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公开(公告)号:US08461182B2
公开(公告)日:2013-06-11
申请号:US13122281
申请日:2009-09-30
IPC分类号: A61K31/04 , C07D215/38
CPC分类号: C07D401/06 , C07D401/14
摘要: PROBLEMTo provide a novel compound, a pharmaceutically acceptable salt or a hydrate thereof useful for preventing or treating for depression, anxiety disorders (such as generalized anxiety disorder, posttraumatic stress disorder, panic disorder, obsessive-compulsive disorder or social anxiety disorder), attention deficit disorder, mania, manic-depressive illness, schizophrenia, mood disorders, stress, sleep disorders, attacks, memory impairment, cognitive impairment, dementia, amnesia, delirium, obesity, eating disorder, appetite disorder, hyperphagia, bulimia, cibophobia, diabetes, cardiovascular diseases, hypertension, dyslipidemia, myocardial infarction, movement disorder (such as Parkinson's disease, epilepsy, convulsion or tremor), drug abuse, drug addiction or sexual dysfunction, based on a melanin-concentrating hormone receptor (MCH receptor) antagonistic action.SOLUTIONA compound, a pharmaceutically acceptable salt or a hydrate thereof represented by the formula (I).
摘要翻译: 提供用于预防或治疗抑郁症,焦虑症(例如广泛性焦虑症,创伤后应激障碍,恐慌症,强迫症或社会焦虑症)的新型化合物,其药学上可接受的盐或水合物,注意力 缺陷障碍,躁狂症,躁狂抑郁症,精神分裂症,情绪障碍,压力,睡眠障碍,攻击,记忆障碍,认知障碍,痴呆,遗忘症,del妄,肥胖,进食障碍,食欲障碍,食欲过盛,贪食症, 基于黑色素浓度激素受体(MCH受体)拮抗作用的心血管疾病,高血压,血脂异常,心肌梗塞,运动障碍(例如帕金森病,癫痫,惊厥或震颤),药物滥用,药物成瘾或性功能障碍。 解决方案由式(I)表示的化合物,其药学上可接受的盐或其水合物。
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公开(公告)号:US20110288293A1
公开(公告)日:2011-11-24
申请号:US13142230
申请日:2009-12-25
申请人: Tetsuo Takayama , Hajime Asanuma , Daisuke Wakasugi , Rie Nishikawa , Yoshinori Sekiguchi , Madoka Kawamura , Naoya Ono , Tetsuya Yabuuchi , Takahiro Oi , Yusuke Oka , Shoichi Kuroda , Fumito Uneuchi , Takeshi Koami
发明人: Tetsuo Takayama , Hajime Asanuma , Daisuke Wakasugi , Rie Nishikawa , Yoshinori Sekiguchi , Madoka Kawamura , Naoya Ono , Tetsuya Yabuuchi , Takahiro Oi , Yusuke Oka , Shoichi Kuroda , Fumito Uneuchi , Takeshi Koami
IPC分类号: C07D413/12 , C07D401/12 , C07D405/12 , C07D217/24 , C07D409/12 , C07D471/04 , C07D401/06 , C07D217/16 , C07D417/12
CPC分类号: C07D217/16 , C07D217/18 , C07D217/20 , C07D401/12 , C07D405/12 , C07D409/12 , C07D417/12 , C07D471/04
摘要: A compound represented by formula (I) or a pharmaceutically acceptable salt thereof has an effect of inhibiting CRTH2 and, therefore, is useful as a preventive or a remedy for allergic diseases such as asthma, atopic dermatitis and allergic rhinitis.
摘要翻译: 由式(I)表示的化合物或其药学上可接受的盐具有抑制CRTH2的作用,因此可用作哮喘,特应性皮炎和过敏性鼻炎等过敏性疾病的预防或治疗。
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公开(公告)号:US20110178304A1
公开(公告)日:2011-07-21
申请号:US13122281
申请日:2009-09-30
IPC分类号: C07D401/10
CPC分类号: C07D401/06 , C07D401/14
摘要: Problem To provide a novel compound, a pharmaceutically acceptable salt or a hydrate thereof useful for preventing or treating for depression, anxiety disorders (such as generalized anxiety disorder, posttraumatic stress disorder, panic disorder, obsessive-compulsive disorder or social anxiety disorder), attention deficit disorder, mania, manic-depressive illness, schizophrenia, mood disorders, stress, sleep disorders, attacks, memory impairment, cognitive impairment, dementia, amnesia, delirium, obesity, eating disorder, appetite disorder, hyperphagia, bulimia, cibophobia, diabetes, cardiovascular diseases, hypertension, dyslipidemia, myocardial infarction, movement disorder (such as Parkinson's disease, epilepsy, convulsion or tremor), drug abuse, drug addiction or sexual dysfunction, based on a melanin-concentrating hormone receptor (MCH receptor) antagonistic action.Solution A compound, a pharmaceutically acceptable salt or a hydrate thereof represented by the formula (I).
摘要翻译: 问题提供用于预防或治疗抑郁症,焦虑症(例如广泛性焦虑症,创伤后应激障碍,恐慌症,强迫症或社会焦虑症)的新型化合物,其药学上可接受的盐或水合物,注意力 缺陷障碍,躁狂症,躁狂抑郁症,精神分裂症,情绪障碍,压力,睡眠障碍,攻击,记忆障碍,认知障碍,痴呆,遗忘症,del妄,肥胖,进食障碍,食欲障碍,食欲过盛,贪食症, 基于黑色素浓度激素受体(MCH受体)拮抗作用的心血管疾病,高血压,血脂异常,心肌梗塞,运动障碍(例如帕金森病,癫痫,惊厥或震颤),药物滥用,药物成瘾或性功能障碍。 溶液由式(I)表示的化合物,其药学上可接受的盐或其水合物。
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公开(公告)号:US20090281292A1
公开(公告)日:2009-11-12
申请号:US12223675
申请日:2007-02-07
申请人: Tomohiro Sugimoto , Kanako Yamamoto , Akira Manaka , Haruhisa Ogita , Jun Kurosaka , Madoka Kawamura , Masato Kashimura , Naoki Sasamoto , Tomoaki Miura , Kenichi Kanemoto , Tomohiro Ozawa , Ken Chikauchi , Eiki Shitara , Dai Kubota
发明人: Tomohiro Sugimoto , Kanako Yamamoto , Akira Manaka , Haruhisa Ogita , Jun Kurosaka , Madoka Kawamura , Masato Kashimura , Naoki Sasamoto , Tomoaki Miura , Kenichi Kanemoto , Tomohiro Ozawa , Ken Chikauchi , Eiki Shitara , Dai Kubota
CPC分类号: C07H17/00 , A61K31/7052
摘要: [Object]: To provide a compound having a novel structure effective against Hemophilus influenzae and erythromycin resistant bacteria (for example, resistant pneumococci and streptococci) as well as against conventional erythromycin sensitive bacteria.[Solution]: A novel 10a-azalide compound represented by the formula (I), a pharmaceutically acceptable salt thereof or a solvate thereof, or an intermediate for the preparation of the same. The compound of the present invention has superior antibacterial activity against Hemophilus influenzae, erythromycin resistant pneumococci and the like, and therefore, the compound can be used as a therapeutic agent of infectious diseases.
摘要翻译: [目的]提供具有抗血友病嗜血杆菌和抗红霉素抗性细菌(例如抗性肺炎球菌和链球菌)以及常规红霉素敏感细菌的新型结构的化合物。 [溶液]:由式(I)表示的新型10a-氮杂化合物,其药学上可接受的盐或其溶剂化物或其制备的中间体。 本发明的化合物对流感嗜血杆菌,抗红霉素的肺炎球菌等具有优异的抗菌活性,因此可用作感染性疾病的治疗剂。
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公开(公告)号:US08124744B2
公开(公告)日:2012-02-28
申请号:US12299229
申请日:2007-05-01
IPC分类号: C07H17/08
CPC分类号: C07H17/08 , A61K31/7048 , A61K31/7052 , C07H17/00
摘要: Compounds represented by formula (I) and the formula (IV) have an inhibitory activity of MMP-9 production, therefore, are useful as a medicine agent with fewer side effects than conventional MMP enzyme activity inhibitors, as a prophylactic and therapeutic drug for oncogenic angiogenesis, chronic rheumatoid arthritis, vascular intimal thickening after a percutaneous coronary transluminal angioplasty, vascular atherosclerosis, hemorrhagic apoplexy, acute myocardial infarction, chronic heart failure, aneurysm, lung cancer metastasis, adult respiratory distress syndrome, asthma, interstitial pulmonary fibrosis, chronic rhinosinusitis, bronchitis or chronic obstructive pulmonary disease (COPD).
摘要翻译: 由式(I)和式(IV)表示的化合物具有抑制MMP-9产生的活性,因此作为一种具有比常规MMP酶活性抑制剂更少副作用的药剂可用作致癌剂的预防和治疗药物 血管生成,慢性类风湿关节炎,经皮冠状动脉腔内血管成形术后血管内膜增厚,血管动脉粥样硬化,出血性中风,急性心肌梗塞,慢性心力衰竭,动脉瘤,肺癌转移,成人呼吸窘迫综合征,哮喘,间质性肺纤维化,慢性鼻鼻窦炎, 支气管炎或慢性阻塞性肺疾病(COPD)。
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公开(公告)号:US08097708B2
公开(公告)日:2012-01-17
申请号:US12223675
申请日:2007-02-07
申请人: Tomohiro Sugimoto , Kanako Yamamoto , Akira Manaka , Haruhisa Ogita , Jun Kurosaka , Madoka Kawamura , Masato Kashimura , Naoki Sasamoto , Tomoaki Miura , Kenichi Kanemoto , Tomohiro Ozawa , Ken Chikauchi , Eiki Shitara , Dai Kubota
发明人: Tomohiro Sugimoto , Kanako Yamamoto , Akira Manaka , Haruhisa Ogita , Jun Kurosaka , Madoka Kawamura , Masato Kashimura , Naoki Sasamoto , Tomoaki Miura , Kenichi Kanemoto , Tomohiro Ozawa , Ken Chikauchi , Eiki Shitara , Dai Kubota
IPC分类号: C07H17/08
CPC分类号: C07H17/00 , A61K31/7052
摘要: [Object]: To provide a compound having a novel structure effective against Hemophilus influenzae and erythromycin resistant bacteria (for example, resistant pneumococci and streptococci) as well as against conventional erythromycin sensitive bacteria.[Solution]: A novel 10a-azalide compound represented by the formula (I), a pharmaceutically acceptable salt thereof or a solvate thereof, or an intermediate for the preparation of the same. The compound of the present invention has superior antibacterial activity against Hemophilus influenzae, erythromycin resistant pneumococci and the like, and therefore, the compound can be used as a therapeutic agent of infectious diseases.
摘要翻译: [目的]提供具有抗血友病嗜血杆菌和抗红霉素抗性细菌(例如抗性肺炎球菌和链球菌)以及常规红霉素敏感细菌的新型结构的化合物。 [溶液]:由式(I)表示的新型10a-氮杂化合物,其药学上可接受的盐或其溶剂化物或其制备的中间体。 本发明的化合物对流感嗜血杆菌,抗红霉素的肺炎球菌等具有优异的抗菌活性,因此可用作感染性疾病的治疗剂。
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公开(公告)号:US20090076253A1
公开(公告)日:2009-03-19
申请号:US12299229
申请日:2007-05-01
IPC分类号: C07H17/08
CPC分类号: C07H17/08 , A61K31/7048 , A61K31/7052 , C07H17/00
摘要: Compounds represented by formula (I) and the formula (IV) have an inhibitory activity of MMP-9 production, therefore, are useful as a medicine agent with fewer side effects than conventional MMP enzyme activity inhibitors, as a prophylactic and therapeutic drug for oncogenic angiogenesis, chronic rheumatoid arthritis, vascular intimal thickening after a percutaneous coronary transluminal angioplasty, vascular atherosclerosis, hemorrhagic apoplexy, acute myocardial infarction, chronic heart failure, aneurysm, lung cancer metastasis, adult respiratory distress syndrome, asthma, interstitial pulmonary fibrosis, chronic rhinosinusitis, bronchitis or chronic obstructive pulmonary disease (COPD).
摘要翻译: 由式(I)和式(IV)表示的化合物具有抑制MMP-9产生的活性,因此作为一种具有比常规MMP酶活性抑制剂更少副作用的药剂可用作致癌剂的预防和治疗药物 血管生成,慢性类风湿关节炎,经皮冠状动脉腔内血管成形术后血管内膜增厚,血管动脉粥样硬化,出血性中风,急性心肌梗塞,慢性心力衰竭,动脉瘤,肺癌转移,成人呼吸窘迫综合征,哮喘,间质性肺纤维化,慢性鼻鼻窦炎, 支气管炎或慢性阻塞性肺疾病(COPD)。
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公开(公告)号:US08461329B2
公开(公告)日:2013-06-11
申请号:US13142230
申请日:2009-12-25
申请人: Tetsuo Takayama , Hajime Asanuma , Daisuke Wakasugi , Rie Nishikawa , Yoshinori Sekiguchi , Madoka Kawamura , Naoya Ono , Tetsuya Yabuuchi , Takahiro Oi , Yusuke Oka , Shoichi Kuroda , Fumito Uneuchi , Takeshi Koami
发明人: Tetsuo Takayama , Hajime Asanuma , Daisuke Wakasugi , Rie Nishikawa , Yoshinori Sekiguchi , Madoka Kawamura , Naoya Ono , Tetsuya Yabuuchi , Takahiro Oi , Yusuke Oka , Shoichi Kuroda , Fumito Uneuchi , Takeshi Koami
IPC分类号: C07D413/12 , C07D401/12 , C07D405/12 , C07D217/24
CPC分类号: C07D217/16 , C07D217/18 , C07D217/20 , C07D401/12 , C07D405/12 , C07D409/12 , C07D417/12 , C07D471/04
摘要: A compound represented by formula (I) or a pharmaceutically acceptable salt thereof has an effect of inhibiting CRTH2 and, therefore, is useful as a preventive or a remedy for allergic diseases such as asthma, atopic dermatitis and allergic rhinitis.
摘要翻译: 由式(I)表示的化合物或其药学上可接受的盐具有抑制CRTH2的作用,因此可用作哮喘,特应性皮炎和过敏性鼻炎等过敏性疾病的预防或治疗。
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公开(公告)号:US20130096310A1
公开(公告)日:2013-04-18
申请号:US13805944
申请日:2011-06-22
IPC分类号: C07D217/18
CPC分类号: C07D217/18 , C07D217/20
摘要: A compound represented by formula (I) or a pharmaceutically acceptable salt thereof has an effect of inhibiting CRTH2 and, therefore, is useful as a pharmaceutical.
摘要翻译: 由式(I)表示的化合物或其药学上可接受的盐具有抑制CRTH2的作用,因此可用作药物。
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