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Exifone

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纯度: 99.95%

货号 T20080Cas号 52479-85-3

别名 依昔苯酮, NSC-680919, NSC680919, NSC 680919

Exifone (NSC-680919) 是一种混合的、非必需的 HDAC1 激活剂,能够与游离酶和底物结合酶结合,从而提高 HDAC1 催化的去乙酰化的相对最大速率。

Exifone
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Exifone

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Rating icon 很棒

纯度: 99.95%

货号 T20080 别名 依昔苯酮, NSC-680919, NSC680919, NSC 680919Cas号 52479-85-3

Exifone (NSC-680919) 是一种混合的、非必需的 HDAC1 激活剂,能够与游离酶和底物结合酶结合,从而提高 HDAC1 催化的去乙酰化的相对最大速率。

规格价格库存数量
5 mg
¥ 287
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25 mg
¥ 513
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50 mg
¥ 769
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100 mg
¥ 1,154
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200 mg
¥ 1,731
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1 mL x 10 mM (in DMSO)
¥ 195
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产品介绍


Exifone AI Summary
Exifone exhibits neurotoxicity on murine HT-22 hippocampal cell culture at maximum tolerated concentrations of 10.0 µM (MTT reduction assay) and 50.0 µM (LDH assay), and TC50 values of 34.0 µM and 91.0 µM respectively in vitro. Despite this, it shows neuroprotective activity against L-homocysteic acid cytotoxicity with a PC50 value above 10.0 µM in both assays. It has also been identified as DILI positive in the Drug Induced Liver Injury Prediction System (DILIps) validation dataset with a score of 1.0, indicating potential for drug-induced liver injury. Additionally, the compound demonstrates moderate and acute liver toxicity, including severe hepatitis and cytolytic liver toxicity. In bioactivity assays, Exifone shows antiviral properties by inhibiting SARS-CoV-2 induced cytotoxicity in Vero E6 cells and Caco-2 cells, albeit with varying inhibition percentages. It has shown potent inhibition of SARS-CoV-2 3CL-Pro protease with an inhibition percentage of 90.77% at a 20 µM concentration and an IC50 value of 4380.0 nM, but no significant inhibition of MERS 3CL-Pro protease. Other antiviral bioactivity includes blocking Ebola virus entry with an AC50 of 1778.3 nM and exhibiting IC50 values from 69.11 nM to 192.37 nM in various cell viability assays. Furthermore, Exifone inhibits human HDAC6 enzyme activity, with 17.44% inhibition in an enzymatic assay using a commercial peptide substrate..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Exifone (NSC-680919) is a mixed, nonessential activator of HDAC1 that is capable of binding to both free and substrate-bound enzyme, resulting in an increased relative maximal rate of HDAC1-catalyzed deacetylation.
别名依昔苯酮, NSC-680919, NSC680919, NSC 680919
化学信息
分子量278.21
分子式C13H10O7
CAS No.52479-85-3
SmilesC(=O)(C1=CC(O)=C(O)C(O)=C1)C2=C(O)C(O)=C(O)C=C2
密度1.759 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: 250 mg/mL (898.6 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM3.5944 mL17.9720 mL35.9441 mL179.7204 mL
5 mM0.7189 mL3.5944 mL7.1888 mL35.9441 mL
10 mM0.3594 mL1.7972 mL3.5944 mL17.9720 mL
20 mM0.1797 mL0.8986 mL1.7972 mL8.9860 mL
50 mM0.0719 mL0.3594 mL0.7189 mL3.5944 mL
100 mM0.0359 mL0.1797 mL0.3594 mL1.7972 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

关键词

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