CAS NO: | 1333207-63-8 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | SAR7334 hydrochloride is a potent and specificTRPC6inhibitor, inhibiting TRPC6 currents withIC50of 7.9 nM. | ||||||||||||||||
IC50& Target | IC50: 7.9 nM (TRPC6 currents)[3] | ||||||||||||||||
体外研究 (In Vitro) | SAR7334 inhibits TRPC6, TRPC3 and TRPC7-mediated Ca2+influx into cells with IC50s of 9.5, 282 and 226 nM[1][2][3], whereas TRPC4 and TRPC5-mediated Ca2+entry is not affected. SAR7334 (1 μM) results in a major block of the Ang II-evoked calcium influx in the podocytes[1]. SAR7334 (1 μM) has negligible effect on SOCE[2]. SAR7334 dose-dependently reduces TRPC6 currents with an IC50of 7.9 nM. SAR7334 (100 nM) substantially reduces TRPC6 currents[3]. | ||||||||||||||||
体内研究 (In Vivo) | SAR7334 (10 mg/kg, p.o.) suppresses TRPC6-dependent acute HPV in isolated perfused lungs from mice. SAR7334 demonstrates that it is suitable for chronic oral administration. In an initial short-term study, SAR7334 does not change mean arterial pressure in spontaneously hypertensive rats (SHR)[3]. | ||||||||||||||||
分子量 | 440.79 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C21H24Cl3N3O | ||||||||||||||||
CAS 号 | 1333207-63-8 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 100 mg/mL(226.87 mM;Need ultrasonic) H2O : 50 mg/mL(113.43 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
|