JP2009530302A5 - - Google Patents

Download PDF

Info

Publication number
JP2009530302A5
JP2009530302A5 JP2009500517A JP2009500517A JP2009530302A5 JP 2009530302 A5 JP2009530302 A5 JP 2009530302A5 JP 2009500517 A JP2009500517 A JP 2009500517A JP 2009500517 A JP2009500517 A JP 2009500517A JP 2009530302 A5 JP2009530302 A5 JP 2009530302A5
Authority
JP
Japan
Prior art keywords
substituted
unsubstituted
compound according
disease
compound
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.)
Granted
Application number
JP2009500517A
Other languages
English (en)
Japanese (ja)
Other versions
JP5306986B2 (ja
JP2009530302A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2007/006685 external-priority patent/WO2007109160A2/en
Publication of JP2009530302A publication Critical patent/JP2009530302A/ja
Publication of JP2009530302A5 publication Critical patent/JP2009530302A5/ja
Application granted granted Critical
Publication of JP5306986B2 publication Critical patent/JP5306986B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2009500517A 2006-03-16 2007-03-16 P2x7調節因子としてのビシクロへテロアリール化合物およびその使用 Expired - Fee Related JP5306986B2 (ja)

Applications Claiming Priority (29)

Application Number Priority Date Filing Date Title
US78277606P 2006-03-16 2006-03-16
US78278106P 2006-03-16 2006-03-16
US78277506P 2006-03-16 2006-03-16
US78297306P 2006-03-16 2006-03-16
US78312106P 2006-03-16 2006-03-16
US78330406P 2006-03-16 2006-03-16
US78278206P 2006-03-16 2006-03-16
US78292306P 2006-03-16 2006-03-16
US78359006P 2006-03-16 2006-03-16
US78374806P 2006-03-16 2006-03-16
US78292206P 2006-03-16 2006-03-16
US60/782,922 2006-03-16
US60/782,973 2006-03-16
US60/783,121 2006-03-16
US60/783,304 2006-03-16
US60/783,590 2006-03-16
US60/782,782 2006-03-16
US60/782,775 2006-03-16
US60/782,776 2006-03-16
US60/783,748 2006-03-16
US60/782,781 2006-03-16
US83141606P 2006-07-17 2006-07-17
US60/831,416 2006-07-17
US84699306P 2006-09-25 2006-09-25
US60/846,993 2006-09-25
US91808607P 2007-03-15 2007-03-15
US60/918,086 2007-03-15
US60/782,923 2007-03-16
PCT/US2007/006685 WO2007109160A2 (en) 2006-03-16 2007-03-16 Bicycloheteroaryl compounds as p2x7 modulators and uses thereof

Publications (3)

Publication Number Publication Date
JP2009530302A JP2009530302A (ja) 2009-08-27
JP2009530302A5 true JP2009530302A5 (enExample) 2011-03-17
JP5306986B2 JP5306986B2 (ja) 2013-10-02

Family

ID=38522992

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009500517A Expired - Fee Related JP5306986B2 (ja) 2006-03-16 2007-03-16 P2x7調節因子としてのビシクロへテロアリール化合物およびその使用

Country Status (9)

Country Link
US (1) US8779144B2 (enExample)
EP (1) EP1937643B1 (enExample)
JP (1) JP5306986B2 (enExample)
BR (1) BRPI0709596A2 (enExample)
CA (1) CA2645551C (enExample)
DK (1) DK1937643T3 (enExample)
ES (1) ES2596532T3 (enExample)
MX (1) MX2008011919A (enExample)
WO (1) WO2007109160A2 (enExample)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7297700B2 (en) * 2005-03-24 2007-11-20 Renovis, Inc. Bicycloheteroaryl compounds as P2X7 modulators and uses thereof
DK2124562T3 (en) * 2007-03-09 2016-08-01 Second Genome Inc BICYCLOHETEROARYLFORBINDELSER AS P2X7 modulators and uses thereof
CA2707441A1 (en) 2008-01-09 2009-07-16 Renovis, Inc. Amide derivatives as ion-channel ligands and pharmaceutical compositions and methods of using the same
EP2105164B1 (en) 2008-03-25 2011-01-12 Affectis Pharmaceuticals AG Novel P2X7R antagonists and their use
AU2009240643B2 (en) * 2008-04-23 2014-03-06 Rigel Pharmaceuticals, Inc. Carboxamide compounds for the treatment of metabolic disorders
EP2362730A4 (en) 2008-11-21 2012-08-29 High Point Pharmaceuticals Llc Adamantyl BENZAMIDE CONNECTIONS
ATE541832T1 (de) 2009-04-14 2012-02-15 Affectis Pharmaceuticals Ag Neuartige p2x7r-antagonisten und ihre verwendung
EP2386541A1 (en) 2010-05-14 2011-11-16 Affectis Pharmaceuticals AG Novel methods for the preparation of P2X7R antagonists
WO2012110190A1 (en) 2011-02-17 2012-08-23 Affectis Pharmaceuticals Ag Novel p2x7r antagonists and their use
WO2012163792A1 (en) 2011-05-27 2012-12-06 Affectis Pharmaceuticals Ag Novel p2x7r antagonists and their use
WO2012163456A1 (en) 2011-05-27 2012-12-06 Affectis Pharmaceuticals Ag Novel p2x7r antagonists and their use
MX2014000894A (es) 2011-07-22 2014-02-27 Actelion Pharmaceuticals Ltd Derivados de amidas heterociclicas como antagonistas de receptores p2x7.
BR112014017735B1 (pt) 2012-01-20 2022-06-28 Idorsia Pharmaceuticals Ltd Compostos derivados de amida heterocíclicos como antagonistas do receptor de p2x7, composição farmacêutica, e, uso de um composto
EP2931717B1 (en) 2012-12-12 2016-12-07 Actelion Pharmaceuticals Ltd. Indole carboxamide derivatives as p2x7 receptor antagonists
CA2891499C (en) * 2012-12-18 2021-07-06 Actelion Pharmaceuticals Ltd Indole carboxamide derivatives as p2x7 receptor antagonists
JP6282017B2 (ja) 2013-01-22 2018-02-21 イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd P2x7受容体アンタゴニストとしての複素環アミド誘導体
CN104918617B (zh) 2013-01-22 2017-05-10 埃科特莱茵药品有限公司 作为p2x7受体拮抗剂的杂环酰胺衍生物
TWI825637B (zh) 2021-03-31 2023-12-11 美商輝瑞股份有限公司 啶-1,6(2h,7h)-二酮
EP4496797A1 (en) * 2022-03-21 2025-01-29 Gasherbrum Bio, Inc. 5,8-dihydro-1,7-naphthyridine derivatives as glp-1 agonists for the treatment of diabetes

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3942893A1 (de) * 1989-12-23 1991-06-27 Bayer Ag Heterocyclische verbindungen
US5484926A (en) * 1993-10-07 1996-01-16 Agouron Pharmaceuticals, Inc. HIV protease inhibitors
US5336674A (en) 1993-01-27 1994-08-09 Merck & Co., Inc. 2-phenanthridinyl carbaphenem antibacterial agent
GB9310700D0 (en) 1993-05-24 1993-07-07 Zeneca Ltd Novel composition
US5670517A (en) * 1993-11-30 1997-09-23 Lg Chemical Limited Irreversible HIV protease inhibitors, compositions containing same and process for the preparation thereof
AR008234A1 (es) * 1996-06-17 1999-12-29 Smithkline Beecham Plc Derivados de benzamidas, procedimiento para su preparacion, composiciones farmaceuticas y su uso para la preparacion de un medicamento
SE9704544D0 (sv) 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
SE9704545D0 (sv) 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
SE9704546D0 (sv) 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
SE9901875D0 (sv) 1999-05-25 1999-05-25 Astra Pharma Prod Novel compounds
TW200303304A (en) * 2002-02-18 2003-09-01 Astrazeneca Ab Chemical compounds
SE0200920D0 (sv) * 2002-03-25 2002-03-25 Astrazeneca Ab Novel compounds
GB0312609D0 (en) 2003-06-02 2003-07-09 Astrazeneca Ab Novel compounds
SE0302139D0 (sv) * 2003-07-28 2003-07-28 Astrazeneca Ab Novel compounds
NZ549449A (en) 2004-03-09 2009-05-31 Merck & Co Inc HIV Integrase inhibitors
WO2005105814A1 (en) 2004-04-28 2005-11-10 Incyte Corporation Tetracyclic inhibitors of janus kinases
SE0401345D0 (sv) 2004-05-25 2004-05-25 Astrazeneca Ab Therapeutic compounds: Pyridine as scaffold
EP1768955A1 (en) 2004-07-12 2007-04-04 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. Amide derivatives as inhibitors of histone deacetylase
UY29101A1 (es) 2004-09-07 2006-03-31 Smithkline Beecham Corp 1,3-diaminas aceclicas y usos de las mismas
JP2006220522A (ja) 2005-02-10 2006-08-24 National Institute For Materials Science Dnaとdna結合分子の結合様式の判定方法及びその判定に使用する試料の作製方法
US7893267B2 (en) 2005-03-14 2011-02-22 High Point Pharmaceuticals, Llc Benzazole derivatives, compositions, and methods of use as β-secretase inhibitors
US7297700B2 (en) 2005-03-24 2007-11-20 Renovis, Inc. Bicycloheteroaryl compounds as P2X7 modulators and uses thereof
JP3928086B2 (ja) 2005-03-29 2007-06-13 塩野義製薬株式会社 3−プロペニルセフェム誘導体
WO2006121831A2 (en) 2005-05-10 2006-11-16 Merck & Co., Inc. Hiv integrase inhibitors
FR2885904B1 (fr) 2005-05-19 2007-07-06 Aventis Pharma Sa Nouveaux derives du fluorene, compositions les contenant et utilisation
JP2009500418A (ja) 2005-07-08 2009-01-08 メルク エンド カムパニー インコーポレーテッド チェックポイントキナーゼの阻害剤
US20090105259A1 (en) 2005-09-08 2009-04-23 Jeong Jae U Acyclic 1,4-Diamines and Uses Thereof
TWI412322B (zh) 2005-12-30 2013-10-21 Du Pont 控制無脊椎害蟲之異唑啉
DK2124562T3 (en) * 2007-03-09 2016-08-01 Second Genome Inc BICYCLOHETEROARYLFORBINDELSER AS P2X7 modulators and uses thereof

Similar Documents

Publication Publication Date Title
JP2009530302A5 (enExample)
JP2009541206A5 (enExample)
JP2009530304A5 (enExample)
JP2010520875A5 (enExample)
JP2010524930A5 (enExample)
JP5306986B2 (ja) P2x7調節因子としてのビシクロへテロアリール化合物およびその使用
JP2008534511A5 (enExample)
ES2639621T3 (es) Derivados de fenilamida del ácido 4-(bencil)-piperazina-1-carboxílico y compuestos relacionados como moduladores de la amida hidrolasa de ácidos grasos (FAAH) para el tratamiento de la ansiedad, el dolor y otras afecciones
JP2007509043A5 (enExample)
JP2008546639A5 (enExample)
IL255752A (en) Novel anti-inflammatory agents
ES2664810T3 (es) Derivados de imidazopiridazina como moduladores de la actividad del receptor GABAA
KR20150013189A (ko) 벤조티오펜 화합물 또는 이의 염의 2수화물, 및 이의 제조 방법
EA200901162A1 (ru) Производные 1,4-дизамещённого 3-цианопиридона и их применение в качестве положительных модуляторов рецептора mglur2
KR20140027160A (ko) 치환된 디아미노카르복스아미드 및 디아미노카르보니트릴 피리미딘, 그의 조성물, 및 그를 사용하는 치료 방법
HRP20200681T1 (hr) Ciklički eter pirazol-4-il-heterociklil-karboksamidni spojevi i postupci njihove upotrebe
ATE517868T1 (de) Pyrazinverbindungen, ihre verwendung und herstellungsverfahren
HRP20110097T1 (hr) Derivati fenilpirazola kao nesteroidni ligandi glukokortikoidnih receptora
JP7167236B2 (ja) せん妄の予防または治療剤
ES2825348T3 (es) Compuestos y composición farmacéutica asociados al sistema ubiquitinación-proteasoma
JP2014520810A5 (enExample)
JP2010520875A (ja) P2x7調節因子としてのビシクロヘテロアリール化合物およびその使用
JP2018529639A (ja) アミノナフトキノン化合物、および疾患におけるユビキチン化−プロテアソーム系をブロックするための薬学的組成物
ES2945062T3 (es) Derivados de ácido barbitúrico novedosos, su preparación y uso de los mismos como inhibidores de la transmigración de leucocitos y para el tratamiento de enfermedades inflamatorias, enfermedades autoinmunitarias y cáncer
CN103497179A (zh) 含苯并咪唑结构单元的嘧啶衍生物及其制备方法和用途