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5,6,7,8-tetrabromo-2,3-dihydrophthalazine-1,4-dione | 1133866-08-6

中文名称
——
中文别名
——
英文名称
5,6,7,8-tetrabromo-2,3-dihydrophthalazine-1,4-dione
英文别名
——
5,6,7,8-tetrabromo-2,3-dihydrophthalazine-1,4-dione化学式
CAS
1133866-08-6
化学式
C8H2Br4N2O2
mdl
——
分子量
477.732
InChiKey
KQFOVSHRRQBKKE-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):
    3.2
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    58.2
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    四溴苯酐一水合肼盐酸 作用下, 以 乙醇 为溶剂, 反应 1.0h, 生成 5,6,7,8-tetrabromo-2,3-dihydrophthalazine-1,4-dione
    参考文献:
    名称:
    Synthesis of new analogs of benzotriazole, benzimidazole and phthalimide—potential inhibitors of human protein kinase CK2
    摘要:
    New derivatives of 4,5,6,7-tetrabromo-1H-1,2,3-benzotriazole (TBBt), 4,5,6,7-tetrabromo-1H-benzimidazole (TBBi), and N-substituted tetrabromophthalimides were synthesized and their effect on the activity of human protein kinase CK2 was examined. The most active were derivatives with N-hydroxypropyl substituents (IC50 in 0.32-0.54 mu M range) whereas derivatives of phthalimide were almost ineffective. (c) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2008.12.071
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文献信息

  • Synthesis of new analogs of benzotriazole, benzimidazole and phthalimide—potential inhibitors of human protein kinase CK2
    作者:Andzelika Najda-Bernatowicz、Maja Łebska、Andrzej Orzeszko、Katarzyna Kopańska、Ewa Krzywińska、Grażyna Muszyńska、Maria Bretner
    DOI:10.1016/j.bmc.2008.12.071
    日期:2009.2
    New derivatives of 4,5,6,7-tetrabromo-1H-1,2,3-benzotriazole (TBBt), 4,5,6,7-tetrabromo-1H-benzimidazole (TBBi), and N-substituted tetrabromophthalimides were synthesized and their effect on the activity of human protein kinase CK2 was examined. The most active were derivatives with N-hydroxypropyl substituents (IC50 in 0.32-0.54 mu M range) whereas derivatives of phthalimide were almost ineffective. (c) 2009 Elsevier Ltd. All rights reserved.
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