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公开(公告)号:EP2022793A4
公开(公告)日:2010-09-08
申请号:EP07744040
申请日:2007-05-24
发明人: KIYOTO TARO , ANDO JUNICHI , TANAKA TADASHI , TSUTSUI YASUHIRO , YOKOTANI MAI , NOGUCHI TOSHIYA , USHIYAMA FUMIHITO , URABE HIROKI , HORIKIRI HIROMASA
IPC分类号: C07D471/04 , A61K31/4375 , A61K31/4985 , A61K31/5365 , A61K31/542 , A61P31/04 , C07D519/00
CPC分类号: C07D471/04 , C07D491/056 , C07D519/00 , Y02P20/55
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公开(公告)号:EP2604602A4
公开(公告)日:2013-12-18
申请号:EP11816483
申请日:2011-08-11
申请人: TAISHO PHARMA CO LTD
发明人: NAKAMURA TOSHIO , SAKAGAMI KAZUNARI , KONISHI KAZUHIDE , YAMAMOTO KANAKO , MASUDA SEIJI , MATSUDA YOHEI , OKADA KUMIKO , SHIBATA TSUYOSHI , OHTA HIROSHI , YASUHARA AKITO , KAWAMOTO HIROSHI , AMADA HIDEAKI , URABE HIROKI , NISHIKAWA RIE , KASHIWA SHUHEI
IPC分类号: C07D403/04 , A61K31/4155 , A61K31/4245 , A61K31/4439 , A61P25/04 , A61P25/08 , A61P25/20 , A61P25/22 , A61P25/28 , A61P25/36 , C07D403/14 , C07D413/04 , C07D413/14
CPC分类号: C07D413/14 , C07D231/38 , C07D403/04 , C07D403/14 , C07D413/04
摘要: A compound represented by formula [I] and a pharmaceutically accepted salt of said compound are a novel compound and a phamaceutically accepted salt thereof which exert antagonistic activity against group II metabotropic glutamate (mGlu) receptors, and are effective as a novel preventive or therapeutic agent for disorders such as mood disorders (depressive disorder, bipolar disorder, etc.), anxiety disorders (generalized anxiety disorder, panic disorder, obsessive-compulsive disorder, social anxiety disorder, posttraumatic stress disorder, a specific phobic disorder, acute stress disorder, etc.), schizophrenia, Alzheimer's disease, cognitive impairment, dementia, drug dependence, convulsions, shivering, pain, sleep disorders, and the like.
摘要翻译: 由式[I]表示的化合物和所述化合物的药学上可接受的盐是对II类代谢型谷氨酸(mGlu)受体发挥拮抗活性的新化合物及其药学上可接受的盐,并且作为新型预防剂或治疗剂 (抑郁症,双相性精神障碍等),焦虑症(广泛性焦虑症,恐慌症,强迫症,社交焦虑症,创伤后应激障碍,特定的恐怖症,急性应激障碍等) ),精神分裂症,阿尔茨海默病,认知障碍,痴呆,药物依赖,惊厥,寒战,疼痛,睡眠障碍等。
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公开(公告)号:EP2562155A4
公开(公告)日:2014-09-10
申请号:EP11772045
申请日:2011-04-20
发明人: TAKASHIMA HAJIME , TSURUTA RISA , YABUUCHI TETSUYA , OKA YUSUKE , URABE HIROKI , SUGA YOICHIRO , TAKAHASHI MASATO , UNEUCHI FUMITO , KOTSUBO HIRONORI , SHOJI MUNEO , KAWAGUCHI YASUKO
IPC分类号: C07C259/06 , A61K31/166 , A61K31/337 , A61K31/341 , A61K31/343 , A61K31/351 , A61K31/357 , A61K31/36 , A61K31/381 , A61K31/397 , A61K31/40 , A61K31/4015 , A61K31/402 , A61K31/403 , A61K31/4035 , A61K31/404 , A61K31/4045 , A61K31/407 , A61K31/415 , A61K31/416
CPC分类号: C07C233/83 , C07C235/84 , C07C237/36 , C07C259/06 , C07C271/22 , C07C271/28 , C07C309/30 , C07C311/08 , C07C317/28 , C07C317/44 , C07C323/41 , C07C323/62 , C07C2601/02 , C07C2601/04 , C07C2601/08 , C07C2601/14 , C07C2601/16 , C07C2601/18 , C07C2602/08 , C07D205/04 , C07D205/12 , C07D207/10 , C07D207/12 , C07D207/27 , C07D207/327 , C07D209/08 , C07D209/12 , C07D209/14 , C07D209/44 , C07D209/52 , C07D211/14 , C07D211/18 , C07D211/38 , C07D211/46 , C07D211/56 , C07D211/70 , C07D213/38 , C07D213/40 , C07D213/54 , C07D213/61 , C07D213/64 , C07D213/65 , C07D213/70 , C07D213/74 , C07D213/81 , C07D215/14 , C07D217/04 , C07D217/12 , C07D231/12 , C07D231/56 , C07D233/61 , C07D235/04 , C07D257/04 , C07D261/08 , C07D263/14 , C07D263/32 , C07D263/56 , C07D265/30 , C07D265/36 , C07D265/38 , C07D267/10 , C07D271/12 , C07D277/20 , C07D277/30 , C07D277/62 , C07D277/66 , C07D285/12 , C07D295/08 , C07D295/12 , C07D295/14 , C07D295/16 , C07D305/06 , C07D305/08 , C07D307/14 , C07D307/18 , C07D307/52 , C07D307/54 , C07D307/78 , C07D307/81 , C07D307/82 , C07D307/87 , C07D309/04 , C07D309/14 , C07D317/30 , C07D317/60 , C07D319/18 , C07D319/20 , C07D333/24 , C07D405/06 , C07D413/06 , C07D471/04 , C07D471/10 , C07D487/08 , C07D491/20 , C07D498/04 , C07D498/08 , C07F9/091
摘要: Provided is a novel compound which is useful as a pharmaceutical composition by inhibiting an LpxC activity, thereby exhibiting potent antimicrobial activity against gram-negative bacteria including Pseudomonas aeruginosa and its drug resistant bacteria. Provided is a hydroxamic acid derivative represented by the following general formula [1] or a pharmaceutically acceptable salt thereof:
摘要翻译: 提供了通过抑制LpxC活性作为药物组合物有用的新型化合物,从而对包括铜绿假单胞菌及其耐药细菌在内的革兰氏阴性细菌表现出有效的抗微生物活性。 提供由以下通式[1]表示的异羟肟酸衍生物或其药学上可接受的盐:
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公开(公告)号:EP2617715A4
公开(公告)日:2014-02-26
申请号:EP11825276
申请日:2011-09-16
申请人: TAISHO PHARMA CO LTD
发明人: MORIYA MINORU , YASUHARA AKITO , SAKAGAMI KAZUNARI , OHTA HIROSHI , ABE KUMI , YAMAMOTO SHUJI , ARAKI YUKO , URABE HIROKI , SUN XIANG-MIN
IPC分类号: C07D233/90 , A61K31/4178 , A61K31/4196 , A61K31/422 , A61K31/4245 , A61K31/427 , A61K31/437 , A61K31/4439 , A61K31/444 , A61K31/4709 , A61K31/4725 , A61K31/497 , A61K31/506 , A61K31/5377 , A61P25/04 , A61P25/08 , A61P25/14 , A61P25/18
CPC分类号: C07D405/14 , C07D233/90 , C07D401/12 , C07D401/14 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12 , C07D417/14 , C07D471/04
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5.NOVEL NAPHTHYRIDINE DERIVATIVE MONOHYDRATE AND METHOD FOR PRODUCING THE SAME 有权
标题翻译: 新的萘并吡啶衍生的一水合物及其生产方法公开(公告)号:EP2221309A4
公开(公告)日:2011-11-09
申请号:EP08855286
申请日:2008-11-25
发明人: KIYOTO TARO , TAKEBAYASHI MASAHIRO , BABA YASUTAKA , SYOJI MUNEO , NOGUCHI TOSHIYA , USHIYAMA FUMIHITO , URABE HIROKI , HORIKIRI HIROMASA
IPC分类号: C07D519/00 , A61K31/4545 , A61P31/04 , C07D309/40 , C07D491/04 , C07D491/056
CPC分类号: C07D519/00 , C07D309/40 , C07D491/04
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公开(公告)号:EP1900732A4
公开(公告)日:2009-11-18
申请号:EP06767173
申请日:2006-06-22
发明人: KIYOTO TARO , TANAKA TADASHI , TSUTSUI YASUHIRO , ANDO JUNICHI , MOTONO MAI , KAWAGUCHI YASUKO , NOGUCHI TOSHIYA , USHIKI YASUNOBU , USHIYAMA FUMIHITO , URABE HIROKI
IPC分类号: C07D401/06 , A61K31/4709 , A61K31/496 , A61P31/04 , C07D401/14 , C07D405/14 , C07D409/14 , C07D491/056
CPC分类号: C07D405/14 , C07D215/227 , C07D401/06 , C07D401/14 , C07D405/12 , C07D409/14 , C07D413/14 , C07D471/04 , C07D491/04 , C07D495/04 , C07D513/04 , C07D519/00
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