| 产品描述: | Bay K 8644是一种高选择性的L型钙离子通道激动剂,EC50为17.3 nM |
| 靶点: |
L-type calcium channel(in the isolated field-stimulated vas deferens of the mouse):17.3nM(EC50);CalciumChannel |
| 体外研究: |
Bay K 8644 作为L型钙离子的激动剂,提高了取自大鼠的肠系膜动脉的静息张力 |
| 体内研究: |
Bay K 8644 可诱导5周龄、3月龄、1年、1.5年龄wistar-kyoto大鼠主动脉的小的收缩,这一现象不受大鼠年龄所影响 |
| 细胞实验: |
Cell lines: 5TGM1 cells Concentrations: 10 nM Incubation Time: 30 minutes Method: Cells were treated with indicated concentration of drug for 30 minutes. |
| 动物实验: |
Animal Models: Male Sprague-Dawley rats Dosages: 1, 10, 50 and 100 µg/kg Administration: Jugular catheters |
| 参考文献: |
1. A J Gonzales,et al. Interactions of calcium antagonists and the calcium channel agonist Bay K 8644 on neurotransmission of the mouse isolated vas deferens. Br J Pharmacol. 1989, 96(2):333-340 2. Sulayma A. Albarwani,et al. Aging Reduces L-Type Calcium Channel Current and the Vasodilatory Response of Small Mesenteric Arteries to Calcium Channel Blockers. Front Physiol. 2016, 7:171. 3. Hernández MC,et al. Effects of Bay K 8644 in aorta from spontaneously hypertensive and Wistar Kyoto rats of different ages. J Auton Pharmacol. 1995, 15(4):257-269. 4. Wang J, et al. Apoptotic Extracellular Vesicles Ameliorate Multiple Myeloma by Restoring Fas-Mediated Apoptosis. ACS Nano. 2021 Sep 28;15(9):14360-14372. 5. Ives N, et al. BAY k 8644, a calcium channel agonist, reverses hypotension in endotoxin-shocked rats. Eur J Pharmacol. 1986 Nov 4;130(3):169-75. |
| 溶解性: |
Soluble in DMSO |
| 保存条件: |
-20℃ |
| 配置溶液浓度参考: |
|
1mg |
5mg |
10mg |
| 1 mM |
2.807 ml |
14.033 ml |
28.067 ml |
| 5 mM |
0.561 ml |
2.807 ml |
5.613 ml |
| 10 mM |
0.281 ml |
1.403 ml |
2.807 ml |
| 50 mM |
0.056 ml |
0.281 ml |
0.561 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。 |