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2-(4-Bromo-butyl)-5H-phenanthridin-6-one | 866403-68-1

中文名称
——
中文别名
——
英文名称
2-(4-Bromo-butyl)-5H-phenanthridin-6-one
英文别名
——
2-(4-Bromo-butyl)-5H-phenanthridin-6-one化学式
CAS
866403-68-1
化学式
C17H16BrNO
mdl
——
分子量
330.224
InChiKey
FDRSBFRGGXIPSD-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):
    4.4
  • 重原子数:
    20.0
  • 可旋转键数:
    4.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    32.86
  • 氢给体数:
    1.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    描述:
    2-(4-Bromo-butyl)-5H-phenanthridin-6-one1,2,3,6-四氢-4-苯基吡啶盐酸盐三乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以29%的产率得到2-[4-(4-Phenyl-3,6-dihydro-2H-pyridin-1-yl)-butyl]-5H-phenanthridin-6-one
    参考文献:
    名称:
    4-Phenyl-1,2,3,6-tetrahydropyridine, an excellent fragment to improve the potency of PARP-1 inhibitors
    摘要:
    We have shown that a 4-phenyl-1,2,3,6-tetrahydropyridine fragment plays an important role in improving inhibitory potency against poly(ADP-ribose) polymerise-1 (PARP-1). Various benzamide analogues linked with this fragment via alkyl spacers have been prepared and evaluated. As a result, some of them have been found to be highly potent PARP-1 inhibitors. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.06.094
  • 作为产物:
    描述:
    [4-(4-Hydroxy-butyl)-phenyl]-carbamic acid ethyl ester 在 四(三苯基膦)钯sodium acetate 、 phosphorus pentoxide 、 三溴化磷sodium carbonate溶剂黄146三氯氧磷 作用下, 以 乙二醇二甲醚乙酸乙酯 为溶剂, 生成 2-(4-Bromo-butyl)-5H-phenanthridin-6-one
    参考文献:
    名称:
    4-Phenyl-1,2,3,6-tetrahydropyridine, an excellent fragment to improve the potency of PARP-1 inhibitors
    摘要:
    We have shown that a 4-phenyl-1,2,3,6-tetrahydropyridine fragment plays an important role in improving inhibitory potency against poly(ADP-ribose) polymerise-1 (PARP-1). Various benzamide analogues linked with this fragment via alkyl spacers have been prepared and evaluated. As a result, some of them have been found to be highly potent PARP-1 inhibitors. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.06.094
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