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21.
公开(公告)号:US08071601B2
公开(公告)日:2011-12-06
申请号:US13008398
申请日:2011-01-18
申请人: Peter Aranyi , Sandor Batori , Geza Timari , Kinga Boer , Zoltan Kapui , Endre Mikus , Katalin Urban-Szabo , Katalin Gerber , Judit Vargane Szeredi , Michel Finet
发明人: Peter Aranyi , Sandor Batori , Geza Timari , Kinga Boer , Zoltan Kapui , Endre Mikus , Katalin Urban-Szabo , Katalin Gerber , Judit Vargane Szeredi , Michel Finet
IPC分类号: A61K31/497 , A61K31/47 , C07D401/04 , C07D453/04
CPC分类号: C07D405/12 , C07C229/50 , C07D215/48 , C07D405/14 , C07D409/12 , C07D409/14 , C07D491/04
摘要: The present invention relates to an adenosine A3 receptor ligand of the general formula (I).
摘要翻译: 本发明涉及通式(I)的腺苷A3受体配体。
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22.
公开(公告)号:US20060211689A1
公开(公告)日:2006-09-21
申请号:US11344440
申请日:2006-01-31
申请人: Peter Aranyi , Sandor Batori , Geza Timari , Kinga Boer , Zoltan Kapui , Endre Mikus , Katalin Urban-Szabo , Katalin Gerber , Judit Vargane Szeredi , Michel Finet
发明人: Peter Aranyi , Sandor Batori , Geza Timari , Kinga Boer , Zoltan Kapui , Endre Mikus , Katalin Urban-Szabo , Katalin Gerber , Judit Vargane Szeredi , Michel Finet
IPC分类号: A61K31/541 , A61K31/5377 , A61K31/496 , A61K31/4709 , C07D417/02 , C07D413/02 , C07D401/02
CPC分类号: C07D405/12 , C07C229/50 , C07D215/48 , C07D405/14 , C07D409/12 , C07D409/14 , C07D491/04
摘要: The present invention relates to an adenosine A3 receptor ligand of the general formula (I), within those preferably to the antagonists, including a salt, solvate or isomer (tautomer, desmotrop, and optically active isomer) thereof, to a pharmaceutical composition containing the ligand, to the use of the ligand, to its preparation, and intermediates of the ligand of the general formula (II″), (III″), (IV″), (V″), (VI″), (VII″), (VIII″) and (XIII″) and their preparation.
摘要翻译: 本发明涉及通式(I)的腺苷A 3 N 3受体配体,其中优选包括盐,溶剂合物或异构体(互变异构体,去质性和光学活性异构体) (II“),(III”),(IV“),(V)的配体的配体的使用,其制备方法和中间体的含有配体的药物组合物, (VI“),(VII”),(VIII“)和(XIII”)及其制备。
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23.
公开(公告)号:US07799922B2
公开(公告)日:2010-09-21
申请号:US12484658
申请日:2009-06-15
申请人: Peter Aranyi , Sandor Batori , Geza Timari , Kinga Boer , Zoltan Kapui , Endre Mikus , Katalin Urban-Szabo , Katalin Gerber , Judit Vargane Szeredi , Michel Finet
发明人: Peter Aranyi , Sandor Batori , Geza Timari , Kinga Boer , Zoltan Kapui , Endre Mikus , Katalin Urban-Szabo , Katalin Gerber , Judit Vargane Szeredi , Michel Finet
IPC分类号: C07D215/38 , C07D215/54 , C07D215/56
CPC分类号: C07D405/12 , C07C229/50 , C07D215/48 , C07D405/14 , C07D409/12 , C07D409/14 , C07D491/04
摘要: The present invention relates to an adenosine A3 receptor ligand of the general formula (I), within those preferably to the antagonists, including a salt, solvate or isomer (tautomer, desmotrop, and optically active isomer) thereof, to a pharmaceutical composition containing the ligand, to the use of the ligand, to its preparation, and intermediates of the ligand of the general formula (II″), (III″), (IV″), (V″), (VI″), (VII″), (VIII″) and (XIII″) and their preparation.
摘要翻译: 本发明涉及通式(I)的腺苷A3受体配体,其中优选包括其盐,溶剂化物或异构体(互变异构体,去质性和旋光异构体)的拮抗剂,包含其中的 通式(II“),(III”),(IV“),(V”),(VI“),(VII”)的配体的配体,配体的使用, ),(VIII“)和(XIII”)及其制备。
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24.
公开(公告)号:US07547696B2
公开(公告)日:2009-06-16
申请号:US11344440
申请日:2006-01-31
申请人: Peter Aranyi , Sandor Batori , Geza Timari , Kinga Boer , Zoltan Kapui , Endre Mikus , Katalin Urban-Szabo , Katalin Gerber , Judit Vargane Szeredi , Michel Finet
发明人: Peter Aranyi , Sandor Batori , Geza Timari , Kinga Boer , Zoltan Kapui , Endre Mikus , Katalin Urban-Szabo , Katalin Gerber , Judit Vargane Szeredi , Michel Finet
IPC分类号: A61K31/535 , C07D413/12
CPC分类号: C07D405/12 , C07C229/50 , C07D215/48 , C07D405/14 , C07D409/12 , C07D409/14 , C07D491/04
摘要: The present invention relates to an adenosine A3 receptor ligand of the general formula (I), within those preferably to the antagonists, including a salt, solvate or isomer (tautomer, desmotrop, and optically active isomer) thereof, to a pharmaceutical composition containing the ligand, to the use of the ligand, to its preparation, and intermediates of the ligand of the general formula (II″), (III″), (IV″), (V″), (VI″), (VII″), (VIII″) and (XIII″) and their preparation.
摘要翻译: 本发明涉及通式(I)的腺苷A3受体配体,其中优选包括其盐,溶剂化物或异构体(互变异构体,去质性和旋光异构体)的拮抗剂,包含其中的 (II“),(III”),(IV“),(V”),(VI“)的配体的中间体,配体的使用,配体的使用, ),(VII“),(VIII”)和(XIII“)及其制备。
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