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Acefylline

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纯度: 99.57%

货号 T2205Cas号 652-37-9

别名 茶碱乙酸, Theophyllineacetic acid, Theophylline-7-acetic acid, Carboxymethyltheophylline, acetyloxytheophylline

Acefylline (Theophylline-7-acetic acid) 是黄嘌呤衍生物,是一种腺苷受体拮抗剂。它是蛋白质精氨酸脱亚氨酶 (PAD) 激活剂,也是一种支气管扩张剂,可抑制大鼠肺 cAMP 磷酸二酯酶同工酶。

Acefylline
其他形式的 “Acefylline”:

Acefylline

一键复制产品信息
Rating icon 很棒

纯度: 99.57%

货号 T2205 别名 茶碱乙酸, Theophyllineacetic acid, Theophylline-7-acetic acid, Carboxymethyltheophylline, acetyloxytheophyllineCas号 652-37-9

Acefylline (Theophylline-7-acetic acid) 是黄嘌呤衍生物,是一种腺苷受体拮抗剂。它是蛋白质精氨酸脱亚氨酶 (PAD) 激活剂,也是一种支气管扩张剂,可抑制大鼠肺 cAMP 磷酸二酯酶同工酶。

规格价格库存数量
25 mg
¥ 132
现货
50 mg
¥ 178
现货
100 mg
¥ 247
现货
500 mg
¥ 572
现货
1 g
¥ 837
现货
1 mL x 10 mM (in DMSO)
¥ 272
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纯度: 99.57%
颜色: 白色
性状: Solid
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产品介绍


Acefylline AI Summary
Acefylline demonstrates a broad spectrum of bioactivities. It binds to the human Adenosine A2B receptor with a Ki value of 27600.0 nM, indicating notable affinity. In cellular assays, it exhibits minimal impact on calcium ion release in PC12 cells, showing only 1.4% of the effect of 1 mM Caffeine. Additionally, it has shown antiviral potentials, particularly against Ebola virus with AC50 values ranging from 39.81 uM to 39810.7 nM for inhibiting viral entry. Against SARS-CoV-2, Acefylline inhibits virus-induced cytotoxicity in Caco-2 cells by 20.97% at 10 uM concentration over 48 hours, and has a hit score of 0.1779 in HRCE cells at MOI 0.4 after 96 hours. It also shows a weak inhibitory effect on SARS-CoV-2 3CL-Pro protease with 12.99% inhibition at 20 µM. However, it displays minimal inhibition of cell viability in Vero E6 cells infected with SARS-CoV-2 and has an IC50 greater than 20000.0 nM in inhibiting SARS-CoV-2 induced cytotoxicity in VERO-6 cells. Lastly, it has shown weak inhibitory activity against human HDAC6, with -7.47% and -3.53% in assays using commercial and custom peptide substrates, respectively..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Acefylline (Theophylline-7-acetic acid), a stimulant drug of the xanthine chemical class, acts as an adenosine receptor antagonist. It is combined with diphenhydramine in the pharmaceutical preparation Etanautine to help offset its stimulant effects
别名茶碱乙酸, Theophyllineacetic acid, Theophylline-7-acetic acid, Carboxymethyltheophylline, acetyloxytheophylline
化学信息
分子量238.2
分子式C9H10N4O4
CAS No.652-37-9
SmilesCN1C2=C(N(CC(O)=O)C=N2)C(=O)N(C)C1=O
密度1.64 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: 50 mg/mL (209.91 mM), Sonication and heating are recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (8.4 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 mM4.1982 mL20.9908 mL41.9815 mL209.9076 mL
5 mM0.8396 mL4.1982 mL8.3963 mL41.9815 mL
10 mM0.4198 mL2.0991 mL4.1982 mL20.9908 mL
20 mM0.2099 mL1.0495 mL2.0991 mL10.4954 mL
50 mM0.0840 mL0.4198 mL0.8396 mL4.1982 mL
100 mM0.0420 mL0.2099 mL0.4198 mL2.0991 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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