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5-Bromo-8-(4-morpholinylsulfonyl)isoquinoline | 862777-70-6

中文名称
——
中文别名
——
英文名称
5-Bromo-8-(4-morpholinylsulfonyl)isoquinoline
英文别名
4-(5-bromoisoquinolin-8-yl)sulfonylmorpholine
5-Bromo-8-(4-morpholinylsulfonyl)isoquinoline化学式
CAS
862777-70-6
化学式
C13H13BrN2O3S
mdl
——
分子量
357.22
InChiKey
JVMIVPXGCPLJQW-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:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    67.9
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • Tetrahydroisoquinolinyl derivatives of quinazoline and isoquinoline
    申请人:Allen Patrick Martin
    公开号:US20050182079A1
    公开(公告)日:2005-08-18
    The invention pertains to substituted quinazoline and isoquinoline compounds that serve as effective phosphodiesterase (PDE) inhibitors. In particular, the invention relates to said compounds which are selective inhibitors of PDE-10. The invention also relates to intermediates for preparation of said compounds; pharmaceutical compositions comprising said compounds; and the use of said compounds in a method for treating certain central nervous system (CNS) or other disorders.
    本发明涉及作为有效的磷酸二酯酶(PDE)抑制剂的取代喹唑啉和异喹啉化合物。特别是,本发明涉及作为PDE-10的选择性抑制剂的上述化合物。本发明还涉及用于制备所述化合物的中间体;包含所述化合物的药物组合物;以及使用所述化合物在治疗某些中枢神经系统(CNS)或其他疾病的方法。
  • TETRAHYDROISOQUINOLINYL DERIVATIVES OF QUINAZOLINE AND ISOQUINOLINE
    申请人:Pfizer Products Incorporated
    公开号:EP1723134A2
    公开(公告)日:2006-11-22
  • US7268142B2
    申请人:——
    公开号:US7268142B2
    公开(公告)日:2007-09-11
  • [EN] TETRAHYDROISOQUINOLINYL DERIVATIVES OF QUINAZOLINE AND ISOQUINOLINE<br/>[FR] DERIVES TETRAHYDROISOQUINOLINYLIQUES DE QUINAZOLINE ET D'ISOQUINOLINE
    申请人:PFIZER PROD INC
    公开号:WO2005082883A2
    公开(公告)日:2005-09-09
    The invention pertains to substituted quinazoline and isoquinoline of formula (I) that serve as effective phosphodiesterase (PDE) inhibitors. In particular, the invention relates to said compounds which are selective inhibitors of PDE-10. The invention also relates to intermediates for preparation of said compounds; pharmaceutical compositions comprising said compounds; and the use of said compounds in a method for treating certain central nervous system (CNS) or other disorders. or a pharmaceutically acceptable salt, solvate or prodrug thereof.
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