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公开(公告)号:US07879839B2
公开(公告)日:2011-02-01
申请号:US11658114
申请日:2005-07-27
申请人: Christopher J. Dinsmore , Jeffrey M. Bergman , Douglas C. Beshore , B. Wesley Trotter , Kausik K. Nanda , Richard Isaacs , Linda S. Payne , Lou Anne Neilson , Zhicai Wu , Mark T. Bilodeau , Peter J. Manley , Adrienne E. Balitza
发明人: Christopher J. Dinsmore , Jeffrey M. Bergman , Douglas C. Beshore , B. Wesley Trotter , Kausik K. Nanda , Richard Isaacs , Linda S. Payne , Lou Anne Neilson , Zhicai Wu , Mark T. Bilodeau , Peter J. Manley , Adrienne E. Balitza
IPC分类号: C07D401/14 , A61K31/438
CPC分类号: C07D213/36 , C07D213/30 , C07D213/32 , C07D213/38 , C07D213/40 , C07D213/42 , C07D213/55 , C07D213/56 , C07D213/64 , C07D401/06 , C07D401/14 , C07D405/14 , C07D409/14 , C07D413/14 , C07D417/14 , C07D471/04 , C07D471/10 , C07D487/08 , C07D491/08
摘要: The present invention relates to compounds having the structure useful as potassium channel inhibitors to treat cardiac arrhythmias, and the like.
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公开(公告)号:US20100216834A1
公开(公告)日:2010-08-26
申请号:US12445594
申请日:2007-10-15
IPC分类号: A61K31/4375 , C07D471/14 , C07D471/04 , A61P31/18
CPC分类号: C07D471/14
摘要: Stereoisomers of compounds of Formula I are disclosed: wherein V1, V2, R5a, R5b, R5c, R8 and R9b are defined herein and wherein the stereoisomer contains 2 chiral centers in the 8-membered ring and one of the chiral centers is due to the presence of a chiral ring carbon. The isomers are inhibitors of HIV integrase and inhibitors of HIV replication, and are useful for the prophylaxis or treatment of infection by HIV and the prophylaxis, treatment, or delay in the onset or progression of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines.
摘要翻译: 公开了式I化合物的立体异构体:其中V1,V2,R5a,R5b,R5c,R8和R9b在本文中定义,其中立体异构体在8元环中含有2个手性中心,并且其中一个手性中心是由于 存在手性环碳。 异构体是HIV整合酶和HIV复制抑制剂的抑制剂,可用于预防或治疗艾滋病毒感染以及艾滋病的发病或进展的预防,治疗或延迟。 这些化合物用作抗感染和艾滋病作为化合物本身或以药学上可接受的盐的形式。 化合物及其盐可以用作药物组合物中的成分,任选与其它抗病毒剂,免疫调节剂,抗生素或疫苗组合使用。
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公开(公告)号:US07781457B2
公开(公告)日:2010-08-24
申请号:US10572343
申请日:2004-09-22
申请人: Richard Isaacs , Christopher J. Dinsmore , Charles J. McIntyre , Linda S. Payne , David A. Claremon
发明人: Richard Isaacs , Christopher J. Dinsmore , Charles J. McIntyre , Linda S. Payne , David A. Claremon
IPC分类号: C07D217/16 , A61K31/47
CPC分类号: C07D217/26 , C07D217/24 , C07D401/04 , C07D401/06 , C07D417/04
摘要: The present invention relates to compounds having the structure formula (I) useful as potassium channel inhibitors to treat cardiac arrhythmias, and the like.
摘要翻译: 本发明涉及具有结构式(I)的化合物,其可用作治疗心律失常的钾通道抑制剂等。
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公开(公告)号:US20090054399A1
公开(公告)日:2009-02-26
申请号:US11920032
申请日:2006-05-05
申请人: Joseph P. Vacca , John S. Wai , Linda S. Payne , Richard C.A. Isaacs , Wei Han , Melissa Egbertson , Richard Pracitto
发明人: Joseph P. Vacca , John S. Wai , Linda S. Payne , Richard C.A. Isaacs , Wei Han , Melissa Egbertson , Richard Pracitto
IPC分类号: A61K31/5383 , C07D471/14 , A61K31/551 , A61K31/4985 , A61K31/4375 , C07D498/14
CPC分类号: C07D471/14 , A61K31/4353 , A61K31/4375 , C07D498/14
摘要: Tricyclic compounds of Formula (I) are inhibitors of HIV integrase and inhibitors of HIV replication: wherein bond a, ring A, R1, R2 and R3 are defined herein. The compounds are useful for the prophylaxis or treatment of infection by HIV and the prophylaxis, treatment, or delay in the onset of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines.
摘要翻译: 式(I)的三环化合物是HIV整合酶和HIV复制抑制剂的抑制剂:其中键A,环A,R 1,R 2和R 3在本文中定义。 该化合物可用于预防或治疗艾滋病毒感染以及艾滋病的预防,治疗或延迟。 这些化合物用作抗感染和艾滋病作为化合物本身或以药学上可接受的盐的形式。 化合物及其盐可以用作药物组合物中的成分,任选与其它抗病毒剂,免疫调节剂,抗生素或疫苗组合使用。
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公开(公告)号:US20110275621A1
公开(公告)日:2011-11-10
申请号:US13107512
申请日:2011-05-13
申请人: Joseph P. Vacca , John S. Wai , Linda S. Payne
发明人: Joseph P. Vacca , John S. Wai , Linda S. Payne
IPC分类号: A61K31/4375 , C07D498/14 , A61P37/00 , A61K31/5383 , A61K31/5377 , A61P31/18 , C07D471/14 , A61K31/4985
CPC分类号: C07D471/14 , A61K31/4353 , A61K31/4375 , C07D498/14
摘要: Tricyclic compounds of Formula I are inhibitors of HIV integrase and inhibitors of HIV replication: wherein bond a, ring A, R1, R2 and R3 are defined herein. The compounds are useful for the prophylaxis or treatment of infection by HIV and the prophylaxis, treatment, or delay in the onset of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines.
摘要翻译: 式I的三环化合物是HIV整合酶和HIV复制抑制剂的抑制剂:其中键A,环A,R 1,R 2和R 3在本文中定义。 该化合物可用于预防或治疗艾滋病毒感染以及艾滋病的预防,治疗或延迟。 这些化合物用作抗感染和艾滋病作为化合物本身或以药学上可接受的盐的形式。 化合物及其盐可以用作药物组合物中的成分,任选与其它抗病毒剂,免疫调节剂,抗生素或疫苗组合使用。
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公开(公告)号:US07968564B2
公开(公告)日:2011-06-28
申请号:US12760638
申请日:2010-04-15
IPC分类号: C07D455/00 , A01N43/42 , A61K31/44
CPC分类号: C07D471/14 , A61K31/4353 , A61K31/4375 , C07D498/14
摘要: Tricyclic compounds of Formula I are inhibitors of HIV integrase and inhibitors of HIV replication: wherein bond a, ring A, R1, R2 and R3 are defined herein. The compounds are useful for the prophylaxis or treatment of infection by HIV and the prophylaxis, treatment, or delay in the onset of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines.
摘要翻译: 式I的三环化合物是HIV整合酶和HIV复制抑制剂的抑制剂:其中键A,环A,R 1,R 2和R 3在本文中定义。 该化合物可用于预防或治疗艾滋病毒感染以及艾滋病的预防,治疗或延迟。 这些化合物用作抗感染和艾滋病作为化合物本身或以药学上可接受的盐的形式。 化合物及其盐可以用作药物组合物中的成分,任选与其它抗病毒剂,免疫调节剂,抗生素或疫苗组合使用。
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公开(公告)号:US20100204201A1
公开(公告)日:2010-08-12
申请号:US12760638
申请日:2010-04-15
IPC分类号: A61K31/553 , C07D471/14 , A61K31/4375 , A61P31/18 , A61K31/551 , A61K31/4985 , A61K31/5365 , C07D498/14
CPC分类号: C07D471/14 , A61K31/4353 , A61K31/4375 , C07D498/14
摘要: Tricyclic compounds of Formula I are inhibitors of HIV integrase and inhibitors of HIV replication: wherein bond a, ring A, R1, R2 and R3 are defined herein. The compounds are useful for the prophylaxis or treatment of infection by HIV and the prophylaxis, treatment, or delay in the onset of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines.
摘要翻译: 式I的三环化合物是HIV整合酶和HIV复制抑制剂的抑制剂:其中键A,环A,R 1,R 2和R 3在本文中定义。 该化合物可用于预防或治疗艾滋病毒感染以及艾滋病的预防,治疗或延迟。 这些化合物用作抗感染和艾滋病作为化合物本身或以药学上可接受的盐的形式。 化合物及其盐可以用作药物组合物中的成分,任选与其它抗病毒剂,免疫调节剂,抗生素或疫苗组合使用。
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公开(公告)号:US07741315B2
公开(公告)日:2010-06-22
申请号:US11920032
申请日:2006-05-05
IPC分类号: A01N43/00 , A61K31/33 , C07D491/00
CPC分类号: C07D471/14 , A61K31/4353 , A61K31/4375 , C07D498/14
摘要: Tricyclic compounds of Formula (I) are inhibitors of HIV integrase and inhibitors of HIV replication: wherein bond a, ring A, R1, R2 and R3 are defined herein. The compounds are useful for the prophylaxis or treatment of infection by HIV and the prophylaxis, treatment, or delay in the onset of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines.
摘要翻译: 式(I)的三环化合物是HIV整合酶和HIV复制抑制剂的抑制剂:其中键A,环A,R 1,R 2和R 3在本文中定义。 该化合物可用于预防或治疗艾滋病毒感染以及艾滋病的预防,治疗或延迟。 这些化合物用作抗感染和艾滋病作为化合物本身或以药学上可接受的盐的形式。 化合物及其盐可以用作药物组合物中的成分,任选与其它抗病毒剂,免疫调节剂,抗生素或疫苗组合使用。
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