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
ATE500234T1 (de) * 2003-11-10 2011-03-15 Merck Sharp & Dohme Substituierte trialzole als blocker des natriumkanals
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
US8299107B2 (en) * 2007-02-08 2012-10-30 Synta Pharmaceuticals Corporation Triazole compounds that modulate HSP90 activity
WO2008124092A2 (en) * 2007-04-03 2008-10-16 E. I. Du Pont De Nemours And Company Substituted benzene fungicides
MX2010004549A (es) * 2007-10-25 2010-07-28 Revalesio Corp Composiciones y métodos bacteriostáticos o bactericidas.
EP2215260A4 (en) * 2007-10-25 2011-04-20 Revalesio Corp COMPOSITIONS AND METHOD FOR MODULATING CELL MEMBRANE-IMPROVED INTRA-CELLULAR SIGNAL TRANSMISSION
KR20100098653A (ko) 2007-11-21 2010-09-08 디코드 제네틱스 이에이치에프 염증의 치료를 위한 바이아릴 pde4 억제제
CA2722582A1 (en) * 2007-11-21 2009-05-28 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
WO2011092290A1 (en) 2010-02-01 2011-08-04 Novartis Ag Pyrazolo[5,1b]oxazole derivatives as crf-1 receptor antagonists
AR080056A1 (es) 2010-02-01 2012-03-07 Novartis Ag Derivados de ciclohexil-amida como antagonistas de los receptores de crf
EP2531490B1 (en) 2010-02-02 2014-10-15 Novartis AG Cyclohexyl amide derivatives as crf receptor antagonists
AR086554A1 (es) 2011-05-27 2014-01-08 Novartis Ag Derivados de la piperidina 3-espirociclica como agonistas de receptores de la ghrelina
JP2015525202A (ja) 2012-05-03 2015-09-03 ノバルティス アーゲー グレリン受容体アゴニストとしての2,7−ジアザ−スピロ[4,5]デカ−7−イル誘導体のl−リンゴ酸塩およびその結晶形態

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
TW533205B (en) * 1996-06-25 2003-05-21 Novartis Ag Substituted 3,5-diphenyl-l,2,4-triazoles and their pharmaceutical composition
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
NZ520875A (en) * 2000-03-24 2005-04-29 Euro Celtique S Aryl substituted pyrazoles, triazoles and tetrazoles as sodium channel blocker
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
US20060183897A1 (en) * 2003-03-18 2006-08-17 Chakravarty Prasun K Biaryl substituted triazoles as sodium channel blockers
MY142651A (en) * 2003-03-18 2010-12-15 Merck Sharp & Dohme Biaryl substituted triazoles as sodium channel blockers
ATE500234T1 (de) * 2003-11-10 2011-03-15 Merck Sharp & Dohme Substituierte trialzole als blocker des natriumkanals

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