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1-(4-bromophenyl)-4-(morpholin-1-yl)phthalazine | 1351858-38-2

中文名称
——
中文别名
——
英文名称
1-(4-bromophenyl)-4-(morpholin-1-yl)phthalazine
英文别名
4-[4-(4-Bromophenyl)phthalazin-1-yl]morpholine;4-[4-(4-bromophenyl)phthalazin-1-yl]morpholine
1-(4-bromophenyl)-4-(morpholin-1-yl)phthalazine化学式
CAS
1351858-38-2
化学式
C18H16BrN3O
mdl
——
分子量
370.249
InChiKey
MIVTWTMTKJHXCH-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):
    3.5
  • 重原子数:
    23
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    38.2
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis and evaluation of anti-proliferative activity of 1,4-disubstituted phthalazines
    摘要:
    A series of new phthalazine derivatives 3a-i and 4a-c were synthesized via the reaction of 1-chlorophthalazine derivative 2 with either N-substituted-piperazines, primary or their secondary amines. The structure of the synthesized, new compounds were characterized by spectral data. The anti-proliferative activity on human breast cancer cell line MCF-7 of the synthesized compounds was determined. The results showed that six of the test compounds (3a, 3g, 3i, and 4a-c) displayed potent cytotoxic activity ranging from 1.4 to 2.3 mu mol.
    DOI:
    10.1007/s00044-011-9874-z
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文献信息

  • Synthesis and evaluation of anti-proliferative activity of 1,4-disubstituted phthalazines
    作者:Khaled A. M. Abouzid、Nadia A. Khalil、Eman M. Ahmed
    DOI:10.1007/s00044-011-9874-z
    日期:2012.10
    A series of new phthalazine derivatives 3a-i and 4a-c were synthesized via the reaction of 1-chlorophthalazine derivative 2 with either N-substituted-piperazines, primary or their secondary amines. The structure of the synthesized, new compounds were characterized by spectral data. The anti-proliferative activity on human breast cancer cell line MCF-7 of the synthesized compounds was determined. The results showed that six of the test compounds (3a, 3g, 3i, and 4a-c) displayed potent cytotoxic activity ranging from 1.4 to 2.3 mu mol.
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