摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4-benzyl-2-(4-bromo-phenyl)-2H-phthalazin-1-one | 66614-92-4

中文名称
——
中文别名
——
英文名称
4-benzyl-2-(4-bromo-phenyl)-2H-phthalazin-1-one
英文别名
4-Benzyl-2-(p-bromphenyl)-phtalazin-1(2H)-on;4-Benzyl-2-(4-bromophenyl)phthalazin-1-one
4-benzyl-2-(4-bromo-phenyl)-2<i>H</i>-phthalazin-1-one化学式
CAS
66614-92-4
化学式
C21H15BrN2O
mdl
——
分子量
391.267
InChiKey
SUJGNEISJVIGTA-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):
    5
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    32.7
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    苯乙酸 、 alkaline earth salt of/the/ methylsulfuric acid 在 sodium acetate 作用下, 生成 4-benzyl-2-(4-bromo-phenyl)-2H-phthalazin-1-one
    参考文献:
    名称:
    Vasorelaxant activity of phthalazinones and related compounds
    摘要:
    Several series of dihydrostilbenamide, imidazo[2,1-a]isoindole, pyrimido[2,1-a]isoindole and phthalazinone derivatives were obtained and their vasorelaxant activity was measured on isolated rat aorta rings pre-contracted with phenylephrine (10(-5) M). Some phthalazinones attained, practically, the total relaxation of the organ at micromolar concentrations. For the most potent compound 9h (EC50 = 0.43 mu M) the affinities for alpha(1A), alpha(1B) and alpha(1D) adrenergic sub-receptors were determined. (C) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.02.003
点击查看最新优质反应信息

文献信息

  • Vasorelaxant activity of phthalazinones and related compounds
    作者:Esther del Olmo、Bianca Barboza、Ma Inés Ybarra、José Luis López-Pérez、Rosalía Carrón、Ma Angeles Sevilla、Cinthia Boselli、Arturo San Feliciano
    DOI:10.1016/j.bmcl.2006.02.003
    日期:2006.5
    Several series of dihydrostilbenamide, imidazo[2,1-a]isoindole, pyrimido[2,1-a]isoindole and phthalazinone derivatives were obtained and their vasorelaxant activity was measured on isolated rat aorta rings pre-contracted with phenylephrine (10(-5) M). Some phthalazinones attained, practically, the total relaxation of the organ at micromolar concentrations. For the most potent compound 9h (EC50 = 0.43 mu M) the affinities for alpha(1A), alpha(1B) and alpha(1D) adrenergic sub-receptors were determined. (C) 2006 Elsevier Ltd. All rights reserved.
查看更多