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A2793 99%+

货号:A919855 同义名: Ethyl [(5-Chloroquinolin-8-yl)oxy]acetate 产品仅供科研

A2793 is an inhibitor of TRESK (IC50 value of 6.8 μM for mTRESK).

A2793 化学结构 CAS号:88349-90-0
A2793 化学结构
CAS号:88349-90-0
A2793 3D分子结构
CAS号:88349-90-0
A2793 化学结构 CAS号:88349-90-0
A2793 3D分子结构 CAS号:88349-90-0
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A2793 纯度/质量文件

货号:A919855 标准纯度:99%+
批次查询: 批次纯度:

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1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

A2793 生物活性

描述 A2793 is a potent dual inhibitor of TWIK-related acid-sensitive K+ channels (TASK)-1 and TRESK, with an IC50 of 6.8 μM for mTRESK. A2764 exhibits greater selectivity for TRESK and only moderately affects TREK-1 and TALK-1 [1]. A2793, at a concentration of 100 µM, inhibits the unstimulated channel by 43.0±8.9% (n=5), while after ionomycin activation, the reduction of the TRESK current is 85.5±2.9% (n=5) [1]. A2793 inhibits TASK-1 (100 µM, 53.4±13.5%, n=5). In contrast, A2764 is more selective for TRESK and has a moderate impact on TREK-1 and TALK-1 [1]. A2793 can serve as a tool to distinguish between resting and activated channels in heterologous expression systems. It also blocks TRESK activated by calcineurin in native cells lacking TASK-1 [1].

A2793 参考文献

[1]Miklós Lengyel, et al. Chemically Modified Derivatives of the Activator Compound Cloxyquin Exert Inhibitory Effect on TRESK (K 2P 18.1) Background Potassium Channel. Mol Pharmacol. 2019 Jun;95(6):652-660.

A2793 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.76mL

0.75mL

0.38mL

18.82mL

3.76mL

1.88mL

37.64mL

7.53mL

3.76mL

A2793 技术信息

CAS号88349-90-0
分子式C13H12ClNO3
分子量265.692
别名 Ethyl [(5-Chloroquinolin-8-yl)oxy]acetate
运输蓝冰
存储条件

粉末 Sealed in dry,Room Temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 105 mg/mL(395.19 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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