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首页 化工产品目录 生物化工 生化试剂 激动剂抑制剂 3-(2-Chlorophenyl)-2-[2-[6-[(diethylamino)methyl]-2-pyridinyl]ethenyl]-6-fluoro-4(3H)-quinazolinonehydrochloride
199655-36-2
3-(2-Chlorophenyl)-2-[2-[6-[(diethylamino)methyl]-2-pyridinyl]ethenyl]-6-fluoro-4(3H)-quinazolinonehydrochloride
产品纠错
CAS号:199655-36-2 | 英文名称:3-(2-Chlorophenyl)-2-[2-[6-[(diethylamino)methyl]-2-pyridinyl]ethenyl]-6-fluoro-4(3H)-quinazolinonehydrochloride
分子式 C26H24ClFN4O
分子量 463
EINECS号 200-158-5
MDL
Smiles
InChIKey
3-(2-Chlorophenyl)-2-[2-[6-[(diethylamino)methyl]-2-pyridinyl]ethenyl]-6-fluoro-4(3H)-quinazolinonehydrochloride化学百科
基本信息
中文名称 CP 465022 HYDROCHLORIDE
英文名称 3-(2-Chlorophenyl)-2-[2-[6-[(diethylamino)methyl]-2-pyridinyl]ethenyl]-6-fluoro-4(3H)-quinazolinonehydrochloride
CAS号 199655-36-2
分子式 C26H24ClFN4O
分子量 462.95
EINECS号 200-158-5
物化性质
沸点 585.0±60.0 °C(Predicted)
密度 1.23±0.1 g/cm3(Predicted)
溶解度 不溶于水; <49.94mg/ml,溶于 DMSO
形态 固体
酸度系数(pKa) 8.51±0.25(Predicted)
颜色 粘黄色
安全信息
生产及用途
CP-465022 hydrochloride 是一种强效的、选择性的、非竞争性的 AMPA受体 拮抗剂,具有抗惊厥活性。CP-465022 对 Kainate 诱导反应具有抑制作用,IC50 为 25 nM。CP-465022 是研究 AMPA 受体在生理和病理方面研究的有效工具。

IC50: 25 nM (rat cortical neurons)

CP-465022 (0.0001 μM-10 μM) inhibits kainate-induced response in relatively slow manner and dependents on compound concentration, exhibiting a calculated IC 50 of 25 nM and essentially complete inhibition at 3.2 µM. CP-465022 1 µM for 10 min has little effect on peak NMDA-induced currents but reduces current measured at 8 s during NMDA application by 26%.CP-465,022 at 10 µM inhibits peak NMDA-induced currents in cortical neurons by 36% and currents measured at 8 s by 70% d in primary cultures of cortical and cerebellar granule neurons. CP-465022 1 µM for 10 min inhibits peak NMDA currents in cultured rat cerebellar granule neurons with mean inhibition of 19% and NMDA currents measured at 8 s by 45%, similar to what is observed in the cortical neurons.CP-465022 (100 nM -10 µM) has inhibitory effects on Kainate-induced whole-cell currents in voltage-clamped rat hippocampal, 100 nM CP465,022 inhibits kainate currents developed over the course of 200s, 500 nM and 1 µM CP-465,022 nearly complete inhibits this time frame (99.3%).

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