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描述 | YM-244769 dihydrochloride is a potent, selective, and orally active inhibitor of the Na+/Ca2+ exchanger (NCX). It exhibits a preference for inhibiting NCX3 and attenuates the unidirectional outward NCX current (Ca2+ entry mode), with IC50s of 18 nM and 50 nM, respectively. Additionally, YM-244769 dihydrochloride effectively protects against hypoxia/reoxygenation-induced damage in SH-SY5Y neuronal cells. Moreover, it can enhance urine volume and urinary electrolyte excretion in mice [1][2][3]. |
Animal study | YM-244769 (0.1-1 mg/kg; pO.; once) demonstrates a dose-dependent natriuretic effect in mice. Additionally, it significantly enhances urinary excretion of Ca2+ as well as Ca2+/Cr ratio[2]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.94mL 0.39mL 0.19mL |
9.68mL 1.94mL 0.97mL |
19.37mL 3.87mL 1.94mL |
CAS号 | 1780390-65-9 |
分子式 | C26H24Cl2FN3O3 |
分子量 | 516.39 |
SMILES Code | O=C(C1=CC=C(OC2=CC=C(OCC3=CC=CC(F)=C3)C=C2)N=C1)NCC4=CC=CC(N)=C4.[H]Cl.[H]Cl |
MDL No. | MFCD23381171 |
别名 | YM-244769 dihydrochloride |
运输 | 蓝冰 |
InChI Key | OCKIUNLKEPKCRE-UHFFFAOYSA-N |
Pubchem ID | 90488952 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Inert atmosphere, 2-8°C |
溶解方案 |
请根据您的动物给药指南选择适当的溶解方案。 以下溶解方案都请先按照体外实验的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,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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