-
公开(公告)号:US08642779B2
公开(公告)日:2014-02-04
申请号:US12634136
申请日:2009-12-09
申请人: Hayley Binch , Simon Everitt , Francesca Mazzei , Daniel Robinson
发明人: Hayley Binch , Simon Everitt , Francesca Mazzei , Daniel Robinson
IPC分类号: C07D231/54 , C07D401/00 , C07D409/00
CPC分类号: C07D487/04 , A61K31/41 , A61K45/06 , A61K2300/00
摘要: The present invention provides compounds of formula I: or a pharmaceutically acceptable derivative thereof, wherein A, B, Q, R1, and R2 are as described in the specification. These compounds are inhibitors of protein kinase, particularly inhibitors of AKT or PDK1 kinase, mammalian protein kinases involved in proliferative and neurodegenerative disorders. The invention also provides pharmaceutical compositions comprising the compounds of the invention, processes for preparing the compounds, and methods of utilizing those compositions in the treatment of various disorders.
摘要翻译: 本发明提供式I化合物或其药学上可接受的衍生物,其中A,B,Q,R 1和R 2如说明书中所述。 这些化合物是蛋白激酶的抑制剂,特别是AKT或PDK1激酶的抑制剂,涉及增殖和神经变性疾病的哺乳动物蛋白激酶。 本发明还提供包含本发明化合物的药物组合物,制备化合物的方法,以及利用这些组合物治疗各种疾病的方法。
-
公开(公告)号:US08268829B2
公开(公告)日:2012-09-18
申请号:US12436407
申请日:2009-05-06
IPC分类号: C07D403/14 , A61K31/4155
CPC分类号: C07D403/14 , C07D239/34 , C07D401/14 , C07D403/12 , C07D453/02
摘要: The present invention provides a facile process for the preparation of tri- and tetra-substituted pyrimidines. The process is useful for preparing inhibitors of protein kinases, especially Aurora kinase. These inhibitors are useful for treating or lessening the severity of Aurora-mediated diseases or conditions.
摘要翻译: 本发明提供了制备三取代和四取代嘧啶的简便方法。 该方法可用于制备蛋白激酶抑制剂,特别是Aurora激酶。 这些抑制剂可用于治疗或减轻Aurora介导的疾病或病症的严重性。
-
公开(公告)号:US20060270660A1
公开(公告)日:2006-11-30
申请号:US11500981
申请日:2006-08-09
IPC分类号: A61K31/551 , A61K31/5377 , A61K31/513 , C07D403/14 , C07D413/14
CPC分类号: C07D403/14 , C07D239/34 , C07D401/14 , C07D403/12 , C07D453/02
摘要: The present invention provides a facile process for the preparation of tri- and tetra-substituted pyrimidines. The process is useful for preparing inhibitors of protein kinases, especially Aurora kinase. These inhibitors are useful for treating or lessening the severity of Aurora-mediated diseases or conditions.
摘要翻译: 本发明提供了制备三取代和四取代嘧啶的简便方法。 该方法可用于制备蛋白激酶抑制剂,特别是Aurora激酶。 这些抑制剂可用于治疗或减轻Aurora介导的疾病或病症的严重性。
-
公开(公告)号:US20100087467A1
公开(公告)日:2010-04-08
申请号:US12634136
申请日:2009-12-09
申请人: Hayley Binch , Simon Everitt , Francesca Mazzei , Daniel Robinson
发明人: Hayley Binch , Simon Everitt , Francesca Mazzei , Daniel Robinson
IPC分类号: A61K31/506 , C07D403/14 , C07D487/04 , A61K31/4162 , A61P35/00
CPC分类号: C07D487/04 , A61K31/41 , A61K45/06 , A61K2300/00
摘要: The present invention provides compounds of formula I: or a pharmaceutically acceptable derivative thereof, wherein A, B, Q, R1, and R2 are as described in the specification. These compounds are inhibitors of protein kinase, particularly inhibitors of AKT or PDK1 kinase, mammalian protein kinases involved in proliferative and neurodegenerative disorders. The invention also provides pharmaceutical compositions comprising the compounds of the invention, processes for preparing the compounds, and methods of utilizing those compositions in the treatment of various disorders.
摘要翻译: 本发明提供式I化合物或其药学上可接受的衍生物,其中A,B,Q,R 1和R 2如说明书中所述。 这些化合物是蛋白激酶的抑制剂,特别是AKT或PDK1激酶的抑制剂,涉及增殖和神经变性疾病的哺乳动物蛋白激酶。 本发明还提供包含本发明化合物的药物组合物,制备化合物的方法,以及利用这些组合物治疗各种疾病的方法。
-
公开(公告)号:US07652135B2
公开(公告)日:2010-01-26
申请号:US10949714
申请日:2004-09-23
申请人: Hayley Binch , Simon Everitt , Francesca Mazzei , Daniel Robinson
发明人: Hayley Binch , Simon Everitt , Francesca Mazzei , Daniel Robinson
IPC分类号: C07D413/00 , C07D211/32
CPC分类号: C07D487/04 , A61K31/41 , A61K45/06 , A61K2300/00
摘要: The present invention provides compounds of formula I: or a pharmaceutically acceptable derivative thereof, wherein A, B, Q, R1, and R2 are as described in the specification. These compounds are inhibitors of protein kinase, particularly inhibitors of AKT or PDK1 kinase, mammalian protein kinases involved in proliferative and neurodegenerative disorders. The invention also provides pharmaceutical compositions comprising the compounds of the invention, processes for preparing the compounds, and methods of utilizing those compositions in the treatment of various disorders.
摘要翻译: 本发明提供式I化合物或其药学上可接受的衍生物,其中A,B,Q,R 1和R 2如说明书中所述。 这些化合物是蛋白激酶的抑制剂,特别是AKT或PDK1激酶的抑制剂,涉及增殖和神经变性疾病的哺乳动物蛋白激酶。 本发明还提供包含本发明化合物的药物组合物,制备化合物的方法,以及利用这些组合物治疗各种疾病的方法。
-
公开(公告)号:US07557106B2
公开(公告)日:2009-07-07
申请号:US11500981
申请日:2006-08-09
IPC分类号: C07D403/14 , A61K31/4155
CPC分类号: C07D403/14 , C07D239/34 , C07D401/14 , C07D403/12 , C07D453/02
摘要: The present invention provides a facile process for the preparation of tri- and tetra-substituted pyrimidines. The process is useful for preparing inhibitors of protein kinases, especially Aurora kinase. These inhibitors are useful for treating or lessening the severity of Aurora-mediated diseases or conditions.
摘要翻译: 本发明提供了制备三取代和四取代嘧啶的简便方法。 该方法可用于制备蛋白激酶抑制剂,特别是Aurora激酶。 这些抑制剂可用于治疗或减轻Aurora介导的疾病或病症的严重性。
-
公开(公告)号:US08779127B2
公开(公告)日:2014-07-15
申请号:US13585861
申请日:2012-08-15
IPC分类号: C07D403/14 , C07D403/12 , C07D417/14
CPC分类号: C07D403/14 , C07D239/34 , C07D401/14 , C07D403/12 , C07D453/02
摘要: The present invention provides a facile process for the preparation of tri- and tetra—substituted pyrimidines. The process is useful for preparing inhibitors of protein kinases, especially Aurora kinase. These inhibitors are useful for treating or lessening the severity of Aurora—mediated diseases or conditions.
摘要翻译: 本发明提供了制备三取代和四取代嘧啶的简便方法。 该方法可用于制备蛋白激酶抑制剂,特别是Aurora激酶。 这些抑制剂可用于治疗或减轻Aurora介导的疾病或病症的严重性。
-
公开(公告)号:US20130066069A1
公开(公告)日:2013-03-14
申请号:US13585861
申请日:2012-08-15
IPC分类号: C07D403/14 , C07D403/04 , C07D403/12 , C07D417/14 , C07D453/02 , C07D239/38 , C07D413/14 , C07D401/14
CPC分类号: C07D403/14 , C07D239/34 , C07D401/14 , C07D403/12 , C07D453/02
摘要: The present invention provides a facile process for the preparation of tri- and tetra-substituted pyrimidines. The process is useful for preparing inhibitors of protein kinases, especially Aurora kinase. These inhibitors are useful for treating or lessening the severity of Aurora-mediated diseases or conditions.
-
公开(公告)号:US20050101594A1
公开(公告)日:2005-05-12
申请号:US10949714
申请日:2004-09-23
申请人: Hayley Binch , Simon Everitt , Francesca Mazzei , Daniel Robinson
发明人: Hayley Binch , Simon Everitt , Francesca Mazzei , Daniel Robinson
IPC分类号: A61K31/41 , A61K31/4162 , A61K31/4745 , A61K31/55 , A61K45/06 , A61P35/00 , C07D487/04
CPC分类号: C07D487/04 , A61K31/41 , A61K45/06 , A61K2300/00
摘要: The present invention provides compounds of formula I: or a pharmaceutically acceptable derivative thereof, wherein A, B, Q, R1, and R2 are as described in the specification. These compounds are inhibitors of protein kinase, particularly inhibitors of AKT or PDK1 kinase, mammalian protein kinases involved in proliferative and neurodegenerative disorders. The invention also provides pharmaceutical compositions comprising the compounds of the invention, processes for preparing the compounds, and methods of utilizing those compositions in the treatment of various disorders.
摘要翻译: 本发明提供式I化合物或其药学上可接受的衍生物,其中A,B,Q,R 1和R 2如说明书所述。 这些化合物是蛋白激酶的抑制剂,特别是AKT或PDK1激酶的抑制剂,涉及增殖和神经变性疾病的哺乳动物蛋白激酶。 本发明还提供包含本发明化合物的药物组合物,制备化合物的方法,以及利用这些组合物治疗各种疾病的方法。
-
公开(公告)号:US20090221602A1
公开(公告)日:2009-09-03
申请号:US12436407
申请日:2009-05-06
IPC分类号: A61K31/506 , C07D403/14 , C12N7/06 , A61P35/00
CPC分类号: C07D403/14 , C07D239/34 , C07D401/14 , C07D403/12 , C07D453/02
摘要: The present invention provides a facile process for the preparation of tri- and tetra-substituted pyrimidines. The process is useful for preparing inhibitors of protein kinases, especially Aurora kinase. These inhibitors are useful for treating or lessening the severity of Aurora-mediated diseases or conditions.
摘要翻译: 本发明提供了制备三取代和四取代嘧啶的简便方法。 该方法可用于制备蛋白激酶抑制剂,特别是Aurora激酶。 这些抑制剂可用于治疗或减轻Aurora介导的疾病或病症的严重性。
-
-
-
-
-
-
-
-
-