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公开(公告)号:US20090048213A1
公开(公告)日:2009-02-19
申请号:US11878556
申请日:2007-07-25
申请人: Teiji Kimura , Koki Kawano , Noritaka Kitazawa , Nobuaki Sato , Toshihiko Kaneko , Koichi Ito , Mamoru Takaishi , Ikuo Kushida
发明人: Teiji Kimura , Koki Kawano , Noritaka Kitazawa , Nobuaki Sato , Toshihiko Kaneko , Koichi Ito , Mamoru Takaishi , Ikuo Kushida
IPC分类号: A61K31/675 , C07D401/02 , C07F9/06 , A61K31/5377 , C07D221/04 , A61K31/5365 , A61P25/28 , C07D498/04 , A61K31/4439 , A61K31/435 , C07D413/02 , A61K31/454
CPC分类号: C07D401/10 , C07F9/65583 , C07F9/6561
摘要: The present invention provides a most suitable prodrug of a cinnamide compound. The prodrug is represented by Formula (I) wherein Ra and Rb each denote a C1-6 alkyl group or the like; Xa denotes a methoxy group or a fluorine atom; Y denotes a phosphono group or the like; and A denotes a cyclic lactam derivative.
摘要翻译: 本发明提供了最合适的肉桂酰胺化合物的前药。 前药由式(I)表示,其中R a和R b各自表示C 1-6烷基等; Xa表示甲氧基或氟原子; Y表示膦酰基等; A表示环状内酰胺衍生物。
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公开(公告)号:US07737141B2
公开(公告)日:2010-06-15
申请号:US11878556
申请日:2007-07-25
申请人: Teiji Kimura , Koki Kawano , Noritaka Kitazawa , Nobuaki Sato , Toshihiko Kaneko , Koichi Ito , Mamoru Takaishi , Ikuo Kushida
发明人: Teiji Kimura , Koki Kawano , Noritaka Kitazawa , Nobuaki Sato , Toshihiko Kaneko , Koichi Ito , Mamoru Takaishi , Ikuo Kushida
IPC分类号: A61K31/535 , A61K31/44 , C07D413/14 , C07D221/02
CPC分类号: C07D401/10 , C07F9/65583 , C07F9/6561
摘要: The present invention provides a most suitable prodrug of a cinnamide compound. The prodrug is represented by Formula (I) wherein Ra and Rb each denote a C1-6 alkyl group or the like; Xa denotes a methoxy group or a fluorine atom; Y denotes a phosphono group or the like; and A denotes a cyclic lactam derivative.
摘要翻译: 本发明提供了最合适的肉桂酰胺化合物的前药。 前药由式(I)表示,其中R a和R b各自表示C 1-6烷基等; Xa表示甲氧基或氟原子; Y表示膦酰基等; A表示环状内酰胺衍生物。
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公开(公告)号:US07713993B2
公开(公告)日:2010-05-11
申请号:US11715440
申请日:2007-03-08
申请人: Teiji Kimura , Noritaka Kitazawa , Toshihiko Kaneko , Nobuaki Sato , Koki Kawano , Koichi Ito , Eriko Doi , Mamoru Takaishi , Takeo Sasaki , Takehiko Miyagawa , Hiroaki Hagiwara , Takashi Doko
发明人: Teiji Kimura , Noritaka Kitazawa , Toshihiko Kaneko , Nobuaki Sato , Koki Kawano , Koichi Ito , Eriko Doi , Mamoru Takaishi , Takeo Sasaki , Takehiko Miyagawa , Hiroaki Hagiwara , Takashi Doko
IPC分类号: C07D471/04 , C07D498/04 , A61K31/5383 , A61K31/5025
CPC分类号: C07D403/10 , C07D471/04 , C07D498/04
摘要: The present invention provides a compound represented by the formula (I): or a pharmacologically acceptable salt thereof, wherein Ar1 represents an imidazolyl group that may be substituted with a C1-6 alkyl group, or the like, Ar2 represents a phenyl group that may be substituted with a C1-6 alkoxy group, or the like, X1 represents a double bond or the like, and Het represents an imidazolyl group that may be substituted with a C1-6 alkyl group, or the like, which is effective as a therapeutic or prophylactic agent for a disease caused by Aβ.
摘要翻译: 本发明提供由式(I)表示的化合物或其药理学上可接受的盐,其中Ar 1表示可被C 1-6烷基取代的咪唑基等,Ar 2表示可以 被C 1-6烷氧基等取代,X 1表示双键等,Het表示可被C 1-6烷基取代的咪唑基等,其作为式 由A&Bgr引起的疾病的治疗或预防剂。
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公开(公告)号:US20100113773A1
公开(公告)日:2010-05-06
申请号:US12522281
申请日:2008-02-27
申请人: Teiji Kimura , Koki Kawano , Eriko Doi , Noritaka Kitazawa , Mamoru Takaishi , Koichi Ito , Toshihiko Kaneko , Takeo Sasaki , Nobuaki Sato , Takehiko Miyagawa , Hiroaki Hagiwara
发明人: Teiji Kimura , Koki Kawano , Eriko Doi , Noritaka Kitazawa , Mamoru Takaishi , Koichi Ito , Toshihiko Kaneko , Takeo Sasaki , Nobuaki Sato , Takehiko Miyagawa , Hiroaki Hagiwara
IPC分类号: C07D498/04
CPC分类号: C07D498/04
摘要: The present invention relates to a compound represented by formula (I): wherein R1 represents a C1-3 alkyl group, R2 represents a hydrogen atom or a C1-3 alkyl group, Ar represents a phenyl group or the like which may be substituted with 1 to 3 substituents, X represents an oxygen atom or the like, n and m are the same or different and integers of 0 to 2, or a pharmacologically acceptable salt, and use thereof as a medicament.
摘要翻译: 本发明涉及由式(I)表示的化合物:其中R1表示C1-3烷基,R2表示氢原子或C1-3烷基,Ar表示可被基团取代的苯基等 1〜3个取代基,X表示氧原子等,n和m相同或不同,为0〜2的整数,或药理学上可接受的盐及其作为药物的用途。
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公开(公告)号:US20110065696A1
公开(公告)日:2011-03-17
申请号:US12950670
申请日:2010-11-19
申请人: Teiji KIMURA , Noritaka Kitazawa , Toshihiko Kaneko , Nobuaki Sato , Koki Kawano , Koichi Ito , Mamoru Takaishi , Takeo Sasaki , Yu Yoshida , Toshiyuki Uemura , Takashi Doko , Daisuke Shinmyo , Daiju Hasegawa , Takehiko Miyagawa , Hiroaki Hagiwara
发明人: Teiji KIMURA , Noritaka Kitazawa , Toshihiko Kaneko , Nobuaki Sato , Koki Kawano , Koichi Ito , Mamoru Takaishi , Takeo Sasaki , Yu Yoshida , Toshiyuki Uemura , Takashi Doko , Daisuke Shinmyo , Daiju Hasegawa , Takehiko Miyagawa , Hiroaki Hagiwara
IPC分类号: A61K31/437 , C07D471/04 , C07D487/04 , C07D498/04 , A61K31/519 , A61K31/4439 , A61K31/5383 , A61P25/00 , A61P25/28
CPC分类号: C07D403/10 , C07D401/14 , C07D403/14 , C07D409/14
摘要: A compound represented by the formula (I): or a pharmacologically acceptable salt thereof, wherein Ar1 represents an imidazolyl group or the like which may be substituted with a C1-6 alkyl group, Ar2 represents a phenyl group or the like which may be substituted with a C1-6 alkoxy group, X1 represents a double bond or the like and Het represents a triazolyl group or the like which may be substituted with a C1-6 alkyl group or the like, is effective as a therapeutic or prophylactic agent for a disease caused by Aβ.
摘要翻译: 由式(I)表示的化合物或其药理学上可接受的盐,其中Ar 1表示可被C 1-6烷基取代的咪唑基等,Ar 2表示可被取代的苯基等 具有C 1-6烷氧基,X 1表示双键等,Het表示可以被C 1-6烷基等取代的三唑基等,作为治疗或预防药物是有效的 A&BGR引起的疾病
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公开(公告)号:US07897632B2
公开(公告)日:2011-03-01
申请号:US12721952
申请日:2010-03-11
申请人: Teiji Kimura , Noritaka Kitazawa , Toshihiko Kaneko , Nobuaki Sato , Koki Kawano , Koichi Ito , Eriko Doi , Mamoru Takaishi , Takeo Sasaki , Takehiko Miyagawa , Hiroaki Hagiwara , Takashi Doko
发明人: Teiji Kimura , Noritaka Kitazawa , Toshihiko Kaneko , Nobuaki Sato , Koki Kawano , Koichi Ito , Eriko Doi , Mamoru Takaishi , Takeo Sasaki , Takehiko Miyagawa , Hiroaki Hagiwara , Takashi Doko
IPC分类号: C07D471/04 , C07D498/04 , A61K31/5383 , A61K31/5025
CPC分类号: C07D403/10 , C07D471/04 , C07D498/04
摘要: The present invention provides a compound represented by the formula (I): or a pharmacologically acceptable salt thereof, wherein Ar1 represents an imidazolyl group that may be substituted with a C1-6 alkyl group, or the like, Ar2 represents a phenyl group that may be substituted with a C1-6 alkoxy group, or the like, X1 represents a double bond or the like, and Het represents an imidazolyl group that may be substituted with a C1-6 alkyl group, or the like, which is effective as a therapeutic or prophylactic agent for a disease caused by Aβ.
摘要翻译: 本发明提供由式(I)表示的化合物或其药理学上可接受的盐,其中Ar 1表示可被C 1-6烷基取代的咪唑基等,Ar 2表示可以 被C 1-6烷氧基等取代,X 1表示双键等,Het表示可被C 1-6烷基取代的咪唑基等,其作为式 由A&Bgr引起的疾病的治疗或预防剂。
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公开(公告)号:US20110009619A1
公开(公告)日:2011-01-13
申请号:US12671873
申请日:2008-08-28
申请人: Teiji Kimura , Noritaka Kitazawa , Toshihiko Kaneko , Nobuaki Sato , Koki Kawano , Koichi Ito , Mamoru Takaishi , Takeo Sasaki , Yu Yoshida , Toshiyuki Uemura , Takashi Doko , Daisuke Shinmyo , Daiju Hasegawa , Takehiko Miyagawa , Hiroaki Hagiwara
发明人: Teiji Kimura , Noritaka Kitazawa , Toshihiko Kaneko , Nobuaki Sato , Koki Kawano , Koichi Ito , Mamoru Takaishi , Takeo Sasaki , Yu Yoshida , Toshiyuki Uemura , Takashi Doko , Daisuke Shinmyo , Daiju Hasegawa , Takehiko Miyagawa , Hiroaki Hagiwara
IPC分类号: C07D487/04 , C07D471/04 , C07D498/04
CPC分类号: C07D403/10 , C07D471/04 , C07D487/04 , C07D498/04
摘要: Disclosed is a compound represented by the formula (I): or a pharmacologically acceptable salt thereof, which is effective as a therapeutic or prophylactic agent for a disease induced by Aβ, wherein Ar1 represents an imidazolyl group which may be substituted with a C1-6 alkyl group, or the like; Ar2 represents a phenyl group which may be substituted with a C1-6 alkoxy group, or the like; X1 represents a double bond, or the like; and Het represents a triazolyl group or the like which may be substituted with a C1-6 alkyl group or the like, or the like.
摘要翻译: 公开了由式(I)表示的化合物或其药理学上可接受的盐,其作为由A&bgr诱导的疾病的治疗或预防剂是有效的,其中Ar1表示可被C1- 6烷基等; Ar 2表示可被C 1-6烷氧基取代的苯基等; X1表示双键等; Het表示可以被C 1-6烷基等取代的三唑基等。
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公开(公告)号:US07935815B2
公开(公告)日:2011-05-03
申请号:US12200731
申请日:2008-08-28
申请人: Teiji Kimura , Noritaka Kitazawa , Toshihiko Kaneko , Nobuaki Sato , Koki Kawano , Koichi Ito , Mamoru Takaishi , Takeo Sasaki , Yu Yoshida , Toshiyuki Uemura , Takashi Doko , Daisuke Shinmyo , Daiju Hasegawa , Takehiko Miyagawa , Hiroaki Hagiwara
发明人: Teiji Kimura , Noritaka Kitazawa , Toshihiko Kaneko , Nobuaki Sato , Koki Kawano , Koichi Ito , Mamoru Takaishi , Takeo Sasaki , Yu Yoshida , Toshiyuki Uemura , Takashi Doko , Daisuke Shinmyo , Daiju Hasegawa , Takehiko Miyagawa , Hiroaki Hagiwara
IPC分类号: C07D491/00 , C07D513/00 , C07D515/00 , C07D265/36 , C07D498/02 , C07D487/00 , C07D513/02 , C07D515/02 , C07D401/00
CPC分类号: C07D403/10 , C07D401/14 , C07D403/14 , C07D409/14
摘要: A compound represented by the formula (I): or a pharmacologically acceptable salt thereof, wherein Ar1 represents an imidazolyl group or the like which may be substituted with a C1-6 alkyl group, Ar2 represents a phenyl group or the like which may be substituted with a C1-6 alkoxy group, X1 represents a double bond or the like and Het represents a triazolyl group or the like which may be substituted with a C1-6 alkyl group or the like, is effective as a therapeutic or prophylactic agent for a disease caused by Aβ.
摘要翻译: 由式(I)表示的化合物或其药理学上可接受的盐,其中Ar 1表示可被C 1-6烷基取代的咪唑基等,Ar 2表示可被取代的苯基等 具有C 1-6烷氧基,X 1表示双键等,Het表示可以被C 1-6烷基等取代的三唑基等,作为治疗或预防药物是有效的 A&BGR引起的疾病
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公开(公告)号:US20090203697A1
公开(公告)日:2009-08-13
申请号:US12301421
申请日:2007-05-18
申请人: Teiji Kimura , Koki Kawano , Eriko Doi , Noritaka Kitazawa , Takehiko Miyagawa , Nobuaki Sato , Toshihiko Kaneko , Kogyoku Shin , Koichi Ito , Mamoru Takaishi , Takeo Sasaki , Hiroaki Hagiwara
发明人: Teiji Kimura , Koki Kawano , Eriko Doi , Noritaka Kitazawa , Takehiko Miyagawa , Nobuaki Sato , Toshihiko Kaneko , Kogyoku Shin , Koichi Ito , Mamoru Takaishi , Takeo Sasaki , Hiroaki Hagiwara
IPC分类号: A61K31/5377 , A61K31/4353 , A61K31/4439 , C07D413/10 , C07D455/02 , C07D401/10 , C07D413/14 , C07D401/14
CPC分类号: C07D249/08 , C07D401/10 , C07D401/14 , C07D413/10 , C07D413/14 , C07D471/04
摘要: Disclosed is a compound represented by the formula (I) below or a pharmacologically acceptable salt thereof. Also disclosed is a use of the compound or salt as a pharmaceutical product. (In the formula, Ar1 represents a triazolyl group or the like which may be substituted with a C1-6 alkyl group or the like; Ar2 represents a phenyl group or the like which may be substituted with a C1-6 alkoxy group or the like; X1 represents —CR3═CR4— (wherein R3 and R4 respectively represent a C1-6 alkyl group or the like); and R1 and R2 respectively represent a C1-6 alkyl group or the like.)
摘要翻译: 公开了由下式(I)表示的化合物或其药理学上可接受的盐。 还公开了化合物或盐作为药物产品的用途。 (式中,Ar 1表示可被C 1-6烷基等取代的三唑基等,Ar 2表示可被C 1-6烷氧基等取代的苯基等) ; X1表示-CR3-CR4-(其中R3和R4分别表示C1-6烷基等),R1和R2分别表示C1-6烷基等)。
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公开(公告)号:US20080207900A1
公开(公告)日:2008-08-28
申请号:US12037315
申请日:2008-02-26
申请人: Teiji KIMURA , Koki Kawano , Eriko Doi , Noritaka Kitazawa , Mamoru Takaishi , Koichi Ito , Toshihiko Kaneko , Takeo Sasaki , Nobuaki Sato , Takehiko Miyagawa , Hiroaki Hagiwara
发明人: Teiji KIMURA , Koki Kawano , Eriko Doi , Noritaka Kitazawa , Mamoru Takaishi , Koichi Ito , Toshihiko Kaneko , Takeo Sasaki , Nobuaki Sato , Takehiko Miyagawa , Hiroaki Hagiwara
IPC分类号: C07D498/04
CPC分类号: C07D498/04
摘要: The present invention relates to a compound represented by formula (I): wherein R1 represents a C1-3 alkyl group, R2 represents a hydrogen atom or a C1-3 alkyl group, Ar represents a phenyl group or the like which may be substituted with 1 to 3 substituents, X represents an oxygen atom or the like, n and m are the same or different and integers of 0 to 2, or a pharmacologically acceptable salt, and use thereof as a medicament.
摘要翻译: 本发明涉及由式(I)表示的化合物:其中R 1表示C 1-3烷基,R 2表示氢原子或C1-3 烷基,Ar表示可被1〜3个取代基取代的苯基等,X表示氧原子等,n和m相同或不同,整数为0〜2,或药理学上可接受的盐 ,及其作为药物的用途。
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