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3-(4-nitro-1H-imidazol-1-yl)-propionic acid-2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl ester | 1214752-92-7

中文名称
——
中文别名
——
英文名称
3-(4-nitro-1H-imidazol-1-yl)-propionic acid-2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl ester
英文别名
2-(2-Methyl-5-nitroimidazol-1-yl)ethyl 3-(2-nitroimidazol-1-yl)propanoate
3-(4-nitro-1H-imidazol-1-yl)-propionic acid-2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl ester化学式
CAS
1214752-92-7
化学式
C12H14N6O6
mdl
——
分子量
338.28
InChiKey
AZCHRUXHCCULJI-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):
    0.1
  • 重原子数:
    24
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    154
  • 氢给体数:
    0
  • 氢受体数:
    8

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:
    2-硝基咪唑2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl acrylate三乙胺 作用下, 以 二氯甲烷1,2-二氯乙烷 为溶剂, 以68%的产率得到3-(4-nitro-1H-imidazol-1-yl)-propionic acid-2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl ester
    参考文献:
    名称:
    Imidazole derivatives as possible microbicides with dual protection
    摘要:
    Twenty seven derivatives (2-28) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethanol were synthesized and evaluated for anti-trichomonas, spermicidal and antifungal activities. Twenty six compounds were active against Trichomonas vaginalis at MIC ranging from 1-42 mu M and seven compounds (9,18,19,22,24,26,28) immobilized 100% human spermatozoa at 1% concentration (w/v). Twenty three compounds (2,3,5,8-26,28) exhibited antifungal activity at 25-50 mu g/mL concentration. Seven compounds (9,18,19,22,24,26,28) showed significant anti-trichomonas and spermicidal activities and also exhibited mild antifungal activity. All the compounds were highly safe towards human cervical cell line (HeLa) as shown by the cell-viability assay of HeLa cells at 200 mu g/mL concentration, whereas nonoxynol-9 (N-9, the marketed spermicidal microbicide) was highly cytotoxic. Therefore, it may be concluded that introduction of the pharmacophore responsible for spermicidal activity into a proven anti-trichomonas structure may lead to a potent dual function microbicide better and safer than N-9. (C) 2009 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2009.10.021
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