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公开(公告)号:US4408372A
公开(公告)日:1983-10-11
申请号:US198726
申请日:1980-10-20
申请人: Teiji Kimura , Shigeru Kimura
发明人: Teiji Kimura , Shigeru Kimura
CPC分类号: F16B21/073 , Y10T24/45775
摘要: A coupler for joining two objects comprises an insertion member attached fast to one of the objects and a reception member attached fast to the other object and used for admitting the insertion member into fast engagement therewith. The insertion member is provided with a setting portion for fast attachment to the aforementioned one object and a shaft extended from the setting portion and possessed of a radially expanded engaging portion at the leading end thereof. The reception member is provided with two generally semicylindrical shells connected to each other through a thin-walled hinge portion and adapted to form one cylindrical shape upon being closed onto each other along the matched edges thereof and a plurality of resilient engaging pieces regularly spaced in the longitudinal direction on the inner wall of each of the shells.
摘要翻译: 用于连接两个物体的联接器包括快速附接到物体之一的插入构件和快速附接到另一物体的接收构件,并用于允许插入构件与其快速接合。 插入构件设置有用于快速附接到上述一个物体的设置部分和从设置部分延伸并且在其前端具有径向扩张的接合部分的轴。 接收构件设置有两个通常半圆柱形壳体,通过薄壁铰链部分相互连接,并且适于在沿其匹配边缘彼此闭合时形成一个圆柱形形状,并且多个弹性接合件在该 每个壳体的内壁上的纵向方向。
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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:US06737425B1
公开(公告)日:2004-05-18
申请号:US09743358
申请日:2001-01-29
申请人: Noboru Yamamoto , Makoto Komatsu , Yuichi Suzuki , Koki Kawano , Teiji Kimura , Koichi Ito , Satoshi Nagato , Yoshihiko Norimine , Tetsuhiro Niidome , Tetsuyuki Teramoto , Yoichi Iimura , Shinji Hatakeyama
发明人: Noboru Yamamoto , Makoto Komatsu , Yuichi Suzuki , Koki Kawano , Teiji Kimura , Koichi Ito , Satoshi Nagato , Yoshihiko Norimine , Tetsuhiro Niidome , Tetsuyuki Teramoto , Yoichi Iimura , Shinji Hatakeyama
IPC分类号: A61K31497
CPC分类号: C07D213/64 , C07D213/57 , C07D215/20 , C07D217/02 , C07D233/54 , C07D239/34 , C07D239/80 , C07D295/15 , C07D317/64 , C07D333/24 , C07D333/38
摘要: The invention provides an N,N-substituted cyclic amine compound represented by the following formula (VIII): wherein A represents an aryl group etc.; E represents a group represented by the formula —CO— or a group represented by the formula —CHOH—; G represents an oxygen atom etc.; J represents an aryl group which may be substituted; R1 represents a lower alkyl group etc.; Alk represents a linear or branched lower alkylene group; n, v, w, x and y are independent of each other and each represents 0 or 1; and p represents 2 or 3, or a pharmacologically acceptable salt thereof. The compound of the present invention or a salt thereof is effective to treat a disease against which calcium antagonism is effective. The disease may include acute ischemic stroke, cerebral apoplexy, cerebral infarction, head trauma, cerebral nerve cell death, Alzheimer disease, Parkinson disease, amyotrophic lateral sclerosis, Huntington disease, cerebral circulatory metabolism disturbance, cerebral function disturbance, pain, spasm, schizophrenia, migraine, epilepsy, maniac-depressive psychosis, nerve degenerative diseases, cerebral ischemia, AIDS dementia complications, edema, anxiety disorder (generalized anxiety disorder) and diabetic neuropathy.
摘要翻译: 本发明提供由下式(VIII)表示的N,N-取代的环胺化合物:其中A表示芳基等; E表示由式-CO-表示的基团或由式-CHOH-表示的基团; G表示氧原子等。 J表示可被取代的芳基; R 1表示低级烷基等。 Alk表示直链或支链低级亚烷基; n,v,w,x和y彼此独立,各自表示0或1; 和p表示2或3,或其药理学上可接受的盐。 本发明的化合物或其盐可有效治疗钙拮抗作用有效的疾病。 该疾病可能包括急性缺血性脑卒中,脑中风,脑梗塞,头部创伤,脑神经细胞死亡,阿尔茨海默病,帕金森病,肌萎缩性侧索硬化,亨廷顿病,脑循环代谢障碍,脑功能障碍,疼痛,痉挛,精神分裂症, 偏头痛,癫痫,疯子抑郁精神病,神经退行性疾病,脑缺血,艾滋病痴呆并发症,水肿,焦虑症(广泛性焦虑症)和糖尿病性神经病变。
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公开(公告)号:US5801180A
公开(公告)日:1998-09-01
申请号:US904260
申请日:1997-07-31
申请人: Yasutaka Takase , Nobuhisa Watanabe , Makoto Matsui , Hironori Ikuta , Teiji Kimura , Takao Saeki , Hideyuki Adachi , Tadakazu Tokumura , Hisatoshi Mochida , Yasunori Akita , Shigeru Souda
发明人: Yasutaka Takase , Nobuhisa Watanabe , Makoto Matsui , Hironori Ikuta , Teiji Kimura , Takao Saeki , Hideyuki Adachi , Tadakazu Tokumura , Hisatoshi Mochida , Yasunori Akita , Shigeru Souda
IPC分类号: C07D215/42 , A61K31/415 , A61K31/4184 , A61K31/4427 , A61K31/443 , A61K31/445 , A61K31/454 , A61K31/4706 , A61K31/4709 , A61K31/496 , A61K31/505 , A61K31/517 , A61K31/519 , A61P9/00 , A61P9/04 , A61P9/10 , A61P9/12 , A61P11/06 , A61P37/00 , A61P43/00 , B60S1/16 , B60S1/24 , C07D215/48 , C07D235/06 , C07D235/08 , C07D239/78 , C07D239/84 , C07D239/86 , C07D239/88 , C07D239/90 , C07D239/94 , C07D239/95 , C07D239/96 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/12 , C07D405/06 , C07D405/12 , C07D405/14 , C07D413/12 , C07D471/04 , C07D491/04 , C07D491/056 , C07D521/00 , F16C7/02 , F16C11/04
CPC分类号: C07D235/06 , C07D215/42 , C07D231/12 , C07D233/56 , C07D239/84 , C07D239/86 , C07D239/88 , C07D239/94 , C07D239/95 , C07D239/96 , C07D249/08 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/12 , C07D405/06 , C07D405/12 , C07D405/14 , C07D413/10 , C07D413/12 , C07D471/04 , C07D491/04
摘要: The present invention provides a nitrogenous heterocyclic compound represented by the following general formula (1) or a pharmacologically acceptable salt thereof which is useful for various ischemic heart diseases and the like: ##STR1## �in formula (1), ring A represents a benzene ring, a pyridine ring or a cyclohexane ring; ring B represents a pyridine ring, a pyrimidine ring or an imidazole ring, R.sup.1, R.sup.2, R.sup.3 and R.sup.4 represent each a hydrogen atom, a halogen atom or a group such as a lower alkoxy group; R.sup.5 represents a group represented by the formula --NR.sup.11 R.sup.12 (wherein R.sup.11 and R.sup.12 represent each a hydrogen atom or a group such as a lower alkyl group) or the like; and R.sup.6 represents a group represented by the formula ##STR2## (wherein R.sup.19 represents a hydrogen atom, a lower alkyl group or the like; R.sup.20, R.sup.21 and R.sup.22 represent each a hydrogen atom, a halogen atom, a hydroxyl group or the like; and r represents 0 or an integer of 1 to 8)!.
摘要翻译: 本发明提供由以下通式(1)表示的含氮杂环化合物或其药理学上可接受的盐,其可用于各种缺血性心脏病等:(1)[式(1)中,环A 表示苯环,吡啶环或环己烷环; 环B表示吡啶环,嘧啶环或咪唑环,R1,R2,R3和R4分别表示氢原子,卤素原子或低级烷氧基等基团。 R5表示由式-NR11R12表示的基团(其中R11和R12各自表示氢原子或低级烷基等基团)等; R 6表示氢原子,低级烷基等,R 20,R 21,R 22分别表示氢原子,卤素原子,羟基等。 和r表示0或1〜8的整数)]。
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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:US07687640B2
公开(公告)日:2010-03-30
申请号:US12497251
申请日:2009-07-02
申请人: Teiji Kimura , Koki Kawano , Eriko Doi , Noritaka Kitazawa , Kogyoku Shin , Takehiko Miyagawa , Toshihiko Kaneko , Koichi Ito , Mamoru Takaishi , Takeo Sasaki , Hiroaki Hagiwara
发明人: Teiji Kimura , Koki Kawano , Eriko Doi , Noritaka Kitazawa , Kogyoku Shin , Takehiko Miyagawa , Toshihiko Kaneko , Koichi Ito , Mamoru Takaishi , Takeo Sasaki , Hiroaki Hagiwara
IPC分类号: C07D233/56 , A01N43/50
CPC分类号: C07D401/10 , C07D401/12 , C07D405/12 , C07D409/12 , C07D409/14 , C07D413/10 , C07D413/12 , C07D413/14 , C07D417/10 , C07D417/12 , C07D417/14 , C07D487/04
摘要: The present invention relates to a process for preparing a compound of formula (6a): wherein Ar1 represents an imidazolyl group which may be substituted with 1 to 3 substituents shown below; Ar2 represents a pyridinyl group, a pyrimidinyl group or a phenyl group which may be substituted with 1 to 3 substituents; and R11 represents a group selected from certain substituents.
摘要翻译: 本发明涉及式(6a)化合物的制备方法:其中Ar 1表示可被1〜3个取代基取代的咪唑基, Ar 2表示吡啶基,嘧啶基或可被1〜3个取代基取代的苯基; R 11表示选自某些取代基的基团。
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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:US06667412B1
公开(公告)日:2003-12-23
申请号:US09914349
申请日:2001-08-27
申请人: Yuichi Suzuki , Noboru Yamamoto , Koki Kawano , Teiji Kimura , Koichi Ito , Satoshi Nagato , Yoshihiko Norimine , Yoichi Iimura
发明人: Yuichi Suzuki , Noboru Yamamoto , Koki Kawano , Teiji Kimura , Koichi Ito , Satoshi Nagato , Yoshihiko Norimine , Yoichi Iimura
IPC分类号: C07C25536
CPC分类号: C07D295/145 , C07C255/36 , C07C255/41 , C07D295/14
摘要: The present invention provides a novel nitrile compound useful as an intermediate for the production of, for example, N,N-substituted cyclic amine derivatives or phenylacetonitrile derivatives that are useful as a medicine. Specifically it provides a nitrile carboxylic acid compound, nitrile ester compound and nitrile alcohol compound. That is, it provides a nitrile compound represented by the following formula (I): wherein R1 and R2 means substituents; m means 0 or an integer of from 1 to 6; n means 0 or an integer of from 1 to 5; and R3 means carboxyl group, a lower alkoxycarbonyl group or hydroxymethyl group.
摘要翻译: 本发明提供了可用作制备例如可用作药物的N,N-取代的环胺衍生物或苯乙腈衍生物的中间体的新型腈化合物。 具体地说,它提供了一种腈羧酸化合物,腈酯化合物和腈醇化合物。 也就是说,它提供由下式(I)表示的腈化合物:其中R 1和R 2表示取代基; m表示0或1〜6的整数; n表示0或1至5的整数; R 3表示羧基,低级烷氧基羰基或羟甲基。
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