FR2607813B1
(fr)
|
1986-12-05 |
1989-03-31 |
Montpellier I Universite |
Alkylamino-8 imidazo (1,2-a) pyrazines et derives, leur preparation et leur application en therapeutique
|
AU622330B2
(en)
|
1989-06-23 |
1992-04-02 |
Takeda Chemical Industries Ltd. |
Condensed heterocyclic compounds having a nitrogen atom in the bridgehead for use as fungicides
|
IL96432A0
(en)
|
1989-11-30 |
1991-08-16 |
Schering Ag |
Pesticidal compositions containing pyridine derivatives and novel pyridine derivatives
|
FR2662163A1
(fr)
|
1990-05-16 |
1991-11-22 |
Lipha |
Nouvelles 8-amino-1,2,4-triazolo(4,3-a) pyrazines, procedes de preparation et medicaments les contenant.
|
ES2130269T3
(es)
|
1992-06-17 |
1999-07-01 |
Upjohn Co |
Oximas sustituidas con piridina, pirrolidina y azepina utiles como agentes contra la aterosclerosis y antihipercolesterolemicos.
|
JP2923139B2
(ja)
*
|
1992-10-05 |
1999-07-26 |
三井化学株式会社 |
製 剤
|
DE4327027A1
(de)
|
1993-02-15 |
1994-08-18 |
Bayer Ag |
Imidazoazine
|
FR2711993B1
(fr)
|
1993-11-05 |
1995-12-01 |
Rhone Poulenc Rorer Sa |
Médicaments contenant des dérivés de 7H-imidazol[1,2-a]pyrazine-8-one, les nouveaux composés et leur préparation.
|
US6451796B1
(en)
|
1997-11-11 |
2002-09-17 |
Ono Pharmaceutical Co., Ltd. |
Fused pyrazine compounds
|
JP2000319277A
(ja)
|
1999-05-11 |
2000-11-21 |
Ono Pharmaceut Co Ltd |
縮合ピラジン化合物およびその化合物を有効成分とする薬剤
|
JP2000319278A
(ja)
|
1999-05-11 |
2000-11-21 |
Ono Pharmaceut Co Ltd |
縮合ピラジン化合物およびその化合物を有効成分とする薬剤
|
JP4032566B2
(ja)
|
1999-06-21 |
2008-01-16 |
東レ株式会社 |
発光素子
|
JP4041624B2
(ja)
|
1999-07-21 |
2008-01-30 |
三井化学株式会社 |
有機電界発光素子
|
JP2001057292A
(ja)
|
1999-08-20 |
2001-02-27 |
Toray Ind Inc |
発光素子
|
DE19948434A1
(de)
|
1999-10-08 |
2001-06-07 |
Gruenenthal Gmbh |
Substanzbibliothek enthaltend bicyclische Imidazo-5-amine und/oder bicyclische Imidazo-3-amine
|
JP4409680B2
(ja)
|
1999-10-18 |
2010-02-03 |
株式会社ヤクルト本社 |
三環性縮合イミダゾール誘導体
|
CN1173975C
(zh)
|
2000-04-27 |
2004-11-03 |
山之内制药株式会社 |
咪唑并吡啶衍生物
|
US6403588B1
(en)
|
2000-04-27 |
2002-06-11 |
Yamanouchi Pharmaceutical Co., Ltd. |
Imidazopyridine derivatives
|
ES2225624T3
(es)
|
2000-06-28 |
2005-03-16 |
Smithkline Beecham Plc |
Procedimiento de molienda por via humeda.
|
WO2002006286A2
(en)
|
2000-07-14 |
2002-01-24 |
Bristol-Myers Squibb Pharma Company |
IMIDAZO[1,2-a]PYRAZINES FOR THE TREATMENT OF NEUROLOGICAL DISORDERS
|
DE10050663A1
(de)
|
2000-10-13 |
2002-04-18 |
Gruenenthal Gmbh |
Verwendung von substituierten Imidazo[1,2-a]pyridin-, -pyrimidin- und pyrazin-3-yl-amin-Derivaten zur Herstellung von Medikamenten zur NOS-Inhibierung
|
AU2001295992A1
(en)
|
2000-10-24 |
2002-05-06 |
Sankyo Company Limited |
Imidazopyridine derivatives
|
JP2002205992A
(ja)
|
2000-11-08 |
2002-07-23 |
Takeda Chem Ind Ltd |
二環式トリアゾロン誘導体およびそれを含有する除草剤
|
WO2002048146A2
(de)
|
2000-12-13 |
2002-06-20 |
Basf Aktiengesellschaft |
Verwendung von substituierten imidazoazinen, neue imidazoazine, verfahren zu deren herstellung, sowie sie enthaltende mittel
|
EP1217000A1
(en)
|
2000-12-23 |
2002-06-26 |
Aventis Pharma Deutschland GmbH |
Inhibitors of factor Xa and factor VIIa
|
TWI312347B
(en)
|
2001-02-08 |
2009-07-21 |
Eisai R&D Man Co Ltd |
Bicyclic nitrogen-containing condensed ring compounds
|
US6951848B2
(en)
|
2001-03-12 |
2005-10-04 |
Millennium Pharmaceuticals, Inc., |
Functionalized heterocycles as modulators of chemokine receptor function and methods of use therefor
|
AR035543A1
(es)
|
2001-06-26 |
2004-06-16 |
Japan Tobacco Inc |
Agente terapeutico para la hepatitis c que comprende un compuesto de anillo condensado, compuesto de anillo condensado, composicion farmaceutica que lo comprende, compuestos de benzimidazol, tiazol y bifenilo utiles como intermediarios para producir dichos compuestos, uso del compuesto de anillo con
|
IL159811A0
(en)
|
2001-07-13 |
2004-06-20 |
Neurogen Corp |
Heteroaryl substituted fused bicyclic heteroaryl compounds as gabaa receptor ligands
|
US6921762B2
(en)
|
2001-11-16 |
2005-07-26 |
Amgen Inc. |
Substituted indolizine-like compounds and methods of use
|
US20050113283A1
(en)
|
2002-01-18 |
2005-05-26 |
David Solow-Cordero |
Methods of treating conditions associated with an EDG-4 receptor
|
JP2005519915A
(ja)
|
2002-01-18 |
2005-07-07 |
セレテック・リミテッド・ライアビリティ・カンパニー |
Edg受容体に関連する症状の処置方法
|
WO2004017950A2
(en)
|
2002-08-22 |
2004-03-04 |
Piramed Limited |
Phosphadidylinositol 3,5-biphosphate inhibitors as anti-viral agents
|
UA80296C2
(en)
|
2002-09-06 |
2007-09-10 |
Biogen Inc |
Imidazolopyridines and methods of making and using the same
|
CN1747949A
(zh)
|
2002-12-20 |
2006-03-15 |
法马西亚公司 |
无环吡唑化合物
|
US7189723B2
(en)
|
2003-02-10 |
2007-03-13 |
Cgi Pharmaceuticals, Inc. |
Certain 8-heteroaryl-6-phenyl-imidazo[1,2-a]pyrazines as modulators of kinase activity
|
US7186832B2
(en)
|
2003-02-20 |
2007-03-06 |
Sugen Inc. |
Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
|
US7157460B2
(en)
|
2003-02-20 |
2007-01-02 |
Sugen Inc. |
Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
|
GB0303910D0
(en)
|
2003-02-20 |
2003-03-26 |
Merck Sharp & Dohme |
Therapeutic agents
|
EP2385040A1
(en)
|
2003-03-14 |
2011-11-09 |
ONO Pharmaceutical Co., Ltd. |
Nitrogen-containing heterocyclic derivatives and drugs containing the same as the active ingredient
|
JP2006522750A
(ja)
|
2003-04-11 |
2006-10-05 |
ノボ ノルディスク アクティーゼルスカブ |
代謝性症候群ならびに関連の疾患および障害を治療するために、11β−ヒドロキシステロイドデヒドロゲナーゼ1型阻害剤および抗高血圧剤を使用する併用療法
|
ATE455547T1
(de)
|
2003-04-11 |
2010-02-15 |
High Point Pharmaceuticals Llc |
Pharmazeutische verwendungen von kondensierten 1, 2,4-triazolen
|
AU2004233828B2
(en)
|
2003-04-24 |
2009-05-28 |
Merck Sharp & Dohme Corp. |
Inhibitors of Akt activity
|
SE0301653D0
(sv)
|
2003-06-05 |
2003-06-05 |
Astrazeneca Ab |
Novel compounds
|
AR045697A1
(es)
|
2003-07-14 |
2005-11-09 |
Arena Pharm Inc |
Aril y heteroaril derivados fusionados como moduladores del metabolismo y la prevencion y tratamiento de trastornos relacionados con el mismo
|
US7538120B2
(en)
|
2003-09-03 |
2009-05-26 |
Array Biopharma Inc. |
Method of treating inflammatory diseases
|
ES2385219T3
(es)
|
2003-09-12 |
2012-07-19 |
Merck Serono Sa |
Derivados de sulfonamida para el tratamiento de diabetes
|
JP2005089352A
(ja)
|
2003-09-16 |
2005-04-07 |
Kissei Pharmaceut Co Ltd |
新規なイミダゾ[1,5−a]ピラジン誘導体、それを含有する医薬組成物およびそれらの用途
|
CA2541832C
(en)
|
2003-10-10 |
2009-11-24 |
Pfizer Products Inc. |
Substituted 2h-[1,2,4]triazolo[4,3-a]pyrazines as gsk-3 inhibitors
|
US7419978B2
(en)
|
2003-10-22 |
2008-09-02 |
Bristol-Myers Squibb Company |
Phenyl-aniline substituted bicyclic compounds useful as kinase inhibitors
|
US7714009B2
(en)
|
2003-10-31 |
2010-05-11 |
Takeda Pharmaceutical Company Limited |
Nitrogen-containing fused heterocyclic compounds
|
WO2005063241A1
(ja)
|
2003-12-26 |
2005-07-14 |
Ono Pharmaceutical Co., Ltd. |
ミトコンドリアベンゾジアゼピン受容体介在性疾患の予防および/または治療剤
|
US20070191395A1
(en)
|
2004-02-16 |
2007-08-16 |
Katsuhiro Kawakami |
Heterocyclic compounds having antifungal activity
|
US7306631B2
(en)
|
2004-03-30 |
2007-12-11 |
The Procter & Gamble Company |
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
|
TW200612918A
(en)
|
2004-07-29 |
2006-05-01 |
Threshold Pharmaceuticals Inc |
Lonidamine analogs
|
MX2007001612A
(es)
|
2004-08-18 |
2007-04-10 |
Upjohn Co |
Compuestos novedosos de triazolopiridina para el tratamiento de la inflamacion.
|
BRPI0516819A
(pt)
|
2004-10-07 |
2008-09-23 |
Warner Lambert Co |
derivados de triazolopiridina e agentes antibacterianos
|
WO2006057946A2
(en)
|
2004-11-22 |
2006-06-01 |
Threshold Pharmaceuticals, Inc. |
Tubulin binding anti cancer agents and prodrugs thereof
|
JP2008521858A
(ja)
|
2004-12-01 |
2008-06-26 |
ラボラトワール セローノ ソシエテ アノニム |
過増殖性疾患を処置するための[1,2,4]トリアゾロ[4,3−a]ピリジン誘導体
|
US20070293456A9
(en)
|
2004-12-30 |
2007-12-20 |
Anthony Hayford |
Method for the synthesis of 3-substituted indolizine and benzoindolizine compounds
|
US7456289B2
(en)
|
2004-12-31 |
2008-11-25 |
National Health Research Institutes |
Anti-tumor compounds
|
GEP20094727B
(en)
|
2005-02-22 |
2009-07-10 |
Pfizer |
Oxyindole derivatives as 5ht4 receptor agonists
|
TW200716594A
(en)
|
2005-04-18 |
2007-05-01 |
Neurogen Corp |
Substituted heteroaryl CB1 antagonists
|
US7579360B2
(en)
|
2005-06-09 |
2009-08-25 |
Bristol-Myers Squibb Company |
Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors
|
US7572807B2
(en)
|
2005-06-09 |
2009-08-11 |
Bristol-Myers Squibb Company |
Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors
|
AU2005332594A1
(en)
|
2005-06-09 |
2006-12-14 |
Oncalis Ag |
Angiogenesis inhibitors
|
US7452892B2
(en)
|
2005-06-17 |
2008-11-18 |
Bristol-Myers Squibb Company |
Triazolopyrimidine cannabinoid receptor 1 antagonists
|
US7572808B2
(en)
|
2005-06-17 |
2009-08-11 |
Bristol-Myers Squibb Company |
Triazolopyridine cannabinoid receptor 1 antagonists
|
TW200800213A
(en)
|
2005-09-02 |
2008-01-01 |
Abbott Lab |
Novel imidazo based heterocycles
|
KR20080074963A
(ko)
|
2005-11-10 |
2008-08-13 |
쉐링 코포레이션 |
단백질 키나제 억제제로서의 이미다조피라진
|
WO2007074491A1
(en)
|
2005-12-28 |
2007-07-05 |
Universita Degli Studi Di Siena |
HETEROTRICYCLIC AMIDE DERIVATIVES AS NEUROKININ-l (NKl) RECEPTOR LIGANDS
|
PE20070978A1
(es)
|
2006-02-14 |
2007-11-15 |
Novartis Ag |
COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE FOSFATIDILINOSITOL 3-QUINASAS (PI3Ks)
|
US8097617B2
(en)
|
2006-03-31 |
2012-01-17 |
Novartis Ag |
Organic compounds
|
US20090175852A1
(en)
|
2006-06-06 |
2009-07-09 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
TW200808802A
(en)
|
2006-06-06 |
2008-02-16 |
Schering Corp |
Imidazopyrazines as protein kinase inhibitors
|
ES2456042T3
(es)
|
2006-06-22 |
2014-04-21 |
Medibeacon, LLC |
Derivados de pirazina y usos de los mismos en la monitorización renal
|
CN101472903A
(zh)
|
2006-06-22 |
2009-07-01 |
马林克罗特公司 |
具有扩展共轭的吡嗪衍生物及其用途
|
AR061664A1
(es)
|
2006-06-29 |
2008-09-10 |
Schering Corp |
Derivados de himbacina como antagonistas del receptor de trombina biciclicos y triciclicos sustituidos. composiciones farmaceuticas.
|
WO2008005423A1
(en)
|
2006-07-03 |
2008-01-10 |
Cambrex Charles City, Inc. |
Improved method of making sufentanil
|
US7501438B2
(en)
|
2006-07-07 |
2009-03-10 |
Forest Laboratories Holdings Limited |
Pyridoimidazole derivatives
|
PE20121506A1
(es)
|
2006-07-14 |
2012-11-26 |
Amgen Inc |
Compuestos triazolopiridinas como inhibidores de c-met
|
US8198448B2
(en)
|
2006-07-14 |
2012-06-12 |
Amgen Inc. |
Fused heterocyclic derivatives and methods of use
|
US8217177B2
(en)
|
2006-07-14 |
2012-07-10 |
Amgen Inc. |
Fused heterocyclic derivatives and methods of use
|
US20080021026A1
(en)
|
2006-07-20 |
2008-01-24 |
Mehmet Kahraman |
Benzothiophene inhibitors of rho kinase
|
US7563797B2
(en)
|
2006-08-28 |
2009-07-21 |
Forest Laboratories Holding Limited |
Substituted imidazo(1,2-A)pyrimidines and imidazo(1,2-A) pyridines as cannabinoid receptor ligands
|
DE102006041292A1
(de)
|
2006-09-01 |
2008-03-06 |
Henkel Kgaa |
Wasserstoffperoxid-Aktivierung mit N-Heterocyclen
|
WO2008037607A1
(de)
|
2006-09-25 |
2008-04-03 |
Basf Se |
Carbonylgruppen-enthaltende heterocyclische verbindungen und deren verwendung zur bekämpfung von phytopathogenen pilzen
|
CA2665195C
(en)
|
2006-10-11 |
2011-08-09 |
Amgen Inc. |
Imidazo- and triazolo-pyridine compounds and methods of use thereof
|
WO2008056176A1
(en)
|
2006-11-10 |
2008-05-15 |
Scottish Biomedical Limited |
Pyrazolopyrimidines as phosphodiesterase inhibitors
|
BRPI0719333A2
(pt)
|
2006-11-22 |
2014-02-04 |
Incyte Corp |
Midazotriazinas e imidazopirimidinas como inbidores de cinase
|
ATE495743T1
(de)
|
2006-12-01 |
2011-02-15 |
Galapagos Nv |
Triazolopyridinverbindungen zur behandlung von degenerations- und entzündungskrankheiten
|
DE102007012645A1
(de)
|
2007-03-16 |
2008-09-18 |
Bayer Healthcare Ag |
Substituierte Imidazo- und Triazolopyrimidine
|
EP1972628A1
(en)
|
2007-03-21 |
2008-09-24 |
Schwarz Pharma Ag |
Indolizines and aza-analog derivatives thereof as CNS active compounds
|
CN101679428A
(zh)
|
2007-04-16 |
2010-03-24 |
利奥制药有限公司 |
用于治疗皮肤疾病的作为磷酸二酯酶抑制剂的三唑并吡啶类
|
JP2010524953A
(ja)
|
2007-04-17 |
2010-07-22 |
ブリストル−マイヤーズ スクイブ カンパニー |
縮合ヘテロ環11−β−ヒドロキシステロイドデヒドロゲナーゼI型阻害剤
|
WO2008141249A1
(en)
|
2007-05-10 |
2008-11-20 |
Acadia Pharmaceuticals Inc. |
Imidazol (1,2-a)pyridines and related compounds with activity at cannabinoid cb2 receptors
|
WO2008143240A1
(ja)
*
|
2007-05-21 |
2008-11-27 |
Toray Industries, Inc. |
特定の有機酸を含有する経口製剤並びに経口製剤の溶出性及び化学的安定性の改善方法
|
MX2009013213A
(es)
|
2007-06-08 |
2010-03-30 |
Abbott Lab |
Indazoles 5-sustituidos 5-heteroarilo como inhibidores de cinasa.
|
US8648069B2
(en)
|
2007-06-08 |
2014-02-11 |
Abbvie Inc. |
5-substituted indazoles as kinase inhibitors
|
CN101772500A
(zh)
|
2007-06-14 |
2010-07-07 |
先灵公司 |
作为蛋白质激酶抑制剂的咪唑并吡嗪
|
CL2008001839A1
(es)
|
2007-06-21 |
2009-01-16 |
Incyte Holdings Corp |
Compuestos derivados de 2,7-diazaespirociclos, inhibidores de 11-beta hidroxil esteroide deshidrogenasa tipo 1; composicion farmaceutica que comprende a dichos compuestos; utiles para tratar la obesidad, diabetes, intolerancia a la glucosa, diabetes tipo ii, entre otras enfermedades.
|
CN101801966A
(zh)
|
2007-07-18 |
2010-08-11 |
诺瓦提斯公司 |
双环杂芳基化合物和它们作为激酶抑制剂的用途
|
BRPI0814874A2
(pt)
|
2007-07-31 |
2019-09-24 |
Schering Corp |
combinação de agente antimitótico e inibidor da aurora quinase como tratamento anticâncer.
|
WO2009017954A1
(en)
|
2007-08-01 |
2009-02-05 |
Phenomix Corporation |
Inhibitors of jak2 kinase
|
EA201000201A1
(ru)
|
2007-08-10 |
2010-12-30 |
ГЛАКСОСМИТКЛАЙН ЭлЭлСи |
Азотсодержащие бициклические химические вещества для лечения вирусных инфекций
|
FR2920091A1
(fr)
|
2007-08-24 |
2009-02-27 |
Oreal |
Composition tinctoriale comprenant une base d'oxydation aminopyrazolopyridine, un coupleur et un polyol particulier.
|
FR2920090A1
(fr)
|
2007-08-24 |
2009-02-27 |
Oreal |
Composition tinctoriale comprenant une base d'oxydation aminopyrazolopyridine particuliere, un coupleur et un tensioactif particulier.
|
US8119658B2
(en)
|
2007-10-01 |
2012-02-21 |
Bristol-Myers Squibb Company |
Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors
|
GB0719803D0
(en)
|
2007-10-10 |
2007-11-21 |
Cancer Rec Tech Ltd |
Therapeutic compounds and their use
|
JP4705695B2
(ja)
|
2007-10-11 |
2011-06-22 |
アストラゼネカ アクチボラグ |
プロテインキナーゼb阻害剤としてのピロロ[2,3−d]ピリミジン誘導体
|
BRPI0818161B8
(pt)
*
|
2007-10-12 |
2021-05-25 |
Novartis Ag |
mistura estável compreendendo agonista de receptores de s1p, sua forma de dosagem final e seu uso
|
CA2710194C
(en)
|
2007-12-19 |
2014-04-22 |
Amgen Inc. |
Inhibitors of p13 kinase
|
WO2009085980A1
(en)
|
2007-12-19 |
2009-07-09 |
Genentech, Inc. |
8-anilin0imidaz0pyridines and their use as anti-cancer and/or anti-inflammatory agents
|
KR20120108042A
(ko)
|
2008-03-11 |
2012-10-04 |
인사이트 코포레이션 |
Jak 억제제로서의 아제티딘 및 시클로부탄 유도체
|
JP5638961B2
(ja)
|
2008-03-13 |
2014-12-10 |
ザ ジェネラル ホスピタル コーポレイション |
Bmpシグナル伝達経路のインヒビター
|
EP2277881A4
(en)
|
2008-04-18 |
2011-09-07 |
Shionogi & Co |
HETEROCYCLIC COMPOUND HAVING INHIBITORY ACTIVITY ON P13K
|
US8349210B2
(en)
|
2008-06-27 |
2013-01-08 |
Transitions Optical, Inc. |
Mesogenic stabilizers
|
WO2010010189A1
(en)
|
2008-07-25 |
2010-01-28 |
Galapagos Nv |
Novel compounds useful for the treatment of degenerative and inflammatory diseases
|
WO2010010188A1
(en)
|
2008-07-25 |
2010-01-28 |
Galapagos Nv |
Novel compounds useful for the treatment of degenerative and inflammatory diseases.
|
WO2010010184A1
(en)
|
2008-07-25 |
2010-01-28 |
Galapagos Nv |
[1, 2, 4] triazolo [1, 5-a] pyridines as jak inhibitors
|
WO2010010187A1
(en)
|
2008-07-25 |
2010-01-28 |
Galapagos Nv |
Novel compounds useful for the treatment of degenerative and inflammatory diseases
|
UY32049A
(es)
|
2008-08-14 |
2010-03-26 |
Takeda Pharmaceutical |
Inhibidores de cmet
|
JP2010070503A
(ja)
|
2008-09-19 |
2010-04-02 |
Daiichi Sankyo Co Ltd |
抗真菌作用2−アミノトリアゾロピリジン誘導体
|
US20120021519A1
(en)
|
2008-09-19 |
2012-01-26 |
Presidents And Fellows Of Harvard College |
Efficient induction of pluripotent stem cells using small molecule compounds
|
US8703778B2
(en)
|
2008-09-26 |
2014-04-22 |
Intellikine Llc |
Heterocyclic kinase inhibitors
|
EP2361242B1
(en)
|
2008-10-17 |
2018-08-01 |
Oryzon Genomics, S.A. |
Oxidase inhibitors and their use
|
WO2010048149A2
(en)
|
2008-10-20 |
2010-04-29 |
Kalypsys, Inc. |
Heterocyclic modulators of gpr119 for treatment of disease
|
JP2012510983A
(ja)
|
2008-12-04 |
2012-05-17 |
プロキシマジェン エルティーディー |
イミダゾピリジン化合物
|
US8450321B2
(en)
|
2008-12-08 |
2013-05-28 |
Gilead Connecticut, Inc. |
6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor
|
US8993808B2
(en)
|
2009-01-21 |
2015-03-31 |
Oryzon Genomics, S.A. |
Phenylcyclopropylamine derivatives and their medical use
|
CA2750517A1
(en)
|
2009-02-04 |
2010-08-12 |
Vitae Pharmaceuticals, Inc. |
Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1
|
WO2010104307A2
(ko)
|
2009-03-07 |
2010-09-16 |
주식회사 메디젠텍 |
세포핵에서 세포질로의 gsk3의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 gsk3 이동에 의해 발생되는 질환의 치료 또는 예방용 약학적 조성물
|
AR076052A1
(es)
|
2009-03-20 |
2011-05-18 |
Incyte Corp |
Derivados de pirimidinas sustituidas, composiciones farmaceuticas que los contienen y uso de los mismos en trastornos asociados con receptores de histamina h4, tales como trastornos inflamatorios, prurito y dolor.
|
WO2010113942A1
(ja)
|
2009-03-31 |
2010-10-07 |
キッセイ薬品工業株式会社 |
インドリジン誘導体及びその医薬用途
|
ES2475091T3
(es)
|
2009-04-16 |
2014-07-10 |
Centro Nacional De Investigaciones Oncol�Gicas (Cnio) |
Imidazopirazinas como inhibidores de proteína cinasas
|
TWI461426B
(zh)
|
2009-05-27 |
2014-11-21 |
Merck Sharp & Dohme |
(二氫)咪唑並異〔5,1-a〕喹啉類
|
JP2012529529A
(ja)
|
2009-06-10 |
2012-11-22 |
スノビオン プハルマセウトイカルス インコーポレイテッド |
ヒスタミンh3インバースアゴニスト及びアンタゴニスト、並びにその使用方法
|
CA2937222C
(en)
|
2009-06-25 |
2019-06-04 |
Alkermes Pharma Ireland Limited |
Prodrugs of nh-acidic compounds
|
KR101721280B1
(ko)
|
2009-08-17 |
2017-03-29 |
인텔리카인, 엘엘씨 |
헤테로사이클릭 화합물 및 이의 용도
|
EP2467359A4
(en)
|
2009-08-18 |
2013-01-09 |
Univ Johns Hopkins |
(BIS-) UREA- AND (BIS-) THIOMINE COMPOUNDS AS EPIGENE MODULATORS OF THE LYSINE-SPECIFIC DEMETHYLASE 1 AND METHODS OF DISEASE TREATMENT THEREWITH
|
WO2011033265A1
(en)
|
2009-09-18 |
2011-03-24 |
Almac Discovery Limited |
Pharmaceutical compounds
|
JP5699152B2
(ja)
|
2009-09-25 |
2015-04-08 |
オリゾン・ジェノミックス・ソシエダッド・アノニマOryzon Genomics S.A. |
リジン特異的デメチラーゼ−1阻害剤およびその使用
|
WO2011042217A1
(en)
|
2009-10-09 |
2011-04-14 |
Oryzon Genomics S.A. |
Substituted heteroaryl- and aryl- cyclopropylamine acetamides and their use
|
WO2011050245A1
(en)
|
2009-10-23 |
2011-04-28 |
Yangbo Feng |
Bicyclic heteroaryls as kinase inhibitors
|
US8541404B2
(en)
|
2009-11-09 |
2013-09-24 |
Elexopharm Gmbh |
Inhibitors of the human aldosterone synthase CYP11B2
|
ES2627703T3
(es)
|
2010-01-22 |
2017-07-31 |
Fundación Centro Nacional De Investigaciones Oncológicas Carlos Iii |
Inhibidores de PI3·quinasa
|
WO2011097607A1
(en)
|
2010-02-08 |
2011-08-11 |
Southern Research Institute |
Anti-viral treatment and assay to screen for anti-viral agent
|
WO2011106574A2
(en)
|
2010-02-24 |
2011-09-01 |
Oryzon Genomics, S.A. |
Inhibitors for antiviral use
|
US9186337B2
(en)
|
2010-02-24 |
2015-11-17 |
Oryzon Genomics S.A. |
Lysine demethylase inhibitors for diseases and disorders associated with Hepadnaviridae
|
TW201200518A
(en)
|
2010-03-10 |
2012-01-01 |
Kalypsys Inc |
Heterocyclic inhibitors of histamine receptors for the treatment of disease
|
CA2793279A1
(en)
|
2010-03-18 |
2011-09-22 |
Ulrich Klar |
Imidazopyrazines
|
MX345762B
(es)
|
2010-03-18 |
2017-02-15 |
Pasteur Institut Korea |
Compuestos antiinfecciosos.
|
CA2793313C
(en)
|
2010-04-02 |
2018-01-23 |
Euroscreen Sa |
Nk-3 receptor selective antagonist compounds, pharmaceutical composition and methods for use in nk-3 receptors mediated disorders
|
PL2560947T3
(pl)
|
2010-04-19 |
2017-04-28 |
Oryzon Genomics, S.A. |
Inhibitory demetylazy specyficznej dla lizyny i ich zastosowanie
|
AU2011244478B2
(en)
|
2010-04-20 |
2014-07-17 |
Fondazione IEO-CCM |
Tranylcypromine derivatives as inhibitors of histone demethylase LSD1 and/or LSD2
|
WO2011141713A1
(en)
|
2010-05-13 |
2011-11-17 |
Centro Nacional De Investigaciones Oncologicas (Cnio) |
New bicyclic compounds as pi3-k and mtor inhibitors
|
BR112012029026A2
(pt)
|
2010-05-13 |
2016-08-02 |
Amgen Inc |
composto heretocíclicos de nitrogênio úteis como inbidores pde10
|
CN102295642B
(zh)
|
2010-06-25 |
2016-04-06 |
中国人民解放军军事医学科学院毒物药物研究所 |
2-芳基咪唑并[1,2-a]吡啶-3-乙酰胺衍生物、其制备方法及用途
|
ES2529119T3
(es)
|
2010-07-02 |
2015-02-17 |
Gilead Sciences, Inc. |
Compuestos heterocíclicos condensados como moduladores de canales iónicos
|
JP5830094B2
(ja)
|
2010-07-12 |
2015-12-09 |
バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH |
置換イミダゾ[1,2−a]ピリミジンおよび−ピリジン
|
WO2012016133A2
(en)
|
2010-07-29 |
2012-02-02 |
President And Fellows Of Harvard College |
Ros1 kinase inhibitors for the treatment of glioblastoma and other p53-deficient cancers
|
EP2598480B1
(en)
|
2010-07-29 |
2019-04-24 |
Oryzon Genomics, S.A. |
Cyclopropylamine derivatives useful as lsd1 inhibitors
|
RU2611437C2
(ru)
|
2010-07-29 |
2017-02-22 |
Оризон Дженомикс С.А. |
Ингибиторы деметилазы lsd1 на основе арилциклопропиламина и их применение в медицине
|
US9527805B2
(en)
|
2010-09-10 |
2016-12-27 |
Robert A. Casero |
Small molecules as epigenetic modulators of lysine-specific demethylase 1 and methods of treating disorders
|
KR20130099064A
(ko)
|
2010-09-29 |
2013-09-05 |
깃세이 야쿠힌 고교 가부시키가이샤 |
(아자)인돌리진 유도체 및 그 의약용도
|
US20130303545A1
(en)
|
2010-09-30 |
2013-11-14 |
Tamara Maes |
Cyclopropylamine derivatives useful as lsd1 inhibitors
|
JP2013540767A
(ja)
|
2010-10-07 |
2013-11-07 |
ザ ジェイ. デヴィッド グラッドストーン インスティテューツ |
免疫不全ウイルス転写を調節するための組成物および方法
|
EP2629614B1
(en)
|
2010-10-18 |
2014-09-17 |
E.I. Du Pont De Nemours And Company |
Nematocidal sulfonamides
|
EP2444084A1
(en)
|
2010-10-21 |
2012-04-25 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Use of PI3K inibitors for the treatment of obesity
|
WO2012052745A1
(en)
|
2010-10-21 |
2012-04-26 |
Centro Nacional De Investigaciones Oncológicas (Cnio) |
Combinations of pi3k inhibitors with a second anti -tumor agent
|
WO2012071469A2
(en)
|
2010-11-23 |
2012-05-31 |
Nevada Cancer Institute |
Histone demethylase inhibitors and uses thereof for treatment o f cancer
|
WO2012072713A2
(en)
|
2010-11-30 |
2012-06-07 |
Oryzon Genomics, S.A. |
Lysine demethylase inhibitors for diseases and disorders associated with flaviviridae
|
WO2012080727A2
(en)
|
2010-12-14 |
2012-06-21 |
Electrophoretics Limited |
Casein kinase 1delta (ck1delta) inhibitors
|
UY33805A
(es)
|
2010-12-17 |
2012-07-31 |
Boehringer Ingelheim Int |
?Derivados de dihidrobenzofuranil-piperidinilo, aza-dihidrobenzofuranilpiperidinilo y diaza-dihidrobenzofuranil-piperidinilo, composiciones farmacéuticas que los contienen y usos de los mismos?.
|
WO2012080234A1
(en)
|
2010-12-17 |
2012-06-21 |
Bayer Pharma Aktiengesellschaft |
Substituted 6-imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
|
US20140187548A1
(en)
|
2010-12-17 |
2014-07-03 |
Bayer Intellectual Property Gmbh |
6 substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
|
EP2651946B1
(en)
|
2010-12-17 |
2015-05-27 |
Bayer Intellectual Property GmbH |
2-substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
|
CA2821819A1
(en)
|
2010-12-17 |
2012-06-21 |
Marcus Koppitz |
6-substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
|
US8987271B2
(en)
|
2010-12-22 |
2015-03-24 |
Eutropics Pharmaceuticals, Inc. |
2,2′-biphenazine compounds and methods useful for treating disease
|
TWI617559B
(zh)
|
2010-12-22 |
2018-03-11 |
江蘇恆瑞醫藥股份有限公司 |
2-芳基咪唑并[1,2-b]嗒.2-苯基咪唑并[1,2-a]吡啶,和2-苯基咪唑并[1,2-a]吡衍生物
|
US20140038953A1
(en)
|
2011-01-21 |
2014-02-06 |
The General Hospital Corporation |
Compositions and methods for cardiovascular disease
|
EP3981395A1
(en)
|
2011-02-08 |
2022-04-13 |
Oryzon Genomics, S.A. |
Lysine demethylase inhibitors for myeloproliferative disorders
|
WO2012107499A1
(en)
|
2011-02-08 |
2012-08-16 |
Oryzon Genomics S.A. |
Lysine demethylase inhibitors for myeloproliferative or lymphoproliferative diseases or disorders
|
JP5808826B2
(ja)
|
2011-02-23 |
2015-11-10 |
インテリカイン, エルエルシー |
複素環化合物およびその使用
|
US9464065B2
(en)
|
2011-03-24 |
2016-10-11 |
The Scripps Research Institute |
Compounds and methods for inducing chondrogenesis
|
EP2688568B1
(en)
|
2011-03-25 |
2019-06-19 |
Glaxosmithkline Intellectual Property (No. 2) Limited |
Cyclopropylamines as lsd1 inhibitors
|
WO2012147890A1
(ja)
|
2011-04-27 |
2012-11-01 |
持田製薬株式会社 |
新規アゾール誘導体
|
EP2741741A2
(en)
|
2011-05-19 |
2014-06-18 |
Oryzon Genomics, S.A. |
Lysine demethylase inhibitors for inflammatory diseases or conditions
|
EP2524918A1
(en)
|
2011-05-19 |
2012-11-21 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Imidazopyrazines derivates as kinase inhibitors
|
US20140296255A1
(en)
|
2011-05-19 |
2014-10-02 |
Oryzong Genomics, S.A. |
Lysine demethylase inhibitors for thrombosis and cardiovascular diseases
|
EA201490042A1
(ru)
|
2011-06-20 |
2014-10-30 |
Инсайт Корпорейшн |
Азетидинил-фенил-, пиридил- или пиразинилкарбоксамидные производные как ингибиторы jak
|
TW201311149A
(zh)
|
2011-06-24 |
2013-03-16 |
Ishihara Sangyo Kaisha |
有害生物防治劑
|
EP2548877A1
(en)
|
2011-07-19 |
2013-01-23 |
MSD Oss B.V. |
4-(5-Membered fused pyridinyl)benzamides as BTK-inhibitors
|
AU2012293223B2
(en)
|
2011-08-09 |
2017-03-02 |
Takeda Pharmaceutical Company Limited |
Cyclopropaneamine compound
|
EA026389B1
(ru)
|
2011-08-15 |
2017-04-28 |
Юниверсити Оф Юта Рисерч Фаундейшн |
Замещенные аналоги (e)-n'-(1-фенилэтилиден)бензогидразида в качестве ингибиторов деметилазы гистонов
|
WO2013033688A1
(en)
|
2011-09-01 |
2013-03-07 |
The Brigham And Women's Hospital, Inc. |
Treatment of cancer
|
JP6067019B2
(ja)
|
2011-09-02 |
2017-01-25 |
プロメガ コーポレイションPromega Corporation |
代謝的に活性な細胞の酸化還元状態を評価するための化合物及び方法、ならびにnad(p)/nad(p)hを測定するための方法
|
MA37958B1
(fr)
|
2011-10-10 |
2018-10-31 |
H Lundbeck As |
Pde9i ayant un squelette imidazo pyrazinone
|
PL2776394T3
(pl)
|
2011-10-20 |
2019-06-28 |
Oryzon Genomics, S.A. |
(hetero)arylowe związki cyklopropyloaminowe jako inhibitory lsd1
|
WO2013057320A1
(en)
|
2011-10-20 |
2013-04-25 |
Oryzon Genomics, S.A. |
(hetero)aryl cyclopropylamine compounds as lsd1 inhibitors
|
ITMI20111971A1
(it)
|
2011-10-28 |
2013-04-29 |
Mesogenics Srl |
Inibitori dell'enzima lsd-1 per l'induzione del differenziamento osteogenico
|
US9266881B2
(en)
|
2011-11-14 |
2016-02-23 |
Merck Sharp & Dohme Corp. |
Triazolopyridinone PDE10 inhibitors
|
EP2787990A4
(en)
|
2011-12-05 |
2015-09-02 |
Univ Brandeis |
TREATMENT OF AMYLOIDOSE BY COMPOUNDS FOR REGULATING RETROMER STABILIZATION
|
AU2013230286B2
(en)
|
2012-03-07 |
2016-12-22 |
Merck Patent Gmbh |
Triazolopyrazine derivatives
|
GB201205669D0
(en)
|
2012-03-30 |
2012-05-16 |
Agency Science Tech & Res |
Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof
|
CN103373996A
(zh)
|
2012-04-20 |
2013-10-30 |
山东亨利医药科技有限责任公司 |
作为crth2受体拮抗剂的二并环衍生物
|
ES2710491T3
(es)
|
2012-06-28 |
2019-04-25 |
Novartis Ag |
Moduladores de la vía del complemento y sus usos
|
GB201212513D0
(en)
|
2012-07-13 |
2012-08-29 |
Ucb Pharma Sa |
Therapeutic agents
|
CN105051005B
(zh)
|
2012-10-12 |
2017-06-13 |
武田药品工业株式会社 |
环丙胺化合物及其用途
|
US9757379B2
(en)
|
2012-11-14 |
2017-09-12 |
The Board Of Regents Of The University Of Texas System |
Inhibition of HIF-2α heterodimerization with HIF1β (ARNT)
|
US9388123B2
(en)
|
2012-11-28 |
2016-07-12 |
Kyoto University |
LSD1-selective inhibitor having lysine structure
|
US9144555B2
(en)
|
2012-11-30 |
2015-09-29 |
Darlene E. McCord |
Hydroxytyrosol and oleuropein compositions for induction of DNA damage, cell death and LSD1 inhibition
|
EP2740474A1
(en)
|
2012-12-05 |
2014-06-11 |
Instituto Europeo di Oncologia S.r.l. |
Cyclopropylamine derivatives useful as inhibitors of histone demethylases kdm1a
|
CN103054869A
(zh)
|
2013-01-18 |
2013-04-24 |
郑州大学 |
含三唑基的氨基二硫代甲酸酯化合物在制备以lsd1为靶标药物中的应用
|
CN103933036B
(zh)
|
2013-01-23 |
2017-10-13 |
中国人民解放军军事医学科学院毒物药物研究所 |
2‑芳基咪唑并[1,2‑α]吡啶‑3‑乙酰胺衍生物在制备防治PTSD的药物中的用途
|
JP2016513112A
(ja)
|
2013-02-18 |
2016-05-12 |
ザ スクリプス リサーチ インスティテュート |
治療的潜在能力を有するバソプレッシン受容体のモジュレーター
|
WO2014164867A1
(en)
|
2013-03-11 |
2014-10-09 |
Imago Biosciences |
Kdm1a inhibitors for the treatment of disease
|
CN105283552A
(zh)
|
2013-03-13 |
2016-01-27 |
澳大利亚核科学和技术组织 |
具有非功能性tspo基因的转基因非人类生物体
|
US20140343118A1
(en)
|
2013-03-14 |
2014-11-20 |
Duke University |
Methods of treatment using arylcyclopropylamine compounds
|
EP3003301B1
(en)
|
2013-05-30 |
2021-02-24 |
Board Of Regents Of The Nevada System Of Higher Education On Behalf Of The University Of Nevada, Las Vegas |
Novel suicidal lsd1 inhibitors targeting sox2-expressing cancer cells
|
JP6525162B2
(ja)
|
2013-06-19 |
2019-06-05 |
ザ ユニバーシティ オブ ユタ リサーチ ファウンデイション |
ヒストン脱メチル化酵素阻害剤としての置換(e)−n’−(1−フェニルエチリデン)ベンゾヒドラジド類似体
|
US9186391B2
(en)
|
2013-08-29 |
2015-11-17 |
Musc Foundation For Research Development |
Cyclic peptide inhibitors of lysine-specific demethylase 1
|
WO2015031564A2
(en)
|
2013-08-30 |
2015-03-05 |
University Of Utah |
Substituted-1h-benzo[d]imidazole series compounds as lysine-specfic demethylase 1 (lsd1) inhibitors
|
KR101568724B1
(ko)
|
2013-11-13 |
2015-11-12 |
서울대학교산학협력단 |
신규한 화합물, 이의 생산 방법, 및 히스톤 디메틸라제 저해제로서 이의 용도
|
FI3080100T3
(fi)
|
2013-12-11 |
2023-03-15 |
Celgene Quanticel Res Inc |
Lysiinispesifisen demetylaasi-1:n estäjät
|
ES2656390T3
(es)
*
|
2014-02-12 |
2018-02-27 |
Omnigen Research, Llc |
Composición y método para promover la reducción de estrés por calor en animales
|
CN111454188A
(zh)
|
2014-02-13 |
2020-07-28 |
因赛特公司 |
作为lsd1抑制剂的环丙胺
|
EP3105219B9
(en)
|
2014-02-13 |
2018-10-03 |
Incyte Corporation |
Cyclopropylamines as lsd1 inhibitors
|
US9493450B2
(en)
|
2014-02-13 |
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|
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|
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|
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|
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|
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|
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|
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