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4-{4-[1-(pyridin-2-yl)-1H-pyrazol-5-yl]phenyl}morpholine | 1345865-44-2

中文名称
——
中文别名
——
英文名称
4-{4-[1-(pyridin-2-yl)-1H-pyrazol-5-yl]phenyl}morpholine
英文别名
4-[4-(2-Pyridin-2-ylpyrazol-3-yl)phenyl]morpholine
4-{4-[1-(pyridin-2-yl)-1H-pyrazol-5-yl]phenyl}morpholine化学式
CAS
1345865-44-2
化学式
C18H18N4O
mdl
——
分子量
306.367
InChiKey
SOWXAMTTWVTJKO-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):
    2.6
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    43.2
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis and biological evaluation of novel pyrazole derivatives with anticancer activity
    摘要:
    We synthesized thirty-six novel pyrazole derivatives and studied their antiproliferative activity in human ovarian adenocarcinoma A2780 cells, human lung carcinoma A549 cells, and murine P388 leukemia cells.Four of these substances were selected because of their higher antiproliferative activity and further analyses showed that they were all able to induce apoptosis, although to a different extent. The expression of p53 and p21(waf1), which induce apoptosis and cell cycle arrest, was evaluated by western blot analysis in cells treated with compound 12d.The analysis of the cell cycle showed that all the selected compounds cause a partial G2/M block and the formation of polyploid cells. Furthermore, the four selected compounds were tested for their interaction with the microtubular cytoskeletal system by docking analysis, tubulin polymerization assay and immunofluorescence staining, demonstrating that the compound 12d, unlike the other active derivatives, was able to significantly bind dimers of alpha- and beta-tubulin, probably causing a molecular distortion resulting in the disassembly of microtubules. (C) 2011 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2011.08.014
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