JP2005537291A5 - - Google Patents

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Publication number
JP2005537291A5
JP2005537291A5 JP2004525375A JP2004525375A JP2005537291A5 JP 2005537291 A5 JP2005537291 A5 JP 2005537291A5 JP 2004525375 A JP2004525375 A JP 2004525375A JP 2004525375 A JP2004525375 A JP 2004525375A JP 2005537291 A5 JP2005537291 A5 JP 2005537291A5
Authority
JP
Japan
Prior art keywords
alkyl
pyridin
methyl
hydrogen
membered
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.)
Pending
Application number
JP2004525375A
Other languages
English (en)
Japanese (ja)
Other versions
JP2005537291A (ja
Filing date
Publication date
Priority claimed from GBGB0217783.0A external-priority patent/GB0217783D0/en
Application filed filed Critical
Publication of JP2005537291A publication Critical patent/JP2005537291A/ja
Publication of JP2005537291A5 publication Critical patent/JP2005537291A5/ja
Pending legal-status Critical Current

Links

JP2004525375A 2002-07-31 2003-07-29 イミダゾ[1,2−a]ピリジン Pending JP2005537291A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0217783.0A GB0217783D0 (en) 2002-07-31 2002-07-31 Compounds
PCT/EP2003/008390 WO2004013138A2 (en) 2002-07-31 2003-07-29 Imidazo`1,2-a!pyridines

Publications (2)

Publication Number Publication Date
JP2005537291A JP2005537291A (ja) 2005-12-08
JP2005537291A5 true JP2005537291A5 (enExample) 2006-09-14

Family

ID=9941484

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004525375A Pending JP2005537291A (ja) 2002-07-31 2003-07-29 イミダゾ[1,2−a]ピリジン

Country Status (11)

Country Link
US (1) US20050234029A1 (enExample)
EP (1) EP1543003B1 (enExample)
JP (1) JP2005537291A (enExample)
AR (1) AR040724A1 (enExample)
AT (1) ATE326467T1 (enExample)
AU (1) AU2003255323A1 (enExample)
DE (1) DE60305332T2 (enExample)
ES (1) ES2259419T3 (enExample)
GB (1) GB0217783D0 (enExample)
TW (1) TW200413366A (enExample)
WO (1) WO2004013138A2 (enExample)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR039241A1 (es) 2002-04-04 2005-02-16 Biogen Inc Heteroarilos trisustituidos y metodos para su produccion y uso de los mismos
EP1539748A1 (en) * 2002-07-31 2005-06-15 Smithkline Beecham Corporation 2-phenylpyridin-4-yl derivatives as alk5 inhibitors
UA80296C2 (en) * 2002-09-06 2007-09-10 Biogen Inc Imidazolopyridines and methods of making and using the same
PA8595001A1 (es) * 2003-03-04 2004-09-28 Pfizer Prod Inc Nuevos compuestos heteroaromaticos condensados que son inhibidores del factor de crecimiento transforante (tgf)
MX2007011453A (es) 2005-04-22 2008-02-12 Alantos Pharmaceuticals Holding Inc Inhibidores de la dipeptidil peptidasa-iv.
EP1928237A4 (en) * 2005-09-02 2011-03-09 Abbott Lab NEW HETEROCYCLES BASED ON IMIDAZO
CN101611007A (zh) 2006-12-20 2009-12-23 先灵公司 新颖的jnk抑制剂
CA2672960A1 (en) * 2006-12-20 2008-07-10 Schering Corporation Novel jnk inhibitors
EA201000615A1 (ru) 2007-10-17 2010-12-30 Новартис Аг Производные имидазо[1,2-а]пиридина, применимые в качестве ингибиторов апк (активиноподобной киназы)
WO2009086123A1 (en) * 2007-12-21 2009-07-09 Wyeth Imidazo [1,2-a] pyridine compounds
EP2307402B1 (en) * 2008-04-29 2012-11-07 Novartis AG Imidazo-pyridine derivatives as activin-like receptor kinase (alk4 or alk5) inhibitors
PH12012500778A1 (en) 2009-10-30 2012-11-26 Janssen Pharmaceutica Nv IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS
WO2011074658A1 (ja) 2009-12-18 2011-06-23 田辺三菱製薬株式会社 新規抗血小板薬
AR080754A1 (es) 2010-03-09 2012-05-09 Janssen Pharmaceutica Nv Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10
WO2011146287A1 (en) 2010-05-20 2011-11-24 Takeda Pharmaceutical Company Limited Pyrazolo[4,3-b]pyridine-7-amine inhibitors of alk5
US20120309796A1 (en) 2011-06-06 2012-12-06 Fariborz Firooznia Benzocycloheptene acetic acids
JP6115962B2 (ja) 2011-06-27 2017-04-19 ヤンセン ファーマシューティカ エヌ.ベー. 1−アリール−4−メチル−[1,2,4]トリアゾロ[4,3−a]キノキサリン誘導体
WO2014001314A1 (en) 2012-06-26 2014-01-03 Janssen Pharmaceutica Nv Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl- [1,2,4] triazolo [4,3-a] quinoxaline compounds and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders
AU2013289284B2 (en) 2012-07-09 2017-03-30 Janssen Pharmaceutica Nv Inhibitors of phosphodiesterase 10 enzyme
CN108341769A (zh) * 2018-05-13 2018-07-31 浙江凯普化工有限公司 多取代的6-氟皮考啉酸的制备方法
CN115975224B (zh) * 2023-03-16 2023-08-08 四川大学 一种pH/ROS双响应的组织粘附载药水凝胶及其制备方法和应用

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11302177A (ja) * 1998-04-27 1999-11-02 Otsuka Pharmaceut Factory Inc 腎炎治療剤
GB0007405D0 (en) * 2000-03-27 2000-05-17 Smithkline Beecham Corp Compounds
PE20020506A1 (es) * 2000-08-22 2002-07-09 Glaxo Group Ltd Derivados de pirazol fusionados como inhibidores de la proteina cinasa
GB0027987D0 (en) * 2000-11-16 2001-01-03 Smithkline Beecham Plc Compounds
EP1349851A4 (en) * 2000-11-16 2004-09-08 Smithkline Beecham Corp COMPOUNDS
GB0100762D0 (en) * 2001-01-11 2001-02-21 Smithkline Beecham Plc Novel use
EP1539748A1 (en) * 2002-07-31 2005-06-15 Smithkline Beecham Corporation 2-phenylpyridin-4-yl derivatives as alk5 inhibitors

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