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2-[(E)-2-(4-chlorophenyl)vinyl]-1-methyl-5-nitro-1H-imidazole | 1161926-01-7

中文名称
——
中文别名
——
英文名称
2-[(E)-2-(4-chlorophenyl)vinyl]-1-methyl-5-nitro-1H-imidazole
英文别名
2-[(E)-2-(4-chlorophenyl)ethenyl]-1-methyl-5-nitroimidazole
2-[(E)-2-(4-chlorophenyl)vinyl]-1-methyl-5-nitro-1H-imidazole化学式
CAS
1161926-01-7
化学式
C12H10ClN3O2
mdl
——
分子量
263.683
InChiKey
SJPPVGKVERANLW-QPJJXVBHSA-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):
    1.9
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    63.6
  • 氢给体数:
    0
  • 氢受体数:
    3

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

  • 作为反应物:
    描述:
    2-[(E)-2-(4-chlorophenyl)vinyl]-1-methyl-5-nitro-1H-imidazole碘甲烷 作用下, 以 硝基苯 为溶剂, 反应 24.0h, 以97%的产率得到C12H10ClN3O2
    参考文献:
    名称:
    Synthesis, Spectroscopic and Structural Studies of New 2-Substituted 4- Nitroimidazoles
    摘要:
    本研究描述了通过硝基的转位反应合成新型 4-硝基-2-取代咪唑衍生物的过程。在碘化甲烷的催化下,5-硝基-2-苯乙醇(苯乙烯基)咪唑衍生物在硝基苯中以良好的收率转化为相应的 4-硝基异构体。报告了五种化合物的光谱研究和单晶 X 射线结构,以了解这些化合物的构象结构。
    DOI:
    10.2174/15701786113106660090
  • 作为产物:
    描述:
    二甲硝咪唑4-氯苯甲醛sodium ethanolate 作用下, 以 乙醇 为溶剂, 以15%的产率得到2-[(E)-2-(4-chlorophenyl)vinyl]-1-methyl-5-nitro-1H-imidazole
    参考文献:
    名称:
    Synthesis and Electrochemistry of 2-Ethenyl and 2-Ethanyl Derivatives of 5-Nitroimidazole and Antimicrobial Activity against Giardia lamblia
    摘要:
    Infections with the diarrheagenic pathogen, Giardia lamblia, are commonly treated with the 5-nitroimidazole (5-NI) metronidazole (Mz), and yet treatment failures and Mz resistance occur. Using a panel of new 2-ethenyl and 2-ethanyl 5-NI derivatives, we found that compounds with a saturated bridge between the 5-NI core and a pendant ring system exhibited only modestly increased antigiardial activity and could not overcome Mz resistance. By contrast, olefins with a conjugated bridge connecting the core and a substituted phenyl or heterocyclic ring showed greatly increased antigiardial activity without toxicity, and several overcame Mz resistance and were more effective than Mz in a murine giardiasis model. Determination of the half-wave potential of the initial one-electron transfer by cyclic voltammetry revealed that easier redox activation correlated with greater antigiardial activity and capacity to overcome Mz resistance. These studies show the potential of combining systematic synthetic approaches with biological and electrochemical evaluations in developing improved 5-NI drugs.
    DOI:
    10.1021/jm900356n
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文献信息

  • [EN] EXPANDED THERAPEUTIC POTENTIAL IN NITROHETEROARYL ANTIMICROBIALS<br/>[FR] POTENTIEL THÉRAPEUTIQUE ÉTENDU DANS DES ANTIMICROBIENS À NITROHÉTÉROARYLE
    申请人:UNIV CALIFORNIA
    公开号:WO2014205414A1
    公开(公告)日:2014-12-24
    Disclosed herein are antimicrobial compounds compositions, pharmaceutical compositions, the use and preparation thereof. Some embodiments relate to imidazole, thiazole, and furan derivatives and their use as therapeutic agents.
    本文披露了抗微生物化合物组合物、药物组合物及其使用和制备。一些实施例涉及咪唑噻唑呋喃生物及其作为治疗剂的用途。
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