在pAxl和pMer中分别为7 nM和7.8 nM。在体内,AZ 14145845呈剂量依赖性地减少Mer和Axl激酶Ba/F3肿瘤异种移植模型中的肿瘤生长。结合抗PD1抗体和电离辐射,AZ 14145845可提高源自MC38细胞的小鼠肿瘤存活率。此外,AZ 14145845可通过口服给药。

AZ 14145845是一种高效且高度选择性的双Mer/Axl激酶抑制剂,其pIC50值在pAxl和pMer中分别为7 nM和7.8 nM。在体内,AZ 14145845呈剂量依赖性地减少Mer和Axl激酶Ba/F3肿瘤异种移植模型中的肿瘤生长。结合抗PD1抗体和电离辐射,AZ 14145845可提高源自MC38细胞的小鼠肿瘤存活率。此外,AZ 14145845可通过口服给药。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 25 mg | ¥ 10,600 | 8-10周 | |
| 50 mg | ¥ 13,800 | 8-10周 | |
| 100 mg | ¥ 17,500 | 8-10周 |
| 产品描述 | AZ 14145845, a potent and highly selective dual Mer/Axl kinase inhibitor (pIC50 = 7 nM and 7.8 nM in pAxl and pMer, respectively), demonstrates significant efficacy in reducing tumor growth in a dose-dependent manner within the Mer and Axl kinase Ba/F3 tumor xenograft model in vivo. When combined with anti-PD1 antibodies and ionizing radiation, this compound enhances survival rates in mice bearing MC38-derived tumors. Additionally, AZ 14145845 is orally bioavailable. |
| 分子量 | 561.68 |
| 分子式 | C32H35N9O |
| CAS No. | 2830555-70-7 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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