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公开(公告)号:US06777416B2
公开(公告)日:2004-08-17
申请号:US10149659
申请日:2002-10-22
申请人: Ulrich Niewöhner , Helmut Haning , Thomas Lampe , Mazen Es-Sayed , Gunter Schmidt , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Karl-Heinz Schlemmer
发明人: Ulrich Niewöhner , Helmut Haning , Thomas Lampe , Mazen Es-Sayed , Gunter Schmidt , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Karl-Heinz Schlemmer
IPC分类号: A61K31519
CPC分类号: C07D498/04 , A01N43/90
摘要: The invention relates to novel isoxazolo pyrimidinones of general formula (I), a method for producing the same and the pharmaceutical use thereof.
摘要翻译: 本发明涉及通式(I)的新的异恶唑嘧啶酮,其制备方法及其药物用途。
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公开(公告)号:US06683081B2
公开(公告)日:2004-01-27
申请号:US10149921
申请日:2002-10-21
申请人: Ulrich Niewöhner , Helmut Haning , Thomas Lampe , Mazen Es-Sayed , Gunter Schmidt , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Karl-Heinz Schlemmer
发明人: Ulrich Niewöhner , Helmut Haning , Thomas Lampe , Mazen Es-Sayed , Gunter Schmidt , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Karl-Heinz Schlemmer
IPC分类号: C07D48704
CPC分类号: C07D487/04
摘要: The invention relates to novel triazolotriazinones of the general formula (I), to a method for their production and to the pharmaceutical use thereof.
摘要翻译: 本发明涉及通式(I)的新型三唑并三嗪酮及其制备方法及其药物用途。
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公开(公告)号:US07091203B2
公开(公告)日:2006-08-15
申请号:US10892984
申请日:2004-07-15
申请人: Ulrich Niewöhner , Helmut Haning , Thomas Lampe , Mazen Es-Sayed , Gunter Schmidt , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Karl-Heinz Schlemmer
发明人: Ulrich Niewöhner , Helmut Haning , Thomas Lampe , Mazen Es-Sayed , Gunter Schmidt , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Karl-Heinz Schlemmer
IPC分类号: A01N43/66 , A61K31/53 , A61K31/535
CPC分类号: C07D487/04
摘要: The invention relates to imidazo[1,3,5]triazinones, a method for their production and methods of use, in particular as inhibitors of cyclic GMP metabolizing phosphodiesterases.
摘要翻译: 本发明涉及咪唑并[1,3,5]三嗪酮,其制备方法和使用方法,特别是作为环状GMP代谢磷酸二酯酶的抑制剂。
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公开(公告)号:US06803365B2
公开(公告)日:2004-10-12
申请号:US10168194
申请日:2002-11-04
申请人: Ulrich Niewöhner , Helmut Haning , Thomas Lampe , Mazen Es-Sayed , Gunter Schmidt , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Karl-Heinz Schlemmer
发明人: Ulrich Niewöhner , Helmut Haning , Thomas Lampe , Mazen Es-Sayed , Gunter Schmidt , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Karl-Heinz Schlemmer
IPC分类号: C07D48704
CPC分类号: C07D487/04
摘要: The invention relates to imidazo[1.3.5]triazinones, a method for their production and methods of use, in particular as inhibitors of cyclic GMP metabolizing phosphodiesterases.
摘要翻译: 本发明涉及咪唑并[1.3.5]三嗪酮,其制备方法和使用方法,特别是作为环状GMP代谢磷酸二酯酶的抑制剂。
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公开(公告)号:US06838459B1
公开(公告)日:2005-01-04
申请号:US10251939
申请日:2002-09-20
申请人: Ulrich Niewöhner , Mazen Es-Sayed , Helmut Haning , Thomas Schenke , Gunter Schmidt , Karl-Heinz Schlemmer , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn
发明人: Ulrich Niewöhner , Mazen Es-Sayed , Helmut Haning , Thomas Schenke , Gunter Schmidt , Karl-Heinz Schlemmer , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn
IPC分类号: A61K31/53 , A61K31/5377 , A61K31/539 , A61K31/55 , A61K31/5513 , A61K31/675 , A61P7/12 , A61P9/00 , A61P9/08 , A61P9/10 , A61P15/00 , A61P15/10 , A61P21/02 , A61P43/00 , C07D487/04 , C07D519/00 , C07F9/6561
CPC分类号: C07D487/04 , C07F9/6561
摘要: The present invention relates to 7-alkyl- and cycloalkyl-substituted imidazotriazinones, to processes for their preparation and to their use as medicaments, in particular as inhibitors of cGMP-metabolizing phosphodiesterases.
摘要翻译: 本发明涉及7-烷基 - 和环烷基取代的咪唑并三嗪酮,其制备方法和用作药物,特别是作为cGMP代谢磷酸二酯酶的抑制剂。
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公开(公告)号:US06476029B1
公开(公告)日:2002-11-05
申请号:US09720051
申请日:2001-03-23
申请人: Ulrich Niewöhner , Mazen Es-Sayed , Helmut Haning , Thomas Schenke , Gunter Schmidt , Karl-Heinz Schlemmer , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn
发明人: Ulrich Niewöhner , Mazen Es-Sayed , Helmut Haning , Thomas Schenke , Gunter Schmidt , Karl-Heinz Schlemmer , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn
IPC分类号: C07D48704
CPC分类号: C07D487/04 , C07F9/6561
摘要: The present invention relates to 7-alkyl- and cycloalkyl-substituted imidazotriazinones, to processes for their preparation and to their use as medicaments, in particular as inhibitors of cGMP-metabolizing phosphodiesterases.
摘要翻译: 本发明涉及7-烷基 - 和环烷基取代的咪唑并三嗪酮,其制备方法和用作药物,特别是作为cGMP代谢磷酸二酯酶的抑制剂。
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公开(公告)号:US06943163B2
公开(公告)日:2005-09-13
申请号:US10850510
申请日:2004-05-20
申请人: Ulrich Niewöhner , Mazen Es-Sayed , Helmut Haning , Thomas Schenke , Gunter Schmidt , Karl-Heinz Schlemmer , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn
发明人: Ulrich Niewöhner , Mazen Es-Sayed , Helmut Haning , Thomas Schenke , Gunter Schmidt , Karl-Heinz Schlemmer , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn
IPC分类号: A61K31/53 , A61K31/5377 , A61K31/539 , A61K31/55 , A61K31/5513 , A61K31/675 , A61P7/12 , A61P9/00 , A61P9/08 , A61P9/10 , A61P15/00 , A61P15/10 , A61P21/02 , A61P43/00 , C07D487/04 , C07D519/00 , C07F9/6561 , A61P9/12 , A61P13/08
CPC分类号: C07D487/04 , C07F9/6561
摘要: The present invention relates to 7-alkyl- and cycloalkyl-substituted imidazotriazinones, to processes for their preparation and to their use as medicaments, in particular as inhibitors of cGMP-metabolizing phosphodiesterases.
摘要翻译: 本发明涉及7-烷基 - 和环烷基取代的咪唑并三嗪酮,其制备方法和用作药物,特别是作为cGMP代谢磷酸二酯酶的抑制剂。
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公开(公告)号:US20050043303A1
公开(公告)日:2005-02-24
申请号:US10892984
申请日:2004-07-15
申请人: Ulrich Niewohner , Helmut Haning , Thomas Lampe , Mazen Es-Sayed , Gunter Schmidt , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Karl-Heinz Schlemmer
发明人: Ulrich Niewohner , Helmut Haning , Thomas Lampe , Mazen Es-Sayed , Gunter Schmidt , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Karl-Heinz Schlemmer
IPC分类号: A61K31/53 , A61K31/5377 , A61K31/539 , A61K31/55 , A61P7/00 , A61P7/02 , A61P9/00 , A61P9/06 , A61P9/10 , A61P9/12 , A61P13/00 , A61P13/02 , A61P13/08 , A61P15/00 , A61P15/08 , A61P15/10 , A61P25/00 , A61P25/20 , A61P25/28 , A61P43/00 , C07D487/04
CPC分类号: C07D487/04
摘要: The invention relates to imidazo[1,3,5]triazinones, a method for their production and methods of use, in particular as inhibitors of cyclic GMP metabolizing phosphodiesterases.
摘要翻译: 本发明涉及咪唑并[1,3,5]三嗪酮,其制备方法和使用方法,特别是作为环状GMP代谢磷酸二酯酶的抑制剂。
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公开(公告)号:US20050267112A1
公开(公告)日:2005-12-01
申请号:US11030605
申请日:2005-01-05
申请人: Ulrich Niewohner , Mazen Es-Sayed , Thomas Lampe , Helmut Haning , Gunter Schmidt , Karl-Heinz Schlemmer , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Maria Niewohner
发明人: Ulrich Niewohner , Mazen Es-Sayed , Thomas Lampe , Helmut Haning , Gunter Schmidt , Karl-Heinz Schlemmer , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn , Maria Niewohner
IPC分类号: A61K31/53 , A61K31/5377 , A61K31/539 , A61K31/662 , A61P7/02 , A61P7/10 , A61P9/00 , A61P9/06 , A61P9/08 , A61P9/10 , A61P9/12 , A61P9/14 , A61P13/00 , A61P13/02 , A61P13/08 , A61P15/00 , A61P15/10 , A61P25/00 , A61P25/14 , A61P25/16 , A61P25/28 , C07D487/04 , C07D519/00 , C07F9/6524
CPC分类号: C07D487/04
摘要: Novel imidazotriazinones of general formula a method for the production and the pharmaceutical use thereof are disclosed.
摘要翻译: 公开了通式的新型咪唑并三嗪酮的制备方法和药物用途。
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10.2-phenyl substituted imidazotriazinones as phosphodiesterase inhibitors 有权
标题翻译: 2-苯基取代的咪唑并三嗪酮作为磷酸二酯酶抑制剂公开(公告)号:US07704999B2
公开(公告)日:2010-04-27
申请号:US12004933
申请日:2007-12-21
申请人: Ulrich Niewöhner , Maria Niewöhner, legal representative , Mazen Es-Sayed , Helmut Haning , Thomas Schenke , Karl-Heinz Schlemmer , Jörg Keldenich , Erwin Bischoff , Elisabeth Perzborn , Klaus Dembowsky , Peter Serno , Marc Nowakowski
发明人: Ulrich Niewöhner , Mazen Es-Sayed , Helmut Haning , Thomas Schenke , Karl-Heinz Schlemmer , Jörg Keldenich , Erwin Bischoff , Elisabeth Perzborn , Klaus Dembowsky , Peter Serno , Marc Nowakowski
CPC分类号: C07D487/04 , C07F9/6561
摘要: The 2-phenyl-substituted imidazotriazinones having short, unbranched alkyl radicals in the 9-position are prepared from the corresponding 2-phenyl-imidazotriazinones by chlorosulphonation and subsequent reaction with the amines. The compounds inhibit cGMP-metabolizing phosphodiesterases and are suitable for use as active compounds in pharmaceuticals, for the treatment of cardiovascular and cerebrovascular disorders and/or disorders of the urogenital system, in particular for the treatment of erectile dysfunction.
摘要翻译: 通过氯磺化和随后与胺的反应,由相应的2-苯基 - 咪唑并三嗪酮制备在9-位上具有短的非支链烷基的2-苯基取代的咪唑并三嗪酮。 所述化合物抑制cGMP代谢磷酸二酯酶,并且适合用作药物中的活性化合物,用于治疗心血管和脑血管障碍和/或泌尿生殖系统疾病,特别是用于治疗勃起功能障碍。
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