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Eticlopride hydrochloride

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纯度: 98%

货号 T4007Cas号 97612-24-3

别名 依替必利盐酸盐

Eticlopride hydrochloride 是一种抗精神病药,是一种选择性多巴胺 D2/D3 受体拮抗剂(Ki:0.5/0.16 nM)。

Eticlopride hydrochloride
其他形式的 “Eticlopride hydrochloride”:

Eticlopride hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 98%

货号 T4007 别名 依替必利盐酸盐Cas号 97612-24-3

Eticlopride hydrochloride 是一种抗精神病药,是一种选择性多巴胺 D2/D3 受体拮抗剂(Ki:0.5/0.16 nM)。

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1 mg
¥ 412
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5 mg
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产品介绍


Eticlopride hydrochloride AI Summary
Eticlopride hydrochloride exhibits a broad range of bioactivities, including antiplasmodial activity against various strains of Plasmodium falciparum with IC50 values ranging from 10000.0 nM to 12589.25 nM after 72 hours, as determined by the SYBR green assay. It has shown potency in inhibiting interactions of HP1-beta chromodomain with methylated histone tails, bacterial growth inhibition, cytotoxicity in TGF-b, cell surface uPA generation, induction of DNA re-replication in breast cells, inhibition of mitochondrial permeability transition pore, inhibition of Glutaminase, inhibition of Hepatitis C Virus, inhibition of ATXN expression, and inhibition of GLP-1 Receptor. Furthermore, Eticlopride hydrochloride induces synthetic lethality in tumor cells producing 2HG, inhibits human tyrosyl-DNA phosphodiesterase 1 (TDP1), and has demonstrated efficacy against Lassa Virus, Marburg Virus, and Ebola Virus by inhibiting their binding or entry into cells. Additionally, Eticlopride hydrochloride has shown antiviral activity against SARS-CoV-2. It inhibits SARS-CoV-2 induced cytotoxicity in Caco-2 cells by 47.59% at a concentration of 10 µM after 48 hours and shows 12.59% inhibition of SARS-CoV-2 3CL-Pro protease at a 20 µM concentration, as determined by FRET-based assay. In Vero E6 cells infected with SARS-CoV-2 (strain BavPat1), it achieved an inhibition index of 0.4234 after a certain multiplicity of infection (MOI) after 72 hours, and demonstrated largely negligible inhibition (-0.09%) of cytotoxicity in VERO-6 cells at the same concentration and exposure duration..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Eticlopride, an antipsychotic, is a Selective dopamine D2/D3 receptor antagonist (Ki: 0.5/0.16 nM).
靶点活性
D2:0.50 nM, D2:0.09 nM (Ki), D3:0.16 nM
别名依替必利盐酸盐
化学信息
分子量377.31
分子式C17H25ClN2O3.HCl
CAS No.97612-24-3
SmilesCl.CCN1CCC[C@H]1CNC(=O)c1c(O)c(CC)cc(Cl)c1OC
密度no data available
储存&溶解度
存储store at low temperature | 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
H2O: 30 mg/mL (79.51 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.3 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
H2O
1mg5mg10mg50mg
1 mM2.6503 mL13.2517 mL26.5034 mL132.5170 mL
5 mM0.5301 mL2.6503 mL5.3007 mL26.5034 mL
10 mM0.2650 mL1.3252 mL2.6503 mL13.2517 mL
20 mM0.1325 mL0.6626 mL1.3252 mL6.6259 mL
50 mM0.0530 mL0.2650 mL0.5301 mL2.6503 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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