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公开(公告)号:US20250051322A1
公开(公告)日:2025-02-13
申请号:US18722917
申请日:2023-01-12
Applicant: Eisai R&D Management Co., Ltd.
Inventor: Ikuo Kushida , Yoko Ito , So Yasui , Takashi Fukuyama , Nobuaki Sato , Taro Asaba
IPC: C07D451/02 , A61K31/506
Abstract: Crystals of compounds represented by formula (I) having potential as drug substances for pharmaceuticals, as well as salts of compounds represented by formula (I) and their crystals.
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公开(公告)号:US20180057499A1
公开(公告)日:2018-03-01
申请号:US15689481
申请日:2017-08-29
Applicant: Eisai R&D Management Co., Ltd.
Inventor: Richard Clark , Tetsuya Kawahara , Daisuke Iida , Shinsuke Hirota , Yasuaki Kamada , Toshiyuki Ohfusa , Naoki Yoneda , Fumiyoshi Matsuura , So Yasui
IPC: C07D487/04
CPC classification number: C07D487/04 , A61K31/519 , A61P17/06 , A61P29/00
Abstract: The compounds represented by formulas (I) to (XVIII) or pharmaceutically acceptable salts thereof.
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公开(公告)号:US11691990B2
公开(公告)日:2023-07-04
申请号:US17058406
申请日:2019-08-14
Applicant: Eisai R&D Management Co., Ltd.
Inventor: Jun Niijima , Hirofumi Kuroda , So Yasui , Yoko Ito , Ikuo Kushida
IPC: C07D519/00 , A61P35/00 , C07F9/6587 , C07H21/00 , A61K31/7084
CPC classification number: C07D519/00 , C07B2200/13
Abstract: The present invention provides crystals of (1R,3R,15E,28R,29R,30R,31R,34R,36R,39S,41R)-29,41-Difluoro-34,39-bis(sulfanyl)-2,33,35,38,40,42-hexaoxa-4,6,9,11,13,18,20,22,25,27-decaaza-34λ5,39λ5-diphosphaoctacyclo[28.6.4.13,36.128,31.04,8.07,12.019,24.023,27]dotetraconta-5,7,9,11,15,19,21,23,25-nonaene-34,39-dione (Compound (I)) ammonium salts, Compound (I) sodium salts, or Compound (I), possessing a potential to be used as drug substance in pharmaceuticals.
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公开(公告)号:US10227349B2
公开(公告)日:2019-03-12
申请号:US15689481
申请日:2017-08-29
Applicant: Eisai R&D Management Co., Ltd.
Inventor: Richard Clark , Tetsuya Kawahara , Daisuke Iida , Shinsuke Hirota , Yasuaki Kamada , Toshiyuki Ohfusa , Naoki Yoneda , Fumiyoshi Matsuura , So Yasui
IPC: C07D487/04 , A61K31/519 , A61P17/06 , A61P29/00
Abstract: The disclosure provides pyrazolo[1,5-a]pyrimidine compounds, and pharmaceutically acceptable salts thereof, having protease-activated receptor 2 (PAR2) inhibitory action, pharmaceutical compositions containing the same, and methods of treatment using the same.
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