NL7013068A
(en)
|
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
(en)
|
1986-12-05 |
1989-03-31 |
Montpellier I Universite |
ALKYLAMINO-8 IMIDAZO (1,2-A) PYRAZINES AND DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
|
JPH032778Y2
(en)
|
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
(en)
|
1989-07-13 |
1999-01-06 |
株式会社科薬 |
Aqueous solution of stable polymyxin antibiotics
|
IL96432A0
(en)
|
1989-11-30 |
1991-08-16 |
Schering Ag |
Pesticidal compositions containing pyridine derivatives and novel pyridine derivatives
|
FR2662163A1
(en)
|
1990-05-16 |
1991-11-22 |
Lipha |
New 8-amino-1,2,4-triazolo[4,3-a]pyrazines, preparation processes and medicaments containing them
|
ATE177426T1
(en)
|
1992-06-17 |
1999-03-15 |
Upjohn Co |
PYRRIDINO-, PYRROLIDINO- AND AZEPINO- SUBSTITUTED OXIMES AS ANTIATHEROSCLEROSIC AGENTS AND ANTIHYPERCHOLESTEROLEMIC AGENTS
|
JP2923139B2
(en)
|
1992-10-05 |
1999-07-26 |
三井化学株式会社 |
Agent
|
DE4327027A1
(en)
|
1993-02-15 |
1994-08-18 |
Bayer Ag |
Imidazoazine
|
FR2711993B1
(en)
|
1993-11-05 |
1995-12-01 |
Rhone Poulenc Rorer Sa |
Drugs containing 7H-imidazol [1,2-a] pyrazine-8-one derivatives, new compounds and their preparation.
|
US5932223A
(en)
|
1996-09-26 |
1999-08-03 |
Merck & Co., Inc. |
Rotavirus vaccine formulations
|
WO1999024434A1
(en)
|
1997-11-11 |
1999-05-20 |
Ono Pharmaceutical Co., Ltd. |
Fused pyrazine compounds
|
JP2000319277A
(en)
|
1999-05-11 |
2000-11-21 |
Ono Pharmaceut Co Ltd |
Condensed pyrazine compound and medicinal agent having the same as active ingredient
|
JP2000319278A
(en)
|
1999-05-11 |
2000-11-21 |
Ono Pharmaceut Co Ltd |
Condensed pyrazine compound and medicinal agent having the same as active ingredient
|
JP4032566B2
(en)
|
1999-06-21 |
2008-01-16 |
東レ株式会社 |
Light emitting element
|
JP4041624B2
(en)
|
1999-07-21 |
2008-01-30 |
三井化学株式会社 |
Organic electroluminescence device
|
JP2001057292A
(en)
|
1999-08-20 |
2001-02-27 |
Toray Ind Inc |
Luminescent element
|
NZ518052A
(en)
|
1999-09-28 |
2005-04-29 |
Panacea Biotec Ltd |
Controlled release compositions comprising nimesulide (4-nitro-2-phenoxymethanesulfonanilide) for a once-a-day oral dosage to treat diseases such as arthritis
|
SE9903611D0
(en)
|
1999-10-06 |
1999-10-06 |
Astra Ab |
Novel compounds III
|
DE19948434A1
(en)
|
1999-10-08 |
2001-06-07 |
Gruenenthal Gmbh |
Substance library containing bicyclic imidazo-5-amines and / or bicyclic imidazo-3-amines
|
JP4409680B2
(en)
|
1999-10-18 |
2010-02-03 |
株式会社ヤクルト本社 |
Tricyclic fused imidazole derivatives
|
US6403588B1
(en)
|
2000-04-27 |
2002-06-11 |
Yamanouchi Pharmaceutical Co., Ltd. |
Imidazopyridine derivatives
|
AU2001252609A1
(en)
|
2000-04-27 |
2001-11-12 |
Imperial Cancer Research Technology Ltd. |
Imidazopyridine derivatives
|
HU230396B1
(en)
|
2000-06-28 |
2016-04-28 |
Smithkline Beecham Plc |
Wet milling process
|
AR029538A1
(en)
|
2000-07-06 |
2003-07-02 |
Wyeth Corp |
PHARMACEUTICAL COMPOSITIONS OF ESTROGEN AGENTS
|
CA2419626A1
(en)
|
2000-07-14 |
2002-01-24 |
Rajagopal Bakthavatachalam |
Imidazo¬1,2-a|pyrazines for the treatment of neurological disorders
|
DE10050663A1
(en)
|
2000-10-13 |
2002-04-18 |
Gruenenthal Gmbh |
Use of amino-substituted imidazo(1,2-a)pyridine, imidazo(1,2-a)pyrimidine and imidazo(1,2-a)pyrazine derivatives as NO synthase inhibitors, e.g. in treatment of migraine and neurodegenerative diseases
|
AU2001295992A1
(en)
|
2000-10-24 |
2002-05-06 |
Sankyo Company Limited |
Imidazopyridine derivatives
|
JP2002205992A
(en)
|
2000-11-08 |
2002-07-23 |
Takeda Chem Ind Ltd |
Bicyclic triazolone derivative and herbicide comprising the same
|
AU1253002A
(en)
|
2000-11-10 |
2002-05-21 |
Merck Sharp & Dohme |
Imidazo-triazine derivatives as ligands for gaba receptors
|
AU2002224927A1
(en)
|
2000-12-13 |
2002-06-24 |
Basf Aktiengesellschaft |
Use of substituted imidazoazines, novel imidazoazines, methods for the production thereof, and agents containing these compounds
|
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
(en)
|
2001-06-26 |
2004-06-16 |
Japan Tobacco Inc |
THERAPEUTIC AGENT FOR HEPATITIS C THAT INCLUDES A CONDENSED RING COMPOUND, CONDENSED RING COMPOUND, PHARMACEUTICAL COMPOSITION THAT UNDERSTANDS, BENZIMIDAZOL, THIAZOL AND BIFENYL COMPOUNDS USED AS INTERMEDIARY COMPARTMENTS OF COMPARTMENTS
|
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
|
WO2003062392A2
(en)
|
2002-01-18 |
2003-07-31 |
Ceretek Llc |
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
|
US20060276339A1
(en)
|
2002-10-16 |
2006-12-07 |
Windsor J B |
Methods and compositions for increasing the efficacy of biologically-active ingredients
|
EP1572682A4
(en)
|
2002-12-20 |
2008-01-23 |
Pharmacia Corp |
Acyclic pyrazole compounds
|
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
|
US7157460B2
(en)
|
2003-02-20 |
2007-01-02 |
Sugen Inc. |
Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
|
US7186832B2
(en)
|
2003-02-20 |
2007-03-06 |
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
|
TWI344955B
(en)
|
2003-03-14 |
2011-07-11 |
Ono Pharmaceutical Co |
Heterocyclic rinf having nitrogen atom derivatives and medicament containing the derivatives as active ingredient
|
JP2006522750A
(en)
|
2003-04-11 |
2006-10-05 |
ノボ ノルディスク アクティーゼルスカブ |
Combination therapy using 11β-hydroxysteroid dehydrogenase type 1 inhibitors and antihypertensive agents to treat metabolic syndrome and related diseases and disorders
|
JP2006522747A
(en)
|
2003-04-11 |
2006-10-05 |
ノボ ノルディスク アクティーゼルスカブ |
Pharmaceutical use of condensed 1,2,4-triazole
|
AU2004233828B2
(en)
|
2003-04-24 |
2009-05-28 |
Merck Sharp & Dohme Corp. |
Inhibitors of Akt activity
|
SE0301653D0
(en)
|
2003-06-05 |
2003-06-05 |
Astrazeneca Ab |
Novel compounds
|
AU2004257267B2
(en)
|
2003-07-14 |
2009-12-03 |
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
(en)
|
2003-09-16 |
2005-04-07 |
Kissei Pharmaceut Co Ltd |
NEW IMIDAZO[1,5-a]PYRAZINE DERIVATIVE, MEDICINE COMPOSITION CONTAINING THE SAME AND THEIR USE
|
DE602004008098T8
(en)
|
2003-10-10 |
2008-04-17 |
Pfizer Products Inc., Groton |
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
|
EP1677791A4
(en)
|
2003-10-31 |
2007-08-15 |
Takeda Pharmaceutical |
Nitrogen-containing fused heterocyclic compounds
|
EP1698335A4
(en)
|
2003-12-26 |
2007-08-01 |
Ono Pharmaceutical Co |
Preventive and/or therapeutic agent for disease in which mitochondrial benzodiazepine receptor participates
|
WO2005077948A1
(en)
|
2004-02-16 |
2005-08-25 |
Daiichi Pharmaceutical Co., Ltd. |
Fungicidal 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
|
BRPI0510319A
(en)
*
|
2004-04-26 |
2007-10-16 |
Pfizer |
hiv integrase enzyme inhibitors
|
US8383154B2
(en)
|
2004-05-11 |
2013-02-26 |
Egalet A/S |
Swellable dosage form comprising gellan gum
|
TW200612918A
(en)
|
2004-07-29 |
2006-05-01 |
Threshold Pharmaceuticals Inc |
Lonidamine analogs
|
MX2007001612A
(en)
|
2004-08-18 |
2007-04-10 |
Upjohn Co |
Triazolopyridine compounds useful for the treatment of inflammation.
|
EP1799671A4
(en)
|
2004-09-02 |
2009-06-10 |
Smithkline Beecham Corp |
Chemical compounds
|
CA2582482A1
(en)
|
2004-10-07 |
2006-04-13 |
Warner-Lambert Company Llc |
Triazolopyridine derivatives as antibacterial agents
|
CA2587210A1
(en)
|
2004-11-22 |
2006-06-01 |
Threshold Pharmaceuticals, Inc. |
Tubulin binding anti cancer agents and prodrugs thereof
|
AU2005311451A1
(en)
|
2004-12-01 |
2006-06-08 |
Merck Serono Sa |
[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
|
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
(en)
|
2005-03-07 |
2005-06-06 |
Alfa Wassermann Spa |
GASTRORESISTIC PHARMACEUTICAL FORMULATIONS CONTAINING RIFAXIMINA
|
AR053712A1
(en)
|
2005-04-18 |
2007-05-16 |
Neurogen Corp |
HETEROARILOS SUBSTITUTED, ANTAGONISTS OF CB1 (RECEIVER 1 CANABINOID)
|
AU2005332594A1
(en)
|
2005-06-09 |
2006-12-14 |
Oncalis Ag |
Angiogenesis inhibitors
|
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
|
US7572808B2
(en)
|
2005-06-17 |
2009-08-11 |
Bristol-Myers Squibb Company |
Triazolopyridine cannabinoid receptor 1 antagonists
|
US7632837B2
(en)
|
2005-06-17 |
2009-12-15 |
Bristol-Myers Squibb Company |
Bicyclic heterocycles as cannabinoid-1 receptor modulators
|
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
(en)
|
2005-09-02 |
2009-02-19 |
アボット・ラボラトリーズ |
New imidazo heterocycle
|
JP2009507843A
(en)
|
2005-09-09 |
2009-02-26 |
シェーリング コーポレイション |
Aza-fused cyclin-dependent kinase inhibitors
|
CA2628455A1
(en)
|
2005-11-10 |
2007-05-24 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
EP1959966B1
(en)
|
2005-11-28 |
2020-06-03 |
Marinus Pharmaceuticals, Inc. |
Ganaxolone formulations and methods for the making and use thereof
|
AU2006331363B2
(en)
|
2005-12-27 |
2012-07-05 |
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
(en)
|
2006-02-14 |
2007-11-15 |
Novartis Ag |
HETEROCICLIC COMPOUNDS AS INHIBITORS OF PHOSPHATIDYLINOSITOL 3-KINASES (PI3Ks)
|
RU2008143179A
(en)
|
2006-03-31 |
2010-05-10 |
Новартис АГ (CH) |
ORGANIC COMPOUNDS
|
AR061229A1
(en)
|
2006-06-06 |
2008-08-13 |
Schering Corp |
IMIDAZOPIRAZINS AS INHIBITORS OF PROTEIN QUINASA
|
US20090175852A1
(en)
|
2006-06-06 |
2009-07-09 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
CN101472903A
(en)
|
2006-06-22 |
2009-07-01 |
马林克罗特公司 |
Pyrazine derivatives with extended conjugation and uses thereof
|
JP2009542662A
(en)
|
2006-06-29 |
2009-12-03 |
シェーリング コーポレイション |
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
|
US8198448B2
(en)
|
2006-07-14 |
2012-06-12 |
Amgen Inc. |
Fused heterocyclic derivatives and methods of use
|
US8217177B2
(en)
|
2006-07-14 |
2012-07-10 |
Amgen Inc. |
Fused heterocyclic derivatives and methods of use
|
PE20121506A1
(en)
|
2006-07-14 |
2012-11-26 |
Amgen Inc |
TRIAZOLOPYRIDINE COMPOUNDS AS C-MET INHIBITORS
|
JP2009544625A
(en)
|
2006-07-20 |
2009-12-17 |
メーメット・カーラマン |
Benzothiophene inhibitors of RHO kinase
|
WO2008027812A2
(en)
|
2006-08-28 |
2008-03-06 |
Forest Laboratories Holdings Limited |
Imidazopyridine and imidazopyrimidine derivatives
|
DE102006041292A1
(en)
|
2006-09-01 |
2008-03-06 |
Henkel Kgaa |
Use of optionally substituted hexagonal heterocycle with a nitrogen in the ring for activating and improving the brightening effect of the hydrogen peroxide for keratin fibers such as fur, wool, feathers and human hair
|
WO2008037607A1
(en)
|
2006-09-25 |
2008-04-03 |
Basf Se |
Heterocyclic compounds containing carbonyl groups, and the use thereof for controlling phytopathogenic fungi
|
EP2086973B1
(en)
|
2006-10-11 |
2012-01-25 |
Amgen Inc., |
Imidazo- and triazolo-pyridine compounds and methods of use therof
|
JP2010509363A
(en)
|
2006-11-08 |
2010-03-25 |
ノババックス,インコーポレイテッド |
Process for the production of multi-phase pharmaceutical compositions in solid dosage forms
|
CN101553487B
(en)
|
2006-11-08 |
2012-06-13 |
纽罗克里生物科学有限公司 |
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
|
WO2008056176A1
(en)
|
2006-11-10 |
2008-05-15 |
Scottish Biomedical Limited |
Pyrazolopyrimidines as phosphodiesterase inhibitors
|
EA026126B1
(en)
|
2006-11-22 |
2017-03-31 |
Инсайт Холдингс Корпорейшн |
Imidazotriazines and imidazopyrimidines as kinase inhibitors
|
ATE495743T1
(en)
|
2006-12-01 |
2011-02-15 |
Galapagos Nv |
TRIAZOLOPYRIDINE COMPOUNDS FOR THE TREATMENT OF DEGENERATIONAL AND INFLAMMATORY DISEASES
|
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
(en)
|
2007-03-16 |
2008-09-18 |
Bayer Healthcare Ag |
Substituted imidazo and triazolopyrimidines
|
EP1972628A1
(en)
|
2007-03-21 |
2008-09-24 |
Schwarz Pharma Ag |
Indolizines and aza-analog derivatives thereof as CNS active compounds
|
EP2146989B1
(en)
|
2007-04-16 |
2012-01-04 |
Leo Pharma A/S |
Triazolopyridines as phosphodiesterase inhibitors for treatment of dermal diseases
|
EP2142551B1
(en)
|
2007-04-17 |
2015-10-14 |
Bristol-Myers Squibb Company |
Fused heterocyclic 11-beta-hydroxysteroid dehydrogenase type i inhibitors
|
US20110206607A1
(en)
|
2007-05-10 |
2011-08-25 |
Roger Olsson |
Imidazol (1,2-a)pyridines and related compounds with activity at cannabinoid cb2 receptors
|
EP2168579B1
(en)
|
2007-05-21 |
2017-10-11 |
Toray Industries, Inc. |
Oral preparation comprising specific organic acid, and method for improvement in dissolution 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
|
JP2010529195A
(en)
|
2007-06-14 |
2010-08-26 |
シェーリング コーポレイション |
Imidazopyrazine as an inhibitor of protein kinase
|
CL2008001839A1
(en)
|
2007-06-21 |
2009-01-16 |
Incyte Holdings Corp |
Compounds derived from 2,7-diazaspirocycles, inhibitors of 11-beta hydroxyl steroid dehydrogenase type 1; pharmaceutical composition comprising said compounds; Useful to treat obesity, diabetes, glucose intolerance, type II diabetes, among other diseases.
|
US20090004281A1
(en)
|
2007-06-26 |
2009-01-01 |
Biovail Laboratories International S.R.L. |
Multiparticulate osmotic delivery system
|
JP2010533680A
(en)
|
2007-07-18 |
2010-10-28 |
ノバルティス アーゲー |
Bicyclic heteroaryl compounds and their use as kinase inhibitors
|
BRPI0814874A2
(en)
|
2007-07-31 |
2019-09-24 |
Schering Corp |
combination of antimitotic agent and aurora kinase inhibitor as anticancer treatment.
|
WO2009017954A1
(en)
|
2007-08-01 |
2009-02-05 |
Phenomix Corporation |
Inhibitors of jak2 kinase
|
EA201000201A1
(en)
|
2007-08-10 |
2010-12-30 |
ГЛАКСОСМИТКЛАЙН ЭлЭлСи |
NITROGEN-CONTAINING BICYCLIC CHEMICALS FOR THE TREATMENT OF 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
(en)
|
2007-08-24 |
2009-02-27 |
Oreal |
Composition for coloring keratin fibers, preferably human hair, comprises amino pyrazolopyridine oxidation bases, couplers, and surfactants comprising alkyl ether carboxylic acid and alkyl polyglucosides
|
FR2920091A1
(en)
|
2007-08-24 |
2009-02-27 |
Oreal |
Composition for coloring keratin fibers, preferably human hair, comprises amino pyrazolopyridine oxidation bases, couplers and polyols comprising hydrocarbon chain carrying two hydroxyl functions, where the chain is free from ether function
|
KR20090022616A
(en)
|
2007-08-31 |
2009-03-04 |
한올제약주식회사 |
Oral administration drug, which contains clopidogrel besylate
|
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
(en)
|
2007-10-11 |
2011-06-22 |
アストラゼネカ アクチボラグ |
Pyrrolo [2,3-D] pyrimidine derivatives as protein kinase B inhibitors
|
SG187458A1
(en)
|
2007-10-12 |
2013-02-28 |
Novartis Ag |
Compositions comprising sphingosine 1 phosphate (s1p) receptor modulators
|
NZ585306A
(en)
|
2007-12-19 |
2012-05-25 |
Genentech Inc |
8-Anilinoimidazopyridines and their use as anti-cancer and/or anti-inflammatory agents
|
WO2009085230A1
(en)
|
2007-12-19 |
2009-07-09 |
Amgen Inc. |
Inhibitors of pi3 kinase
|
KR100988233B1
(en)
|
2007-12-26 |
2010-10-18 |
한미홀딩스 주식회사 |
Pharmaceutical composition and formulation comprising clopidogrel 1,5-naphthalene disulfonate or hydrate thereof
|
PT2288610T
(en)
|
2008-03-11 |
2016-10-17 |
Incyte Holdings Corp |
Azetidine and cyclobutane derivatives as jak inhibitors
|
PL2262505T3
(en)
|
2008-03-12 |
2015-04-30 |
Intra Cellular Therapies Inc |
Substituted heterocycle fused gamma-carbolines solid
|
US8507501B2
(en)
|
2008-03-13 |
2013-08-13 |
The Brigham And Women's Hospital, Inc. |
Inhibitors of the BMP signaling pathway
|
WO2009114870A2
(en)
|
2008-03-14 |
2009-09-17 |
Intellikine, Inc. |
Kinase inhibitors and methods of use
|
JPWO2009128520A1
(en)
|
2008-04-18 |
2011-08-04 |
塩野義製薬株式会社 |
Heterocyclic compounds having PI3K inhibitory activity
|
DE102008023801A1
(en)
|
2008-05-15 |
2009-11-19 |
Bayer Schering Pharma Aktiengesellschaft |
Substituted imidazo and triazolopyrimidines, imidazo and pyrazolopyrazines and imidazotriazines
|
US8349210B2
(en)
|
2008-06-27 |
2013-01-08 |
Transitions Optical, Inc. |
Mesogenic stabilizers
|
WO2010010187A1
(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.
|
WO2010010189A1
(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
(en)
|
2008-08-14 |
2010-03-26 |
Takeda Pharmaceutical |
CMET INHIBITORS
|
TR200806298A2
(en)
|
2008-08-22 |
2010-03-22 |
Bi̇lgi̇ç Mahmut |
Pharmaceutical formulation
|
JP2010070503A
(en)
|
2008-09-19 |
2010-04-02 |
Daiichi Sankyo Co Ltd |
Antifungal 2-amino-triazolopyridine derivative
|
WO2010033906A2
(en)
|
2008-09-19 |
2010-03-25 |
President And Fellows Of Harvard College |
Efficient induction of pluripotent stem cells using small molecule compounds
|
CA2738429C
(en)
|
2008-09-26 |
2016-10-25 |
Intellikine, Inc. |
Heterocyclic kinase inhibitors
|
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
|
ES2403633T3
(en)
|
2008-12-04 |
2013-05-20 |
Proximagen Limited |
Imidazopyridine Compounds
|
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
|
US20100209489A1
(en)
|
2009-02-04 |
2010-08-19 |
Supernus Pharmaceuticals, Inc. |
Formulations of desvenlafaxine
|
EP2393813B1
(en)
|
2009-02-04 |
2013-07-31 |
Vitae Pharmaceuticals, Inc. |
Cyclic inhibitors of 11 ß-hydroxysteroid dehydrogenase 1 useful for the treatment of diseases related to elevated level of cortisol
|
TR200900878A2
(en)
|
2009-02-05 |
2010-08-23 |
Bi̇lgi̇ç Mahmut |
Pharmaceutical formulations combined in a single dosage form
|
TR200900879A2
(en)
|
2009-02-05 |
2010-08-23 |
Bi̇lgi̇ç Mahmut |
Pharmaceutical compositions in which the active ingredients are combined in a single dosage form
|
CA2752114C
(en)
|
2009-02-13 |
2017-06-20 |
Bayer Pharma Aktiengesellschaft |
Fused pyrimidines as akt inhibitors
|
WO2010104307A2
(en)
|
2009-03-07 |
2010-09-16 |
주식회사 메디젠텍 |
Pharmaceutical compositions for treating or preventing diseases caused by the translocation of gsk3 from the cell nucleus to the cytoplasm, containing compounds for inhibiting the translocation of gsk3 from the cell nucleus to the cytoplasm
|
WO2010107404A1
(en)
|
2009-03-16 |
2010-09-23 |
Mahmut Bilgic |
Stable pharmaceutical combinations
|
AR076052A1
(en)
|
2009-03-20 |
2011-05-18 |
Incyte Corp |
DERIVATIVES OF REPLACED PYRIMIDINS, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND USE OF THE SAME IN ASSOCIATED DISORDERS WITH RECEPTORS OF H4 HISTAMINE, SUCH AS INFLAMMATORY DISORDERS, PRURITE AND PAIN.
|
SI2415771T1
(en)
|
2009-03-31 |
2013-12-31 |
Kissei Pharmaceutical Co., Ltd. |
Indolizine derivative and use thereof for medical purposes
|
BRPI1014572B8
(en)
|
2009-04-16 |
2022-07-19 |
Fundacion Centro Nac De Investigaciones Oncologicas Carlos Iii |
IMIDAZOPYRAZINES FOR USE AS KINASE INHIBITORS
|
TWI461426B
(en)
|
2009-05-27 |
2014-11-21 |
Merck Sharp & Dohme |
(dihydro)imidazoiso[5,1-a]quinolines
|
BRPI1012097A2
(en)
|
2009-06-10 |
2016-03-22 |
Sunovion Pharmaceuticals Inc |
h3 histamine antagonists and inverse antagonists and methods of their use.
|
AU2010266040B2
(en)
|
2009-06-25 |
2015-01-15 |
Alkermes Pharma Ireland Limited |
Prodrugs of NH-acidic compounds
|
NZ598220A
(en)
|
2009-08-17 |
2014-02-28 |
Intellikine Llc |
Heterocyclic compounds and uses thereof
|
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
|
US8546376B2
(en)
|
2009-09-18 |
2013-10-01 |
Almac Discovery Limited |
Pharmaceutical compounds
|
KR101736218B1
(en)
|
2009-09-25 |
2017-05-16 |
오리존 지노믹스 에스.에이. |
Lysine Specific Demethylase-1 INHIBITORS THEIR USE
|
EP2486002B1
(en)
|
2009-10-09 |
2019-03-27 |
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
|
CA2787714C
(en)
|
2010-01-22 |
2019-04-09 |
Joaquin Pastor Fernandez |
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
|
WO2011106105A2
(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
|
WO2011113862A1
(en)
|
2010-03-18 |
2011-09-22 |
Bayer Pharma Aktiengesellschaft |
Imidazopyrazines
|
NZ602311A
(en)
|
2010-03-18 |
2014-08-29 |
Pasteur Institut Korea |
Anti-infective compounds
|
DK2552920T3
(en)
|
2010-04-02 |
2017-06-12 |
Ogeda Sa |
UNKNOWN UNKNOWN NK-3 RECEPTOR SELECTIVE ANTAGONIST RELATIONS, PHARMACEUTICAL COMPOSITION AND METHODS FOR USE IN NK-3 RECEPTOR-MEDIUM DISORDERS
|
ES2607081T3
(en)
|
2010-04-19 |
2017-03-29 |
Oryzon Genomics, S.A. |
Lysine-1 specific demethylase inhibitors and their use
|
EP2560949B1
(en)
|
2010-04-20 |
2015-12-02 |
Università degli Studi di Roma "La Sapienza" |
Tranylcypromine derivatives as inhibitors of histone demethylase lsd1 and/or lsd2
|
AU2011246067A1
(en)
|
2010-04-28 |
2012-09-27 |
Daiichi Sankyo Company, Limited |
[5,6] heterocyclic compound
|
WO2011141713A1
(en)
|
2010-05-13 |
2011-11-17 |
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
(en)
|
2010-05-20 |
2011-11-23 |
上海亚盛医药科技有限公司 |
Apogossypolone self-emulsifying drug delivery system and preparation method thereof
|
EP2575808A1
(en)
|
2010-05-28 |
2013-04-10 |
Mahmut Bilgic |
Combination of antihypertensive agents
|
CN102295642B
(en)
|
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-Aryimidazole is [1,2-a] pyridine-3-acetamide, Preparation Method And The Use also
|
MX2012015096A
(en)
|
2010-07-02 |
2013-05-28 |
Gilead Sciences Inc |
Fused heterocyclic compounds as ion channel modulators.
|
WO2012007345A2
(en)
|
2010-07-12 |
2012-01-19 |
Bayer Pharma Aktiengesellschaft |
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
(en)
|
2010-07-16 |
2013-04-03 |
钟术光 |
Solid preparation and preparation method thereof
|
CN101987081B
(en)
|
2010-07-16 |
2012-08-08 |
钟术光 |
Controlled release preparation
|
HUE037937T2
(en)
*
|
2010-07-29 |
2021-11-29 |
Oryzon Genomics Sa |
Arylcyclopropylamine based demethylase inhibitors of lsd1 and their medical use
|
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
|
CN102397552B
(en)
|
2010-09-10 |
2016-06-08 |
广州自远生物科技有限公司 |
A kind of medicine compound preparation of quinolone containing class and its preparation method and application
|
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
|
EP2623505B1
(en)
|
2010-09-29 |
2015-07-29 |
Kissei Pharmaceutical Co., Ltd. |
(aza)indolizine derivatives as xanthine oxidase inhibitors
|
US20130303545A1
(en)
|
2010-09-30 |
2013-11-14 |
Tamara Maes |
Cyclopropylamine derivatives useful as lsd1 inhibitors
|
JP2013540767A
(en)
|
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 |
Compositions and methods for modulating immunodeficiency virus transcription
|
WO2012054233A1
(en)
|
2010-10-18 |
2012-04-26 |
E. I. Du Pont De Nemours And Company |
Nematocidal sulfonamides
|
EP2444084A1
(en)
|
2010-10-21 |
2012-04-25 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Use of PI3K inibitors for the treatment of obesity
|
CN103282365B
(en)
|
2010-10-21 |
2017-12-29 |
麦迪韦逊科技有限公司 |
(8S, 9R) 5 fluorine 8 (4 fluorophenyl) 9 (base of 1 methyl 1H, 1,2,4 triazoles 5) 8,9 dihydro 2H pyridos [4,3,2 de] phthalazines 3 (7H) ketone toluene fulfonate of crystallization
|
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
|
ES2650744T3
(en)
|
2010-12-14 |
2018-01-22 |
Electrophoretics Limited |
Casein kinase 1 delta inhibitors (CK1delta)
|
EP2651945A1
(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
|
CN103443100B
(en)
|
2010-12-17 |
2016-03-23 |
拜耳知识产权有限责任公司 |
The 6-Imidazopyrazines of the replacement of MPS-1 and TKK inhibitor is used as in the treatment of hyperproliferative disorders
|
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
|
CN103370322B
(en)
|
2010-12-17 |
2016-02-10 |
拜耳知识产权有限责任公司 |
The Imidazopyrazines that the 2-being used as MPS-1 and TKK inhibitor in the treatment of hyperproliferative disorders replaces
|
UY33805A
(en)
|
2010-12-17 |
2012-07-31 |
Boehringer Ingelheim Int |
? Dihydrobenzofuranyl-piperidinyl, aza-dihydrobenzofuranylpiperidinyl and diaza-dihydrobenzofuranyl-piperidinyl derivatives, pharmaceutical compositions containing them and uses thereof?
|
TWI617559B
(en)
|
2010-12-22 |
2018-03-11 |
江蘇恆瑞醫藥股份有限公司 |
2-arylimidazo[1,2-b]pyridazine, 2-phenylimidazo[1,2-a]pyridine, and 2-phenylimidazo[1,2-a]pyrazine derivatives
|
WO2012088438A1
(en)
|
2010-12-22 |
2012-06-28 |
Eutropics Pharmaceuticals, Inc. |
Compositions and methods useful for treating diseases
|
EP2665726A4
(en)
|
2011-01-21 |
2014-09-03 |
Gen Hospital Corp |
Compositions and methods for cardiovascular disease
|
BRPI1100101B1
(en)
|
2011-01-28 |
2020-10-20 |
Universidade De São Paulo Usp |
eight articulated ring
|
US20140163041A1
(en)
|
2011-02-08 |
2014-06-12 |
Oryzon Genomics S.A. |
Lysine demethylase inhibitors for myeloproliferative or lymphoproliferative diseases or disorders
|
WO2012107498A1
(en)
|
2011-02-08 |
2012-08-16 |
Oryzon Genomics S.A. |
Lysine demethylase inhibitors for myeloproliferative disorders
|
JP5808826B2
(en)
|
2011-02-23 |
2015-11-10 |
インテリカイン, エルエルシー |
Heterocyclic compounds and uses thereof
|
WO2012129562A2
(en)
|
2011-03-24 |
2012-09-27 |
The Scripps Research Institute |
Compounds and methods for inducing chondrogenesis
|
PE20141322A1
(en)
|
2011-03-25 |
2014-10-05 |
Glaxosmithkline Intellectual Property (N 2) Limited |
CYCLOPROPYLAMINES AS INHIBITORS OF LYSINE-SPECIFIC DESMETILASE 1
|
WO2012147890A1
(en)
|
2011-04-27 |
2012-11-01 |
持田製薬株式会社 |
Novel azole derivative
|
US20140296255A1
(en)
|
2011-05-19 |
2014-10-02 |
Oryzong Genomics, S.A. |
Lysine demethylase inhibitors for thrombosis and cardiovascular diseases
|
EP2524918A1
(en)
|
2011-05-19 |
2012-11-21 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Imidazopyrazines derivates as kinase inhibitors
|
EP2741741A2
(en)
|
2011-05-19 |
2014-06-18 |
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
|
AR086983A1
(en)
|
2011-06-20 |
2014-02-05 |
Incyte Corp |
DERIVATIVES OF AZETIDINIL FENIL, PIRIDIL OR PIRAZINIL CARBOXAMIDA AS JAK INHIBITORS
|
TW201311149A
(en)
|
2011-06-24 |
2013-03-16 |
Ishihara Sangyo Kaisha |
Pesticide
|
EP2548877A1
(en)
|
2011-07-19 |
2013-01-23 |
MSD Oss B.V. |
4-(5-Membered fused pyridinyl)benzamides as BTK-inhibitors
|
US9278931B2
(en)
|
2011-08-09 |
2016-03-08 |
Takeda Pharmaceutical Company Limited |
Cyclopropaneamine compound
|
CA2843609C
(en)
|
2011-08-15 |
2020-12-08 |
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
|
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
|
SG11201502728WA
(en)
|
2011-10-10 |
2015-05-28 |
Lundbeck & Co As H |
Pde9i with imidazo pyrazinone backbone
|
PE20141692A1
(en)
|
2011-10-20 |
2014-11-08 |
Oryzon Genomics Sa |
(HETERO) ARYL CYCLOPROPYLAMINE COMPOUNDS AS INHIBITORS OF LSD1
|
EP2768805B1
(en)
|
2011-10-20 |
2020-03-25 |
Oryzon Genomics, S.A. |
(hetero)aryl cyclopropylamine compounds as lsd1 inhibitors
|
CL2014000988A1
(en)
|
2011-10-20 |
2014-11-03 |
Oryzon Genomics Sa |
Compounds derived from (aryl or heteroaryl) cyclopropylamide, lsd1 inhibitors; procedure to prepare them; pharmaceutical composition that includes them; and method to treat or prevent cancer, a neurological disease, a viral infection and viral reactivation after latency.
|
ITMI20111971A1
(en)
|
2011-10-28 |
2013-04-29 |
Mesogenics Srl |
LSD-1 ENZYME INHIBITORS FOR THE INDUCTION OF OSTEOGENIC DIFFERENTIATION
|
EP2785183B1
(en)
|
2011-11-14 |
2018-12-19 |
Merck Sharp & Dohme Corp. |
Triazolopyridinone pde10 inhibitors
|
WO2013085877A1
(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
|
CN102579381B
(en)
|
2012-03-30 |
2013-07-10 |
河南中帅医药科技发展有限公司 |
Guanidine hydrochloride sustained release preparation and preparation method thereof
|
GB201205669D0
(en)
|
2012-03-30 |
2012-05-16 |
Agency Science Tech & Res |
Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof
|
CN103373996A
(en)
|
2012-04-20 |
2013-10-30 |
山东亨利医药科技有限责任公司 |
Bicyclic derivatives serving as CRTH2 receptor antagonist
|
ES2704744T3
(en)
*
|
2012-06-13 |
2019-03-19 |
Incyte Holdings Corp |
Substituted tricyclic compounds as FGFR inhibitors
|
US9815819B2
(en)
|
2012-06-28 |
2017-11-14 |
Novartis Ag |
Complement pathway modulators and uses thereof
|
CN102772444A
(en)
|
2012-07-06 |
2012-11-14 |
周明千 |
Method for processing traditional Chinese medicinal ultramicro wall-broken oral tablet slices
|
GB201212513D0
(en)
|
2012-07-13 |
2012-08-29 |
Ucb Pharma Sa |
Therapeutic agents
|
AU2013324396B2
(en)
|
2012-09-28 |
2018-10-04 |
Vanderbilt University |
Fused heterocyclic compounds as selective BMP inhibitors
|
WO2014055955A1
(en)
|
2012-10-05 |
2014-04-10 |
Rigel Pharmaceuticals, Inc. |
Gdf-8 inhibitors
|
WO2014058071A1
(en)
|
2012-10-12 |
2014-04-17 |
武田薬品工業株式会社 |
Cyclopropanamine compound and use thereof
|
EP2919770A4
(en)
|
2012-11-14 |
2017-03-08 |
The Board of Regents of The University of Texas System |
Inhibition of hif-2 heterodimerization with hif1 (arnt)
|
US9388123B2
(en)
|
2012-11-28 |
2016-07-12 |
Kyoto University |
LSD1-selective inhibitor having lysine structure
|
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
|
MX360420B
(en)
|
2012-12-19 |
2018-10-31 |
Wockhardt Ltd |
A stable aqueous composition comprising human insulin or an analogue or derivative thereof.
|
CN103054869A
(en)
|
2013-01-18 |
2013-04-24 |
郑州大学 |
Application of amino dithio formic ester compound with triazolyl in preparing medicine taking LSD1 (Lysine Specificity Demethylase 1) as target
|
CN103933036B
(en)
|
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 Aryimidazoles simultaneously the acetamide derivative of [1,2 α] pyridine 3 prepare preventing and treating PTSD medicine in purposes
|
JP2016513112A
(en)
|
2013-02-18 |
2016-05-12 |
ザ スクリプス リサーチ インスティテュート |
Vasopressin receptor modulators 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
|
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 treating cancer
|
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
|
BR112015032113B1
(en)
|
2013-06-19 |
2019-01-29 |
University Of Utah Research Foundation |
(e) -n '- (1-phenylethylidene) benzohydrazide analogs substituted as histone demethylase inhibitors
|
DK3010910T3
(en)
|
2013-06-21 |
2020-02-17 |
Myokardia Inc |
PYRIMIDINDION COMPOUNDS AGAINST HEART CONDITIONS
|
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
|
EP3043778B1
(en)
|
2013-09-13 |
2017-09-06 |
Bayer Pharma Aktiengesellschaft |
Pharmaceutical compositions containing refametinib
|
KR101568724B1
(en)
|
2013-11-13 |
2015-11-12 |
서울대학교산학협력단 |
Novel compound, a preparing method thereof, and a use thereof as inhibitors of histone demethylase
|
ES2935746T3
(en)
|
2013-12-11 |
2023-03-09 |
Celgene Quanticel Res Inc |
Lysine-specific demethylase-1 inhibitors
|
US9428470B2
(en)
|
2014-02-13 |
2016-08-30 |
Takeda Pharmaceutical Company Limited |
Heterocyclic compound
|
US9670210B2
(en)
|
2014-02-13 |
2017-06-06 |
Incyte Corporation |
Cyclopropylamines as LSD1 inhibitors
|
US9346776B2
(en)
|
2014-02-13 |
2016-05-24 |
Takeda Pharmaceutical Company Limited |
Fused heterocyclic compound
|
TWI720451B
(en)
|
2014-02-13 |
2021-03-01 |
美商英塞特控股公司 |
Cyclopropylamines as lsd1 inhibitors
|
WO2015123437A1
(en)
|
2014-02-13 |
2015-08-20 |
Incyte Corporation |
Cyclopropylamines as lsd1 inhibitors
|
EP3392244A1
(en)
|
2014-02-13 |
2018-10-24 |
Incyte Corporation |
Cyclopropylamines as lsd1 inhibitors
|
WO2015145145A1
(en)
|
2014-03-24 |
2015-10-01 |
Cipla Limited |
Pharmaceutical composition comprising lapatinib
|
CN103893163B
(en)
|
2014-03-28 |
2016-02-03 |
中国药科大学 |
The application of 2-([1,1 '-biphenyl]-4-base) 2-oxoethyl 4-((the chloro-4-aminomethyl phenyl of 3-) is amino)-4-oxobutanoic acid esters in preparation LSD1 inhibitor medicaments
|
PL3126351T3
(en)
|
2014-04-02 |
2019-03-29 |
Bristol-Myers Squibb Company |
Biaryl kinase inhibitors
|
UA122205C2
(en)
|
2014-04-11 |
2020-10-12 |
Такеда Фармасьютікал Компані Лімітед |
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
|
WO2015155297A1
(en)
|
2014-04-11 |
2015-10-15 |
Sanovel Ilac Sanayi Ve Ticaret A.S. |
Pharmaceutical combinations of dabigatran and h2-receptor antagonists
|
CN103961340B
(en)
|
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 |
A kind of LSD1 inhibitor and its application
|
JP6320570B2
(en)
|
2014-05-30 |
2018-05-09 |
イエオ−イスティトゥート・エウロペオ・ディ・オンコロジア・エッセ・エッレ・エッレ |
Cyclopropylamine compounds as histone demethylase inhibitors
|
CN104119280B
(en)
|
2014-06-27 |
2016-03-16 |
郑州大学 |
Containing the pyrimidine derivatives of amino urea and Terminal Acetylenes structural unit, preparation method and application
|
TWI687419B
(en)
|
2014-07-10 |
2020-03-11 |
美商英塞特公司 |
Imidazopyridines and imidazopyrazines as LSD1 inhibitors
|
US9695167B2
(en)
|
2014-07-10 |
2017-07-04 |
Incyte Corporation |
Substituted triazolo[1,5-a]pyridines and triazolo[1,5-a]pyrazines as LSD1 inhibitors
|
US9758523B2
(en)
|
2014-07-10 |
2017-09-12 |
Incyte Corporation |
Triazolopyridines and triazolopyrazines as LSD1 inhibitors
|
WO2016007736A1
(en)
|
2014-07-10 |
2016-01-14 |
Incyte Corporation |
Imidazopyrazines as lsd1 inhibitors
|
GB201417828D0
(en)
|
2014-10-08 |
2014-11-19 |
Cereno Scient Ab |
New methods and compositions
|
CN104173313B
(en)
|
2014-08-25 |
2017-05-17 |
杭州朱养心药业有限公司 |
Rivaroxaban troche pharmaceutical composition
|
JP6653116B2
(en)
|
2014-08-27 |
2020-02-26 |
日本ケミファ株式会社 |
Olmesartan prodrug formulations
|
UA122061C2
(en)
|
2014-10-08 |
2020-09-10 |
Ф. Хоффманн-Ля Рош Аг |
Spirodiamine derivatives as aldosterone synthase inhibitors
|
EA201792205A1
(en)
|
2015-04-03 |
2018-02-28 |
Инсайт Корпорейшн |
HETEROCYCLIC COMPOUNDS AS LSD1 INHIBITORS
|
BR112017020935A2
(en)
|
2015-04-03 |
2018-07-10 |
Mutabilis |
"compounds, pharmaceutical composition and assembly"
|
MX2017012738A
(en)
|
2015-04-03 |
2017-11-15 |
Bristol Myers Squibb Co |
Inhibitors of indoleamine 2,3-dioxygenase for the treatment of cancer.
|
AU2016306555B2
(en)
|
2015-08-12 |
2021-01-28 |
Incyte Holdings Corporation |
Salts of an LSD1 inhibitor
|
CN105232488B
(en)
|
2015-10-15 |
2021-05-04 |
上海凌凯医药科技有限公司 |
Solid pharmaceutical composition containing rivaroxaban
|
CN108884029B
(en)
|
2015-12-29 |
2021-10-26 |
米拉蒂医疗股份有限公司 |
LSD1 inhibitors
|
WO2017130933A1
(en)
|
2016-01-25 |
2017-08-03 |
国立大学法人熊本大学 |
Therapeutic agent for neurodegenerative diseases
|
US10166221B2
(en)
|
2016-04-22 |
2019-01-01 |
Incyte Corporation |
Formulations of an LSD1 inhibitor
|
US20200054643A1
(en)
|
2017-01-18 |
2020-02-20 |
Vanderbilt University |
Fused heterocyclic compounds as selective bmp inhibitors
|
EP3575301A4
(en)
|
2017-03-16 |
2020-08-05 |
Jiangsu Hengrui Medicine Co., Ltd. |
Heteroaryl[4,3-c]pyrimidine-5-amine derivative, preparation method therefor, and medical uses thereof
|
EP3818063A1
(en)
|
2018-07-05 |
2021-05-12 |
Incyte Corporation |
Fused pyrazine derivatives as a2a / a2b inhibitors
|
WO2020047198A1
(en)
|
2018-08-31 |
2020-03-05 |
Incyte Corporation |
Salts of an lsd1 inhibitor and processes for preparing the same
|