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Imidazolidinyl urea

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纯度: 98.6%

货号 T0430Cas号 39236-46-9

别名 咪唑烷基脲, Imidurea

Imidazolidinyl urea (Imidurea) 在化妆品中作为抗菌防腐剂, 也用作甲醛释放剂。

Imidazolidinyl urea
其他形式的 “Imidazolidinyl urea”:

Imidazolidinyl urea

一键复制产品信息
Rating icon 很棒

纯度: 98.6%

货号 T0430 别名 咪唑烷基脲, ImidureaCas号 39236-46-9

Imidazolidinyl urea (Imidurea) 在化妆品中作为抗菌防腐剂, 也用作甲醛释放剂。

规格价格库存数量
500 mg
¥ 108
现货
1 g
¥ 147
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5 g
¥ 316
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10 g
¥ 455
现货
1 mL x 10 mM (in DMSO)
¥ 108
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产品介绍


Imidazolidinyl urea AI Summary
Imidazolidinyl urea exhibits a range of bioactivities in various assays. It shows inhibition against HIV-1 integrase, with an inhibition greater than 50.0% at 1 mM, and less than 50.0% at 200 µM and 25 µM. In a qHTS assay, it inhibited RanGTP induced Rango-Importin beta complex dissociation with a potency of 7.3 nM, acted as a delayed death inhibitor for the malarial parasite plastid with a potency of 18,526.0 nM, and inhibited HP1-beta Chromodomain interactions at 100,000.0 nM. In terms of antiviral activity, Imidazolidinyl urea inhibits SARS-CoV-2. It showed moderate bioactivity on infected Vero E6 cells with an inhibition index of 0.7579 compared to arbidol, and demonstrated 3.89% inhibition of virus-induced cytotoxicity in Caco-2 cells at 10 µM concentration over 48 hours. However, its activity against SARS-CoV-2 3CL-Pro protease was minimal, showing a 1.165% inhibition at 20 µM. The compound also inhibited transglutaminase in human keratinocytes by 35.0% in the presence of retinal, and likewise, inhibited human HDAC6 enzyme activity with rates of 38.7% and 7.67% using commercial and custom peptide substrates, respectively. This profile suggests its potential as both a HIV-1 integrase and HDAC6 inhibitor, as well as an antiviral agent with specific activities against SARS-CoV-2..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Imidazolidinyl urea (Imidurea) is an antimicrobial preservative used in cosmetics.
别名咪唑烷基脲, Imidurea
化学信息
分子量388.29
分子式C11H16N8O8
CAS No.39236-46-9
SmilesN(C(NCNC(NC1N(CO)C(=O)NC1=O)=O)=O)C2N(CO)C(=O)NC2=O
密度1.85g/cm3
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: 250 mg/mL (643.85 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.15 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 mM2.5754 mL12.8770 mL25.7539 mL128.7697 mL
5 mM0.5151 mL2.5754 mL5.1508 mL25.7539 mL
10 mM0.2575 mL1.2877 mL2.5754 mL12.8770 mL
20 mM0.1288 mL0.6438 mL1.2877 mL6.4385 mL
50 mM0.0515 mL0.2575 mL0.5151 mL2.5754 mL
100 mM0.0258 mL0.1288 mL0.2575 mL1.2877 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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