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Temgicoluril

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纯度: 99.8%

货号 T9424Cas号 10095-06-4

别名 Tetramethylglycoluril, mebikar

Temgicoluril (mebikar) 具有抗焦虑活性,作用于GABA 受体。

Temgicoluril

Temgicoluril

一键复制产品信息
Rating icon 很棒

纯度: 99.8%

货号 T9424 别名 Tetramethylglycoluril, mebikarCas号 10095-06-4

Temgicoluril (mebikar) 具有抗焦虑活性,作用于GABA 受体。

规格价格库存数量
10 mg
¥ 133
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25 mg
¥ 206
现货
50 mg
¥ 296
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产品介绍


Temgicoluril AI Summary
Temgicoluril exhibits antiviral activity against SARS-CoV-2 by inhibiting virus-induced cytotoxicity in both Caco-2 and VERO-6 cells. Specifically, it inhibits SARS-CoV-2 induced cytotoxicity in Caco-2 cells at a 10 µM concentration with a 4.43% inhibition after 48 hours, as determined by high content imaging. In VERO-6 cells, the inhibition was -0.21% under the same conditions. Moreover, the compound demonstrates moderate antiviral activity against the SARS-CoV-2 USA-WA1/2020 strain in HRCE cells with a hit score of 0.1618. It also acts as an inhibitor of the SARS-CoV-2 3CL-Pro protease, showing 12.24% inhibition at 20 µM concentration. However, its potency in terms of inhibition is limited, with an IC50 value greater than 20000 nM in VERO-6 cells. In enzymatic assays, Temgicoluril has a moderate inhibitory effect on human HDAC6 activity with an inhibition of 6.15% using a commercial peptide substrate and -1.23% using a custom substrate. The compound displays binding affinity towards various receptors and transporters but exhibits minimal bioactivity, with AC50 values greater than 30,000 nM for all tested targets, indicating low or no activity in these assays..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Temgicoluril (mebikar) acts on GABA Receptor.
别名Tetramethylglycoluril, mebikar
化学信息
分子量198.22
分子式C8H14N4O2
CAS No.10095-06-4
SmilesCN1C2C(N(C)C1=O)N(C)C(=O)N2C
密度1.237 g/cm3 (Predicted)
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: 125 mg/mL (630.61 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (20.18 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 mM5.0449 mL25.2245 mL50.4490 mL252.2450 mL
5 mM1.0090 mL5.0449 mL10.0898 mL50.4490 mL
10 mM0.5045 mL2.5224 mL5.0449 mL25.2245 mL
20 mM0.2522 mL1.2612 mL2.5224 mL12.6122 mL
50 mM0.1009 mL0.5045 mL1.0090 mL5.0449 mL
100 mM0.0504 mL0.2522 mL0.5045 mL2.5224 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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