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7-Benzyloxy-1-(3,5-dimethoxy-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methyl ester | 682778-82-1

中文名称
——
中文别名
——
英文名称
7-Benzyloxy-1-(3,5-dimethoxy-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methyl ester
英文别名
——
7-Benzyloxy-1-(3,5-dimethoxy-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methyl ester化学式
CAS
682778-82-1
化学式
C26H23NO6
mdl
——
分子量
445.472
InChiKey
UPBIHWPZZUPSTC-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

物化性质

  • 沸点:
    628.0±55.0 °C(Predicted)
  • 密度:
    1.274±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.37
  • 重原子数:
    33.0
  • 可旋转键数:
    7.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    75.99
  • 氢给体数:
    0.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    描述:
    7-Benzyloxy-1-(3,5-dimethoxy-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methyl estersodium hydroxide 作用下, 以 乙醇 为溶剂, 以100%的产率得到7-Benzyloxy-1-(3,5-dimethoxy-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid
    参考文献:
    名称:
    A novel class of apical sodium-dependent bile acid transporter inhibitors: the amphiphilic 4-oxo-1-phenyl-1,4-dihydroquinoline derivatives
    摘要:
    A series of 4-oxo-1-phenyl-1,4-dihydroquinolines possessing a linker and an ammonio moiety were synthesized and found to inhibit the apical sodium-dependent bile acid transporter (ASBT). The potency of ASBT inhibition varied with the position and length of the linking tether. Compound 21e effectively lowered the total serum cholesterol levels in hamsters. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2003.12.063
  • 作为产物:
    参考文献:
    名称:
    A novel class of apical sodium-dependent bile acid transporter inhibitors: the amphiphilic 4-oxo-1-phenyl-1,4-dihydroquinoline derivatives
    摘要:
    A series of 4-oxo-1-phenyl-1,4-dihydroquinolines possessing a linker and an ammonio moiety were synthesized and found to inhibit the apical sodium-dependent bile acid transporter (ASBT). The potency of ASBT inhibition varied with the position and length of the linking tether. Compound 21e effectively lowered the total serum cholesterol levels in hamsters. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2003.12.063
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