NL7013068A
(hu)
|
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
(hu)
|
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.
|
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.
|
US5932223A
(en)
|
1996-09-26 |
1999-08-03 |
Merck & Co., Inc. |
Rotavirus vaccine formulations
|
US6451796B1
(en)
|
1997-11-11 |
2002-09-17 |
Ono Pharmaceutical Co., Ltd. |
Fused pyrazine compounds
|
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
|
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
|
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
|
CZ20021076A3
(cs)
|
1999-09-28 |
2002-08-14 |
Panacea Biotec Limited |
Prostředky s kontrolovaným uvolňováním obsahující nimesulid
|
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
|
DK1277754T3
(da)
|
2000-04-27 |
2005-11-14 |
Astellas Pharma Inc |
Imidazopyridinderivater
|
US6403588B1
(en)
|
2000-04-27 |
2002-06-11 |
Yamanouchi Pharmaceutical Co., Ltd. |
Imidazopyridine derivatives
|
CA2413330A1
(en)
|
2000-06-28 |
2002-01-03 |
Smithkline Beecham P.L.C. |
Wet milling process
|
AR029538A1
(es)
|
2000-07-06 |
2003-07-02 |
Wyeth Corp |
Composiciones farmaceuticas de agentes estrogenicos
|
AU2001276903A1
(en)
|
2000-07-14 |
2002-01-30 |
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
|
WO2002034748A1
(en)
|
2000-10-24 |
2002-05-02 |
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
|
JP4302980B2
(ja)
|
2000-11-10 |
2009-07-29 |
メルク シャープ エンド ドーム リミテッド |
Gaba受容体リガンドとしてのイミダゾ−トリアジン誘導体
|
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
|
EP1377549A1
(en)
|
2001-03-12 |
2004-01-07 |
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
|
CA2473740A1
(en)
|
2002-01-18 |
2003-07-31 |
David Solow-Cordero |
Methods of treating conditions associated with an edg receptor
|
AU2003255845A1
(en)
|
2002-08-22 |
2004-03-11 |
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
|
CA2502148A1
(en)
|
2002-10-16 |
2005-02-17 |
Board Of Regents, The University Of Texas System |
Methods and compositions for increasing the efficacy of biologically-active ingredients
|
MXPA05006569A
(es)
|
2002-12-20 |
2005-09-22 |
Pharmacia Corp |
Compuestos que inhiben la proteina cinasa-2 activada por la proteina cinasa activada por el mitogeno.
|
US7160885B2
(en)
|
2003-02-10 |
2007-01-09 |
Cgi Pharmaceuticals, Inc. |
Certain 6, 8-(heteroaryl or aryl) disubstituted imidazo[1,2-a]pyrazines as modulators of Hsp90 complex 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
|
TW201018661A
(en)
|
2003-03-14 |
2010-05-16 |
Ono Pharmaceutical Co |
Heterocyclic rinf having nitrogen atom derivatives and medicament containing the derivatives as active ingredient
|
DE602004025220D1
(de)
|
2003-04-11 |
2010-03-11 |
High Point Pharmaceuticals Llc |
Pharmazeutische verwendungen von kondensierten 1,2,4-triazolen
|
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
|
CN1809354A
(zh)
|
2003-04-24 |
2006-07-26 |
麦克公司 |
Akt活性抑制剂
|
SE0301653D0
(sv)
|
2003-06-05 |
2003-06-05 |
Astrazeneca Ab |
Novel compounds
|
CA2532971A1
(en)
|
2003-07-14 |
2005-01-27 |
Arena Pharmaceuticals, Inc. |
Fused-aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto
|
US7538120B2
(en)
|
2003-09-03 |
2009-05-26 |
Array Biopharma Inc. |
Method of treating inflammatory diseases
|
WO2005025558A1
(en)
|
2003-09-12 |
2005-03-24 |
Applied Reserach Systems Ars Holding N.V. |
Sulfonamide derivatives for the treatment of 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
|
CA2543707A1
(en)
|
2003-10-31 |
2005-05-19 |
Takeda Pharmaceutical Company Limited |
Nitrogen-containing fused heterocyclic compounds
|
US20080249154A1
(en)
|
2003-12-26 |
2008-10-09 |
Ono Pharmaceutical Co., Ltd. |
Preventive and/or Therapeutic Agent For Disease In Which Mitochondrial Benzodiazephine Receptor Participates
|
EP1717238A4
(en)
|
2004-02-16 |
2008-03-05 |
Daiichi Seiyaku Co |
FUNGICIDES HETEROCYCLIC COMPOUNDS
|
US7306631B2
(en)
|
2004-03-30 |
2007-12-11 |
The Procter & Gamble Company |
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
|
WO2005103003A2
(en)
*
|
2004-04-26 |
2005-11-03 |
Pfizer Inc. |
Pyrrolopyridine derivatives and their use as hiv-integrase inhibitors
|
ATE516019T1
(de)
|
2004-05-11 |
2011-07-15 |
Egalet Ltd |
Quellbare dosierform mit gellan-gummit
|
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
|
WO2006026703A2
(en)
|
2004-09-02 |
2006-03-09 |
Smithkline Beecham Corporation |
Chemical compounds
|
MX2007004179A
(es)
|
2004-10-07 |
2007-06-07 |
Warner Lambert Co |
Derivados de triazolpiridina como agentes antibacterianos.
|
EP1819338A4
(en)
|
2004-11-22 |
2009-11-04 |
Threshold Pharmaceuticals Inc |
ANTICANCER TUBULIN-BINDING AGENTS AND THEIR PRODUCTS
|
US20070299103A1
(en)
|
2004-12-01 |
2007-12-27 |
Ulrich Abel |
[1,2,4]Triazolo[4,3-A]Pyridine Derivatives for the Treatment of Hyperproliferative Diseases
|
WO2007149479A1
(en)
|
2006-06-22 |
2007-12-27 |
Mallinckrodt Inc. |
Pyrazine derivatives and uses thereof in renal monitoring
|
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
|
KR100908547B1
(ko)
|
2005-02-22 |
2009-07-20 |
화이자 인코포레이티드 |
5ht4 수용체 작용제로서의 옥시인돌 유도체
|
ITBO20050123A1
(it)
|
2005-03-07 |
2005-06-06 |
Alfa Wassermann Spa |
Formulazioni farmaceutiche gastroresistenti contenenti rifaximina
|
AU2006236387A1
(en)
|
2005-04-18 |
2006-10-26 |
Neurogen Corporation |
Subtituted heteroaryl CB1 antagonists
|
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
|
US7579360B2
(en)
|
2005-06-09 |
2009-08-25 |
Bristol-Myers Squibb Company |
Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors
|
US7632837B2
(en)
|
2005-06-17 |
2009-12-15 |
Bristol-Myers Squibb Company |
Bicyclic heterocycles as cannabinoid-1 receptor modulators
|
TW200726765A
(en)
|
2005-06-17 |
2007-07-16 |
Bristol Myers Squibb Co |
Triazolopyridine cannabinoid receptor 1 antagonists
|
US7452892B2
(en)
|
2005-06-17 |
2008-11-18 |
Bristol-Myers Squibb Company |
Triazolopyrimidine cannabinoid receptor 1 antagonists
|
TW200800213A
(en)
|
2005-09-02 |
2008-01-01 |
Abbott Lab |
Novel imidazo based heterocycles
|
ATE478852T1
(de)
|
2005-09-09 |
2010-09-15 |
Schering Corp |
Neue 4-cyano-, 4-amino-, und 4- aminomethylderivative von pyrazoloä1,5- aüpyridinen, pyrazoloä1,5-cüpyrimidinen und 2h- indazolverbindungen und 5-cyano-, 5-amino- und 5- aminomethylderivative von imidazoä1,2-aüpyridinen,und imidazoä1,5-aüpyrazinverbindungen als inhibitoren der cyclinabhänggen kinase
|
KR20080074963A
(ko)
|
2005-11-10 |
2008-08-13 |
쉐링 코포레이션 |
단백질 키나제 억제제로서의 이미다조피라진
|
US7858609B2
(en)
|
2005-11-28 |
2010-12-28 |
Marinus Pharmaceuticals |
Solid ganaxolone formulations and methods for the making and use thereof
|
WO2007074089A1
(en)
|
2005-12-27 |
2007-07-05 |
F. Hoffmann-La Roche Ag |
Aryl-isoxazol-4-yl-imidazo[1, 5-a]pyridine derivatives
|
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)
|
BRPI0710110A2
(pt)
|
2006-03-31 |
2011-08-02 |
Novartis Ag |
compostos orgánicos
|
US20090175852A1
(en)
|
2006-06-06 |
2009-07-09 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
CA2654202A1
(en)
|
2006-06-06 |
2007-12-21 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
JP2009541323A
(ja)
|
2006-06-22 |
2009-11-26 |
マリンクロット インコーポレイテッド |
拡張された共役を有するピラジン誘導体およびその使用
|
US8022088B2
(en)
|
2006-06-29 |
2011-09-20 |
Schering Corporation |
Substituted bicyclic and tricyclic thrombin receptor antagonists
|
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
|
PE20080403A1
(es)
|
2006-07-14 |
2008-04-25 |
Amgen Inc |
Derivados heterociclicos fusionados y metodos de uso
|
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
|
CA2658764A1
(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
|
JP2010509363A
(ja)
|
2006-11-08 |
2010-03-25 |
ノババックス,インコーポレイテッド |
固体剤形の多相医薬組成物の製造方法
|
WO2008056176A1
(en)
|
2006-11-10 |
2008-05-15 |
Scottish Biomedical Limited |
Pyrazolopyrimidines as phosphodiesterase inhibitors
|
ME02372B
(me)
|
2006-11-22 |
2016-06-20 |
Incyte Holdings Corp |
Imidazotriazini i imidazopiramidini kao inhibitori kinaze
|
ATE495743T1
(de)
|
2006-12-01 |
2011-02-15 |
Galapagos Nv |
Triazolopyridinverbindungen zur behandlung von degenerations- und entzündungskrankheiten
|
AU2007338631A1
(en)
|
2006-12-22 |
2008-07-03 |
Combinatorx, Incorporated |
Pharmaceutical compositions for treatment of parkinson's disease and related disorders
|
EP2118101B1
(en)
|
2007-03-09 |
2012-09-26 |
Probiodrug AG |
Imidazo [1,5-a] pyridine derivatives as inhibitors of glutaminyl cyclase
|
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
|
ATE540037T1
(de)
|
2007-04-16 |
2012-01-15 |
Leo Pharma As |
Triazolopyridine als phosphodiesterasehemmer zur behandlung von hautkrankheiten
|
WO2008130951A1
(en)
|
2007-04-17 |
2008-10-30 |
Bristol-Myers Squibb Company |
Fused heterocyclic 11-beta-hydroxysteroid dehydrogenase type i inhibitors
|
WO2008141239A1
(en)
|
2007-05-10 |
2008-11-20 |
Acadia Pharmaceuticals Inc. |
Imidazol [1,2-a] pyridines and related compounds with activity at cannabinoid cb2 receptors
|
US9084817B2
(en)
|
2007-05-21 |
2015-07-21 |
Toray Industries, Inc. |
Oral preparation comprising specific organic acid, and method for improvement in elution property and chemical stability of oral preparation
|
AU2008262038A1
(en)
|
2007-06-08 |
2008-12-18 |
AbbVie Deutschland GmbH & Co. KG |
5-heteroaryl substituted indazoles as kinase inhibitors
|
US8648069B2
(en)
|
2007-06-08 |
2014-02-11 |
Abbvie Inc. |
5-substituted indazoles as kinase inhibitors
|
WO2008156614A2
(en)
|
2007-06-14 |
2008-12-24 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
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
|
JP2010533680A
(ja)
|
2007-07-18 |
2010-10-28 |
ノバルティス アーゲー |
二環ヘテロアリール化合物およびそれらのキナーゼ阻害剤としての使用
|
RU2010106878A
(ru)
|
2007-07-31 |
2011-09-10 |
Шеринг Корпорейшн (US) |
Комбинация антимитотического агента и ингибитора аврора киназы как средство для лечения рака
|
WO2009017954A1
(en)
|
2007-08-01 |
2009-02-05 |
Phenomix Corporation |
Inhibitors of jak2 kinase
|
US20120121540A1
(en)
|
2007-08-10 |
2012-05-17 |
Franz Ulrich Schmitz |
Certain Nitrogen Containing Bicyclic Chemical Entities For Treating Viral Infections
|
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
|
FR2920090A1
(fr)
|
2007-08-24 |
2009-02-27 |
Oreal |
Composition tinctoriale comprenant une base d'oxydation aminopyrazolopyridine particuliere, un coupleur et un tensioactif particulier.
|
FR2920091A1
(fr)
|
2007-08-24 |
2009-02-27 |
Oreal |
Composition tinctoriale comprenant une base d'oxydation aminopyrazolopyridine, un coupleur et un polyol 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
|
WO2009047563A1
(en)
|
2007-10-11 |
2009-04-16 |
Astrazeneca Ab |
Pyrrolo [2, 3 -d] pyrimidin derivatives as protein kinase b inhibitors
|
TW200927142A
(en)
|
2007-10-12 |
2009-07-01 |
Novartis Ag |
Compositions comprising sphingosine 1 phosphate (S1P) receptor modulators
|
DK2231662T3
(da)
|
2007-12-19 |
2011-08-29 |
Genentech Inc |
8-Anilinoimidazopyridiner og deres anvendelse som anticancer- og/eller antiinflammatoriske midler
|
WO2009085230A1
(en)
|
2007-12-19 |
2009-07-09 |
Amgen Inc. |
Inhibitors of pi3 kinase
|
KR100988233B1
(ko)
|
2007-12-26 |
2010-10-18 |
한미홀딩스 주식회사 |
클로피도그렐 1,5-나프탈렌 다이술폰산 염 또는 이의수화물의 약학 조성물 및 제제
|
SG191660A1
(en)
|
2008-03-11 |
2013-07-31 |
Incyte Corp |
Azetidine and cyclobutane derivatives as jak inhibitors
|
US8507501B2
(en)
|
2008-03-13 |
2013-08-13 |
The Brigham And Women's Hospital, Inc. |
Inhibitors of the BMP signaling pathway
|
JP5547099B2
(ja)
|
2008-03-14 |
2014-07-09 |
インテリカイン, エルエルシー |
キナーゼ阻害剤および使用方法
|
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
(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
|
WO2010010189A1
(en)
|
2008-07-25 |
2010-01-28 |
Galapagos Nv |
Novel compounds useful for the treatment of degenerative and inflammatory diseases
|
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
|
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
|
US20120021519A1
(en)
|
2008-09-19 |
2012-01-26 |
Presidents And Fellows Of Harvard College |
Efficient induction of pluripotent stem cells using small molecule compounds
|
JP5731978B2
(ja)
|
2008-09-26 |
2015-06-10 |
インテリカイン, エルエルシー |
複素環キナーゼ阻害剤
|
WO2010043721A1
(en)
|
2008-10-17 |
2010-04-22 |
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
|
EP2389362B1
(en)
|
2009-01-21 |
2019-12-11 |
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
|
US20100209489A1
(en)
|
2009-02-04 |
2010-08-19 |
Supernus Pharmaceuticals, Inc. |
Formulations of desvenlafaxine
|
TR200900879A2
(tr)
|
2009-02-05 |
2010-08-23 |
Bi̇lgi̇ç Mahmut |
Aktif maddelerin tek bir dozaj formunda kombine edildiği farmasötik bileşimler
|
TR200900878A2
(tr)
|
2009-02-05 |
2010-08-23 |
Bi̇lgi̇ç Mahmut |
Tek bir dozaj formunda kombine edilen farmasötik formülasyonlar
|
US20130310362A1
(en)
|
2009-02-13 |
2013-11-21 |
Bayer Pharma Aktiegesellschaft |
Fused pyrimidines
|
WO2010104306A2
(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
|
WO2010107404A1
(en)
|
2009-03-16 |
2010-09-23 |
Mahmut Bilgic |
Stable pharmaceutical combinations
|
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.
|
BRPI1013432B1
(pt)
|
2009-03-31 |
2019-12-17 |
Kissei Pharmaceutical |
derivado de indolizina e composição farmacêutica
|
WO2010119264A1
(en)
|
2009-04-16 |
2010-10-21 |
Centro Nacional De Investigaciones Oncólogicas (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
|
AU2010258785A1
(en)
|
2009-06-10 |
2012-01-19 |
Sunovion Pharmaceuticals Inc. |
Histamine H3 inverse agonists and antagonists and methods of use thereof
|
US8686009B2
(en)
|
2009-06-25 |
2014-04-01 |
Alkermes Pharma Ireland Limited |
Prodrugs of NH-acidic compounds
|
MY162604A
(en)
|
2009-08-17 |
2017-06-30 |
Intellikine Llc |
Heterocyclic compounds and uses thereof
|
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
|
WO2011035941A1
(en)
|
2009-09-25 |
2011-03-31 |
Oryzon Genomics S.A. |
Lysine specific demethylase-1 inhibitors and their use
|
US8946296B2
(en)
|
2009-10-09 |
2015-02-03 |
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
|
US8614315B2
(en)
|
2009-12-25 |
2013-12-24 |
Mahmut Bilgic |
Cefdinir and cefixime formulations and uses thereof
|
US9073927B2
(en)
|
2010-01-22 |
2015-07-07 |
Fundacion Centro Nacional De Investigaciones Oncologicas Carlos Iii |
Inhibitors of PI3 kinase
|
US20130085133A1
(en)
|
2010-02-08 |
2013-04-04 |
Sourthern Research Institute Office of Commercialization and Intellectual Prop. |
Anti-viral treatment and assay to screenfor 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
|
WO2011113862A1
(en)
|
2010-03-18 |
2011-09-22 |
Bayer Pharma Aktiengesellschaft |
Imidazopyrazines
|
SG184073A1
(en)
|
2010-03-18 |
2012-10-30 |
Pasteur Institut Korea |
Anti-infective compounds
|
EP2552920B1
(en)
|
2010-04-02 |
2017-03-15 |
Ogeda Sa |
Novel nk-3 receptor selective antagonist compounds, pharmaceutical composition and methods for use in nk-3 receptors mediated disorders
|
EP3133059A1
(en)
|
2010-04-19 |
2017-02-22 |
Oryzon Genomics, S.A. |
Lysine specific demethylase-1 inhibitors and their use
|
CN102985402B
(zh)
|
2010-04-20 |
2015-04-29 |
罗马大学 |
反苯环丙胺衍生物作为组蛋白去甲基酶lsd1和/或lsd2的抑制剂
|
AU2011246067A1
(en)
|
2010-04-28 |
2012-09-27 |
Daiichi Sankyo Company, Limited |
[5,6] heterocyclic compound
|
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
|
WO2011141713A1
(en)
|
2010-05-13 |
2011-11-17 |
Centro Nacional De Investigaciones Oncologicas (Cnio) |
New bicyclic compounds as pi3-k and mtor inhibitors
|
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
|
EP2575808A1
(en)
|
2010-05-28 |
2013-04-10 |
Mahmut Bilgic |
Combination of antihypertensive agents
|
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
|
MX2012015096A
(es)
|
2010-07-02 |
2013-05-28 |
Gilead Sciences Inc |
Compuestos heterociclicos fusionados como moduladores del canal ion.
|
CN103097384B
(zh)
|
2010-07-12 |
2017-02-15 |
拜耳知识产权有限责任公司 |
取代的咪唑并[1,2‑a]嘧啶和吡啶
|
WO2012009475A1
(en)
|
2010-07-14 |
2012-01-19 |
Oregon Health & Science University |
Methods of treating cancer with inhibition of lysine-specific demethylase 1
|
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
|
US9006449B2
(en)
|
2010-07-29 |
2015-04-14 |
Oryzon Genomics, S.A. |
Cyclopropylamine derivatives useful as LSD1 inhibitors
|
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
|
WO2012013728A1
(en)
|
2010-07-29 |
2012-02-02 |
Oryzon Genomics S.A. |
Arylcyclopropylamine based demethylase inhibitors of lsd1 and their medical use
|
WO2012034116A2
(en)
|
2010-09-10 |
2012-03-15 |
The Johns Hopkins University |
Small molecules as epigenetic modulators of lysine-specific demethylase 1 and methods of treating disorders
|
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
|
ES2549926T3
(es)
|
2010-09-29 |
2015-11-03 |
Kissei Pharmaceutical Co., Ltd. |
Derivados (aza)indolizínicos como inhibidores de la xantina-oxidasa
|
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
|
KR101941300B1
(ko)
|
2010-10-18 |
2019-01-22 |
이 아이 듀폰 디 네모아 앤드 캄파니 |
살선충성 설폰아미드
|
TWI557123B
(zh)
|
2010-10-21 |
2016-11-11 |
梅迪維新技術公司 |
結晶型(8S,9R)-5-氟-8-(4-氟苯基)-9-(1-甲基-1H-1,2,4-三唑-5-基)-8,9-二氫-2H-吡啶并[4,3,2-de]呔-3(7H)-酮甲苯磺酸鹽
|
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
|
ES2553610T3
(es)
|
2010-12-14 |
2015-12-10 |
Electrophoretics Limited |
Inhibidores de la caseína cinasa 1 delta (CK1delta)
|
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?.
|
CN103370322B
(zh)
|
2010-12-17 |
2016-02-10 |
拜耳知识产权有限责任公司 |
在过度增殖性病症的治疗中用作mps-1和tkk抑制剂的2-取代的咪唑并吡嗪
|
EP2651950A1
(en)
|
2010-12-17 |
2013-10-23 |
Bayer Intellectual Property GmbH |
6 substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
|
EP2651944B1
(en)
|
2010-12-17 |
2015-09-23 |
Bayer Intellectual Property GmbH |
Substituted 6-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
|
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
|
WO2012088438A1
(en)
|
2010-12-22 |
2012-06-28 |
Eutropics Pharmaceuticals, Inc. |
Compositions and methods useful for treating diseases
|
US20140038953A1
(en)
|
2011-01-21 |
2014-02-06 |
The General Hospital Corporation |
Compositions and methods for cardiovascular disease
|
EP2712316A1
(en)
|
2011-02-08 |
2014-04-02 |
Oryzon Genomics, S.A. |
Lysine demethylase inhibitors for myeloproliferative or lymphoproliferative diseases or disorders
|
EP3981395A1
(en)
|
2011-02-08 |
2022-04-13 |
Oryzon Genomics, S.A. |
Lysine demethylase inhibitors for myeloproliferative disorders
|
US9127000B2
(en)
|
2011-02-23 |
2015-09-08 |
Intellikine, LLC. |
Heterocyclic compounds and uses thereof
|
WO2012129562A2
(en)
|
2011-03-24 |
2012-09-27 |
The Scripps Research Institute |
Compounds and methods for inducing chondrogenesis
|
SG193241A1
(en)
|
2011-03-25 |
2013-10-30 |
Glaxosmithkline Ip No 2 Ltd |
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
|
US20140329833A1
(en)
|
2011-05-19 |
2014-11-06 |
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
|
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
|
WO2012177606A1
(en)
|
2011-06-20 |
2012-12-27 |
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
(en)
|
2011-07-19 |
2013-01-23 |
MSD Oss B.V. |
4-(5-Membered fused pyridinyl)benzamides as BTK-inhibitors
|
SG2014009161A
(en)
|
2011-08-09 |
2014-04-28 |
Takeda Pharmaceutical |
Cyclopropaneamine compound
|
WO2013025805A1
(en)
|
2011-08-15 |
2013-02-21 |
University Of Utah Research Foundation |
Substituted (e)-n'-(1-phenylethylidene) benzohydrazide analogs as histone demethylase inhiitors
|
WO2013033688A1
(en)
|
2011-09-01 |
2013-03-07 |
The Brigham And Women's Hospital, Inc. |
Treatment of cancer
|
EP2751089B1
(en)
|
2011-09-02 |
2018-11-14 |
Promega Corporation |
Compounds and methods for assaying redox state of metabolically active cells and methods for measuring nad(p)/nad(p)h
|
CN104703987B
(zh)
|
2011-10-10 |
2017-05-03 |
H.隆德贝克有限公司 |
具有咪唑并吡嗪酮骨架的pde9抑制剂
|
JP6046154B2
(ja)
|
2011-10-20 |
2016-12-14 |
オリソン ヘノミクス エセ. アー. |
Lsd1阻害剤としての(ヘテロ)アリールシクロプロピルアミン化合物
|
AU2012324803B9
(en)
|
2011-10-20 |
2017-08-24 |
Oryzon Genomics, S.A. |
(hetero)aryl cyclopropylamine compounds as LSD1 inhibitors
|
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.
|
ITMI20111971A1
(it)
|
2011-10-28 |
2013-04-29 |
Mesogenics Srl |
Inibitori dell'enzima lsd-1 per l'induzione del differenziamento osteogenico
|
WO2013074390A1
(en)
|
2011-11-14 |
2013-05-23 |
Merck Sharp & Dohme Corp. |
Triazolopyridinone pde10 inhibitors
|
US20140288145A1
(en)
|
2011-12-05 |
2014-09-25 |
Brandeis University |
Treatment of amyloidosis by compounds that regulate retromer stabilization
|
ES2579981T3
(es)
|
2012-03-07 |
2016-08-18 |
Merck Patent Gmbh |
Derivados de triazolopirazina
|
CN102587054B
(zh)
|
2012-03-13 |
2014-05-07 |
机械科学研究总院先进制造技术研究中心 |
缸盖自动锁紧装置及包括该装置的筒子纱染色机
|
GB201205669D0
(en)
|
2012-03-30 |
2012-05-16 |
Agency Science Tech & Res |
Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof
|
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
|
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
|
US9815819B2
(en)
|
2012-06-28 |
2017-11-14 |
Novartis Ag |
Complement pathway modulators and uses thereof
|
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
|
ES2660051T3
(es)
|
2012-09-28 |
2018-03-20 |
Vanderbilt University |
Compuestos heterocíclicos condensados como inhibidores selectivos de BMP
|
BR112015007182A2
(pt)
|
2012-10-05 |
2017-07-04 |
Rigel Pharmaceuticals Inc |
inibidores de gdf-8
|
JP6325449B2
(ja)
*
|
2012-10-12 |
2018-05-16 |
武田薬品工業株式会社 |
シクロプロパンアミン化合物およびその用途
|
WO2014078479A2
(en)
|
2012-11-14 |
2014-05-22 |
The Board Of Regents Of The University Of Texas System |
INHIBITION OF HIF-2α HETERODIMERIZATION WITH HIF1β (ARNT)
|
WO2014084298A1
(ja)
|
2012-11-28 |
2014-06-05 |
京都府公立大学法人 |
リシン構造を有するlsd1選択的阻害薬
|
EP2925307B1
(en)
|
2012-11-30 |
2020-10-28 |
McCord, Darlene E. |
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
|
CA2889165A1
(en)
|
2012-12-19 |
2014-06-26 |
Wockhardt Limited |
A stable aqueous composition comprising human insulin or an analogue or derivative thereof
|
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
|
WO2014127350A1
(en)
|
2013-02-18 |
2014-08-21 |
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
(en)
|
2013-03-11 |
2014-10-09 |
Imago Biosciences |
Kdm1a inhibitors for the treatment of disease
|
US20160050895A1
(en)
|
2013-03-13 |
2016-02-25 |
Australian Nuclear Science And Technology Organization |
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
|
WO2014194280A2
(en)
|
2013-05-30 |
2014-12-04 |
The Board of Regents of the Nevada System of Higher Education on behalf of the University of |
Novel suicidal lsd1 inhibitors targeting sox2-expressing cancer cells
|
NZ715331A
(en)
|
2013-06-19 |
2019-09-27 |
The Univ Of Utah Research Foundation |
Substituted (e)-n’-(1-phenylethylidene) benzohydrazide analogs as histone demethylase inhibitors
|
ES2773250T3
(es)
|
2013-06-21 |
2020-07-10 |
Myokardia Inc |
Compuestos de pirimidindiona contra afecciones cardíacas
|
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
|
US9770514B2
(en)
|
2013-09-03 |
2017-09-26 |
ExxPharma Therapeutics LLC |
Tamper-resistant pharmaceutical dosage forms
|
ES2648267T3
(es)
|
2013-09-13 |
2017-12-29 |
Bayer Pharma Aktiengesellschaft |
Composiciones farmacéuticas que contienen refametinib
|
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
|
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
|
CR20200199A
(es)
|
2014-02-13 |
2020-06-19 |
Incyte Corp |
CICLOPROPILAMINA COMO INHIBIDOR DE LA LSD1 (Divisional 2016-0396)
|
US9493442B2
(en)
|
2014-02-13 |
2016-11-15 |
Incyte Corporation |
Cyclopropylamines as LSD1 inhibitors
|
EP3105226B1
(en)
|
2014-02-13 |
2019-09-04 |
Incyte Corporation |
Cyclopropylamines as lsd1 inhibitors
|
US9428470B2
(en)
|
2014-02-13 |
2016-08-30 |
Takeda Pharmaceutical Company Limited |
Heterocyclic compound
|
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
|
ES2700549T3
(es)
|
2014-04-02 |
2019-02-18 |
Bristol Myers Squibb Co |
Inhibidores de biaril quinasa
|
US10053456B2
(en)
|
2014-04-11 |
2018-08-21 |
Takeda Pharmaceutical Company Limited |
Cyclopropanamine compound and use thereof
|
WO2015155281A1
(en)
|
2014-04-11 |
2015-10-15 |
Sanovel Ilac Sanayi Ve Ticaret A.S. |
Pharmaceutical combinations of dabigatran and proton pump inhibitors
|
EP2929884A1
(en)
|
2014-04-11 |
2015-10-14 |
Sanovel Ilac Sanayi ve Ticaret A.S. |
Pharmaceutical combinations of dabigatran and h2-receptor antagonists
|
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
|
US10233165B2
(en)
|
2014-05-30 |
2019-03-19 |
Istituto Europeo Di Oncologia S.R.L. |
Cyclopropylamine compounds as histone demethylase inhibitors
|
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
|
WO2016007727A1
(en)
|
2014-07-10 |
2016-01-14 |
Incyte Corporation |
Triazolopyridines and triazolopyrazines as lsd1 inhibitors
|
WO2016007722A1
(en)
|
2014-07-10 |
2016-01-14 |
Incyte Corporation |
Triazolopyridines and triazolopyrazines as lsd1 inhibitors
|
WO2016007736A1
(en)
|
2014-07-10 |
2016-01-14 |
Incyte Corporation |
Imidazopyrazines as lsd1 inhibitors
|
WO2016007731A1
(en)
|
2014-07-10 |
2016-01-14 |
Incyte Corporation |
Imidazopyridines and imidazopyrazines as lsd1 inhibitors
|
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
|
CN106852142B
(zh)
|
2014-10-08 |
2020-08-21 |
豪夫迈·罗氏有限公司 |
作为醛固酮合酶抑制剂的螺二胺衍生物
|
AU2016243939B2
(en)
|
2015-04-03 |
2020-09-03 |
Incyte Holdings Corporation |
Heterocyclic compounds as LSD1 inhibitors
|
RU2714197C2
(ru)
|
2015-04-03 |
2020-02-13 |
Мутабилис |
Гетероциклические соединения и их применение для предупреждения или лечения бактериальных инфекций
|
JP2018519245A
(ja)
|
2015-04-03 |
2018-07-19 |
ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company |
癌の治療のためのインドールアミン−2,3−ジオキシゲナーゼの阻害剤およびそれらの使用方法
|
TWI765860B
(zh)
|
2015-08-12 |
2022-06-01 |
美商英塞特公司 |
Lsd1抑制劑之鹽
|
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
|
AU2016382463B2
(en)
|
2015-12-29 |
2021-05-27 |
Mirati Therapeutics, Inc. |
LSD1 inhibitors
|
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
|
JP6999574B2
(ja)
|
2016-04-22 |
2022-01-18 |
インサイト・コーポレイション |
Lsd1阻害剤の製剤
|
CN110430880A
(zh)
|
2017-01-18 |
2019-11-08 |
范德比尔特大学 |
作为选择性bmp抑制剂的稠合杂环化合物
|
US11312705B2
(en)
|
2017-03-16 |
2022-04-26 |
Jiangsu Hengrui Medicine Co., Ltd. |
Heteroaryl[4,3-C]pyrimidine-5-amine derivative, preparation method therefor, and medical uses thereof
|
TWI829716B
(zh)
|
2018-07-05 |
2024-01-21 |
美商英塞特公司 |
作為a2a/a2b 抑制劑之稠合吡嗪衍生物
|
US10968200B2
(en)
|
2018-08-31 |
2021-04-06 |
Incyte Corporation |
Salts of an LSD1 inhibitor and processes for preparing the same
|