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1.
公开(公告)号:US08232297B2
公开(公告)日:2012-07-31
申请号:US11992015
申请日:2006-09-08
申请人: Thomas Maier , Thomas Beckers , Rolf-Peter Hummel , Martin Feth , Matthias Müller , Thomas Bär , Jürgen Volz
发明人: Thomas Maier , Thomas Beckers , Rolf-Peter Hummel , Martin Feth , Matthias Müller , Thomas Bär , Jürgen Volz
IPC分类号: A61K31/40 , A61K31/4439 , A61K31/4025 , C07D207/34 , C07D401/14 , C07D403/14
CPC分类号: C07D207/48 , C07D403/12 , C07D409/12
摘要: Compounds of a certain formula I, in which R1, R2, R3, R4, R5, R6 and R7 have the meanings indicated in the description, as well as salts thereof are novel effective HDAC inhibitors.
摘要翻译: 其中R 1,R 2,R 3,R 4,R 5,R 6和R 7具有说明书中所示含义的某种式I化合物及其盐是新的有效的HDAC抑制剂。
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2.Sulphonylpyrrole Hydrochloride Salts as Histone Deacetylases Inhibitors 失效
标题翻译: 磺酰吡唑盐酸盐作为组蛋白脱乙酰酶抑制剂公开(公告)号:US20090297473A1
公开(公告)日:2009-12-03
申请号:US11992018
申请日:2006-09-08
申请人: Thomas Maier , Thomas Beckers , Rolf-Peter Hummel , Martin Feth , Matthias Müller , Thomas Bär
发明人: Thomas Maier , Thomas Beckers , Rolf-Peter Hummel , Martin Feth , Matthias Müller , Thomas Bär
IPC分类号: A61K31/40 , C07D403/02 , C07D207/48 , C07D409/14 , A61K31/4439 , A61K31/404 , A61K39/395 , A61K31/7088 , A61K38/00 , A61K38/21 , A61P35/00
CPC分类号: C07D207/48
摘要: Compounds of a certain formula 1, in which R1, R2, R3, R4, R5, R6 and R7 have the meanings indicated in the description, as well as salts thereof are novel effective HDAC inhibitors.
摘要翻译: 其中R 1,R 2,R 3,R 4,R 5,R 6和R 7具有说明书中所述含义的某种式1化合物及其盐是新的有效的HDAC抑制剂。
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3.Sulphonylpyrrole hydrochloride salts as histone deacetylases inhibitors 失效
标题翻译: 磺酰吡咯盐酸盐作为组蛋白脱乙酰酶抑制剂公开(公告)号:US08188138B2
公开(公告)日:2012-05-29
申请号:US11992018
申请日:2006-09-08
申请人: Thomas Maier , Thomas Beckers , Rolf-Peter Hummel , Martin Feth , Matthias Müller , Thomas Bär
发明人: Thomas Maier , Thomas Beckers , Rolf-Peter Hummel , Martin Feth , Matthias Müller , Thomas Bär
IPC分类号: C07D403/12 , C07D409/14 , C07D207/48 , A61K31/4439 , A61K31/4045 , A61K31/40
CPC分类号: C07D207/48
摘要: Compounds of a certain formula I, in which R1, R2, R3, R4, R5, R6 and R7 have the meanings indicated in the description, as well as salts thereof are novel effective HDAC inhibitors.
摘要翻译: 其中R 1,R 2,R 3,R 4,R 5,R 6和R 7具有说明书中所示含义的某种式I化合物及其盐是新的有效的HDAC抑制剂。
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4.(E)-N-(2-amino-phenyl)-3-{1-[4-(l-methyl-1H-pyrazol-4-yl)-benzenesulfonyl]-1H-pyrrol-3-yl}-acrylamide salts 有权
标题翻译: (E)-N-(2-氨基 - 苯基)-3- {1- [4-(1-甲基-1H-吡唑-4-基) - 苯磺酰基] -1H-吡咯-3-基} - 丙烯酰胺盐公开(公告)号:US08557858B2
公开(公告)日:2013-10-15
申请号:US12921889
申请日:2009-03-11
申请人: Jürgen Volz , Martin Feth , Rolf-Peter Hummel , Matthias Müller , Thomas Maier , Bernd Müller
发明人: Jürgen Volz , Martin Feth , Rolf-Peter Hummel , Matthias Müller , Thomas Maier , Bernd Müller
IPC分类号: A61K31/4155 , C07D231/12
CPC分类号: C07D403/12
摘要: A salt of (E)-N-{2-amino-phenyl)-3-{1-[4-(1-methyl-1 H-pyrazol-4-yl)-beπzenesulfonyl]-1 H-pyrrol-3-yl)-acrylamide selected from the group consisting of the hydrobromide, methansulfonate, hemi ethane-1,2-disulfonate, benzenesulfonate, toiuenesulfonate and 2-naphthalenesulfonate.
摘要翻译: (E)-N- {2-氨基 - 苯基)-3- {1- [4-(1-甲基-1H-吡唑-4-基) - 对苯磺酰基] -1H-吡咯-3-基] 吡咯烷-1-基) - 丙烯酰胺,其选自氢溴酸盐,甲磺酸盐,半乙烷-1,2-二磺酸盐,苯磺酸盐,甲苯磺酸盐和2-萘磺酸盐。
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公开(公告)号:US20110086897A1
公开(公告)日:2011-04-14
申请号:US12921889
申请日:2009-03-11
申请人: Jürgen Volz , Martin Feth , Rolf-Peter Hummel , Matthias Muller , Thomas Maier , Bernd Muller
发明人: Jürgen Volz , Martin Feth , Rolf-Peter Hummel , Matthias Muller , Thomas Maier , Bernd Muller
IPC分类号: A61K31/4155 , C07D403/10 , A61P35/00
CPC分类号: C07D403/12
摘要: A salt of (E)-N-{2-amino-phenyl)-3-{1-[4-(1-methyl-1H-pyrazol-4-yl)-beπzenesulfonyl]-1H-pyrrol-3-yl)-acrylamide selected from the group consisting of the hydrobromide, methansulfonate, hemi ethane-1,2-disulfonate, benzenesulfonate, toiuenesulfonate and 2-naphthalenesulfonate.
摘要翻译: (E)-N- {2-氨基 - 苯基)-3- {1- [4-(1-甲基-1H-吡唑-4-基) - 对 - 磺酰基] -1H-吡咯-3-基] 吡咯烷-1-基) - 丙烯酰胺,其选自氢溴酸盐,甲磺酸盐,半乙烷-1,2-二磺酸盐,苯磺酸盐,甲苯磺酸盐和2-萘磺酸盐。
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6.Novel Sulphonylpyrroles as Inhibitors of Hdac S Novel Sulphonylpyrroles 有权
标题翻译: 新型磺酰吡啶作为Hdac S新型磺酰基吡咯的抑制剂公开(公告)号:US20090263353A1
公开(公告)日:2009-10-22
申请号:US11992015
申请日:2006-09-08
申请人: Thomas Maier , Thomas Beckers , Rolf-Peter Hummel , Martin Feth , Matthias Muller , Thomas Bar , Jurgen Volz
发明人: Thomas Maier , Thomas Beckers , Rolf-Peter Hummel , Martin Feth , Matthias Muller , Thomas Bar , Jurgen Volz
IPC分类号: A61K38/21 , C07D207/48 , A61K31/40 , C07D209/04 , A61K31/404 , C07D401/02 , A61K31/4439 , C07D403/02 , A61K31/415 , C07D413/02 , A61K31/5377 , A61K39/395 , A61K31/7052 , A61K38/14 , A61P35/00
CPC分类号: C07D207/48 , C07D403/12 , C07D409/12
摘要: Compounds of a certain formula I, in which R1, R2, R3, R4, R5, R6 and R7 have the meanings indicated in the description, as well as salts thereof are novel effective HDAC inhibitors.
摘要翻译: 其中R 1,R 2,R 3,R 4,R 5,R 6和R 7具有说明书中所示含义的某种式I化合物及其盐是新的有效的HDAC抑制剂。
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公开(公告)号:US08865745B2
公开(公告)日:2014-10-21
申请号:US13618026
申请日:2012-09-14
申请人: Beate Schmidt , Christian Scheufler , Juergen Volz , Martin Feth , Rolf-Peter Hummel , Armin Hatzelmann , Christof Zitt , Andrea Wohlsen , Degenhard Marx , Hans-Peter Kley , Deborah Ockert , Anke Heuser , Johannes A. M. Christiaans , Geert Jan Sterk , Wiro M. P. B. Menge
发明人: Beate Schmidt , Christian Scheufler , Juergen Volz , Martin Feth , Rolf-Peter Hummel , Armin Hatzelmann , Christof Zitt , Andrea Wohlsen , Degenhard Marx , Hans-Peter Kley , Deborah Ockert , Anke Heuser , Johannes A. M. Christiaans , Geert Jan Sterk , Wiro M. P. B. Menge
IPC分类号: A01N43/40 , A61K31/445 , C07D401/00 , C07D401/14
CPC分类号: C07D401/14 , A61K31/4152
摘要: The compound 1-(2-{4-[3-(3,4-dimethoxyphenyl)-4,4-dimethyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl]piperidin-1-yl}-2-oxoethyl)pyrrolidine-2,5-dione is a novel effective inhibitor of the type 4 phosphodiesterase.
摘要翻译: 化合物1-(2- {4- [3-(3,4-二甲氧基苯基)-4,4-二甲基-5-氧代-4,5-二氢-1H-吡唑-1-基]哌啶-1-基 } -2-氧代乙基)吡咯烷-2,5-二酮是4型磷酸二酯酶的新型有效抑制剂。
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公开(公告)号:US08304436B2
公开(公告)日:2012-11-06
申请号:US12451348
申请日:2008-05-14
申请人: Beate Schmidt , Christian Scheufler , Juergen Volz , Martin Feth , Rolf-Peter Hummel , Armin Hatzelmann , Christof Zitt , Andrea Wohlsen , Degenhard Marx , Hans-Peter Kley , Deborah Ockert , Anke Heuser , Johannes A. M. Christiaans , Geert Jan Sterk , Wiro M. P. B. Menge
发明人: Beate Schmidt , Christian Scheufler , Juergen Volz , Martin Feth , Rolf-Peter Hummel , Armin Hatzelmann , Christof Zitt , Andrea Wohlsen , Degenhard Marx , Hans-Peter Kley , Deborah Ockert , Anke Heuser , Johannes A. M. Christiaans , Geert Jan Sterk , Wiro M. P. B. Menge
IPC分类号: A01N43/40 , A61K31/445 , C07D401/00 , C07D231/00 , C07D403/00 , C07D403/02
CPC分类号: C07D401/14 , A61K31/4152
摘要: The compounds of a certain formula 1, in which R1, R7, R8, R9 and n have the meanings as given in the description, are novel effective inhibitors of the type 4 phosphodiesterase.
摘要翻译: R1,R7,R8,R9和n具有如说明书中给出的含义的某种式1的化合物是4型磷酸二酯酶的新型有效抑制剂。
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公开(公告)号:US20100120757A1
公开(公告)日:2010-05-13
申请号:US12451348
申请日:2008-05-14
申请人: Beate Schmidt , Christian Scheufler , Juergen Volz , Martin Feth , Rolf-Peter Hummel , Armin Hatzelmann , Christof Zitt , Andrea Wohlsen , Degenhard Marx , Hans-Peter Kley , Deborah Ockert , Anke Heuser , Johannes A.M. Christiaans , Geert Jan Sterk , Wiro M.P.B. Menge
发明人: Beate Schmidt , Christian Scheufler , Juergen Volz , Martin Feth , Rolf-Peter Hummel , Armin Hatzelmann , Christof Zitt , Andrea Wohlsen , Degenhard Marx , Hans-Peter Kley , Deborah Ockert , Anke Heuser , Johannes A.M. Christiaans , Geert Jan Sterk , Wiro M.P.B. Menge
IPC分类号: A61K31/541 , C07D401/04 , A61K31/454 , C07D413/14 , A61K31/5377 , C07D417/14
CPC分类号: C07D401/14 , A61K31/4152
摘要: The compounds of a certain formula 1, in which R1, R7, R8, R9 and n have the meanings as given in the description, are novel effective inhibitors of the type 4 phosphodiesterase.
摘要翻译: R1,R7,R8,R9和n具有如说明书中给出的含义的某种式1的化合物是4型磷酸二酯酶的新型有效抑制剂。
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公开(公告)号:US20100120737A1
公开(公告)日:2010-05-13
申请号:US12292045
申请日:2008-11-10
申请人: Martin Feth , Rolf-Peter Hummel , Jurgen Volz , Peter Zimmermann , Beate Schmidt
发明人: Martin Feth , Rolf-Peter Hummel , Jurgen Volz , Peter Zimmermann , Beate Schmidt
CPC分类号: C07D317/70
摘要: The present invention relates to amorphous ciclesonide, methods to prepare the same, pharmaceutical compositions comprising amorphous ciclesonide as active ingredient, and methods of treatment using amorphous ciclesonide.
摘要翻译: 本发明涉及无定形环索奈德,其制备方法,包含无定形环索奈德作为活性成分的药物组合物,以及使用无定形环索奈德治疗的方法。
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