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公开(公告)号:EP2007789B1
公开(公告)日:2015-05-20
申请号:EP07811837.9
申请日:2007-04-09
申请人: Novartis AG , Novartis Pharma GmbH
发明人: BRANDL, Trixi , FU, Jiping , LENOIR, Francois , PARKER, David Thomas , PATANE, Michael , RADETICH, Branko , RAMAN, Prakash , RIGOLLIER, Pascal , SEEPERSAUD, Mohindra , SIMIC, Oliver , YIFRU, Aregahegn , ZHENG, Rui
IPC分类号: C07K5/078 , C07K5/083 , C07K5/087 , C07K5/103 , C07K5/107 , A61K38/05 , A61P31/14 , C07D401/12 , C07D403/12 , C07D409/12 , C07D405/12 , C07D413/12 , C07D417/12 , C07D487/10 , C07D491/20 , C07D495/10 , C07D498/10 , C07D209/96 , C07K5/065 , C07K5/062
CPC分类号: A61K38/07 , A61K38/00 , A61K38/06 , A61K45/06 , C07D209/96 , C07D401/12 , C07D401/14 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14 , C07D487/10 , C07D491/20 , C07D495/10 , C07D498/04 , C07D498/10 , C07K5/06034 , C07K5/06078 , C07K5/06165 , C07K5/0808 , C07K5/0812 , C07K5/101 , C07K5/1016
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公开(公告)号:EP2007789A2
公开(公告)日:2008-12-31
申请号:EP07811837.9
申请日:2007-04-09
发明人: BRANDL, Trixi , FU, Jiping , LENOIR, Francois , PARKER, David Thomas , PATANE, Michael , RADETICH, Branko , RAMAN, Prakash , RIGOLLIER, Pascal , SEEPERSAUD, Mohindra , SIMIC, Oliver , YIFRU, Aregahegn , ZHENG, Rui
IPC分类号: C07K5/06 , C07K5/078 , C07K5/08 , C07K5/083 , C07K5/087 , C07K5/10 , C07K5/103 , C07K5/107 , A61K38/05 , A61K38/06 , A61K38/07 , A61P31/12 , A61P31/14 , A61P31/18
CPC分类号: A61K38/07 , A61K38/00 , A61K38/06 , A61K45/06 , C07D209/96 , C07D401/12 , C07D401/14 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14 , C07D487/10 , C07D491/20 , C07D495/10 , C07D498/04 , C07D498/10 , C07K5/06034 , C07K5/06078 , C07K5/06165 , C07K5/0808 , C07K5/0812 , C07K5/101 , C07K5/1016
摘要: The present application describes organic compounds of formula (I): that are useful for the treatment, prevention and/or amelioration of human diseases such as HCV and HIV.
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3.3-PYRIMIDIN-4-YL-OXAZOLIDIN-2-ONES AS INHIBITORS OF MUTANT IDH 有权
标题翻译: 3-(吡啶二酮-4-YL)-OXAZOLIDIN-2-ONE ALS INHIBITOREN VON IDH-MUTATIONEN公开(公告)号:EP2771337A1
公开(公告)日:2014-09-03
申请号:EP12784701.0
申请日:2012-09-26
申请人: Novartis AG
发明人: CHO, Young Shin , LEVELL, Julian Roy , TOURE, Bakary-Barry , YANG, Fan , CAFERRO, Thomas , LEI, Huangshu , LENOIR, Francois , LIU, Gang , PALERMO, Mark G. , SCHULTZ, Michael David , SMITH, Troy , COSTALES, Abran Q. , PFISTER, Keith Bruce , SENDZIK, Martin , SCHAFER, Cynthia , SUTTON, James , ZHAO, Qian
IPC分类号: C07D413/04 , C07D413/14 , C07D417/14 , C07D471/04 , C07D487/04 , C07D498/10 , C07D513/04 , A61K31/506 , A61P35/00
CPC分类号: C07D413/14 , C07D413/04 , C07D417/14 , C07D471/04 , C07D487/04 , C07D487/08 , C07D498/10 , C07D513/04
摘要: The invention is directed to a compound of formula (I) or a pharmaceutically acceptable salt thereof, wherein R
1 -R
6 are defined herein. The invention is also directed to compositions containing a compound of formula (I) and to the use of such compounds in the inhibition of mutant IDH proteins having a neomorphic activity. The invention is further directed to the use of a compound of formual (I) in the treatment of diseases or disorders associated with such mutant IDH proteins including, but not limited to, cell-proliferation disorders, such as cancer.摘要翻译: 本发明涉及式(I)化合物或其药学上可接受的盐,其中R 1 -R 6在本文中定义。 本发明还涉及含有式(I)化合物的组合物以及这些化合物在抑制具有新形态活性的突变体IDH蛋白质中的用途。 本发明进一步涉及式(I)化合物在治疗与这种突变型IDH蛋白相关的疾病或病症中的用途,包括但不限于细胞增殖病症如癌症。
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4.3-(PYRIMIDIN-4-YL)-OXAZOLIDIN-2-ONES AS INHIBITORS OF MUTANT IDH 有权
标题翻译: 3-(嘧啶-4-基) - 恶唑烷-2-酮作为突变IDH的抑制剂公开(公告)号:EP2771337B1
公开(公告)日:2017-08-02
申请号:EP12784701.0
申请日:2012-09-26
申请人: Novartis AG
发明人: CHO, Young Shin , LEVELL, Julian Roy , TOURE, Bakary-Barry , YANG, Fan , CAFERRO, Thomas , LEI, Huangshu , LENOIR, Francois , LIU, Gang , PALERMO, Mark G. , SHULTZ, Michael David , SMITH, Troy , COSTALES, Abran Q. , PFISTER, Keith Bruce , SENDZIK, Martin , SHAFER, Cynthia , SUTTON, James , ZHAO, Qian
IPC分类号: C07D413/04 , C07D413/14 , C07D417/14 , C07D471/04 , C07D487/04 , C07D498/10 , C07D513/04 , A61K31/506 , A61P35/00
CPC分类号: C07D413/14 , C07D413/04 , C07D417/14 , C07D471/04 , C07D487/04 , C07D487/08 , C07D498/10 , C07D513/04
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5.ORGANIC COMPOUNDS FOR APPLICATIONS IN BACTERIAL INFECTIONS TREATMENT 审中-公开
标题翻译: ORGANISCHE VERBINDUNGENFÜRANWENDUNGEN BEI DER BEHANDLUNG BAKTERIELLER INFEKTIONEN公开(公告)号:EP2340241A1
公开(公告)日:2011-07-06
申请号:EP09782998.0
申请日:2009-09-15
申请人: Novartis AG
发明人: DOBLER, Markus, Rolf , LENOIR, Francois , PARKER, David, Thomas , PENG, Yunshan , PIIZZI, Grazia , WATTANASIN, Sompong
IPC分类号: C07C259/06 , C07C321/28 , C07D211/34 , C07D213/56 , C07D307/16 , C07D307/81 , C07D309/22 , A61P31/04 , A61K31/166
CPC分类号: C07D309/22 , C07B2200/05 , C07C259/06 , C07C323/62 , C07C2601/02 , C07C2601/04 , C07C2601/08 , C07C2601/10 , C07C2601/14 , C07C2601/16 , C07D211/70 , C07D213/30 , C07D307/42 , C07D307/80
摘要: The present application describes organic compounds of a general formula: and salts, and isomers thereof, wherein R, R2 and R3 are defined in the specification. The compounds are useful for treating a gram-negative bacterial infection.
摘要翻译: 本申请描述了通式为的有机化合物及其盐及其异构体,其中R,R 2和R 3在本说明书中定义。 该化合物可用于治疗革兰氏阴性细菌感染。
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