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公开(公告)号:WO2009094866A1
公开(公告)日:2009-08-06
申请号:PCT/CN2008/071014
申请日:2008-05-20
IPC: C07D403/12 , C07D209/52 , A61K31/4025 , A61P3/10
CPC classification number: C07D209/52 , C07D403/12
Abstract: Disclosed are new dicycloazaalkane derivates represented by general formula (I), preparation processes and pharmaceutical compositions containing them, and the uses for treatment especially for dipeptidyl peptidase inhibitor(DPPIV), in which each substituent group of general formula (I) is as defined in specification.
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公开(公告)号:WO2008138232A1
公开(公告)日:2008-11-20
申请号:PCT/CN2008/001352
申请日:2008-05-14
IPC: C07D519/00 , C07D487/04 , C07D471/04 , A61K31/41 , A61K31/437 , A61P9/00 , A61P35/00 , A61P41/00
CPC classification number: C07D471/04 , C07D487/04 , C07D519/00
Abstract: The invention provides new pyrrolo-nitrogenous heterocyclic derivatives represented by formula (I) or their salts, the preparation thereof, pharmaceutical compositions containing such derivatives and the use of such derivatives as therapeutic agents, especially as protein kinase inhibitors, wherein each substituent in formula (I) is same as defined in the description.
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公开(公告)号:WO2008148279A1
公开(公告)日:2008-12-11
申请号:PCT/CN2007/070927
申请日:2007-10-19
IPC: C07D209/52 , A61K31/403 , A61P3/10
CPC classification number: C07D209/52 , C07D403/06
Abstract: A novel cyclobutyl-fused pyrrolidine derivatives of formula (I) in which the substituents are defined in the description, their preparation methods, their compositions and their use as therapeutical agent, particularly as dipeptidyl peptidase IV (DPPIV) inhibitor.
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公开(公告)号:WO2008138184A1
公开(公告)日:2008-11-20
申请号:PCT/CN2007/003080
申请日:2007-10-30
IPC: C07D487/04 , C07D519/00 , A61K31/55 , A61K31/407 , A61P35/02 , A61P3/10 , A61P37/02 , A61P17/06 , A61P19/02 , A61P9/00 , A61P29/00 , A61P35/04 , A61P43/00
CPC classification number: C07D487/04
Abstract: The new derivatives of pyrroloazacycles represented by formula (I) or salts thereof, the method of making them and pharmaceutical compositions containing them, as well as the use thereof as therapeutical agents especially as inhibitors of protein kinases, wherein the substitutes in formula (I) have the same meanings as what are mentioned in the descriptions.
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公开(公告)号:WO2008089636A1
公开(公告)日:2008-07-31
申请号:PCT/CN2007/070990
申请日:2007-10-30
IPC: A61K31/403 , C07D417/14 , C07D417/04 , C07D403/14 , C07D403/04 , C07D209/52 , A61P3/10
CPC classification number: C07D403/12 , C07D209/52
Abstract: Derivatives of azabicyclo octane presented by formula (I), the method of making them, and the compositions containing the same and the uses thereof as inhibitors of dipeptidyl peptidase IV (DPP-IV), wherein the substitutes in formula (I) have the same meanings as what is mentioned in the descriptions.
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公开(公告)号:WO2007112669A1
公开(公告)日:2007-10-11
申请号:PCT/CN2007/001008
申请日:2007-03-28
IPC: C07D207/16 , C07D275/03 , A61K31/426 , A61P3/10 , C07C49/345
CPC classification number: C07D207/16 , C07C45/59 , C07C49/345 , C07C49/513 , C07C49/517 , C07C49/747 , C07D277/06
Abstract: The present invention relates to new dicyclooctane derivates represented by general formula (I), preparation processes and pharmaceutical compositions containing them, and to the uses for treatment especially for dipeptidyl peptidase inhibitor(DPPIV), in which each substituent group of general formula (I) is as defined in specification.
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公开(公告)号:WO2010139231A1
公开(公告)日:2010-12-09
申请号:PCT/CN2010/072787
申请日:2010-05-14
Applicant: 北京纳通投资有限公司 , 郑诚功 , 柴鹏 , 赵富强 , 刘建祥
CPC classification number: A61F2/4425 , A61F2002/30062 , A61F2002/30079 , A61F2002/302 , A61F2002/305 , A61F2002/30502 , A61F2002/30504 , A61F2002/30505 , A61F2002/30566 , A61F2002/30604 , A61F2002/30607 , A61F2002/30647 , A61F2002/30649 , A61F2002/30662 , A61F2002/30841 , A61F2230/0065 , Y10T29/49826
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公开(公告)号:WO2009024016A1
公开(公告)日:2009-02-26
申请号:PCT/CN2008/001388
申请日:2008-07-29
Applicant: 上海恒瑞医药有限公司 , 邓炳初 , 杨家亮 , 苏熠东 , 赵富强
IPC: C07D417/04 , C07D209/30 , C07D209/04 , A61K31/437 , A61P33/00
CPC classification number: C07D471/04
Abstract: Pyrrolo[3,2-c]pyridine-4-one-2-indolinone compounds, especially 2-(2-oxoindoline-3-ylidene)methyl-5- (2-hydroxy-3-morpholin-4-yl -propyl)-6,7-dihydro -1H-pyrrol[3,2-c]pyridine-4(5H)-one compounds. Their preparation and pharmaceutical composition , and pharmaceutical use as protein kinase inhibitors.
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