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1-Methylimidazole

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纯度: 99.50%

货号 T0575Cas号 616-47-7

别名 N-甲基咪唑

1-Methylimidazole 是1-methyl-2-thioimidazole (methimazole)的代谢物,可抑制骨吸收。

1-Methylimidazole
其他形式的 “1-Methylimidazole”:

1-Methylimidazole

一键复制产品信息
Rating icon 很棒

纯度: 99.50%

货号 T0575 别名 N-甲基咪唑Cas号 616-47-7

1-Methylimidazole 是1-methyl-2-thioimidazole (methimazole)的代谢物,可抑制骨吸收。

规格价格库存数量
1 g
¥ 99
现货
1 mL x 10 mM (in DMSO)
¥ 99
现货
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纯度: 99.50%
颜色: 无色透明
性状: Liquid
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产品介绍


1-Methylimidazole AI Summary
1-Methylimidazole is a multi-functional bioactive compound with diverse properties and activities. It has a dissociation constant (pKa) of 7.12, indicating specific behaviors related to ionization and protonation at certain pH levels. It enhances styrene oxide hydrolase activity at pH 8.7, with an efficiency of E100 = 0.012 M, achieving maximum enhancement at a concentration of 0.05 M. Additionally, it enhances epoxide hydrolase activity with a Log 1/E100 value of 1.94 and has a partition coefficient (logP) value of 0.28. 1-Methylimidazole also exhibits germicidal activity against Staphylococcus aureus, Pseudomonas aeruginosa, and Streptococcus pyogenes at a concentration of 254 ppm with a sterilization time of over 0.5 hours. It acts as an inhibitor of CYP3A4 with an IC50 value greater than 10,000 nM, indicating its role as a retinoic acid metabolism blocking agent (RAMBA). Moreover, it demonstrates inhibitory effects on the SARS-CoV-2 3CL-Pro protease with an inhibition rate of 21.78% at a 20 µM concentration and exhibits antiviral activity against SARS-CoV-2 by inhibiting virus-induced cytotoxicity in VERO-6 cells at 10 µM after 48 hours of virus exposure. In cellular assays, 1-Methylimidazole acts as both an agonist and antagonist of the NFkB signaling pathway with a potency of 6.3 nM. It inhibits multiple enzymes including APE1, HADH2, Histone Lysine Methyltransferase G9a, FEN1, Human D2 Dopamine Receptor, and Arylsulfatase A with varying potencies from 794.3 nM to 37685.8 nM. Overall, 1-Methylimidazole shows potential in various biochemical and pharmacological applications due to its diverse bioactive properties..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
1-Methylimidazole is a metabolite of 1-methyl-2-thioimidazole (methimazole) which inhibits bone resorption.
别名N-甲基咪唑
化学信息
分子量82.10
分子式C4H6N2
CAS No.616-47-7
SmilesCN1C=CN=C1
密度1.035 g/cm3. Temperature:20 °C.;1.017 g/cm3. Temperature:40 °C.
储存&溶解度
存储In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 45 mg/mL (548.11 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM12.1803 mL60.9013 mL121.8027 mL609.0134 mL
5 mM2.4361 mL12.1803 mL24.3605 mL121.8027 mL
10 mM1.2180 mL6.0901 mL12.1803 mL60.9013 mL
20 mM0.6090 mL3.0451 mL6.0901 mL30.4507 mL
50 mM0.2436 mL1.2180 mL2.4361 mL12.1803 mL
100 mM0.1218 mL0.6090 mL1.2180 mL6.0901 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:
比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL, 一共给药动物10只,您使用的配方为 10% DMSO + 40% PEG300 + 5% Tween 80 + 45% Saline / PBS / ddH2O, 那么您的工作液浓度为2 mg/mL
母液配置方法:2 mg 药物溶于 100 μL DMSO ( 母液浓度为 20 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:100 μL DMSO 母液, 添加 400 μL PEG300 混匀澄清, 再加 50 μL Tween 80, 混匀澄清, 再加 450 μL Saline / PBS / ddH2O 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: DMSOPEG300PEG400Tween 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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