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11.
公开(公告)号:US10323027B2
公开(公告)日:2019-06-18
申请号:US15735418
申请日:2016-06-23
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Takahiro Sugimoto , Shinkichi Suzuki , Hiroki Sakamoto , Masami Yamada , Minoru Nakamura , Makoto Kamata , Kenichiro Shimokawa , Masataka Murakami , Jinichi Yonemori , Takuto Kojima
IPC: C07D413/14 , C07D413/04 , C07D413/06 , C07D413/10 , C07D417/06 , C07D471/04 , C07D265/22 , C07D491/107 , C07F7/02 , A61P25/28 , C07D417/10 , C07F7/08
Abstract: The present invention provides a compound having a cholinergic muscarinic M1 receptor positive allosteric modulator activity, which may be useful as a prophylactic or therapeutic drug for Alzheimer's disease, schizophrenia, pain, sleep disorder, Parkinson's disease dementia, dementia with Lewy bodies and the like. The present invention relates to a compound represented by the formula (I) or a salt thereof: wherein each symbol is as defined in the attached DESCRIPTION.
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公开(公告)号:US10131653B2
公开(公告)日:2018-11-20
申请号:US15568644
申请日:2016-04-22
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Taku Kamei , Yasuyoshi Arikawa , Tomohiro Ohashi , Toshihiro Imaeda , Ikuo Fujimori , Takashi Miki , Jinichi Yonemori , Yuya Oguro , Takahiro Sugimoto , Masaki Seto , Goushi Nishida , Makoto Kamata , Hiroshi Imoto
IPC: C07D413/14 , C07D409/14 , C07D413/04 , C07D417/14 , A61P25/20 , A61P25/28 , A61P25/30 , A61P25/22 , A61P25/18 , A61P25/24 , A61K31/553
Abstract: The present invention provide a compound having an orexin receptor antagonistic activity, which is expected to be useful as medicaments such as agents for the prophylaxis or treatment of sleep disorder, depression, anxiety disorder, panic disorder, schizophrenia, drug dependence, Alzheimer's disease and the like.The present invention relates to a compound represented by the formula (I): wherein each symbol is as defined in the specification, or a salt thereof.
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公开(公告)号:US09789084B2
公开(公告)日:2017-10-17
申请号:US15608565
申请日:2017-05-30
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Masami Yamada , Shinkichi Suzuki , Takahiro Sugimoto , Minoru Nakamura , Hiroki Sakamoto , Makoto Kamata
IPC: C07D209/46 , C07D401/10 , C07D401/14 , C07D403/04 , C07D403/10 , C07D405/04 , C07D405/14 , A61K31/4035 , A61K31/4406 , A61K31/045 , C07D471/04
CPC classification number: C07D405/14 , A61K31/045 , A61K31/13 , A61K31/325 , A61K31/4035 , A61K31/4155 , A61K31/4406 , A61K31/4439 , A61K31/445 , A61K31/55 , C07D209/46 , C07D401/06 , C07D401/10 , C07D401/14 , C07D403/04 , C07D403/10 , C07D405/04 , C07D471/04
Abstract: The present invention provides a compound having a cholinergic muscarinic M1 receptor positive allosteric modulator activity and useful as an agent for the prophylaxis or treatment of Alzheimer's disease, schizophrenia, pain, sleep disorder, Parkinson's disease dementia, dementia with Lewy bodies, and the like.The present invention relates to a compound represented by the formula (I) or a salt thereof. wherein each symbol is as described in the specification, or a salt thereof.
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公开(公告)号:US09403802B2
公开(公告)日:2016-08-02
申请号:US14382390
申请日:2013-02-28
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Hiroki Sakamoto , Takahiro Sugimoto
IPC: C07D401/14 , C07D209/12 , C07D401/04 , C07D405/12 , C07D215/56 , C07D401/10 , C07D401/12 , C07D237/28 , C07D401/06 , C07D403/10
CPC classification number: C07D405/12 , C07D215/56 , C07D237/28 , C07D401/06 , C07D401/10 , C07D401/12 , C07D403/10
Abstract: The present invention provides a compound having a cholinergic muscarinic M1 receptor positive allosteric modulator activity, and useful as a prophylactic or therapeutic drug for Alzheimer's disease, schizophrenia, pain, a sleep disorder and the like. The present invention relates to a compound represented by the formula (I): wherein R1 is an optionally substituted amino group or an optionally substituted cyclic amino group, R2 and R3 are each independently a hydrogen atom or a substituent, X is —CH═ or —N═, and ring A is an optionally substituted 5- to 10-membered ring, or a salt thereof.
Abstract translation: 本发明提供具有胆碱能毒蕈碱M1受体阳性变构调节剂活性的化合物,可用作阿尔茨海默病,精神分裂症,疼痛,睡眠障碍等的预防或治疗药物。 本发明涉及由式(I)表示的化合物:其中R 1为任选取代的氨基或任选取代的环状氨基,R 2和R 3各自独立地为氢原子或取代基,X为-CH =或 -N =,环A为任选取代的5至10元环或其盐。
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公开(公告)号:US12091410B2
公开(公告)日:2024-09-17
申请号:US17413473
申请日:2019-12-11
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Yuichi Kajita , Yuhei Miyanohana , Tatsuki Koike , Yasutaka Hoashi , Yasushi Hattori , Norihito Tokunaga , Tsuneo Oda , Tohru Miyazaki , Dilhumar Uyghur , Yoshiteru Ito , Kohei Takeuchi , Keisuke Imamura , Takahiro Sugimoto , Koichiro Fukuda , Yasuhisa Kohara , Rei Okamoto , Taiichi Ohra , Naoki Miyamoto , Yoshito Terao , Masanori Kawasaki
IPC: C07D471/04 , C07D215/38 , C07D231/56 , C07D277/64 , C07D401/14
CPC classification number: C07D471/04 , C07D215/38 , C07D231/56 , C07D277/64 , C07D401/14
Abstract: The present invention provides a heterocyclic compound having an orexin type 2 receptor agonist activity.
A compound represented by the formula (I):
wherein each symbol is as described in the description, or a salt thereof has an orexin type 2 receptor agonist activity, and is useful as an agent for the prophylaxis or treatment of narcolepsy.-
公开(公告)号:US12071434B2
公开(公告)日:2024-08-27
申请号:US17413469
申请日:2019-12-11
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Yuhei Miyanohana , Yuichi Kajita , Tatsuki Koike , Yasutaka Hoashi , Yasushi Hattori , Norihito Tokunaga , Tsuneo Oda , Tohru Miyazaki , Dilhumar Uyghur , Yoshiteru Ito , Kohei Takeuchi , Keisuke Imamura , Takahiro Sugimoto , Koichiro Fukuda , Yasuhisa Kohara , Rei Okamoto , Taiichi Ohra , Naoki Miyamoto , Jun Chiba , Yoshito Terao , Masanori Kawasaki
IPC: C07D455/02 , A61P25/26 , C07D217/24 , C07D237/32 , C07D239/90 , C07D401/06 , C07D401/10 , C07D403/10 , C07D417/06 , C07D471/04 , C07D498/04
CPC classification number: C07D455/02 , A61P25/26 , C07D217/24 , C07D237/32 , C07D239/90 , C07D401/06 , C07D401/10 , C07D403/10 , C07D417/06 , C07D471/04 , C07D498/04 , C07B2200/05
Abstract: The present invention provides a heterocyclic compound having an orexin type 2 receptor agonist activity.
A compound represented by the formula (I):
wherein each symbol is as described in the description, or a salt thereof has an orexin type 2 receptor agonist activity, and is useful as an agent for the prophylaxis or treatment of narcolepsy.-
公开(公告)号:US11655241B2
公开(公告)日:2023-05-23
申请号:US16973320
申请日:2019-06-27
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Tsuneo Oda , Yoshiteru Ito , Tohru Miyazaki , Kohei Takeuchi , Norihito Tokunaga , Yasutaka Hoashi , Yasushi Hattori , Keisuke Imamura , Yuichi Kajita , Yuhei Miyanohana , Takahiro Sugimoto , Tatsuki Koike , Dilhumar Uyghur
IPC: C07D405/12 , C07D207/14 , C07D211/56 , C07D401/06 , C07D401/14 , C07D403/06 , C07D405/06 , C07D405/14 , C07D417/06 , C07D417/14
CPC classification number: C07D405/12 , C07D207/14 , C07D211/56 , C07D401/06 , C07D401/14 , C07D403/06 , C07D405/06 , C07D405/14 , C07D417/06 , C07D417/14
Abstract: The present invention provides a heterocyclic compound having an orexin type 2 receptor agonist activity.
A compound represented by the formula (I):
wherein each symbol is as described in the specification, or a salt thereof has an orexin type 2 receptor agonist activity, and is useful as an agent for the prophylaxis or treatment of narcolepsy.-
公开(公告)号:US10584097B2
公开(公告)日:2020-03-10
申请号:US16577449
申请日:2019-09-20
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Yuichi Kajita , Yuhei Miyanohana , Tatsuki Koike , Kohei Takeuchi , Yoshiteru Ito , Norihito Tokunaga , Takahiro Sugimoto , Tohru Miyazaki , Tsuneo Oda , Yasutaka Hoashi , Yasushi Hattori , Keisuke Imamura
IPC: C07D211/56 , C07D405/06 , C07D205/04 , C07D207/14 , C07D401/06 , C07D401/10 , C07D401/14 , C07D403/06 , C07D405/10 , C07D405/12 , C07D413/06 , C07D417/06 , C07D417/14 , C07D211/36 , A61P25/00
Abstract: The present invention provides a heterocyclic compound having an orexin type 2 receptor agonist activity.A compound represented by the formula (I): wherein each symbol is as described in the specification, or a salt thereof, is useful as an agent for the prophylaxis or treatment of narcolepsy.
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公开(公告)号:US10428056B2
公开(公告)日:2019-10-01
申请号:US16113635
申请日:2018-08-27
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Takahiro Sugimoto , Shinkichi Suzuki , Hiroki Sakamoto , Masami Yamada , Minoru Nakamura , Makoto Kamata , Kenichiro Shimokawa , Masataka Murakami , Jinichi Yonemori , Takuto Kojima
IPC: C07D471/04 , C07D413/14 , C07D413/04 , C07D413/06 , C07D413/10 , C07D417/06 , C07D265/22 , C07D491/107 , C07F7/02 , A61P25/28 , C07D417/10 , C07F7/08
Abstract: The present invention provides a compound having a cholinergic muscarinic M1 receptor positive allosteric modulator activity, which may be useful as a prophylactic or therapeutic drug for Alzheimer's disease, schizophrenia, pain, sleep disorder, Parkinson's disease dementia, dementia with Lewy bodies and the like. The present invention relates to a compound represented by the formula (I) or a salt thereof: wherein each symbol is as defined in the attached DESCRIPTION.
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公开(公告)号:US09868725B2
公开(公告)日:2018-01-16
申请号:US15306012
申请日:2015-04-22
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Masami Yamada , Shinkichi Suzuki , Takahiro Sugimoto , Minoru Nakamura , Hiroki Sakamoto , Makoto Kamata
IPC: C07D209/46 , C07D401/10 , C07D401/14 , C07D403/04 , C07D403/10 , C07D405/04 , C07D405/14 , C07D401/06 , A61K31/4035 , A61K31/4155 , A61K31/4439
CPC classification number: C07D405/14 , A61K31/045 , A61K31/13 , A61K31/325 , A61K31/4035 , A61K31/4155 , A61K31/4406 , A61K31/4439 , A61K31/445 , A61K31/55 , C07D209/46 , C07D401/06 , C07D401/10 , C07D401/14 , C07D403/04 , C07D403/10 , C07D405/04 , C07D471/04
Abstract: The present invention provides a compound having a cholinergic muscarinic M1 receptor positive allosteric modulator activity and useful as an agent for the prophylaxis or treatment of Alzheimer's disease, schizophrenia, pain, sleep disorder, Parkinson's disease dementia, dementia with Lewy bodies, and the like. The present invention relates to a compound represented by the formula (I) or a salt thereof. (I) wherein each symbol is as described in the specification, or a salt thereof.
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