| 产品描述: | Capadenoson is a selective agonist of adenosine-A1 receptor. |
| 靶点: |
Adenosine A1 receptor;AdenosineReceptor |
| 体内研究: |
In the in vivo experiments, Wistar rats and SHR are pre-treated with Capadenoson at a concentration of 0.15 mg/kg for 5 days. On day 5, a stress test (physical restraint) is performed for 2 hours. The plasma concentration of Capadenoson measured 3 hours after drug intake remains constant in the 5 days prior to the restraint stress test and averaged 7.63 µg/L on day 4 and 5, respectively |
| 参考文献: |
1. Bott-Flügel L, et al. Selective attenuation of norepinephrine release and stress-induced heart rate increase by partial adenosine A1 agonism. PLoS One. 2011 Mar 28;6(3):e18048. 2. Bailey IR, et al. Optimization of Thermolytic Response to A1 Adenosine Receptor Agonists in Rats. J Pharmacol Exp Ther. 2017 Sep;362(3):424-430. |
| 溶解性: |
Soluble in DMSO |
| 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 |
1.923 ml |
9.615 ml |
19.23 ml |
| 5 mM |
0.385 ml |
1.923 ml |
3.846 ml |
| 10 mM |
0.192 ml |
0.961 ml |
1.923 ml |
| 50 mM |
0.038 ml |
0.192 ml |
0.385 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。 |