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公开(公告)号:US07026479B2
公开(公告)日:2006-04-11
申请号:US10199755
申请日:2002-07-19
IPC分类号: C07D239/70 , C07D237/02
CPC分类号: C07D401/04 , C07D213/57
摘要: The invention provides a process for the production of a compound of formula (A), or a pharmaceutically acceptable salt or solvate thereof, wherein R1, R2, R3, and R4 are as defined herein.
摘要翻译: 本发明提供了制备式(A)化合物或其药学上可接受的盐或溶剂合物的方法,其中R 1,R 2,R 2, > 3 SUP>,而R 4 4如本文所定义。
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公开(公告)号:US06313312B1
公开(公告)日:2001-11-06
申请号:US09467871
申请日:1999-12-20
申请人: Bernard Joseph Banks , Robert James Crook , Stephen Paul Gibson , Graham Lunn , Alan John Pettman
发明人: Bernard Joseph Banks , Robert James Crook , Stephen Paul Gibson , Graham Lunn , Alan John Pettman
IPC分类号: C07D20952
CPC分类号: C07D401/04 , C07D209/52 , C07D401/06 , C07D401/10 , C07D401/12 , C07D403/04 , C07D403/06 , C07D403/10 , C07D403/12 , C07D405/06 , C07D409/06 , C07D409/10 , C07D413/12 , C07D417/06
摘要: Compounds of formula (I), their salts and prodrugs thereof, where the substituents are as defined herein are disclosed as opiate binding agents useful in the treatment of opiate-mediated conditions. Also described are processes for making such substances.
摘要翻译: 公开了其中取代基如本文所定义的式(I)化合物及其盐和前药,其用作阿片剂结合剂,其用于治疗阿片剂介导的病症。 还描述了制备这些物质的方法。
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公开(公告)号:US06737430B2
公开(公告)日:2004-05-18
申请号:US10000985
申请日:2001-10-31
IPC分类号: A61K314439
CPC分类号: C07D401/12 , A61K31/4422 , A61K31/4439 , A61K2300/00
摘要: The present invention relates to a mutual prodrug of amlodipine and atorvastatin, pharmaceutically acceptable acid addition salts thereof, pharmaceutical compositions thereof and the use of said prodrug and its salts in the manufacture of medicaments for the treatment of atherosclerosis, angina pectoris, combined hypertension and hyperlipidaemia and the management of cardiac risk.
摘要翻译: 本发明涉及氨氯地平和阿托伐他汀的互用前药,其药学上可接受的酸加成盐,其药物组合物以及所述前药及其盐在制备用于治疗动脉粥样硬化,心绞痛,联合高血压和高脂血症的药物中的用途 和心脏风险的管理。
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公开(公告)号:US07049444B2
公开(公告)日:2006-05-23
申请号:US10214658
申请日:2002-08-07
申请人: Bernard Joseph Banks , Robert James Crook , Stephen Paul Gibson , Graham Lunn , Alan John Pettman
发明人: Bernard Joseph Banks , Robert James Crook , Stephen Paul Gibson , Graham Lunn , Alan John Pettman
IPC分类号: C07D209/52
CPC分类号: C07D401/04 , C07D209/52 , C07D401/06 , C07D401/10 , C07D401/12 , C07D403/04 , C07D403/06 , C07D403/10 , C07D403/12 , C07D405/06 , C07D409/06 , C07D409/10 , C07D413/12 , C07D417/06
摘要: Compounds of formula (I), their salts and prodrugs thereof, where the substituents are as defined herein are disclosed as opiate binding agents useful in the treatment of opiate-mediated conditions. Also described are processes for making such substances.
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公开(公告)号:US06333326B1
公开(公告)日:2001-12-25
申请号:US09367303
申请日:1999-08-02
IPC分类号: C07D40114
CPC分类号: C07D401/14
摘要: This invention relates to 2,3(1H,4H)-quinoxalinedione derivatives which are selective antagonists of N-methyl-D-aspartate receptors. More particularly, this invention relates to 5-triazolyl-2,3(1H,4H)-quinoxalinedione derivatives and to the preparation of, compositions containing, and the uses of, such derivatives. It also relates to a method for treating acute neurodegeneration disorders and chronic neurological disorders.
摘要翻译: 本发明涉及作为N-甲基-D-天冬氨酸受体的选择性拮抗剂的2,3(1H,4H) - 喹喔啉二酮衍生物。 更具体地说,本发明涉及5-三唑基-2,3(1H,4H) - 喹喔啉二酮衍生物及其制备方法,含有这些衍生物的用途和用途。 它还涉及治疗急性神经变性疾病和慢性神经障碍的方法。
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