申请人:Andrés-Gil José Ignacio
公开号:US20100105694A1
公开(公告)日:2010-04-29
The present invention concerns substituted pyrazinone derivatives according to the general Formula (I) a pharmaceutically acceptable acid or base addition salt thereof, a stereochemically isomeric form thereof, an N-oxide form thereof or a quaternary ammonium salt thereof, wherein the variables are defined in claim
1
, having selective 2C-adrenoceptor antagonist activity. It further relates to their preparation, compositions comprising them and their use as a medicine. The compounds according to the invention are useful for the prevention and/or treatment of central nervous system disorders, mood disorders, anxiety disorders, stress-related disorders associated with depression and/or anxiety, cognitive disorders, personality disorders, schizoaffective disorders, Parkinson's disease, dementia of the Alzheimer's type, chronic pain conditions, neurodegenerative diseases, addiction disorders, mood disorders and sexual dysfunction.
本发明涉及通式(I)的取代吡唑酮衍生物,其为药学上可接受的酸性或碱性盐、立体化学异构体形式、N-氧化物形式或季铵盐,其中变量在权利要求1中定义,具有选择性2C-肾上腺素受体拮抗剂活性。本发明还涉及它们的制备、包含它们的组合物及其用作药物。根据本发明的化合物对于预防和/或治疗中枢神经系统疾病、情绪障碍、焦虑症、与抑郁和/或焦虑有关的应激相关障碍、认知障碍、人格障碍、情感性精神病、帕金森病、阿尔茨海默病型痴呆、慢性疼痛症状、神经退行性疾病、成瘾障碍、情感障碍和性功能障碍方面具有用处。