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1-[(E)-(quinolin-3-ylimino)methyl]phenol | 129855-32-9

中文名称
——
中文别名
——
英文名称
1-[(E)-(quinolin-3-ylimino)methyl]phenol
英文别名
2-[(E)-(quinolin-3-ylimino)methyl]phenol;2-[(E)-(3-quinolinylimino)methyl]phenol;H-QMP
1-[(E)-(quinolin-3-ylimino)methyl]phenol化学式
CAS
129855-32-9
化学式
C16H12N2O
mdl
——
分子量
248.284
InChiKey
ORSPJBCSWFMOPT-LICLKQGHSA-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):
    3.69
  • 重原子数:
    19.0
  • 可旋转键数:
    2.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    45.48
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

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

  • 作为反应物:
    参考文献:
    名称:
    Synthesis, characterization and distinct butyrylcholinesterase activities of transition metal complexes of 2-[(E)-(quinolin-3-ylimino)methyl]phenol
    摘要:
    2-[(E)-(Quinolin-3-ylimino) methyl] phenol (H-QMP) was synthesized by condensing salicylaldehyde with 2-aminoquinoline and fully characterized by mass spectrometry, H-1 and C-13{H-1} NMR, and IR spectroscopies. The metal complexes [M(QMP)(OAc)]H2O where M = Cu(II) and Zn(II) and [M(QMP)(2)] where M = Ni and Co(II) were prepared from the metal acetates. All transition metal complexes were assigned geometries based on the UV-Vis spectra, conductivity and magnetic susceptibilities. [M(QMP)(2)], {where M = Ni and Co(II)}, were further characterized by single crystal X-ray diffraction and were found to be pseudo-octahedral with interquinoline interaction to the metal center. The complexes were screened for acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). Only cobalt and copper containing complexes were found to be active against BChE with IC50 = 69 +/- 0.0112 and 5 +/- 0.0004 mu M +/- SEM, respectively. Surprisingly no activity was observed for AChE, therefore selective BChE inhibition was observed for copper and cobalt complexes only. (C) 2012 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2012.04.036
  • 作为产物:
    描述:
    3-氨基喹啉水杨醛乙醇 为溶剂, 反应 6.0h, 生成 1-[(E)-(quinolin-3-ylimino)methyl]phenol
    参考文献:
    名称:
    Development of novel ruthenium(ii)–arene complexes displaying potent anticancer effects in glioblastoma cells
    摘要:
    设计了两种生物活性的Ru(ii)-p-环戊烯配合物,进行了结构分析,并研究了它们在体外对人类胶质母细胞瘤(GB)细胞的治疗潜力。
    DOI:
    10.1039/d0dt02167a
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