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公开(公告)号:US09101588B2
公开(公告)日:2015-08-11
申请号:US13496778
申请日:2010-09-10
IPC分类号: C07C309/00 , A01N33/00 , A61K31/13 , A61K31/16 , A61K31/185
CPC分类号: A61K31/185
摘要: A composition for lowering a blood uric acid level is characterized by comprising taurine as an active ingredient.
摘要翻译: 用于降低血液尿酸水平的组合物的特征在于包含牛磺酸作为活性成分。
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公开(公告)号:US09035059B2
公开(公告)日:2015-05-19
申请号:US14004950
申请日:2012-03-14
申请人: Tsuyoshi Busujima , Takahiro Oi , Hiroaki Tanaka , Yoshihisa Shirasaki , Kanako Iwakiri , Nagaaki Sato , Shigeru Tokita
发明人: Tsuyoshi Busujima , Takahiro Oi , Hiroaki Tanaka , Yoshihisa Shirasaki , Kanako Iwakiri , Nagaaki Sato , Shigeru Tokita
IPC分类号: C07D401/14 , C07D209/44 , C07D217/04 , C07D223/16 , C07D405/12 , C07D409/06 , C07D413/06 , C07D417/10 , A61K31/4035 , A61K31/454 , A61K31/472 , A61K31/497 , C07D217/18 , C07D217/06 , C07D217/22 , C07D401/06 , C07D401/10 , C07D401/12 , C07D403/12 , C07D405/06 , C07D413/12 , C07D417/06 , A61K9/16 , A61K9/20 , A61K9/48 , C07D217/20 , C07D217/26 , C07D405/14 , C07D409/14 , C07D417/12 , C07D417/14 , C07D495/04 , C07D217/10 , C07D401/08
CPC分类号: C07D217/18 , A61K9/1623 , A61K9/2018 , A61K9/4858 , C07D209/44 , C07D217/04 , C07D217/06 , C07D217/10 , C07D217/20 , C07D217/22 , C07D217/26 , C07D223/16 , C07D401/06 , C07D401/08 , C07D401/10 , C07D401/12 , C07D401/14 , C07D403/12 , C07D405/06 , C07D405/12 , C07D405/14 , C07D409/06 , C07D409/14 , C07D413/06 , C07D413/12 , C07D417/06 , C07D417/10 , C07D417/12 , C07D417/14 , C07D495/04
摘要: There are provided compounds represented by the following general formula (I) or pharmaceutically acceptable salts of thereof, which have a superior monoacylglycerol acyltransferase 2 inhibitory action: wherein Ring A represents a partially saturated heteroaryl group, an aryl group or a heteroaryl group, RB represents a C4-18 alkyl group, a C3-8 cycloalkyl group, a partially saturated aryl group, an aryl group, or the following formula (II): wherein V represents the formula —CR11R12—, —CO—, —CO—O—, or —CO—NH—, W represents a single bond or a C1-3 alkylene group, and Ring B represents a C3-8 cycloalkyl group, a C3-8 cycloalkenyl group, a partially saturated heteroaryl group, a saturated heterocyclyl group, an aryl group, or a heteroaryl group, Y represents a nitrogen atom or the formula N+(RF), RF represents a C1-4 alkyl group, and m and n, which may be the same or different, each represent an integer of 0 or 1.
摘要翻译: 提供具有优异的单酰基甘油酰基转移酶2抑制作用的由以下通式(I)表示的化合物或其药学上可接受的盐:其中环A表示部分饱和的杂芳基,芳基或杂芳基,RB表示 C4-18烷基,C3-8环烷基,部分饱和芳基,芳基或下式(Ⅱ)表示:其中V表示式-CR11R12-,-CO-,-CO-O- 或-CO-NH-,W表示单键或C1-3亚烷基,环B表示C3-8环烷基,C3-8环烯基,部分饱和杂芳基,饱和杂环基, 芳基或杂芳基,Y表示氮原子或式N +(RF),RF表示C1-4烷基,m和n可相同或不同,分别表示0以上的整数 或1。
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公开(公告)号:US20140330010A1
公开(公告)日:2014-11-06
申请号:US14362939
申请日:2012-12-07
发明人: Toshio Nakamura , Seiji Masuda
IPC分类号: C07D491/107 , C07D413/14 , C07D403/12 , C07D401/12
CPC分类号: A61K31/454 , A61K31/4025 , A61K31/5377 , C07D401/12 , C07D403/12 , C07D413/14 , C07D491/107
摘要: Provided are novel compounds that are useful in the prevention or treatment of such diseases as dementia, Alzheimer's disease, attention-deficient hyperactivity disorder, schizophrenia, epilepsy, central convulsion, obesity, diabetes mellitus, hyperlipidemia, narcolepsy, idiopathic hypersomnia, behaviorally induced insufficient sleep syndrome, sleep apnea syndrome, circadian rhythm disorder, parasomnia, sleep related movement disorder, insomnia, and depression, or allergic rhinitis, or pharmaceutically acceptable salts of such compounds. Specifically, there are provided phenylpyrrole compounds represented by the following formula (I) or pharmaceutically acceptable salts thereof:Formula (I) [wherein Q refers to a group represented by the following formula (A) or (B):
摘要翻译: 提供了可用于预防或治疗诸如痴呆,阿尔茨海默病,注意缺陷多动障碍,精神分裂症,癫痫,中枢抽搐,肥胖症,糖尿病,高脂血症,发作性睡眠,特发性睡眠过度,行为诱发的不足睡眠等疾病的新型化合物 综合征,睡眠呼吸暂停综合征,昼夜节律紊乱,睡眠睡眠,睡眠相关的运动障碍,失眠和抑郁症,或过敏性鼻炎,或这些化合物的药学上可接受的盐。 具体地,提供下式(I)表示的苯基吡咯化合物或其药学上可接受的盐:式(I)[其中Q表示由下式(A)或(B)表示的基团:
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公开(公告)号:US08822503B2
公开(公告)日:2014-09-02
申请号:US13081201
申请日:2011-04-06
申请人: Takanori Kawaguchi , Kengo Watatani , Keiko Fusegi , Masahiro Bohno , Hajime Asanuma , Shoichi Kuroda , Yudai Imai , Tomomichi Chonan , Nagaaki Sato , Shigeru Tokita , Shigetada Sasako , Takumi Okada , Keishi Hayashi , Shin Itoh , Noriko Saito , Rui Jibiki , Seishi Ishiyama , Hirofumi Ota
发明人: Takanori Kawaguchi , Kengo Watatani , Keiko Fusegi , Masahiro Bohno , Hajime Asanuma , Shoichi Kuroda , Yudai Imai , Tomomichi Chonan , Nagaaki Sato , Shigeru Tokita , Shigetada Sasako , Takumi Okada , Keishi Hayashi , Shin Itoh , Noriko Saito , Rui Jibiki , Seishi Ishiyama , Hirofumi Ota
IPC分类号: A61K31/4439 , C07D401/06
CPC分类号: C07D401/10 , C07D213/64 , C07D401/12 , C07D401/14 , C07D405/10 , C07D413/06 , C07D417/06 , C07D417/14
摘要: A 2-pyridone compound represented by the formula [1]: {wherein in the formula [1], the ring represented by A represents a benzene ring or a pyridine ring, X represents any of the structures represented by the formulas [3] shown below: V represents a single bond or a lower alkylene group, and W represents a single bond, an ether bond or a lower alkylene group (wherein the lower alkylene group may contain an ether bond)}, a tautomer or stereoisomer of the compound, a pharmaceutically acceptable salt thereof, or a solvate thereof is a compound that has an excellent GK activating effect and is useful as a pharmaceutical.
摘要翻译: 由式[1]表示的2-吡啶酮化合物:其中,在式[1]中,由A表示的环表示苯环或吡啶环,X表示由式[3]表示的任何结构 V表示单键或低级亚烷基,W表示单键,醚键或低级亚烷基(其中低级亚烷基可以含有醚键)},化合物的互变异构体或立体异构体, 其药学上可接受的盐或其溶剂合物是具有优异的GK活化作用并可用作药物的化合物。
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公开(公告)号:US08796272B2
公开(公告)日:2014-08-05
申请号:US14000261
申请日:2012-02-21
申请人: Minoru Moriya , Hiroshi Ohta , Shuji Yamamoto , Kumi Abe , Yuko Araki , Xiang-Min Sun , Daisuke Wakasugi
发明人: Minoru Moriya , Hiroshi Ohta , Shuji Yamamoto , Kumi Abe , Yuko Araki , Xiang-Min Sun , Daisuke Wakasugi
IPC分类号: A61K31/50 , A61K31/501
CPC分类号: C07D401/04 , C07D401/14 , C07D413/14 , C07D417/14
摘要: The present invention relates to novel compounds of formula [I] or pharmaceutically acceptable salts thereof: The compounds of the present invention are useful in the prevention or treatment of diseases such as schizophrenia, Alzheimer's disease, cognitive impairment, dementia, anxiety disorders (e.g., generalized anxiety disorder, panic disorder, obsessive-compulsive disorder, social anxiety disorder, post-traumatic stress disorder, specific phobias, acute stress disorder), depression, drug dependence, spasm, tremor, pain, Parkinson's disease, attention deficit hyperactivity disorder, bipolar disorder, eating disorder, or sleep disorders, which is based on the glycine uptake-inhibiting action.
摘要翻译: 本发明涉及式[I]的新化合物或其药学上可接受的盐:本发明的化合物可用于预防或治疗诸如精神分裂症,阿尔茨海默氏病,认知障碍,痴呆,焦虑症(例如, 广泛性焦虑症,恐慌症,强迫症,社交焦虑症,创伤后应激障碍,特异性恐惧症,急性应激障碍),抑郁症,药物依赖性,痉挛,震颤,疼痛,帕金森病,注意缺陷多动障碍,双相 紊乱,进食障碍或睡眠障碍,其基于甘氨酸摄取抑制作用。
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公开(公告)号:US08609847B2
公开(公告)日:2013-12-17
申请号:US13144591
申请日:2010-02-05
申请人: Toshio Nakamura , Seiji Masuda , Aya Futamura
发明人: Toshio Nakamura , Seiji Masuda , Aya Futamura
IPC分类号: C07D215/38
CPC分类号: C07D401/12 , C07D401/14 , C07D405/14 , C07D413/14 , C07D471/04
摘要: The present invention provides a prophylactic or therapeutic agent for dementia, Alzheimer's disease, attention-deficit hyperactivity disorder, schizophrenia, eating disorders, obesity, diabetes, hyperlipidemia, sleep disorders, narcolepsy, sleep apnea syndrome, circadian rhythm disorder, depression, allergic rhinitis or other diseases.A dihydroquinolinone derivative represented by formula (1) or a pharmaceutically acceptable salt thereof: {wherein Q represents the following formula (A) or (B)}
摘要翻译: 本发明提供了用于痴呆,阿尔茨海默病,注意缺陷多动障碍,精神分裂症,进食障碍,肥胖,糖尿病,高脂血症,睡眠障碍,发作性睡眠障碍,睡眠呼吸暂停综合征,昼夜节律紊乱,抑郁,过敏性鼻炎或 其他疾病 由式(1)表示的二氢喹啉酮衍生物或其药学上可接受的盐:其中Q表示下式(A)或(B)}
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公开(公告)号:US20130281465A1
公开(公告)日:2013-10-24
申请号:US13994043
申请日:2011-12-16
申请人: Dai Nozawa , Ryo Suzuki , Aya Futamura , Rie Shimono , Masahito Abe , Hiroshi Ohta , Yuko Araki
发明人: Dai Nozawa , Ryo Suzuki , Aya Futamura , Rie Shimono , Masahito Abe , Hiroshi Ohta , Yuko Araki
IPC分类号: C07D403/12 , C07D405/14 , A61K31/4439 , A61K31/506 , A61K31/4192 , C07D401/14
CPC分类号: A61K31/4192 , A61K31/4439 , A61K31/506 , C07D401/14 , C07D403/12 , C07D405/14
摘要: A compound represented by formula (IA) or a pharmaceutically acceptable salt thereof, which is useful for the treatment or prevention of diseases such sleep disorder, depression, anxiety disorder, panic disorder, schizophrenia, drug dependence, Alzheimer's disease, Parkinson's disease, Huntington's chorea, eating disorder, pain, gastrointestinal diseases, epilepsy, inflammation, immune-related diseases, endocrine-related diseases, and hypertension, and of which the action relies on an orexin (OX) receptor antagonistic activity.
摘要翻译: 由式(IA)表示的化合物或其药学上可接受的盐,其可用于治疗或预防睡眠障碍,抑郁症,焦虑障碍,恐慌症,精神分裂症,药物依赖,阿尔茨海默氏病,帕金森病,亨廷顿舞蹈病 ,饮食失调,疼痛,胃肠道疾病,癫痫,炎症,免疫相关疾病,内分泌相关疾病和高血压,其作用依赖于食欲素(OX)受体拮抗作用。
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公开(公告)号:US08524738B2
公开(公告)日:2013-09-03
申请号:US13463434
申请日:2012-05-03
申请人: Taro Kiyoto , Tadashi Tanaka , Yasuhiro Tsutsui , Junichi Ando , Mai Motono , Yasuko Kawaguchi , Toshiya Noguchi , Yasunobu Ushiki , Fumihito Ushiyama , Hiroki Urabe
发明人: Taro Kiyoto , Tadashi Tanaka , Yasuhiro Tsutsui , Junichi Ando , Mai Motono , Yasuko Kawaguchi , Toshiya Noguchi , Yasunobu Ushiki , Fumihito Ushiyama , Hiroki Urabe
IPC分类号: A61K31/47
CPC分类号: C07D405/14 , C07D215/227 , C07D401/06 , C07D401/14 , C07D405/12 , C07D409/14 , C07D413/14 , C07D471/04 , C07D491/04 , C07D495/04 , C07D513/04 , C07D519/00
摘要: A nitrogen-containing heterocyclic compound or pharmaceutically acceptable salt thereof represented by the general formula: which have a potent antibacterial activity and a high safety. Thus, the compounds are useful as antibacterial agents against gram-positive bacteria, gram-negative bacteria and drug resistant bacteria.
摘要翻译: 由通式表示的含氮杂环化合物或其药学上可接受的盐,其具有强的抗菌活性和高安全性。 因此,这些化合物可用作抗革兰氏阳性细菌,革兰氏阴性细菌和耐药细菌的抗菌剂。
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公开(公告)号:US08367831B2
公开(公告)日:2013-02-05
申请号:US13468140
申请日:2012-05-10
申请人: Taro Kiyoto , Junichi Ando , Tadashi Tanaka , Yasuhiro Tsutsui , Mai Yokotani , Toshiya Noguchi , Fumihito Ushiyama , Hiroki Urabe , Hiromasa Horikiri
发明人: Taro Kiyoto , Junichi Ando , Tadashi Tanaka , Yasuhiro Tsutsui , Mai Yokotani , Toshiya Noguchi , Fumihito Ushiyama , Hiroki Urabe , Hiromasa Horikiri
IPC分类号: C07D471/04
CPC分类号: C07D471/04 , C07D491/056 , C07D519/00 , Y02P20/55
摘要: Disclosed is a compound represented by the general formula: wherein R1 represents an aryl or heterocyclic group which may be substituted or the like; X1 represents a C2-C4 alkylene group or the like; X2, X3 and X5 independently represent NH, a bond or the like; X4 represents a lower alkylene group, a bond or the like; Y1 represents a bivalent alicyclic hydrocarbon residue which may be substituted or a bivalent alicyclic amine residue which may be substituted; and Z1, Z2, Z3, Z4, Z5 and Z6 independently represent a nitrogen atom, a group represented by the formula: CH, or the like, provided that at least one of Z3, Z4, Z5 and Z6 represents a nitrogen atom, or a salt thereof, which is useful as an antibacterial agent.
摘要翻译: 公开了由以下通式表示的化合物:其中R1表示可被取代的芳基或杂环基等; X1表示C2-C4亚烷基等; X2,X3和X5独立地表示NH,键等; X 4表示低级亚烷基,键等; Y1表示可以被取代的二价脂环族烃残基或可以被取代的二价脂环族胺残基; 并且Z 1,Z 2,Z 3,Z 4,Z 5和Z 6独立地表示氮原子,由式CH表示的基团等,条件是Z 3,Z 4,Z 5和Z 6中的至少一个表示氮原子,或 其盐,其可用作抗菌剂。
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公开(公告)号:US08183387B2
公开(公告)日:2012-05-22
申请号:US12951964
申请日:2010-11-22
申请人: Toshio Nakamura , Makoto Tatsuzuki , Dai Nozawa , Tomoko Tamita , Seiji Masuda , Hiroshi Ohta , Shuhei Kashiwa , Aya Fujino , Shigeyuki Chaki , Toshiharu Shimazaki
发明人: Toshio Nakamura , Makoto Tatsuzuki , Dai Nozawa , Tomoko Tamita , Seiji Masuda , Hiroshi Ohta , Shuhei Kashiwa , Aya Fujino , Shigeyuki Chaki , Toshiharu Shimazaki
IPC分类号: C07D231/10
CPC分类号: C07D231/14 , C07D231/40 , C07D401/04 , C07D401/14 , C07D403/04 , C07D403/06 , C07D403/12 , C07D403/14 , C07D413/04 , C07D413/14
摘要: The present invention provides a prophylactic or therapeutic agent for dementia, Alzheimer's disease, attention-deficit hyperactivity disorder, schizophrenia, eating disorders, obesity, diabetes, hyperlipidemia, sleep disorders, narcolepsy, sleep apnea syndrome, circadian rhythm disorder, depression, allergic rhinitis or other diseases.A phenylpyrazole derivative represented by formula (1) or a pharmaceutically acceptable salt thereof: {wherein R1 and R2, which may be the same or different, each represent C1-C6 alkyl or C3-C8 cycloalkyl, or R1 and R2 are attached to each other together with their adjacent nitrogen atom to form a 4- to 7-membered saturated heterocyclic ring (wherein said saturated heterocyclic ring may be substituted with halogen or C1-C6 alkyl), n represents an integer of 0 to 2, T represents a hydrogen atom, halogen or C1-C6 alkyl, and R represents formula (I): or the like}.
摘要翻译: 本发明提供了用于痴呆,阿尔茨海默病,注意缺陷多动障碍,精神分裂症,进食障碍,肥胖症,糖尿病,高脂血症,睡眠障碍,发作性睡眠障碍,睡眠呼吸暂停综合征,昼夜节律紊乱,抑郁,过敏性鼻炎或 其他疾病 由式(1)表示的苯基吡唑衍生物或其药学上可接受的盐:其中可以相同或不同的R 1和R 2各自表示C 1 -C 6烷基或C 3 -C 8环烷基,或者R 1和R 2各自连接 与其相邻的氮原子一起形成4-至7-元饱和杂环(其中所述饱和杂环可被卤素或C 1 -C 6烷基取代),n表示0至2的整数,T表示氢 原子,卤素或C 1 -C 6烷基,R表示式(I):等)。
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