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IK1 inhibitor PA-6
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。
IK1 inhibitor PA-6图片
规格:98%
分子量:492.61
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议

产品介绍
IK1 inhibitor PA-6 (PA-6) 是一种喷他脒类似物,是有效的、选择性的 IK1 (KIR2.x离子通道携带向内整流电流) 抑制剂,人和老鼠中对KIR2.x 电流的 IC50 值为 12-15 nM。IK1 inhibitor PA-6 (PA-6) 可上调 KIR2.1 的蛋白表达,诱导细胞内KIR2.1 的蛋白的积累。IK1 inhibitor PA-6 (PA-6) 有治疗房颤和心律失常的潜力。
货号:ajcx29408
CAS:500715-03-7
分子式:C31H32N4O2
分子量:492.61
溶解度:DMSO: 125 mg/mL (253.75 mM)
纯度:98%
存储:Store at -20°C
库存:现货

Background:

IK1 inhibitor PA-6 (PA-6), a pentamidine analogue, is a selective and potent IK1 (KIR2.x ion-channel-carried inward rectifier current) inhibitor, with IC50 values of 12-15 nM for human and mouse KIR2.x currents. IK1 inhibitor PA-6 (PA-6) elevates KIR2.1 protein expression and induces intracellular KIR2.1 accumulation. IK1 inhibitor PA-6 (PA-6) has the potential to treat atrial fibrillation and arrhythmia[1][2][3].


[1]. Takanari H, et al. Efficient and specific cardiac IK? inhibition by a new pentamidine analogue. Cardiovasc Res. 2013 Jul 1;99(1):203-14. [2]. Ji Y, et al. The inward rectifier current inhibitor PA-6 terminates atrial fibrillation and does not cause ventricular arrhythmias in goat and dog models. Br J Pharmacol. 2017 Aug;174(15):2576-2590. [3]. Ji Y, et al. PA-6 inhibits inward rectifier currents carried by V93I and D172N gain-of-function KIR2.1 channels, but increases channel protein expression. J Biomed Sci. 2017 Jul 15;24(1):44.