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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 2025/08/19 20:20:55
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(dòng)劑抑制劑

物理化學(xué)性質(zhì)

熔點(diǎn)141-143°C
閃點(diǎn)11 °C
儲(chǔ)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
InChIInChI=1S/C20H26N2.C4H4O4/c1-16(14-21(2)3)15-22-19-10-6-4-8-17(19)12-13-18-9-5-7-11-20(18)22;5-3(6)1-2-4(7)8/h4-11,16H,12-15H2,1-3H3;1-2H,(H,5,6)(H,7,8)/b;2-1-
InChIKeyYDGHCKHAXOUQOS-BTJKTKAUSA-N
SMILESN1(CC(C)CN(C)C)C2C(=CC=CC=2)CCC2C=CC=CC1=2.C(/C(=O)O)=C/C(=O)O
EPA化學(xué)物質(zhì)信息Trimipramine maleate (521-78-8)

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)有害 (GHS07)健康危害 (GHS08)
GHS07,GHS08
警示詞警告
危險(xiǎn)性描述H302-H315-H319-H335-H361
危險(xiǎn)品標(biāo)志Xn,T,F
危險(xiǎn)品運(yùn)輸編號(hào)3249
WGK Germany3
RTECS號(hào)HN9260000
危險(xiǎn)等級(jí)6.1(b)
包裝類別III
海關(guān)編碼2933996100
存儲(chǔ)類別11 - Combustible Solids
危險(xiǎn)性類別Acute Tox. 4 Oral
Eye Irrit. 2
Repr. 2
Skin Irrit. 2
STOT SE 3
馬來酸三甲丙咪嗪價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2026/06/05HY-B1213R馬來酸三甲丙咪嗪
Trimipramine maleate (Standard)
521-78-810 mg360元
2026/06/05HY-B1213R馬來酸三甲丙咪嗪
Trimipramine maleate (Standard)
521-78-825 mg660元
2026/06/05HY-B1213R馬來酸三甲丙咪嗪
Trimipramine maleate (Standard)
521-78-850 mg1000元

常見問題列表

生物活性
Trimipramine maleate 是 5-HT 受體的拮抗劑,其對(duì) 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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