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Iopanoic acid

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纯度: 97.06%

货号 T0960Cas号 96-83-3

别名 碘番酸, Iodopanoic acid, Acidum iopanoicum

Iopanoic acid 是一种碘造影剂,也是一种 5'-Deiodinase 抑制剂。

Iopanoic acid
其他形式的 “Iopanoic acid”:

Iopanoic acid

一键复制产品信息
Rating icon 很棒

纯度: 97.06%

货号 T0960 别名 碘番酸, Iodopanoic acid, Acidum iopanoicumCas号 96-83-3

Iopanoic acid 是一种碘造影剂,也是一种 5'-Deiodinase 抑制剂。

规格价格库存数量
25 mg
¥ 169
现货
50 mg
¥ 233
现货
100 mg
¥ 328
现货
500 mg
¥ 783
现货
1 mL x 10 mM (in DMSO)
¥ 129
现货
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产品介绍


Iopanoic acid AI Summary
Iopanoic acid shows rapid distribution in various organs of female rats following intravenous administration, with detectable percentages in blood, heart, kidney, lung, and liver at both 5 and 30 minutes post-administration. Analysis through polyacrylamide gel electrophoresis indicates its presence in different plasma components such as low-density lipoprotein, high-density lipoprotein, and albumin at multiple time points. Bioactivity studies reveal that Iopanoic acid inhibits enzymes including Histone Lysine Methyltransferase G9a, ELG1-dependent DNA repair, and human tyrosyl-DNA phosphodiesterase 1 (TDP1), among others. It also exhibits antagonistic activity against cAMP-regulated guanine nucleotide exchange factor 2 (EPAC2) and blocks Ebola Virus entry under different screening conditions. Additionally, it inhibits sodium fluorescein uptake in OATP1B3- and OATP1B1-transfected CHO cells at a 10 µM concentration. Toxicologically, Iopanoic acid induces moderate to acute liver toxicity demonstrated by elevated clinical-chemistry markers (ALT and AST). However, there are no indications of chronic liver diseases or related conditions such as cirrhosis or cancer. In terms of antiviral activity, Iopanoic acid inhibits SARS-CoV-2 induced cytotoxicity in VERO-6 cells and Caco-2 cells, although with relatively high IC50 values exceeding 20,000 nM. It also exhibits minimal inhibition of the SARS-CoV-2 3CL-Pro protease. Furthermore, Iopanoic acid shows inhibitory potential on the human HDAC6 enzyme and antagonistic activity towards human TBXA2R and CHRM1 receptors, with agonist activity at human ADRA1A receptor. While it demonstrates binding to various receptors and enzymes, significant bioactivity is largely absent at target sites tested, as indicated by AC50 values above 30,000 nM for most targets except a few..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Iopanoic acid is an iodine contrast agent and a 5'-Deiodinase inhibitor.
别名碘番酸, Iodopanoic acid, Acidum iopanoicum
化学信息
分子量570.93
分子式C11H12I3NO2
CAS No.96-83-3
SmilesCCC(Cc1c(I)cc(I)c(N)c1I)C(O)=O
密度2.426g/cm3
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: 55 mg/mL (96.33 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (3.5 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 mM1.7515 mL8.7576 mL17.5153 mL87.5764 mL
5 mM0.3503 mL1.7515 mL3.5031 mL17.5153 mL
10 mM0.1752 mL0.8758 mL1.7515 mL8.7576 mL
20 mM0.0876 mL0.4379 mL0.8758 mL4.3788 mL
50 mM0.0350 mL0.1752 mL0.3503 mL1.7515 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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