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521-78-8

中文名稱 馬來酸三甲丙咪嗪
英文名稱 TRIMIPRAMINE MALEATE SALT
CAS 521-78-8
分子式 C24H30N2O4
分子量 410.51
MOL 文件 521-78-8.mol
更新日期 2024/06/17 17:25:36
521-78-8 結(jié)構(gòu)式 521-78-8 結(jié)構(gòu)式

基本信息

中文別名
馬來酸三甲丙咪嗪
英文別名
Trimipramina
surmontilmaleate
Einecs 208-318-3
trimepriminemaleate
TRIMIPRAMINE MALEATE
TRIMIPRAMINEMALEATE,BP
Trimeprimine Monomaleat
trimipramineacidmaleate
trimepriminemonomaleate
TRIMIPRAMINE MALEATE SALT
所屬類別
生物化工:激動劑抑制劑

物理化學(xué)性質(zhì)

熔點(diǎn)141-143°C
閃點(diǎn)11 °C
儲存條件2-8°C
溶解度氯仿:可溶,50mg/ml,透明,無色至淡黃色
形態(tài)powder
顏色white
EPA化學(xué)物質(zhì)信息Trimipramine maleate (521-78-8)

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
警示詞警告
危險品標(biāo)志Xn,T,F
危險品運(yùn)輸編號3249
WGK Germany3
RTECS號HN9260000
危險等級6.1(b)
包裝類別III
海關(guān)編碼2933996100
馬來酸三甲丙咪嗪價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/08/19HY-B1213馬來酸三甲丙咪嗪
Trimipramine maleate
521-78-8100mg500元
2024/08/19HY-B1213馬來酸三甲丙咪嗪
Trimipramine maleate
521-78-810mM * 1mLin DMSO550元

常見問題列表

生物活性
Trimipramine maleate 是 5-HT 受體的拮抗劑,其對 5-HT1C,5-HT2 和 5-HT1A 受體的 pKi 值分別為 6.39,8.10,4.66。
靶點(diǎn)

5-HT 1C Receptor

6.39 (pKi)

5-HT 2 Receptor

8.10 (pKi)

sPLA2

4.66 (pKi)

體外研究

Trimipramine displays much higher affinity for 5-HT 2 than for 5-HT 1C receptors.

體內(nèi)研究

The chronic administration of Trimipramine (5 mg/kg/day), as delivered by the osmotic minipump in 14 days produce significant increases in the regional concentration of 5-HT. The increases are highest in the frontal cortex and the hippocampus, followed by the olfactory tubercles and the hypothalamus. The Trimipramine treatment also produces marked increases in brain 5-HIAA concentrations ranging from 63% in the hippocampus to 25% in the nucleus accumbens with intermediate values for the hypothalamus, olfactory tubercles, frontal cortex and nucleus accumbens. Trimipramine treatment produces significant increases in DA concentrations in the nucleus accumbens, striaturn, and olfactory tubercles reaching 43, 21 and 11% respectively. Chronic administration of Trimipramine produces a marked reduction in the number of frontal cortex 5-HT 2 and striatal DA D 2 receptors. The chronic administration of Trimipramine produces an increase in the brain regional level of monoamines and metabolites indicating a greater synthesis rate for DA and 5-HT coinciding with an adaptive down regulation of 5-HT 2 and DA D 2 receptors.

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