hSMG-1 inhibitor 11j
规格
| Cas Number | 1402452-15-6 |
| 规格或纯度 | ≥99% |
| 纯度 | ≥99% |
| 包装 | 10mg 或 5mg |
产品信息
| 品牌 | 阿拉丁 |
| 溶解性 | DMSO : 80 mg/mL (141.33 mM; Need ultrasonic) |
| 过滤标签 | CDK,GSK-3,mTOR,PI3K,Cell Cycle/DNA Damage,Stem Cell/Wnt,PI3K/Akt/mTOR |
| 储存温度 | 2-8°C储存,避光,干燥 |
| 运输条件 | 冰袋运输 |
| 生化和生理学机理 | hSMG-1 抑制剂 11j 是一种嘧啶衍生物，是一种强效的 hSMG-1 选择性抑制剂，其 IC 50 为 0.11 nM。 |
| 英文描述 |
hSMG-1 inhibitor 11j, a pyrimidine derivative, is a potent and selective inhibitor of hSMG-1 , with an IC 50 of 0.11 nM. hSMG-1 inhibitor 11j exhibits >455-fold selectivity for hSMG-1 over mTOR ( IC 50 =50 nM), PI3Kα/γ ( IC 50 =92/60 nM) and CDK1/CDK2 ( IC 50 =32/7.1 μM). hSMG-1 inhibitor 11j can be used for the research of cancer In Vitro hSMG-1 inhibitor 11j (0.3-3 μM; 6 h) significantly reduces UPF1 phosphorylation at 0.3 μM, and eliminates it at 1 μM in MDA 361 cells. hSMG-1 inhibitor 11j inhibits MDA468 cell proliferation, with an IC 50 of 75 nM. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid IC50& Target:hSMG-1 0.11 nM (IC 50 ) mTOR 50 nM (IC 50 ) PI3Kγ 60 nM (IC 50 ) PI3Kα 92 nM (IC 50 ) GSKα 260 (IC 50 ) GSKβ 330 (IC 50 ) CDK2 7.1 μM (IC 50 ) CDK1 32 μM (IC 50 ) |