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公开(公告)号:EP2157090A4
公开(公告)日:2011-09-07
申请号:EP08765775
申请日:2008-06-20
发明人: UMEMIYA HIROKI , WATATANI KENGO , KAWAGUCHI TAKANORI , KAWABE KENICHI , OKADA TAKUMI , SASAKO SHIGETADA , SAITO NORIKO
IPC分类号: C07D403/12 , A61K31/497 , A61K31/501 , A61P3/04 , A61P3/10 , A61P43/00 , C07D401/14 , C07D403/14 , C07D413/14 , C07D417/14
CPC分类号: C07D401/14 , C07D403/12 , C07D403/14 , C07D413/14 , C07D417/14
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公开(公告)号:EP3173408A4
公开(公告)日:2017-12-06
申请号:EP15825310
申请日:2015-07-24
申请人: TAISHO PHARMA CO LTD
发明人: KURODA SHOICHI , KAWABE KENICHI , USHIKI YASUNOBU , OHTA HIROSHI , UNEUCHI FUMITO , SHIBATA TSUYOSHI , TABUSE HIDEAKI , MUNETOMO EIJI , CHONAN SUMI
IPC分类号: C07D401/10 , A61K31/4725 , A61P1/10 , A61P13/12 , A61P19/00 , A61P43/00 , C07D401/14 , C07D403/14 , C07D405/10 , C07D413/10 , C07D413/14 , C07D417/10
CPC分类号: C07D417/10 , A61K31/4725 , C07D401/10 , C07D401/14 , C07D403/14 , C07D405/10 , C07D413/10 , C07D413/14
摘要: The present invention provides a compound represented by the following formula [1] or a pharmaceutically acceptable salt thereof which has an excellent NHE3 inhibitory effect: €ƒ€ƒ€ƒ€ƒ€ƒ€ƒ€ƒ€ƒ[Formula 15]€ƒ€ƒ€ƒ€ƒ€ƒA-Y [1] wherein A represents a structure represented by the following formula [2]: wherein R 11 and R 12 each represent a halogen atom or the like, R 2 represents C 1-6 alkyl or the like, ring E represents triazole, tetrazole, pyrimidine, or the like, R 31 and R 32 each represent a hydrogen atom, C 1-6 alkyl, C 1-6 alkoxy, or the like, and W represents a single bond, the formula -NH-, the formula -O-, or the formula -CONH-, and Y represents a hydrogen atom or a structure represented by the following formula [3']:
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公开(公告)号:EP2607360A4
公开(公告)日:2014-01-08
申请号:EP11818240
申请日:2011-08-19
申请人: TAISHO PHARMA CO LTD
发明人: KAKINUMA HIROYUKI , KOBASHI YOHEI , CHONAN TOMOMICHI , SHIOZAWA FUMIYASU , IWATA YUKI , OI TAKAHIRO , KAWABE KENICHI
IPC分类号: C07D309/10 , A61K31/351 , A61P3/10 , A61P43/00
CPC分类号: A61K31/7034 , A61K31/351 , C07D309/10
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公开(公告)号:EP2881384A4
公开(公告)日:2015-12-23
申请号:EP13825784
申请日:2013-07-29
申请人: TAISHO PHARMA CO LTD
发明人: TAKAYAMA TETSUO , SHIBATA TSUYOSHI , SHIOZAWA FUMIYASU , KAWABE KENICHI , SHIMIZU YUKI , HAMADA MAKOTO , HIRATATE AKIRA , TAKAHASHI MASATO , USHIYAMA FUMIHITO , OI TAKAHIRO , SHIRASAKI YOSHIHISA , MATSUDA DAISUKE , KOIZUMI CHIE , KATO SOTA
IPC分类号: C07D207/36 , A61K31/4015 , A61K31/4412 , A61K31/4418 , A61K31/443 , A61K31/4436 , A61K31/4439 , A61K31/444 , A61K31/4545 , A61K31/4704 , A61K31/4709 , A61K31/496 , A61K31/497 , A61K31/501 , A61K31/506 , A61K31/5377 , A61K31/55 , A61P7/06 , A61P43/00
CPC分类号: C07D211/90 , C07D207/36 , C07D209/54 , C07D215/56 , C07D221/20 , C07D401/06 , C07D401/10 , C07D401/12 , C07D401/14 , C07D405/06 , C07D409/06 , C07D409/10 , C07D413/06 , C07D413/10 , C07D413/12 , C07D417/06 , C07D417/10 , C07D417/12 , C07D471/10 , C07D491/107 , C07D498/04
摘要: There are provided compounds having a superior PHD2 inhibitory effect that are represented by general formula (I'): (in the above-mentioned general formula (I'), W, Y, R 2 , R 3 , R 4 , and Y 4 are as described hereinabove), or pharmaceutically acceptable salts thereof.
摘要翻译: 提供由通式(I')表示的具有优异PHD2抑制作用的化合物:(在上述通式(I')中,W,Y,R 2,R 3,R 4和Y 4 如上所述)或其药学上可接受的盐。
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公开(公告)号:EP2103607A4
公开(公告)日:2011-01-05
申请号:EP07850604
申请日:2007-12-14
申请人: TAISHO PHARMA CO LTD
发明人: KAKINUMA HIROYUKI , OI TAKAHIRO , HASHIMOTO YUKO , TAKAHASHI HITOMI , KOBAYASHI YOHEI , IWATA YUKI , KAWABE KENICHI , TAKAHASHI MASATO
IPC分类号: C07D335/02 , A61K31/382 , A61P3/04 , A61P3/06 , A61P3/08 , A61P3/10 , A61P7/10 , A61P9/04 , A61P9/10 , A61P9/12 , A61P13/12 , A61P19/06 , A61P25/00 , A61P27/02 , A61P31/04 , A61P43/00
CPC分类号: C07D335/02
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