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3-(4-((8-(3-Methoxyphenyl)quinolin-6-yl)methoxy)phenyl)propanenitrile | 1252807-63-8

中文名称
——
中文别名
——
英文名称
3-(4-((8-(3-Methoxyphenyl)quinolin-6-yl)methoxy)phenyl)propanenitrile
英文别名
3-[4-[[8-(3-methoxyphenyl)quinolin-6-yl]methoxy]phenyl]propanenitrile
3-(4-((8-(3-Methoxyphenyl)quinolin-6-yl)methoxy)phenyl)propanenitrile化学式
CAS
1252807-63-8
化学式
C26H22N2O2
mdl
——
分子量
394.473
InChiKey
MKNJREMNOZKXPS-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):
    5.2
  • 重原子数:
    30
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    55.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3-(4-羟基苯基)丙酸 、 6-(bromomethyl)-8-(3-methoxyphenyl)quinoline 在 caesium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 3-(4-((8-(3-Methoxyphenyl)quinolin-6-yl)methoxy)phenyl)propanenitrile
    参考文献:
    名称:
    The discovery and synthesis of highly potent subtype selective phosphodiesterase 4D inhibitors
    摘要:
    The SAR study of a series of 6-aryloxymethyl-8-aryl substituted quinolines is described. Optimization of the series led to the discovery of compound 26b, a highly potent (IC(50) = 0.6 nM) and selective PDE4D inhibitor with a 75-fold selectivity over the A, B, and C subtypes and over 18,000-fold selectivity against other PDE family members. Rat pharmacokinetics and tissue distribution are also summarized. (c) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.07.076
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文献信息

  • The discovery and synthesis of highly potent subtype selective phosphodiesterase 4D inhibitors
    作者:Renee Aspiotis、Denis Deschênes、Daniel Dubé、Yves Girard、Zheng Huang、France Laliberté、Susana Liu、Robert Papp、Donald W. Nicholson、Robert N. Young
    DOI:10.1016/j.bmcl.2010.07.076
    日期:2010.9
    The SAR study of a series of 6-aryloxymethyl-8-aryl substituted quinolines is described. Optimization of the series led to the discovery of compound 26b, a highly potent (IC(50) = 0.6 nM) and selective PDE4D inhibitor with a 75-fold selectivity over the A, B, and C subtypes and over 18,000-fold selectivity against other PDE family members. Rat pharmacokinetics and tissue distribution are also summarized. (c) 2010 Elsevier Ltd. All rights reserved.
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