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4-(2-(naphthalen-2-ylformyloxyl)ethoxy)-3-phenylfuran-2(5H)-one | 1450824-33-5

中文名称
——
中文别名
——
英文名称
4-(2-(naphthalen-2-ylformyloxyl)ethoxy)-3-phenylfuran-2(5H)-one
英文别名
2-[(5-oxo-4-phenyl-2H-furan-3-yl)oxy]ethyl naphthalene-2-carboxylate
4-(2-(naphthalen-2-ylformyloxyl)ethoxy)-3-phenylfuran-2(5H)-one化学式
CAS
1450824-33-5
化学式
C23H18O5
mdl
——
分子量
374.393
InChiKey
KGWCRXRYXVZOJG-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):
    4.3
  • 重原子数:
    28
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    61.8
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    苯乙酸 在 sodium hydride 、 三乙胺 、 sodium hydroxide 作用下, 以 四氢呋喃二甲基亚砜丙酮 为溶剂, 生成 4-(2-(naphthalen-2-ylformyloxyl)ethoxy)-3-phenylfuran-2(5H)-one
    参考文献:
    名称:
    3-Aryl-4-acyloxyethoxyfuran-2(5H)-ones as inhibitors of tyrosyl-tRNA synthetase: Synthesis, molecular docking and antibacterial evaluation
    摘要:
    Thirty-eight 3-aryl-4-acyloxyethoxyfuran-2(5H)-ones were designed, prepared and tested for antibacterial activities. Some of them showed significant antibacterial activity against Gram-positive organism, Gram-negative organism and fungus. Out of these compounds, 4-(2-(3-chlorophenylformyloxy)ethoxy)-3-(4-chlorophenyl)furan-2(5H)-one (d40) showed the widest spectrum of activity with MIC50 of 2.0 mu g/mL against Staphylococcus aureus, 4.3 mu g/mL against Escherichia coli, 1.5 mu g/mL against Pseudomonas aeruginosa and 1.2 mu g/mL against Candida albicans. Our data disclosed that MIC50 values against whole cell bacteria are positive correlation with MIC50 values against tyrosyl-tRNA synthetase. Meanwhile, molecular docking of d40 into S. aureus tyrosyl-tRNA synthetase active site was also performed, and the inhibitor tightly fitting the active site might be an important reason why it has high antimicrobial activity. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.06.066
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文献信息

  • 3-Aryl-4-acyloxyethoxyfuran-2(5H)-ones as inhibitors of tyrosyl-tRNA synthetase: Synthesis, molecular docking and antibacterial evaluation
    作者:Xu-Dong Wang、Rui-Cheng Deng、Jing-Jun Dong、Zhi-Yun Peng、Xiao-Ming Gao、Shu-Ting Li、Wan-Qiang Lin、Chun-Lei Lu、Zhu-Ping Xiao、Hai-Liang Zhu
    DOI:10.1016/j.bmc.2013.06.066
    日期:2013.9
    Thirty-eight 3-aryl-4-acyloxyethoxyfuran-2(5H)-ones were designed, prepared and tested for antibacterial activities. Some of them showed significant antibacterial activity against Gram-positive organism, Gram-negative organism and fungus. Out of these compounds, 4-(2-(3-chlorophenylformyloxy)ethoxy)-3-(4-chlorophenyl)furan-2(5H)-one (d40) showed the widest spectrum of activity with MIC50 of 2.0 mu g/mL against Staphylococcus aureus, 4.3 mu g/mL against Escherichia coli, 1.5 mu g/mL against Pseudomonas aeruginosa and 1.2 mu g/mL against Candida albicans. Our data disclosed that MIC50 values against whole cell bacteria are positive correlation with MIC50 values against tyrosyl-tRNA synthetase. Meanwhile, molecular docking of d40 into S. aureus tyrosyl-tRNA synthetase active site was also performed, and the inhibitor tightly fitting the active site might be an important reason why it has high antimicrobial activity. (C) 2013 Elsevier Ltd. All rights reserved.
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