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公开(公告)号:US08629132B2
公开(公告)日:2014-01-14
申请号:US12945629
申请日:2010-11-12
申请人: Jaekyoo Lee , Ho-Juhn Song , Jong Sung Koh , Hee Kyu Lee , Youngsam Kim , Hong Woo Kim , Sunhwa Chang , Sun-Hee Lim , Jang-Sik Choi , Jung-Ho Kim , Se-Won Kim
发明人: Jaekyoo Lee , Ho-Juhn Song , Jong Sung Koh , Hee Kyu Lee , Youngsam Kim , Hong Woo Kim , Sunhwa Chang , Sun-Hee Lim , Jang-Sik Choi , Jung-Ho Kim , Se-Won Kim
IPC分类号: A61K31/33 , A61K31/55 , A61K31/535 , A61K31/501 , C07D413/06 , C07D403/04 , C07D243/08
CPC分类号: A61K31/505 , C07D403/04 , C07D403/14 , C07D405/14 , C07D417/14 , C07D487/08
摘要: The present invention provides a new group of protein kinase inhibitors, pyrropyrimidine and pyrazolopyrimidine derivatives, and pharmaceutically acceptable salts and prodrugs thereof that are useful for treating cell proliferative disease and disorder such as cancer, autoimmune diseases, infection, cardiovascular disease and neurodegenerative disease and disorder. The present invention provides methods for synthesizing and administering the protein kinase inhibitor compounds. The present invention also provides pharmaceutical formulations comprising at least one of the protein kinase inhibitor compounds together with a pharmaceutically acceptable carrier, diluent or excipient therefor. The invention also provides useful intermediates generated during the syntheses of the pyrropyrimidine and pyrazolopyrimidine derivatives.
摘要翻译: 本发明提供了可用于治疗细胞增殖性疾病和病症如癌症,自身免疫性疾病,感染,心血管疾病和神经变性疾病和病症的新组蛋白激酶抑制剂,嘧啶嘧啶和吡唑并嘧啶衍生物及其药学上可接受的盐和前药 。 本发明提供了合成和给予蛋白激酶抑制剂化合物的方法。 本发明还提供了包含至少一种蛋白激酶抑制剂化合物以及药学上可接受的载体,稀释剂或赋形剂的药物制剂。 本发明还提供了在嘧啶嘧啶和吡唑并嘧啶衍生物的合成过程中产生的有用的中间体。
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公开(公告)号:US08404677B2
公开(公告)日:2013-03-26
申请号:US12916368
申请日:2010-10-29
申请人: Hong Woo Kim , Jong Sung Koh , Jaekyoo Lee , Ho-Juhn Song , Youngsam Kim , Hee Kyu Lee , Jang-Sik Choi , Sun-Hee Lim , Sunhwa Chang
发明人: Hong Woo Kim , Jong Sung Koh , Jaekyoo Lee , Ho-Juhn Song , Youngsam Kim , Hee Kyu Lee , Jang-Sik Choi , Sun-Hee Lim , Sunhwa Chang
IPC分类号: C07D471/04 , C07D211/86 , A61K31/519 , A61K31/4375
CPC分类号: A61K31/519 , C07D471/04
摘要: The present invention provides a new group of protein kinase inhibitors, pyrido[4,3,-d]pyrimidin-5-one derivatives, and pharmaceutically acceptable salts thereof that are useful for intreating cell proliferative disease and disorder such as cancer, autoimmune diseases, infection, cardiovascular disease and neurodegenerative disease and disorder. The present invention provides methods for synthesizing and administering the protein kinase inhibitor compounds. The present invention also provides pharmaceutical formulations comprising at least one of the protein kinase inhibitor compounds together with a pharmaceutically acceptable carrier, diluent or excipient therefor. The invention also provides useful intermediates generated during the syntheses of the pyrido[4,3,-d]pyrimidin-5-one derivatives.
摘要翻译: 本发明提供了一组新的蛋白激酶抑制剂,吡啶并[4,3,-d]嘧啶-5-酮衍生物及其药学上可接受的盐,其可用于促进细胞增殖性疾病和病症如癌症,自身免疫性疾病, 感染,心血管疾病和神经退行性疾病和障碍。 本发明提供了合成和施用蛋白激酶抑制剂化合物的方法。 本发明还提供了包含至少一种蛋白激酶抑制剂化合物以及药学上可接受的载体,稀释剂或赋形剂的药物制剂。 本发明还提供了在吡啶并[4,3, - d]嘧啶-5-酮衍生物的合成过程中产生的有用的中间体。
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公开(公告)号:US20110269739A1
公开(公告)日:2011-11-03
申请号:US12916368
申请日:2010-10-29
申请人: Hong Woo Kim , Jong Sung Koh , Jaekyoo Lee , Ho-Juhn Song , Youngsam Kim , Hee Kyu Lee , Jang-Sik Choi , Sun-Hee Lim , Sunhwa Chang
发明人: Hong Woo Kim , Jong Sung Koh , Jaekyoo Lee , Ho-Juhn Song , Youngsam Kim , Hee Kyu Lee , Jang-Sik Choi , Sun-Hee Lim , Sunhwa Chang
IPC分类号: A61K31/397 , A61K31/519 , C07D413/14 , A61K31/5377 , A61K31/496 , C07D417/14 , A61K31/541 , A61K31/5513 , A61P35/00 , A61P11/06 , A61P11/00 , A61P17/00 , A61P17/06 , A61P19/02 , A61P25/28 , A61P19/10 , A61P9/00 , A61P31/00 , A61P31/12 , C12N5/09 , C07D471/04
CPC分类号: A61K31/519 , C07D471/04
摘要: The present invention provides a new group of protein kinase inhibitors, pyrido[4,3,-d]pyrimidin-5-one derivatives, and pharmaceutically acceptable salts thereof that are useful for intreating cell proliferative disease and disorder such as cancer, autoimmune diseases, infection, cardiovascular disease and neurodegenerative disease and disorder. The present invention provides methods for synthesizing and administering the protein kinase inhibitor compounds. The present invention also provides pharmaceutical formulations comprising at least one of the protein kinase inhibitor compounds together with a pharmaceutically acceptable carrier, diluent or excipient therefor. The invention also provides useful intermediates generated during the syntheses of the pyrido[4,3,-d]pyrimidin-5-one derivatives.
摘要翻译: 本发明提供了一组新的蛋白激酶抑制剂,吡啶并[4,3,-d]嘧啶-5-酮衍生物及其药学上可接受的盐,其可用于促进细胞增殖性疾病和病症如癌症,自身免疫性疾病, 感染,心血管疾病和神经退行性疾病和障碍。 本发明提供了合成和施用蛋白激酶抑制剂化合物的方法。 本发明还提供了包含至少一种蛋白激酶抑制剂化合物以及药学上可接受的载体,稀释剂或赋形剂的药物制剂。 本发明还提供了在吡啶并[4,3, - d]嘧啶-5-酮衍生物的合成过程中产生的有用的中间体。
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公开(公告)号:US20110281841A1
公开(公告)日:2011-11-17
申请号:US12945629
申请日:2010-11-12
申请人: Jaekyoo Lee , Ho-Juhn Song , Jong Sung Kon , Hee Kyu Lee , Yougsam Kim , Hong Woo Kim , Sunhwa Chang , Sun-Hee Lim , Jang-Sik Choi , Jung-Ho Kim , Se-Won Kim
发明人: Jaekyoo Lee , Ho-Juhn Song , Jong Sung Kon , Hee Kyu Lee , Yougsam Kim , Hong Woo Kim , Sunhwa Chang , Sun-Hee Lim , Jang-Sik Choi , Jung-Ho Kim , Se-Won Kim
IPC分类号: A61K31/506 , C07D403/14 , C07D401/14 , C07D413/14 , A61K31/496 , A61K31/551 , A61K31/5377 , A61P11/00 , A61P11/06 , A61P1/04 , A61P1/00 , A61P17/00 , A61P17/06 , A61P19/02 , A61P35/00 , A61P25/16 , A61P25/28 , A61P19/10 , A61P19/08 , A61P3/10 , A61P9/10 , A61P9/04 , A61P9/12 , A61P31/12 , A61P31/10 , C12N5/09 , C07D403/04
CPC分类号: A61K31/505 , C07D403/04 , C07D403/14 , C07D405/14 , C07D417/14 , C07D487/08
摘要: The present invention provides a new group of protein kinase inhibitors, pyrropyrimidine and pyrazolopyrimidine derivatives, and pharmaceutically acceptable salts and prodrugs thereof that are useful for treating cell proliferative disease and disorder such as cancer, autoimmune diseases, infection, cardiovascular disease and neurodegenerative disease and disorder. The present invention provides methods for synthesizing and administering the protein kinase inhibitor compounds. The present invention also provides pharmaceutical formulations comprising at least one of the protein kinase inhibitor compounds together with a pharmaceutically acceptable carrier, diluent or excipient therefor. The invention also provides useful intermediates generated during the syntheses of the pyrropyrimidine and pyrazolopyrimidine derivatives.
摘要翻译: 本发明提供了可用于治疗细胞增殖性疾病和病症如癌症,自身免疫性疾病,感染,心血管疾病和神经变性疾病和病症的新组蛋白激酶抑制剂,嘧啶嘧啶和吡唑并嘧啶衍生物及其药学上可接受的盐和前药 。 本发明提供了合成和施用蛋白激酶抑制剂化合物的方法。 本发明还提供了包含至少一种蛋白激酶抑制剂化合物以及药学上可接受的载体,稀释剂或赋形剂的药物制剂。 本发明还提供了在嘧啶嘧啶和吡唑并嘧啶衍生物的合成过程中产生的有用的中间体。
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