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公开(公告)号:US5679672A
公开(公告)日:1997-10-21
申请号:US646249
申请日:1996-05-14
申请人: John J. Baldwin , David A. Claremon , Jason M. Elliott , Nigel Liverton , David C. Remy , Harold G. Selnick
发明人: John J. Baldwin , David A. Claremon , Jason M. Elliott , Nigel Liverton , David C. Remy , Harold G. Selnick
IPC分类号: A61K31/395 , A61K31/415 , A61K31/55 , A61P9/06 , C07D487/04 , C07D498/04 , C07D513/04
CPC分类号: C07D487/04
摘要: Compounds of structures (I) and (Ia) are Class III antiarrhythmic agents ##STR1##
摘要翻译: PCT No.PCT / US94 / 13546 Sec。 371日期:1996年5月14日 102(e)日期1996年5月14日PCT 1994年11月21日PCT PCT。 出版物WO95 / 14694 日期:1995年6月1日结构(I)和(Ia)的化合物是III类抗心律失常药物(I)
(Ia) -
公开(公告)号:US5441952A
公开(公告)日:1995-08-15
申请号:US42963
申请日:1993-04-05
申请人: David A. Claremon , Nigel Liverton
发明人: David A. Claremon , Nigel Liverton
IPC分类号: C07D243/24 , A61K31/55 , A61K31/551 , A61P7/02 , C07D401/06 , C07D211/62 , A61K38/00
CPC分类号: C07D401/06
摘要: Fibrinogen receptor antagonists of the ##STR1## are disclosed for use in inhibiting the binding of fibrinogen to blood platelets and for inhibiting the aggregation of blood platelets, for example ##STR2##
摘要翻译: 公开了用于抑制纤维蛋白原与血小板结合和抑制血小板聚集的纤维蛋白原受体拮抗剂,例如
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公开(公告)号:US5426185A
公开(公告)日:1995-06-20
申请号:US156331
申请日:1993-11-22
申请人: John J. Baldwin , David A. Claremon , Jason M. Elliott , Nigel Liverton , David C. Remy , Harold G. Selnick
发明人: John J. Baldwin , David A. Claremon , Jason M. Elliott , Nigel Liverton , David C. Remy , Harold G. Selnick
IPC分类号: A61K31/5513 , A61K31/55 , A61K31/551 , A61K38/00 , A61P9/00 , A61P9/06 , C07D243/14 , C07D243/24 , C07D401/04 , C07D401/12 , C07D403/12 , C07D405/04 , C07D405/12 , C07D409/12 , C07D413/10 , C07D413/12 , C07D471/04 , C07D487/04 , C07D495/04 , C07K5/06 , C07K5/078 , C07D243/12
CPC分类号: C07D401/04 , A61K31/55 , C07D243/14 , C07D243/24 , C07D401/12 , C07D403/12 , C07D405/04 , C07D405/12 , C07D409/12 , C07D413/10 , C07D413/12 , C07D471/04 , C07D487/04 , C07D495/04 , C07K5/06026 , C07K5/06139 , A61K38/00 , Y10S514/821
摘要: Benzo-(1,5)-diazepine derivatives with an amide or urea function in the 3-position are useful in the treatment of arrhythmia. The compounds have structural formulae: ##STR1##
摘要翻译: 具有3-位氨基或脲官能团的苯并(1,5) - 二氮杂衍生物可用于治疗心律失常。 化合物具有结构式:
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公开(公告)号:US06303637B1
公开(公告)日:2001-10-16
申请号:US09422500
申请日:1999-10-21
申请人: Jianming Bao , Andrew Kotliar , Frank Kayser , William H. Parsons , Kathleen M. Rupprecht , Christopher F. Claiborne , David A. Claremon , Nigel Liverton , Wayne J. Thompson
发明人: Jianming Bao , Andrew Kotliar , Frank Kayser , William H. Parsons , Kathleen M. Rupprecht , Christopher F. Claiborne , David A. Claremon , Nigel Liverton , Wayne J. Thompson
IPC分类号: A61K31445
CPC分类号: C07D211/96 , A61K31/445 , A61K31/47 , A61K31/52 , A61K31/535 , A61K31/70 , A61K38/13 , A61K45/06 , C07D211/26 , A61K31/365 , A61K31/16 , A61K2300/00
摘要: The present invention relates to a class of heterocyclic compounds of Formula I that are useful as potassium channel inhibitors to treat autoimmune disorders, cardiac arrhythmias, and the like.
摘要翻译: 本发明涉及可用作治疗自身免疫性疾病,心律失常等的钾通道抑制剂的一类式I的杂环化合物。
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公开(公告)号:US06194458B1
公开(公告)日:2001-02-27
申请号:US09422499
申请日:1999-10-21
申请人: Robert K. Baker , Jianming Bao , Frank Kayser , Andrew Kotliar , William H. Parsons , Kathleen M. Rupprecht , Christopher F. Claiborne , David A. Claremon , Nigel Liverton , Wayne J. Thompson
发明人: Robert K. Baker , Jianming Bao , Frank Kayser , Andrew Kotliar , William H. Parsons , Kathleen M. Rupprecht , Christopher F. Claiborne , David A. Claremon , Nigel Liverton , Wayne J. Thompson
IPC分类号: A61K3122
CPC分类号: C07D307/79 , A61K45/06 , C07C235/60 , C07C271/20
摘要: This invention relates to benzamide potassium channel inhibitors of general structural Formula I. The compounds of this invention are useful in the treatment of autoimmune diseases, the prevention of rejection of foreign organ transplants and related afflictions, diseases and illnesses, and cardiac arrhythmias. Also within the scope of this invention are pharmaceutical formulations comprising a compound of Formula I and a pharmaceutical carrier, as well as pharmaceutical formulations comprising a compound of Formula I, one or more immunosuppressive compounds and a pharmaceutical carrier.
摘要翻译: 本发明涉及一般结构式I的苯甲酰胺钾通道抑制剂。本发明的化合物可用于治疗自身免疫性疾病,预防外来器官移植排斥和相关疾病,疾病和疾病以及心律失常。 也包括本发明范围的药物制剂,其包含式I化合物和药物载体,以及包含式I化合物,一种或多种免疫抑制化合物和药物载体的药物制剂。
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6.N-(2,4-Dioxo-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3yl) -3- amides 失效
标题翻译: N-(2,4-二氧代-2,3,4,5-四氢-1H-1,5-苯并二氮杂-3基)-3-酰胺公开(公告)号:US5691331A
公开(公告)日:1997-11-25
申请号:US474801
申请日:1995-06-07
IPC分类号: A61P9/06 , A61K31/55 , C07D243/12
CPC分类号: C07D243/12
摘要: This invention is concerned with novel compounds represented by structural formula I ##STR1## which are useful in the treatment of arrhythmia.
摘要翻译: 本发明涉及可用于治疗心律失常的结构式I表示的新化合物。
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公开(公告)号:US5631251A
公开(公告)日:1997-05-20
申请号:US481662
申请日:1995-06-07
IPC分类号: A61K31/55 , A61K31/551 , A61P9/06 , C07D243/14 , C07D243/24
CPC分类号: C07D243/14
摘要: This invention is concerned with novel compounds represented by structural formula I ##STR1## Z is C.sub.0-6 alkyl; and R.sup.1 is phenyl or mono or disubstituted phenyl, where the substitutents are Cl, and CF.sub.3,or pharmaceutically acceptable salts, hydrates and crystal forms thereof which are useful in the treatment of arrhythmia.
摘要翻译: 本发明涉及由结构式I表示的新化合物,其中Z是C0-6烷基; 并且R 1是苯基或单取代或二取代的苯基,其中取代基是Cl,和CF 3,或其药学上可接受的盐,水合物和晶体形式,其可用于治疗心律失常。
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公开(公告)号:US5428157A
公开(公告)日:1995-06-27
申请号:US155670
申请日:1993-11-22
申请人: John J. Baldwin , David A. Claremon , Jason M. Elliott , Nigel Liverton , David C. Remy , Harold G. Selnick
发明人: John J. Baldwin , David A. Claremon , Jason M. Elliott , Nigel Liverton , David C. Remy , Harold G. Selnick
IPC分类号: A61K31/55 , A61K31/551 , A61P9/06 , A61P9/08 , A61P9/10 , C07D243/14 , C07D243/12
CPC分类号: C07D243/14
摘要: 3-Acylamino-5-Aminobenzo[1,5]diazepines are useful in the treatment of arrhythmia. The compounds have structural formulae: ##STR1##
摘要翻译: 3-酰基氨基-5-氨基苯并[1,5]二氮杂可用于治疗心律失常。 化合物具有结构式:
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公开(公告)号:US08338449B2
公开(公告)日:2012-12-25
申请号:US12753572
申请日:2010-04-02
申请人: B. Wesley Trotter , Christopher Claiborne , Gerald S. Ponticello , Charles J. McIntyre , Nigel Liverton , David A. Claremon
发明人: B. Wesley Trotter , Christopher Claiborne , Gerald S. Ponticello , Charles J. McIntyre , Nigel Liverton , David A. Claremon
IPC分类号: C07D471/02 , A61K31/47
CPC分类号: C07D217/24 , C07D455/04 , C07D471/04
摘要: The present invention relates to compounds having the structure useful as potassium channel inhibitors to treat cardiac arrhythmias, and the like.
摘要翻译: 本发明涉及具有用作治疗心律失常的钾通道抑制剂的结构的化合物等。
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公开(公告)号:US20100256698A1
公开(公告)日:2010-10-07
申请号:US12753572
申请日:2010-04-02
申请人: B. Wesley Trotter , Christopher Claiborne , Gerald S. Ponticello , Charles J. McIntyre , Nigel Liverton , David A. Claremon
发明人: B. Wesley Trotter , Christopher Claiborne , Gerald S. Ponticello , Charles J. McIntyre , Nigel Liverton , David A. Claremon
IPC分类号: A61N1/36 , C07D217/24 , A61K31/4745 , A61K31/4704 , A61K31/70 , A61K31/616 , A61K31/727 , A61K31/4365 , A61P9/00
CPC分类号: C07D217/24 , C07D455/04 , C07D471/04
摘要: The present invention relates to compounds having the structure useful as potassium channel inhibitors to treat cardiac arrhythmias, and the like.
摘要翻译: 本发明涉及具有用作治疗心律失常的钾通道抑制剂的结构的化合物等。
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