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1-(2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl)-4-(N-benzyl,N-methylaminomethyl)-1H-1,2,3-triazole

中文名称
——
中文别名
——
英文名称
1-(2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl)-4-(N-benzyl,N-methylaminomethyl)-1H-1,2,3-triazole
英文别名
N-methyl-N-[[1-[2-(2-methyl-5-nitroimidazol-1-yl)ethyl]triazol-4-yl]methyl]-1-phenylmethanamine
1-(2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl)-4-(N-benzyl,N-methylaminomethyl)-1H-1,2,3-triazole化学式
CAS
——
化学式
C17H21N7O2
mdl
——
分子量
355.399
InChiKey
BCZNROBVAHFDTF-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):
    1.3
  • 重原子数:
    26
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    97.6
  • 氢给体数:
    0
  • 氢受体数:
    6

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:
    甲硝唑 在 sodium azide 、 copper(II) sulfate 、 sodium ascorbate三乙胺 作用下, 以 甲醇二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 22.33h, 生成 1-(2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl)-4-(N-benzyl,N-methylaminomethyl)-1H-1,2,3-triazole
    参考文献:
    名称:
    Metronidazole-triazole conjugates: Activity against Clostridium difficile and parasites
    摘要:
    Metronidazole has been used clinically for over 50 years as an antiparasitic and broad-spectrum antibacterial agent effective against anaerobic bacteria. However resistance to metronidazole in parasites and bacteria has been reported, and improved second-generation metronidazole analogues are needed. The copper catalysed Huigsen azide-alkyne 1,3-dipolar cycloaddition offers a way to efficiently assemble new libraries of metronidazole analogues. Several new metronidazole-triazole conjugates (Mtz-triazoles) have been identified with excellent broad spectrum antimicrobial and antiparasitic activity targeting Clostridium difficile, Entamoeba histolytica and Giardia lambda. Cross resistance to metronidazole was observed against stable metronidazole resistant C. difficile and G.. lamblia strains. However for the most potent Mtz-triazoles, the activity remained in a therapeutically relevant window. (C) 2015 The Authors. Published by Elsevier Masson SAS. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
    DOI:
    10.1016/j.ejmech.2015.06.019
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文献信息

  • Metronidazole-triazole conjugates: Activity against Clostridium difficile and parasites
    作者:Angie M. Jarrad、Tomislav Karoli、Anjan Debnath、Chin Yen Tay、Johnny X. Huang、Geraldine Kaeslin、Alysha G. Elliott、Yukiko Miyamoto、Soumya Ramu、Angela M. Kavanagh、Johannes Zuegg、Lars Eckmann、Mark A.T. Blaskovich、Matthew A. Cooper
    DOI:10.1016/j.ejmech.2015.06.019
    日期:2015.8
    Metronidazole has been used clinically for over 50 years as an antiparasitic and broad-spectrum antibacterial agent effective against anaerobic bacteria. However resistance to metronidazole in parasites and bacteria has been reported, and improved second-generation metronidazole analogues are needed. The copper catalysed Huigsen azide-alkyne 1,3-dipolar cycloaddition offers a way to efficiently assemble new libraries of metronidazole analogues. Several new metronidazole-triazole conjugates (Mtz-triazoles) have been identified with excellent broad spectrum antimicrobial and antiparasitic activity targeting Clostridium difficile, Entamoeba histolytica and Giardia lambda. Cross resistance to metronidazole was observed against stable metronidazole resistant C. difficile and G.. lamblia strains. However for the most potent Mtz-triazoles, the activity remained in a therapeutically relevant window. (C) 2015 The Authors. Published by Elsevier Masson SAS. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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