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PNU-120596
| 品牌 | 厂商性质 | 产地 | 货期 |
|---|---|---|---|
| 阿拉丁 | 生产商 | 上海 | 现货 |
产品参数
| 货号 | CAS号 | 操作 |
|---|---|---|
| P125212-50mg | 501925-31-1 | 询价 |
| P125212-10mg | 501925-31-1 | 询价 |
产品介绍
- 分子式 C13H14ClN3O4
- 分子量311.72
- MDL号 MFCD00095313
属性
| 溶解性 | Soluble in DMSO (62 mg/ml), methanol (1 mg/ml), acetonitrile (0.5 mg/ml), ethanol (1 mg/ml), and water (<1 mg/ml). |
| 存贮条件 | 储存温度-20°C |
描述
| 应用 | A type II positive allosteric modulator. |
| 产品介绍 | PNU-120596是一种有效的α7 nAChR变构调节剂，EC50为216 nM。 |
| 备注 | PNU-120596 is a positive allosteric modulator of α7 nAChR with EC50 of 216 nM. |
| 生化机理 | PNU 120596 is a type II positive allosteric modulator of α7 neuronal nicotinic acetylcholine receptor (AChR) located on the somatodendritic membrane of hippocampal interneurons. This modulator increases the frequency of acetylcholine-evoked GABAergic postsynaptic currents in pyramidal neurons, which can be suppressed by TTX. In addition, studies show that PNU 120596 increases the average time the channel of AChR is open, but does not have any effect on the selectivity of ions flowing through the channel. Furthermore, PNU 120596 has little effect on α4β2, α3β4 and α9α10 receptors. Alternate studies indicate that PNU 120596 increases the effects of choline on native α7-containing AChRs activating these receptors, thus producing single ion channel openings which result in an influx of calcium ions, that can be inhibited with the addition of methyllycaconitine |
| 别名 | N-(5-氯-2,4-二甲氧基苯基)-N'-(5-甲基-3-异噁唑基)脲;PNU 120596; PNU120596; NSC 216666;PNU 120596; PNU120596; NSC 216666;N-(5-Chloro-2,4-dimethoxyphenyl)-N′-(5-methyl-3-isoxazolyl)-urea |
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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