CAS NO: | 477775-14-7 |
生物活性 | AT2 receptoragonist C21 is a druglike selectiveangiotensin IIAT2 receptoragonist withKivalues of 0.4 nM and >10 μM for theAT2 receptorandAT1 receptor, respectively[1]. | ||||||||||||||||
IC50& Target | Ki: 0.4 nM (AT2) and >10 μM (AT1)[1] | ||||||||||||||||
体内研究 (In Vivo) | AT2 receptor agonist C21, with a bioavailability of 20-30% after oral administration and a half-life estimated to 4 h in rat, induces outgrowth of neurite cells, stimulates p42/p44mapk, enhances in vivo duodenal alkaline secretion in Sprague-Dawley rats, and lowers the mean arterial blood pressure in anesthetized, spontaneously hypertensive rats[1]. | ||||||||||||||||
分子量 | 475.62 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C23H29N3O4S2 | ||||||||||||||||
CAS 号 | 477775-14-7 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
| ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 100 mg/mL(210.25 mM;Need ultrasonic) 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。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
|
维奥蛋白资源库 - 中文蛋白资源 CopyRight © 2010-2024 |