iMDK,99.34%
产品编号:Bellancom-110171| CAS NO:881970-80-5| 分子式:C21H13FN2O2S| 分子量:376.40
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iMDK
| 产品介绍 | iMDK 是一种有效的 PI3K 抑制剂,可抑制生长因子 MDK(也称为中期因子或 MK)。iMDK 与 MEK 抑制剂协同抑制非小细胞肺癌 (NSCLC),而不会伤害正常细胞和小鼠。 | ||||||||||||||||
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| 生物活性 | iMDK is a potent PI3K inhibitor and inhibits the growth factor MDK (also known as midkine or MK). iMDK suppresses non-small cell lung cancer (NSCLC) cooperatively with A MEK inhibitor without harming normal cells and mice. | ||||||||||||||||
| 体外研究 |
iMDK (50–500 nM) suppressed AKT phosphorylation in a dose-dependent manner in H441 lung adenocarcinoma cells after treatment for 72 h. In contrast, iMDK robustly increases p-ERK. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability Assay
Western Blot Analysis
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| 体内研究 (In Vivo) |
The combination treatment of iMDK ( (9 mg/kg/day; intraperitoneally injected with 100 μl) and PD0325901 (5 mg/kg; orally administered) effectively reduced lung tumor growth in a xenograft mouse model. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.
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| 体内研究 |
The combination treatment of iMDK ( (9 mg/kg/day; intraperitoneally injected with 100 μl) and PD0325901 (5 mg/kg; orally administered) effectively reduced lung tumor growth in a xenograft mouse model. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.
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| 体内研究 |
The combination treatment of iMDK ( (9 mg/kg/day; intraperitoneally injected with 100 μl) and PD0325901 (5 mg/kg; orally administered) effectively reduced lung tumor growth in a xenograft mouse model. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.
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| 性状 | Solid | ||||||||||||||||
| 溶解性数据 |
In Vitro:
DMSO : 3.33 mg/mL (8.85 mM; ultrasonic and warming and heat to 60°C) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 | ||||||||||||||||
| 运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
| 储存方式 |
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| 参考文献 |

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