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5-(2,4-dihydroxybenzylidene)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)- trione | 373376-98-8

中文名称
——
中文别名
——
英文名称
5-(2,4-dihydroxybenzylidene)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)- trione
英文别名
5-(2,4-dihydroxybenzylidene)-1,3-dimethyl-2,4,6(1H,3H,5H)pyrimidinetrione;5-[(2,4-Dihydroxyphenyl)methylidene]-1,3-dimethyl-1,3-diazinane-2,4,6-trione
5-(2,4-dihydroxybenzylidene)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)- trione化学式
CAS
373376-98-8
化学式
C13H12N2O5
mdl
——
分子量
276.249
InChiKey
URHHHNHYJAANDR-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    20
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    98.2
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    1,3-二甲基巴比妥酸2,4-二羟基苯甲醛 为溶剂, 反应 0.5h, 以72%的产率得到5-(2,4-dihydroxybenzylidene)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)- trione
    参考文献:
    名称:
    Synthesis and DPPH Radical Scavenging Activity of 5-Arylidene-N,Ndimethylbarbiturates
    摘要:
    对24种N,N-二甲基巴比妥酸衍生物1-24进行了DPPH自由基清除活性筛选。这些化合物显示出优异的抗氧化活性。讨论了结构-活性关系,同时所有合成化合物均通过光谱技术和元素分析进行了表征。
    DOI:
    10.2174/157340611795564231
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文献信息

  • Synthesis and DPPH Radical Scavenging Activity of 5-Arylidene-N,Ndimethylbarbiturates
    作者:Khalid Mohammed Khan、Momin Khan、Muhammad Ali、Muhammad Taha、Abdul Hameed、Sajjad Ali、Shahnaz Perveen、M. Iqbal Choudhary
    DOI:10.2174/157340611795564231
    日期:2011.5.1
    Twenty-four derivatives of N,N-dimethylbarbituric acid 1-24 were screened for their DPPH radical scavenging activity. These compounds showed an excellent antioxidant activity. A structure-activity relationship has been discussed, while all the synthetic compounds were characterized by spectroscopic techniques and elemental analysis.
    对24种N,N-二甲基巴比妥酸衍生物1-24进行了DPPH自由基清除活性筛选。这些化合物显示出优异的抗氧化活性。讨论了结构-活性关系,同时所有合成化合物均通过光谱技术和元素分析进行了表征。
  • Synthesis and antifungal activity of substituted 2,4,6-pyrimidinetrione carbaldehyde hydrazones
    作者:Donna M. Neumann、Amy Cammarata、Gregory Backes、Glen E. Palmer、Branko S. Jursic
    DOI:10.1016/j.bmc.2013.12.010
    日期:2014.1
    Opportunistic fungal infections caused by the Candida spp. are the most common human fungal infections, often resulting in severe systemic infections-a significant cause of morbidity and mortality in at-risk populations. Azole antifungals remain the mainstay of antifungal treatment for candidiasis, however development of clinical resistance to azoles by Candida spp. limits the drugs' efficacy and highlights the need for discovery of novel therapeutics. Recently, it has been reported that simple hydrazone derivatives have the capability to potentiate antifungal activities in vitro. Similarly, pyrimidinetrione analogs have long been explored by medicinal chemists as potential therapeutics, with more recent focus being on the potential for pyrimidinetrione antimicrobial activity. In this work, we present the synthesis of a class of novel hydrazone-pyrimidinetrione analogs using novel synthetic procedures. In addition, structure-activity relationship studies focusing on fungal growth inhibition were also performed against two clinically significant fungal pathogens. A number of derivatives, including phenylhydrazones of 5-acylpyrimidinetrione exhibited potent growth inhibition at or below 10 mu M with minimal mammalian cell toxicity. In addition, in vitro studies aimed at defining the mechanism of action of the most active analogs provide preliminary evidence that these compound decrease energy production and fungal cell respiration, making this class of analogs promising novel therapies, as they target pathways not targeted by currently available antifungals. (C) 2013 Elsevier Ltd. All rights reserved.
  • Khan, Khalid Mohammed; Khan, Momin; Karim, Aneela, Journal of the Chemical Society of Pakistan, 2013, vol. 35, # 2, p. 495 - 498
    作者:Khan, Khalid Mohammed、Khan, Momin、Karim, Aneela、Taha, Muhammad、Ambreen, Nida、Gojayev, Anar、Perveen, Shahnaz、Choudhary, Muhammad Iqbal
    DOI:——
    日期:——
  • Khan, Khalid Mohammed; Khan, Momin; Khan, Ajmal, Journal of the Chemical Society of Pakistan, 2014, vol. 36, # 3, p. 524 - 527
    作者:Khan, Khalid Mohammed、Khan, Momin、Khan, Ajmal、Perveen, Shahnaz、Naz, Farzana、Choudhary, M. Iqbal
    DOI:——
    日期:——
  • Khan, Khalid Mohammed; Khan, Momin; Ahmad, Aqeel, Journal of the Chemical Society of Pakistan, 2014, vol. 36, # 6, p. 1153 - 1157
    作者:Khan, Khalid Mohammed、Khan, Momin、Ahmad, Aqeel、Irshad, Aisha、Kardono, Leonardus Broto Sugeng、Rahim, Fazal、Haider, Syed Moazzam、Ahmed, Sumbul、Parveen, Shahnaz
    DOI:——
    日期:——
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