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1. 发明申请

US20050171070A1 Stable salts of o-acetylsalicylic acid containing basic amino acids II 审中-公开
标题翻译：含有碱性氨基酸的邻乙酰水杨酸的稳定盐II
公开(公告)号：US20050171070A1
公开(公告)日：2005-08-04
申请号：US10501677
申请日：2003-01-07
申请人： Felix Ecker , Ralf Bullesbach , Wolfram Ledwoch , Gerhard Franckowiak , Marianne Petersen-Braun
发明人： Felix Ecker , Ralf Bullesbach , Wolfram Ledwoch , Gerhard Franckowiak , Marianne Petersen-Braun
IPC分类号： A61K9/00 , A61K9/16 , A61K9/20 , A61K9/48 , A61K31/192 , A61K45/00 , A61K47/10 , A61K47/18 , A61K47/26 , A61K47/46 , A61P1/16 , A61P3/10 , A61P9/00 , A61P9/10 , A61P19/02 , A61P21/00 , A61P25/04 , A61P25/06 , A61P25/28 , A61P29/00 , A61P31/04 , A61P31/18 , A61P35/00 , C07C69/157 , C07C229/26 , A61K31/60 , A61K31/198
CPC分类号： A61K9/1688 , A61K9/0056 , A61K9/2018 , C07C229/26
摘要： The present invention relates to improved compositions comprising stable salts of O-acetylsalicylic acid with basic amino acids, to pharmaceuticals comprising them and to their use for preparing pharmaceuticals.
摘要翻译：本发明涉及包含O-乙酰水杨酸与碱性氨基酸的稳定盐的改进组合物，包括它们的药物及其制备药物的用途。

2. 发明授权

US06773724B2 Stable salts of O-acetylsalicylic acid with basic amino acids 有权
标题翻译： O-乙酰水杨酸与碱性氨基酸的稳定盐
公开(公告)号：US06773724B2
公开(公告)日：2004-08-10
申请号：US09906497
申请日：2001-07-16
申请人： Gerhard Franckowiak , Hubert Appolt , Gregor Leifker , Hans-Peter Wirges , Wolfram Ledwoch
发明人： Gerhard Franckowiak , Hubert Appolt , Gregor Leifker , Hans-Peter Wirges , Wolfram Ledwoch
IPC分类号： A61K914
CPC分类号： A61K31/616 , C07C229/26
摘要： The present invention relates to stable salts of O-acetylsalicylic acid with basic amino acids, a process for their preparation and their use as medicaments.
摘要翻译：本发明涉及O-乙酰水杨酸与碱性氨基酸的稳定盐，其制备方法及其作为药物的用途。

3. 发明授权

US08063243B2 Stable active compound complex of salts of o-acetylsalicylic acid with basic amino acids and glycine 有权
标题翻译：邻乙酰水杨酸与碱性氨基酸和甘氨酸的稳定的活性复合物
公开(公告)号：US08063243B2
公开(公告)日：2011-11-22
申请号：US11921339
申请日：2006-05-20
申请人： Gerhard Franckowiak , Wolfram Ledwoch , Eberhard Schweinheim , Yutaka Hayauchi
发明人： Gerhard Franckowiak , Wolfram Ledwoch , Eberhard Schweinheim , Yutaka Hayauchi
IPC分类号： C07C65/10
CPC分类号： A61K31/616 , A61K31/198 , C07C69/157 , C07C227/42 , C07C229/08 , C07C229/26
摘要： The present invention relates to stable active compound complexes of salts of o-acetylsalicylic acid with basic amino acids and glycine, to a process for their preparation and to their use as medicaments.
摘要翻译：本发明涉及邻乙酰水杨酸与碱性氨基酸和甘氨酸的稳定的活性化合物络合物，其制备方法和用作药物。

4. 发明申请

US20090306024A1 Combination preparations of o-acetylsalicylic acid salts 审中-公开
标题翻译：邻乙酰水杨酸盐的组合制剂
公开(公告)号：US20090306024A1
公开(公告)日：2009-12-10
申请号：US12090179
申请日：2006-10-04
申请人： Wolfram Ledwoch , Claus Gert Haase , Gerhard Franckowiak , Heike Wagner , Yutaka Hayauchi
发明人： Wolfram Ledwoch , Claus Gert Haase , Gerhard Franckowiak , Heike Wagner , Yutaka Hayauchi
IPC分类号： A61K31/60 , A61P9/00
CPC分类号： A61K9/2077 , A61K9/2054 , A61K9/4808 , A61K9/5084 , A61K31/366 , A61K31/40 , A61K31/44 , A61K31/60 , A61K47/542 , A61K2300/00
摘要： The present invention relates to a fixed combination comprising a salt of o-acetylsalicylic acid with a basic amino acid as component A and an HMG-CoA reductase inhibitor as component B, a medicament comprising this combination and a process for its production.
摘要翻译：本发明涉及包含邻乙酰水杨酸与碱性氨基酸作为组分A的盐和作为组分B的HMG-CoA还原酶抑制剂的固定组合物，包含该组合的药物及其生产方法。

5. 发明申请

US20090226524A1 Stable active compound complex of salts of o-acetylsalicylic acid with basic amino acids and glycine 有权
标题翻译：邻乙酰水杨酸与碱性氨基酸和甘氨酸的稳定的活性复合物
公开(公告)号：US20090226524A1
公开(公告)日：2009-09-10
申请号：US11921339
申请日：2006-05-20
申请人： Gerhard Franckowiak , Wolfram Ledwoch , Eberhard Schweinheim , Yutaka Hayauchi
发明人： Gerhard Franckowiak , Wolfram Ledwoch , Eberhard Schweinheim , Yutaka Hayauchi
IPC分类号： A61K9/14 , A61K31/60 , A61P9/10
CPC分类号： A61K31/616 , A61K31/198 , C07C69/157 , C07C227/42 , C07C229/08 , C07C229/26
摘要： The present invention relates to stable active compound complexes of salts of o-acetylsalicylic acid with basic amino acids and glycine, to a process for their preparation and to their use as medicaments.
摘要翻译：本发明涉及邻乙酰水杨酸与碱性氨基酸和甘氨酸的稳定的活性化合物络合物，其制备方法和用作药物。

6. 发明授权

US07449198B2 Stable salts of O-acetylsalicylic acid with basic amino acids 失效
标题翻译： O-乙酰水杨酸与碱性氨基酸的稳定盐
公开(公告)号：US07449198B2
公开(公告)日：2008-11-11
申请号：US10915652
申请日：2004-08-09
申请人： Gerhard Franckowiak , Hubert Appolt , Gregor Leifker , Hans-Peter Wirges , Wolfram Ledwoch
发明人： Gerhard Franckowiak , Hubert Appolt , Gregor Leifker , Hans-Peter Wirges , Wolfram Ledwoch
IPC分类号： A61K9/14 , A61K9/50 , A61K9/00
CPC分类号： A61K31/616 , C07C229/26
摘要： The present invention relates to stable salts of O-acetylsalicylic acid with basic amino acids, a process for their preparation and their use as medicaments.
摘要翻译：本发明涉及O-乙酰水杨酸与碱性氨基酸的稳定盐，其制备方法及其作为药物的用途。

7. 发明申请

US20050009791A1 Stable salts of O-acetylsalicylic acid with basic amino acids 失效
标题翻译： O-乙酰水杨酸与碱性氨基酸的稳定盐
公开(公告)号：US20050009791A1
公开(公告)日：2005-01-13
申请号：US10915652
申请日：2004-08-09
申请人： Gerhard Franckowiak , Hubert Appolt , Gregor Leifker , Hans-Peter Wirges , Wolfram Ledwoch
发明人： Gerhard Franckowiak , Hubert Appolt , Gregor Leifker , Hans-Peter Wirges , Wolfram Ledwoch
IPC分类号： A61K9/16 , A61K31/616 , A61K45/00 , A61K47/18 , A61P9/10 , A61P19/00 , A61P19/02 , A61P25/00 , A61P25/04 , A61P25/06 , A61P29/00 , C07C69/157 , C07C229/26 , C07D233/64 , A61K31/60
CPC分类号： A61K31/616 , C07C229/26
摘要： The present invention relates to stable salts of O-acetylsalicylic acid with basic amino acids, a process for their preparation and their use as medicaments.
摘要翻译：本发明涉及O-乙酰水杨酸与碱性氨基酸的稳定盐，其制备方法及其作为药物的用途。

8. 发明授权

US4645775A Positive inotropic 3-nitro-5-substituted ester and thioester-1,4-dihydropyridines 失效
标题翻译：正性收缩性3-硝基-5-取代酯和硫酯-1,4-二氢吡啶
公开(公告)号：US4645775A
公开(公告)日：1987-02-24
申请号：US734502
申请日：1985-05-15
申请人： Jurgen Stoltefuss , Fred R. Heiker , Gerhard Franckowiak , Matthias Schramm , Gunter Thomas , Rainer Gross
发明人： Jurgen Stoltefuss , Fred R. Heiker , Gerhard Franckowiak , Matthias Schramm , Gunter Thomas , Rainer Gross
IPC分类号： A61K31/4427 , A61K31/455 , A61P9/04 , A61P9/12 , C07D211/90 , C07D401/12 , C07D413/04
CPC分类号： C07D401/12 , C07D211/90 , C07D413/04
摘要： Novel 3-nitro-dihydropyridine derivatives of the formula ##STR1## in which R.sub.1 and R.sub.2 each independently is hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.12 -alkoxy, C.sub.1 -C.sub.4 -halogenoalkoxy, halogen, nitro, C.sub.1 -C.sub.4 -halogenoalkyl, C.sub.1 -C.sub.4 -halogenoalkylmercapto, ##STR2## Z is oxygen or sulphur, R.sub.4 and R.sub.5 each independently is hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.6 -alkoxy, halogen, C.sub.1 -C.sub.4 -halogenoalkyl, C.sub.1 -C.sub.4 -halogenoalkoxy or nitro, orR.sub.1 and R.sub.2, together with 2 C atoms of the phenyl ring form the ring ##STR3## X is oxygen or sulphur, A is a hydrocarbon radical with up to 12 C atoms which optionally contains one or two identical or different chain members from the group comprising O, S and CO and/or which is optionally substituted by hydroxyl or aliphatic acyloxy with up to 4 C atoms,R.sub.3 is --O--COR.sub.6, --S--CO--R.sub.6, SH, OH , NH.sub.2, ##STR4## NH--COR.sub.6, COOR.sub.6, NR.sub.7 R.sub.8 or CONR.sub.7 R.sub.8, R.sub.6 is hydrogen or an aliphatic radical with up to 6 C atoms or a phenyl radical, andR.sub.7 and R.sub.8 each independently is hydrogen or an aliphatic radical with up to 6 C atoms or a phenyl radical,or a physiologically acceptable salts thereof, which are active in circulation and exhibit positive inotropic activity.
摘要翻译：其中R 1和R 2各自独立地为氢，C 1 -C 4 - 烷基，C 1 -C 12 - 烷氧基，C 1 -C 4 - 卤代烷氧基，卤素，硝基，C 1 -C 4 - 卤代烷基的新颖的3-硝基 - 二氢吡啶衍生物，C 1 -C 4卤代烷基巯基，Z为氧或硫，R 4和R 5各自独立地为氢，C 1 -C 4 - 烷基，C 1 -C 6 - 烷氧基，卤素，C 1 -C 4 - 卤代烷基，C 1 -C 4卤代烷氧基或硝基或R1和R2与苯环的2 C原子一起形成环，X是氧或硫，A是具有至多12个C原子的烃基，其任选地含有一个或两个相同或不同的链成员由包含O，S和CO的基团和/或其任选被具有至多4个C原子的羟基或脂族酰氧基取代，R 3是-O-COR 6，-S-CO-R 6，SH，OH，NH 2， > NH-COR 6，COOR 6，NR 7 R 8或CONR 7 R 8，R 6是氢或具有至多6个C原子或苯基的脂族基团，并且R 7和R 8各自独立地为氢或至多6个碳原子的脂族基团 oms或苯基或其生理上可接受的盐，其在循环中具有活性并表现出正性肌力活性。

9. 发明授权

US4540684A 3-Nitro-5-amide-1,4-dihydropyridines with positive inotropic activity 失效
标题翻译：具有正性肌力活性的3-硝基-5-酰胺-1,4-二氢吡啶
公开(公告)号：US4540684A
公开(公告)日：1985-09-10
申请号：US612093
申请日：1984-05-18
申请人： Jurgen Stoltefuss , Gerhard Franckowiak , Horst Boshagen , Siegfried Goldmann , Matthias Schramm , Gunter Thomas , Rainer Gross
发明人： Jurgen Stoltefuss , Gerhard Franckowiak , Horst Boshagen , Siegfried Goldmann , Matthias Schramm , Gunter Thomas , Rainer Gross
IPC分类号： A61K31/455 , A61P3/08 , A61P9/02 , A61P9/04 , C07D211/90 , C07D211/98 , A61K31/70 , C07D405/12
CPC分类号： C07D211/90
摘要： A 1,4-dihydropyridine derivative of the formula ##STR1## in which R and R.sub.1 each independently is hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 to C.sub.12 -alkoxy, C.sub.1 -C.sub.4 -halogenoalkoxy, halogen, nitro, trifluoromethyl, ##STR2## X is oxygen or sulphur, R.sub.4 and R.sub.5 each independently is hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.6 -alkoxy, halogen, trifluoromethyl, amino or nitro, andR.sub.2 and R.sub.3 each independently is hydrogen, a C.sub.1 -C.sub.10 -alkyl, C.sub.2 -C.sub.10 -alkenyl or C.sub.3 -C.sub.10 -alkinyl radical which is optionally substituted by halogen, hydroxyl, C.sub.1 -C.sub.4 -alkoxy, amino, mono- and di-C.sub.1 -C.sub.4 -alkylamino, carbo-C.sub.1 -C.sub.6 -alkoxy and/or nitro, a C.sub.3 to C.sub.6 -membered cycloalkyl radical, a phenyl radical which is optionally substituted by C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.6 -alkoxy, halogen, amino and/or nitro, or a phenyl-C.sub.1 -C.sub.3 -alkyl radical, or a carbohydrate radical which is optionally bonded via a C.sub.1 -C.sub.8 -alkyl chain to the amide nitrogen atomor a pharmaceutically acceptable acid addition salt thereof, which improves the contractility of the heart, raises the blood pressure, lowers the blood sugar, reduces the swelling of mucous membranes and affects the salt and fluid balances of a patient.
摘要翻译：其中R和R 1各自独立地为氢，C 1 -C 4 - 烷基，C 1 -C 12 - 烷氧基，C 1 -C 4卤代烷氧基，卤素，硝基，三氟甲基， X是氧或硫，R4和R5各自独立地是氢，C1-C4-烷基，C1-C6-烷氧基，卤素，三氟甲基，氨基或硝基，R2和R3各自独立地是氢，C1-C10 - 烷基，C 2 -C 10 - 烯基或C 3 -C 10 - 炔基，其任选被卤素，羟基，C 1 -C 4 - 烷氧基，氨基，单 - 和二-C 1 -C 4 - 烷基氨基，C 1 -C 6 - 和/或硝基，C3至C6元环烷基，任选被C 1 -C 4 - 烷基，C 1 -C 6 - 烷氧基，卤素，氨基和/或硝基取代的苯基，或苯基-C 1 -C 3 - 烷基或通过C1-C8烷基链任选与酰胺氮原子键合的碳水化合物基团或其药学上可接受的酸加成盐，其改善心脏的收缩力，使血压升高 ure，降低血糖，减少粘膜肿胀，影响患者的盐和液体平衡。

10. 发明授权

US4537881A 5-Nitro 1,4-dihydropyridines having a positive inotropic effect 失效
标题翻译：具有正性肌力作用的5-硝基1,4-二氢吡啶类
公开(公告)号：US4537881A
公开(公告)日：1985-08-27
申请号：US627596
申请日：1984-07-03
申请人： Fred R. Heiker , Jurgen Stoltefuss , Gerhard Franckowiak , Matthias Schramm , Gunter Thomas , Rainer Gross
发明人： Fred R. Heiker , Jurgen Stoltefuss , Gerhard Franckowiak , Matthias Schramm , Gunter Thomas , Rainer Gross
IPC分类号： A61K31/70 , A61K31/7028 , A61P3/08 , A61P9/04 , A61P9/12 , C07H15/04 , C07H15/06 , C07H15/12 , C07H15/14 , C07H15/26 , A61K31/41 , A61K31/395 , C07D405/12
CPC分类号： C07H15/06 , C07H15/04 , C07H15/14 , C07H15/26
摘要： Novel 1,4-dihydropyridines of the fomula ##STR1## in which R.sub.1 and R.sub.2 each independently is hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.12 -alkoxy, C.sub.1 -C.sub.4 -halogenoalkoxy, halogen, nitro, C.sub.1 -C.sub.4 -halogenoalkyl, C.sub.1 -C.sub.4 -halogenoalkylmercapto, ##STR2## in which Z is oxygen or sulphur, andR.sub.4 and R.sub.5 each independently is hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.6 -alkoxy, halogen, C.sub.1 -C.sub.4 -halogenoalkyl, C.sub.1 -C.sub.4 -halogenoalkoxy or nitro, orR.sub.1 and R.sub.2, together with 2 C atoms of the phenyl ring, form the ring ##STR3## X is oxygen, sulphur or the radical NR.sub.6, R.sub.6 is a C.sub.1 -C.sub.6 -alkyl group,A is a C.sub.2 -C.sub.10 -alkylene group, it being necessary that at least two C atoms are located in the alkylene chain which connects the carbonyloxy group to X, andR.sub.3 is a monosaccharide or disaccharide moiety or a protected monosaccharide or disaccharide moiety,or pharmaceutically acceptable addition salts thereof, which exhibit positive inotropic activity and are useful in treating circulatory disorders.
摘要翻译： R1和R2各自独立地为氢，C1-C4-烷基，C1-C12-烷氧基，C1-C4-卤代烷氧基，卤素，硝基，C1-C4-卤代烷基， C1-C4卤代烷基巯基，其中Z是氧或硫，R4和R5各自独立地是氢，C1-C4-烷基，C1-C6-烷氧基，卤素，C1-C4-卤代烷基，C1-C4-卤代烷基，卤代烷氧基或硝基，或R 1和R 2与苯环的2 C原子一起形成环，X为氧，硫或基团NR 6，R 6为C 1 -C 6 - 烷基，A为C 2 - C10亚烷基，必须至少两个C原子位于将羰氧基连接到X的亚烷基链中，R3是单糖或二糖部分或受保护的单糖或二糖部分，或其药学上可接受的加成盐，其表现出正性肌力活性并且可用于治疗循环障碍。

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