JP2010529203A5 - - Google Patents

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Publication number
JP2010529203A5
JP2010529203A5 JP2010512313A JP2010512313A JP2010529203A5 JP 2010529203 A5 JP2010529203 A5 JP 2010529203A5 JP 2010512313 A JP2010512313 A JP 2010512313A JP 2010512313 A JP2010512313 A JP 2010512313A JP 2010529203 A5 JP2010529203 A5 JP 2010529203A5
Authority
JP
Japan
Prior art keywords
alkyl
aryl
compound
heteroaryl
selection
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
JP2010512313A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010529203A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2008/066510 external-priority patent/WO2008154563A1/en
Publication of JP2010529203A publication Critical patent/JP2010529203A/ja
Publication of JP2010529203A5 publication Critical patent/JP2010529203A5/ja
Withdrawn legal-status Critical Current

Links

JP2010512313A 2007-06-11 2008-06-11 1,3−ジヒドロキシ置換フェニルアミドグルコキナーゼ活性化剤 Withdrawn JP2010529203A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US94309207P 2007-06-11 2007-06-11
PCT/US2008/066510 WO2008154563A1 (en) 2007-06-11 2008-06-11 1, 3 - dihydroxy substituted phenylamide glucokinase activators

Publications (2)

Publication Number Publication Date
JP2010529203A JP2010529203A (ja) 2010-08-26
JP2010529203A5 true JP2010529203A5 (enExample) 2011-07-07

Family

ID=39713941

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010512313A Withdrawn JP2010529203A (ja) 2007-06-11 2008-06-11 1,3−ジヒドロキシ置換フェニルアミドグルコキナーゼ活性化剤

Country Status (5)

Country Link
US (1) US8222285B2 (enExample)
EP (1) EP2170852A1 (enExample)
JP (1) JP2010529203A (enExample)
CN (1) CN101711238A (enExample)
WO (1) WO2008154563A1 (enExample)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2170852A1 (en) 2007-06-11 2010-04-07 Bristol-Myers Squibb Company 1, 3 - dihydroxy substituted phenylamide glucokinase activators
JP5572549B2 (ja) 2007-08-13 2014-08-13 リガンド・ファーマシューティカルズ・インコーポレイテッド グルコキナーゼの新規な活性化剤
CA2774373A1 (en) * 2009-09-17 2011-03-24 Vanderbilt University Substituted heteroarylamide analogs as mglur5 negative allosteric modulators and methods of making and using the same
AU2010343102B2 (en) 2009-12-29 2016-03-24 Dana-Farber Cancer Institute, Inc. Type II Raf kinase inhibitors
WO2011095997A1 (en) 2010-02-08 2011-08-11 Advinus Therapeutics Private Limited Benzamide compounds as glucokinase activators and their pharmaceutical application
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
CA2800498C (en) 2010-03-31 2021-11-16 The Scripps Research Institute Reprogramming cells
US8530413B2 (en) 2010-06-21 2013-09-10 Sanofi Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
WO2013045413A1 (en) 2011-09-27 2013-04-04 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
CA2931097A1 (en) 2013-11-19 2015-05-28 Vanderbilt University Substituted imidazopyridine and triazolopyridine compounds as negative allosteric modulators of mglur5
US9533982B2 (en) 2014-03-20 2017-01-03 Vanderbilt University Substituted bicyclic heteroaryl carboxamide analogs as mGluR5 negative allosteric modulators
US9550778B2 (en) 2014-10-03 2017-01-24 Vanderbilt University Substituted 6-aryl-imidazopyridine and 6-aryl-triazolopyridine carboxamide analogs as negative allosteric modulators of mGluR5
CA2972239A1 (en) 2014-12-23 2016-06-30 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
CN105837599A (zh) * 2015-01-14 2016-08-10 中国科学院上海药物研究所 N-取代-3,5-二取代苯甲酰胺类化合物及其制备方法和应用
CN107427521B (zh) 2015-03-27 2021-08-03 达纳-法伯癌症研究所股份有限公司 细胞周期蛋白依赖性激酶的抑制剂
KR102513342B1 (ko) 2016-07-22 2023-03-22 브리스톨-마이어스 스큅 컴퍼니 글루코키나제 활성화제 및 그의 사용 방법
MX392031B (es) 2016-11-03 2025-03-21 Corvus Pharmaceuticals Inc Compuestos y métodos para modular la cinasa de linfocitos t inducible por interleucina 2
US11174253B2 (en) 2017-08-02 2021-11-16 Alphala Co., Ltd. Compound and pharmaceutical composition containing the same
CA3093189A1 (en) 2018-03-07 2019-09-12 Bayer Aktiengesellschaft Identification and use of erk5 inhibitors
CN111446449B (zh) * 2020-03-10 2021-07-09 西安交通大学 一种多电子传输钒基氧代氟磷酸钠电池材料及其制备方法

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5594016A (en) 1992-12-28 1997-01-14 Mitsubishi Chemical Corporation Naphthalene derivatives
WO1999020618A1 (en) 1997-10-21 1999-04-29 Active Biotech Ab Thiadiazoles amides useful as antiinflammatory agents
US6022884A (en) * 1997-11-07 2000-02-08 Amgen Inc. Substituted pyridine compounds and methods of use
DE19851421A1 (de) * 1998-11-07 2000-05-11 Boehringer Ingelheim Pharma Neue Pyrimidine, deren Herstellung und Verwendung
US6548529B1 (en) 1999-04-05 2003-04-15 Bristol-Myers Squibb Company Heterocyclic containing biphenyl aP2 inhibitors and method
TWI302149B (en) 1999-09-22 2008-10-21 Bristol Myers Squibb Co Substituted acid derivatives useful as antiodiabetic and antiobesity agents and method
US6414002B1 (en) 1999-09-22 2002-07-02 Bristol-Myers Squibb Company Substituted acid derivatives useful as antidiabetic and antiobesity agents and method
IL144507A0 (en) 2000-07-31 2002-05-23 Pfizer Prod Inc Use of glycogen phosphorylase inhibitors to inhibit tumor growth
SE0102764D0 (sv) * 2001-08-17 2001-08-17 Astrazeneca Ab Compounds
NZ564608A (en) 2005-07-09 2009-09-25 Astrazeneca Ab Heteroaryl benzamide derivatives for use as GLK activators in the treatment of diabetes
US7910747B2 (en) 2006-07-06 2011-03-22 Bristol-Myers Squibb Company Phosphonate and phosphinate pyrazolylamide glucokinase activators
US7888504B2 (en) 2006-07-06 2011-02-15 Bristol-Myers Squibb Company Glucokinase activators and methods of using same
EP2170852A1 (en) 2007-06-11 2010-04-07 Bristol-Myers Squibb Company 1, 3 - dihydroxy substituted phenylamide glucokinase activators
JP2010534722A (ja) 2007-07-27 2010-11-11 ブリストル−マイヤーズ スクイブ カンパニー 新規グルコキナーゼ活性化薬およびその使用方法

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