| 产品描述: | Dorsomorphin 2HCl是一种有效的,可逆的AMPK选择性抑制剂,Ki为109 nM,对一些结构相关的激酶,包括ZAPK, SYK, PKCθ, PKA和JAK3没有显著的抑制作用。同时抑制了BMP一型受体作用。 |
| 体内研究: |
Dorsomorphin (化合物 C; 10 mg/kg; 静脉注射一次) dihydrochloride 处理导致总血清铁浓度增加 60%,降低成年小鼠铁调素表达的基础水平并增加血清铁浓度。 Dorsomorphin (0.2 mg/kg,静脉注射,LPS 注射前 30 分钟) dihydrochloride 降低注射 LPS 的大鼠主动脉中的 ICAM-1 和 VCAM-1 表达。 Dorsomorphin (25 mg/kg;腹腔注射,在雄性 BALB/c 小鼠中) dihydrochloride 在注射脂多糖 (LPS) 之前进行处理,与仅接受 LPS 处理的动物相比,显著降低了致死率。 |
| 参考文献: |
1. Zhou G, et al. Role of AMP-activated protein kinase in mechanism of action. J Clin Invest. 2001 Oct;108(8):1167-74.
2. Saito S, et al. Compound C prevents the unfolded protein response during glucose deprivation through a mechanism independent of AMPK and BMP signaling. PLoS One. 2012;7(9):e45845.
3. Yu PB, et al. Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism. Nat Chem Biol. 2008 Jan;4(1):33-41.
4. Kim YM, et al. Compound C independent of AMPK inhibits ICAM-1 and VCAM-1 expression in inflammatory stimulants-activated endothelial cells in vitro and in vivo. Atherosclerosis. 2011 Nov;219(1):57-64.
5. Guo Y, et al. AMPK inhibition blocks ROS-NFκB signaling and attenuates endotoxemia-induced liver injury. PLoS One. 2014 Jan 24;9(1):e86881. |
| 溶解性: |
H2O:20mg/ml |
| 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 |
2.117 ml |
10.584 ml |
21.168 ml |
| 5 mM |
0.423 ml |
2.117 ml |
4.234 ml |
| 10 mM |
0.212 ml |
1.058 ml |
2.117 ml |
| 50 mM |
0.042 ml |
0.212 ml |
0.423 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。 |