|
NL7013068A
(fr)
|
1969-09-17 |
1971-03-19 |
|
|
|
US4537889A
(en)
|
1982-12-27 |
1985-08-27 |
Eli Lilly And Company |
Inotropic agents
|
|
US4625040A
(en)
|
1984-09-24 |
1986-11-25 |
Pennwalt Corporation |
N-(phenyl) or N-(phenylcyclopropyl)-2,5-dihydro-2-oxo-4[(substituted phenyl)amino]-3-furancarboxamide derivatives
|
|
US4614810A
(en)
|
1984-09-24 |
1986-09-30 |
Pennwalt Corporation |
4,5-dihydro-4-oxo-2-[(2-trans-phenylcyclopropyl)amino]-3-furancarboxylic acids and derivatives thereof
|
|
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
|
|
JPH032778Y2
(fr)
|
1986-12-15 |
1991-01-24 |
|
|
|
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
|
|
JP2844351B2
(ja)
|
1989-07-13 |
1999-01-06 |
株式会社科薬 |
安定なポリミキシン系抗生物質水性溶液
|
|
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.
|
|
JPH07507796A
(ja)
|
1992-06-17 |
1995-08-31 |
ファルマシア・アンド・アップジョン・カンパニー |
抗−アテローム性動脈硬化剤および抗−高コレステロール血症剤として有用なピリジノ−,ピロリジノ−,およびアゼピノ−置換オキシム類
|
|
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.
|
|
US5932223A
(en)
|
1996-09-26 |
1999-08-03 |
Merck & Co., Inc. |
Rotavirus vaccine formulations
|
|
CA2310072A1
(fr)
|
1997-11-11 |
1999-05-20 |
Hiroyuki Ohno |
Composes de pyrazine condenses
|
|
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
|
|
PT1218889E
(pt)
|
1999-09-28 |
2010-03-08 |
Panacea Biotec Ltd |
Composições de libertação controlada compreendendo nimesulida
|
|
SE9903611D0
(sv)
|
1999-10-06 |
1999-10-06 |
Astra Ab |
Novel compounds III
|
|
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
|
|
EP1277754B8
(fr)
|
2000-04-27 |
2005-09-28 |
Astellas Pharma Inc. |
Derives d'imidazopyridine
|
|
US6403588B1
(en)
|
2000-04-27 |
2002-06-11 |
Yamanouchi Pharmaceutical Co., Ltd. |
Imidazopyridine derivatives
|
|
EP1294358B1
(fr)
|
2000-06-28 |
2004-08-18 |
Smithkline Beecham Plc |
Procede de broyage par voie humide
|
|
AR029538A1
(es)
|
2000-07-06 |
2003-07-02 |
Wyeth Corp |
Composiciones farmaceuticas de agentes estrogenicos
|
|
EP1301511A2
(fr)
|
2000-07-14 |
2003-04-16 |
Bristol-Myers Squibb Pharma Company |
Imidazo 1,2-a]pyrazines destinees au traitement d'affections neurologiques
|
|
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
|
|
WO2002034748A1
(fr)
|
2000-10-24 |
2002-05-02 |
Sankyo Company, Limited |
Derives d'imidazopyridine
|
|
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
|
|
AU1253002A
(en)
|
2000-11-10 |
2002-05-21 |
Merck Sharp & Dohme |
Imidazo-triazine derivatives as ligands for gaba receptors
|
|
WO2002048146A2
(fr)
|
2000-12-13 |
2002-06-20 |
Basf Aktiengesellschaft |
Utilisation d'imidazoazines substituees, nouvelles imidazoazines, procede permettant de les produire et agents les contenant
|
|
EP1217000A1
(fr)
|
2000-12-23 |
2002-06-26 |
Aventis Pharma Deutschland GmbH |
Inhibiteurs du factor Xa et factor VIIa
|
|
TWI312347B
(en)
|
2001-02-08 |
2009-07-21 |
Eisai R&D Man Co Ltd |
Bicyclic nitrogen-containing condensed ring compounds
|
|
WO2002072549A1
(fr)
|
2001-03-12 |
2002-09-19 |
Millennium Pharmaceuticals, Inc. |
Heterocycles fonctionnalises en tant que modulateurs de la fonction du recepteur de chimiokines et procedes de mise en oeuvre
|
|
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
|
|
CA2473740A1
(fr)
|
2002-01-18 |
2003-07-31 |
David Solow-Cordero |
Procedes pour traiter des pathologies associees a un recepteur d'edg
|
|
US20050113283A1
(en)
|
2002-01-18 |
2005-05-26 |
David Solow-Cordero |
Methods of treating conditions associated with an EDG-4 receptor
|
|
WO2004017950A2
(fr)
|
2002-08-22 |
2004-03-04 |
Piramed Limited |
Inhibiteurs de phosphatidylinositol 3,5-biphosphate en tant qu'agents antiviraux
|
|
UA80296C2
(en)
|
2002-09-06 |
2007-09-10 |
Biogen Inc |
Imidazolopyridines and methods of making and using the same
|
|
WO2005014777A2
(fr)
|
2002-10-16 |
2005-02-17 |
Board Of Regents, The University Of Texas System |
Procedes et compositions pour augmenter l'efficacite de substances actives d'un point de vue biologique
|
|
BR0317430A
(pt)
|
2002-12-20 |
2005-10-25 |
Pharmacia Corp |
Compostos inibidores de quinase-2 de proteìna ativada por quinase de proteìna ativada por mitógeno
|
|
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
|
|
GB0303910D0
(en)
|
2003-02-20 |
2003-03-26 |
Merck Sharp & Dohme |
Therapeutic agents
|
|
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
|
|
JP4736043B2
(ja)
|
2003-03-14 |
2011-07-27 |
小野薬品工業株式会社 |
含窒素複素環誘導体およびそれらを有効成分とする薬剤
|
|
ATE455547T1
(de)
|
2003-04-11 |
2010-02-15 |
High Point Pharmaceuticals Llc |
Pharmazeutische verwendungen von kondensierten 1, 2,4-triazolen
|
|
WO2004089416A2
(fr)
|
2003-04-11 |
2004-10-21 |
Novo Nordisk A/S |
Polytherapie utilisant un inhibiteur de type 1 de la 11beta-hydroxysteroide deshydrogenase et un agent hypotenseur dans le traitement du syndrome metabolique et des troubles et maladies associes
|
|
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
|
|
KR20060056944A
(ko)
|
2003-07-14 |
2006-05-25 |
아레나 파마슈티칼스, 인크. |
대사 조절제로서 융합된 아릴 및 헤테로아릴 유도체 및이에 관련된 장애의 예방 또는 치료
|
|
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
|
|
MXPA06004043A
(es)
|
2003-10-10 |
2006-06-28 |
Pfizer Prod Inc |
2h-[1,2,4]triazolo[4,3-a]pirazinas sustituidas como inhibidores de la glucogeno sintetasa cinasa 3.
|
|
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
|
|
JPWO2005063241A1
(ja)
|
2003-12-26 |
2007-07-19 |
小野薬品工業株式会社 |
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
|
|
WO2005077948A1
(fr)
|
2004-02-16 |
2005-08-25 |
Daiichi Pharmaceutical Co., Ltd. |
Composes heterocycliques fongicides
|
|
US7306631B2
(en)
|
2004-03-30 |
2007-12-11 |
The Procter & Gamble Company |
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
|
|
US8383154B2
(en)
|
2004-05-11 |
2013-02-26 |
Egalet A/S |
Swellable dosage form comprising gellan gum
|
|
WO2006131003A1
(fr)
|
2005-06-09 |
2006-12-14 |
Oncalis Ag |
Inhibiteurs d'angiogenese
|
|
TW200612918A
(en)
|
2004-07-29 |
2006-05-01 |
Threshold Pharmaceuticals Inc |
Lonidamine analogs
|
|
JP2008509985A
(ja)
|
2004-08-18 |
2008-04-03 |
ファルマシア アンド アップジョン カンパニー リミテッド ライアビリティ カンパニー |
炎症治療用の新規トリアゾロピリジン化合物
|
|
EP1799671A4
(fr)
|
2004-09-02 |
2009-06-10 |
Smithkline Beecham Corp |
Composes chimiques
|
|
EP1799680A2
(fr)
|
2004-10-07 |
2007-06-27 |
Warner-Lambert Company LLC |
Derives de triazolopyridine comme agents antibacteriens
|
|
JP2008520719A
(ja)
|
2004-11-22 |
2008-06-19 |
スレショルド ファーマシューティカルズ インコーポレイティッド |
チューブリン結合抗癌剤およびそれらのプロドラッグ
|
|
ES2330872T3
(es)
|
2004-12-01 |
2009-12-16 |
Merck Serono Sa |
Derivados de (1,2,4)triazolo(4,3-a)piridina para el tratamiento de enfermedades hiperproliferativas.
|
|
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
|
|
AU2006217534B8
(en)
|
2005-02-22 |
2011-12-08 |
Pfizer Inc. |
Oxyindole derivatives as 5HT4 receptor agonists
|
|
ITBO20050123A1
(it)
|
2005-03-07 |
2005-06-06 |
Alfa Wassermann Spa |
Formulazioni farmaceutiche gastroresistenti contenenti rifaximina
|
|
EP1871762A2
(fr)
|
2005-04-18 |
2008-01-02 |
Neurogen Corporation |
Antagonistes cb1 heteroaryle substitue
|
|
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
|
|
US7452892B2
(en)
|
2005-06-17 |
2008-11-18 |
Bristol-Myers Squibb Company |
Triazolopyrimidine cannabinoid receptor 1 antagonists
|
|
TW200726765A
(en)
|
2005-06-17 |
2007-07-16 |
Bristol Myers Squibb Co |
Triazolopyridine cannabinoid receptor 1 antagonists
|
|
US7632837B2
(en)
|
2005-06-17 |
2009-12-15 |
Bristol-Myers Squibb Company |
Bicyclic heterocycles as cannabinoid-1 receptor modulators
|
|
EP1928237A4
(fr)
|
2005-09-02 |
2011-03-09 |
Abbott Lab |
Nouveaux heterocycles a base imidazo
|
|
CA2621983A1
(fr)
|
2005-09-09 |
2007-03-22 |
Schering Corporation |
Nouveaux derives 4-cyano, 4-amino, et 4-aminomethyl des composes pyrazolo[1,5-a]pyridine, pyrazolo[1,5-c]pyrimidine et 2h-indazole, et nouveaux derives 5-cyano, 5-amino, et 5-aminomethyl des composes imidazo[1,2-a]pyridine, et imidazo[1,5-a]pyrazine pouvant servir d'inhibiteurs d
|
|
EP1945644A2
(fr)
|
2005-11-10 |
2008-07-23 |
Schering Corporation |
Imidazopyrazines inhibant la proteine kinase
|
|
ES2812250T3
(es)
|
2005-11-28 |
2021-03-16 |
Marinus Pharmaceuticals Inc |
Formulaciones de ganaxolona y procedimientos para la preparación y uso de las mismas
|
|
ATE537171T1
(de)
|
2005-12-27 |
2011-12-15 |
Hoffmann La Roche |
Aryl-isoxazol-4-yl-imidazoä1,5-aüpyridin-deriva e
|
|
WO2007074491A1
(fr)
|
2005-12-28 |
2007-07-05 |
Universita Degli Studi Di Siena |
Derives d’amide heterotricycliques en tant que ligands du recepteur de neurokinine-1 (nk1)
|
|
PE20070978A1
(es)
|
2006-02-14 |
2007-11-15 |
Novartis Ag |
COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE FOSFATIDILINOSITOL 3-QUINASAS (PI3Ks)
|
|
JP2009531390A
(ja)
|
2006-03-31 |
2009-09-03 |
ノバルティス アクチエンゲゼルシャフト |
有機化合物
|
|
JP2009539840A
(ja)
|
2006-06-06 |
2009-11-19 |
シェーリング コーポレイション |
プロテインキナーゼ阻害剤としてのイミダゾピラジン
|
|
US20090175852A1
(en)
|
2006-06-06 |
2009-07-09 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
|
JP2009534396A
(ja)
|
2006-06-22 |
2009-09-24 |
マリンクロッド・インコーポレイテッド |
ピラジン誘導体および腎臓の監視におけるその使用
|
|
US9216963B2
(en)
|
2006-06-22 |
2015-12-22 |
Medibeacon Inc. |
Pyrazine derivatives with extended conjugation and methods of using the same in optical applications
|
|
CA2655720A1
(fr)
|
2006-06-29 |
2008-01-10 |
Schering Corporation |
Antagonistes de recepteur de la thrombine bicycliques et tricycliques substitues
|
|
WO2008005423A1
(fr)
|
2006-07-03 |
2008-01-10 |
Cambrex Charles City, Inc. |
Méthode améliorée de fabrication de sufentanil
|
|
US7501438B2
(en)
|
2006-07-07 |
2009-03-10 |
Forest Laboratories Holdings Limited |
Pyridoimidazole derivatives
|
|
US8217177B2
(en)
|
2006-07-14 |
2012-07-10 |
Amgen Inc. |
Fused heterocyclic derivatives and methods of use
|
|
US8198448B2
(en)
|
2006-07-14 |
2012-06-12 |
Amgen Inc. |
Fused heterocyclic derivatives and methods of use
|
|
PE20121506A1
(es)
|
2006-07-14 |
2012-11-26 |
Amgen Inc |
Compuestos triazolopiridinas como inhibidores de c-met
|
|
BRPI0713187A2
(pt)
|
2006-07-20 |
2012-10-16 |
Mehmet Kahraman |
método de inibir rho-quinase, método de tratamento de doença mediada por rho-quinase, composto e composição farmacêutica
|
|
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
(fr)
|
2006-09-25 |
2008-04-03 |
Basf Se |
Composés hétérocycliques à teneur en groupe carbonyle et leur utilisation pour lutter contre des champignons phytopathogènes
|
|
EP2086973B1
(fr)
|
2006-10-11 |
2012-01-25 |
Amgen Inc., |
Composés d'imidazo- et de triazolo-pyridine et leurs procédés d'utilisation
|
|
DK2081929T3
(da)
|
2006-11-08 |
2013-04-15 |
Neurocrine Biosciences Inc |
Substituerede 3-isobutyl-9,10-dimethoxy-1,3,4,6,7,11B-hexahydro-2H-pyrido[2,1-A]isoquinolin-2-ol-forbindelser og fremgangsmåder angående disse
|
|
CA2669094A1
(fr)
|
2006-11-08 |
2008-05-29 |
Novavax,Inc. |
Procede pour preparer des formes de dosage solides de compositions pharmaceutiques a plusieurs phases
|
|
WO2008056176A1
(fr)
|
2006-11-10 |
2008-05-15 |
Scottish Biomedical Limited |
Pyrazolopyrimidines utiles comme inhibiteurs de la phosphodiestérase
|
|
GEP20125658B
(en)
|
2006-11-22 |
2012-10-10 |
Incyte Corp |
Imidazotriazines and imidazo pyrimidines as kinase inhibitors
|
|
ATE495743T1
(de)
|
2006-12-01 |
2011-02-15 |
Galapagos Nv |
Triazolopyridinverbindungen zur behandlung von degenerations- und entzündungskrankheiten
|
|
CA2673511A1
(fr)
|
2006-12-22 |
2008-07-03 |
Combinatorx, Incorporated |
Compositions pharmaceutiques pour le traitement de la maladie de parkinson et de troubles apparentes
|
|
WO2008110523A1
(fr)
|
2007-03-09 |
2008-09-18 |
Probiodrug Ag |
Dérivés d'imidazo [1,5-a] pyridine comme inhibiteurs de la glutaminyl cyclase
|
|
DE102007012645A1
(de)
|
2007-03-16 |
2008-09-18 |
Bayer Healthcare Ag |
Substituierte Imidazo- und Triazolopyrimidine
|
|
EP1972628A1
(fr)
|
2007-03-21 |
2008-09-24 |
Schwarz Pharma Ag |
Indolizines et leurs dérivés aza analogues en tant que composés actifs du SNC
|
|
JP2010523725A
(ja)
|
2007-04-16 |
2010-07-15 |
レオ ファーマ アクティーゼルスカブ |
皮膚疾患処置用ホスホジエステラーゼ阻害剤としてのトリアゾロピリジン
|
|
US8546394B2
(en)
*
|
2007-04-17 |
2013-10-01 |
Bristol-Myers Squibb Company |
Substituted [1,2,4]triazolo[4,3-A]pyrazine 11-beta-hydroxysteroid dehydrogenase inhibitors
|
|
WO2008141239A1
(fr)
|
2007-05-10 |
2008-11-20 |
Acadia Pharmaceuticals Inc. |
Imidazole [1,2-a] pyridines et composés présentant une activité au niveau des récepteurs cb2 cannabinoïdes
|
|
WO2008143240A1
(fr)
|
2007-05-21 |
2008-11-27 |
Toray Industries, Inc. |
Préparation orale renfermant un acide organique spécifique et procédé d'amélioration de la propriété d'élution et de la stabilité chimique de la préparation orale
|
|
US8648069B2
(en)
|
2007-06-08 |
2014-02-11 |
Abbvie Inc. |
5-substituted indazoles as kinase inhibitors
|
|
CN101790526A
(zh)
|
2007-06-08 |
2010-07-28 |
雅培制药有限公司 |
用作激酶抑制剂的5-杂芳基取代的吲唑化合物
|
|
PE20090365A1
(es)
|
2007-06-14 |
2009-04-04 |
Schering Corp |
Imidazopirazinas como inhibidores de proteina quinasa
|
|
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.
|
|
US20090004281A1
(en)
|
2007-06-26 |
2009-01-01 |
Biovail Laboratories International S.R.L. |
Multiparticulate osmotic delivery system
|
|
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
|
|
KR20100042287A
(ko)
|
2007-07-31 |
2010-04-23 |
쉐링 코포레이션 |
항암요법으로서의 항-유사분열제 및 아우로라 키나제 억제제 조합물
|
|
WO2009017954A1
(fr)
|
2007-08-01 |
2009-02-05 |
Phenomix Corporation |
Inhibiteurs de kinase jak2
|
|
CN101842098A
(zh)
|
2007-08-10 |
2010-09-22 |
基因实验室技术有限公司 |
用于治疗病毒感染的含氮的二环化学实体
|
|
US20090047336A1
(en)
|
2007-08-17 |
2009-02-19 |
Hong Kong Baptist University |
novel formulation of dehydrated lipid vesicles for controlled release of active pharmaceutical ingredient via inhalation
|
|
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.
|
|
KR20090022616A
(ko)
|
2007-08-31 |
2009-03-04 |
한올제약주식회사 |
베실산클로피도그렐 함유 경구투여용 약제
|
|
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
|
|
BRPI0818533B8
(pt)
|
2007-10-11 |
2021-05-25 |
Astrazeneca Ab |
composto, composição farmacêutica, uso de um composto, e, processo para a preparação de um composto
|
|
WO2009048993A2
(fr)
|
2007-10-12 |
2009-04-16 |
Novartis Ag |
Compositions comprenant des modulateurs du récepteur de sphingosine 1-phosphate (s1p)
|
|
EP2231662B1
(fr)
|
2007-12-19 |
2011-06-22 |
Genentech, Inc. |
8-anilinoimidazopyridines et leur utilisation en tant qu'agents anticancéreux et/ou anti-inflammatoires
|
|
US7820665B2
(en)
|
2007-12-19 |
2010-10-26 |
Amgen Inc. |
Imidazopyridazine inhibitors of PI3 kinase for cancer treatment
|
|
KR100988233B1
(ko)
|
2007-12-26 |
2010-10-18 |
한미홀딩스 주식회사 |
클로피도그렐 1,5-나프탈렌 다이술폰산 염 또는 이의수화물의 약학 조성물 및 제제
|
|
MY165582A
(en)
|
2008-03-11 |
2018-04-05 |
Incyte Holdings Corp |
Azetidine and cyclobutane derivatives as jak inhibitors
|
|
ES2530090T3
(es)
|
2008-03-12 |
2015-02-26 |
Intra-Cellular Therapies, Inc. |
Sólido de gamma-carbolinas fusionadas con heterociclo sustituido
|
|
EP2265603B1
(fr)
|
2008-03-13 |
2014-05-07 |
The General Hospital Corporation |
Inhibiteurs de la voie de signalisation bmp
|
|
WO2009114870A2
(fr)
|
2008-03-14 |
2009-09-17 |
Intellikine, Inc. |
Inhibiteurs de kinases, et procédés d’utilisation associés
|
|
US20110105457A1
(en)
|
2008-04-18 |
2011-05-05 |
Shionogi & Co., Ltd. |
Heterocyclic compound having inhibitory activity on pi3k
|
|
DE102008023801A1
(de)
|
2008-05-15 |
2009-11-19 |
Bayer Schering Pharma Aktiengesellschaft |
Substituierte Imidazo- und Triazolopyrimidine, Imidazo- und Pyrazolopyrazine und Imidazotriazine
|
|
US8349210B2
(en)
|
2008-06-27 |
2013-01-08 |
Transitions Optical, Inc. |
Mesogenic stabilizers
|
|
WO2010010188A1
(fr)
|
2008-07-25 |
2010-01-28 |
Galapagos Nv |
Nouveaux composés utiles pour le traitement de maladies dégénératives et inflammatoires
|
|
WO2010010189A1
(fr)
|
2008-07-25 |
2010-01-28 |
Galapagos Nv |
Nouveaux composés utiles pour le traitement de maladies dégénératives et inflammatoires
|
|
WO2010010187A1
(fr)
|
2008-07-25 |
2010-01-28 |
Galapagos Nv |
Nouveaux composés utiles pour le traitement de maladies dégénératives et inflammatoires
|
|
WO2010010184A1
(fr)
|
2008-07-25 |
2010-01-28 |
Galapagos Nv |
[1, 2, 4]triazolo[1, 5-a]pyridines utilisées comme inhibiteurs de jak
|
|
UY32049A
(es)
|
2008-08-14 |
2010-03-26 |
Takeda Pharmaceutical |
Inhibidores de cmet
|
|
TR200806298A2
(tr)
|
2008-08-22 |
2010-03-22 |
Bi̇lgi̇ç Mahmut |
Farmasötik formülasyon
|
|
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
|
|
WO2010033906A2
(fr)
|
2008-09-19 |
2010-03-25 |
President And Fellows Of Harvard College |
Induction efficace de cellules souches pluripotentes au moyen de composés à petite molécule
|
|
WO2010036380A1
(fr)
|
2008-09-26 |
2010-04-01 |
Intellikine, Inc. |
Inhibiteurs hétérocycliques de kinases
|
|
WO2010043721A1
(fr)
|
2008-10-17 |
2010-04-22 |
Oryzon Genomics, S.A. |
Inhibiteurs d’oxydases et leur utilisation
|
|
WO2010048149A2
(fr)
|
2008-10-20 |
2010-04-29 |
Kalypsys, Inc. |
Modulateurs hétérocycliques de gpr119 pour le traitement d'une maladie
|
|
ES2403633T3
(es)
|
2008-12-04 |
2013-05-20 |
Proximagen Limited |
Compuestos de imidazopiridina
|
|
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
|
|
WO2010090991A1
(fr)
|
2009-02-04 |
2010-08-12 |
Supernus Pharmaceuticals, Inc. |
Formulations de desvenlafaxine
|
|
US8598163B2
(en)
|
2009-02-04 |
2013-12-03 |
Vitae Pharmaceuticals, Inc. |
Derivatives of [1,3]Oxazin-2-one useful for the treatment of metabolic diseases such as lipid disorders
|
|
TR200900878A2
(tr)
|
2009-02-05 |
2010-08-23 |
Bi̇lgi̇ç Mahmut |
Tek bir dozaj formunda kombine edilen farmasötik formülasyonlar
|
|
TR200900879A2
(tr)
|
2009-02-05 |
2010-08-23 |
Bi̇lgi̇ç Mahmut |
Aktif maddelerin tek bir dozaj formunda kombine edildiği farmasötik bileşimler
|
|
US20130310362A1
(en)
|
2009-02-13 |
2013-11-21 |
Bayer Pharma Aktiegesellschaft |
Fused pyrimidines
|
|
WO2010104306A2
(fr)
|
2009-03-07 |
2010-09-16 |
주식회사 메디젠텍 |
Compositions pharmaceutiques pour traiter ou prévenir des maladies causées par la translocation de gsk3 du noyau cellulaire au cytoplasme, contenant des composés inhibant la translocation de gsk3 du noyau cellulaire au cytoplasme
|
|
WO2010107404A1
(fr)
|
2009-03-16 |
2010-09-23 |
Mahmut Bilgic |
Combinaisons pharmaceutiques stables
|
|
TW201035078A
(en)
|
2009-03-20 |
2010-10-01 |
Incyte Corp |
Substituted heterocyclic compounds
|
|
BRPI1013432B1
(pt)
|
2009-03-31 |
2019-12-17 |
Kissei Pharmaceutical |
derivado de indolizina e composição farmacêutica
|
|
NZ596185A
(en)
|
2009-04-16 |
2013-01-25 |
Ct Nac Investigaciones Oncologicas Cnio |
Imidazopyrazines for use as kinase inhibitors
|
|
TWI461426B
(zh)
|
2009-05-27 |
2014-11-21 |
Merck Sharp & Dohme |
(二氫)咪唑並異〔5,1-a〕喹啉類
|
|
KR20120035183A
(ko)
|
2009-06-10 |
2012-04-13 |
선오비온 파마슈티컬스 인코포레이티드 |
히스타민 h3 역 작용제 및 길항제, 및 이의 사용 방법
|
|
JP5732453B2
(ja)
|
2009-06-25 |
2015-06-10 |
アルカーメス ファーマ アイルランド リミテッド |
Nh酸性化合物のプロドラッグ
|
|
UA111579C2
(uk)
|
2009-08-17 |
2016-05-25 |
Інтеллікіне Ллк |
ГЕТЕРОЦИКЛІЧНІ ПОХІДНІ 2-АМІНОБЕНЗО[d]ОКСАЗОЛУ, ФАРМАЦЕВТИЧНА КОМПОЗИЦІЯ НА ЇХ ОСНОВІ ТА ЇХ ЗАСТОСУВАННЯ ДЛЯ ЛІКУВАННЯ ЗАХВОРЮВАННЯ, ПОВ'АНОГО З РІ3-КІНАЗОЮ
|
|
AU2010284221B2
(en)
|
2009-08-18 |
2016-09-22 |
Casero, Robert A |
(bis) urea and (bis) thiourea compounds as epigenic modulators of lysine-specific demethylase 1 and methods of treating disorders
|
|
EP2473495A1
(fr)
|
2009-09-18 |
2012-07-11 |
Almac Discovery Limited |
Composés pharmaceutiques
|
|
WO2011035941A1
(fr)
|
2009-09-25 |
2011-03-31 |
Oryzon Genomics S.A. |
Inhibiteurs de déméthylase-1 spécifique de la lysine et leur utilisation
|
|
US8946296B2
(en)
|
2009-10-09 |
2015-02-03 |
Oryzon Genomics S.A. |
Substituted heteroaryl- and aryl-cyclopropylamine acetamides and their use
|
|
WO2011050245A1
(fr)
|
2009-10-23 |
2011-04-28 |
Yangbo Feng |
Hétéroaryles bicycliques formant inhibiteurs de la kinase
|
|
US8541404B2
(en)
|
2009-11-09 |
2013-09-24 |
Elexopharm Gmbh |
Inhibitors of the human aldosterone synthase CYP11B2
|
|
US8614315B2
(en)
|
2009-12-25 |
2013-12-24 |
Mahmut Bilgic |
Cefdinir and cefixime formulations and uses thereof
|
|
CA2787714C
(fr)
|
2010-01-22 |
2019-04-09 |
Joaquin Pastor Fernandez |
Inhibiteurs de la pi3 kinase
|
|
WO2011097607A1
(fr)
|
2010-02-08 |
2011-08-11 |
Southern Research Institute |
Traitement antiviral et dosage pour cribler des antiviraux
|
|
WO2011106574A2
(fr)
|
2010-02-24 |
2011-09-01 |
Oryzon Genomics, S.A. |
Inhibiteurs destinés à une utilisation antivirale
|
|
WO2011106106A2
(fr)
|
2010-02-24 |
2011-09-01 |
Oryzon Genomics, S.A. |
Inhibiteurs de lysine déméthylase pour lutter contre les maladies et troubles associés à l'hepadnaviridae
|
|
TW201200518A
(en)
|
2010-03-10 |
2012-01-01 |
Kalypsys Inc |
Heterocyclic inhibitors of histamine receptors for the treatment of disease
|
|
RU2576662C2
(ru)
|
2010-03-18 |
2016-03-10 |
Энститю Пастер Корея |
Противоинфекционные соединения
|
|
ES2551407T3
(es)
|
2010-03-18 |
2015-11-18 |
Bayer Intellectual Property Gmbh |
Imidazopirazinas
|
|
CA2793313C
(fr)
|
2010-04-02 |
2018-01-23 |
Euroscreen Sa |
Composes antagonistes selectifs du recepteur nk-3, composition pharmaceutique et methodes pour une utilisation dans des troubles a mediation par des recepteurs nk-3
|
|
RS55348B1
(sr)
|
2010-04-19 |
2017-03-31 |
Oryzon Gnomics S A |
Inhibitori lizin specifične demetilaze-1 i njihova upotreba
|
|
US8765820B2
(en)
|
2010-04-20 |
2014-07-01 |
Universita Degli Studi Di Roma “La Sapienza” |
Tranylcypromine derivatives as inhibitors of histone demethylases LSD1 and/or LSD2
|
|
JPWO2011136264A1
(ja)
|
2010-04-28 |
2013-07-22 |
第一三共株式会社 |
[5,6]複素環化合物
|
|
US20130131057A1
(en)
|
2010-05-13 |
2013-05-23 |
Centro Nacional De Investigaciones Oncologicas (Cnio |
New bicyclic compounds as pi3-k and mtor inhibitors
|
|
CN103221404B
(zh)
|
2010-05-13 |
2015-12-16 |
安姆根有限公司 |
可用作pde10抑制剂的不饱和氮杂环化合物
|
|
CN102247321A
(zh)
|
2010-05-20 |
2011-11-23 |
上海亚盛医药科技有限公司 |
一种阿朴棉子酚酮自乳化药物传递系统及其制备方法
|
|
WO2011149438A1
(fr)
|
2010-05-28 |
2011-12-01 |
Mahmut Bilgic |
Combinaison d'agents antihypertenseurs
|
|
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
|
|
EP2588197B1
(fr)
|
2010-07-02 |
2014-11-05 |
Gilead Sciences, Inc. |
Composés hétérocycliques condensés en tant que modulateurs des canaux ioniques
|
|
CA2804845A1
(fr)
|
2010-07-12 |
2012-01-19 |
Stuart Ince |
Imidazo[1,2-a]pyrimidines et -pyridines substitues
|
|
WO2012009475A1
(fr)
|
2010-07-14 |
2012-01-19 |
Oregon Health & Science University |
Méthodes de traitement du cancer par inhibition de la déméthylase 1 spécifique de la lysine
|
|
CN101987082B
(zh)
|
2010-07-16 |
2013-04-03 |
钟术光 |
固体制剂及其制备方法
|
|
CN101987081B
(zh)
|
2010-07-16 |
2012-08-08 |
钟术光 |
一种控释制剂
|
|
DK2598482T3
(en)
|
2010-07-29 |
2018-06-14 |
Oryzon Genomics Sa |
ARYLCYCLOPROPYLAMINE-BASED DEMETHYLASE INHIBITORS OF LSD1 AND THEIR MEDICAL USE
|
|
WO2012016133A2
(fr)
|
2010-07-29 |
2012-02-02 |
President And Fellows Of Harvard College |
Inhibiteurs de la ros1 kinase pour le traitement de glioblastome et d'autres cancers déficients en p53
|
|
EP2598480B1
(fr)
|
2010-07-29 |
2019-04-24 |
Oryzon Genomics, S.A. |
Dérivés de cyclopropylamine utiles en tant qu'inhibiteurs de lsd1
|
|
WO2012034116A2
(fr)
|
2010-09-10 |
2012-03-15 |
The Johns Hopkins University |
Petites molécules à titre de modulateurs épigénétiques de la déméthylase 1 spécifique de la lysine et méthodes de traitement de troubles
|
|
CN102397552B
(zh)
|
2010-09-10 |
2016-06-08 |
广州自远生物科技有限公司 |
一种含喹诺酮类的药物复合制剂及其制备方法和应用
|
|
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
|
|
US20120108500A1
(en)
|
2010-10-07 |
2012-05-03 |
Naoki Sakane |
Compositions and Methods for Modulating Immunodeficiency Virus Transcription
|
|
KR101941300B1
(ko)
|
2010-10-18 |
2019-01-22 |
이 아이 듀폰 디 네모아 앤드 캄파니 |
살선충성 설폰아미드
|
|
EP2444084A1
(fr)
|
2010-10-21 |
2012-04-25 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Utilisation d'inhibiteurs de PI3K pour le traitement de l'obésité
|
|
CN103282365B
(zh)
|
2010-10-21 |
2017-12-29 |
麦迪韦逊科技有限公司 |
结晶的(8S,9R)‑5‑氟‑8‑(4‑氟苯基)‑9‑(1‑甲基‑1H‑1,2,4‑三唑‑5‑基)‑8,9‑二氢‑2H‑吡啶并[4,3,2‑de]酞嗪‑3(7H)‑酮甲苯磺酸盐
|
|
WO2012052745A1
(fr)
|
2010-10-21 |
2012-04-26 |
Centro Nacional De Investigaciones Oncológicas (Cnio) |
Combinaisons d'inhibiteurs de pi3k avec un second agent antitumoral
|
|
WO2012071469A2
(fr)
|
2010-11-23 |
2012-05-31 |
Nevada Cancer Institute |
Inhibiteurs d'histone déméthylase et utilisations de ceux-ci pour le traitement de cancer
|
|
WO2012072713A2
(fr)
|
2010-11-30 |
2012-06-07 |
Oryzon Genomics, S.A. |
Inhibiteurs de la déméthylase spécifique de la lysine pour des maladies et troubles liés aux flaviviridés
|
|
EP2651405A2
(fr)
|
2010-12-14 |
2013-10-23 |
Electrophoretics Limited |
Inhibiteurs de caséine kinase 1 (ck1 )
|
|
US20140135319A1
(en)
|
2010-12-17 |
2014-05-15 |
Bayer Intellectual Property Gmbh |
6-substituted 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
|
|
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?.
|
|
US9284317B2
(en)
|
2010-12-17 |
2016-03-15 |
Bayer Intellectual Property Gmbh |
Substituted imidazo[1,2-a]pyrazines as MPS-1 inhibitors
|
|
WO2012080232A1
(fr)
|
2010-12-17 |
2012-06-21 |
Bayer Pharma Aktiengesellschaft |
Imidazopyrazines 2-substituées pour l'utilisation en tant qu'inhibiteurs de mps-1 et de tkk dans le traitement de troubles d'hyperprolifération
|
|
EP2655334B1
(fr)
|
2010-12-22 |
2018-10-03 |
Eutropics Pharmaceuticals, Inc. |
Compositions et méthodes utilisables en vue du traitement de maladies
|
|
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
|
|
JP2014504604A
(ja)
|
2011-01-21 |
2014-02-24 |
ザ ジェネラル ホスピタル コーポレイション |
心血管疾患のための組成物および方法
|
|
US20140163041A1
(en)
|
2011-02-08 |
2014-06-12 |
Oryzon Genomics S.A. |
Lysine demethylase inhibitors for myeloproliferative or lymphoproliferative diseases or disorders
|
|
EP2712315B1
(fr)
|
2011-02-08 |
2021-11-24 |
Oryzon Genomics, S.A. |
Inhibiteurs de lysine déméthylase pour des troubles myéloprolifératifs
|
|
WO2012116237A2
(fr)
|
2011-02-23 |
2012-08-30 |
Intellikine, Llc |
Composés hétérocycliques et leurs utilisations
|
|
BRPI1101013A2
(pt)
|
2011-03-03 |
2013-06-04 |
Luciano Rabinowicz |
composiÇço para preparo de bebida energÉtica e bebida energÉtica
|
|
WO2012129562A2
(fr)
|
2011-03-24 |
2012-09-27 |
The Scripps Research Institute |
Composés et procédés pour l'induction de la chondrogenèse
|
|
MX347913B
(es)
|
2011-03-25 |
2017-05-17 |
Glaxosmithkline Intellectual Property (No 2) Ltd |
Ciclopropilaminas como inhibidores de desmetilasa 1 especifica de lisina.
|
|
WO2012147890A1
(fr)
|
2011-04-27 |
2012-11-01 |
持田製薬株式会社 |
Nouveau dérivé d'azole
|
|
WO2012156531A2
(fr)
|
2011-05-19 |
2012-11-22 |
Oryzon Genomics, S.A. |
Inhibiteurs de la lysine déméthylase destinés au traitement de maladies ou états inflammatoires
|
|
EP2750671A2
(fr)
|
2011-05-19 |
2014-07-09 |
Oryzon Genomics, S.A. |
Inhibiteurs de la lysine déméthylase destinés au traitement de la thrombose et de maladies cardiovasculaires
|
|
EP2524918A1
(fr)
|
2011-05-19 |
2012-11-21 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Imidazopyrazines en tant qu'inhibiteurs de kinase
|
|
CN103687496A
(zh)
|
2011-06-07 |
2014-03-26 |
Spai集团有限公司 |
用于改善敏感性食品添加剂及其食品产品的稳定性并且延长其货架期的组合物和方法
|
|
US8691807B2
(en)
|
2011-06-20 |
2014-04-08 |
Incyte Corporation |
Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as JAK inhibitors
|
|
TW201311149A
(zh)
|
2011-06-24 |
2013-03-16 |
Ishihara Sangyo Kaisha |
有害生物防治劑
|
|
EP2548877A1
(fr)
|
2011-07-19 |
2013-01-23 |
MSD Oss B.V. |
Dérivés de 4-(pyridine condensée à 5 chaînons)benzamide comme inhibiteurs de BTK
|
|
BR112014002939A2
(pt)
|
2011-08-09 |
2017-03-01 |
Takeda Pharmaceuticals Co |
composto, medicamento, método para profilaxia ou tratamento de doença, a doença sendo esquizofrenia, alzheimer, parkinson ou huntington, uso do composto, e, método para inibir o lsd1
|
|
AU2012296639B2
(en)
|
2011-08-15 |
2016-06-09 |
University Of Utah Research Foundation |
Substituted (E)-N'-(1-phenylethylidene) benzohydrazide analogs as histone demethylase inhibitors
|
|
US9289415B2
(en)
|
2011-09-01 |
2016-03-22 |
The Brigham And Women's Hospital, Inc. |
Treatment of cancer
|
|
US9273343B2
(en)
|
2011-09-02 |
2016-03-01 |
Promega Corporation |
Compounds and methods for assaying redox state of metabolically active cells and methods for measuring NAD(P)/NAD(P)H
|
|
MX381326B
(es)
|
2011-10-10 |
2025-03-12 |
H Lundbeck As |
Derivados de 7h-imidazo[1-5-a]pirazin-8-ona como inhibidores de la fosfodiesterasa 9(pde9); y el uso de los mismos en el tratamiento de trastornos neurodegenerativos
|
|
CL2014000988A1
(es)
|
2011-10-20 |
2014-11-03 |
Oryzon Genomics Sa |
Compuestos derivados de (aril o heteroaril) ciclopropilamida, inhibidores de lsd1; procedimiento para prepararlos; composicion farmaceutica que los comprende; y metodo para tratar o prevenir cancer, una enfermedad neurologica, una infeccion viral y la reactivacion viral despues de la latencia.
|
|
US9469597B2
(en)
|
2011-10-20 |
2016-10-18 |
Oryzon Genomics S.A. |
(Hetero)aryl cyclopropylamine compounds as LSD1 inhibitors
|
|
AU2012324803B9
(en)
|
2011-10-20 |
2017-08-24 |
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
|
|
WO2013074390A1
(fr)
|
2011-11-14 |
2013-05-23 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de pde10 de triazolopyridinone
|
|
CA2857964A1
(fr)
|
2011-12-05 |
2013-06-13 |
Brandeis University |
Traitement de l'amyloidose au moyen de composes qui regulent la stabilisation de retromeres
|
|
EP2822948B1
(fr)
|
2012-03-07 |
2016-04-06 |
Merck Patent GmbH |
Dérivés de triazolopyrazine
|
|
CN102579381B
(zh)
|
2012-03-30 |
2013-07-10 |
河南中帅医药科技发展有限公司 |
盐酸胍法辛缓释制剂及其制备方法
|
|
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
|
|
WO2014002051A2
(fr)
|
2012-06-28 |
2014-01-03 |
Novartis Ag |
Modulateurs de la voie du complément et leurs utilisations
|
|
CN102772444A
(zh)
|
2012-07-06 |
2012-11-14 |
周明千 |
中药超微破壁口服片剂饮片的加工方法
|
|
GB201212513D0
(en)
|
2012-07-13 |
2012-08-29 |
Ucb Pharma Sa |
Therapeutic agents
|
|
JP6430383B2
(ja)
|
2012-09-28 |
2018-11-28 |
ヴァンダービルト ユニバーシティーVanderbilt University |
選択的bmp阻害剤としての縮合複素環化合物
|
|
JP6457942B2
(ja)
|
2012-10-05 |
2019-01-23 |
ライジェル ファーマシューティカルズ, インコーポレイテッド |
Gdf−8阻害剤
|
|
EP2907802B1
(fr)
|
2012-10-12 |
2019-08-07 |
Takeda Pharmaceutical Company Limited |
Composé de cyclopropanamine et utilisation de celui-ci
|
|
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)
|
|
WO2014084298A1
(fr)
|
2012-11-28 |
2014-06-05 |
京都府公立大学法人 |
Inhibiteur sélectif de lsd1 à structure lysine
|
|
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
(fr)
|
2012-12-05 |
2014-06-11 |
Instituto Europeo di Oncologia S.r.l. |
Dérivés de cyclopropylamine utiles comme inhibiteurs d'histone-déméthylases kdm1a
|
|
MX360420B
(es)
|
2012-12-19 |
2018-10-31 |
Wockhardt Ltd |
Una composicion acuosa estable que comprende insulina humana o un analogo o derivado de la misma.
|
|
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
|
|
US20150376198A1
(en)
|
2013-02-18 |
2015-12-31 |
The Scripps Research Institute |
Modulators of vasopressin receptors with therapeutic potential
|
|
US8558008B2
(en)
|
2013-02-28 |
2013-10-15 |
Dermira, Inc. |
Crystalline glycopyrrolate tosylate
|
|
WO2014164867A1
(fr)
|
2013-03-11 |
2014-10-09 |
Imago Biosciences |
Inhibiteurs de kdm1a pour le traitement d'une maladie
|
|
AU2014231768A1
(en)
|
2013-03-13 |
2015-09-24 |
Australian Nuclear Science And Technology Organisation |
Transgenic non-human organisms with non-functional TSPO genes
|
|
JP2016517434A
(ja)
|
2013-03-14 |
2016-06-16 |
エピザイム,インコーポレイティド |
癌を処置するための併用療法
|
|
US20140343118A1
(en)
|
2013-03-14 |
2014-11-20 |
Duke University |
Methods of treatment using arylcyclopropylamine compounds
|
|
US9918983B2
(en)
|
2013-05-30 |
2018-03-20 |
The Board Of Regents Of The Nevada System Of Higher Education On Behalf Of The University Of Nevada, Las Vegas |
Suicidal LSD1 inhibitors targeting SOX2-expressing cancer cells
|
|
CN105555784B
(zh)
|
2013-06-19 |
2019-03-15 |
犹他大学研究基金会 |
作为组蛋白去甲基化酶抑制剂的被取代的(e)-n’-(1-苯亚乙基)苯甲酰肼类似物
|
|
SMT202000071T1
(it)
|
2013-06-21 |
2020-03-13 |
Myokardia Inc |
Composti di pirimidinadione contro le condizioni cardiache
|
|
US9186391B2
(en)
|
2013-08-29 |
2015-11-17 |
Musc Foundation For Research Development |
Cyclic peptide inhibitors of lysine-specific demethylase 1
|
|
WO2015031564A2
(fr)
|
2013-08-30 |
2015-03-05 |
University Of Utah |
Composés de la série des 1h-benzo[d]imidazoles substitués à titre d'inhibiteurs de déméthylase 1 spécifique de la lysine (lsd1)
|
|
US9770514B2
(en)
|
2013-09-03 |
2017-09-26 |
ExxPharma Therapeutics LLC |
Tamper-resistant pharmaceutical dosage forms
|
|
EP3043778B1
(fr)
|
2013-09-13 |
2017-09-06 |
Bayer Pharma Aktiengesellschaft |
Compositions pharmaceutiques contenant du refametinib
|
|
KR101568724B1
(ko)
|
2013-11-13 |
2015-11-12 |
서울대학교산학협력단 |
신규한 화합물, 이의 생산 방법, 및 히스톤 디메틸라제 저해제로서 이의 용도
|
|
CA3161836A1
(fr)
|
2013-12-11 |
2015-06-18 |
Celgene Quanticel Research, Inc. |
Inhibiteur de la demethylase-1 specifique de la lysine
|
|
PT3110437T
(pt)
|
2014-02-12 |
2018-01-16 |
Omnigen Res Llc |
Composição e método para promover a redução do stress térmico em animais
|
|
EP3392244A1
(fr)
|
2014-02-13 |
2018-10-24 |
Incyte Corporation |
Cyclopropylamines en tant qu'inhibiteurs de lsd1
|
|
US9428470B2
(en)
|
2014-02-13 |
2016-08-30 |
Takeda Pharmaceutical Company Limited |
Heterocyclic compound
|
|
WO2015123424A1
(fr)
|
2014-02-13 |
2015-08-20 |
Incyte Corporation |
Cyclopropylamines en tant qu'inhibiteurs de lsd1
|
|
US9346776B2
(en)
|
2014-02-13 |
2016-05-24 |
Takeda Pharmaceutical Company Limited |
Fused heterocyclic compound
|
|
US9527835B2
(en)
|
2014-02-13 |
2016-12-27 |
Incyte Corporation |
Cyclopropylamines as LSD1 inhibitors
|
|
LT3105218T
(lt)
|
2014-02-13 |
2019-12-10 |
Incyte Corp |
Ciklopropilaminai kaip lsd1 inhibitoriai
|
|
WO2015145145A1
(fr)
|
2014-03-24 |
2015-10-01 |
Cipla Limited |
Composition pharmaceutique contenant du lapatinib
|
|
CN103893163B
(zh)
|
2014-03-28 |
2016-02-03 |
中国药科大学 |
2-([1,1′-联苯]-4-基)2-氧代乙基4-((3-氯-4-甲基苯基)氨基)-4-氧代丁酸酯在制备lsd1抑制剂药物中的应用
|
|
CA2944466C
(fr)
|
2014-04-02 |
2020-06-09 |
Bristol-Myers Squibb Company |
Inhibiteurs biaryle de kinase
|
|
NZ725262A
(en)
|
2014-04-11 |
2023-01-27 |
Takeda Pharmaceuticals Co |
Cyclopropanamine compound and use thereof
|
|
EP2929884A1
(fr)
|
2014-04-11 |
2015-10-14 |
Sanovel Ilac Sanayi ve Ticaret A.S. |
Combinaisons pharmaceutiques de dabigatran et antagonistes du récepteur de h2
|
|
US10130618B2
(en)
|
2014-04-11 |
2018-11-20 |
Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi |
Pharmaceutical combinations of dabigatran and proton pump inhibitors
|
|
CN103961340B
(zh)
|
2014-04-30 |
2019-06-25 |
南通中国科学院海洋研究所海洋科学与技术研究发展中心 |
一类lsd1抑制剂及其应用
|
|
MX375102B
(es)
|
2014-05-30 |
2025-03-06 |
Ieo St Europeo Di Oncologia S R L |
Compuestos de ciclopropilamina como inhibidores de histona demetilasa
|
|
CN104119280B
(zh)
|
2014-06-27 |
2016-03-16 |
郑州大学 |
含氨基类脲与端炔结构单元的嘧啶衍生物、制备方法及应用
|
|
WO2016007736A1
(fr)
*
|
2014-07-10 |
2016-01-14 |
Incyte Corporation |
Imidazopyrazines en tant qu'inhibiteurs de lsd1
|
|
US9758523B2
(en)
|
2014-07-10 |
2017-09-12 |
Incyte Corporation |
Triazolopyridines and triazolopyrazines as LSD1 inhibitors
|
|
WO2016007722A1
(fr)
|
2014-07-10 |
2016-01-14 |
Incyte Corporation |
Triazolopyridines et triazolopyrazines utilisables comme inhibiteurs de lsd1
|
|
WO2016007731A1
(fr)
*
|
2014-07-10 |
2016-01-14 |
Incyte Corporation |
Imidazopyridines et imidazopyrazines à utiliser en tant qu'inhibiteurs de lsd1
|
|
GB201417828D0
(en)
|
2014-10-08 |
2014-11-19 |
Cereno Scient Ab |
New methods and compositions
|
|
CN104173313B
(zh)
|
2014-08-25 |
2017-05-17 |
杭州朱养心药业有限公司 |
利伐沙班片剂药物组合物
|
|
JP6653116B2
(ja)
|
2014-08-27 |
2020-02-26 |
日本ケミファ株式会社 |
オルメサルタンのプロドラッグ製剤
|
|
CR20170118A
(es)
|
2014-10-08 |
2017-07-10 |
Hoffmann La Roche |
Derivados espirodiamina como inhibidores de la aldosterona sintasa
|
|
EA201792205A1
(ru)
|
2015-04-03 |
2018-02-28 |
Инсайт Корпорейшн |
Гетероциклические соединения как ингибиторы lsd1
|
|
MX2017012738A
(es)
|
2015-04-03 |
2017-11-15 |
Bristol Myers Squibb Co |
Inhibidores de indolamina 2.3-dioxigenasa (ido) para el tratamiento de cancer.
|
|
EP3277277B1
(fr)
|
2015-04-03 |
2021-01-06 |
Mutabilis |
Nouveaux composés hétérocycliques et leur utilisation dans la prévention ou le traitement d'infections bactériennes
|
|
DK3334709T3
(da)
|
2015-08-12 |
2025-02-03 |
Incyte Holdings Corp |
Salte af en lsd1-hæmmer
|
|
CN105232488B
(zh)
|
2015-10-15 |
2021-05-04 |
上海凌凯医药科技有限公司 |
一种含有利伐沙班的固体药物组合物
|
|
KR102720551B1
(ko)
|
2015-12-29 |
2024-10-21 |
미라티 테라퓨틱스, 인크. |
Lsd1 억제제
|
|
JPWO2017130933A1
(ja)
|
2016-01-25 |
2018-11-29 |
国立大学法人 熊本大学 |
神経変性疾患治療剤
|
|
CA3021678A1
(fr)
|
2016-04-22 |
2017-10-26 |
Incyte Corporation |
Formulations d'un inhibiteur de lsd1
|
|
US20200054643A1
(en)
|
2017-01-18 |
2020-02-20 |
Vanderbilt University |
Fused heterocyclic compounds as selective bmp inhibitors
|
|
KR20190129851A
(ko)
|
2017-03-16 |
2019-11-20 |
지앙수 헨그루이 메디슨 컴퍼니 리미티드 |
헤테로아릴[4,3-c]피리미딘-5-아민 유도체, 이의 제조 방법 및 이의 의학적 용도
|
|
CN117304191A
(zh)
|
2018-07-05 |
2023-12-29 |
因赛特公司 |
作为a2a/a2b抑制剂的稠合吡嗪衍生物
|
|
US10968200B2
(en)
|
2018-08-31 |
2021-04-06 |
Incyte Corporation |
Salts of an LSD1 inhibitor and processes for preparing the same
|