发明公开
EP0830359A1 NOVEL SUBSTITUTED ARYL AND CYCLOALKYL IMIDAZOLONES; A NEW CLASS OF GABA BRAIN RECEPTOR LIGANDS 失效
取代的芳基和环烷基咪唑啉酮,配体GABA受体在脑中的一类

  • 专利标题: NOVEL SUBSTITUTED ARYL AND CYCLOALKYL IMIDAZOLONES; A NEW CLASS OF GABA BRAIN RECEPTOR LIGANDS
  • 专利标题(中): 取代的芳基和环烷基咪唑啉酮,配体GABA受体在脑中的一类
  • 申请号: EP96919393.0
    申请日: 1996-06-04
  • 公开(公告)号: EP0830359A1
    公开(公告)日: 1998-03-25
  • 发明人: DESIMONE, Robert, W.BLUM, Charles, A.
  • 申请人: NEUROGEN CORPORATION
  • 申请人地址: 35 N.E. Industrial Road Branford, CT 06405 US
  • 专利权人: NEUROGEN CORPORATION
  • 当前专利权人: NEUROGEN CORPORATION
  • 当前专利权人地址: 35 N.E. Industrial Road Branford, CT 06405 US
  • 代理机构: Vossius, Volker, Dr., et al
  • 优先权: US19950461641 19950605; US19950462674 19950605
  • 国际公布: WO1996039404 19961212
  • 主分类号: C07D413
  • IPC分类号: C07D413 C07D417
NOVEL SUBSTITUTED ARYL AND CYCLOALKYL IMIDAZOLONES; A NEW CLASS OF GABA BRAIN RECEPTOR LIGANDS
摘要:
Disclosed are compounds of formula (I) wherein: T is NH, O, or S; X is hydrogen, hydroxyl, lower alkyl, or an optionally substituted amide; the W ring is an optionally substituted aryl or heteroaryl group; and (a) represents an optionally substituted benzo group or an optionally substituted 5, 6, 7, or 8 membered ring. These compounds are highly selective agonists, antagonists or inverse agonists for GABAa brain receptors or prodrugs of agonists, antagonists or inverse agonists for GABAa brain receptors. These compouns are useful in the diagnosis and treatment of anxiety, sleep and seizure disorders, overdose with benzodiazepine drugs and for enhancement of memory.
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