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521-78-8

中文名称 马来酸三甲丙咪嗪
英文名称 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 2024/04/02 22:44:43
521-78-8 结构式 521-78-8 结构式

基本信息

中文别名
马来酸三甲丙咪嗪
英文别名
Trimipramina
surmontilmaleate
Einecs 208-318-3
trimepriminemaleate
TRIMIPRAMINE MALEATE
TRIMIPRAMINEMALEATE,BP
Trimeprimine Monomaleat
trimipramineacidmaleate
trimepriminemonomaleate
TRIMIPRAMINE MALEATE SALT
所属类别
生物化工:激动剂抑制剂

物理化学性质

熔点141-143°C
闪点11 °C
储存条件2-8°C
溶解度氯仿:可溶,50mg/ml,透明,无色至淡黄色
形态powder
颜色white
EPA化学物质信息Trimipramine maleate (521-78-8)

安全数据

危险性符号(GHS)
GHS07,GHS08
警示词警告
危险品标志Xn,T,F
危险品运输编号3249
WGK Germany3
RTECS号HN9260000
危险等级6.1(b)
包装类别III
海关编码2933996100
马来酸三甲丙咪嗪价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-B1213马来酸三甲丙咪嗪
Trimipramine maleate
521-78-8100mg500元
2024/04/30HY-B1213马来酸三甲丙咪嗪
Trimipramine maleate
521-78-810mM * 1mLin DMSO550元

常见问题列表

生物活性
Trimipramine maleate 是 5-HT 受体的拮抗剂,其对 5-HT1C,5-HT2 和 5-HT1A 受体的 pKi 值分别为 6.39,8.10,4.66。
靶点

5-HT 1C Receptor

6.39 (pKi)

5-HT 2 Receptor

8.10 (pKi)

sPLA2

4.66 (pKi)

体外研究

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

体内研究

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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