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SAR7334
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
SAR7334图片
CAS NO:1333210-07-3
包装与价格:
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

产品介绍
SAR7334 是一种有效的TRPC6特异性抑制剂,能够抑制 TRPC6 电流,IC50值为 7.9 nM。
生物活性

SAR7334 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

367.87

性状

Solid

Formula

C21H22ClN3O

CAS 号

1333210-07-3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : ≥ 370 mg/mL(1005.79 mM)

*"≥" means soluble, but saturation unknown.

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM2.7184 mL13.5918 mL27.1835 mL
5 mM0.5437 mL2.7184 mL5.4367 mL
10 mM0.2718 mL1.3592 mL2.7184 mL
*

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
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。