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公开(公告)号:US06284771B1
公开(公告)日:2001-09-04
申请号:US09403061
申请日:2000-04-03
IPC分类号: A61K3144
CPC分类号: A61K31/44
摘要: The present invention provides a method for treating a condition selected from the group consisting of schizophrenia, schizoaffective disorder, and schizophreniform disorder in a patient using a Compound (I).
摘要翻译: 本发明提供了使用化合物(I)在患者中治疗选自精神分裂症,分裂情感障碍和精神分裂症状障碍的病症的方法。
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公开(公告)号:US5998434A
公开(公告)日:1999-12-07
申请号:US91143
申请日:1998-06-04
IPC分类号: A61K31/41 , A61K31/4245 , A61K31/433 , A61K31/439 , A61K31/44 , A61K31/485 , A61K31/495 , A61K31/497 , A61K31/55 , C07D241/18 , C07D285/10 , C07D417/12 , C07D453/02 , C07D471/08 , C07D487/08
CPC分类号: C07D285/10 , A61K31/4245 , A61K31/433 , A61K31/439 , A61K31/497 , C07D241/18 , C07D417/12 , C07D453/02 , C07D471/08 , C07D487/08
摘要: The present invention provides a composition and method for treating pain using Selected Muscarinic Compounds and one or more compounds selected from the group consisting of Nonsteroidal Anti-inflammatory drugs, acetaminophen, opioids, and alpha-adrenergic compounds.
摘要翻译: PCT No.PCT / US96 / 19229 Sec。 371日期:1998年6月4日 102(e)1998年6月4日PCT 1996年12月5日PCT PCT。 公开号WO97 / 20819 日期:1997年6月12日本发明提供了使用选择毒蕈碱化合物和一种或多种选自非甾体抗炎药,对乙酰氨基酚,阿片样物质和α-肾上腺素能化合物的化合物治疗疼痛的组合物和方法。
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公开(公告)号:US5821371A
公开(公告)日:1998-10-13
申请号:US470788
申请日:1995-06-06
申请人: Charles A. Alt , Leander Merritt , Gary A. Rhodes , Roger L. Robey , Eldon E. Van Meter , John S. Ward , Charles H. Mitch
发明人: Charles A. Alt , Leander Merritt , Gary A. Rhodes , Roger L. Robey , Eldon E. Van Meter , John S. Ward , Charles H. Mitch
IPC分类号: C07D285/06 , A61K31/41 , A61K31/425 , A61K31/433 , A61K31/435 , A61K31/445 , A61K31/46 , A61P1/00 , A61P25/00 , A61P25/08 , A61P25/18 , A61P25/20 , A61P25/24 , A61P25/26 , A61P25/28 , A61P27/02 , A61P43/00 , C07D285/10 , C07D417/12 , C07D451/02 , C07D451/04 , C07D451/06 , C07D453/02 , C07D453/06 , C07D471/04 , C07D471/08 , C07D487/08
CPC分类号: C07D285/10 , C07D417/12 , C07D451/06 , C07D453/02 , C07D453/06 , C07D471/04 , C07D471/08 , C07D487/08
摘要: The present invention relates to therapeutically active azacyclic or azabicyclic compounds, a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful in treating diseases in the central nervous system caused by malfunctioning of the muscarinic cholinergic system.
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公开(公告)号:US5773452A
公开(公告)日:1998-06-30
申请号:US513851
申请日:1995-10-31
IPC分类号: A61K31/4439 , A61K31/445 , A61K31/4545 , A61K31/5377 , A61P25/04 , A61P25/20 , A61P25/28 , A61P27/02 , A61P27/06 , A61P29/00 , A61P43/00 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , A61K31/44
CPC分类号: C07D413/04 , C07D417/04 , C07D417/14 , Y10S514/913
摘要: The present invention relates to therapeutically active azabicyclic compounds of formula (1), wherein Z1 is oxygen or sulphur, a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful as stimulants of the cognitive function of forebrain and hippocampus of mammals and especially in the treatment of Alzheimer's disease, severe painful conditions and glaucoma. ##STR1##
摘要翻译: PCT No.PCT / DK94 / 00095 Sec。 371日期1995年10月31日 102(e)日期1995年10月31日PCT 1994年4月4日PCT PCT。 出版物WO94 / 20495 日期:1994年9月15日本发明涉及治疗活性的式(1)的氮杂双环化合物,其中Z1是氧或硫,其制备方法和包含该化合物的药物组合物。 新化合物可用作哺乳动物前脑和海马的认知功能的兴奋剂,特别是治疗阿尔茨海默病,严重的疼痛病症和青光眼。 (一)
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公开(公告)号:US5672709A
公开(公告)日:1997-09-30
申请号:US470789
申请日:1995-06-06
申请人: Charles A. Alt , Leander Merritt , Gary A. Rhodes , Roger L. Robey , Eldon E. Van Meter , John S. Ward , Charles H. Mitch
发明人: Charles A. Alt , Leander Merritt , Gary A. Rhodes , Roger L. Robey , Eldon E. Van Meter , John S. Ward , Charles H. Mitch
IPC分类号: C07D285/06 , A61K31/41 , A61K31/425 , A61K31/433 , A61K31/435 , A61K31/445 , A61K31/46 , A61P1/00 , A61P25/00 , A61P25/08 , A61P25/18 , A61P25/20 , A61P25/24 , A61P25/26 , A61P25/28 , A61P27/02 , A61P43/00 , C07D285/10 , C07D417/12 , C07D451/02 , C07D451/04 , C07D451/06 , C07D453/02 , C07D453/06 , C07D471/04 , C07D471/08 , C07D487/08 , C07F7/10
CPC分类号: C07D285/10 , C07D417/12 , C07D451/06 , C07D453/02 , C07D453/06 , C07D471/04 , C07D471/08 , C07D487/08
摘要: The present invention relates to therapeutically active azacyclic or azabicyclic compounds, a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful in treating diseases in the central nervous system caused by malfunctioning of the muscarinic cholinergic system.
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公开(公告)号:US5658932A
公开(公告)日:1997-08-19
申请号:US453605
申请日:1995-05-30
IPC分类号: A61K31/4439 , A61K31/445 , A61K31/4545 , A61K31/5377 , A61P25/04 , A61P25/20 , A61P25/28 , A61P27/02 , A61P27/06 , A61P29/00 , A61P43/00 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , A61K31/42 , A61K31/425
CPC分类号: C07D413/04 , C07D417/04 , C07D417/14 , Y10S514/913
摘要: The present invention relates to therapeutically active azacyclic compounds, a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful as stimulants of the cognitive function of the forebrain and hippocampus of mammals and especially in the treatment of Alzheimer's disease, severe painful conditions and glaucoma.
摘要翻译: 本发明涉及治疗活性的azacyclic化合物,其制备方法和包含该化合物的药物组合物。 新化合物可用作哺乳动物的前脑和海马的认知功能的兴奋剂,特别是在治疗阿尔茨海默病,严重的疼痛病症和青光眼中。
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公开(公告)号:US5559136A
公开(公告)日:1996-09-24
申请号:US455300
申请日:1995-05-30
IPC分类号: A61K31/4439 , A61K31/445 , A61K31/4545 , A61K31/5377 , A61P25/04 , A61P25/20 , A61P25/28 , A61P27/02 , A61P27/06 , A61P29/00 , A61P43/00 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , A61K31/44 , A61K31/41 , A61K31/425
CPC分类号: C07D413/04 , C07D417/04 , C07D417/14 , Y10S514/913
摘要: The present invention relates to therapeutically active azacyclic compounds. The novel compounds are useful as stimulants of the cognitive function of the forebrain and hippocampus of mammals and especially in the treatment of Alzheimer's disease, severe painful conditions and glaucoma.
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公开(公告)号:US5319087A
公开(公告)日:1994-06-07
申请号:US939794
申请日:1992-09-03
IPC分类号: C07D211/22 , C07D409/06 , C07D211/20
CPC分类号: C07D409/06 , C07D211/22
摘要: This invention provides trans-3,4 1-substituted-3-substituted-4-methyl-4-(3-substituted phenyl)piperidines as opioid antagonists capable of blocking the mu or kappa receptors in the brain.
摘要翻译: 本发明提供反式-3,4- 1-取代-3-取代-4-甲基-4-(3-取代苯基)哌啶作为能阻断脑中μ或κ受体的阿片样物质拮抗剂。
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公开(公告)号:US06429317B1
公开(公告)日:2002-08-06
申请号:US09117089
申请日:2000-09-05
申请人: Sean P. Hollinshead , Michael A. Staszak , John S. Ward , Joseph W. Wilson , Bret E. Huff , Philip F. Hughes , Jose S. Mendoza , Charles H. Mitch
发明人: Sean P. Hollinshead , Michael A. Staszak , John S. Ward , Joseph W. Wilson , Bret E. Huff , Philip F. Hughes , Jose S. Mendoza , Charles H. Mitch
IPC分类号: C07D20708
CPC分类号: C07D213/82 , C07C257/12 , C07C311/20 , C07C2602/08 , C07C2602/10 , C07D295/13 , C07D333/38 , C07D333/70 , C40B40/00
摘要: The present invention provides novel indane-like compounds which can be useful for treating psychosis and other conditions associated with the modulation of a muscarinic receptor. The invention provides formulations and methods for using the novel compounds.
摘要翻译: 本发明提供了可用于治疗与调节毒蕈碱受体相关的精神病和其它病症的新型吲哚类化合物。 本发明提供了使用新化合物的制剂和方法。
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公开(公告)号:US5665745A
公开(公告)日:1997-09-09
申请号:US470791
申请日:1995-06-06
申请人: Charles A. Alt , Leander Merritt , Gary A. Rhodes , Roger L. Robey , Eldon E. Van Meter , John S. Ward , Charles H. Mitch
发明人: Charles A. Alt , Leander Merritt , Gary A. Rhodes , Roger L. Robey , Eldon E. Van Meter , John S. Ward , Charles H. Mitch
IPC分类号: C07D285/06 , A61K31/41 , A61K31/425 , A61K31/433 , A61K31/435 , A61K31/445 , A61K31/46 , A61P1/00 , A61P25/00 , A61P25/08 , A61P25/18 , A61P25/20 , A61P25/24 , A61P25/26 , A61P25/28 , A61P27/02 , A61P43/00 , C07D285/10 , C07D417/12 , C07D451/02 , C07D451/04 , C07D451/06 , C07D453/02 , C07D453/06 , C07D471/04 , C07D471/08 , C07D487/08 , C07D417/14
CPC分类号: C07D285/10 , C07D417/12 , C07D451/06 , C07D453/02 , C07D453/06 , C07D471/04 , C07D471/08 , C07D487/08
摘要: The present invention relates to therapeutically active azacyclic or azabicyclic compounds, a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful in treating diseases in the central nervous system caused by malfunctioning of the muscarinic cholinergic system.
摘要翻译: 本发明涉及治疗活性的氮杂环或氮杂双环化合物,其制备方法和包含该化合物的药物组合物。 新型化合物可用于治疗由毒蕈碱胆碱能系统功能障碍引起的中枢神经系统疾病。
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