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1-(2-chloro-phenyl)-3-[2-(6-nitro-4-oxo-2-phenyl-4H-quinazolin-3-yl)ethyl]urea | 1367326-30-4

中文名称
——
中文别名
——
英文名称
1-(2-chloro-phenyl)-3-[2-(6-nitro-4-oxo-2-phenyl-4H-quinazolin-3-yl)ethyl]urea
英文别名
1-(2-Chlorophenyl)-3-[2-(6-nitro-4-oxo-2-phenyl-quinazolin-3-yl)ethyl]urea;1-(2-chlorophenyl)-3-[2-(6-nitro-4-oxo-2-phenylquinazolin-3-yl)ethyl]urea
1-(2-chloro-phenyl)-3-[2-(6-nitro-4-oxo-2-phenyl-4H-quinazolin-3-yl)ethyl]urea化学式
CAS
1367326-30-4
化学式
C23H18ClN5O4
mdl
——
分子量
463.88
InChiKey
LYOFZRJXYDFHBM-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):
    3.7
  • 重原子数:
    33
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    120
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis, characterization, and pharmacological evaluation of 1-[2-(6-nitro-4-oxo-2-phenyl-4H-quinazolin-3-yl)-ethyl]-3-phenyl ureas
    摘要:
    In the present communication, a series based on 1-[2-(6-nitro-4-oxo-2-phenyl-4H-quinazolin-3-yl)-ethyl]-3- phenyl-urea have been synthesized by an efficient synthetic protocol. The synthesized compounds were characterized by IR, H-1 NMR, C-13 NMR spectroscopy, ESI Mass spectrometry, and elemental analysis. The antibacterial and antifungal activity of the compounds were studied against selected strains (Pseudomonas aeruginosa ATCC 27853, Escherichia coli ATCC 25922, Staphylococcus aureus ATCC 25923, Bacillus subtilis ATCC 11774, and Candida albicans ATCC 66027) by using Kirby Bauer disk diffusion technique and broth dilution technique. All the synthesized compounds showed good antifungal potency against strain C. albicans.
    DOI:
    10.1007/s00044-012-0004-3
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文献信息

  • Synthesis, characterization, and pharmacological evaluation of 1-[2-(6-nitro-4-oxo-2-phenyl-4H-quinazolin-3-yl)-ethyl]-3-phenyl ureas
    作者:Aniruddhasinh M. Rana、Kishor R. Desai、Smita Jauhari
    DOI:10.1007/s00044-012-0004-3
    日期:2013.1
    In the present communication, a series based on 1-[2-(6-nitro-4-oxo-2-phenyl-4H-quinazolin-3-yl)-ethyl]-3- phenyl-urea have been synthesized by an efficient synthetic protocol. The synthesized compounds were characterized by IR, H-1 NMR, C-13 NMR spectroscopy, ESI Mass spectrometry, and elemental analysis. The antibacterial and antifungal activity of the compounds were studied against selected strains (Pseudomonas aeruginosa ATCC 27853, Escherichia coli ATCC 25922, Staphylococcus aureus ATCC 25923, Bacillus subtilis ATCC 11774, and Candida albicans ATCC 66027) by using Kirby Bauer disk diffusion technique and broth dilution technique. All the synthesized compounds showed good antifungal potency against strain C. albicans.
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