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公开(公告)号:US20070287689A1
公开(公告)日:2007-12-13
申请号:US11576972
申请日:2005-10-13
CPC分类号: A61K45/06 , A61K31/277 , A61K31/357 , A61K31/4409 , A61K31/4427 , A61K31/443 , A61K31/4433 , A61K31/496 , A61K31/573 , A61K31/58 , A61K2300/00
摘要: The present invention provides: a therapeutic and/or preventive agent for chronic skin diseases which comprises (a) a phosphodiesterase (PDE)-IV inhibitor or a pharmaceutically acceptable salt thereof and (b) a steroid agent as active ingredients; a therapeutic and/or preventive agent for chronic skin diseases to be administered simultaneously or separately with an interval which comprises (a) a PDE-IV inhibitor or a pharmaceutically acceptable salt thereof and (b) a steroid agent, as active ingredients; a kit for treating and/or preventing chronic skin diseases characterized by comprising (a) a first component comprising a PDE-IV inhibitor or a pharmaceutically acceptable salt thereof and (b) a second component comprising a steroid agent; and the like.
摘要翻译: 本发明提供:慢性皮肤病的治疗和/或预防剂,其包含(a)磷酸二酯酶(PDE)-IV抑制剂或其药学上可接受的盐和(b)作为活性成分的类固醇剂; 用于与(a)PDE-IV抑制剂或其药学上可接受的盐和(b)类固醇剂)作为活性成分的间隔同时或分开施用的慢性皮肤病的治疗和/或预防剂。 用于治疗和/或预防慢性皮肤疾病的试剂盒,其特征在于包含(a)包含PDE-IV抑制剂或其药学上可接受的盐的第一组分和(b)包含类固醇剂的第二组分; 等等。
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公开(公告)号:US07271176B2
公开(公告)日:2007-09-18
申请号:US10487168
申请日:2002-11-13
申请人: Jay R. Luly , Yoshisuke Nakasato , Etsuo Ohshima , Geraldine C. B. Harriman , Kenneth G. Carson , Shomir Ghosh , Amy M. Elder , Karen M. Mattia
发明人: Jay R. Luly , Yoshisuke Nakasato , Etsuo Ohshima , Geraldine C. B. Harriman , Kenneth G. Carson , Shomir Ghosh , Amy M. Elder , Karen M. Mattia
IPC分类号: A01N43/42 , A61K31/44 , C07D401/00 , C07D451/00 , C07D453/00
CPC分类号: C07D211/46 , C07D211/52 , C07D313/12 , C07D401/06 , C07D405/06 , C07D409/06 , C07D471/04 , C07D491/04 , C07D495/04
摘要: Disclosed are novel compounds and a method of treating a disease associated with aberrant leukocyte recruitment and/or activation. The method comprises administering to a subject in need an effective amount of a compound represented by: formula (1) or physiologically acceptable salt thereof
摘要翻译: 公开了新型化合物和治疗与异常白细胞募集和/或激活相关的疾病的方法。 该方法包括向有需要的受试者施用有效量的由式(1)表示的化合物或其生理学上可接受的盐
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公开(公告)号:US20070037834A1
公开(公告)日:2007-02-15
申请号:US10516750
申请日:2003-06-06
申请人: Hitoshi Arai , Tsutomu Matsumura , Hiroshi Ishida , Yosuke Yamaura , Seiji Aratake , Etsuo Ohshima , Koji Yanagawa , Motoki Miyama , Koji Suzuki , Ari Kawabe , Satoshi Nakanishi , Katsuya Kobayashi , Takashi Sato , Ichiro Miki , Kimihisa Ueno , Shinya Fujii , Miho Iwase
发明人: Hitoshi Arai , Tsutomu Matsumura , Hiroshi Ishida , Yosuke Yamaura , Seiji Aratake , Etsuo Ohshima , Koji Yanagawa , Motoki Miyama , Koji Suzuki , Ari Kawabe , Satoshi Nakanishi , Katsuya Kobayashi , Takashi Sato , Ichiro Miki , Kimihisa Ueno , Shinya Fujii , Miho Iwase
IPC分类号: A61K31/519 , C07D487/02
CPC分类号: C07D263/58 , C07D471/04 , C07D487/04
摘要: [wherein m and n may be the same or different and each represents an integer of 1 to 3 wherein m+n is 4 or less; R1 represents —NR4R5 (wherein R4 and R5 may be the same or different and each represents a hydrogen atom, substituted or unsubstituted lower alkyl, substituted or unsubstituted aralkyl or the like); R2 represents the above Formula (II), Formula (IV) or the like; A represents a single bond, —C(═O)—, —SO2—, —OC(═O)— or the like; and R3 represents substituted or unsubstituted lower alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aralkyl or the like]Bicyclic pyrimidine derivatives represented by the above Formula (I), or quaternary ammonium salts thereof, or pharmaceutically acceptable salts thereof, or the like, are provided. These have anti-inflammatory activities or modulation activities on the functions of TARC and/or MDC and are useful for treating and/or preventing a disease which is related to T cells, such as an allergic disease, an autoimmune disease or transplant rejection.
摘要翻译: [其中m和n可以相同或不同,并且各自表示1〜3的整数,其中m + n为4以下; R 1表示-NR 4 R 5(其中R 4,R 5和R 5) 可以相同或不同,各自表示氢原子,取代或未取代的低级烷基,取代或未取代的芳烷基等); R 2表示上述式(II),式(IV)等; A表示单键,-C(-O) - , - SO 2 - , - OC(-O) - 等; 和R 3表示取代或未取代的低级烷基,取代或未取代的环烷基,取代或未取代的芳烷基等〕由上式(I)表示的双环嘧啶衍生物或其季铵盐或药学上可接受的盐 可接受的盐等。 它们具有对TARC和/或MDC的功能的抗炎活性或调节活性,并且可用于治疗和/或预防与T细胞相关的疾病,例如过敏性疾病,自身免疫疾病或移植排斥反应。
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公开(公告)号:US20060239927A1
公开(公告)日:2006-10-26
申请号:US10551248
申请日:2004-03-31
申请人: Etsuo Ohshima , Haruhiko Manabe , Motoya Mie , Harunobu Tahara , Kazuo Yamaguchi , Yasuhiro Ishikawa
发明人: Etsuo Ohshima , Haruhiko Manabe , Motoya Mie , Harunobu Tahara , Kazuo Yamaguchi , Yasuhiro Ishikawa
IPC分类号: A61K31/4747 , A61L9/04
CPC分类号: A61K9/0078 , A61K9/0075 , A61K9/008 , A61K31/443 , C07D405/06
摘要: An agent for intra-airway administration comprising a compound having a PDE-IV inhibitory activity or the pharmaceutically acceptable salt thereof as an active ingredient which shows its concentration in lung tissues 350-times or more higher than its concentration in plasma when administered into the airway is provided. An agent for intra-airway administration, wherein the compound having a PDE-IV inhibitory activity is, for example, a benzofuran derivative or a 1,3-benzodioxole derivative is provided.
摘要翻译: 用于气道内施用的药剂,其包含具有PDE-IV抑制活性的化合物或其药学上可接受的盐作为活性成分,其在肺组织中的浓度当其施用于气道时在血浆中的浓度高于其浓度的350倍或更高 被提供。 用于气道内施用的药剂,其中具有PDE-IV抑制活性的化合物是例如苯并呋喃衍生物或1,3-苯并间二氧杂环戊烯衍生物。
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公开(公告)号:US20060194811A1
公开(公告)日:2006-08-31
申请号:US10546215
申请日:2004-02-20
申请人: Etsuo Ohshima , Motoki Miyama , Koji Yanagawa , Seiji Aratake , Ichiro Miki , Katsuya Kobayashi
发明人: Etsuo Ohshima , Motoki Miyama , Koji Yanagawa , Seiji Aratake , Ichiro Miki , Katsuya Kobayashi
IPC分类号: A61K31/506 , C07D403/02
CPC分类号: C07D401/04
摘要: A pyrimidine derivative represented by Formula (I) wherein Ar represents substituted or unsubstituted aryl, R1 represents —NR2R3 and wherein R2 represents a hydrogen atom or substituted or unsubstituted lower alkyl and R3 represents substituted or unsubstituted lower alkyl, substituted or unsubstituted aralkyl, A represents a single bond, Formula (III) wherein m1 is 0 to 2, n1 is 0 to 4, a1 is from 0 to a substitutable number, R5 represents substituted or unsubstituted lower alkyl, and each R5 may be the same or different when a1 is 2 or more), and Q represents —NR6R7 (wherein R6 and R7 may be the same or different and each represents a hydrogen atom, a substituted or unsubstituted heteroalicyclic group, a substituted or unsubstituted heteroalicyclic group, substituted or unsubstituted piperidin-4-ylamino, or quaternary ammonium salts thereof, or pharmaceutically acceptable salts thereof.
摘要翻译: 由式(I)表示的嘧啶衍生物,其中Ar表示取代或未取代的芳基,R 1表示-NR 2 R 3,并且其中R 1, O 2表示氢原子或取代或未取代的低级烷基,R 3表示取代或未取代的低级烷基,取代或未取代的芳烷基,A表示单键,式(III)其中 m 1是0至2,n 1是0至4,a 1是0至可取代数,R 5 代表取代或未取代的低级烷基,并且每个R 5可以相同或不同,当O 1为2或更多时),并且Q表示-NR 其中R 6和R 7可以相同或不同,并且各自表示氢原子, 取代或未取代的杂脂环基,取代或未取代的杂脂环基,取代或未取代的哌啶-4-基氨基或季铵 其盐或其药学上可接受的盐。
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公开(公告)号:US5607955A
公开(公告)日:1997-03-04
申请号:US431425
申请日:1995-05-01
申请人: Etsuo Ohshima , Fumihiko Kanai , Hideyuki Sato , Hiroyuki Obase , Toshiaki Kumazawa , Shiho Takahara , Tetsuji Ohno , Tomoko Ishikawa , Koji Yamada
发明人: Etsuo Ohshima , Fumihiko Kanai , Hideyuki Sato , Hiroyuki Obase , Toshiaki Kumazawa , Shiho Takahara , Tetsuji Ohno , Tomoko Ishikawa , Koji Yamada
IPC分类号: C07D403/06 , C07D403/12 , C07D403/14 , C07D405/06 , C07D471/04 , C07D521/00 , A61K31/41 , A61K31/415 , C07D233/54 , C07D235/04 , C07D257/04
CPC分类号: C07D249/08 , C07D231/12 , C07D233/56 , C07D403/06 , C07D403/12 , C07D403/14 , C07D405/06 , C07D471/04
摘要: A tricyclic compound represented by the following formula (I): ##STR1## exhibits antagonism to angiotensin II receptors.
摘要翻译: 由下式(I)表示的三环化合物:显示对血管紧张素II受体的拮抗作用。
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公开(公告)号:US08192736B2
公开(公告)日:2012-06-05
申请号:US11666695
申请日:2005-10-28
IPC分类号: A61K38/00 , A61K39/395 , C07K16/24 , C07K16/28 , C07K14/54 , C07K14/715
CPC分类号: C07K16/244 , A61K31/00 , A61K2039/505 , C07K16/2866
摘要: The present invention provides a therapeutic agent for endometriosis comprising an interleukin-5 antagonist as an active ingredient.
摘要翻译: 本发明提供了一种含有白细胞介素-5拮抗剂作为活性成分的子宫内膜异位症治疗剂。
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公开(公告)号:US07541365B2
公开(公告)日:2009-06-02
申请号:US11595653
申请日:2006-11-10
申请人: Jay R. Luly , Yoshisuke Nakasato , Etsuo Ohshima , Geraldine C. B. Harriman , Kenneth G. Carson , Shomir Ghosh , Amy M. Elder , Karen M. Mattia
发明人: Jay R. Luly , Yoshisuke Nakasato , Etsuo Ohshima , Geraldine C. B. Harriman , Kenneth G. Carson , Shomir Ghosh , Amy M. Elder , Karen M. Mattia
IPC分类号: A01N43/42 , A61K31/44 , C07D455/04 , C07D491/00 , C07D221/00 , C07D221/06
CPC分类号: C07D519/00 , C07D211/44 , C07D211/46 , C07D211/52 , C07D401/06 , C07D401/14 , C07D405/06 , C07D409/06 , C07D471/04 , C07D491/04 , C07D491/044 , C07D493/04 , C07D495/04 , C07D497/04 , C07D513/04
摘要: Disclosed are novel compounds and a method of treating a disease associated with aberrant leukocyte recruitment and/or activation. The method comprises administering to a subject in need an effective amount of a compound represented by: or physiologically acceptable salt thereof.
摘要翻译: 公开了新型化合物和治疗与异常白细胞募集和/或激活相关的疾病的方法。 该方法包括向有需要的受试者施用有效量的由其表示的化合物或其生理上可接受的盐。
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公开(公告)号:US07186729B2
公开(公告)日:2007-03-06
申请号:US10487168
申请日:2002-11-13
申请人: Jay R. Luly , Yoshisuke Nakasato , Etsuo Ohshima , Geraldine C. B. Harriman , Kenneth G. Carson , Shomir Ghosh , Amy M. Elder , Karen M. Mattia
发明人: Jay R. Luly , Yoshisuke Nakasato , Etsuo Ohshima , Geraldine C. B. Harriman , Kenneth G. Carson , Shomir Ghosh , Amy M. Elder , Karen M. Mattia
IPC分类号: A01N43/42 , A61K31/44 , C07D401/00 , C07D451/00 , C07D453/00
摘要: Disclosed are novel compounds and a method of treating a disease associated with aberrant leukocyte recruitment and/or activation. The method comprises administering to a subject in need an effective amount of a compound represented by: formula (1) or physiologically acceptable salt thereof
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公开(公告)号:US20050070549A1
公开(公告)日:2005-03-31
申请号:US10487168
申请日:2002-11-13
申请人: Jay Luly , Yoshisuke Nakasato , Etsuo Ohshima , Geraldine Harriman , Kenneth Carson , Shomir Ghosh , Amy Elder , Karen Mattia
发明人: Jay Luly , Yoshisuke Nakasato , Etsuo Ohshima , Geraldine Harriman , Kenneth Carson , Shomir Ghosh , Amy Elder , Karen Mattia
IPC分类号: A61P1/00 , A61P3/10 , A61P29/00 , C07D211/46 , C07D211/52 , C07D313/12 , C07D401/06 , C07D405/06 , C07D409/06 , C07D471/04 , C07D491/04 , C07D495/04 , C07D519/00 , A61K31/495 , A61K31/445 , C07D211/18 , C07D241/04
CPC分类号: C07D211/46 , C07D211/52 , C07D313/12 , C07D401/06 , C07D405/06 , C07D409/06 , C07D471/04 , C07D491/04 , C07D495/04
摘要: Disclosed are novel compounds and a method of treating a disease associated with aberrant leukocyte recruitment and/or activation. The method comprises administering to a subject in need an effective amount of a compound represented by: formula (1) or physiologically acceptable salt thereof.
摘要翻译: 公开了新型化合物和治疗与异常白细胞募集和/或激活相关的疾病的方法。 该方法包括向有需要的受试者施用有效量的由式(1)表示的化合物或其生理学上可接受的盐。
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