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N-(2-chlorobenzyl)-2-(4-((E)-2-(1-(2-hydroxyethyl)-5-nitro-1H-imidazol-2-yl)vinyl)benzylidene)hydrazine-1-carbothioamide | 1078661-98-9

中文名称
——
中文别名
——
英文名称
N-(2-chlorobenzyl)-2-(4-((E)-2-(1-(2-hydroxyethyl)-5-nitro-1H-imidazol-2-yl)vinyl)benzylidene)hydrazine-1-carbothioamide
英文别名
——
N-(2-chlorobenzyl)-2-(4-((E)-2-(1-(2-hydroxyethyl)-5-nitro-1H-imidazol-2-yl)vinyl)benzylidene)hydrazine-1-carbothioamide 化学式
CAS
1078661-98-9
化学式
C22H21ClN6O3S
mdl
——
分子量
484.966
InChiKey
RBGUDJWFYCPIFD-WVIOECCYSA-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):
    3.61
  • 重原子数:
    33.0
  • 可旋转键数:
    9.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    117.61
  • 氢给体数:
    3.0
  • 氢受体数:
    7.0

反应信息

  • 作为产物:
    描述:
    2-(4-formylstyryl)-1-(β-hydroxyethyl)-5-nitroimidazole 、 4-<2-Chlor-benzyl>-thiosemicarbazid乙醇 为溶剂, 以37%的产率得到N-(2-chlorobenzyl)-2-(4-((E)-2-(1-(2-hydroxyethyl)-5-nitro-1H-imidazol-2-yl)vinyl)benzylidene)hydrazine-1-carbothioamide
    参考文献:
    名称:
    Synthesis and antiamoebic activity of metronidazole thiosemicarbazone analogues
    摘要:
    Repeated treatment of Entamoeba histolytica infection with commonly used antiamoebic drugs results in not only increasing the toxicity potential but also leads to the development of clinical resistance. Thus new effective agents with less toxicity against amoebiasis are urgently required. With this view, metronidazole thiosemicarbazone analogues 1-11 were synthesized wherein thioamide moiety was substituted by different cyclic and aromatic amines. These compounds were screened against HMI:IMSS strain of E. histolytica parasite cultured in vitro and the sensitivity of the parasite to the metronidazole thiosemicarbazones was evaluated using the microdilution method. Eight compounds (1-4, 7-9 and 11) were found better inhibitors of E. histolytica growth since IC50 values elicited by these compounds were much lower than metronidazole with compound 4 showing the most promising antiamoebic activity (IC50 = 0.56 mu M). The study suggests the beneficial potential of these leads that need to be further explored in order to discover and develop better and yet safer therapeutic agents for amoebiasis. (C) 2007 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2007.12.007
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