JP2012528839A5 - - Google Patents

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Publication number
JP2012528839A5
JP2012528839A5 JP2012513673A JP2012513673A JP2012528839A5 JP 2012528839 A5 JP2012528839 A5 JP 2012528839A5 JP 2012513673 A JP2012513673 A JP 2012513673A JP 2012513673 A JP2012513673 A JP 2012513673A JP 2012528839 A5 JP2012528839 A5 JP 2012528839A5
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JP
Japan
Prior art keywords
optionally substituted
benzyl
oxo
chloro
formula
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Application number
JP2012513673A
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English (en)
Japanese (ja)
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JP5684800B2 (ja
JP2012528839A (ja
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Priority claimed from GBGB0909671.0A external-priority patent/GB0909671D0/en
Application filed filed Critical
Publication of JP2012528839A publication Critical patent/JP2012528839A/ja
Publication of JP2012528839A5 publication Critical patent/JP2012528839A5/ja
Application granted granted Critical
Publication of JP5684800B2 publication Critical patent/JP5684800B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2012513673A 2009-06-04 2010-06-04 化合物 Active JP5684800B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB0909671.0A GB0909671D0 (en) 2009-06-04 2009-06-04 Compounds
GB0909671.0 2009-06-04
PCT/GB2010/001092 WO2010139953A1 (en) 2009-06-04 2010-06-04 Compounds

Publications (3)

Publication Number Publication Date
JP2012528839A JP2012528839A (ja) 2012-11-15
JP2012528839A5 true JP2012528839A5 (enExample) 2013-07-18
JP5684800B2 JP5684800B2 (ja) 2015-03-18

Family

ID=40936942

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012513673A Active JP5684800B2 (ja) 2009-06-04 2010-06-04 化合物

Country Status (5)

Country Link
US (1) US8399481B2 (enExample)
EP (1) EP2438044B1 (enExample)
JP (1) JP5684800B2 (enExample)
GB (1) GB0909671D0 (enExample)
WO (1) WO2010139953A1 (enExample)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2720368T3 (es) 2008-03-27 2019-07-19 Purdue Research Foundation Peptidoglicanos sintéticos de enlace a colágeno, preparación y método de utilización
GB0909672D0 (en) * 2009-06-04 2009-07-22 Xention Discovery Ltd Compounds
LT2714718T (lt) * 2011-05-24 2017-04-10 Symic Ip, Llc Hialurono rūgštį surišantys sintetiniai peptidoglikanai, gamyba ir panaudojimo būdai
JP6603650B2 (ja) 2013-03-15 2019-11-06 パーデュー・リサーチ・ファウンデーション 細胞外マトリックス結合性合成ペプチドグリカン
WO2015164822A1 (en) 2014-04-25 2015-10-29 Purdue Research Foundation Collagen binding synthetic peptidoglycans for treatment of endothelial dysfunction
WO2018010142A1 (en) * 2016-07-14 2018-01-18 Shanghai Meton Pharmaceutical Co., Ltd Iso-citrate dehydrogenase (idh) inhibitor
EP3315551B1 (en) * 2016-10-25 2021-03-03 Borealis AG Heterophasic polypropylene composition with improved mechanical and optical properties
KR20240148963A (ko) 2017-07-07 2024-10-11 시믹 아이피, 엘엘씨 합성 생체접합체
CN114555597B (zh) * 2019-10-12 2024-06-04 浙江迈同生物医药有限公司 异柠檬酸脱氢酶(idh)抑制剂

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5741819A (en) 1995-06-07 1998-04-21 3-Dimensional Pharmaceuticals, Inc. Arylsulfonylaminobenzene derivatives and the use thereof as factor Xa inhibitors
US6083986A (en) * 1996-07-26 2000-07-04 Icagen, Inc. Potassium channel inhibitors
US6077680A (en) 1996-11-27 2000-06-20 The University Of Florida ShK toxin compositions and methods of use
DE19727117A1 (de) 1997-06-26 1999-01-07 Boehringer Ingelheim Pharma Phenylalkylderivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
US6194458B1 (en) 1998-10-30 2001-02-27 Merck & Co., Inc. Benzamide potassium channel inhibitors
MY125533A (en) 1999-12-06 2006-08-30 Bristol Myers Squibb Co Heterocyclic dihydropyrimidine compounds
WO2003082205A2 (en) 2002-03-27 2003-10-09 Smithkline Beecham Corporation Compounds and methods
TW200503994A (en) 2003-01-24 2005-02-01 Novartis Ag Organic compounds
AU2004276268B2 (en) * 2003-09-23 2009-01-29 Merck Sharp & Dohme Corp. Isoquinoline potassium channel inhibitors
KR100793095B1 (ko) 2003-10-01 2008-01-10 주식회사 프로메디텍 Bace 저해효능을 가진 신규한 술폰 아미드 유도체
AU2005265270B2 (en) * 2004-06-22 2011-09-22 Vertex Pharmaceuticals Incorporated Heterocyclic derivatives for modulation of calcium channels
US20100160304A1 (en) 2005-01-19 2010-06-24 Dainippon Sumitomo Pharma Co., Ltd Aromatic sulfone compound as aldosterone receptor modulator
CA2620171A1 (en) 2005-08-25 2007-03-01 Schering Corporation Imidazole derivatives as functionally selective alpha2c adrenoreceptor agonists
WO2007056078A2 (en) 2005-11-02 2007-05-18 Cytokinetics, Inc. Certain chemical entities, compositions, and methods
US8110681B2 (en) * 2006-03-17 2012-02-07 The United States Of America As Represented By The Secretary, Department Of Health And Human Services Compounds for the treatment of spinal muscular atrophy and other uses
DE102006013957A1 (de) 2006-03-27 2007-10-04 Bayer Healthcare Aktiengesellschaft Substituierte N-Benzyl-N-phenylbenzolsulfonamide
GB0619176D0 (en) * 2006-09-29 2006-11-08 Lectus Therapeutics Ltd Ion channel modulators & uses thereof
DE102007012284A1 (de) 2007-03-16 2008-09-18 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue substituierte Arylsulfonylglycine, deren Herstellung und deren Verwendung als Arzneimittel
GB0710844D0 (en) 2007-06-06 2007-07-18 Lectus Therapeutics Ltd Potassium ion channel modulators & uses thereof
GB0815782D0 (en) * 2008-08-29 2008-10-08 Xention Ltd Novel potassium channel blockers
GB0815781D0 (en) * 2008-08-29 2008-10-08 Xention Ltd Novel potassium channel blockers
GB0815784D0 (en) * 2008-08-29 2008-10-08 Xention Ltd Novel potassium channel blockers
GB0909672D0 (en) * 2009-06-04 2009-07-22 Xention Discovery Ltd Compounds

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