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7-[(4-溴苯基)甲氧基]-4-氧代-1H-喹啉-3-羧酸 | 78112-21-7

中文名称
7-[(4-溴苯基)甲氧基]-4-氧代-1H-喹啉-3-羧酸
中文别名
——
英文名称
7-(4-Bromo-benzyloxy)-4-hydroxy-quinoline-3-carboxylic acid
英文别名
7-[(4-bromophenyl)methoxy]-4-oxo-1H-quinoline-3-carboxylic acid
7-[(4-溴苯基)甲氧基]-4-氧代-1H-喹啉-3-羧酸化学式
CAS
78112-21-7
化学式
C17H12BrNO4
mdl
——
分子量
374.191
InChiKey
SWTMBXHEWHOJEQ-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):
    4
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    75.6
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    3-<(4-bromobenzyl)oxy>-1-nitrobenzene盐酸sodium hydroxide 、 tin(ll) chloride 作用下, 以 二苯醚乙醇甲苯 为溶剂, 反应 8.63h, 生成 7-[(4-溴苯基)甲氧基]-4-氧代-1H-喹啉-3-羧酸
    参考文献:
    名称:
    4-Hydroxyquinoline-3-carboxylic acids as inhibitors of cell respiration. 2. Quantitative structure-activity relationship of dehydrogenase enzyme and Ehrlich ascites tumor cell inhibitions
    摘要:
    Studies on dehydrogenase enzyme inhibition have been extended with the design, synthesis, and correlation analysis of 7-[(substituted-benzyl)oxy]-, 7-[(substituted-phenethyl)oxy]-, and 7([substituted-phenoxy)ethoxy]-4-hydroxyquinoline-3-carboxylic acids. Sixteen new congeners and the fifteen molecules previously synthesized have been tested against cytoplasmic malate dehydrogenase and lactate dehydrogenase, as well as against mitochondrial malate dehydrogenase. The lipophilic congeners show a clear specificity for inhibition of the mitochondrial enzyme. Correlation analysis of the data on the three enzymes allows a comparison of the binding sites in quantitative terms, while examination of the data on inhibition of ascites tumor cell respiration affords an indication of membrane transport. A newly developed high-pressure liquid chromatography based retention index is compared to the octanol-water pi constant as a model for hydrophobic interactions.
    DOI:
    10.1021/jm00343a011
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