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9-[2-(3-bromophenyl)-2-oxoethyl]-8-phenyl-2-pyridin-4-yl-7,8-dihydro-6H-pyrimido[1,2-a]pyrimidin-4-one

中文名称
——
中文别名
——
英文名称
9-[2-(3-bromophenyl)-2-oxoethyl]-8-phenyl-2-pyridin-4-yl-7,8-dihydro-6H-pyrimido[1,2-a]pyrimidin-4-one
英文别名
——
9-[2-(3-bromophenyl)-2-oxoethyl]-8-phenyl-2-pyridin-4-yl-7,8-dihydro-6H-pyrimido[1,2-a]pyrimidin-4-one化学式
CAS
——
化学式
C26H21BrN4O2
mdl
——
分子量
501.4
InChiKey
ZWIGYTCEFZPKKQ-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):
    3.8
  • 重原子数:
    33
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    65.9
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • Substituted 8-Pyridinyl-6,7,8,9-Tetrahydropyrimido[1,2-a]Pyrimidin-4-one and 8-Phenyl-6-7,8,9-Tetrahydropyrimido[1,2-a]Pyrimidin-4-one derivatives
    申请人:SANOFI-SYNTHELABO
    公开号:EP1460075A1
    公开(公告)日:2004-09-22
    The invention relates to substituted-pyrimidone derivatives represented by formula (I) or a salt thereof: wherein: X represents two hydrogen atoms, a sulfur atom, an oxygen atom or a C1-2 alkyl group and a hydrogen atom; Y represents a bond, a carbonyl group, a methylene group optionally substituted; R1 represents a 2, 3 or 4-pyridine ring or a 2, 4 or 5-pyrimidine ring, the rings being optionally substituted; R2 represents a phenyl group or a naphthalene ring; the phenyl group and the naphthalene ring being optionally substituted; R3 represents a hydrogen atom or a C1-6 alkyl group; R4 represents a phenyl group, a pyridinyl group or a naphthalene ring, the groups and the ring being optionally substituted; R5 represents a hydrogen atom, a C1-6 alkyl group or a halogen atom; n represents 0 to 3; and p+q=0-3. The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β, such as Alzheimer disease.
    该发明涉及由式(I)表示的取代嘧啶酮衍生物或其盐:其中:X代表两个氢原子、一个硫原子、一个氧原子或一个C1-2烷基基团和一个氢原子;Y代表一个键、一个羰基、一个可选择取代的亚甲基基团;R1代表一个2、3或4-吡啶环或一个2、4或5-嘧啶环,环可选择取代;R2代表一个苯基或一个萘环;苯基和萘环可选择取代;R3代表一个氢原子或一个C1-6烷基基团;R4代表一个苯基、一个吡啶基团或一个萘环,基团和环可选择取代;R5代表一个氢原子、一个C1-6烷基基团或一个卤原子;n表示0到3;p+q=0-3。该发明还涉及一种药物,包括所述衍生物或其盐作为活性成分,用于预防和/或治疗由GSK3β异常活性引起的神经退行性疾病,如阿尔茨海默病。
  • 8-Substituted-6,7,8,9-tetrahydropyrimido [1,2-a] pyrimidin-4-one derivatives
    申请人:Lochead Alistair
    公开号:US20060035885A1
    公开(公告)日:2006-02-16
    The invention relates to substituted-pyrimidone derivatives represented by formula (I) or a salt thereof: wherein X, Y, R1, R2, R3, R4, R5, n, p and q are as defined herein. The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β, such as Alzheimer's disease.
    本发明涉及由式(I)或其盐所代表的取代嘧啶酮衍生物:其中X、Y、R1、R2、R3、R4、R5、n、p和q如本文所定义。本发明还涉及一种药物,其包含所述衍生物或其盐作为活性成分,用于预防和/或治疗由GSK3β异常活性引起的神经退行性疾病,如阿尔茨海默病。
  • USE OF 8-SUBSTITUTED-6,7,8,9-TETRAHYDROPYRIMIDO[1,2-a] PYRIMIDIN-4-ONE DERIVATIVES
    申请人:LOCHEAD Alistair
    公开号:US20080021046A1
    公开(公告)日:2008-01-24
    The invention relates to use of substituted-pyrimidone derivatives represented by formula (I) or a salt thereof: wherein X, Y, R1, R2, R3, R4, R5, n, p and q are as defined herein. More specifically, the invention relates to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a disease caused by abnormal activity of GSK3β, such as Pick's disease among various other diseases as claimed herein.
    本发明涉及使用式(I)或其盐所代表的取代嘧啶酮衍生物,其中X,Y,R1,R2,R3,R4,R5,n,p和q如本文所定义。更具体地,本发明涉及一种药物,其包含所述衍生物或其盐作为活性成分,用于预防和/或治疗由GSK3β异常活性引起的疾病,例如Pick氏病以及其他各种疾病。
  • 8-SUBSTITUTED-6, 7, 8,9-TETRAHY9DROPYRIMIDO (1,2- a) PYRIMIDIN-4-ONE DERIVATIVES
    申请人:Sanofi-Aventis
    公开号:EP1608654B1
    公开(公告)日:2009-12-23
  • US7247638B2
    申请人:——
    公开号:US7247638B2
    公开(公告)日:2007-07-24
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