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公开(公告)号:US20210340114A1
公开(公告)日:2021-11-04
申请号:US17226854
申请日:2021-04-09
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Yoshihiro Banno , Masahiro Kamaura , Kazuaki Takami , Koichiro Fukuda , Shigekazu Sasaki
IPC: C07D263/46 , A61K31/4418 , A61P27/02 , A61K31/421 , C07D231/22 , C07D239/34 , A61K31/505 , C07D263/38 , C07D213/70 , C07D213/65 , C07D231/12 , A61K31/415 , C07K14/47 , C12N15/09
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.-
公开(公告)号:US10544111B2
公开(公告)日:2020-01-28
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 , A61K31/415 , A61K31/421 , A61K31/4418 , A61K31/505 , C07D231/12 , C07D231/22 , C07D239/34 , C07D263/38 , C07D213/65 , A61P27/02 , C07D213/70 , C07K14/47 , C12N15/09
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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公开(公告)号:US20160159808A1
公开(公告)日:2016-06-09
申请号:US14907139
申请日:2014-07-23
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Masanori Kawasaki , Satoshi Mikami , Shinji Nakamura , Nobuyuki Negoro , Shuhei Ikeda , Izumi Nomura , Tomoko Ashizawa , Toshihiro Imaeda , Masaki Seto , Shigekazu Sasaki , Shogo Marui , Takahiko Taniguchi
IPC: C07D487/04 , C07D498/08 , C07D491/08 , C07D471/04 , C07D473/00
CPC classification number: C07D487/04 , C07D471/04 , C07D473/00 , C07D491/08 , C07D498/08
Abstract: A compound represented by the formula (I): wherein each symbol is as described in the SPECIFICATION, or a salt thereof has a PDE2A inhibitory action, and is useful as a prophylactic or therapeutic drug for schizophrenia, Alzheimer's disease and the like.
Abstract translation: 由式(I)表示的化合物:其中每个符号如说明书所述,或其盐具有PDE2A抑制作用,并且可用作精神分裂症,阿尔茨海默氏病等的预防或治疗药物。
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公开(公告)号:US10975043B2
公开(公告)日:2021-04-13
申请号:US16773720
申请日:2020-01-27
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Yoshihiro Banno , Masahiro Kamaura , Kazuaki Takami , Koichiro Fukuda , Shigekazu Sasaki
IPC: A61K31/4418 , A61K31/505 , C07D239/34 , C07D213/65 , C07D213/70 , C07D263/46 , A61K31/415 , A61K31/421 , C07D231/12 , C07D231/22 , C07D263/38 , A61P27/02 , C07K14/47 , C12N15/09
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.-
公开(公告)号:US10017508B2
公开(公告)日:2018-07-10
申请号:US15264213
申请日:2016-09-13
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Satoshi Mikami , Shinji Nakamura , Tomoko Ashizawa , Shigekazu Sasaki , Takahiko Taniguchi , Izumi Nomura , Masanori Kawasaki
IPC: C07D241/36 , A61K31/498 , C07D471/04 , C07D519/00 , A61K9/20 , A61K31/555 , C07F7/18
CPC classification number: C07D471/04 , A61K9/20 , A61K31/498 , A61K31/555 , C07D519/00 , C07F7/1804
Abstract: The present invention provides a compound having a PDE2A selective inhibitory action, which is useful as an agent for the prophylaxis or treatment of schizophrenia, Alzheimer's disease and the like.The present invention is a compound represented by the formula (1): wherein each symbol is as described in the specification, or a salt thereof.
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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:US09556200B2
公开(公告)日:2017-01-31
申请号:US14381347
申请日:2013-03-06
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Tomokazu Kusumoto , Shigekazu Sasaki , Hironobu Maezaki
IPC: A61K31/55 , C07D487/06 , C07D495/06 , C07D491/06
CPC classification number: C07D495/06 , C07D487/06 , C07D491/06
Abstract: The present invention provides a compound having a superior serotonin 5-HT2C receptor activating action.The present invention relates to a compound represented by the formula (1) wherein ring A is an aromatic carbocycle optionally having substituent(s) or an aromatic heterocycle optionally having substituent(s), X is —N(R1)—, —O— or the like, when ring A is an aromatic carbocycle optionally having substituent(s), then R1 is a hydrogen atom, an alkyl group optionally having substituent(s), or the like, and when ring A is an aromatic heterocycle optionally having substituent(s), then R1 is a hydrogen atom, an alkyl group optionally having substituent(s), a cycloalkyl group optionally having substituent(s), or the like, is a single bond or a double bond, and n is an integer of 0, 1 or 2, or a salt thereof.
Abstract translation: 本发明提供具有优良的5-羟色胺5-HT 2c受体激活作用的化合物。 本发明涉及由式(1)表示的化合物,其中环A是任选具有取代基的芳族碳环或任选具有取代基的芳族杂环,X是-N(R 1) - , - O - 当环A为任选具有取代基的芳族碳环,则R 1为氢原子,任选具有取代基的烷基等,当环A为任选的芳香族杂环时, 具有取代基,则R 1为氢原子,任选具有取代基的烷基,任选具有取代基的环烷基等为单键或双键,n为 0,1或2的整数,或其盐。
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公开(公告)号:US20230295628A1
公开(公告)日:2023-09-21
申请号:US18163506
申请日:2023-02-02
Applicant: National University Corporation Tokyo Medical and Dental University , Takeda Pharmaceutical Company Limited
Inventor: Takanori Yokota , Tetsuya Nagata , Hideki Furukawa , Yasuo Nakagawa , Takatoshi Yogo , Ryosuke Tokunoh , Shigekazu Sasaki , Kosuke Hidaka , Tomohiro Seki , Kenichi Miyata , Akio Uchida
IPC: C12N15/113 , A61P25/00
CPC classification number: C12N15/113 , A61P25/00 , C12N2310/11 , C12N2310/341
Abstract: Developed and provided is: a nucleic acid agent that is efficiently delivered to the central nervous system, to which drug delivery is inhibited by the blood brain barrier mechanism, and that provides an antisense effect to a target transcription product at the delivery site; and a composition containing such a nucleic acid agent. Provided is a double-stranded nucleic acid complex consisting of a first nucleic acid strand and a second nucleic acid strand that are annealed to each other; wherein the first nucleic acid strand hybridizes with part of a target transcription product and has an antisense effect on the target transcription product; and wherein the second nucleic acid strand includes a base sequence complementary to the first nucleic acid strand and is conjugated to a phosphatidylethanolamine or an analog thereof.
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公开(公告)号:US11597928B2
公开(公告)日:2023-03-07
申请号:US16980191
申请日:2019-03-13
Applicant: National University Corporation Tokyo Medical and Dental University , Takeda Pharmaceutical Company Limited
Inventor: Takanori Yokota , Tetsuya Nagata , Hideki Furukawa , Yasuo Nakagawa , Takatoshi Yogo , Ryosuke Tokunoh , Shigekazu Sasaki , Kosuke Hidaka , Tomohiro Seki , Kenichi Miyata , Akio Uchida
IPC: C07H21/04 , C12N15/113 , A61P25/00
Abstract: Developed and provided is: a nucleic acid agent that is efficiently delivered to the central nervous system, to which drug delivery is inhibited by the blood brain barrier mechanism, and that provides an antisense effect to a target transcription product at the delivery site; and a composition containing such a nucleic acid agent.
Provided is a double-stranded nucleic acid complex consisting of a first nucleic acid strand and a second nucleic acid strand that are annealed to each other; wherein the first nucleic acid strand hybridizes with part of a target transcription product and has an antisense effect on the target transcription product; and wherein the second nucleic acid strand includes a base sequence complementary to the first nucleic acid strand and is conjugated to a phosphatidylethanolamine or an analog thereof.-
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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