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公开(公告)号:US08673908B2
公开(公告)日:2014-03-18
申请号:US13128516
申请日:2009-11-09
申请人: Nobuyoshi Amishiro , Yuichi Fukuda , Keisuke Kimpara , Motoya Mie , Hisashi Tagaya , Takeshi Takahashi
发明人: Nobuyoshi Amishiro , Yuichi Fukuda , Keisuke Kimpara , Motoya Mie , Hisashi Tagaya , Takeshi Takahashi
IPC分类号: A61K31/535 , A01N43/58 , A01N43/60 , A61K31/495 , A61K31/50 , C07D413/00 , C07D491/00 , C07D241/02
CPC分类号: C07D241/22 , A61K31/4965 , A61K31/497 , A61K31/498 , A61K31/4985 , A61K31/5377 , C07D241/20 , C07D241/44 , C07D401/12 , C07D403/12 , C07D407/12 , C07D407/14 , C07D409/12 , C07D413/12 , C07D413/14 , C07D417/12 , C07D453/02 , C07D471/04
摘要: Provided is a kynurenine production inhibitor comprising a nitrogen-containing heterocyclic compound represented by formula (I): (wherein R50 and R51 may be the same or different and each represent a hydrogen atom or the like, G1 and G2 may be the same or different and each represent a nitrogen atom or the like, X represents formula (III): (wherein m1 and m2 may be the same or different and each represent an integer of 0 or 1, Y represents an oxygen atom or the like, and R6 and R7 may be the same or different and each represent a hydrogen atom or the like), R1 represents optionally substituted lower alkyl or the like, R2 represents a hydrogen atom or the like, and R3 represents optionally substituted lower alkyl or the like), and the like.
摘要翻译: 本发明提供了含有由式(I)表示的含氮杂环化合物的犬尿氨酸生产抑制剂:其中R50和R51可以相同或不同,各自表示氢原子等,G1和G2可以相同或不同 各自表示氮原子等,X表示式(III):(其中,m1和m2可以相同或不同,表示0或1的整数,Y表示氧原子等,R6和 R 7可以相同或不同,各自表示氢原子等),R 1表示任选取代的低级烷基等,R 2表示氢原子等,R 3表示任选取代的低级烷基等),和 类似。
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公开(公告)号:US20110237584A1
公开(公告)日:2011-09-29
申请号:US13128516
申请日:2009-11-09
申请人: Nobuyoshi Amishiro , Yuichi Fukuda , Keisuke Kinpara , Motoya Mie , Hisashi Tagaya , Takeshi Takahashi
发明人: Nobuyoshi Amishiro , Yuichi Fukuda , Keisuke Kinpara , Motoya Mie , Hisashi Tagaya , Takeshi Takahashi
IPC分类号: A61K31/4965 , C07D401/12 , A61K31/497 , C07D241/22 , C07D471/04 , A61K31/4985 , C07D409/12 , C07D405/14 , C07D413/14 , C07D405/12 , A61K31/5377 , C07D417/12 , C07D417/14 , C07D403/12 , A61P35/00
CPC分类号: C07D241/22 , A61K31/4965 , A61K31/497 , A61K31/498 , A61K31/4985 , A61K31/5377 , C07D241/20 , C07D241/44 , C07D401/12 , C07D403/12 , C07D407/12 , C07D407/14 , C07D409/12 , C07D413/12 , C07D413/14 , C07D417/12 , C07D453/02 , C07D471/04
摘要: Provided is a kynurenine production inhibitor comprising a nitrogen-containing heterocyclic compound represented by formula (I): (wherein R50 and R51 may be the same or different and each represent a hydrogen atom or the like, G1 and G2 may be the same or different and each represent a nitrogen atom or the like, X represents formula (III): (wherein m1 and m2 may be the same or different and each represent an integer of 0 or 1, Y represents an oxygen atom or the like, and R6 and R7 may be the same or different and each represent a hydrogen atom or the like), R1 represents optionally substituted lower alkyl or the like, R2 represents a hydrogen atom or the like, and R3 represents optionally substituted lower alkyl or the like), and the like.
摘要翻译: 本发明提供了含有由式(I)表示的含氮杂环化合物的犬尿氨酸生产抑制剂:其中R50和R51可以相同或不同,各自表示氢原子等,G1和G2可以相同或不同 各自表示氮原子等,X表示式(III):(其中,m1和m2可以相同或不同,表示0或1的整数,Y表示氧原子等,R6和 R 7可以相同或不同,各自表示氢原子等),R 1表示任选取代的低级烷基等,R 2表示氢原子等,R 3表示任选取代的低级烷基等),和 类似。
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公开(公告)号:US07745641B2
公开(公告)日:2010-06-29
申请号:US11918778
申请日:2006-04-19
申请人: Chikara Murakata , Nobuyoshi Amishiro , Toshiyuki Atsumi , Yoshinori Yamashita , Takeshi Takahashi , Ryuichiro Nakai , Hisashi Tagaya , Hiroko Takahashi , Jun Funahashi , Junichiro Yamamoto , Yuichi Fukuda
发明人: Chikara Murakata , Nobuyoshi Amishiro , Toshiyuki Atsumi , Yoshinori Yamashita , Takeshi Takahashi , Ryuichiro Nakai , Hisashi Tagaya , Hiroko Takahashi , Jun Funahashi , Junichiro Yamamoto , Yuichi Fukuda
IPC分类号: C07D207/00 , A61K31/40
CPC分类号: C07D209/46 , C07D209/48 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/04 , C07D405/14 , C07D409/04 , C07D409/14 , C07D471/04
摘要: The present invention provides a nitrogen-containing heterocyclic compound represented by formula (I): {wherein W represents a nitrogen atom or —CH—; X represents —C(═O)— or —CHR4— (wherein R4 represents a hydrogen atom, or the like}; R1 represents a group represented by the following formula: [wherein Q1 represents a nitrogen atom or —CR8— (wherein R8 represents a hydrogen atom, substituted or unsubstituted lower alkyl, or the like). Q2 represents —NR15— (wherein R15 represents a hydrogen atom, or the like) and R5 and R6 may be the same or different and each represents a hydrogen atom, substituted or unsubstituted lower alkyl, or the like]; and R2 and R3 may be the same or different and each represents a hydrogen atom, halogen, substituted or unsubstituted lower alkyl, or the like} or a pharmaceutically acceptable salt thereof, and the like.
摘要翻译: 本发明提供由式(I)表示的含氮杂环化合物:其中W表示氮原子或-CH-; X表示-C(= O) - 或-CHR 4 - (其中R 4表示氢原子等); R 1表示由下式表示的基团:[其中Q1表示氮原子或-CR 8 - (其中R 8 表示氢原子,取代或未取代的低级烷基等),Q2表示-NR15-(式中,R15表示氢原子等),R5和R6可以相同或不同,表示氢原子, 取代或未取代的低级烷基等); R 2和R 3可以相同或不同,各自表示氢原子,卤素,取代或未取代的低级烷基等,或其药学上可接受的盐等 。
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公开(公告)号:US20090054407A1
公开(公告)日:2009-02-26
申请号:US11918778
申请日:2006-04-19
申请人: Chikara Murakata , Nobuyoshi Amishiro , Toshiyuki Atsumi , Yoshinori Yamashita , Takeshi Takahashi , Ryuichiro Nakai , Hisashi Tagaya , Hiroko Takahashi , Jun Funahashi , Junichiro Yamamoto , Yuichi Fukuda
发明人: Chikara Murakata , Nobuyoshi Amishiro , Toshiyuki Atsumi , Yoshinori Yamashita , Takeshi Takahashi , Ryuichiro Nakai , Hisashi Tagaya , Hiroko Takahashi , Jun Funahashi , Junichiro Yamamoto , Yuichi Fukuda
IPC分类号: A61K31/55 , C07D209/04 , A61K31/404 , C07D403/14 , A61K31/496 , C07D401/14 , A61K31/541 , A61K31/506 , A61P35/00 , C07D417/14 , A61K31/454 , C07D413/14 , A61K31/5377 , A61K31/4439
CPC分类号: C07D209/46 , C07D209/48 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/04 , C07D405/14 , C07D409/04 , C07D409/14 , C07D471/04
摘要: The present invention provides a nitrogen-containing heterocyclic compound represented by formula (I): {wherein W represents a nitrogen atom or —CH—; X represents —C(═O)— or —CHR4— (wherein R4 represents a hydrogen atom, or the like); R1 represents a group represented by the following formula: [wherein Q1 represents a nitrogen atom or —CR8— (wherein R8 represents a hydrogen atom, substituted or unsubstituted lower alkyl, or the like). Q2 represents —NR15— (wherein R15 represents a hydrogen atom, or the like) and R5 and R6 may be the same or different and each represents a hydrogen atom, substituted or unsubstituted lower alkyl, or the like]; and R2 and R3 may be the same or different and each represents a hydrogen atom, halogen, substituted or unsubstituted lower alkyl, or the like} or a pharmaceutically acceptable salt thereof, and the like.
摘要翻译: 本发明提供由式(I)表示的含氮杂环化合物:其中W表示氮原子或-CH-; X表示-C(-O) - 或-CHR 4 - (其中R 4表示氢原子等); R1表示由下式表示的基团:[其中Q1表示氮原子或-CR8-(其中R8表示氢原子,取代或未取代的低级烷基等)。 Q2表示-NR15-(其中R15表示氢原子等),R5和R6可以相同或不同,表示氢原子,取代或未取代的低级烷基等]。 R 2和R 3可以相同或不同,各自表示氢原子,卤素,取代或未取代的低级烷基等}或其药学上可接受的盐等。
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公开(公告)号:US20090054508A1
公开(公告)日:2009-02-26
申请号:US11814753
申请日:2006-01-27
申请人: Yutaka Kanda , Hiromi Ando , Keiko Kawashima , Takamasa Sugita , Masayo Suzuki , Hisashi Tagaya , Tomoyuki Nakazato , Yoshinori Yamashita , Takeshi Takahashi , Shinji Nara , Hiroaki Nakamura
发明人: Yutaka Kanda , Hiromi Ando , Keiko Kawashima , Takamasa Sugita , Masayo Suzuki , Hisashi Tagaya , Tomoyuki Nakazato , Yoshinori Yamashita , Takeshi Takahashi , Shinji Nara , Hiroaki Nakamura
IPC分类号: A61K31/416 , A61P3/10
CPC分类号: C07D231/56 , C07D401/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12 , C07D491/10 , C07D495/04
摘要: The present invention provides a type I insulin-like growth factor receptor (IGF-1R) inhibitor comprising, as an active ingredient, an indazole derivative represented by Formula (I): {wherein R1 represents —NR4R5 [wherein R4 represents a hydrogen atom or the like, R5 represents substituted or unsubstituted lower alkyl, —C(═O)R6 (wherein R6 represents substituted or unsubstituted lower alkyl, substituted or unsubstituted aryl or the like), or the like], or the like, and R2 and R3 may be the same or different and each represents a hydrogen atom, hydroxy, substituted or unsubstituted lower alkoxy, or the like} or a pharmaceutically acceptable salt thereof, and the like.
摘要翻译: 本发明提供一种I型胰岛素样生长因子受体(IGF-1R)抑制剂,其包含作为活性成分的由式(I)表示的吲唑衍生物:其中R 1表示-NR 4 R 5 [其中R 4表示氢原子或 R 5表示取代或未取代的低级烷基,-C(-O)R 6(其中R 6表示取代或未取代的低级烷基,取代或未取代的芳基等)等,等等,R2和R3 可以相同或不同,各自表示氢原子,羟基,取代或未取代的低级烷氧基等}或其药学上可接受的盐等。
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公开(公告)号:US07605272B2
公开(公告)日:2009-10-20
申请号:US11814753
申请日:2006-01-27
申请人: Yutaka Kanda , Hiromi Ando , Keiko Kawashima , Takamasa Sugita , Masayo Suzuki , Hisashi Tagaya , Tomoyuki Nakazato , Yoshinori Yamashita , Takeshi Takahashi , Shinji Nara , Hiroaki Nakamura
发明人: Yutaka Kanda , Hiromi Ando , Keiko Kawashima , Takamasa Sugita , Masayo Suzuki , Hisashi Tagaya , Tomoyuki Nakazato , Yoshinori Yamashita , Takeshi Takahashi , Shinji Nara , Hiroaki Nakamura
IPC分类号: C07D231/56 , C07D211/06 , C07D413/10 , C07D403/10 , A61K31/416 , A61K31/4439 , A61K31/496 , A61K31/5355 , A61K31/5377
CPC分类号: C07D231/56 , C07D401/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12 , C07D491/10 , C07D495/04
摘要: The present invention provides a type I insulin-like growth factor receptor (IGF-1R) inhibitor comprising, as an active ingredient, an indazole derivative represented by Formula (I): {wherein R1 represents —NR4R5 [wherein R4 represents a hydrogen atom or the like, R5 represents substituted or unsubstituted lower alkyl, —C(═O)R6 (wherein R6 represents substituted or unsubstituted lower alkyl, substituted or unsubstituted aryl or the like), or the like], or the like, and R2 and R3 may be the same or different and each represents a hydrogen atom, hydroxy, substituted or unsubstituted lower alkoxy, or the like} or a pharmaceutically acceptable salt thereof, and the like.
摘要翻译: 本发明提供一种I型胰岛素样生长因子受体(IGF-1R)抑制剂,其包含作为活性成分的由式(I)表示的吲唑衍生物:其中R 1表示-NR 4 R 5 [其中R 4表示氢原子或 R 5表示取代或未取代的低级烷基,-C(-O)R 6(其中R 6表示取代或未取代的低级烷基,取代或未取代的芳基等),R 2和R 3可以相同 或不同的,并且各自表示氢原子,羟基,取代或未取代的低级烷氧基等}或其药学上可接受的盐等。
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