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N-ethyl-N-(6-methoxypyridin-3-yl)-2-(naphthalen-2-yloxy)acetamide | 1221899-02-0

中文名称
——
中文别名
——
英文名称
N-ethyl-N-(6-methoxypyridin-3-yl)-2-(naphthalen-2-yloxy)acetamide
英文别名
N-ethyl-N-(6-methoxypyridin-3-yl)-2-naphthalen-2-yloxyacetamide
N-ethyl-N-(6-methoxypyridin-3-yl)-2-(naphthalen-2-yloxy)acetamide化学式
CAS
1221899-02-0
化学式
C20H20N2O3
mdl
——
分子量
336.39
InChiKey
YBHKPXVKKBKYFR-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):
    3.8
  • 重原子数:
    25
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    51.7
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    参考文献:
    名称:
    Identification of amide bioisosteres of triazole Oxytocin antagonists
    摘要:
    A series of amides were investigated as potential bioisosteres of previously reported triazole Oxytocin antagonists. A range of potent analogues were identified, although SAR for potency and selectivity over the related V(1A) and V(2) receptors was found to be somewhat divergent from that observed for the corresponding triazole series. The high synthetic accessibility of this new amide series also facilitated the identification of a range of alternative left hand side (biaryl replacement) substituents which gave good levels of Oxytocin antagonism. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.02.018
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文献信息

  • Identification of amide bioisosteres of triazole Oxytocin antagonists
    作者:Alan Brown、Dave Ellis、Olga Wallace、Michael Ralph
    DOI:10.1016/j.bmcl.2010.02.018
    日期:2010.4
    A series of amides were investigated as potential bioisosteres of previously reported triazole Oxytocin antagonists. A range of potent analogues were identified, although SAR for potency and selectivity over the related V(1A) and V(2) receptors was found to be somewhat divergent from that observed for the corresponding triazole series. The high synthetic accessibility of this new amide series also facilitated the identification of a range of alternative left hand side (biaryl replacement) substituents which gave good levels of Oxytocin antagonism. (C) 2010 Elsevier Ltd. All rights reserved.
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