上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。
PRL-3 Inhibitor I 纯度: 98.73%
PRL-3 Inhibitor I 是一种有效的 PRL-3 抑制剂,IC50 为 0.9 μM。PRL-3 Inhibitor I 在细胞检测中显示降低侵袭性。
PRL-3 Inhibitor I Chemical Structure
CAS No. : 893449-38-2
| 规格 | 价格 | 是否有货 | 数量 |
|---|---|---|---|
| 10 mM * 1 mL in DMSO | ¥660 | In-stock | |
| 5 mg | ¥600 | In-stock | |
| 10 mg | ¥1000 | In-stock | |
| 25 mg | ¥2000 | In-stock | |
| 50 mg | ¥3000 | In-stock | |
| 100 mg | ¥4500 | In-stock | |
| 200 mg | 询价 | ||
| 500 mg | 询价 |
* Please select Quantity before adding items.
PRL-3 Inhibitor I 相关产品
•相关化合物库:
- Bioactive Compound Library Plus
- Metabolism/Protease Compound Library
- Anti-Cancer Compound Library
- Phosphatase Inhibitor Library
| 生物活性 |
PRL-3 Inhibitor I is a potent PRL-3 inhibitor with an IC50 of 0.9 μM. PRL-3 Inhibitor I shows a reduced invasion in cell-based assay[1]. |
IC50 & Target |
IC50: 0.9 μM (PRL-3)[1] |
||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 体外研究 (In Vitro) |
PRL-3 Inhibitor I (compound 5e) reduces the invasion of mouse melanoma B16F10 cells in a cell-based assay[1]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. |
||||||||||||||||
| 分子量 |
485.21 |
||||||||||||||||
| Formula |
C17H11Br2NO2S2 |
||||||||||||||||
| CAS 号 |
893449-38-2 |
||||||||||||||||
| 运输条件 |
Room temperature in continental US; may vary elsewhere. |
||||||||||||||||
| 储存方式 |
4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) |
||||||||||||||||
| 溶解性数据 |
In Vitro:
DMSO : 41.67 mg/mL (85.88 mM; ultrasonic and warming and heat to 60°C) H2O : < 0.1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble) 配制储备液
*
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。 |
||||||||||||||||
| 参考文献 |
|
所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务