|
NL7013068A
(enExample)
|
1969-09-17 |
1971-03-19 |
|
|
|
US4537889A
(en)
|
1982-12-27 |
1985-08-27 |
Eli Lilly And Company |
Inotropic agents
|
|
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
|
|
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
|
|
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
(enExample)
|
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.
|
|
EP0649425B1
(en)
|
1992-06-17 |
1999-03-10 |
PHARMACIA & UPJOHN COMPANY |
Pyridino-, pyrrolidino- and azepino-substituted oximes useful as anti-atherosclerosis and anti-hypercholesterolemic agents
|
|
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
|
|
TR200001728T2
(tr)
|
1997-11-11 |
2000-09-21 |
Ono Pharmaceutical Co., Ltd. |
Birleşik pirazin türevleri
|
|
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
|
|
UA80667C2
(en)
|
1999-09-28 |
2007-10-25 |
Panacea Biotec Ltd |
Controlled release composition comprising nimesulide and process for the preparation thereof
|
|
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
|
|
ES2244613T3
(es)
|
2000-04-27 |
2005-12-16 |
Astellas Pharma Inc. |
Derivados de imidazopiridina.
|
|
US6403588B1
(en)
|
2000-04-27 |
2002-06-11 |
Yamanouchi Pharmaceutical Co., Ltd. |
Imidazopyridine derivatives
|
|
EP1294358B1
(en)
|
2000-06-28 |
2004-08-18 |
Smithkline Beecham Plc |
Wet milling process
|
|
AR029538A1
(es)
|
2000-07-06 |
2003-07-02 |
Wyeth Corp |
Composiciones farmaceuticas de agentes estrogenicos
|
|
HUP0301801A2
(hu)
|
2000-07-14 |
2003-09-29 |
Bristol-Myers Squibb Pharma Company |
Imidazo[1,2-a]pirazin-származékok és az ezeket tartalmazó gyógyszerkészítmények
|
|
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
|
|
ES2251518T3
(es)
|
2000-11-10 |
2006-05-01 |
MERCK SHARP & DOHME LTD. |
Derivados de imidazo-triazina como ligandos para receptores gaba.
|
|
EP1343785A2
(de)
|
2000-12-13 |
2003-09-17 |
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
|
|
EP1513522A2
(en)
|
2002-01-18 |
2005-03-16 |
Sri International |
Methods of treating conditions associated with an edg receptor
|
|
US20050113283A1
(en)
|
2002-01-18 |
2005-05-26 |
David Solow-Cordero |
Methods of treating conditions associated with an EDG-4 receptor
|
|
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
|
|
US20060276339A1
(en)
|
2002-10-16 |
2006-12-07 |
Windsor J B |
Methods and compositions for increasing the efficacy of biologically-active ingredients
|
|
AU2003301226A1
(en)
|
2002-12-20 |
2004-07-22 |
Pharmacia Corp |
Acyclic pyrazole compounds for the inhibition of mitogen activated protein kinase-activated protein kinase-2
|
|
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
|
|
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
|
|
US7186832B2
(en)
|
2003-02-20 |
2007-03-06 |
Sugen Inc. |
Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
|
|
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
|
|
ES2338656T3
(es)
|
2003-04-11 |
2010-05-11 |
High Point Pharmaceuticals, Llc |
Uso farmaceutico de 1,2,4-triazoles fusionados.
|
|
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
|
|
US7132426B2
(en)
|
2003-07-14 |
2006-11-07 |
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
|
|
EP1663193B1
(en)
|
2003-09-12 |
2012-04-04 |
Merck Serono SA |
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
|
|
ATE369370T1
(de)
|
2003-10-10 |
2007-08-15 |
Pfizer Prod Inc |
Substituierte 2h-(1,2,4)triazolo(4,3-a)pyrazine als gsk-3-inhibitoren
|
|
US7419978B2
(en)
|
2003-10-22 |
2008-09-02 |
Bristol-Myers Squibb Company |
Phenyl-aniline substituted bicyclic compounds useful as kinase inhibitors
|
|
WO2005044793A2
(en)
|
2003-10-31 |
2005-05-19 |
Takeda Pharmaceutical Company Limited |
Nitrogen-containing fused heterocyclic compounds
|
|
EP1698335A4
(en)
|
2003-12-26 |
2007-08-01 |
Ono Pharmaceutical Co |
AGENT FOR PREVENTING AND / OR TREATING DISEASES INVOLVING A MITOCHONDRIAL BENZODIAZEPINE RECEPTOR
|
|
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
|
|
CA2564356A1
(en)
*
|
2004-04-26 |
2005-11-03 |
Pfizer Inc. |
Pyrrolopyridine derivatives and their use as hiv-integrase inhibitors
|
|
JP5154924B2
(ja)
|
2004-05-11 |
2013-02-27 |
エガレット エイ/エス |
ジェランガムを含む膨張可能な投与形態
|
|
WO2006015263A2
(en)
|
2004-07-29 |
2006-02-09 |
Threshold Pharmaceuticals, Inc. |
Lonidamine analogs
|
|
WO2006018727A2
(en)
|
2004-08-18 |
2006-02-23 |
Pharmacia & Upjohn Company Llc |
Triazolopyridine compounds useful for the treatment of inflammation
|
|
WO2006026703A2
(en)
|
2004-09-02 |
2006-03-09 |
Smithkline Beecham Corporation |
Chemical compounds
|
|
US7524860B2
(en)
|
2004-10-07 |
2009-04-28 |
Pfizer Inc. |
Antibacterial agents
|
|
AU2005309761A1
(en)
|
2004-11-22 |
2006-06-01 |
Threshold Pharmaceuticals, Inc. |
Tubulin binding anti cancer agents and prodrugs thereof
|
|
ATE443063T1
(de)
|
2004-12-01 |
2009-10-15 |
Merck Serono Sa |
Ä1,2,4ütriazoloä4,3-aüpyridin-derivative zur behandlung hyperproliferativer erkrankungen
|
|
WO2006073938A2
(en)
|
2004-12-30 |
2006-07-13 |
East Carolina University |
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
|
|
AP2007004067A0
(en)
|
2005-02-22 |
2007-08-31 |
Pfizer |
Oxyindole derivatives as 5HT4 receptor agonists
|
|
ITBO20050123A1
(it)
|
2005-03-07 |
2005-06-06 |
Alfa Wassermann Spa |
Formulazioni farmaceutiche gastroresistenti contenenti rifaximina
|
|
JP2008536950A
(ja)
|
2005-04-18 |
2008-09-11 |
ニューロジェン・コーポレーション |
置換ヘテロアリールのcb1拮抗薬
|
|
US7572807B2
(en)
|
2005-06-09 |
2009-08-11 |
Bristol-Myers Squibb Company |
Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors
|
|
US7579360B2
(en)
|
2005-06-09 |
2009-08-25 |
Bristol-Myers Squibb Company |
Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors
|
|
EP1901748B1
(en)
|
2005-06-09 |
2010-09-08 |
Oncalis AG |
Angiogenesis inhibitors
|
|
US7632837B2
(en)
|
2005-06-17 |
2009-12-15 |
Bristol-Myers Squibb Company |
Bicyclic heterocycles as cannabinoid-1 receptor modulators
|
|
US7572808B2
(en)
|
2005-06-17 |
2009-08-11 |
Bristol-Myers Squibb Company |
Triazolopyridine cannabinoid receptor 1 antagonists
|
|
US7452892B2
(en)
|
2005-06-17 |
2008-11-18 |
Bristol-Myers Squibb Company |
Triazolopyrimidine cannabinoid receptor 1 antagonists
|
|
TWI255587B
(en)
|
2005-07-04 |
2006-05-21 |
Quanta Comp Inc |
Multi-frequency planar antenna
|
|
JP2009507032A
(ja)
|
2005-09-02 |
2009-02-19 |
アボット・ラボラトリーズ |
新規なイミダゾ系複素環
|
|
US7700773B2
(en)
|
2005-09-09 |
2010-04-20 |
Schering Corporation |
4-cyano, 4-amino, and 4-aminomethyl derivatives of pyrazolo[1,5-a]pyridines, pyrazolo[1,5-c]pyrimidines and 2H-indazole compounds and 5-cyano, 5-amino, and 5-aminomethyl derivatives of imidazo[1,2-a]pyridines, and imidazo[1,5-a]pyrazines as cyclin dependent kinase inhibitors
|
|
AR056785A1
(es)
|
2005-11-10 |
2007-10-24 |
Schering Corp |
COMPUESTOS DE IMIDAZO[1,2-A]PIRAZINAS, uTILES COMO INHIBIDORES, REGULADORES O MODULADORES DE PROTEINQUINASAS
|
|
EP1959966B1
(en)
|
2005-11-28 |
2020-06-03 |
Marinus Pharmaceuticals, Inc. |
Ganaxolone formulations and methods for the making and use thereof
|
|
CA2633536A1
(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)
|
|
WO2007113226A1
(en)
|
2006-03-31 |
2007-10-11 |
Novartis Ag |
Organic compounds
|
|
US20090175852A1
(en)
|
2006-06-06 |
2009-07-09 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
|
AR061229A1
(es)
|
2006-06-06 |
2008-08-13 |
Schering Corp |
Imidazopirazinas como inhibidores de la proteina quinasa
|
|
DK2029554T3
(da)
|
2006-06-22 |
2014-06-10 |
Medibeacon Llc |
Pyrazinderivater og anvendelser heraf til nyreovervågning
|
|
CA2655857C
(en)
|
2006-06-22 |
2014-12-02 |
Mallinckrodt Inc. |
Pyrazine derivatives with extended conjugation and uses thereof
|
|
EP2032560B1
(en)
|
2006-06-29 |
2013-05-01 |
Merck Sharp & Dohme Corp. |
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
|
|
US8217177B2
(en)
|
2006-07-14 |
2012-07-10 |
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
|
|
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
|
|
AU2007307031B2
(en)
|
2006-10-11 |
2011-11-24 |
Amgen Inc. |
Imidazo- and triazolo-pyridine compounds and methods of use therof
|
|
AU2007317242B2
(en)
|
2006-11-08 |
2013-08-01 |
Neurocrine Biosciences, Inc. |
Substituted 3-isobutyl-9, 10-dimethoxy-1,3,4,6,7,11B-hexahydro-2H-pyrido[2,1-a] isoquinolin-2-ol compounds and methods relating thereto
|
|
CN101646419A
(zh)
|
2006-11-08 |
2010-02-10 |
诺瓦瓦克斯股份有限公司 |
制备多相药物组合物的固体剂型的方法
|
|
WO2008056176A1
(en)
|
2006-11-10 |
2008-05-15 |
Scottish Biomedical Limited |
Pyrazolopyrimidines as phosphodiesterase inhibitors
|
|
GEP20125658B
(en)
|
2006-11-22 |
2012-10-10 |
Incyte Corp |
Imidazotriazines and imidazo pyrimidines as kinase inhibitors
|
|
DE602007012133D1
(de)
|
2006-12-01 |
2011-03-03 |
Andrew Burritt |
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
|
|
US7803810B2
(en)
|
2007-03-09 |
2010-09-28 |
Probiodrug Ag |
Inhibitors
|
|
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
|
|
ES2380395T3
(es)
|
2007-04-16 |
2012-05-11 |
Leo Pharma A/S |
Triazolopiridinas como inhibidores de fosfodiesterasa para el tratamiento de enfermedades dérmicas
|
|
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
|
|
EP2155747B1
(en)
|
2007-05-10 |
2012-10-24 |
GE Healthcare Limited |
Imidazol (1,2-a)pyridines and related compounds with activity at cannabinoid cb2 receptors
|
|
JP5343845B2
(ja)
|
2007-05-21 |
2013-11-13 |
東レ株式会社 |
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
|
|
WO2008154241A1
(en)
|
2007-06-08 |
2008-12-18 |
Abbott Laboratories |
5-heteroaryl substituted indazoles as kinase inhibitors
|
|
US8648069B2
(en)
|
2007-06-08 |
2014-02-11 |
Abbvie Inc. |
5-substituted indazoles as kinase inhibitors
|
|
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
|
|
AR067562A1
(es)
|
2007-07-18 |
2009-10-14 |
Novartis Ag |
Compuestos heterociclicos inhibidores de kinasa
|
|
KR20100042287A
(ko)
|
2007-07-31 |
2010-04-23 |
쉐링 코포레이션 |
항암요법으로서의 항-유사분열제 및 아우로라 키나제 억제제 조합물
|
|
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
|
|
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
|
|
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
|
|
EP3733161A1
(en)
|
2007-10-12 |
2020-11-04 |
Novartis AG |
Compositions comprising sphingosine 1 phosphate (s1p) receptor modulators
|
|
CA2710194C
(en)
|
2007-12-19 |
2014-04-22 |
Amgen Inc. |
Inhibitors of p13 kinase
|
|
CA2704125A1
(en)
|
2007-12-19 |
2009-07-09 |
Genentech, Inc. |
8-anilinoimidazopyridines and their use as anti-cancer and/or anti-inflammatory agents
|
|
KR100988233B1
(ko)
|
2007-12-26 |
2010-10-18 |
한미홀딩스 주식회사 |
클로피도그렐 1,5-나프탈렌 다이술폰산 염 또는 이의수화물의 약학 조성물 및 제제
|
|
MX2010010012A
(es)
|
2008-03-11 |
2010-10-20 |
Incyte Corp |
Derivados de azetidina y ciclobutano como inhibidores de jak.
|
|
PL2262505T3
(pl)
|
2008-03-12 |
2015-04-30 |
Intra Cellular Therapies Inc |
Podstawione heterocykliczne skondensowane gamma-karboliny w postaci stałej
|
|
EP2265603B1
(en)
|
2008-03-13 |
2014-05-07 |
The General Hospital Corporation |
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
|
|
JPWO2009128520A1
(ja)
|
2008-04-18 |
2011-08-04 |
塩野義製薬株式会社 |
Pi3k阻害活性を有する複素環化合物
|
|
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
|
|
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.
|
|
WO2010010187A1
(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
|
|
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
|
|
US20120021519A1
(en)
|
2008-09-19 |
2012-01-26 |
Presidents And Fellows Of Harvard College |
Efficient induction of pluripotent stem cells using small molecule compounds
|
|
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
|
|
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
|
|
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
|
|
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
|
|
WO2010090991A1
(en)
|
2009-02-04 |
2010-08-12 |
Supernus Pharmaceuticals, Inc. |
Formulations of desvenlafaxine
|
|
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
|
|
ES2435804T3
(es)
|
2009-02-13 |
2013-12-23 |
Bayer Intellectual Property Gmbh |
Pirimidinas condensadas como inhibidores de Akt
|
|
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
|
|
WO2010107404A1
(en)
|
2009-03-16 |
2010-09-23 |
Mahmut Bilgic |
Stable pharmaceutical combinations
|
|
TW201035078A
(en)
|
2009-03-20 |
2010-10-01 |
Incyte Corp |
Substituted heterocyclic compounds
|
|
KR101772963B1
(ko)
|
2009-03-31 |
2017-08-31 |
깃세이 야쿠힌 고교 가부시키가이샤 |
인돌리진 유도체 및 그 의약용도
|
|
CN102428087B
(zh)
|
2009-04-16 |
2015-06-17 |
卡洛斯三世国家癌症研究中心基金会 |
用作激酶抑制剂的咪唑并吡嗪类化合物
|
|
TWI461426B
(zh)
|
2009-05-27 |
2014-11-21 |
Merck Sharp & Dohme |
(二氫)咪唑並異〔5,1-a〕喹啉類
|
|
RU2011153723A
(ru)
|
2009-06-10 |
2013-07-20 |
Суновион Фармасьютикалз Инк. |
Обратные агонисты и антагонисты н3 рецепторов гистамина и способы их применения
|
|
AU2010266040B2
(en)
|
2009-06-25 |
2015-01-15 |
Alkermes Pharma Ireland Limited |
Prodrugs of NH-acidic compounds
|
|
HRP20190016T1
(hr)
|
2009-08-17 |
2019-03-08 |
Intellikine, Llc |
Heterociklički spojevi i njihova upotreba
|
|
US9708255B2
(en)
|
2009-08-18 |
2017-07-18 |
Robert A. Casero |
(bis)urea and (bis)thiourea compounds as epigenic modulators of lysine-specific demethylase 1 and methods of treating disorders
|
|
EP2473495A1
(en)
|
2009-09-18 |
2012-07-11 |
Almac Discovery Limited |
Pharmaceutical compounds
|
|
KR101736218B1
(ko)
|
2009-09-25 |
2017-05-16 |
오리존 지노믹스 에스.에이. |
라이신 특이적 디메틸라아제-1 억제제 및 이의 용도
|
|
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
|
|
EP2526102B1
(en)
|
2010-01-22 |
2017-03-08 |
Fundación Centro Nacional de Investigaciones Oncológicas Carlos III |
Inhibitors of PI3 kinase
|
|
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
|
|
WO2011106573A2
(en)
|
2010-02-24 |
2011-09-01 |
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
|
|
AU2011229423B2
(en)
|
2010-03-18 |
2015-12-10 |
Institut National De La Sante Et De La Recherche Medicale (Inserm) |
Anti-infective compounds
|
|
CA2793279A1
(en)
|
2010-03-18 |
2011-09-22 |
Ulrich Klar |
Imidazopyrazines
|
|
MX342161B
(es)
|
2010-04-02 |
2016-09-19 |
Euroscreen Sa |
Compuestos antagonistas selectivos de receptor nk-3 novedosos, composicion farmaceutica y metodos para utilizarse en trastornos transmitidos por receptores nk-3.
|
|
BR122019020471B1
(pt)
|
2010-04-19 |
2021-06-22 |
Oryzon Genomics S.A. |
Inibidores da desmetilase específica para lisina 1, seus usos e método para sua identificação, e composições farmacêuticas
|
|
PL2560949T3
(pl)
|
2010-04-20 |
2017-01-31 |
Università Degli Studi Di Roma "La Sapienza" |
Pochodne tranylocyprominy jako inhibitory demetylazy histonowej LSD1 i/lub LSD2
|
|
MX2012012145A
(es)
|
2010-04-28 |
2012-11-21 |
Daiichi Sankyo Co Ltd |
Compuestos [5, 6] heterociclico.
|
|
US20130131057A1
(en)
|
2010-05-13 |
2013-05-23 |
Centro Nacional De Investigaciones Oncologicas (Cnio |
New bicyclic compounds as pi3-k and mtor inhibitors
|
|
SG185515A1
(en)
|
2010-05-13 |
2012-12-28 |
Amgen Inc |
Nitrogen heterocyclic compounds useful as pde10 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
|
|
WO2011149438A1
(en)
|
2010-05-28 |
2011-12-01 |
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
|
|
NZ604478A
(en)
|
2010-07-02 |
2014-12-24 |
Gilead Sciences Inc |
Fused heterocyclic compounds as ion channel modulators
|
|
EP2593451B1
(en)
|
2010-07-12 |
2015-08-19 |
Bayer Intellectual Property GmbH |
Substituted imidazo[1,2-a]pyrimidines and -pyridines
|
|
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
|
|
WO2012013728A1
(en)
*
|
2010-07-29 |
2012-02-02 |
Oryzon Genomics S.A. |
Arylcyclopropylamine based demethylase inhibitors of lsd1 and their medical use
|
|
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
|
|
US9006449B2
(en)
|
2010-07-29 |
2015-04-14 |
Oryzon Genomics, S.A. |
Cyclopropylamine derivatives useful as LSD1 inhibitors
|
|
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
|
|
CN103221412B
(zh)
|
2010-09-29 |
2015-08-19 |
橘生药品工业株式会社 |
(氮杂)中氮茚衍生物及其药物用途
|
|
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
|
|
ES2525441T3
(es)
|
2010-10-18 |
2014-12-23 |
E.I. Du Pont De Nemours And Company |
Sulfonamidas nematocidas
|
|
ES2816600T3
(es)
|
2010-10-21 |
2021-04-05 |
Medivation Tech Llc |
Sal tosilato de (8S,9R)-5-fluoro-8-(4-fluorofenil)-9-(1-metil-1H-1,2,4-triazol-5-il)-8,9-dihidro-2H-pirido[4,3,2-de]ftalazin-3(7H)-ona cristalina
|
|
WO2012052745A1
(en)
|
2010-10-21 |
2012-04-26 |
Centro Nacional De Investigaciones Oncológicas (Cnio) |
Combinations of pi3k inhibitors with a second anti -tumor agent
|
|
EP2444084A1
(en)
|
2010-10-21 |
2012-04-25 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Use of PI3K inibitors for the treatment of obesity
|
|
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
|
|
WO2012080729A2
(en)
|
2010-12-14 |
2012-06-21 |
Electrophoretics Limited |
CASEIN KINASE 1δ (CK1δ) INHIBITORS
|
|
WO2012080230A1
(en)
|
2010-12-17 |
2012-06-21 |
Bayer Pharma Aktiengesellschaft |
6 substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
|
|
WO2012080236A1
(en)
|
2010-12-17 |
2012-06-21 |
Bayer Pharma Aktiengesellschaft |
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?.
|
|
JP5822944B2
(ja)
|
2010-12-17 |
2015-11-25 |
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 |
過剰増殖性障害の治療におけるmps−1およびtkk阻害剤として使用するための2置換イミダゾピラジン
|
|
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
|
|
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
|
|
EP2655334B1
(en)
|
2010-12-22 |
2018-10-03 |
Eutropics Pharmaceuticals, Inc. |
Compositions and methods useful for treating diseases
|
|
WO2012100229A2
(en)
|
2011-01-21 |
2012-07-26 |
The General Hospital Corporation |
Compositions and methods for cardiovascular disease
|
|
BRPI1100101B1
(pt)
|
2011-01-28 |
2020-10-20 |
Universidade De São Paulo Usp |
anel oito articulado
|
|
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
|
|
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
|
|
PE20141322A1
(es)
|
2011-03-25 |
2014-10-05 |
Glaxosmithkline Intellectual Property (N 2) Limited |
Ciclopropilaminas como inhibidores de desmetilasa 1 especifica de lisina
|
|
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
|
|
EP2524918A1
(en)
|
2011-05-19 |
2012-11-21 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Imidazopyrazines derivates as kinase inhibitors
|
|
WO2012156537A2
(en)
|
2011-05-19 |
2012-11-22 |
Oryzon Genomics, S.A. |
Lysine demethylase inhibitors for thrombosis and cardiovascular diseases
|
|
WO2012156531A2
(en)
|
2011-05-19 |
2012-11-22 |
Oryzon Genomics, S.A. |
Lysine demethylase inhibitors for inflammatory diseases or conditions
|
|
AU2012265842A1
(en)
|
2011-06-07 |
2014-01-23 |
SPAI Group Ltd. |
Compositions and methods for improving stability and extending shelf life of sensitive food additives and food products thereof
|
|
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
(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
|
|
BR112014003382B1
(pt)
|
2011-08-15 |
2022-03-15 |
University Of Utah Research Foundation |
Análogos de (e)-n-(1-feniletilideno) benzo-hidrazida substituída como inibidores de histona desmetilase e composições farmacêuticas compreendendo-os
|
|
WO2013033688A1
(en)
|
2011-09-01 |
2013-03-07 |
The Brigham And Women's Hospital, Inc. |
Treatment of cancer
|
|
WO2013033515A1
(en)
|
2011-09-02 |
2013-03-07 |
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
|
|
CN104203914B
(zh)
|
2011-10-20 |
2017-07-11 |
奥瑞泽恩基因组学股份有限公司 |
作为lsd1抑制剂的(杂)芳基环丙胺化合物
|
|
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.
|
|
UA116765C2
(uk)
|
2011-10-20 |
2018-05-10 |
Орізон Джіномікс, С.А. |
(гетеро)арилциклопропіламіни як інгібітори lsd1
|
|
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
|
|
CA2857964A1
(en)
|
2011-12-05 |
2013-06-13 |
Brandeis University |
Treatment of amyloidosis by compounds that regulate retromer stabilization
|
|
WO2013131609A1
(en)
|
2012-03-07 |
2013-09-12 |
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
|
|
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
|
|
PE20190736A1
(es)
*
|
2012-06-13 |
2019-05-23 |
Incyte Holdings Corp |
Compuestos triciclicos sustituidos como inhibidores del receptor del factor de crecimiento de fibroblastos (fgfr)
|
|
JP6273274B2
(ja)
|
2012-06-28 |
2018-01-31 |
ノバルティス アーゲー |
補体経路モジュレーターおよびその使用
|
|
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
|
|
CA2886187C
(en)
|
2012-09-28 |
2020-04-14 |
Vanderbilt University |
Fused heterocyclic compounds as selective bmp inhibitors
|
|
MX2015004151A
(es)
|
2012-10-05 |
2015-07-06 |
Rigel Pharmaceuticals Inc |
Inhibidores del factor de diferenciacion de crecimiento-8 (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
|
|
WO2014085613A1
(en)
|
2012-11-30 |
2014-06-05 |
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
|
|
RU2015129087A
(ru)
|
2012-12-19 |
2017-02-02 |
Вокхардт Лимитед |
Стабильная водная композиция, содержащая инсулин человека или его аналог или производное
|
|
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
|
|
EP2956441A4
(en)
|
2013-02-18 |
2016-11-02 |
Scripps Research Inst |
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
|
|
JP2016516399A
(ja)
|
2013-03-13 |
2016-06-09 |
オーストラリアン ニュークリア サイエンス アンド テクノロジー オーガニゼーション |
非機能性tspo遺伝子を有するトランスジェニック非ヒト生物
|
|
US20140343118A1
(en)
|
2013-03-14 |
2014-11-20 |
Duke University |
Methods of treatment using arylcyclopropylamine compounds
|
|
EP2968343A4
(en)
|
2013-03-14 |
2016-11-02 |
Epizyme Inc |
COMBINATION THERAPY FOR THE TREATMENT OF CANCER
|
|
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
|
|
AU2014281398B2
(en)
|
2013-06-19 |
2018-10-04 |
University Of Utah Research Foundation |
Substituted (E)-N'-(1-phenylethylidene) benzohydrazide analogs as histone demethylase inhibitors
|
|
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
|
|
US9556170B2
(en)
|
2013-08-30 |
2017-01-31 |
University Of Utah Research Foundation |
Substituted-1H-benzo[d]imidazole series compounds as lysine-specific demethylase 1 (LSD1) inhibitors
|
|
US9770514B2
(en)
|
2013-09-03 |
2017-09-26 |
ExxPharma Therapeutics LLC |
Tamper-resistant pharmaceutical dosage forms
|
|
DK3043778T3
(da)
|
2013-09-13 |
2017-11-27 |
Bayer Pharma AG |
Farmaceutiske sammensætninger, der indeholder refametinib
|
|
KR101568724B1
(ko)
|
2013-11-13 |
2015-11-12 |
서울대학교산학협력단 |
신규한 화합물, 이의 생산 방법, 및 히스톤 디메틸라제 저해제로서 이의 용도
|
|
LT3080100T
(lt)
|
2013-12-11 |
2023-02-27 |
Celgene Quanticel Research, Inc. |
Lizinui specifinės demetilazės-1 inhibitoriai
|
|
US9527835B2
(en)
|
2014-02-13 |
2016-12-27 |
Incyte Corporation |
Cyclopropylamines as LSD1 inhibitors
|
|
US9428470B2
(en)
|
2014-02-13 |
2016-08-30 |
Takeda Pharmaceutical Company Limited |
Heterocyclic compound
|
|
US9346776B2
(en)
|
2014-02-13 |
2016-05-24 |
Takeda Pharmaceutical Company Limited |
Fused heterocyclic compound
|
|
DK3105226T3
(da)
|
2014-02-13 |
2019-10-14 |
Incyte Corp |
Cyclopropylaminer som lsd1-inhibitorer
|
|
PT3105218T
(pt)
|
2014-02-13 |
2019-12-05 |
Incyte Corp |
Ciclopropilaminas como inibidores de lsd1
|
|
EP3105219B9
(en)
|
2014-02-13 |
2018-10-03 |
Incyte Corporation |
Cyclopropylamines as lsd1 inhibitors
|
|
WO2015145145A1
(en)
|
2014-03-24 |
2015-10-01 |
Cipla Limited |
Pharmaceutical composition comprising 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
|
|
KR102379518B1
(ko)
|
2014-04-02 |
2022-03-25 |
브리스톨-마이어스 스큅 컴퍼니 |
비아릴 키나제 억제제
|
|
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
|
|
TN2016000418A1
(en)
|
2014-04-11 |
2018-04-04 |
Takeda Pharmaceuticals Co |
Cyclopropanamine compound and use thereof.
|
|
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
|
|
DK3148974T3
(en)
|
2014-05-30 |
2018-10-29 |
St Europeo Di Oncologia S R L |
CYCLOPROPYLAMINE COMPOUNDS AS HYDONDEMETHYLASE 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
|
|
WO2016007722A1
(en)
|
2014-07-10 |
2016-01-14 |
Incyte Corporation |
Triazolopyridines and triazolopyrazines as lsd1 inhibitors
|
|
US9758523B2
(en)
|
2014-07-10 |
2017-09-12 |
Incyte Corporation |
Triazolopyridines and triazolopyrazines as LSD1 inhibitors
|
|
TW201613925A
(en)
|
2014-07-10 |
2016-04-16 |
Incyte Corp |
Imidazopyrazines as LSD1 inhibitors
|
|
TWI687419B
(zh)
|
2014-07-10 |
2020-03-11 |
美商英塞特公司 |
作為lsd1抑制劑之咪唑并吡啶及咪唑并吡嗪
|
|
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
|
|
KR102550852B1
(ko)
|
2014-10-08 |
2023-07-05 |
에프. 호프만-라 로슈 아게 |
알도스테론 신타아제 억제제로서의 스피로다이아민 유도체
|
|
WO2016161279A1
(en)
|
2015-04-03 |
2016-10-06 |
Bristol-Myers Squibb Company |
Inhibitors of indoleamine 2,3-dioxygenase for the treatment of cancer
|
|
BR112017020935A2
(pt)
|
2015-04-03 |
2018-07-10 |
Mutabilis |
?compostos, composição farmacêutica e conjunto?
|
|
EP3626720A1
(en)
|
2015-04-03 |
2020-03-25 |
Incyte Corporation |
Heterocyclic compounds as lsd1 inhibitors
|
|
KR102710120B1
(ko)
|
2015-08-12 |
2024-09-27 |
인사이트 홀딩스 코포레이션 |
Lsd1 저해제의 염
|
|
CN112656772B
(zh)
|
2015-10-15 |
2022-05-20 |
浙江东日药业有限公司 |
利伐沙班药物组合物
|
|
MX384792B
(es)
|
2015-12-29 |
2025-03-14 |
Mirati Therapeutics Inc |
Inhibidores de desmetilasa especifica de lisina 1 (lsd1).
|
|
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
|
|
PE20190377A1
(es)
|
2016-04-22 |
2019-03-08 |
Incyte Corp |
Formulaciones de un inhibidor de lsd 1
|
|
EP3570843A1
(en)
|
2017-01-18 |
2019-11-27 |
Vanderbilt University |
Fused heterocyclic compounds as selective bmp inhibitors
|
|
CN109963854B
(zh)
|
2017-03-16 |
2022-04-12 |
江苏恒瑞医药股份有限公司 |
杂芳基并[4,3-c]嘧啶-5-胺类衍生物、其制备方法及其在医药上的应用
|
|
MA53097A
(fr)
|
2018-07-05 |
2021-05-12 |
Incyte Corp |
Dérivés de pyrazine fusionnés en tant qu'inhibiteurs d'a2a/a2b
|
|
US10968200B2
(en)
|
2018-08-31 |
2021-04-06 |
Incyte Corporation |
Salts of an LSD1 inhibitor and processes for preparing the same
|