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202578-52-7

中文名称 202578-52-7
英文名称 DMP 696
CAS 202578-52-7
分子式 C18H21Cl2N5O2
分子量 410.3
MOL 文件 202578-52-7.mol
202578-52-7 结构式 202578-52-7 结构式

基本信息

中文别名
化合物 T15145
英文别名
DMP 696
4-chloro-8-(2,4-dichlorophenyl)-2,7-dimethylpyrazolo[1,5-a][1,3,5]triazine
Pyrazolo[1,5-a]-1,3,5-triazin-4-amine, 8-(2,4-dichlorophenyl)-N-[2-methoxy-1-(methoxymethyl)ethyl]-2,7-dimethyl-

物理化学性质

熔点120-121 °C
密度1.39±0.1 g/cm3(Predicted)
储存条件-20°C储存
溶解度溶于二甲基亚砜
酸度系数(pKa)1.98±0.30(Predicted)
形态Solid

常见问题列表

生物活性
DMP 696 是一种促肾上腺素皮质激素释放激素受体1 (CRHR1) 拮抗剂,常用于焦虑和抑郁症的研究。
体内研究

DMP696 (3 mg/kg, p.o.) attenuates consolidation of remote fear memories of mice, without affecting their expression and retention. WT mice treated with DMP696 for 1 week starting 24 h after foot shock also show reduced synaptosomal GluR1 levels than do shocked vehicle-treated controls. Rats treated with different doses of DMP696 (1, 3, 10, 30 mg/kg) show very little freezing during the 2-minute preshock interval. Rats treated with DMP696 exhibit a significant overall reduction in CREB phosphorylation, in both the LA, and BLA, but not in the CeA. DMP696 treatment reduces levels of LA and BLA pCREB across all time intervals that do not differ significantly from homecage pCREB levels (P>0.05). In the CeA, both vehicle- and DMP696-treated rats exhibit significantly higher pCREB expression at each post-conditioning time interval than homecage pCREB levels. Rats in the 30 ng DMP696 group exhibit significantly less freezing in comparison to vehicle-treated animals.

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