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2-[4-(1-Methyl-6-oxo-4-pyrimidin-4-ylpyrimidin-2-yl)morpholin-2-yl]benzonitrile

中文名称
——
中文别名
——
英文名称
2-[4-(1-Methyl-6-oxo-4-pyrimidin-4-ylpyrimidin-2-yl)morpholin-2-yl]benzonitrile
英文别名
——
2-[4-(1-Methyl-6-oxo-4-pyrimidin-4-ylpyrimidin-2-yl)morpholin-2-yl]benzonitrile化学式
CAS
——
化学式
C20H18N6O2
mdl
——
分子量
374.4
InChiKey
HJVFOWMJHMSRQA-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):
    0.3
  • 重原子数:
    28
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    94.7
  • 氢给体数:
    0
  • 氢受体数:
    6

文献信息

  • 3-Substituted-4-pyrimidone derivatives
    申请人:Uehara Fumiaki
    公开号:US20050130967A1
    公开(公告)日:2005-06-16
    A pyrimidone derivative represented by formula (I) or a salt thereof, or a solvate thereof or a hydrate thereof having inhibitory activity against tau protein kinase 1: wherein R 1 represents a C 1 -C 12 alkyl group which may be substituted; R represents, for example, a group represented by the following formula (II): wherein R2 and R 3 independently represent a hydrogen atom or a C 1 -C 8 alkyl group; R 4 represents a benzene ring which may be substituted, a naphthalene ring which may be substituted, an indan ring which may be substituted, a tetrahydronaphthalene ring which may be substituted, or an optionally substituted heterocyclic ring having 1 to 4 hetero atoms selected from the group consisting of oxygen atom, sulfur atom and nitrogen atom, and having 5 to 10 ring-constituting atoms in total.
    一种由式(I)表示的吡啶酮衍生物或其盐,或其溶剂化物或合物,具有对tau蛋白激酶1的抑制活性:其中,R1代表可取代的C1-C12烷基;R代表例如由以下式子(II)表示的基团:其中,R2和R3独立地表示氢原子或C1-C8烷基;R4代表可取代的苯环、可取代的环、可取代的萘烷环、可取代的四氢环或选择自氧原子、原子和氮原子组成的1至4个杂环原子,并且总共有5至10个环构成原子的可选取代的杂环。
  • 3-SUBSTITUTED-4-PYRIMIDONE DERIVATIVES
    申请人:Mitsubishi Pharma Corporation
    公开号:EP1427709B1
    公开(公告)日:2005-12-14
  • US7572793B2
    申请人:——
    公开号:US7572793B2
    公开(公告)日:2009-08-11
  • [EN] 3-SUBSTITUTED-4-PYRIMIDONE DERIVATIVES<br/>[FR] DERIVES DE 3-SUBSTITUTE-4-PYRIMIDONE
    申请人:MITSUBISHI PHARMA CORP
    公开号:WO2003027080A1
    公开(公告)日:2003-04-03
    A pyrimidone derivative represented by formula (I) or a salt thereof, or a solvate thereof or a hydrate thereof having inhibitory activity against tau protein kinase 1:wherein R1 represents a C1-C12 alkyl group which may be substituted;R represents, for example, a group represented by the following formula (II):wherein R2 and R3 independently represent a hydrogen atom or a C1-C8 alkyl group; R4 represents a benzene ring which may be substituted, a naphthalene ring which may be substituted, an indan ring which may be substituted, a tetrahydronaphthalene ring which may be substituted, or an optionally substituted heterocyclic ring having 1 to 4 hetero atoms selected from the group consisting of oxygen atom, sulfur atom and nitrogen atom, and having 5 to 10 ring-constituting atoms in total.
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