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1.ENANTIOMERICALLY PURE AMINOHETEROARYL COMPOUNDS AS PROTEIN KINASE INHIBITORS 有权
标题翻译: 纯化纯化蛋白作为蛋白激酶抑制剂公开(公告)号:US20120263706A1
公开(公告)日:2012-10-18
申请号:US13537759
申请日:2012-06-29
申请人: Jingrong Jean Cui , Lee Andrew Funk , Lei Jia , Pei-Pei Kung , Jerry Jialun Meng , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube
发明人: Jingrong Jean Cui , Lee Andrew Funk , Lei Jia , Pei-Pei Kung , Jerry Jialun Meng , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube
IPC分类号: A61K31/4418 , C07D403/10 , C07D401/10 , C07D213/73 , C07D401/14 , C07D401/04 , C07D403/04 , C07D521/00 , A61K31/4965 , A61K31/497 , A61K31/496 , A61K31/4545 , A61K31/4439 , A61K39/395 , A61P35/00 , A61P35/02 , C07D241/20
CPC分类号: C07D403/04 , A61K31/4418 , A61K31/4439 , A61K31/4545 , A61K31/496 , A61K31/4965 , A61K31/497 , A61K45/06 , C07D213/73 , C07D213/76 , C07D241/20 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/14
摘要: Enantiomerically pure compound of formula 1 are provided, as well as methods for their synthesis and use. Preferred compounds are potent inhibitors of the c-Met protein kinase, and are useful in the treatment of abnormal cell growth disorders, such as cancers.
摘要翻译: 提供了对映异构体纯的式1化合物,以及它们合成和使用的方法。 优选的化合物是c-Met蛋白激酶的有效抑制剂,并且可用于治疗异常细胞生长障碍如癌症。
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2.Enantiomerically pure aminoheteroaryl compounds as protein kinase inhibitors 有权
标题翻译: 对映异构纯氨基杂芳基化合物作为蛋白激酶抑制剂公开(公告)号:US07858643B2
公开(公告)日:2010-12-28
申请号:US11212331
申请日:2005-08-26
申请人: Jingrong Jean Cui , Lee Andrew Funk , Lei Jia , Pei-Pei Kung , Jerry Jialun Meng , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube
发明人: Jingrong Jean Cui , Lee Andrew Funk , Lei Jia , Pei-Pei Kung , Jerry Jialun Meng , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube
IPC分类号: C07D213/65 , C07D401/14 , A61K31/4412 , C07D401/04 , A61K31/496 , A61K31/4465
CPC分类号: C07D403/04 , A61K31/4418 , A61K31/4439 , A61K31/4545 , A61K31/496 , A61K31/4965 , A61K31/497 , A61K45/06 , C07D213/73 , C07D213/76 , C07D241/20 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/14
摘要: Enantiomerically pure compound of formula 1 are provided, as well as methods for their synthesis and use. Preferred compounds are potent inhibitors of the c-Met protein kinase, and are useful in the treatment of abnormal cell growth disorders, such as cancers.
摘要翻译: 提供了对映异构体纯的式1化合物,以及它们合成和使用的方法。 优选的化合物是c-Met蛋白激酶的有效抑制剂,并且可用于治疗异常细胞生长障碍如癌症。
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3.Enantiomerically pure aminoheteroaryl compounds as protein kinase inhibitors 有权
标题翻译: 对映异构纯氨基杂芳基化合物作为蛋白激酶抑制剂公开(公告)号:US08785632B2
公开(公告)日:2014-07-22
申请号:US13537759
申请日:2012-06-29
申请人: Jingrong Jean Cui , Lee Andrew Funk , Lei Jia , Pei-Pei Kung , Jerry Jialun Meng , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube
发明人: Jingrong Jean Cui , Lee Andrew Funk , Lei Jia , Pei-Pei Kung , Jerry Jialun Meng , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube
IPC分类号: C07D401/10 , C07D401/04 , C07D401/14 , C07D213/73 , A61P35/00
CPC分类号: C07D403/04 , A61K31/4418 , A61K31/4439 , A61K31/4545 , A61K31/496 , A61K31/4965 , A61K31/497 , A61K45/06 , C07D213/73 , C07D213/76 , C07D241/20 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/14
摘要: Enantiomerically pure compound of formula 1 are provided, as well as methods for their synthesis and use. Preferred compounds are potent inhibitors of the c-Met protein kinase, and are useful in the treatment of abnormal cell growth disorders, such as cancers.
摘要翻译: 提供了对映异构体纯的式1化合物,以及它们合成和使用的方法。 优选的化合物是c-Met蛋白激酶的有效抑制剂,并且可用于治疗异常细胞生长障碍如癌症。
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4.ENANTIOMERICALLY PURE AMINOHETEROARYL COMPOUNDS AS PROTEIN KINASE INHIBITORS 审中-公开
标题翻译: 纯化纯化蛋白作为蛋白激酶抑制剂公开(公告)号:US20100324061A1
公开(公告)日:2010-12-23
申请号:US12874073
申请日:2010-09-01
申请人: Jingrong Jean Cui , Lee Andrew Funk , Lei Jia , Pei-Pei Kung , Jerry Jialun Meng , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube
发明人: Jingrong Jean Cui , Lee Andrew Funk , Lei Jia , Pei-Pei Kung , Jerry Jialun Meng , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube
IPC分类号: A61K31/497 , C07D241/20 , C07D403/10 , C07D401/10 , C07D401/14 , C07D213/73 , C07D401/04 , C07D403/04 , A61K31/4965 , A61K31/4412 , A61K31/496 , A61K31/4545 , A61K31/4439 , A61P35/00
CPC分类号: C07D403/04 , A61K31/4418 , A61K31/4439 , A61K31/4545 , A61K31/496 , A61K31/4965 , A61K31/497 , A61K45/06 , C07D213/73 , C07D213/76 , C07D241/20 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/14
摘要: Enantiomerically pure compound of formula 1 are provided, as well as methods for their synthesis and use. Preferred compounds are potent inhibitors of the c-Met protein kinase, and are useful in the treatment of abnormal cell growth disorders, such as cancers.
摘要翻译: 提供了对映异构体纯的式1化合物,以及它们合成和使用的方法。 优选的化合物是c-Met蛋白激酶的有效抑制剂,并且可用于治疗异常细胞生长障碍如癌症。
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公开(公告)号:US08106197B2
公开(公告)日:2012-01-31
申请号:US11598765
申请日:2006-11-14
申请人: Jingrong Jean Cui , Dilip Bhumralkar , Iriny Botrous , Ji Yu Chu , Lee A. Funk , Cathleen Elizabeth Hanau , G. Davis Harris , Lei Jia , Joanne Johnson , Stephen A. Kolodziej , Pei-Pei Kung , Xiaoyuan (Sharon) Li , Jason (Qishen) Lin , Jerry Jialun Meng , Mitchell David Nambu , Christopher G. Nelson , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube , Allison Walter , Fang-Jie Zhang , Jennifer Zhang
发明人: Jingrong Jean Cui , Dilip Bhumralkar , Iriny Botrous , Ji Yu Chu , Lee A. Funk , Cathleen Elizabeth Hanau , G. Davis Harris , Lei Jia , Joanne Johnson , Stephen A. Kolodziej , Pei-Pei Kung , Xiaoyuan (Sharon) Li , Jason (Qishen) Lin , Jerry Jialun Meng , Mitchell David Nambu , Christopher G. Nelson , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube , Allison Walter , Fang-Jie Zhang , Jennifer Zhang
IPC分类号: C07D241/02
CPC分类号: C07D213/73 , A61K45/06 , C07D401/12 , C07D413/12
摘要: Aminopyridine and aminopyrazine compounds of formula (1), compositions including these compounds, and methods of their use are provided. Preferred compounds of formula 1 have activity as protein kinase inhibitors, including as inhibitors of c-MET.
摘要翻译: 提供式(1)的氨基吡啶和氨基吡嗪化合物,包括这些化合物的组合物及其使用方法。 优选的式1化合物具有作为蛋白激酶抑制剂的活性,包括作为c-MET的抑制剂。
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公开(公告)号:US07230098B2
公开(公告)日:2007-06-12
申请号:US10786610
申请日:2004-02-26
申请人: Jingrong Jean Cui , Dilip Bhumralkar , Iriny Botrous , Ji Yu Chu , Lee A. Funk , Cathleen Elizabeth Hanau , G. Davis Harris , Lei Jia , Joanne Johnson , Stephen A. Kolodziej , Pei-Pei Kung , Xiaoyuan (Sharon) Li , Jason (Qishen) Lin , Jerry Jialun Meng , Mitchell David Nambu , Christopher G. Nelson , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube , Allison Walter , Fang-Jie Zhang , Jennifer Zhang
发明人: Jingrong Jean Cui , Dilip Bhumralkar , Iriny Botrous , Ji Yu Chu , Lee A. Funk , Cathleen Elizabeth Hanau , G. Davis Harris , Lei Jia , Joanne Johnson , Stephen A. Kolodziej , Pei-Pei Kung , Xiaoyuan (Sharon) Li , Jason (Qishen) Lin , Jerry Jialun Meng , Mitchell David Nambu , Christopher G. Nelson , Mason Alan Pairish , Hong Shen , Michelle Tran-Dube , Allison Walter , Fang-Jie Zhang , Jennifer Zhang
IPC分类号: C07D417/00 , C07D413/00 , C07D401/00 , C07D211/68 , C07D211/72
CPC分类号: C07D213/73 , A61K45/06 , C07D401/12 , C07D413/12
摘要: Aminopyridine and aminopyrazine compounds of formula (1), compositions including these compounds, and methods of their use are provided. Preferred compounds of formula 1 have activity as protein kinase inhibitors, including as inhibitors of c-MET
摘要翻译: 提供式(1)的氨基吡啶和氨基吡嗪化合物,包括这些化合物的组合物及其使用方法。 优选的式1化合物具有作为蛋白激酶抑制剂的活性,包括作为c-MET的抑制剂
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公开(公告)号:US07732604B2
公开(公告)日:2010-06-08
申请号:US11745921
申请日:2007-05-08
申请人: Hengmiao Cheng , Jingrong Jean Cui , Jacqui Elizabeth Hoffman , Lei Jia , Mary Catherine Johnson , Robert Steven Kania , Phuong Thi Quy Le , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Bich Tran-Dubé
发明人: Hengmiao Cheng , Jingrong Jean Cui , Jacqui Elizabeth Hoffman , Lei Jia , Mary Catherine Johnson , Robert Steven Kania , Phuong Thi Quy Le , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Bich Tran-Dubé
IPC分类号: C07D471/00 , C07D487/00 , C07D491/00 , C07D495/00 , C07D497/00
CPC分类号: C07D487/04
摘要: The invention relates to compounds of the formula I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3 and R4 are as defined herein. The invention also relates to pharmaceutical compositions containing the compounds of formula I and to methods of treating hyperproliferative disorders in a mammal by administering the compounds of formula I.
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 2,R 3和R 4如本文所定义。 本发明还涉及含有式I化合物的药物组合物和通过施用式I化合物来治疗哺乳动物中过度增殖性疾病的方法。
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公开(公告)号:US20100105656A1
公开(公告)日:2010-04-29
申请号:US12651984
申请日:2010-01-04
申请人: Hengmiao Cheng , Jingrong Jean Cui , Jacqui Elizabeth Hoffman , Lei Jia , Mary Catherine Johnson , Robert Steven Kania , Phuong Thi Quy Le , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Bich Tran-Dubé
发明人: Hengmiao Cheng , Jingrong Jean Cui , Jacqui Elizabeth Hoffman , Lei Jia , Mary Catherine Johnson , Robert Steven Kania , Phuong Thi Quy Le , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Bich Tran-Dubé
IPC分类号: A61K31/397 , A61K31/551 , A61K31/5377 , A61K31/4985 , A61P35/02 , A61P35/00
CPC分类号: C07D487/04
摘要: The invention relates to compounds of the formula I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3 and R4 are as defined herein. The invention also relates to pharmaceutical compositions containing the compounds of formula I and to methods of treating hyperproliferative disorders in a mammal by administering the compounds of formula I.
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 2,R 3和R 4如本文所定义。 本发明还涉及含有式I化合物的药物组合物和通过施用式I化合物来治疗哺乳动物中过度增殖性疾病的方法。
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公开(公告)号:US20070265272A1
公开(公告)日:2007-11-15
申请号:US11745921
申请日:2007-05-08
申请人: Hengmiao Cheng , Jingrong Jean Cui , Jacqui Elizabeth Hoffman , Lei Jia , Mary Catherine Johnson , Robert Steven Kania , Phuong Thi Quy Le , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Bich Tran-Dube
发明人: Hengmiao Cheng , Jingrong Jean Cui , Jacqui Elizabeth Hoffman , Lei Jia , Mary Catherine Johnson , Robert Steven Kania , Phuong Thi Quy Le , Mitchell David Nambu , Mason Alan Pairish , Hong Shen , Michelle Bich Tran-Dube
IPC分类号: A61K31/495 , C07D487/00
CPC分类号: C07D487/04
摘要: The invention relates to compounds of the formula I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3 and R4 are as defined herein. The invention also relates to pharmaceutical compositions containing the compounds of formula I and to methods of treating hyperproliferative disorders in a mammal by administering the compounds of formula I.
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 2,R 3和R 2 > 4 SUP>如本文所定义。 本发明还涉及含有式I化合物的药物组合物和通过施用式I化合物来治疗哺乳动物中过度增殖性疾病的方法。
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公开(公告)号:US07696213B2
公开(公告)日:2010-04-13
申请号:US11854999
申请日:2007-09-13
申请人: Hengmiao Cheng , Dilip Bhumralkar , Klaus Ruprecht Dress , Jacqui Elizabeth Hoffman , Mary Catherine Johnson , Robert Steven Kania , Phuong Thi Quy Le , Mitchell David Nambu , Mason Alan Pairish , Michael Bruno Plewe , Khanh Tuan Tran
发明人: Hengmiao Cheng , Dilip Bhumralkar , Klaus Ruprecht Dress , Jacqui Elizabeth Hoffman , Mary Catherine Johnson , Robert Steven Kania , Phuong Thi Quy Le , Mitchell David Nambu , Mason Alan Pairish , Michael Bruno Plewe , Khanh Tuan Tran
IPC分类号: C07D471/04 , C07D487/04 , A61K31/519 , A61P35/00
CPC分类号: C07D471/04
摘要: The present invention is directed to novel 4-methylpyridopyrimidinone compounds of Formula (I), and to salts thereof, their synthesis, and their use as inhibitors of phosphoinositide 3-kinase alpha (PI3-Kα).
摘要翻译: 本发明涉及新的式(I)的4-甲基吡啶并嘧啶酮化合物及其盐,它们的合成及其作为磷酸肌醇3-激酶α(PI3-Kα)抑制剂的用途。
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