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2-(4-isopropyl-phenyl)-4-oxo-4H-chromene-6-carboxylic acid | 66848-84-8

中文名称
——
中文别名
——
英文名称
2-(4-isopropyl-phenyl)-4-oxo-4H-chromene-6-carboxylic acid
英文别名
4-Oxo-2-(4-propan-2-ylphenyl)chromene-6-carboxylic acid
2-(4-isopropyl-phenyl)-4-oxo-4<i>H</i>-chromene-6-carboxylic acid化学式
CAS
66848-84-8
化学式
C19H16O4
mdl
——
分子量
308.334
InChiKey
VLTPRNORGYFZAV-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):
    4.6
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    63.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    4-hydroxy-3-[(E)-3-(4-propan-2-ylphenyl)prop-2-enoyl]benzoic acid 在 氢氧化钾 作用下, 以 乙醇溶剂黄146 为溶剂, 反应 7.0h, 生成 2-(4-isopropyl-phenyl)-4-oxo-4H-chromene-6-carboxylic acid
    参考文献:
    名称:
    Inhibition of histamine-induced gastric secretion by flavone-6-carboxylic acids
    摘要:
    Twenty-five flavone-6-carboxylic acids were synthesized and tested as to their ability to inhibit histamine-induced gastric acid secretion in the rat. 3-Isopropoxy-4'-methoxyflavone-6-carboxylic acid (41) showed consistent oral activity while being devoid of any other noteworthy pharmacological effects. In vitro, this compound was found to be inactive as a histamine H2 antagonist, and its mode of action remains unknown.
    DOI:
    10.1021/jm00177a029
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文献信息

  • DORIA G.; ROMEO C.; GIRALDI P.; LAURIA F.; SBERZE P.; TIBOLLA M.; CORNO M+, EUR. J. MED. CHEM., 1978, 13, NO 1, 33-39
    作者:DORIA G.、 ROMEO C.、 GIRALDI P.、 LAURIA F.、 SBERZE P.、 TIBOLLA M.、 CORNO M+
    DOI:——
    日期:——
  • Inhibition of histamine-induced gastric secretion by flavone-6-carboxylic acids
    作者:Juerg R. Pfister、Walter E. Wymann、Margery E. Schuler、Adolph P. Roszkowski
    DOI:10.1021/jm00177a029
    日期:1980.3
    Twenty-five flavone-6-carboxylic acids were synthesized and tested as to their ability to inhibit histamine-induced gastric acid secretion in the rat. 3-Isopropoxy-4'-methoxyflavone-6-carboxylic acid (41) showed consistent oral activity while being devoid of any other noteworthy pharmacological effects. In vitro, this compound was found to be inactive as a histamine H2 antagonist, and its mode of action remains unknown.
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