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NMDAR/TRPM4-IN-2 是一种有效的 NMDAR/TRPM4 相互作用界面抑制剂。NMDAR/TRPM4-IN-2 保护小鼠免受 MCAO 诱导的脑损伤和 NMDA 诱导的视网膜神经节细胞丢失。NMDAR/TRPM4-IN-2 具有神经保护活性, 可预防 NMDA 诱导的海马神经元细胞死亡和线粒体功能障碍,其 IC50 值为 2.1 μM。
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NMDAR/TRPM4-IN-2 是一种有效的 NMDAR/TRPM4 相互作用界面抑制剂。NMDAR/TRPM4-IN-2 保护小鼠免受 MCAO 诱导的脑损伤和 NMDA 诱导的视网膜神经节细胞丢失。NMDAR/TRPM4-IN-2 具有神经保护活性, 可预防 NMDA 诱导的海马神经元细胞死亡和线粒体功能障碍,其 IC50 值为 2.1 μM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 185 | 现货 | |
5 mg | ¥ 398 | 现货 | |
10 mg | ¥ 617 | 现货 | |
25 mg | ¥ 893 | 现货 | |
50 mg | ¥ 1,180 | 现货 | |
100 mg | ¥ 1,770 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 462 | 现货 |
产品描述 | NMDAR/TRPM4-IN-2 is a potent interfacial inhibitor of NMDAR/TRPM4 interaction.NMDAR/TRPM4-IN-2 protects against MCAO-induced brain damage and NMDA-induced retinal ganglion cell loss in mice.NMDAR/TRPM4-IN-2 has neuroprotective activity against NMDA-induced hippocampal neuronal cell death and mitochondrial dysfunction. NMDAR/TRPM4-IN-2 showed neuroprotective activity against NMDA-induced cell death and mitochondrial dysfunction in hippocampal neurons with an IC50 value of 2.1 μM. |
体外活性 | NMDAR/TRPM4-IN-2(0-10 μM)消除了CREB关闭途径,恢复了ERK1/2激活和IEG诱导,同时不影响NMDARs的突触活动驱动的转录促进活动。此外,NMDAR/TRPM4-IN-2按剂量依赖的方式减少了GluN2A和GluN2B与TRPM4的相互作用。 |
分子量 | 330.092 |
分子式 | C11H19BrCl2N2 |
CAS No. | 2243506-33-2 |
Smiles | Cl.Cl.CCN(CCN)Cc1cccc(Br)c1 |
存储 | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 112.5 mg/mL (340.8 mM), Sonication is recommended. H2O: 90.0 mg/mL (272.7 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
H2O/DMSO
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