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Aklomide

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纯度: 99.65%

货号 T0390Cas号 3011-89-0

别名 阿克洛胺, Alkomide, 2-Chloro-4-nitrobenzamide

Aklomide (2-Chloro-4-nitrobenzamide) 用于家禽治疗寄生虫。

Aklomide

Aklomide

一键复制产品信息
Rating icon 很棒

纯度: 99.65%

货号 T0390 别名 阿克洛胺, Alkomide, 2-Chloro-4-nitrobenzamideCas号 3011-89-0

Aklomide (2-Chloro-4-nitrobenzamide) 用于家禽治疗寄生虫。

规格价格库存数量
100 mg
¥ 163
现货
500 mg
¥ 475
现货
1 g
¥ 693
现货
1 mL x 10 mM (in DMSO)
¥ 179
现货
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产品介绍


Aklomide AI Summary
Aklomide exhibits a broad spectrum of bioactivity and inhibitory effects in various assays. It acts as an inhibitor of the MLL CXXC domain-DNA interaction with a potency of 50118.7 nM. In the context of malarial research, it functions as a delayed death inhibitor of the malarial parasite plastid, demonstrating potencies of 10691.0 nM and 19011.5 nM after 96-hour and 48-hour incubation assays, respectively. In virology, Aklomide blocks the entry of the Ebola virus with AC50 values ranging from 707.9 nM to 0.7079 µM. It also shows significant antiviral activity against SARS-CoV-2 by inhibiting virus-induced cytotoxicity in Caco-2 and VERO-6 cells at a 10 µM concentration after 48 hours, with inhibition rates of 0.1% and -0.15%, respectively. The compound demonstrates 17.03% inhibition of the SARS-CoV-2 3CL-Pro protease at 20 µM. However, its IC50 value against SARS-CoV-2 in VERO-6 cells is greater than 19952.62 nM, indicating moderate to low potency. Additionally, a hit score of 0.1103 was reported in HRCE cells under specific conditions, suggesting potential efficacy. Moreover, Aklomide potently inhibits sodium fluorescein uptake in OATP1B3 and OATP1B1-transfected CHO cells at 10 µM with inhibition percentages of 100.21% and 115.49%, respectively. The compound also exhibits weak inhibition of the human BSEP transporter with an IC50 value greater than 1000000.0 nM, suggesting a limited effect on ATP-dependent [3H]-taurocholate transport. Lastly, in enzymatic assays for human HDAC6, it shows 8.11% and 3.17% inhibition using commercial and custom peptide substrates, respectively, indicating limited enzymatic inhibition activity..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Aklomide (2-Chloro-4-nitrobenzamide) is used in poultry to treat parasites.
别名阿克洛胺, Alkomide, 2-Chloro-4-nitrobenzamide
化学信息
分子量200.58
分子式C7H5ClN2O3
CAS No.3011-89-0
SmilesNC(=O)C1=C(Cl)C=C(C=C1)[N+]([O-])=O
密度1.52 g/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 (224.35 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (24.93 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 mM4.9855 mL24.9277 mL49.8554 mL249.2771 mL
5 mM0.9971 mL4.9855 mL9.9711 mL49.8554 mL
10 mM0.4986 mL2.4928 mL4.9855 mL24.9277 mL
20 mM0.2493 mL1.2464 mL2.4928 mL12.4639 mL
50 mM0.0997 mL0.4986 mL0.9971 mL4.9855 mL
100 mM0.0499 mL0.2493 mL0.4986 mL2.4928 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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