化合物YM-244769 T9888
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
2 mg | 838819-70-8 | ¥468.00 | 询底价 |
5 mg | 838819-70-8 | ¥788.00 | 询底价 |
Product Introduction
Bioactivity
英文名: YM-244769
描述: YM-244769 (3-Pyridinecarboxamide, N-[(3-aminophenyl)methyl]-6-[4-[(3-fluorophenyl)methoxy]phenoxy]-) 是一种有效的 Na+/Ca2+ exchange 3 (NCX3) 抑制剂,IC50 为 18 nM。 YM-244769 对神经元和肾脏具有有效的保护作用。
体外活性: YM-244769 (0.3 or 1 μM) efficiently suppresses the hypoxia/reoxygenation-induced cell damage in SH-SY5Y cells treated with NCX1 antisense (i.e., SH-SY5Y cells primarily expressing NCX3) more than in those treated with NCX3 antisense (i.e., SH-SY5Y cells primarily expressing NCX1). YM-244769 (0.003-1 μM) inhibits the initial rates of 45 Ca 2+ uptake into NCX1, NCX2, and NCX3 transfectants with IC 50 values of 68±2.9, 96±3.5, and 18±1.0 nM, respectively, indicating that YM-244769 is approximately four to five times more selective to NCX3 than other isoforms[1].
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 245 mg/mL (552.46 mM)
关键字: nicotinamide | Na+/Ca2+ exchange | neuroprotective | YM244769 | NCX3 | SH-SY5Y cells | YM-244769 | Inhibitor | anti-ischemic | inhibit | LLC-PK1 cells | Na+/Ca2+ Exchanger | YM 244769
相关产品: 15-Methoxypinusolidic acid | CCR4 antagonist 2 | Calcicludine | Amlodipine | Flunarizine dihydrochloride | Oxatomide | Tamolarizine | Gallopamil hydrochloride | (-)-Denudatin B | Urolithin C
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途