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202578-52-7

中文名稱 202578-52-7
英文名稱 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 結(jié)構(gòu)式 202578-52-7 結(jié)構(gòu)式

基本信息

中文別名
化合物 T15145
英文別名
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-

物理化學(xué)性質(zhì)

熔點120-121 °C
密度1.39±0.1 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度溶于二甲基亞砜
酸度系數(shù)(pKa)1.98±0.30(Predicted)
形態(tài)Solid

常見問題列表

生物活性
DMP 696 是一種促腎上腺素皮質(zhì)激素釋放激素受體1 (CRHR1) 拮抗劑,常用于焦慮和抑郁癥的研究。
體內(nèi)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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