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6-(2-methylphenyl)pyridazin-3(2H)-one | 1105194-00-0

中文名称
——
中文别名
——
英文名称
6-(2-methylphenyl)pyridazin-3(2H)-one
英文别名
3-(2-methylphenyl)-1H-pyridazin-6-one
6-(2-methylphenyl)pyridazin-3(2H)-one化学式
CAS
1105194-00-0
化学式
C11H10N2O
mdl
MFCD12143090
分子量
186.213
InChiKey
GGEYYRLJDZNPQZ-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):
    1.6
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    41.5
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 下游产品
    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:
    描述:
    6-(2-methylphenyl)pyridazin-3(2H)-one铁粉caesium carbonate溶剂黄146 作用下, 以 乙醇N,N-二甲基甲酰胺 为溶剂, 反应 8.0h, 生成 2-[(3-Aminophenyl)methyl]-6-(2-methylphenyl)pyridazin-3-one
    参考文献:
    名称:
    Discovery of novel 2,6-disubstituted pyridazinone derivatives as acetylcholinesterase inhibitors
    摘要:
    2,6-Disubstituted pyridazinone 4 was identified by HTS as a novel acetylcholinesterase (AChE) inhibitor. Under SAR development, compound 17e stood out as displaying high AChE inhibitory activity and AChE/butyrylcholinesterase (BuChE) selectivity in vitro. Docking studies revealed that 17e might interact with the catalytic active site (CAS) and the peripheral anionic site (PAS) simultaneously. Based on this novel binding information, 6-ortho-tolylamino and N-ethyl-N-isopropylacetamide substituted piperidine were disclosed as new PAS and CAS binders. (c) 2013 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2013.01.056
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文献信息

  • Discovery of novel 2,6-disubstituted pyridazinone derivatives as acetylcholinesterase inhibitors
    作者:Weiqiang Xing、Yan Fu、Zhangxing Shi、Dong Lu、Haiyan Zhang、Youhong Hu
    DOI:10.1016/j.ejmech.2013.01.056
    日期:2013.5
    2,6-Disubstituted pyridazinone 4 was identified by HTS as a novel acetylcholinesterase (AChE) inhibitor. Under SAR development, compound 17e stood out as displaying high AChE inhibitory activity and AChE/butyrylcholinesterase (BuChE) selectivity in vitro. Docking studies revealed that 17e might interact with the catalytic active site (CAS) and the peripheral anionic site (PAS) simultaneously. Based on this novel binding information, 6-ortho-tolylamino and N-ethyl-N-isopropylacetamide substituted piperidine were disclosed as new PAS and CAS binders. (c) 2013 Elsevier Masson SAS. All rights reserved.
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