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5-Amino-4-imidazolecarboxamide

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纯度: 99.17%

货号 T1722Cas号 21299-72-9

别名 5-氨基-1H-咪唑-4-酰胺

5-Amino-4-imidazolecarboxamide 是一种咪唑衍生物。

5-Amino-4-imidazolecarboxamide
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5-Amino-4-imidazolecarboxamide

一键复制产品信息
Rating icon 很棒

纯度: 99.17%

货号 T1722 别名 5-氨基-1H-咪唑-4-酰胺Cas号 21299-72-9

5-Amino-4-imidazolecarboxamide 是一种咪唑衍生物。

规格价格库存数量
10 mg
¥ 138
现货
25 mg
¥ 279
现货
50 mg
¥ 447
现货
100 mg
¥ 581
现货
200 mg
¥ 819
现货
1 mL x 10 mM (in DMSO)
¥ 99
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纯度: 99.17%
颜色: 黄色
性状: Solid
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产品介绍


5-Amino-4-imidazolecarboxamide AI Summary
5-Amino-4-imidazolecarboxamide is an inhibitor with broad bioactivity across various targets and applications. It inhibits Escherichia coli recombinant DNA gyrase-mediated supercoiling of relaxed pRSET A-DNA with an IC50 value of 814,000 nM, and also targets GDA (Glyceraldehyde-3-phosphate dehydrogenase) with a Ki of 4440 nM based on colorimetric assays. This compound has demonstrated diverse activities including inhibiting interactions with methylated histone tails, malarial parasite plastid, ARNT/TAC3 interactions, and TDP-43, inducing DNA re-replication in colon adenocarcinoma cells, and being investigated for its potential in antimalarial drug development via inhibition of AMA1-RON. In cytotoxicity assessments, compound 458904 exhibits a 20% growth inhibition rate in human KB cells at 1 mM after 96 hours as per the CellTitre-Blue fluorescence assay. Moreover, it shows moderate bioactivity in mouse brain tissue with a significant level of drug uptake (52%) in the soluble tissue fraction at 10 μM after 1 hour, and a fraction unbound of 0.48 in the insoluble tissue fraction. Finally, compound 458904 exhibits antiviral activity against SARS-CoV-2, with IC50 values above 20000 nM, suggesting potential antiviral effects at high concentrations..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
5-Amino-4-imidazolecarboxamide is an imidazole derivative.
别名5-氨基-1H-咪唑-4-酰胺
化学信息
分子量126.12
分子式C4H6N4O
CAS No.21299-72-9
SmilesNC(=O)c1[nH]cnc1N
密度1.538g/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: 45 mg/mL (356.8 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM7.9290 mL39.6448 mL79.2896 mL396.4478 mL
5 mM1.5858 mL7.9290 mL15.8579 mL79.2896 mL
10 mM0.7929 mL3.9645 mL7.9290 mL39.6448 mL
20 mM0.3964 mL1.9822 mL3.9645 mL19.8224 mL
50 mM0.1586 mL0.7929 mL1.5858 mL7.9290 mL
100 mM0.0793 mL0.3964 mL0.7929 mL3.9645 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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