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Ethyl (E)-3-{5-chloro-2-[(6-chloro-2-naphthyl)methyl]phenyl}-2-propenoate | 244103-46-6

中文名称
——
中文别名
——
英文名称
Ethyl (E)-3-{5-chloro-2-[(6-chloro-2-naphthyl)methyl]phenyl}-2-propenoate
英文别名
ethyl (E)-3-[5-chloro-2-[(6-chloronaphthalen-2-yl)methyl]phenyl]prop-2-enoate
Ethyl (E)-3-{5-chloro-2-[(6-chloro-2-naphthyl)methyl]phenyl}-2-propenoate化学式
CAS
244103-46-6
化学式
C22H18Cl2O2
mdl
——
分子量
385.29
InChiKey
VADNUTFIINZBGB-JXMROGBWSA-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):
    7
  • 重原子数:
    26
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    5-溴-2-甲氧基苯磺酰胺Ethyl (E)-3-{5-chloro-2-[(6-chloro-2-naphthyl)methyl]phenyl}-2-propenoatesodium hydroxide4-二甲氨基吡啶1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 作用下, 以 四氢呋喃甲醇二氯甲烷 为溶剂, 生成 5-bromo-N-{3-[5-chloro-2-(6-chloronaphthalen-2-ylmethyl)phenyl]acryloyl}-2-methoxybenzenesulfonamide
    参考文献:
    名称:
    Structure–activity relationship of cinnamic acylsulfonamide analogues on the human EP3 prostanoid receptor
    摘要:
    Potent and selective antagonists of the human EP3 receptor have been identified. The structure-activity relationship of the chemical series was conducted and we found several analogues displaying sub-nanomolar K-i values at the EP3 receptor and micromolar activities at the EP1, EP2 and EP4 receptors. The effect of added human serum albumin (HSA) on the binding affinity at the EP3 receptor was also investigated. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(01)00110-9
  • 作为产物:
    描述:
    3-(2-bromomethyl-5-chlorophenyl)acrylic acid ethyl ester 、 Trifluoro-methanesulfonic acid 6-chloro-naphthalen-2-yl ester 在 1,1'-双(二苯基膦)二茂铁 、 bis(dibenzylideneacetone)-palladium(0) 作用下, 以 N,N-二甲基甲酰胺四氢呋喃 为溶剂, 反应 0.5h, 生成 Ethyl (E)-3-{5-chloro-2-[(6-chloro-2-naphthyl)methyl]phenyl}-2-propenoate
    参考文献:
    名称:
    Structure–activity relationship of cinnamic acylsulfonamide analogues on the human EP3 prostanoid receptor
    摘要:
    Potent and selective antagonists of the human EP3 receptor have been identified. The structure-activity relationship of the chemical series was conducted and we found several analogues displaying sub-nanomolar K-i values at the EP3 receptor and micromolar activities at the EP1, EP2 and EP4 receptors. The effect of added human serum albumin (HSA) on the binding affinity at the EP3 receptor was also investigated. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(01)00110-9
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