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5-{[4-(5-amino-2-methoxyphenyl)piperazin-1-yl]sulfonyl}-N,N-dimethylnaphthalen-1-amine | 1246948-38-8

中文名称
——
中文别名
——
英文名称
5-{[4-(5-amino-2-methoxyphenyl)piperazin-1-yl]sulfonyl}-N,N-dimethylnaphthalen-1-amine
英文别名
5-[4-(5-amino-2-methoxyphenyl)piperazin-1-yl]sulfonyl-N,N-dimethylnaphthalen-1-amine
5-{[4-(5-amino-2-methoxyphenyl)piperazin-1-yl]sulfonyl}-N,N-dimethylnaphthalen-1-amine化学式
CAS
1246948-38-8
化学式
C23H28N4O3S
mdl
——
分子量
440.566
InChiKey
VBSOJRCWOKAYIO-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):
    3.3
  • 重原子数:
    31
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    87.5
  • 氢给体数:
    1
  • 氢受体数:
    7

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
  • 下游产品
    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:
    5-{[4-(5-amino-2-methoxyphenyl)piperazin-1-yl]sulfonyl}-N,N-dimethylnaphthalen-1-amine5-氯-3-甲基苯并(B)噻吩-2-磺酰氯吡啶 作用下, 以 二氯甲烷 为溶剂, 反应 12.0h, 以210 mg的产率得到5-Chloro-N-[3-(4-{[5-(dimethylamino)-1-naphthyl]sulfonyl}-piperazin-1-yl)-4-methoxyphenyl]-3-methyl-1-benzothiophene-2-sulfonamide
    参考文献:
    名称:
    Development of Molecular Probes for the Human 5-HT6 Receptor
    摘要:
    In this work we report the synthesis of a set of labeled ligands targeting the human 5-HT6, receptor (h5-HT6R). Among the synthesized compounds, fluorescent probe 10 (K-i = 175 nM and Phi(f) = 0.21 and biotinylated derivative 15 (K-i = 90 nM) deserve special attention because they enable direct observation of the h5-HT6R in cells. Thus, they represent the first molecular probes for 5-HT6R visualization. These results are the starting point for introducing a variety of tags in these or other 5-HT6R ligand scaffolds aimed at the development of optimized probes with tailored profiles in terms of fluorescence, affinity, or selectivity.
    DOI:
    10.1021/jm1007177
  • 作为产物:
    描述:
    5-{[4-(2-methoxy-5-nitrophenyl)piperazin-1-yl]sulfonyl}-N,N-dimethylnaphthalen-1-amine 在 palladium 10% on activated carbon 、 氢气 作用下, 以 乙醇 为溶剂, 20.0 ℃ 、275.8 kPa 条件下, 反应 16.0h, 生成 5-{[4-(5-amino-2-methoxyphenyl)piperazin-1-yl]sulfonyl}-N,N-dimethylnaphthalen-1-amine
    参考文献:
    名称:
    Development of Molecular Probes for the Human 5-HT6 Receptor
    摘要:
    In this work we report the synthesis of a set of labeled ligands targeting the human 5-HT6, receptor (h5-HT6R). Among the synthesized compounds, fluorescent probe 10 (K-i = 175 nM and Phi(f) = 0.21 and biotinylated derivative 15 (K-i = 90 nM) deserve special attention because they enable direct observation of the h5-HT6R in cells. Thus, they represent the first molecular probes for 5-HT6R visualization. These results are the starting point for introducing a variety of tags in these or other 5-HT6R ligand scaffolds aimed at the development of optimized probes with tailored profiles in terms of fluorescence, affinity, or selectivity.
    DOI:
    10.1021/jm1007177
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文献信息

  • Development of Molecular Probes for the Human 5-HT<sub>6</sub> Receptor
    作者:Henar Vázquez-Villa、Juan A. González-Vera、Bellinda Benhamú、Alma Viso、Roberto Fernández de la Pradilla、Elena Junquera、Emilio Aicart、María L. López-Rodríguez、Silvia Ortega-Gutiérrez
    DOI:10.1021/jm1007177
    日期:2010.10.14
    In this work we report the synthesis of a set of labeled ligands targeting the human 5-HT6, receptor (h5-HT6R). Among the synthesized compounds, fluorescent probe 10 (K-i = 175 nM and Phi(f) = 0.21 and biotinylated derivative 15 (K-i = 90 nM) deserve special attention because they enable direct observation of the h5-HT6R in cells. Thus, they represent the first molecular probes for 5-HT6R visualization. These results are the starting point for introducing a variety of tags in these or other 5-HT6R ligand scaffolds aimed at the development of optimized probes with tailored profiles in terms of fluorescence, affinity, or selectivity.
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