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公开(公告)号:US06174891B1
公开(公告)日:2001-01-16
申请号:US09117052
申请日:1998-08-24
申请人: Hiroshi Nagase , Jun Utsumi , Takashi Endoh , Toshiaki Tanaka , Junzo Kamei , Kuniaki Kawamura
发明人: Hiroshi Nagase , Jun Utsumi , Takashi Endoh , Toshiaki Tanaka , Junzo Kamei , Kuniaki Kawamura
IPC分类号: A61K31485
CPC分类号: A61K31/541 , A61K31/40 , A61K31/4025 , A61K31/435 , A61K31/485 , A61K31/5377 , C07D489/00 , C07D489/08
摘要: This invention provides an antipruritic comprising an opiate &kgr; receptor agonist as an effective component, a new morphinan quaternary ammonium salt derivative and a new morphinan-N-oxide derivative which are useful in treating pruritus complicated with some diseases.
摘要翻译: 本发明提供了含有鸦片类κ受体激动剂作为有效成分的止痒剂,新的吗啡喃季铵盐衍生物和新的吗啡喃-N-氧化物衍生物,其可用于治疗与某些疾病并发的瘙痒。
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公开(公告)号:US06440987B1
公开(公告)日:2002-08-27
申请号:US09970978
申请日:2001-10-04
IPC分类号: A61K31485
CPC分类号: A61K31/541 , A61K31/40 , A61K31/4025 , A61K31/435 , A61K31/485 , A61K31/5377 , C07D489/00 , C07D489/08
摘要: This invention provides an antipuritic comprising an opiate &kgr; receptor agonist as an effective component, a new morphian quaternary ammonium salt derivative and a new morphian-N-oxide derivative which are useful in treating puritus complicated with some diseases.
摘要翻译: 本发明提供了含有鸦片类κ受体激动剂作为有效成分的抗炎药,可用于治疗与某些疾病并发的荨麻疹的新的吗啉季铵盐衍生物和新的吗啉-N-氧化物衍生物。
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公开(公告)号:US06316461B1
公开(公告)日:2001-11-13
申请号:US09615540
申请日:2000-07-13
申请人: Hiroshi Nagase , Jun Utsumi , Takashi Endoh , Toshiaki Tanaka , Junzo Kamei , Kuniaki Kawamura
发明人: Hiroshi Nagase , Jun Utsumi , Takashi Endoh , Toshiaki Tanaka , Junzo Kamei , Kuniaki Kawamura
IPC分类号: A61K31485
CPC分类号: A61K31/541 , A61K31/40 , A61K31/4025 , A61K31/435 , A61K31/485 , A61K31/5377 , C07D489/00 , C07D489/08
摘要: This invention provides an antipruritc comprising an opiate &kgr; receptor agonist as an effective component, a new morphinan quaternary ammonium salt derivative and a new morphinan-N-oxide derivative which are useful in treating pruritus complicated with some diseases.
摘要翻译: 本发明提供了含有鸦片类κ受体激动剂作为有效成分的止痒剂,新的吗啡喃季铵盐衍生物和新的吗啡喃-N-氧化物衍生物,其可用于治疗与某些疾病并发的瘙痒。
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公开(公告)号:US06583151B2
公开(公告)日:2003-06-24
申请号:US09297364
申请日:1999-07-12
申请人: Hiroshi Nagase , Takashi Endoh , Tsutomu Suzuki , Kuniaki Kawamura , Koji Oshima , Hideaki Inada
发明人: Hiroshi Nagase , Takashi Endoh , Tsutomu Suzuki , Kuniaki Kawamura , Koji Oshima , Hideaki Inada
IPC分类号: A61K314748
CPC分类号: A61K31/485 , C07D489/08
摘要: A method for treating drug dependence comprising administering, as the active ingredient, an opioid &kgr; receptor agonist of a compound represented by the following formula, is disclosed wherein A and the R terms are herein defined.
摘要翻译: 一种治疗药物依赖性的方法,包括给予作为活性成分的由下式表示的化合物的阿片样物质κ受体激动剂,其中A和R术语在本文中定义。
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公开(公告)号:US06277859B1
公开(公告)日:2001-08-21
申请号:US09541793
申请日:2000-03-31
申请人: Hiroshi Nagase , Koji Kawai , Kuniaki Kawamura , Jun Hayakawa , Takashi Endoh
发明人: Hiroshi Nagase , Koji Kawai , Kuniaki Kawamura , Jun Hayakawa , Takashi Endoh
IPC分类号: C07D48900
CPC分类号: C07D405/12 , C07D409/12 , C07D413/12 , C07D489/08
摘要: A morphinan derivative or its pharmacologically allowed acid addition salt represented with compound I, an analgesic and diuretic having its derivative or its salt as the active ingredient, and its production process are described. The compound of the present invention possesses strong analgesic activity and diuretic action as a highly selective &kgr;-opioid agonist, allowing it to be used as a useful analgesic and diuretic.
摘要翻译: 描述了以化合物I表示的吗啡喃衍生物或其药理学允许的酸加成盐,其衍生物或其盐作为活性成分的止痛剂和利尿剂及其制备方法。 本发明化合物作为高度选择性的κ-阿片样物质激动剂具有强的止痛活性和利尿作用,可用作有用的镇痛和利尿剂。
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公开(公告)号:US06177438B1
公开(公告)日:2001-01-23
申请号:US08754750
申请日:1996-11-21
申请人: Hiroshi Nagase , Jun Hayakawa , Kuniaki Kawamura , Koji Kawai , Takashi Endoh
发明人: Hiroshi Nagase , Jun Hayakawa , Kuniaki Kawamura , Koji Kawai , Takashi Endoh
IPC分类号: C07D49108
CPC分类号: C07D489/08 , C07D489/00
摘要: A morphinan derivative or its pharmaceutically acceptable acid addition salt represented with, for example, and an analgesic, diuretic, antitussive and brain cell protector having its derivative or its salt as the active ingredient are described. The compound of the present invention possesses strong analgesic activity, diuretic action and antitussive action as a highly selective &kgr;-opioid agonist, allowing it to be used as a useful analgesic, diuretic and antitussive. On the other hand, the compound of the present invention also possesses remarkable cerebro-neuroprotective activity, thus allowing it be used as a useful cerebro-neuroprotective agents.
摘要翻译: 描述了以其衍生物或其盐作为活性成分代表的吗啡喃衍生物或其药学上可接受的酸加成盐和镇痛药,利尿剂,镇咳药和脑细胞保护剂。本发明化合物具有强的止痛活性 ,利尿作用和镇咳作用作为高度选择性的κ-阿片样物质激动剂,使其可用作有用的止痛剂,利尿剂和镇咳药。 另一方面,本发明的化合物也具有显着的脑血管保护作用,因此可用作有用的脑血管保护剂。
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公开(公告)号:US06323212B1
公开(公告)日:2001-11-27
申请号:US08108643
申请日:1997-02-10
申请人: Hiroshi Nagase , Koji Kawai , Kuniaki Kawamura , Jun Hayakawa , Takashi Endoh
发明人: Hiroshi Nagase , Koji Kawai , Kuniaki Kawamura , Jun Hayakawa , Takashi Endoh
IPC分类号: C07D48900
CPC分类号: C07D405/12 , C07D409/12 , C07D413/12 , C07D489/08
摘要: A morphinan derivative or its pharmacologically allowed acid addition salt represented with compound I, an analgesic and diuretic having its derivative or its salt as the active ingredient, and its production process are described. The compound of the present invention possesses strong analgesic activity and diuretic action as a highly selective &kgr;-opioid agonist, allowing it to be used as a useful analgesic and diuretic.
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8.
公开(公告)号:US20060094741A1
公开(公告)日:2006-05-04
申请号:US11206489
申请日:2005-08-18
申请人: Hiroshi Nagase , Takashi Endo , Kuniaki Kawamura , Toshiaki Tanaka , Tomohiko Suzuki , Tsutomu Suzuki , Yasushi Kuraishi , Kimiyasu Shiraki
发明人: Hiroshi Nagase , Takashi Endo , Kuniaki Kawamura , Toshiaki Tanaka , Tomohiko Suzuki , Tsutomu Suzuki , Yasushi Kuraishi , Kimiyasu Shiraki
IPC分类号: A61K31/4745 , A61K49/00 , C07D471/04
CPC分类号: A61K31/485 , A61K31/4745 , C07D489/08
摘要: The present invention relates to a therapeutic agent for neuropathic pain containing, as an active ingredient, a compound represented by general formula (I) or a pharmacologically acceptable acid addition salt thereof: (wherein R1, R2, R3, R4, R5, R6, R7, R8, A, and B have the same definitions as those described in the specification), and an animal model produced by administering (+)-4a-(3-hydroxyphenyl)-2-methyl-1,2,3,4,4a,5,12,12a-octohydro-trans-quinolino[2,3-g]isoquinoline. The present invention makes it possible to perform drug treatment for neuropathic pain. The therapeutic effect of a compound against neuropathic pain can also be evaluated.
摘要翻译: 本发明涉及神经性疼痛治疗剂,其含有作为活性成分的通式(I)表示的化合物或其药理学上可接受的酸加成盐:(其中R 1,R 2, R 2,R 3,R 4,R 5,R 6,R 6, A +和B B具有与说明书中描述的那些相同的定义)和通过给予(+) - 4a-(3- 羟基苯基)-2-甲基-1,2,3,4,4a,5,12,12a-八氢 - 反 - 喹啉并[2,3-g]异喹啉。 本发明使得可以进行神经性疼痛的药物治疗。 也可以评价化合物对神经性疼痛的治疗作用。
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9.
公开(公告)号:US08637539B2
公开(公告)日:2014-01-28
申请号:US11206489
申请日:2005-08-18
申请人: Hiroshi Nagase , Takashi Endo , Kuniaki Kawamura , Toshiaki Tanaka , Tomohiko Suzuki , Tsutomu Suzuki , Yasushi Kuraishi , Kimiyasu Shiraki
发明人: Hiroshi Nagase , Takashi Endo , Kuniaki Kawamura , Toshiaki Tanaka , Tomohiko Suzuki , Tsutomu Suzuki , Yasushi Kuraishi , Kimiyasu Shiraki
CPC分类号: A61K31/485 , A61K31/4745 , C07D489/08
摘要: The present invention relates to a therapeutic agent for neuropathic pain containing, as an active ingredient, a compound represented by general formula (I) or a pharmacologically acceptable acid addition salt thereof: (wherein R1, R2, R3, R4, R5, R6, R7, R8, A, and B have the same definitions as those described in the specification), and an animal model produced by administering (+)-4a-(3-hydroxyphenyl)-2-methyl-1,2,3,4,4a,5,12,12a-octohydro-trans-quinolino[2,3-g]isoquinoline. The present invention makes it possible to perform drug treatment for neuropathic pain. The therapeutic effect of a compound against neuropathic pain can also be evaluated.
摘要翻译: 本发明涉及神经性疼痛治疗剂,其含有作为活性成分的通式(I)表示的化合物或其药理学上可接受的酸加成盐:(其中R1,R2,R3,R4,R5,R6, R7,R8,A和B具有与说明书中描述的定义相同的定义)和通过给予(+) - 4a-(3-羟基苯基)-2-甲基-1,2,3,4 ,4a,5,12,12a-八氢 - 反 - 喹啉并[2,3-g]异喹啉。 本发明使得可以进行神经性疼痛的药物治疗。 也可以评价化合物对神经性疼痛的治疗效果。
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公开(公告)号:US06803366B2
公开(公告)日:2004-10-12
申请号:US10148489
申请日:2002-05-30
申请人: Kuniaki Kawamura , Hiroshi Nagase , Noriyuki Hirano , Junzo Kamei
发明人: Kuniaki Kawamura , Hiroshi Nagase , Noriyuki Hirano , Junzo Kamei
IPC分类号: A61K314375
CPC分类号: C07D471/04 , A61K31/4738 , A61K31/4745 , A61K31/498
摘要: Disclosed is an agent for improving learning and/or memory, which is useful for therapy of dementia accompanying disorder of memory due to a cerebrovascular disease, neurodegenerative disease such as Alzheimer's disease, endocrine disease, nutritional or metabolic disorder, infectious disease, drug addiction or the like. The agent for improving learning and/or memory according to the present invention comprises as an effective ingredient an isoquinoline derivative having a specific structure, such as (4aR, 12aR)-2-methyl-4a-(3-hydroxyphenyl)-1,2,3,4,4a,5,12,12a-octahydro-quinoline[2,3-g]isoquinoline or a pharmaceutically acceptable salt thereof.
摘要翻译: 公开了一种用于改善学习和/或记忆的药剂,其用于治疗由于脑血管疾病,神经变性疾病如阿尔茨海默病,内分泌疾病,营养或代谢障碍,感染性疾病,药物成瘾引起的记忆障碍的痴呆症 类似。 根据本发明的用于改善学习和/或记忆的药剂包括作为有效成分的具有特定结构的异喹啉衍生物,例如(4aR,12aR)-2-甲基-4a-(3-羟基苯基)-1,2 ,3,4,4a,5,12,12a-八氢 - 喹啉[2,3-g]异喹啉或其药学上可接受的盐。
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