JP2007507465A5 - - Google Patents

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Publication number
JP2007507465A5
JP2007507465A5 JP2006530262A JP2006530262A JP2007507465A5 JP 2007507465 A5 JP2007507465 A5 JP 2007507465A5 JP 2006530262 A JP2006530262 A JP 2006530262A JP 2006530262 A JP2006530262 A JP 2006530262A JP 2007507465 A5 JP2007507465 A5 JP 2007507465A5
Authority
JP
Japan
Prior art keywords
pyridin
het1
salts
oxides
compounds
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Withdrawn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
JP2006530262A
Other languages
English (en)
Japanese (ja)
Other versions
JP2007507465A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2004/052376 external-priority patent/WO2005030769A1/en
Publication of JP2007507465A publication Critical patent/JP2007507465A/ja
Publication of JP2007507465A5 publication Critical patent/JP2007507465A5/ja
Withdrawn legal-status Critical Current

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JP2006530262A 2003-10-01 2004-09-30 誘導性noシンターゼ阻害剤としてのイミダゾピリジン誘導体 Withdrawn JP2007507465A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP03022064 2003-10-01
PCT/EP2004/052376 WO2005030769A1 (en) 2003-10-01 2004-09-30 Imidazopyridine-derivatives as inducible no-synthase inhibitors

Publications (2)

Publication Number Publication Date
JP2007507465A JP2007507465A (ja) 2007-03-29
JP2007507465A5 true JP2007507465A5 (https=) 2007-11-15

Family

ID=34384572

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006530262A Withdrawn JP2007507465A (ja) 2003-10-01 2004-09-30 誘導性noシンターゼ阻害剤としてのイミダゾピリジン誘導体

Country Status (17)

Country Link
US (1) US20080125460A1 (https=)
EP (1) EP1673371B1 (https=)
JP (1) JP2007507465A (https=)
KR (1) KR20060092222A (https=)
CN (1) CN1856494A (https=)
AT (1) ATE403655T1 (https=)
AU (1) AU2004276013A1 (https=)
BR (1) BRPI0414873A (https=)
CA (1) CA2540242A1 (https=)
DE (1) DE602004015628D1 (https=)
EA (1) EA200600609A1 (https=)
IL (1) IL173809A0 (https=)
MX (1) MXPA06003554A (https=)
NO (1) NO20061316L (https=)
RS (1) RS20060195A (https=)
WO (1) WO2005030769A1 (https=)
ZA (1) ZA200601552B (https=)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA200600607A1 (ru) 2003-10-01 2006-10-27 Алтана Фарма Аг Производные имидазопиридина в качестве ингибиторов индуцируемой no-синтазы
BRPI0414972A (pt) 2003-10-01 2006-11-07 Altana Pharma Ag derivados de imidazopiridinas como inibidores de no-sintase induzìvel
DE602004014523D1 (de) 2003-10-01 2008-07-31 Nycomed Gmbh Imidazoä4,5-büpyridinderivate als inhibitoren der induzierbaren no-synthase
RS20060206A (sr) 2003-10-01 2008-08-07 Altana Pharma Ag., Derivati aminopiridina kao inhibitori inducibilne no-sintaze
WO2009029625A1 (en) * 2007-08-27 2009-03-05 Kalypsys, Inc. 4- [heterocyclyl-methyl] -8-fluoro-quinolin-2-ones useful as nitric oxide synthase inhibitors
NZ603789A (en) * 2010-05-26 2015-03-27 Sunovion Pharmaceuticals Inc Heteroaryl compounds and methods of use thereof
CA2889906A1 (en) * 2012-11-29 2014-06-05 Sunovion Pharmaceuticals Inc. Triazolo-pyrazine derivatives useful in the treatment of disorders of the central nervous system
GB201512635D0 (en) 2015-07-17 2015-08-26 Ucl Business Plc Uses of therapeutic compounds

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4045564A (en) * 1974-02-18 1977-08-30 Ab Hassle Benzimidazole derivatives useful as gastric acid secretion inhibitors
SE418966B (sv) * 1974-02-18 1981-07-06 Haessle Ab Analogiforfarande for framstellning av foreningar med magsyrasekretionsinhiberande verkan
GB8307865D0 (en) * 1983-03-22 1983-04-27 Fujisawa Pharmaceutical Co Benzimidazole derivatives
AUPP873799A0 (en) * 1999-02-17 1999-03-11 Fujisawa Pharmaceutical Co., Ltd. Pyridine compounds
NZ535959A (en) * 2002-03-27 2006-05-26 Altana Pharma Ag Novel alkoxypyridine-derivatives as selective inhibitors of inducible nitric oxidase synthase NOS

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