中文名 | A2793 |
英文名 | A2793 |
别名 | 2-((5-氯喹啉-8-基)氧基)乙酸乙酯 2-[(5-氯-8-喹啉基)氧基]乙酸乙酯 |
英文别名 | A2793 ST072042 ethyl 2-[(5-chloro-8-quinolyl)oxy]acetate ethyl 2-(5-chloroquinolin-8-yl)oxyacetate ethyl [(5-chloroquinolin-8-yl)oxy]acetate ethyl 2-(5-chloroquinolin-8-yl)oxyethanoate 2-[(5-chloro-8-quinolyl)oxy]acetic acid ethyl ester Acetic acid, 2-[(5-chloro-8-quinolinyl)oxy]-, ethyl ester |
CAS | 88349-90-0 |
化学式 | C13H12ClNO3 |
分子量 | 265.69 |
密度 | 1.291±0.06 g/cm3(Predicted) |
沸点 | 393.4±27.0 °C(Predicted) |
溶解度 | 溶于DMSO |
酸度系数 | 1.97±0.29(Predicted) |
存储条件 | -20℃ |
体外研究 | A2793 (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). A2793 inhibits TASK-1 (100 µM, 53.4±13,5%, n=5), while A2764 is more selective for TRESK, it only moderately influences TREK-1 and TALK-1. A2793 may be considered as a tool to discriminate between the resting and activated channels in heterologous expression systems, and to block TRESK activated by calcineurin in the native cells which do not express TASK-1. |
参考资料 展开查看 | [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. |
1mg | 5mg | 10mg | |
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1 mM | 0 ml | 0 ml | 0 ml |
5 mM | 0 ml | 0 ml | 0 ml |
10 mM | 0 ml | 0 ml | 0 ml |
5 mM | 0 ml | 0 ml | 0 ml |
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