-
1.Pyrrolo (2.1a)dihydroisoquinolines and their use as phosphodiesterase 10a inhibitors 失效
标题翻译: 吡咯(2.1a)二氢异喹啉及其作为磷酸二酯酶10a抑制剂的用途公开(公告)号:US06930114B2
公开(公告)日:2005-08-16
申请号:US10451707
申请日:2001-12-04
申请人: Maria Theresia Niewöhner , Marcus Bauser , Jens-Kerim Ergüden , Dietmar Flubacher , Paul Naab , Thorsten-Oliver Repp , Jürgen Stoltefuss , Nils Burkhardt , Andrea Sewing , Michael Schauer , Karl-Heinz Schlemmer , Olaf Weber , Stephen J. Boyer , Mark Miglarese
发明人: Ulrich Niewöhner
IPC分类号: A61K31/4745 , A61P35/00 , A61P43/00 , C07D471/04
CPC分类号: C07D471/04
摘要: The present invention relates to pyrrolo[2.1-a]dihydroisoquinolines which are inhibitors of phosphodiesterase 10a and can be used for combating cancer.
摘要翻译: 本发明涉及吡咯并[2.1-a]二氢异喹啉,它们是磷酸二酯酶10a的抑制剂,可用于抗癌。
-
公开(公告)号:US06936609B2
公开(公告)日:2005-08-30
申请号:US10481281
申请日:2002-06-10
申请人: Jens-Kerim Ergüden , Marcus Bauser , Nils Burkhardt , Dietmar Flubacher , Arno Friedl , Irene Gerlach , Volker Hinz , Reinhard Jork , Paul Naab , Maria Theresia Niewöhner , Thorsten Oliver Repp , Karl-Heinz Schlemmer , Jürgen Stoltefuss , David Brückner , Martin Hendrix , Dagmar Schauss , Adrian Tersteegen
发明人: Ulrich Niewöhner
IPC分类号: A61K31/53 , A61K31/5377 , A61P25/00 , A61P25/16 , A61P25/28 , C07D487/04 , A61K31/415
CPC分类号: C07D487/04
摘要: The invention relates to new imidazotriazines, processes for their preparation, and their use for the production of medicaments for the treatment and/or prophylaxis of neurodegenerative disorders, in particular Parkinson's disease.
摘要翻译: 本发明涉及新的咪唑三嗪,其制备方法及其用于生产用于治疗和/或预防神经变性疾病,特别是帕金森病的药物的用途。
-
公开(公告)号:US06696451B1
公开(公告)日:2004-02-24
申请号:US09673592
申请日:2000-10-18
申请人: Jürgen Stoltefuss , Siegfired Goldmann , Thomas Krämer , Karl-Heinz Schlemmer , Ulrich Niewöhner , Arnold Paessens , Erwin Graef , Stefan Lettmann , Karl Deres , Olaf Weber , Jörn Stölting
发明人: Jürgen Stoltefuss , Siegfired Goldmann , Thomas Krämer , Karl-Heinz Schlemmer , Ulrich Niewöhner , Arnold Paessens , Erwin Graef , Stefan Lettmann , Karl Deres , Olaf Weber , Jörn Stölting
IPC分类号: C07D40104
CPC分类号: C07D239/22 , C07D213/78 , C07D213/84 , C07D401/04 , C07D401/14
摘要: The invention relates to compounds of the general formulae (I) and (Ia) The invention furthermore relates to processes for preparing the compounds of the formulae (I) and (Ia) and to their use as medicaments, in particular for the treatment and prophylaxis of hepatitis B.
摘要翻译: 本发明涉及通式(I)和(Ia)的化合物。本发明还涉及制备式(I)和(Ia)化合物的方法及其作为药物的用途,特别是用于治疗和预防 的乙型肝炎
-
公开(公告)号:US07115602B2
公开(公告)日:2006-10-03
申请号:US10160352
申请日:2002-05-30
申请人: Cristina Alonso-Alija , Heike Gielen , Martin Hendrix , Maria Niewöhner , Dagmar Schauss , Hilmar Bischoff , Nils Burkhardt , Volker Geiss , Karl-Heinz Schlemmer , Nigel J. Cuthbert , Mary F. Fitzgerald , Graham Sturton
发明人: Ulrich Niewöhner
IPC分类号: A01N43/64 , A61K31/53 , C07D487/00
CPC分类号: C07D253/07 , C07D487/04
摘要: The invention relates to 7-(4-tert butyl-cyclohexyl)-imidazotriazinones, processes for their preparation and their use in medicaments, esp. for the treatment and/or prophylaxis of inflammatory processes and/or immune diseases.
摘要翻译: 本发明涉及7-(4-叔丁基 - 环己基) - 咪唑并三嗪酮,其制备方法及其在药物中的应用, 用于治疗和/或预防炎症过程和/或免疫疾病。
-
公开(公告)号:US07514565B2
公开(公告)日:2009-04-07
申请号:US11639955
申请日:2006-12-15
申请人: Jürgen Stoltefuβ , Siegfried Goldmann , Thomas Krämer , Karl-Heinz Schlemmer , Ulrich Niewöhner , Maria Niewöhner , Arnold Paeβens , Erwin Graef , Stefan Lottmann , Karl Deres , Olaf Weber , Jörn Stölting
发明人: Jürgen Stoltefuβ , Siegfried Goldmann , Thomas Krämer , Karl-Heinz Schlemmer , Ulrich Niewöhner , Maria Niewöhner , Arnold Paeβens , Erwin Graef , Stefan Lottmann , Karl Deres , Olaf Weber , Jörn Stölting
IPC分类号: C07D213/58
CPC分类号: C07D239/22 , C07D213/78 , C07D213/84 , C07D401/04 , C07D401/14
摘要: The invention relates to compounds of the formule
摘要翻译: 本发明涉及形式的化合物
-
公开(公告)号:US06930108B2
公开(公告)日:2005-08-16
申请号:US10483462
申请日:2002-07-17
申请人: Maria Theresia Niewöhner , Erwin Bischoff , Helmut Haning , Afssaneh Rahbar , Tiemo-Joerg Bandel , Wolfgang Barth
发明人: Ulrich Niewöhner
IPC分类号: C07D487/04 , A61K31/00 , A61K31/53 , A61K31/5377 , A61K31/675 , A61P1/00 , A61P3/10 , A61P9/04 , A61P9/12 , A61P11/00 , A61P11/12 , A61P13/08 , A61P13/10 , A61P13/12 , A61P15/00 , A61P15/06 , A61P15/08 , A61P17/06 , A61P17/14 , A61P23/00 , A61P25/04 , A61P25/16 , A61P27/06 , A61P27/16 , A61P35/00 , C07D519/00
CPC分类号: A61K31/53 , A61K31/5377
摘要: The present invention relates to the use of known 2-phenyl-substituted imidazotriazinones having short, unbranched alkyl radicals in the 9-position and cGMP PDE-inhibitory properties for the production of medicaments for the treatment of cardiac insufficiency, psoriasis, female infertility, cancer, diabetes, ophthalmic disorders such as glaucoma, disorders of gastric motility, cystic fibrosis, premature labour, pulmonary hypertension, bladder disorders, prostate hyperplasia, nitrate-induced tolerance, pre-eclampsia, alopecia, Parkinson's disease, pain, tinnitus or the renal syndrome.
摘要翻译: 本发明涉及在9位具有短的无支链烷基的已知2-苯基取代的咪唑并三氮嗪酮和cGMP PDE抑制性质用于生产用于治疗心功能不全的药物,牛皮癣,女性不育症,癌症 糖尿病,眼科疾病如青光眼,胃动力障碍,囊性纤维化,早产,肺动脉高压,膀胱疾病,前列腺增生,硝酸盐诱导的耐受,先兆子痫,脱发,帕金森病,疼痛,耳鸣或肾综合征 。
-
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。
-
公开(公告)号:US06878708B2
公开(公告)日:2005-04-12
申请号:US10220560
申请日:2001-02-20
申请人: Maria Niewöhner , Mazen Es-Sayed , Thomas Lampe , Helmut Haning , Gunter Schmidt , Karl-Heinz Schlemmer , Erwin Bischoff , Klaus Dembowsky , Elisabeth Perzborn
发明人: Ulrich Niewöhner
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 , A61K31/4188
CPC分类号: C07D487/04
摘要: Novel imidazotriazinones of general formula (I), a method for the production and the pharmaceutical use thereof are disclosed.
摘要翻译: 公开了通式(I)的新型咪唑并三嗪酮,其制备方法和药物用途。
-
9.2-PHENYL SUBSTITUTED IMIDAZOTRIAZINONES AS PHOSPHODIESTERASE INHIBITORS 审中-公开
标题翻译: 作为磷酸二酯酶抑制剂的2-苯基取代的咪达唑仑公开(公告)号:US20110009367A1
公开(公告)日:2011-01-13
申请号:US12717443
申请日:2010-03-04
申请人: Ulrich Niewöhner , Maria Niewöhner , 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 , Maria Niewöhner , Mazen Es-Sayed , Helmut Haning , Thomas Schenke , Karl-Heinz Schlemmer , Jörg Keldenich , Erwin Bischoff , Elisabeth Perzborn , Klaus Dembowsky , Peter Serno , Marc Nowakowski
IPC分类号: A61K31/53 , C07D487/04 , A61K31/5377 , C07D491/113 , A61K31/683 , A61K31/551 , A61P9/00 , A61P13/00
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。
-
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。
-
-
-
-
-
-
-
-
-