JP2007510741A5 - - Google Patents

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Publication number
JP2007510741A5
JP2007510741A5 JP2006539729A JP2006539729A JP2007510741A5 JP 2007510741 A5 JP2007510741 A5 JP 2007510741A5 JP 2006539729 A JP2006539729 A JP 2006539729A JP 2006539729 A JP2006539729 A JP 2006539729A JP 2007510741 A5 JP2007510741 A5 JP 2007510741A5
Authority
JP
Japan
Prior art keywords
compound
pharmaceutically acceptable
pharmaceutical composition
alkyl
composition according
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.)
Ceased
Application number
JP2006539729A
Other languages
English (en)
Japanese (ja)
Other versions
JP2007510741A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2004/037280 external-priority patent/WO2005047270A2/en
Publication of JP2007510741A publication Critical patent/JP2007510741A/ja
Publication of JP2007510741A5 publication Critical patent/JP2007510741A5/ja
Ceased legal-status Critical Current

Links

JP2006539729A 2003-11-10 2004-11-05 ナトリウムチャンネル遮断薬としての置換トリアゾール類 Ceased JP2007510741A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US51889003P 2003-11-10 2003-11-10
PCT/US2004/037280 WO2005047270A2 (en) 2003-11-10 2004-11-05 Substituted triazoles as sodium channel blockers

Publications (2)

Publication Number Publication Date
JP2007510741A JP2007510741A (ja) 2007-04-26
JP2007510741A5 true JP2007510741A5 (https=) 2007-12-20

Family

ID=34590316

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006539729A Ceased JP2007510741A (ja) 2003-11-10 2004-11-05 ナトリウムチャンネル遮断薬としての置換トリアゾール類

Country Status (17)

Country Link
US (2) US20090074890A1 (https=)
EP (1) EP1694654B1 (https=)
JP (1) JP2007510741A (https=)
KR (1) KR20060123739A (https=)
CN (1) CN1922156A (https=)
AT (1) ATE500234T1 (https=)
AU (1) AU2004289694B2 (https=)
BR (1) BRPI0416319A (https=)
CA (1) CA2545254A1 (https=)
DE (1) DE602004031667D1 (https=)
IL (1) IL175522A0 (https=)
IS (1) IS8438A (https=)
NO (1) NO20062676L (https=)
NZ (1) NZ547044A (https=)
RU (1) RU2372339C2 (https=)
WO (1) WO2005047270A2 (https=)
ZA (1) ZA200603583B (https=)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MY142651A (en) * 2003-03-18 2010-12-15 Merck Sharp & Dohme Biaryl substituted triazoles as sodium channel blockers
CN1922156A (zh) * 2003-11-10 2007-02-28 默克公司 作为钠通道阻断剂的取代的三唑
GB0525068D0 (en) 2005-12-08 2006-01-18 Novartis Ag Organic compounds
GB0603008D0 (en) * 2006-02-14 2006-03-29 Portela & Ca Sa Method
KR100808551B1 (ko) 2006-12-01 2008-03-03 한국생명공학연구원 트리아졸 유도체를 유효성분으로 함유하는 대사성 질환 예방 및 치료용 약학적 조성물
PL2118077T3 (pl) * 2007-02-08 2015-05-29 Synta Pharmaceuticals Corp Związki triazolowe modulujące aktywność hsp90
WO2008124092A2 (en) * 2007-04-03 2008-10-16 E. I. Du Pont De Nemours And Company Substituted benzene fungicides
CA2703672A1 (en) * 2007-10-25 2009-04-30 Revalesio Corporation Compositions and methods for modulating cellular membrane-mediated intracellular signal transduction
WO2009055620A1 (en) * 2007-10-25 2009-04-30 Revalesio Corporation Bacteriostatic or bacteriocidal compositions and methods
JP2011504505A (ja) 2007-11-21 2011-02-10 デコード ジェネティクス イーエイチエフ 肺および心血管障害を治療するためのビアリールpde4抑制剤
EP2222638A2 (en) * 2007-11-21 2010-09-01 Decode Genetics EHF Biaryl pde4 inhibitors for treating inflammation
US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
JP2013518085A (ja) 2010-02-01 2013-05-20 ノバルティス アーゲー CRF−1受容体アンタゴニストとしてのピラゾロ[5,1b]オキサゾール誘導体
AR080056A1 (es) 2010-02-01 2012-03-07 Novartis Ag Derivados de ciclohexil-amida como antagonistas de los receptores de crf
JP5748777B2 (ja) 2010-02-02 2015-07-15 ノバルティス アーゲー Crf受容体アンタゴニストとしてのシクロヘキシルアミド誘導体
UY34094A (es) 2011-05-27 2013-01-03 Novartis Ag Derivados de la piperidina 3-espirocíclica como agonistas de receptores de la ghrelina
CA2867043A1 (en) 2012-05-03 2013-11-07 Novartis Ag L-malate salt of 2,7-diaza-spiro[4.5]dec-7-yle derivatives and crystalline forms thereof as ghrelin receptor agonists

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3682075B2 (ja) * 1993-04-16 2005-08-10 クミアイ化学工業株式会社 トリアゾール誘導体及び殺虫、殺ダニ剤
MY129541A (en) * 1996-06-25 2007-04-30 Novartis Ag Substituded 3,5-diphenyl-1,2,4-triazoles and their use as pharmaceutical metal chelators
DE19816880A1 (de) * 1998-04-17 1999-10-21 Boehringer Ingelheim Pharma Neue Diphenyl-substituierte 5-Ring-Heterocyclen, Verfahren zu ihrer Herstellung sowie deren Verwendung als Arzneimittel
AR029489A1 (es) * 2000-03-10 2003-07-02 Euro Celtique Sa Piridinas, pirimidinas, pirazinas, triazinas sustituidas por arilo, composiciones farmaceuticas y el uso de las mismas para la manufactura de un medicamento
AU4589701A (en) * 2000-03-24 2001-10-08 Cocensys Inc Aryl substituted pyrazoles, triazoles and tetrazoles, and the use thereof
AR037233A1 (es) * 2001-09-07 2004-11-03 Euro Celtique Sa Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamento
MY142651A (en) * 2003-03-18 2010-12-15 Merck Sharp & Dohme Biaryl substituted triazoles as sodium channel blockers
US20060183897A1 (en) * 2003-03-18 2006-08-17 Chakravarty Prasun K Biaryl substituted triazoles as sodium channel blockers
CN1922156A (zh) * 2003-11-10 2007-02-28 默克公司 作为钠通道阻断剂的取代的三唑

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