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1. 发明授权

US5039675A Benzimidazoles and pharmaceutical preparations containing these compounds 失效
标题翻译：苯并咪唑和含有这些化合物的药物制剂
公开(公告)号：US5039675A
公开(公告)日：1991-08-13
申请号：US497223
申请日：1990-03-22
申请人： Peter Morsdorf , Helmut Schickaneder , Rolf Herter , Volker Pfanhlert , Geidrun Engler , Kurt H. Ahrens
发明人： Peter Morsdorf , Helmut Schickaneder , Rolf Herter , Volker Pfanhlert , Geidrun Engler , Kurt H. Ahrens
IPC分类号： A61K31/505 , A61P9/06 , C07D403/04 , C07D403/14
CPC分类号： C07D403/04
摘要： New benzimidazoles correponding to the general formula I ##STR1## are described, in which the pyridazinone ring is attached in the 5- or 6- position of the benzimidazole ring and R.sup.1 denotes a hydrogen atom or a straight chained or branched C.sub.1 to C.sub.4 alkyl group, R.sup.2 denotes a hydrogen atom, a straight chained or branched C.sub.1 to C.sub.4 alkyl group, a C.sub.1 to C.sub.4 alkoxy group, a hydroxy group, a halogen atom, an amino group or a nitro group, A denotes a hydrogen atom, a group of the formula ##STR2## wherein R.sup.3 denotes a hydrogen atom, an optionally substituted C.sub.1 to C.sub.4 alkyl group or a C.sub.1 to C.sub.4 alkoxy group and B denotes a cyano group, a benzoyl group or a phenylsulphonyl group, or A denotes a group of the formula ##STR3## in which m has the value 2 or 3 and n represents an integer from 1 to 6, and the physiologically acceptable salts thereof as well as processes for their preparation and pharmaceutical preparations. containing these compounds These compounds are new, effective, positive inotropic substances which do not act by the mechanism of phosphodiesterase inhibition.

2. 发明授权

US4957920A Benzimidazoles, and pharmaceutical preparations containing these compounds 失效
标题翻译：苯并咪唑和含有这些化合物的药物制剂
公开(公告)号：US4957920A
公开(公告)日：1990-09-18
申请号：US168273
申请日：1988-03-15
申请人： Peter Morsdorf , Helmut Schickaneder , Rolf Herter , Volker Pfahlert , Heidrun Engler , Kurt H. Ahrens
发明人： Peter Morsdorf , Helmut Schickaneder , Rolf Herter , Volker Pfahlert , Heidrun Engler , Kurt H. Ahrens
IPC分类号： A61K31/505 , A61P9/06 , C07D403/04 , C07D403/14
CPC分类号： C07D403/04
摘要： New benzimidazoles corresponding to the general formula I ##STR1## are described, in which the pyridazinone ring is attached in the 5- or 6- position of the benzimidazole ring and R.sup.1 denotes a hydrogen atom or a straight chained or branched C.sub.1 to C.sub.4 alkyl group, R.sup.2 denotes a hydrogen atom, a straight chained or branched C.sub.1 to C.sub.4 alkyl group, a C.sub.1 to C.sub.4 alkoxy group, a hydroxy group, a halogen atom, an amino group or a nitro group, A denotes a hydrogen atom, a group of the formula ##STR2## wherein R.sup.3 denotes a hydrogen atom, an optionally substituted C.sub.1 to C.sub.4 alkyl group or a C.sub.1 to C.sub.4 alkoxy group and B denotes a cyano group, a benzoyl group or a phenylsulphonyl group, or A denotes a group of the formula ##STR3## in which m has the value of 2 or 3 and n represents an integer from 1 to 6, and the physiologically acceptable salts thereof as well as processes for their preparation and pharmaceutical preparations containing these compounds. These compounds are new, effective, positive inotropic substances which do not act by the mechanism of phosphodiesterase inhibition.
摘要翻译：描述了对应于通式I（I）的新的苯并咪唑，其中哒嗪酮环连接在苯并咪唑环的5-或6-位，R1表示氢原子或直链或支链C1至 C4烷基，R2表示氢原子，直链或支链C1〜C4烷基，C1〜C4烷氧基，羟基，卤素原子，氨基或硝基，A表示氢原子，式中，R 3表示氢原子，可以具有取代基的C1〜C4烷基或C1〜C4烷氧基，B表示氰基，苯甲酰基或苯基磺酰基，A表示基团其中m具有2或3的数值，n表示1至6的整数，以及其生理上可接受的盐以及其制备方法和含有这些化合物的药物制剂。这些化合物是新的，有效的正性肌力物质，不受磷酸二酯酶抑制机制的作用。

3. 发明授权

US4666921A Pyrazole derivatives, processes for their preparation and pharmaceutical preparations containing these compounds 失效
标题翻译：吡唑衍生物，其制备方法和含有这些化合物的药物制剂
公开(公告)号：US4666921A
公开(公告)日：1987-05-19
申请号：US787114
申请日：1985-10-15
申请人： Rolf Herter , Helmut Schickaneder , Peter Morsdorf , Stefan Postius , Istvan Szelenyi , Kurt H. Ahrens
发明人： Rolf Herter , Helmut Schickaneder , Peter Morsdorf , Stefan Postius , Istvan Szelenyi , Kurt H. Ahrens
IPC分类号： C07D231/52 , A61K31/445 , A61K31/415 , C07D401/12 , C07D403/12
CPC分类号： C07D231/52
摘要： Special pyrazole derivatives corresponding to the general formula I which have a highly selective action on histamine-H.sub.2 receptors are described. Compared with other drugs known to be effective in their action on histamine-H.sub.2 receptors, these compounds have improved pharmacological properties. A method of preparation of these compounds is also described.
摘要翻译：描述对应于对组胺-H 2受体具有高度选择性作用的通式I的特殊的吡唑衍生物。与已知对其组胺-H 2受体的作用有效的其它药物相比，这些化合物具有改善的药理学性质。还描述了这些化合物的制备方法。

4. 发明授权

US4599346A Propan-2-ol derivatives, a process for their production and medicaments containing these compounds 失效
标题翻译：丙-2-醇衍生物，其生产方法和含有这些化合物的药物
公开(公告)号：US4599346A
公开(公告)日：1986-07-08
申请号：US630963
申请日：1984-07-16
申请人： Helmut Schickaneder , Stefan Postius , Rolf Herter , Peter Morsdorf , Istvan Szelenyi , Kurt H. Ahrens
发明人： Helmut Schickaneder , Stefan Postius , Rolf Herter , Peter Morsdorf , Istvan Szelenyi , Kurt H. Ahrens
IPC分类号： C07D295/08 , A61K31/435 , A61K31/445 , A61P1/04 , A61P43/00 , C07D209/48 , C07D285/10 , C07D295/096 , C07D405/06 , A61K31/41 , C07D211/06 , C07D417/12
CPC分类号： C07D209/48 , C07D285/10 , C07D295/096 , C07D405/06
摘要： The invention relates to new propan-2-ol derivatives corresponding to the following general formula ##STR1## in which R represents ##STR2## and to salts thereof with pharmacologically acceptable acids. These compounds have a selective effect on histamine-H.sub.2 -receptors.
摘要翻译：本发明涉及对应于下列通式（I）的新的丙-2-醇衍生物，其中R代表“IMAGE”，以及其与药理学上可接受的酸的盐。这些化合物对组胺-H 2受体具有选择性作用。

5. 发明授权

US4659721A Alkanol derivatives, and pharmaceutical preparation containing these compounds 失效
标题翻译：烷醇衍生物和含有这些化合物的药物制剂
公开(公告)号：US4659721A
公开(公告)日：1987-04-21
申请号：US693204
申请日：1985-01-22
申请人： Helmut Schickaneder , Stefan Postius , Istvan Szelenyi , Peter Morsdorf , Rolf Herter , Kurt H. Ahrens
发明人： Helmut Schickaneder , Stefan Postius , Istvan Szelenyi , Peter Morsdorf , Rolf Herter , Kurt H. Ahrens
IPC分类号： A61K31/41 , A61K31/425 , A61K31/426 , A61K31/433 , A61K31/445 , A61P1/04 , C07C67/00 , C07C213/00 , C07C215/28 , C07C217/48 , C07C239/00 , C07C279/28 , C07C313/00 , C07C323/29 , C07D209/48 , C07D249/14 , C07D275/02 , C07D275/03 , C07D277/20 , C07D277/26 , C07D277/48 , C07D285/10 , C07D295/08 , C07D295/096 , C07D303/36 , C07D307/52 , C07D333/00 , C07D333/20 , C07D405/12 , C07D409/12 , C07D417/12
CPC分类号： C07D209/48 , C07D249/14 , C07D275/03 , C07D285/10 , C07D295/096 , C07D303/36 , C07D333/20 , C07D405/12 , C07D409/12 , C07D417/12
摘要： Alkanol derivatives corresponding to the general formula IR.sup.1 R.sup.2 N--(CH.sub.2).sub.m --Q--CH.sub.2 X--CH.sub.2 --Y--(CH.sub.2).sub.n --NHR.sup.3 (I)which have a highly selective action on histamine-H.sub.2 receptors are described. Due to this action, these compounds may advantageously be used for treatment of diseases caused by raised gastric secretion.
摘要翻译：描述对应于对组胺-H 2受体具有高度选择性作用的通式I R1R2N-（CH2）m-Q-CH2X-CH2-Y-（CH2）n-NHR3（I）的烷醇衍生物。由于这种作用，这些化合物可有利地用于治疗由升高的胃分泌引起的疾病。

6. 发明授权

US4559344A Pyridine-pyrimidinone derivatives, a process for their production and H.sub. -antagonist medicament containing these compounds 失效
标题翻译：吡啶 - 嘧啶酮衍生物，其制备方法和含有这些化合物的H 2拮抗剂药物
公开(公告)号：US4559344A
公开(公告)日：1985-12-17
申请号：US574077
申请日：1984-01-26
申请人： Helmut Schickaneder , Peter Morsdorf , Stefan Postius , Istvan Szelenyi , Rolf Herter , Herbert Hansen , Kurt H. Ahrens
发明人： Helmut Schickaneder , Peter Morsdorf , Stefan Postius , Istvan Szelenyi , Rolf Herter , Herbert Hansen , Kurt H. Ahrens
IPC分类号： C07D295/08 , C07D213/55 , C07D307/38 , C07D401/06 , C07D405/14 , C07D409/14 , C07D417/14 , A61K31/505 , C07D239/02
CPC分类号： C07D401/06
摘要： The invention relates to new pyridine-pyrimidinone derivatives corresponding to the following general formula ##STR1## wherein R.sup.1 represents linear C.sub.1-6 alkyl or cycloalkyl and R.sup.2 represents linear C.sub.1-6 alkyl or R.sup.1 and R.sup.2 together with the nitrogen atom form a pyrrolidine or piperidine ring;Alk represents a linear alkylene chain C.sub.1-6 ;Q represents a benzene ring, furan ring, thiophene ring or thiazole ring;X represents oxygen, Y is a single bond and m is 2, 3 or 4 when Q represents benzene;X represents methylene, Y represents sulfur and m is 2 or 3 when Q is furan, thiophene or thiazole; andR.sup.3 represents a hydrogen atom or a lower alkyl group.These compounds show improved H.sub.2 -antagonistic activity.
摘要翻译：本发明涉及对应于以下通式的新的吡啶 - 嘧啶酮衍生物，其中R 1表示直链C 1-6烷基或环烷基，R 2表示直链C 1-6烷基或R 1和R 2与氮原子一起形成吡咯烷或哌啶环; Alk表示直链亚烷基链C 1-6; Q表示苯环，呋喃环，噻吩环或噻唑环; X表示氧，Y为单键，当Q表示苯时m为2,3或4; X表示亚甲基，Y表示硫，当Q为呋喃，噻吩或噻唑时，m为2或3; 并且R 3表示氢原子或低级烷基。这些化合物显示出改善的H2拮抗活性。

7. 发明授权

US4656180A Diamine derivatives and pharmaceutical preparations containing these compounds 失效
标题翻译：含有这些化合物的二胺衍生物和药物制剂
公开(公告)号：US4656180A
公开(公告)日：1987-04-07
申请号：US708239
申请日：1985-03-05
申请人： Stefan Postius , Rolf Herter , Peter Morsdorf , Helmut Schickaneder , Istvan Szelenyi , Kurt H. Ahrens
发明人： Stefan Postius , Rolf Herter , Peter Morsdorf , Helmut Schickaneder , Istvan Szelenyi , Kurt H. Ahrens
IPC分类号： C07D295/08 , A61K31/135 , A61K31/34 , A61K31/341 , A61K31/425 , A61K31/426 , A61K31/433 , A61K31/445 , A61P43/00 , C07C67/00 , C07C213/00 , C07C217/48 , C07C217/58 , C07C217/76 , C07C217/84 , C07C313/00 , C07C323/29 , C07C323/32 , C07D209/48 , C07D277/28 , C07D285/10 , C07D295/096 , C07D295/135 , C07D295/155 , C07D303/36 , C07D307/52 , C07D333/20 , C07D409/12 , C07D401/14
CPC分类号： C07D209/48 , C07D285/10 , C07D295/096 , C07D295/135 , C07D295/155 , C07D303/36 , C07D307/52 , C07D333/20 , C07D409/12
摘要： Diamine derivatives corresponding to the general formula IR.sup.1 R.sup.2 N--(CH.sub.2).sub.m --Q--A--NH--R--NH--B--Q'--(CH.sub.2).sub.n NR.sup.3 R.sup.4 (I)which have a highly selective action on histamine-H.sub.2 receptors and are therefore suitable for use as anti-ulcerative agents are described. Processes for the preparation of these compounds and pharmaceutical preparations containing these compounds are also described.
摘要翻译：对应于通式I R1R2N-（CH2）mQA-NH-R-NH-B-Q' - （CH2）nNR3R4（I）的二胺衍生物，其对组胺-H 2受体具有高选择性作用，因此适用于作为抗溃疡剂。还描述了制备这些化合物的方法和含有这些化合物的药物制剂。

8. 发明授权

US4921856A Dihydropyridazinone derivatives, a process for their preparation and pharmaceutical preparations containing these compounds 失效
标题翻译：二氢哒嗪酮衍生物，其制备方法和含有这些化合物的药物制剂
公开(公告)号：US4921856A
公开(公告)日：1990-05-01
申请号：US176689
申请日：1988-04-01
申请人： Helmut Schickaneder , Peter Morsdorf , Volker Pfahlert , Heidrun Engler , Kurt H. Ahrens
发明人： Helmut Schickaneder , Peter Morsdorf , Volker Pfahlert , Heidrun Engler , Kurt H. Ahrens
IPC分类号： A61K31/50 , A61P9/04 , C07D237/04 , C07D403/10 , C07D403/12
CPC分类号： C07D403/10 , C07D237/04 , C07D403/12
摘要： New dihydropryidazinone derivatives corresponding to the following formula ##STR1## and a process for their preparation and pharmaceutical preparations containing these compounds are described. These compounds are effective positively inotropic substances with an improved therapeutic profile.
摘要翻译：描述了对应于下式（I）的新的二氢哒嗪酮衍生物及其制备方法和含有这些化合物的药物制剂。这些化合物是具有改善的治疗特征的有效的正性肌力物质。

9. 发明授权

US4833141A 4-[4-[[2-(halophenyl)-2-[1H-tr:azol(or diazol)-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-piperazine-1-carbi mic acids having antimycotic activity 失效
标题翻译： 4- [4 - [[2-（卤代苯基）-2- [1H-tr：氮杂（或二唑）-1-基甲基）-1,3-二氧戊环-4-基]甲氧基]苯基] 具有抗真菌活性的碳水化合物
公开(公告)号：US4833141A
公开(公告)日：1989-05-23
申请号：US69159
申请日：1987-07-02
申请人： Helmut Schickaneder , Rolf Herter , Hartmut Vergin , Heidrun Engler , Kurt H. Ahrens
发明人： Helmut Schickaneder , Rolf Herter , Hartmut Vergin , Heidrun Engler , Kurt H. Ahrens
IPC分类号： C07D413/06 , A61K31/41 , A61P31/04 , C07D521/00
CPC分类号： C07D249/08 , C07D231/12 , C07D233/56
摘要： The invention relates to new 1,4-piperazine compounds corresponding to the following general formula ##STR1## which show improved antimycotic activity in relation to the known compounds miconazol and ketoconazol.
摘要翻译：本发明涉及对应于以下通式“IMAGE”的新的1,4-哌嗪化合物，其与已知的化合物咪康唑和酮康唑相比显示出改进的抗真菌活性。

10. 发明授权

US4738960A 1,3,4-Thiadiazole derivatives and pharmaceutical preparations useful as inhibitors for histamine-H.sub.2 receptors 失效
标题翻译： 1,3,4-噻二唑衍生物和可用作组胺-H 2受体抑制剂的药物制剂
公开(公告)号：US4738960A
公开(公告)日：1988-04-19
申请号：US799691
申请日：1985-11-19
申请人： Helmut Schickaneder , Rolf Herter , Kurt Wegner , Walter Schunack , Istvan Szelenyi , Stefan Postius , Kurt H. Ahrens
发明人： Helmut Schickaneder , Rolf Herter , Kurt Wegner , Walter Schunack , Istvan Szelenyi , Stefan Postius , Kurt H. Ahrens
IPC分类号： A61K31/41 , A61K31/433 , A61K31/44 , A61K31/445 , A61P1/04 , A61P43/00 , C07D285/12 , C07D285/135 , C07D417/12 , C07D417/14 , A61K31/38
CPC分类号： C07D285/135 , C07D417/12
摘要： 1,3,4-Thiadiazole derivatives corresponding to the general formula I ##STR1## which constitute highly effective inhibitors for histamine-H.sub.2 receptors are described. These compounds in addition have a cytoprotective action.
摘要翻译：描述了构成组胺-H 2受体的高效抑制剂的对应于通式I（I）的1,3,4-噻二唑衍生物。这些化合物另外具有细胞保护作用。

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