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1-(3-acetylphenyl)-2-imidazolidinone | 1012040-98-0

中文名称
——
中文别名
——
英文名称
1-(3-acetylphenyl)-2-imidazolidinone
英文别名
1-(3-Acetylphenyl)imidazolidin-2-one
1-(3-acetylphenyl)-2-imidazolidinone化学式
CAS
1012040-98-0
化学式
C11H12N2O2
mdl
MFCD23745056
分子量
204.228
InChiKey
UZFFTBDDWBVGFL-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

物化性质

  • 密度:
    1?+-.0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.272
  • 拓扑面积:
    49.4
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    参考文献:
    名称:
    Quinoline and quinazoline derivatives having affinity for 5ht1-type receptors
    摘要:
    提供式(I)的化合物和药学上可接受的盐:其中R1,m,X,R2,n,W,p,Y,Z,R3,R4,R5和q的含义如描述中所定义。还公开了制备方法以及在治疗中的用途,特别是用于中枢神经系统疾病,如抑郁症或焦虑症。
    公开号:
    US20060229312A1
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文献信息

  • [EN] QUINOLINE AND QUINAZOLINE DERIVATIVES HAVING AFFINITY FOR 5HT1-TYPE RECEPTORS<br/>[FR] DERIVES DE QUINOLINE ET DE QUINAZOLINE PRESENTANT UNE AFFINITE VIS-A-VIS DES RECEPTEURS DU TYPE 5HT1
    申请人:GLAXO GROUP LTD
    公开号:WO2005014552A1
    公开(公告)日:2005-02-17
    Compounds of formula (I) and pharmaceutically acceptable salts thereof are provided: wherein R1, m, X, R2, n, W, p, Y, Z, R3, R4, R5 and q have the meanings as defined in the description. Methods of preparation and uses thereof in therapy, particularly for CNS disorders such as depression or anxiety, are also disclosed.
    提供了式(I)的化合物及其药用盐:其中R1、m、X、R2、n、W、p、Y、Z、R3、R4、R5和q的含义如描述中所定义。还公开了制备方法以及在治疗中的用途,特别是用于抑郁症或焦虑等中枢神经系统疾病。
  • Quinoline and quinazoline derivatives having affinity for 5HT1-type receptors
    申请人:Glaxo Group Limited
    公开号:US07279481B2
    公开(公告)日:2007-10-09
    Compounds of formula (I) and pharmaceutically acceptable salts thereof are provided: wherein R1, m, X, R2, n, W, p, Y, Z, R3, R4, R5 and q have the meanings as defined in the description. Methods of preparation and uses thereof in therapy, particularly for CNS disorders such as depression or anxiety, are also disclosed.
    提供化学式(I)的化合物及其药学上可接受的盐: 其中R1,m,X,R2,n,W,p,Y,Z,R3,R4,R5和q的含义如描述中所定义。还公开了其制备方法和在治疗中的用途,特别是用于中枢神经系统疾病,如抑郁症或焦虑症。
  • QUINOLINE AND QUINAZOLINE DERIVATIVES HAVING AFFINITY FOR 5HT1-TYPE RECEPTORS
    申请人:Bergauer Markus
    公开号:US20070167423A1
    公开(公告)日:2007-07-19
    Compounds of formula (I) and pharmaceutically acceptable salts thereof are provided: wherein R 1 , m, X, R 2 , n, W, p, Y, Z, R 3 , R 4 , R 5 and q have the meanings as defined in the description. Methods of preparation and uses thereof in therapy, particularly for CNS disorders such as depression or anxiety, are also disclosed.
    提供了式(I)的化合物及其药学上可接受的盐: 其中,R1、m、X、R2、n、W、p、Y、Z、R3、R4、R5和q的含义如描述中定义的那样。还公开了其制备方法和在治疗中的用途,特别是用于中枢神经系统疾病如抑郁症或焦虑症。
  • Quinoline and Quinazoline Derivatives Having Affinity for 5HT1-Type Receptors
    申请人:Bergauer Markus
    公开号:US20100204273A1
    公开(公告)日:2010-08-12
    Disclosed are methods for use of compounds of formula (I) in the treatment of CNS disorders such as dysthymia, schizophrenia, panic disorder, obsessive compulsive disorder, post-traumatic stress disorder, pain, and memory disorders: wherein R 1 , m, X, R 2 , n, W, p, Y, Z, R 3 , R 4 , R 5 and q have the meanings as defined in the description.
    本发明揭示了使用式(I)化合物治疗中枢神经系统疾病,如心境不良、精神分裂症、惊恐障碍、强迫症、创伤后应激障碍、疼痛和记忆障碍的方法:其中R1,m,X,R2,n,W,p,Y,Z,R3,R4,R5和q的含义如描述中定义的那样。
  • US7279481B2
    申请人:——
    公开号:US7279481B2
    公开(公告)日:2007-10-09
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