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3-Acetylcoumarin

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纯度: 99.31%

货号 Fr12596Cas号 3949-36-8

别名 3-乙酰基羟基香豆素

3-Acetylcoumarin 作为室温下铜催化 CN 偶联反应的实用配体。它具有神经保护和杀螨特性。

3-Acetylcoumarin

3-Acetylcoumarin

一键复制产品信息
Rating icon 很棒

纯度: 99.31%

货号 Fr12596 别名 3-乙酰基羟基香豆素Cas号 3949-36-8

3-Acetylcoumarin 作为室温下铜催化 CN 偶联反应的实用配体。它具有神经保护和杀螨特性。

规格价格库存数量
500 mg
¥ 99
现货
1 mL x 10 mM (in DMSO)
¥ 149
现货
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产品介绍


3-Acetylcoumarin AI Summary
3-Acetylcoumarin demonstrates a variety of bioactivities across multiple biological systems. It induces NAD(P)H quinone reductase activity in Hepa 1c1c7 murine hepatoma cells at a concentration of 200.0 µM, suggesting antioxidant properties. The compound exhibits DPPH radical scavenging activity of 0.83% at 25 µg/mL after 30 minutes and shows ABTS free radical inhibition by 63.58%. Moreover, it inhibits rat intestinal alpha-glucosidase by 53.19% at 100 µg/mL and displays inhibitory activity against Human Jumonji Domain Containing 2E (JMJD2E) with a potency of 10,000.0 nM. Additionally, 3-Acetylcoumarin acts in a cytochrome panel assay with an AC50 of 199.53 nM and inhibits human recombinant MAO-B with an IC50 value of 14,450.0 nM, showing selectivity over MAO-A. In cancer research, it inhibits growth in various human tumor cell lines with GI50 values between 36,224.3 nM and 100,000.0 nM across different cancer types such as breast, melanoma, lung, prostate, colon, leukemia, central nervous system, ovarian, and renal cells. The compound also protects against pesticide-induced gastric lesions in Swiss albino mice, reducing lesions by 66.0% at a dose of 20 mg/kg orally. It shows moderate inhibitory activity against human CA9 with a Ki value of 151.8 nM and strong inhibitory activity against human CA12 with a Ki value of 7.8 nM. 3-Acetylcoumarin also inhibits the aggregation of HFIP-induced amyloid beta (1-42 residues), with inhibition rates between 40.0% to 59.0%, as measured by ThT fluorescence and turbidity assays. It demonstrates cytotoxicity against human SH-SY5Y cells with an IC50 of 75,000.0 nM and neuroprotective effects against amyloid beta-induced toxicity in the same cells with an activity level of 77.0%. Additionally, the compound shows antiviral activity against SARS-CoV-2 in VERO-6 cells, although with an IC50 value greater than 20,000.0 nM, it may not be highly potent in this assay..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
3-Acetylcoumarin as a practical ligand for copper-catalyzed CN coupling reactions at room temperature. It has neuroprotective and acaricidal properties.
别名3-乙酰基羟基香豆素
化学信息
分子量188.18
分子式C11H8O3
CAS No.3949-36-8
SmilesCC(=O)c1cc2ccccc2oc1=O
密度1.285g/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: 25 mg/mL (132.85 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM5.3141 mL26.5703 mL53.1406 mL265.7031 mL
5 mM1.0628 mL5.3141 mL10.6281 mL53.1406 mL
10 mM0.5314 mL2.6570 mL5.3141 mL26.5703 mL
20 mM0.2657 mL1.3285 mL2.6570 mL13.2852 mL
50 mM0.1063 mL0.5314 mL1.0628 mL5.3141 mL
100 mM0.0531 mL0.2657 mL0.5314 mL2.6570 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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