| 靶点: |
IC50: 22 nM (LSD1). |
| 体内研究: |
T-448 has minimal impact on the LSD1-GFI1B complex and a superior hematological safety profile in mice via the generation of a compact formyl-FAD adduct. T-448 increases brain H3K4 methylation and partially restored learning function in mice with NMDA receptor hypofunction. T-448 increases H3K4 methylation in the brain without causing hematological side effects even at 100 mg/kg. |
| 参考文献: |
1. Matsuda S, et al. T-448, a specific inhibitor of LSD1 enzyme activity, improves learning function without causing thrombocytopenia in mice. Neuropsychopharmacology. 2018 Dec 22. |
| 保存条件: |
-80℃(运输条件:冰袋低温运输) |
| 配置溶液浓度参考: |
|
1mg |
5mg |
10mg |
| 1 mM |
2.587 ml |
12.937 ml |
25.873 ml |
| 5 mM |
0.517 ml |
2.587 ml |
5.175 ml |
| 10 mM |
0.259 ml |
1.294 ml |
2.587 ml |
| 50 mM |
0.052 ml |
0.259 ml |
0.517 ml |
|
| 注意: |
部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。 |