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DHQ

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纯度: 99.89%

货号 T20436Cas号 15804-19-0

别名 2,3-二羟基喹喔啉, 2,3-dihydroxy-quinoxalin

DHQ (2,3-dihydroxy-quinoxalin) 是单纯疱疹病毒胸苷激酶的 ATPase 活性诱导剂。

DHQ
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DHQ

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Rating icon 很棒

纯度: 99.89%

货号 T20436 别名 2,3-二羟基喹喔啉, 2,3-dihydroxy-quinoxalinCas号 15804-19-0

DHQ (2,3-dihydroxy-quinoxalin) 是单纯疱疹病毒胸苷激酶的 ATPase 活性诱导剂。

规格价格库存数量
25 mg
¥ 161
现货
50 mg
¥ 265
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100 mg
¥ 419
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500 mg
¥ 1,120
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1 mL x 10 mM (in DMSO)
¥ 99
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产品介绍


DHQ AI Summary
DHQ demonstrates a diverse range of bioactivities across several targets. It inhibits the binding of [3H]DCKA to the NMDA receptor in rat brain membranes with an IC50 value of 9800.0 nM and also inhibits [3H]glycine binding at the NMDA receptor glycine site, with various IC50 values reported (up to 39000.0 nM). It exhibits a binding affinity with a Kb value of 16500.0 nM towards the glycine site of the NMDA receptor and a significantly lower affinity towards other glutamate receptors. Additionally, DHQ shows inhibition of [3H]AMPA binding to AMPA receptors with low affinity (Ki > 100,000.0 nM), suggesting minimal effect on AMPA receptor activity. Apart from its activity on NMDA and AMPA receptors, the compound also shows inhibition of Human Jumonji Domain Containing 2E (JMJD2E) and the malarial parasite plastid, with respective potencies of 25118.9 nM and 10417.9 nM. It acts as an agonist of the mutation responsible for Fibrous Dysplasia/McCune-Albright Syndrome with a potency of 5011.9 nM and exhibits dose-dependent inhibition of TPA-induced Epstein-Barr virus early antigen activation in human Raji cells while also displaying cytotoxicity at higher concentrations. Additionally, 27688 inhibits D-amino acid oxidase in porcine kidney homogenate (IC50: 33600.0 nM) and activates Trypanosoma cruzi cruzain. It shows an inhibitory effect on Cryptosporidium hominis TS-DHFR and on HIV-1 subtype B reverse transcriptase, albeit with low inhibition percentages at higher concentrations..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
DHQ (2,3-dihydroxy-quinoxalin) is an inducer of ATPase activity that of Herpes Simplex Virus thymidine kinase.
别名2,3-二羟基喹喔啉, 2,3-dihydroxy-quinoxalin
化学信息
分子量162.15
分子式C8H6N2O2
CAS No.15804-19-0
SmilesOC1=NC2=CC=CC=C2N=C1O
密度1.336g/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: 60 mg/mL (370.03 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM6.1671 mL30.8356 mL61.6713 mL308.3565 mL
5 mM1.2334 mL6.1671 mL12.3343 mL61.6713 mL
10 mM0.6167 mL3.0836 mL6.1671 mL30.8356 mL
20 mM0.3084 mL1.5418 mL3.0836 mL15.4178 mL
50 mM0.1233 mL0.6167 mL1.2334 mL6.1671 mL
100 mM0.0617 mL0.3084 mL0.6167 mL3.0836 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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