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4-(1-(4-iodophenyl)-1H-1,2,3-triazol-4-yl)-N-methylbenzenamine | 946052-55-7

中文名称
——
中文别名
——
英文名称
4-(1-(4-iodophenyl)-1H-1,2,3-triazol-4-yl)-N-methylbenzenamine
英文别名
4-[1-(4-iodophenyl)triazol-4-yl]-N-methylaniline
4-(1-(4-iodophenyl)-1H-1,2,3-triazol-4-yl)-N-methylbenzenamine化学式
CAS
946052-55-7
化学式
C15H13IN4
mdl
——
分子量
376.2
InChiKey
IOKFQOKMKXKIFI-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):
    3.6
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    42.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    4-(1-(4-iodophenyl)-1H-1,2,3-triazol-4-yl)-N-methylbenzenamine六正丁基二锡四(三苯基膦)钯 作用下, 以 甲苯 为溶剂, 反应 4.0h, 以45%的产率得到N-methyl-4-[1-(4-tributylstannylphenyl)-1H-1,2,3-triazol-4-yl]benzenamine
    参考文献:
    名称:
    WO2008/131148
    摘要:
    公开号:
  • 作为产物:
    描述:
    4-乙炔基苯胺 在 copper(II) sulfate sodium methylatesodium ascorbate 作用下, 以 甲醇叔丁醇 为溶剂, 反应 27.0h, 生成 4-(1-(4-iodophenyl)-1H-1,2,3-triazol-4-yl)-N-methylbenzenamine
    参考文献:
    名称:
    Quick Assembly of 1,4-Diphenyltriazoles as Probes Targeting β-Amyloid Aggregates in Alzheimer's Disease
    摘要:
    Accumulation of beta-amyloid aggregates (A beta) in the brain is linked to the pathogenesis of Alzheimer's disease (AD). We report a novel approach for producing 1,4-diphenyltriazoles as probes for targeting A beta aggregates in the brain. The imaging probes, a series of substituted tricyclic 1,4-diphenyltriazoles showing excellent binding affinities to A beta aggregates (K-i = 4-30 nM), were conveniently assembled by "click chemistry." Two radioiodinated probes, [I-125]10a and [I-125]10b, and two radiofluorinated probes, [F-18]17a and [F-18]17b, exhibited moderate lipophilicities and showed excellent initial brain penetrations and fast washouts from the normal mouse brain. In vitro autoradiography of postmortem AD brain sections and homogenates showed that these triazoles were binding to A beta plaques. Preliminary results strongly suggest that use of click chemistry, which led to a 1,4-diphenyltriazole-based core, is a highly convenient and flexible approach for assembling novel imaging agents for targeting A beta aggregates in senile plaques in the living human brain.
    DOI:
    10.1021/jm070467l
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文献信息

  • DIPHENYL-HETEROARYL DERIVATIVES AND THEIR USE FOR BINDING AND IMAGING AMYLOID PLAQUES
    申请人:Kung Hank F.
    公开号:US20110158907A1
    公开(公告)日:2011-06-30
    This invention relates to a method of imaging amyloid deposits and to diphenyl-heteroaryl compounds, and methods of making radiolabeled diphenyl-heteroaryl compounds useful in imaging amyloid deposits. This invention also relates to compounds, and methods of making compounds for inhibiting the aggregation of amyloid proteins to form amyloid deposits, and a method of delivering a therapeutic agent to amyloid deposits.
  • Quick Assembly of 1,4-Diphenyltriazoles as Probes Targeting β-Amyloid Aggregates in Alzheimer's Disease
    作者:Wenchao Qu、Mei-Ping Kung、Catherine Hou、Shunichi Oya、Hank F. Kung
    DOI:10.1021/jm070467l
    日期:2007.7.1
    Accumulation of beta-amyloid aggregates (A beta) in the brain is linked to the pathogenesis of Alzheimer's disease (AD). We report a novel approach for producing 1,4-diphenyltriazoles as probes for targeting A beta aggregates in the brain. The imaging probes, a series of substituted tricyclic 1,4-diphenyltriazoles showing excellent binding affinities to A beta aggregates (K-i = 4-30 nM), were conveniently assembled by "click chemistry." Two radioiodinated probes, [I-125]10a and [I-125]10b, and two radiofluorinated probes, [F-18]17a and [F-18]17b, exhibited moderate lipophilicities and showed excellent initial brain penetrations and fast washouts from the normal mouse brain. In vitro autoradiography of postmortem AD brain sections and homogenates showed that these triazoles were binding to A beta plaques. Preliminary results strongly suggest that use of click chemistry, which led to a 1,4-diphenyltriazole-based core, is a highly convenient and flexible approach for assembling novel imaging agents for targeting A beta aggregates in senile plaques in the living human brain.
  • WO2008/131148
    申请人:——
    公开号:——
    公开(公告)日:——
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