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公开(公告)号:EP2562155B1
公开(公告)日:2019-06-05
申请号:EP11772045.8
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:
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公开(公告)号:EP2935216B1
公开(公告)日:2018-06-27
申请号:EP13828824.6
申请日:2013-12-17
IPC分类号: C07D213/74 , C07D471/04 , C07D211/56 , C07D213/61
CPC分类号: C07D487/04 , C07D211/56 , C07D213/61 , C07D213/74 , C07D471/04
摘要: The present invention provides compounds of Formula III and Formula VI, and processes for their preparation. The present invention further provides use of the compounds of Formula III and Formula VI for the preparation of tofacitinib or isomers or a mixture of isomers or salts thereof.
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公开(公告)号:EP3162810A4
公开(公告)日:2018-01-24
申请号:EP14896077
申请日:2014-12-19
申请人: MARUISHI PHARMA
发明人: MURAYAMA ASAMI , KANO TAKAAKI
CPC分类号: C07D211/56 , C07D211/02 , C07D211/28 , C07K1/128 , C07K5/1016 , C07K7/02
摘要: Provided are a method for industrially advantageously producing a highly purified pentapeptide and an intermediate thereof. A compound represented by the following formula (1) or a salt thereof: wherein R 1 represents an alkyl group or an aralkyl group.
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4.
公开(公告)号:EP3148518A2
公开(公告)日:2017-04-05
申请号:EP15800492.9
申请日:2015-06-01
CPC分类号: C07D211/42 , A61K31/445 , A61K45/06 , C07C59/64 , C07D205/04 , C07D207/09 , C07D207/12 , C07D211/46 , C07D211/56 , C07D211/58 , C07D213/75 , C07D265/30 , C07D453/04
摘要: The present invention also discloses compounds of formula (1) along with other pharmaceutical acceptable excipients and use of the compounds as anti-tubercular agents.
摘要翻译: 本发明涉及式(1)的新型化合物:本发明还公开了式(1)的化合物以及其它药学上可接受的赋形剂以及该化合物作为抗结核剂的用途。
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5.SUBSTITUTED AMINOINDANES AND ANALOGS THEREOF, AND THE PHARMACEUTICAL USE THEREOF 有权
标题翻译: 取代的茚满及其类似物和它们的药物用途公开(公告)号:EP2342178B1
公开(公告)日:2016-09-28
申请号:EP09778082.9
申请日:2009-08-25
申请人: SANOFI
发明人: RACKELMANN, Nils , BIALY, Laurent , ENGLERT, Heinrich , WIRTH, Klaus , ARNDT, Petra , WESTON, John , HEINELT, Uwe , FOLLMANN, Markus
IPC分类号: C07D207/08 , C07D401/12 , C07D403/12 , C07D413/12 , C07D417/12 , A61K31/4523 , A61P1/00 , A61P3/00 , A61P9/00
CPC分类号: C07D487/10 , C07D205/04 , C07D207/08 , C07D211/56 , C07D243/08 , C07D401/12 , C07D403/04 , C07D403/12 , C07D405/12 , C07D411/12 , C07D413/12 , C07D417/12 , C07D487/04 , C07D487/08
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6.KETONE LIGANDS FOR MODULATING THE EXPRESSION OF EXOGENOUS GENES VIA AN ECDYSONE RECEPTOR COMPLEX 有权
标题翻译: KETONLIGANDENFÜRDIE调制剂表达异黄酮基因BER EINEN ECDYSON-REZEPTOR-KOMPLEX公开(公告)号:EP1534658B1
公开(公告)日:2016-09-07
申请号:EP03763259.3
申请日:2003-07-05
申请人: Intrexon Corporation
IPC分类号: C07C49/04 , C07C49/20 , C07C49/527 , C07C69/00 , C07C225/02 , C07C229/02 , C07C237/00 , A61K31/12 , A61K31/16 , A61K31/18
CPC分类号: C07D487/04 , C07C233/31 , C07C233/76 , C07C235/46 , C07C235/48 , C07C235/50 , C07C235/54 , C07C237/32 , C07C271/20 , C07C275/24 , C07C311/20 , C07C2601/02 , C07C2601/08 , C07C2601/14 , C07D207/14 , C07D211/56 , C07D211/58 , C07D309/14 , C07D317/54 , C07D319/18 , C07D321/08 , C07D335/02 , C07F9/36 , C07K14/70567 , C07K14/721 , C12Q1/6897
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公开(公告)号:EP2858500A4
公开(公告)日:2016-04-06
申请号:EP13800631
申请日:2013-06-07
发明人: HOPKINS BRIAN T , CAI XIONGWEI , CHAN TIMOTHY R , CONLON PATRICK , HUMORA MICHAEL , JENKINS TRACY J , MACPHEE J MICHAEL , SHI XIANGLIN , MILLER ROSS A , THOMPSON ANDREW
IPC分类号: A61K31/435 , A61K31/445 , C07D401/14
CPC分类号: C07D401/14 , C07B2200/13 , C07D207/16 , C07D207/28 , C07D211/56 , C07D401/04
摘要: The present invention provides a compound, solid forms, and compositions thereof, which are useful as inhibitors of Bruton's tyrosine kinase and which exhibit desirable characteristics for the same. The present invention also provides methods of making provided compound and solid forms.
摘要翻译: 本发明提供了一种化合物,固体形式及其组合物,其可用作Bruton酪氨酸激酶的抑制剂,并且对其表现出期望的特性。 本发明还提供了制备所提供的化合物和固体形式的方法。
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8.
公开(公告)号:EP2890678A4
公开(公告)日:2016-01-27
申请号:EP13833184
申请日:2013-08-29
IPC分类号: C07D211/56 , A61K31/445 , A61K31/4523 , A61P25/28 , C07D401/06 , C07D417/06 , C07H13/02 , C12N9/24
CPC分类号: C07D211/56 , A61K31/445 , A61K31/4523 , C07D401/06 , C07D417/06
摘要: The invention provides compounds of Formula (I) for inhibiting gh cosidases, prodrugs of the compounds, and pharmaceutical compositions comprising the compounds or prodrugs of the compounds. The invention also provides method of treating diseases and disorders related to deficiency or over-expression of O-gh coprotein 2-acetamido-2-deoxy-&bgr;-D-glucopyranosidase (O-GlcNAcase), accumulation or deficiency of 2-acetamido-2-deoxy-&bgr;-D-glucopyranoside (O-GlcNAc).
摘要翻译: 本发明提供式(I)化合物,其用于抑制gh辅酶,化合物的前药和包含化合物的化合物或前药的药物组合物。 本发明还提供了治疗与O-gh蛋白2-乙酰氨基-2-脱氧-α-D-吡喃葡萄糖苷酶(O-GlcNAcase)的缺乏或过度表达相关的疾病和病症的方法,2-乙酰氨基-2- 2-脱氧-β-D-吡喃葡萄糖苷(O-GlcNAc)。
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公开(公告)号:EP1757582B1
公开(公告)日:2015-12-30
申请号:EP05743307.0
申请日:2005-05-27
发明人: MIYAZAKI, Hiroshi c/o Tanabe Seiyaku Co., Ltd , TSUBAKIMOTO, Junko c/o Tanabe Seiyaku Co., Ltd , YASUDA,Kosuke c/o Tanabe Seiyaku Co., Ltd , TAKAMURO,Iwao c/o Tanabe Seiyaku Co., Ltd , SAKURAI, Osamu c/o Tanabe Seiyaku Co., Ltd , YANAGIDA,Tetsuya, c/o Tanabe Seiyaku Co., Ltd , HISADA,Yutaka c/o Tanabe Seiyaku Co., Ltd
IPC分类号: C07D205/04 , A61K31/397 , A61K31/40 , A61K31/402 , A61K31/4025 , A61K31/404 , A61K31/415 , A61K31/4184 , A61K31/4192 , A61K31/427 , A61K31/4439
CPC分类号: C07D207/14 , C07D205/04 , C07D207/16 , C07D207/27 , C07D207/327 , C07D207/335 , C07D207/34 , C07D211/56 , C07D401/04 , C07D401/06 , C07D401/10 , C07D401/12 , C07D403/06 , C07D403/10 , C07D405/12 , C07D409/06 , C07D409/12 , C07D417/04 , C07D417/06 , C07H17/02
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10.PROCESS FOR PREPARING HETEROCYCLIC COMPOUNDS INCLUDING TRANS-7-OXO-6-(SULPHOOXY)-1,6-DIAZABICYCLO[3,2,1]OCTANE-2-CARBOXAMIDE AND SALTS THEREOF 有权
标题翻译: 用于生产杂环化合物与反式-7-氧代-6-(磺)-1,6-二氮杂双环[3.2.1]辛烷-2-甲酰胺和它们的盐公开(公告)号:EP2721005B1
公开(公告)日:2015-11-25
申请号:EP12727922.2
申请日:2012-06-15
申请人: AstraZeneca AB
发明人: BOYD, Alistair John , CHERRYMAN, Janette Helen , GOLDEN, Michael , KALYAN, Yuriy B. , LAWTON, Graham Richard , MILNE, David , PHILLIPS, Andrew John , RACHA, Saibaba , RONSHEIM, Melanie Simone , TELFORD, Alexander , ZHOU, Shao Hong , DEDHIYA, Mahendra G.
IPC分类号: C07D211/60 , C07D471/08
CPC分类号: C07D211/60 , A61K31/439 , A61K31/445 , C07D211/56 , C07D471/08 , Y02P20/55
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