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 (US07794700-20100914-C00152.png) 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 (US07794700-20100914-C00152.png)
EP (1) EP1694654B1 (US07794700-20100914-C00152.png)
JP (1) JP2007510741A (US07794700-20100914-C00152.png)
KR (1) KR20060123739A (US07794700-20100914-C00152.png)
CN (1) CN1922156A (US07794700-20100914-C00152.png)
AT (1) ATE500234T1 (US07794700-20100914-C00152.png)
AU (1) AU2004289694B2 (US07794700-20100914-C00152.png)
BR (1) BRPI0416319A (US07794700-20100914-C00152.png)
CA (1) CA2545254A1 (US07794700-20100914-C00152.png)
DE (1) DE602004031667D1 (US07794700-20100914-C00152.png)
IL (1) IL175522A0 (US07794700-20100914-C00152.png)
IS (1) IS8438A (US07794700-20100914-C00152.png)
NO (1) NO20062676L (US07794700-20100914-C00152.png)
NZ (1) NZ547044A (US07794700-20100914-C00152.png)
RU (1) RU2372339C2 (US07794700-20100914-C00152.png)
WO (1) WO2005047270A2 (US07794700-20100914-C00152.png)
ZA (1) ZA200603583B (US07794700-20100914-C00152.png)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR044503A1 (es) * 2003-03-18 2005-09-14 Merck & Co Inc Triazoles sustituidos con biarilo como bloqueantes del canal de sodio
WO2005047270A2 (en) * 2003-11-10 2005-05-26 Merck & Co., Inc. Substituted triazoles as sodium channel blockers
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
BRPI0807219A2 (pt) 2007-02-08 2015-05-26 Synta Pharmaceuticals Corp Composto de tiazol que modulam a atividade de hsp90
BR122015028990B8 (pt) * 2007-04-03 2017-12-26 Du Pont composto, composições fungicidas e método de controle de doenças das plantas
EP2215260A4 (en) * 2007-10-25 2011-04-20 Revalesio Corp COMPOSITIONS AND METHOD FOR MODULATING CELL MEMBRANE-IMPROVED INTRA-CELLULAR SIGNAL TRANSMISSION
CA2703648A1 (en) * 2007-10-25 2009-04-30 Revalesio Corporation Bacteriostatic or bacteriocidal compositions and methods
US20090324569A1 (en) 2007-11-21 2009-12-31 Decode Genetics Ehf Biaryl pde4 inhibitors for treating inflammatory, cardiovascular and cns disorders
JP2011505341A (ja) * 2007-11-21 2011-02-24 デコード ジェネティクス イーエイチエフ 炎症性、心血管およびcns障害を治療するビアリールpde4抑制剤
US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
WO2011092293A2 (en) 2010-02-01 2011-08-04 Novartis Ag Cyclohexyl amide derivatives as crf receptor antagonists
AR080055A1 (es) 2010-02-01 2012-03-07 Novartis Ag Derivados de pirazolo-[5,1-b]-oxazol como antagonistas de los receptores de crf -1
CN102753527B (zh) 2010-02-02 2014-12-24 诺华股份有限公司 用作crf受体拮抗剂的环己基酰胺衍生物
AR086554A1 (es) 2011-05-27 2014-01-08 Novartis Ag Derivados de la piperidina 3-espirociclica como agonistas de receptores de la ghrelina
EP2852591A1 (en) 2012-05-03 2015-04-01 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 (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
CN1321112C (zh) * 2000-03-24 2007-06-13 欧洲凯尔特股份有限公司 作为钠通道阻滞剂的芳基取代的吡唑、三唑和四唑化合物
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
AR044503A1 (es) * 2003-03-18 2005-09-14 Merck & Co Inc Triazoles sustituidos con biarilo como bloqueantes del canal de sodio
US20060183897A1 (en) * 2003-03-18 2006-08-17 Chakravarty Prasun K Biaryl substituted triazoles as sodium channel blockers
WO2005047270A2 (en) * 2003-11-10 2005-05-26 Merck & Co., Inc. Substituted triazoles as sodium channel blockers

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