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(Z)-3-(3-Cyano-phenyl)-pent-2-enoic acid ethyl ester | 474334-43-5

中文名称
——
中文别名
——
英文名称
(Z)-3-(3-Cyano-phenyl)-pent-2-enoic acid ethyl ester
英文别名
——
(Z)-3-(3-Cyano-phenyl)-pent-2-enoic acid ethyl ester化学式
CAS
474334-43-5
化学式
C14H15NO2
mdl
——
分子量
229.279
InChiKey
WSWXDGBZDCUUPD-XFXZXTDPSA-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):
    2.91
  • 重原子数:
    17.0
  • 可旋转键数:
    4.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    50.09
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Design, synthesis, and SAR of substituted acrylamides as factor Xa inhibitors
    摘要:
    Substituted acrylamides were used as templates that bridge P1 and P4 binding elements, resulting in a series of potent sub-nanomolar) and selective factor Xa inhibitors. In this template, cis-geometry of P1 and P4 ligands is highly preferred. SAR on the substituting groups, as well as on modification of P1 and P4 moieties is described. Compounds in this series show good in vivo efficacy in animal models. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(02)00199-3
  • 作为产物:
    参考文献:
    名称:
    Design, synthesis, and SAR of substituted acrylamides as factor Xa inhibitors
    摘要:
    Substituted acrylamides were used as templates that bridge P1 and P4 binding elements, resulting in a series of potent sub-nanomolar) and selective factor Xa inhibitors. In this template, cis-geometry of P1 and P4 ligands is highly preferred. SAR on the substituting groups, as well as on modification of P1 and P4 moieties is described. Compounds in this series show good in vivo efficacy in animal models. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(02)00199-3
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