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Idazoxan hydrochloride

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纯度: 99.84%

货号 T0115Cas号 79944-56-2

别名 盐酸咪唑克生, RX 781094

Idazoxan hydrochloride (RX 781094) 是一种 α2-肾上腺素受体拮抗剂,改善帕金森氏病、L-DOPA 引起的运动障碍和实验性帕金森病的运动症状。它也是咪唑啉受体拮抗剂,可竞争性拮抗唑啉样药物的中枢性降压作用。

Idazoxan hydrochloride
其他形式的 “Idazoxan hydrochloride”:
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Idazoxan hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 99.84%

货号 T0115 别名 盐酸咪唑克生, RX 781094Cas号 79944-56-2

Idazoxan hydrochloride (RX 781094) 是一种 α2-肾上腺素受体拮抗剂,改善帕金森氏病、L-DOPA 引起的运动障碍和实验性帕金森病的运动症状。它也是咪唑啉受体拮抗剂,可竞争性拮抗唑啉样药物的中枢性降压作用。

规格价格库存数量
1 mg
¥ 169
现货
5 mg
¥ 413
现货
10 mg
¥ 662
现货
25 mg
¥ 1,200
现货
50 mg
¥ 1,830
现货
100 mg
¥ 2,730
现货
200 mg
¥ 3,920
现货
1 mL x 10 mM (in DMSO)
¥ 215
现货
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产品介绍


Idazoxan hydrochloride AI Summary
Idazoxan hydrochloride exhibits a diverse range of bioactivities across various biological systems. It has a LogD value of 0.33 and shows significant antagonistic activity against the Alpha-2 adrenergic receptor with a Kd value of 15.85 nM, while also demonstrating agonistic activity against the Alpha-1 adrenergic receptor with a Kd value of 1584.89 nM. The compound displays selectivity with a ratio of 100.0 towards the Alpha-2 adrenergic receptor over the Alpha-1 receptor. Furthermore, in murine and rat assays, it shows alpha-2 adrenergic receptor agonist activity with a Kd value of 10.47 nM and alpha-1 adrenergic receptor agonist activity with a Kd value of 501.19 nM, respectively, suggesting a selectivity ratio of 50.0 in these models. In terms of antiplasmodial activity, Idazoxan hydrochloride effectively inhibits various strains of Plasmodium falciparum, with IC50 values ranging from 10,000.0 nM to 12,589.25 nM. The compound also affects the proliferation of different lines of Plasmodium falciparum and demonstrates multiple molecular modulations such as Lamin A splicing, JMJD2E inhibition, Tau fibril formation inhibition, and interactions with proteins and receptors like Neuropeptide S Receptor, Jumonji Domain Containing 2E, Histone Lysine Methyltransferase G9a, and BLM, among others. Idazoxan hydrochloride has demonstrated antiviral activity notably against SARS-CoV-2. It inhibits the viability of Vero E6 cells and Caco-2 cells infected with SARS-CoV-2, showing an inhibition index of 1.162 and an inhibition rate of 7.58% at 10 µM after 48 hours, respectively. Additionally, it inhibits the SARS-CoV-2 3CL-Pro protease by 14.22% at a concentration of 20 µM. However, the inhibitive effect on VERO-6 cells cytotoxicity is relatively lower at 0.37% inhibition rate. This multi-target activity underscores Idazoxan hydrochloride’s potential as a therapeutic agent across different disease areas..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Idazoxan hydrochloride (RX 781094) is a benzodioxane-linked imidazole. It has alpha-2 adrenoceptor antagonist activity.
别名盐酸咪唑克生, RX 781094
化学信息
分子量240.69
分子式C11H12N2O2·HCl
CAS No.79944-56-2
SmilesCl.C1CN=C(N1)C1COC2=C(O1)C=CC=C2
密度no data available
颜色White
物理性状Solid
储存&溶解度
存储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 (415.47 mM), Sonication and heating are recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (16.62 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
1mg5mg10mg50mg
1 mM4.1547 mL20.7736 mL41.5472 mL207.7361 mL
5 mM0.8309 mL4.1547 mL8.3094 mL41.5472 mL
10 mM0.4155 mL2.0774 mL4.1547 mL20.7736 mL
20 mM0.2077 mL1.0387 mL2.0774 mL10.3868 mL
50 mM0.0831 mL0.4155 mL0.8309 mL4.1547 mL
100 mM0.0415 mL0.2077 mL0.4155 mL2.0774 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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