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Imipramine hydrochloride

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纯度: 99.98%

货号 T7941Cas号 113-52-0

别名 盐酸丙米嗪, 盐酸丙咪嗪, Tofranil, Melipramine, Imipramine HCl, Imipramine (hydrochloride), G 22355

Imipramine hydrochloride (Imipramine HCl) 可抑制血清素转运蛋白,IC50=32 nM。它可阻止胰酶的易位,阻碍 MV 和外泌体的分泌。

Imipramine hydrochloride
其他形式的 “Imipramine hydrochloride”:

Imipramine hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 99.98%

货号 T7941 别名 盐酸丙米嗪, 盐酸丙咪嗪, Tofranil, Melipramine, Imipramine HCl, Imipramine (hydrochloride), G 22355Cas号 113-52-0

Imipramine hydrochloride (Imipramine HCl) 可抑制血清素转运蛋白,IC50=32 nM。它可阻止胰酶的易位,阻碍 MV 和外泌体的分泌。

规格价格库存数量
25 mg
¥ 198
现货
50 mg
¥ 289
现货
100 mg
¥ 413
现货
500 mg
¥ 986
5日内发货
1 mL x 10 mM (in DMSO)
¥ 455
现货
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产品介绍


Imipramine hydrochloride AI Summary
Imipramine hydrochloride exhibits a multifaceted bioactivity profile. It shows significant antidepressant effects in various behavioral assays in mice, such as inhibiting tetrabenazine-induced depression of motor activity (ED50 = 0.58 mg/kg) and ptosis (ED50 = 0.98 mg/kg), and reducing immobility time in the forced swim test. The compound also inhibits the norepinephrine transporter with a Ki of 12.0 nM and demonstrates modest activity against serotonin uptake (Ki = 41.8 nM). In pharmacokinetic studies, Imipramine hydrochloride shows high protein binding affinity and consistent distribution ratios across species. It exhibits a bioavailability of 42.0%, a clearance rate of 13.0 mL/min/kg, and a half-life of 16.0 hours in humans. The compound's metabolism results in glucuronide concentrations in bile and urine, indicating substantial metabolic processing. Additionally, Imipramine hydrochloride exhibits antiplasmodial activity against various strains of Plasmodium falciparum, with IC50 values ranging from 1258.93 nM to 15848.93 nM. It also demonstrates antiviral properties, albeit with modest efficacy in inhibiting SARS-CoV-2-induced cytotoxicity in Caco-2 cells and inhibiting the SARS-CoV-2 3CL-Pro protease by 30.25% at 20µM. The compound also exhibits modest antifungal and antibacterial activities, with specific but low inhibition rates against Candida albicans, Cryptococcus neoformans, and different bacterial strains including Klebsiella pneumoniae and Staphylococcus aureus MRSA. Furthermore, Imipramine hydrochloride influences various cell types differently, inhibiting growth in HEK293T and human fibroblast cells but promoting growth in U2OS cells. The combined bioactivities and pharmacokinetic properties highlight the compound's potential for therapeutic applications across a range of conditions, including depression, infectious diseases, and central nervous system disorders..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Imipramine hydrochloride (Imipramine HCl) is a first generation tricyclic antidepressant that acts primarily as an inhibitor of serotonin and norepinephrine transporters (Kds = 1.4 and 37 nM, respectively).Imipramine hydrochloride is reported to prevent the translocation of aSMase, inhibiting MV and exosomes secretion
靶点活性
5-HT:32 nM (IC50)
别名盐酸丙米嗪, 盐酸丙咪嗪, Tofranil, Melipramine, Imipramine HCl, Imipramine (hydrochloride), G 22355
化学信息
分子量316.87
分子式C19H25ClN2
CAS No.113-52-0
SmilesCN(C)CCCN1c2ccccc2CCc2ccccc21.Cl
密度1.041g/cm3
颜色White
物理性状Solid
储存&溶解度
存储store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 100 mg/mL (315.59 mM), Sonication is recommended.
H2O: 100 mg/mL (315.59 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (12.62 mM), Sonication is recommended.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
DMSO/H2O
1mg5mg10mg50mg
1 mM3.1559 mL15.7793 mL31.5587 mL157.7934 mL
5 mM0.6312 mL3.1559 mL6.3117 mL31.5587 mL
10 mM0.3156 mL1.5779 mL3.1559 mL15.7793 mL
20 mM0.1578 mL0.7890 mL1.5779 mL7.8897 mL
50 mM0.0631 mL0.3156 mL0.6312 mL3.1559 mL
100 mM0.0316 mL0.1578 mL0.3156 mL1.5779 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

方案所需的各类助溶剂如: DMSOPEG300 / PEG400Tween 80SBE-β-CD玉米油 等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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