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75450-34-9

中文名称 CGP 37157
英文名称 7-CHLORO-5-(2-CHLOROPHENYL)-1,5-DIHYDRO-4,1-BENZOTHIAZEPIN-2(3H)-ONE
CAS 75450-34-9
分子式 C15H11Cl2NOS
分子量 324.22
MOL 文件 75450-34-9.mol
更新日期 2024/11/20 09:32:44
75450-34-9 结构式 75450-34-9 结构式

基本信息

中文别名
CGP-37157 CALBIOCHEM
英文别名
CGP 37157
CGP-37157 - CAS 75450-34-9 - Calbiochem
7-chloro-5-(2-chlorophenyl)benzo[e][1,4]thiazepin-2(1H,3H,5H)-one
7-CHLORO-5-(2-CHLOROPHENYL)-1,5-DIHYDRO-4,1-BENZOTHIAZEPIN-2(3H)-ONE
7-Chloro-5-(2-chlorophenyl)-1,5-dihydro-4,1-benzothiazepine-2(3H)-one
4,1-Benzothiazepin-2(3H)-one, 7-chloro-5-(2-chlorophenyl)-1,5-dihydro-

物理化学性质

沸点479.8±45.0 °C(Predicted)
密度1.384±0.06 g/cm3(Predicted)
储存条件2-8°C
溶解度二甲基亚砜:≥20mg/mL
酸度系数(pKa)12.20±0.40(Predicted)
形态白色固体
颜色白色
稳定性可在-20°C下DMSO溶液保存长达3个月。

安全数据

危险性符号(GHS)GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS09
警示词警告
危险性描述H400-H302
危险品标志Xn,N
危险类别码22-50
安全说明61
WGK Germany3

常见问题列表

生物活性
CGP37157 是一种 Na+/Ca2+ exchanger 抑制剂,可抑制豚鼠心脏线粒体 Na+ 诱导的 Ca2+ 的释放,IC50 值为 0.8 μM。
靶点

IC50: 0.8 μM (Na + /Ca 2+ exchanger)

体外研究

CGP37157 (Compound XVI) is a potent, selective inhibitor of Na + /Ca 2+ exchanger, inhibiting the Na + -induced Ca 2+ -release from guinea-pig heart mitochondria, with an IC 50 of 0.8 μM. CGP37157 (10 μM) shows inhibitory effect on mitochondrial Na + /Ca 2+ exchanger in cortical neurons, modulates intracellular Ca 2+ levels via suppresssing voltage-gated calcium channels, and reduces NMDA-induced cytosolic and mitochondrial Ca 2+ overloads. CGP37157 (10 μM) also reduces NMDA-induced excitotoxicity, and such an effect is via attenuating mitochondrial damage and calpain activity in neurons. CGP37157 (10 μM) in combination with salinomycin significantly attenuates cell viability and increases apoptosis of FaDu and HLaC79 cells. Moreover, CGP37157 has no inhibitory effect on salinomycin tumor toxicity.

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