| CAS: | 331253-86-2 | ||
| 分子式: | C10H4N6O | ||
| 分子量: | 224.182 | ||
| 英文名称: |
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| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||
| K872093 | MACKLIN | KP372-1(PDK1/Akt/Flt Dual Inhibitor) | ≥98% | 1009元/1mg; | 咨询 | ||||||||||||||||||||||||||
储存:-20℃ | |||||||||||||||||||||||||||||||
| 521275 | Sigma-Aldrich | PDK1/Akt/Flt Dual Pathway Inhibitor-CAS 331253-86-2-Calbiochem | The PDK1/Akt/Flt Dual Pathway Inhibitor, also referenced under CAS 331253-86-2, controls the biological activity of PDK1/Akt/Flt. This small molecule/inhibitor is primarily used for Phosphorylation &a | 5307.21元/5 MG; | 咨询 | ||||||||||||||||||||||||||
产品说明 一般描述 A cell-permeable compound that selectively induces apoptosis in AML (Acute Myelogenous Leukemia) with little effect on normal CD34+ AML progenitor cells. Shown to directly inhibit both PDK1 and Akt activities in in vitro kinase assays in a dose-dependent manner and block cellular phosphorylation of Akt at both Ser473 and Thr308. The dual inhibition nature against both PDK1/Akt and Flt3/PIM signaling pathways allows effective killing of AML cells (Average IC50 = 1.05, 1.91, and 0.43 µM for AML with wild-type Flt3, single mutant ITD/D835, and double mutant Flt3-ITD-TDK, respectively) that are otherwise resistant to inhibitors that target only the PDK1/Akt pathway. 包装 5 mg in Plastic ampoule 生化/生理作用 Cell permeable: yes 警告 Toxicity: Irritant (B) 其他说明 Zeng, Z., et al. 2006. Cancer Res.66, 3737. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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