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公开(公告)号:US09975903B2
公开(公告)日:2018-05-22
申请号:US15539607
申请日:2015-12-24
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Minoru Sasaki , Fumiaki Kikuchi , Zenichi Ikeda , Keiko Kakegawa , Yoichi Nishikawa , Shigekazu Sasaki , Koichiro Fukuda , Kazuaki Takami , Yoshihiro Banno , Masahiro Kamaura
IPC: C07D493/04 , C07D495/04 , C07D321/00 , C07D405/06 , C07D321/12 , C07D413/06 , C07D323/00 , C07D491/044 , C07D313/00 , C07D313/20
CPC classification number: C07D495/04 , A61K31/365 , A61K31/381 , A61K31/4025 , A61K31/422 , A61K31/662 , C07D313/00 , C07D313/20 , C07D321/00 , C07D321/12 , C07D323/00 , C07D405/06 , C07D409/12 , C07D413/06 , C07D491/044 , C07D493/04 , C07F9/655
Abstract: The present invention relates to a condensed heterocyclic compound that has an enteropeptidase inhibitory effect and is useful in the treatment or prevention of obesity, diabetes mellitus, or the like, and a medicament containing the same. Specifically, the present invention relates to a compound represented by the following formula (I) or a salt thereof, and a medicament containing the same [in the formula, each symbol is as defined in the specification].
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公开(公告)号:US20170226137A1
公开(公告)日:2017-08-10
申请号:US15421702
申请日:2017-02-01
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Tatsuhiko Fujimoto , Kentaro Rikimaru , Koichiro Fukuda , Hiromichi Sugimoto , Takahiro Matsumoto , Norihito Tokunaga , Mariko Hirozane
IPC: C07F7/18 , C07D211/24 , C07D401/14 , C07D405/06 , C07D413/06 , C07D405/14 , C07D401/06 , C07D409/12 , C07D401/12 , C07D405/12 , C07D417/06 , C07D417/14 , C07D211/56 , C07D409/06
CPC classification number: C07F7/1804 , C07D211/24 , C07D211/36 , C07D211/56 , C07D401/06 , C07D401/12 , C07D401/14 , C07D405/06 , C07D405/12 , C07D405/14 , C07D409/06 , C07D409/12 , C07D413/06 , C07D417/06 , C07D417/14
Abstract: Provided is a substituted piperidine 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 a prophylactic or therapeutic agent for narcolepsy.
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公开(公告)号:US12077522B2
公开(公告)日:2024-09-03
申请号:US17256330
申请日:2019-06-27
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Tatsuhiko Fujimoto , Koichiro Fukuda , Hiromichi Sugimoto , Kentaro Rikimaru , Yoshihiro Banno , Takahiro Matsumoto , Norihito Tokunaga , Yoshihide Tomata , Yuji Ishichi , Shogo Marui , Tsuneo Oda , Tohru Miyazaki , Yasutaka Hoashi , Yasushi Hattori , Yuichi Kajita , Yuhei Miyanohana , Tatsuki Koike
IPC: C07D401/14 , C07D211/56 , C07D405/14
CPC classification number: C07D401/14 , C07D211/56 , C07D405/14
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:US10508083B2
公开(公告)日:2019-12-17
申请号:US16075240
申请日:2017-02-01
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Tatsuhiko Fujimoto , Kentaro Rikimaru , Koichiro Fukuda , Hiromichi Sugimoto , Takahiro Matsumoto
IPC: C07D211/36 , A61P25/00
Abstract: Provided is a substituted piperidine 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 a prophylactic or therapeutic agent for narcolepsy.
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公开(公告)号:US20190119225A1
公开(公告)日:2019-04-25
申请号:US16230634
申请日:2018-12-21
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Yoshihiro Banno , Masahiro Kamaura , Kazuaki Takami , Koichiro Fukuda , Shigekazu Sasaki
IPC: C07D263/46 , C07D213/70 , A61P27/02 , C07D239/34 , A61K31/421 , C07D213/65 , C07D263/38 , A61K31/415 , C07D231/22 , C07D231/12 , A61K31/505 , A61K31/4418
Abstract: Provided is a heterocyclic compound having a superior RBP4-lowering action and useful as a medicament for the prophylaxis or treatment of a disease or symptom mediated by an increase in RBP4 or retinol supplied by RBP4.A compound represented by the formula (I): wherein each symbol is as defined in the Description, or a salt thereof has a superior RBP4-lowering action, and is useful as a medicament for the prophylaxis or treatment of a disease or symptom mediated by an increase in RBP4 or retinol supplied by RBP4.
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