2-[4-(4-chlorophenylsulfonyl)methyl-2-methyl-5-nitro-1H-imidazol-1-yl]ethanol

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2-[4-(4-chlorophenylsulfonyl)methyl-2-methyl-5-nitro-1H-imidazol-1-yl]ethanol
• 英文别名: 1h-Imidazole-1-ethanol,4-[[(4-chlorophenyl)sulfonyl]methyl]-2-methyl-5-nitro-；2-[4-[(4-chlorophenyl)sulfonylmethyl]-2-methyl-5-nitroimidazol-1-yl]ethanol
• 化学式: C₁₃H₁₄ClN₃O₅S
• 分子量: 359.79
• InChiKey: WLHWBCXNICDODE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  23
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  126
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  sodium p-chlorobenzenesulphinate 在 氢氧化钾 作用下， 以 二甲基亚砜 为溶剂， 反应 12.17h， 生成 2-[4-(4-chlorophenylsulfonyl)methyl-2-methyl-5-nitro-1H-imidazol-1-yl]ethanol
  参考文献：
  名称：

  Rapid Synthesis of New 5‐Nitroimidazoles as Potential Antibacterial Drugs via VNS Procedure

  摘要：

  Original 4-arylsulfonylmethyl-5-nitroimidazoles were prepared by reacting four chloromethylaryl sulfones with 5-nitroimidazole derivatives via a vicarious nucleophilic substitution (VNS) of hydrogen reaction.

  DOI：

  10.1080/00397910600943873

文献信息

• Lowering of 5-nitroimidazole's mutagenicity: Towards optimal antiparasitic pharmacophore
  作者：Maxime D. Crozet、Céline Botta、Monique Gasquet、Christophe Curti、Vincent Rémusat、Sébastien Hutter、Olivier Chapelle、Nadine Azas、Michel De Méo、Patrice Vanelle

  DOI：10.1016/j.ejmech.2008.05.015

  日期：2009.2

  To improve the antiparasitic pharmacophore, 20 5-nitroimidazoles bearing an arylsulfonylmethyl group were prepared from commercial imidazoles. The antiparasitic activity of these molecules was assessed against Trichomonas vaginalis, the in vitro cytotoxicity was evaluated on human monocytes and the mutagenicity was determined by the Salmonella mutagenicity assay. All IC50 on T. vaginalis were below the one of metronidazole. The determination of the specificity indexes (SIs), defined as the ratios of the cytotoxic activity and the antitrichomonas activity, indicated that 11 derivatives had a SI over the one of metronidazole. Molecules, bearing an additional methyl group on the 2-position, showed a lower mutagenicity than metronidazole. Moreover, three derivatives were characterized by a low mutagenicity and an efficient antitrichomonas activity. (C) 2008 Elsevier Masson SAS. All rights reserved.