|
IL73534A
(en)
|
1983-11-18 |
1990-12-23 |
Riker Laboratories Inc |
1h-imidazo(4,5-c)quinoline-4-amines,their preparation and pharmaceutical compositions containing certain such compounds
|
|
JP2890448B2
(ja)
|
1988-04-26 |
1999-05-17 |
日産化学工業株式会社 |
ピラゾロピリジン系メバロノラクトン類
|
|
US5658889A
(en)
|
1989-01-24 |
1997-08-19 |
Gensia Pharmaceuticals, Inc. |
Method and compounds for aica riboside delivery and for lowering blood glucose
|
|
CA2011504C
(en)
|
1989-03-07 |
1998-06-02 |
Kenji Ohmori |
Imidazoquinolone derivatives
|
|
US5721356A
(en)
*
|
1989-09-15 |
1998-02-24 |
Gensia, Inc. |
Orally active adenosine kinase inhibitors
|
|
US5763596A
(en)
|
1989-09-15 |
1998-06-09 |
Metabasis Therapeutics, Inc. |
C-4' modified adenosine kinase inhibitors
|
|
US5763597A
(en)
|
1989-09-15 |
1998-06-09 |
Metabasis Therapeutics, Inc. |
Orally active adenosine kinase inhibitors
|
|
US5674998A
(en)
|
1989-09-15 |
1997-10-07 |
Gensia Inc. |
C-4' modified adenosine kinase inhibitors
|
|
US5795977A
(en)
|
1989-09-15 |
1998-08-18 |
Metabasis Therapeutics, Inc. |
Water soluble adenosine kinase inhibitors
|
|
US5646128A
(en)
|
1989-09-15 |
1997-07-08 |
Gensia, Inc. |
Methods for treating adenosine kinase related conditions
|
|
US5864033A
(en)
|
1989-09-15 |
1999-01-26 |
Metabasis Therapeutics, Inc. |
Adenosine kinase inhibitors
|
|
US5726302A
(en)
|
1989-09-15 |
1998-03-10 |
Gensia Inc. |
Water soluble adenosine kinase inhibitors
|
|
JPH03271289A
(ja)
|
1990-03-16 |
1991-12-03 |
Nissan Chem Ind Ltd |
ピラゾロピリジン誘導体の製造法及びジヒドロピラゾロピリジン誘導体
|
|
US5389640A
(en)
|
1991-03-01 |
1995-02-14 |
Minnesota Mining And Manufacturing Company |
1-substituted, 2-substituted 1H-imidazo[4,5-c]quinolin-4-amines
|
|
JP3130342B2
(ja)
|
1991-10-04 |
2001-01-31 |
日産化学工業株式会社 |
動脈硬化性血管内膜肥厚抑制薬
|
|
JP3271289B2
(ja)
|
1992-02-28 |
2002-04-02 |
スズキ株式会社 |
4サイクルエンジンのバルブ駆動装置
|
|
ATE197051T1
(de)
|
1992-04-03 |
2000-11-15 |
Upjohn Co |
Pharmazeutisch wirksame bicyclisch heterocyclische amine
|
|
US5502187A
(en)
|
1992-04-03 |
1996-03-26 |
The Upjohn Company |
Pharmaceutically active bicyclic-heterocyclic amines
|
|
JPH05310700A
(ja)
|
1992-05-12 |
1993-11-22 |
Sagami Chem Res Center |
縮合ピリジン系メバロノラクトン中間体及びその製法
|
|
WO1995011898A1
(en)
|
1992-05-12 |
1995-05-04 |
Nissan Chemical Industries Ltd. |
Condensed pyridine type mevalonolactone intermediate and process for its production
|
|
JPH0641114A
(ja)
|
1992-05-25 |
1994-02-15 |
Nissan Chem Ind Ltd |
新規メバロノラクトン類とその製法
|
|
JPH06116239A
(ja)
|
1992-10-05 |
1994-04-26 |
Nissan Chem Ind Ltd |
7−置換−3,5−ジヒドロキシヘプタ−6−イン酸類
|
|
BR9307264A
(pt)
|
1992-10-16 |
1999-05-11 |
Nippon Soda Co |
Derivados de pirimidina herbicida e fungicida
|
|
ATE239797T1
(de)
|
1993-01-25 |
2003-05-15 |
Takeda Chemical Industries Ltd |
Antikörper gegen beta-amyloid oder derivative davon und seine verwendung
|
|
CA2154681A1
(en)
|
1993-02-03 |
1994-08-18 |
Mark David Erion |
Adenosine kinase inhibitors comprising lyxofuranosyl derivatives
|
|
DE4304455A1
(de)
|
1993-02-15 |
1994-08-18 |
Bayer Ag |
Heterocyclisch substituierte Phenyl-cyclohexan-carbonsäurederivate
|
|
JP3119758B2
(ja)
|
1993-02-24 |
2000-12-25 |
日清製粉株式会社 |
7−アザインドール誘導体及びこれを有効成分とする抗潰瘍薬
|
|
JP3350739B2
(ja)
|
1993-06-10 |
2002-11-25 |
コニカ株式会社 |
黒白ハロゲン化銀写真感光材料の現像処理方法
|
|
CN1102644A
(zh)
|
1993-11-11 |
1995-05-17 |
财团法人相模中央化学研究所 |
缩合吡啶型甲羟戊酸内酯中间体及其制备方法
|
|
JPH07281365A
(ja)
|
1994-04-07 |
1995-10-27 |
Konica Corp |
写真感光材料の処理方法
|
|
DE59500788D1
(de)
|
1994-05-03 |
1997-11-20 |
Ciba Geigy Ag |
Pyrrolopyrimidinderivate mit antiproliferativer Wirkung
|
|
JP3448724B2
(ja)
|
1995-11-29 |
2003-09-22 |
コニカ株式会社 |
ハロゲン化銀写真感光材料用現像剤及びその処理方法
|
|
GB9604361D0
(en)
|
1996-02-29 |
1996-05-01 |
Pharmacia Spa |
4-Substituted pyrrolopyrimidine compounds as tyrosine kinase inhibitors
|
|
ES2203793T3
(es)
*
|
1996-03-15 |
2004-04-16 |
Novartis Ag |
N-7-heterociclil-pirrolo(2,3-d)pirimidinas y su empleo.
|
|
JPH10213887A
(ja)
|
1996-11-26 |
1998-08-11 |
Konica Corp |
黒白ハロゲン化銀写真感光材料の処理方法
|
|
IL129825A0
(en)
*
|
1996-11-27 |
2000-02-29 |
Pfizer |
Fused bicyclic pyrimidine derivatives
|
|
EP0846981A1
(en)
|
1996-12-03 |
1998-06-10 |
Konica Corporation |
Method for processing black-and-white silver halide photographic light-sensitive material
|
|
JP3543249B2
(ja)
|
1996-12-18 |
2004-07-14 |
コニカミノルタホールディングス株式会社 |
黒白ハロゲン化銀写真感光材料の処理方法
|
|
SI0994728T1
(sl)
|
1997-04-09 |
2009-02-28 |
Intellect Neurosciences Inc |
Rekombinantna protitelesa, specifična za beta-amiloidne konce, kodirana z DNA ter postopki za njihovo uporabo
|
|
US8173127B2
(en)
|
1997-04-09 |
2012-05-08 |
Intellect Neurosciences, Inc. |
Specific antibodies to amyloid beta peptide, pharmaceutical compositions and methods of use thereof
|
|
TWI239847B
(en)
|
1997-12-02 |
2005-09-21 |
Elan Pharm Inc |
N-terminal fragment of Abeta peptide and an adjuvant for preventing and treating amyloidogenic disease
|
|
US6905686B1
(en)
|
1997-12-02 |
2005-06-14 |
Neuralab Limited |
Active immunization for treatment of alzheimer's disease
|
|
JP4666762B2
(ja)
*
|
1998-06-19 |
2011-04-06 |
ファイザー・プロダクツ・インク |
ピロロ[2.3−d]ピリミジン化合物
|
|
PA8474101A1
(es)
|
1998-06-19 |
2000-09-29 |
Pfizer Prod Inc |
Compuestos de pirrolo [2,3-d] pirimidina
|
|
YU25500A
(sh)
|
1999-05-11 |
2003-08-29 |
Pfizer Products Inc. |
Postupak za sintezu analoga nukleozida
|
|
US6309811B2
(en)
|
1999-07-21 |
2001-10-30 |
Eastman Kodak Company |
Color photographic element containing nitrogen heterocycle derivative and inhibitor releasing coupler
|
|
EP3150633A1
(en)
|
2000-02-24 |
2017-04-05 |
Washington University St. Louis |
Humanized antibodies that sequester amyloid beta peptide
|
|
JP2001302515A
(ja)
|
2000-04-18 |
2001-10-31 |
Sumitomo Pharmaceut Co Ltd |
ポリ(adp−リボース)ポリメラーゼ阻害剤
|
|
AU2001264313A1
(en)
|
2000-06-20 |
2002-01-02 |
Japan Tobacco Inc. |
Pyrazolopyridine compounds and use thereof as drugs
|
|
AU2002239764B2
(en)
|
2000-11-03 |
2007-06-21 |
Proteotech, Inc. |
Methods of isolating amyloid-inhibiting compounds and use of compounds isolated from uncaria tomentosa and related plants
|
|
WO2002051837A2
(en)
|
2000-12-22 |
2002-07-04 |
Wyeth |
Heterocyclindazole and azaindazole compounds as 5-hydroxytryptamine-6 ligands
|
|
GB0111186D0
(en)
|
2001-05-08 |
2001-06-27 |
Smithkline Beecham Plc |
Novel compounds
|
|
EP1463742A4
(en)
*
|
2001-06-21 |
2006-05-10 |
Ariad Pharma Inc |
NEW PYRAZOLO AND PYRROLO PYRIMIDINES AND THEIR USES
|
|
JP2005503789A
(ja)
|
2001-08-17 |
2005-02-10 |
イーライ・リリー・アンド・カンパニー |
抗Aβ抗体
|
|
US20030195205A1
(en)
|
2001-11-02 |
2003-10-16 |
Pfizer Inc. |
PDE9 inhibitors for treating cardiovascular disorders
|
|
AU2002339230A1
(en)
|
2002-03-08 |
2003-09-22 |
Decode Genetics Ehf. |
A susceptibility gene for late-onset idiopathic parkinson's disease
|
|
MXPA05001688A
(es)
|
2002-08-12 |
2005-04-19 |
Sugen Inc |
3-pirrolil-piridopirazoles y 3-pirrolil-indazoles como inhibidores de cinasa novedosos.
|
|
SE0202463D0
(sv)
|
2002-08-14 |
2002-08-14 |
Astrazeneca Ab |
Novel compounds
|
|
DE10238724A1
(de)
|
2002-08-23 |
2004-03-04 |
Bayer Ag |
Alkyl-substituierte Pyrazolpyrimidine
|
|
DE10238723A1
(de)
|
2002-08-23 |
2004-03-11 |
Bayer Ag |
Phenyl-substituierte Pyrazolyprimidine
|
|
WO2004032868A2
(en)
|
2002-10-09 |
2004-04-22 |
Rinat Neuroscience Corp. |
Methods of treating alzheimer's disease using antibodies directed against amyloid beta peptide and compositions thereof
|
|
DE10259382A1
(de)
|
2002-12-18 |
2004-07-01 |
Abbott Gmbh & Co. Kg |
3-Substituierte 3,4-Dihydro-thieno[2,3-d]pyrimidin-4-on-Derivate, ihre Herstellung und Verwendung
|
|
US20040220186A1
(en)
|
2003-04-30 |
2004-11-04 |
Pfizer Inc. |
PDE9 inhibitors for treating type 2 diabetes,metabolic syndrome, and cardiovascular disease
|
|
EP1638935A1
(en)
|
2003-06-19 |
2006-03-29 |
Pfizer Products Inc. |
Nk1 antagonist
|
|
WO2005044181A2
(en)
|
2003-09-09 |
2005-05-19 |
Temple University-Of The Commonwealth System Of Higher Education |
Protection of tissues and cells from cytotoxic effects of ionizing radiation by abl inhibitors
|
|
WO2005025616A1
(ja)
|
2003-09-09 |
2005-03-24 |
Takeda Pharmaceutical Company Limited |
抗体の用途
|
|
SI1696920T1
(sl)
|
2003-12-19 |
2015-02-27 |
Plexxikon Inc. |
Spojine in postopki za razvoj modulatorjev ret
|
|
US20050153989A1
(en)
*
|
2004-01-13 |
2005-07-14 |
Ambit Biosciences Corporation |
Pyrrolopyrimidine derivatives and analogs and their use in the treatment and prevention of diseases
|
|
JP2007519707A
(ja)
|
2004-02-02 |
2007-07-19 |
ファイザー・プロダクツ・インク |
ヒスタミン−3受容体モジュレーター
|
|
SI1735278T1
(sl)
|
2004-04-01 |
2010-05-31 |
Lilly Co Eli |
Agenti histamin h receptorja priprava in terapevtska uporaba
|
|
JP5019612B2
(ja)
|
2004-04-02 |
2012-09-05 |
バーテックス ファーマシューティカルズ インコーポレイテッド |
Rockの阻害剤として有用なアザインドールおよび他のプロテインキナーゼ
|
|
US7456164B2
(en)
|
2004-05-07 |
2008-11-25 |
Pfizer, Inc |
3- or 4-monosubtituted phenol and thiophenol derivatives useful as H3 ligands
|
|
EP1595881A1
(en)
|
2004-05-12 |
2005-11-16 |
Pfizer Limited |
Tetrahydronaphthyridine derivates useful as histamine H3 receptor ligands
|
|
JP4069159B2
(ja)
|
2004-05-25 |
2008-04-02 |
ファイザー・プロダクツ・インク |
テトラアザベンゾ[e]アズレン誘導体及びそれらのアナログ
|
|
EP1773880A4
(en)
|
2004-06-08 |
2009-09-09 |
Novartis Vaccines & Diagnostic |
ENV POLYPEPTIDE COMPLEXES AND METHOD FOR THEIR USE
|
|
MXPA06015237A
(es)
|
2004-06-29 |
2007-12-10 |
Amgen Inc |
Pirrolo[2-3-d]pirimidinas que modulan la actividad de ack1 y lck.
|
|
AP2007003890A0
(en)
|
2004-07-30 |
2007-02-28 |
Rinat Neuroscience Corp |
Antibodies directed against amy-loid-beta peptide and methods using same
|
|
WO2006042102A2
(en)
|
2004-10-05 |
2006-04-20 |
Neurogen Corporation |
Pyrrolo-pyridine, pyrrolo-pyrimidine and related heterocyclic compounds
|
|
US8029986B2
(en)
|
2004-10-21 |
2011-10-04 |
Helmholtz Zentrum Muenchen Deutsches Forschungszentrum fuer Gesundheit und Umwelt(GmbH) |
KASPP (LRRK2) gene, its production and use for the detection and treatment of neurodegenerative disorders
|
|
WO2006052568A2
(en)
|
2004-11-10 |
2006-05-18 |
Eli Lilly And Company |
Tgf-beta inhibitors
|
|
DE102004054634A1
(de)
|
2004-11-12 |
2006-05-18 |
Schwarz Pharma Ag |
Azaindolcarboxamide
|
|
EP1827493A4
(en)
|
2004-12-22 |
2009-09-30 |
Univ St Louis |
USE OF ANTI-ABETA ANTIBODIES FOR THE TREATMENT OF BRAIN TRAUMA
|
|
CA2598639A1
(en)
|
2005-02-23 |
2006-08-31 |
Coley Pharmaceutical Group, Inc. |
Hydroxyalkyl substituted imidazonaphthyridines
|
|
PE20061323A1
(es)
|
2005-04-29 |
2007-02-09 |
Rinat Neuroscience Corp |
Anticuerpos dirigidos contra el peptido amiloide beta y metodos que utilizan los mismos
|
|
ATE488496T1
(de)
|
2005-06-22 |
2010-12-15 |
Pfizer Prod Inc |
Histamin-3-rezeptorantagonisten
|
|
US8158673B2
(en)
|
2005-10-27 |
2012-04-17 |
Pfizer Inc. |
Histamine-3 receptor antagonists
|
|
WO2007052124A1
(en)
|
2005-11-04 |
2007-05-10 |
Pfizer Limited |
Tetrahydronaphthyridine derivative
|
|
WO2007063385A2
(en)
|
2005-12-01 |
2007-06-07 |
Pfizer Products Inc. |
Spirocyclic amine histamine-3 receptor antagonists
|
|
WO2007069053A1
(en)
|
2005-12-14 |
2007-06-21 |
Pfizer Products Inc. |
Benzimidazole antagonists of the h-3 receptor
|
|
EP1968568A4
(en)
|
2005-12-22 |
2011-04-13 |
Glaxosmithkline Llc |
HEMMER OF NUTS ACTIVITY
|
|
ES2408318T3
(es)
|
2005-12-23 |
2013-06-20 |
Glaxosmithkline Llc |
Inhibidores de azaindol de las cinasas Aurora
|
|
WO2007088450A2
(en)
|
2006-02-01 |
2007-08-09 |
Pfizer Products Inc. |
Chromane antagonist of the h-3 receptor
|
|
WO2007088462A1
(en)
|
2006-02-01 |
2007-08-09 |
Pfizer Products Inc. |
Spirochromane antagonists of the h-3 receptor
|
|
WO2007099423A1
(en)
|
2006-03-02 |
2007-09-07 |
Pfizer Products Inc. |
1-pyrrolidine indane derivatives as histamine-3 receptor antagonists
|
|
CA2643055A1
(en)
|
2006-03-13 |
2007-09-20 |
Pfizer Products Inc. |
Tetralines antagonists of the h-3 receptor
|
|
ATE431426T1
(de)
|
2006-03-14 |
2009-05-15 |
Cellzome Ag |
Verfahren zur identifizierung von lrrk2 interagierenden molekülen und zur reinigung von lrrk2
|
|
WO2007124096A2
(en)
|
2006-04-21 |
2007-11-01 |
The Trustees Of Columbia University In The City Of New York |
Lrrk2 regulaton of neuronal process morphology
|
|
GB0610317D0
(en)
|
2006-05-24 |
2006-07-05 |
Medical Res Council |
Antiparasitic compounds and compositions
|
|
WO2007138431A2
(en)
|
2006-05-30 |
2007-12-06 |
Pfizer Products Inc. |
Azabicyclic ether histamine-3 antagonists
|
|
CA2657980A1
(en)
*
|
2006-06-20 |
2007-12-27 |
Novartis Ag |
Biomarkers for the progression of alzheimer's disease
|
|
AU2007332143B2
(en)
|
2006-12-11 |
2012-11-08 |
Bionomics Limited |
Chemical compounds and processes
|
|
WO2008075007A1
(en)
*
|
2006-12-21 |
2008-06-26 |
Cancer Research Technology Limited |
Morpholino-substituted bicycloheteroaryl compounds and their use as anti cancer agents
|
|
BRPI0806473A2
(pt)
|
2007-01-22 |
2011-09-27 |
Pfizer Prod Inc |
sal de tosilato de um composto terapêutico e composições farmacêuticas do mesmo
|
|
WO2008091799A2
(en)
|
2007-01-22 |
2008-07-31 |
The Trustees Of Columbia University In The City Of New York |
Cell-based methods for identifying inhibitors of parkinson's disease-associated lrrk2 mutants
|
|
FR2912744B1
(fr)
|
2007-02-16 |
2012-09-07 |
Centre Nat Rech Scient |
Composes pyrrolo°2,3-b!pyridine,composes azaindoles utiles dans la synthese de ces composes pyrrolo°2,3-b!pyridine, leurs procedes de fabrication et leurs utilisations.
|
|
GB0706709D0
(en)
|
2007-04-05 |
2007-05-16 |
Medical Res Council |
Methods
|
|
JP2010523712A
(ja)
*
|
2007-04-13 |
2010-07-15 |
スーパージェン, インコーポレイテッド |
癌または過剰増殖の治療に有用なaxlキナーゼ阻害剤
|
|
WO2008139293A1
(en)
|
2007-05-11 |
2008-11-20 |
Pfizer Inc. |
Amino-heterocyclic compounds
|
|
CL2008001540A1
(es)
|
2007-05-29 |
2009-05-22 |
Sgx Pharmaceuticals Inc |
Compuestos derivados de pirrolopiridinas y pirazolopiridinas; composicion farmaceutica; y uso en el tratamiento del cancer.
|
|
DE102007028515A1
(de)
|
2007-06-21 |
2008-12-24 |
Merck Patent Gmbh |
6-(Pyrrolopyridinyl)-pyrimidinyl-2-amin-derivate
|
|
WO2009000319A1
(de)
|
2007-06-22 |
2008-12-31 |
Schulz Hans M |
Handeingabegerät
|
|
WO2009005730A1
(en)
|
2007-06-27 |
2009-01-08 |
Cornell University |
Transgenic animal models of parkinson's disease
|
|
WO2009030270A1
(en)
|
2007-09-03 |
2009-03-12 |
Novartis Ag |
Dihydroindole derivatives useful in parkinson's disease
|
|
EP2197877B1
(en)
|
2007-09-14 |
2013-05-15 |
Sanofi |
3-methyl-2- ( (2s) -2- (4- (3-methyl-1, 2, 4-oxadiazol-5-yl) phenyl) morpholino) -6- (pyrimidin-4-yl) pyrimidin-4 (3h) -one as tau protein kinase inhibitor
|
|
US20090118276A1
(en)
|
2007-11-02 |
2009-05-07 |
Wyeth |
Thienopyrimidines, thienopyridines, and pyrrolopyrimidines as b-raf inhibitors
|
|
ATE535241T1
(de)
|
2007-12-05 |
2011-12-15 |
Univ Mainz Johannes Gutenberg |
Verwendung von 3-(indolyl)- oder 3-(azaindolyl)-4-arylmaleimid-derivaten bei der behandlung von leukämie
|
|
WO2009127642A2
(en)
|
2008-04-15 |
2009-10-22 |
Cellzome Limited |
Use of lrrk2 inhibitors for neurodegenerative diseases
|
|
CA2723185A1
(en)
|
2008-04-22 |
2009-10-29 |
Portola Pharmaceuticals, Inc. |
Inhibitors of protein kinases
|
|
EP2276346B1
(en)
|
2008-04-30 |
2016-11-23 |
National Health Research Institutes |
Fused bicyclic pyrimidine compounds as aurora kinase inhibitors
|
|
DE102008025751A1
(de)
|
2008-05-29 |
2009-12-03 |
Merck Patent Gmbh |
4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-pyridin-2-ylamin-derivate
|
|
AR072008A1
(es)
|
2008-06-13 |
2010-07-28 |
Merck & Co Inc |
Compuestos heterobiciclicos como agentes de inhibicion de quinasa p38
|
|
EP2320895A2
(en)
|
2008-07-03 |
2011-05-18 |
Exelixis, Inc. |
Cdk modulators
|
|
DE102008031517A1
(de)
|
2008-07-03 |
2010-01-07 |
Merck Patent Gmbh |
Pyrrolopyridinyl-pyrimidin-2-yl-amin-derivate
|
|
DE102008038221A1
(de)
|
2008-08-18 |
2010-02-25 |
Merck Patent Gmbh |
7-Azaindolderivate
|
|
FR2935712A1
(fr)
|
2008-09-05 |
2010-03-12 |
Ct Hospitalier Regional Univer |
Methode de detection de l'expression differentielle d'un ensemble de marqueurs moleculaires associee a la maladie de parkinson
|
|
GB2463656B
(en)
|
2008-09-18 |
2010-10-13 |
Medical Res Council |
Substrate of LRRK2 and methods of assessing LRRK2 activity
|
|
EP2346508B1
(en)
|
2008-09-26 |
2016-08-24 |
Intellikine, LLC |
Heterocyclic kinase inhibitors
|
|
US20100175140A1
(en)
|
2008-12-19 |
2010-07-08 |
The Johns Hopkins University |
Leucine-rich repeat kinase (LRRK2) drosophila model for parkinson's disease: wildtype1 (WT1) and G2019S mutant flies
|
|
JP5908728B2
(ja)
|
2009-01-06 |
2016-04-26 |
ダナ ファーバー キャンサー インスティテュート インコーポレイテッド |
ピリミド−ジアゼピノンキナーゼ骨格化合物及び疾患を治療する方法
|
|
EP2210887A1
(en)
|
2009-01-14 |
2010-07-28 |
Isdin, S.A. |
Bis resorcinyl triazine derivatives as protecting agents against UV radiation
|
|
US20100273769A1
(en)
|
2009-01-26 |
2010-10-28 |
Hanno Roder |
Composition and method for the treatment of parkinson's disease
|
|
WO2010093191A2
(en)
|
2009-02-13 |
2010-08-19 |
Lg Life Sciences Ltd. |
Novel compounds effective as xanthine oxidase inhibitors, method for preparing the same, and pharmaceutical composition containing the same
|
|
PE20120506A1
(es)
*
|
2009-03-19 |
2012-05-14 |
Medical Res Council Technology |
Derivados de pirazolopiridina como inhibidores de quinasas
|
|
TW201040191A
(en)
|
2009-03-27 |
2010-11-16 |
Abbott Gmbh & Co Kg |
Heterocyclic compounds and their use as glycogen synthase kinase-3 inhibitors
|
|
KR20100116765A
(ko)
|
2009-04-23 |
2010-11-02 |
인제대학교 산학협력단 |
파킨슨병 치료제 스크리닝 방법
|
|
DE102009019962A1
(de)
|
2009-05-05 |
2010-11-11 |
Merck Patent Gmbh |
3-([1,2,3]Triazol-4-yl)-pyrrolo[2,3-b]pyridinderivate
|
|
CN102482277B
(zh)
|
2009-05-05 |
2017-09-19 |
达纳-法伯癌症研究所有限公司 |
表皮生长因子受体抑制剂及治疗障碍的方法
|
|
US20120083476A1
(en)
|
2009-06-05 |
2012-04-05 |
Janssen Pharmaceutica Nv |
Heteroaryl-substituted spirocyclic diamine urea modulators of fatty acid amide hydrolase
|
|
CA2775753A1
(en)
|
2009-09-29 |
2011-04-07 |
Paula Louise Nichols |
Lrrk2 kinase inhibitors
|
|
FR2951172B1
(fr)
|
2009-10-13 |
2014-09-26 |
Pf Medicament |
Derives pyrazolopyridines en tant qu'agent anticancereux
|
|
BR112012010085B1
(pt)
|
2009-10-29 |
2020-02-04 |
Genosco |
composto, quantidade terapeuticamente eficaz de um composto, formulação farmacêutica
|
|
KR20110049217A
(ko)
|
2009-11-04 |
2011-05-12 |
다우어드밴스드디스플레이머티리얼 유한회사 |
신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자
|
|
WO2011057204A2
(en)
*
|
2009-11-06 |
2011-05-12 |
The Johns Hopkins University |
Lrrk2-mediated neuronal toxicity
|
|
CN102811619B
(zh)
|
2009-11-13 |
2015-04-22 |
金纳斯克公司 |
激酶抑制剂
|
|
EP2338486A1
(en)
|
2009-12-18 |
2011-06-29 |
Johannes Gutenberg-Universität Mainz |
3-(indolyl)- or 3-(azaindolyl)-4-arylmaleimide derivatives for use in the treatment of colon and gastric adenocarcinoma
|
|
CA2986631C
(en)
|
2009-12-21 |
2020-06-02 |
Samumed, Llc |
1h-pyrazolo[3,4-.beta.]pyridines and thereapeutic uses thereof
|
|
WO2011106168A1
(en)
|
2010-02-24 |
2011-09-01 |
Dcam Pharma Inc |
Purine compounds for treating autoimmune and demyelinating diseases
|
|
US8367349B2
(en)
|
2010-04-19 |
2013-02-05 |
Medical Research Council |
Methods for identifying modulators of LRRK2
|
|
EP2563125A4
(en)
|
2010-04-27 |
2013-10-02 |
Merck Sharp & Dohme |
AZAINDOLE AS JANUSKINASE HEMMER
|
|
GB201008134D0
(en)
|
2010-05-14 |
2010-06-30 |
Medical Res Council Technology |
Compounds
|
|
US8895581B2
(en)
|
2010-05-17 |
2014-11-25 |
Boehringer Ingelheim International Gmbh |
1H-imidazo[4,5-c]quinolines
|
|
WO2011149827A1
(en)
|
2010-05-24 |
2011-12-01 |
Glaxosmithkline Llc |
Compounds and methods
|
|
US9303322B2
(en)
|
2010-05-24 |
2016-04-05 |
Integran Technologies Inc. |
Metallic articles with hydrophobic surfaces
|
|
JP5713367B2
(ja)
|
2010-06-04 |
2015-05-07 |
エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft |
Lrrk2モジュレーターとしてのアミノピリミジン誘導体
|
|
KR101208198B1
(ko)
|
2010-08-27 |
2012-12-04 |
인제대학교 산학협력단 |
Lrrk2 인산화효소 억제 활성을 갖는 화합물을 유효성분으로 함유하는 파킨슨병 치료 또는 예방용 약학조성물
|
|
JP5781611B2
(ja)
|
2010-09-02 |
2015-09-24 |
グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited |
Lrrk2キナーゼ阻害剤としての2−(ベンジルオキシ)ベンズアミド類
|
|
CA2810708A1
(en)
|
2010-09-16 |
2012-03-22 |
Hutchison Medipharma Limited |
Fused heteroaryls and their uses
|
|
GB201015949D0
(en)
|
2010-09-22 |
2010-11-03 |
Medical Res Council Technology |
Compounds
|
|
JP5310700B2
(ja)
|
2010-10-27 |
2013-10-09 |
パナソニック株式会社 |
Ledパッケージ製造システムおよびledパッケージ製造システムにおける樹脂塗布方法
|
|
US9233977B2
(en)
|
2010-10-29 |
2016-01-12 |
Merck Sharp & Dohme Corp. |
Leucine-rich repeat kinase enzyme activity
|
|
HUE037844T2
(hu)
|
2010-11-10 |
2018-09-28 |
Genentech Inc |
Pirazol-aminopirimidin-származékok mint LRRK2 modulátorok
|
|
CA2818428A1
(en)
|
2010-11-30 |
2012-06-07 |
Genentech, Inc. |
Assays and biomarkers for lrrk2
|
|
US20130338106A1
(en)
|
2011-02-28 |
2013-12-19 |
John A. McCauley |
Compounds inhibiting leucine-rich repeat kinase enzyme activity
|
|
US9493452B2
(en)
|
2011-03-24 |
2016-11-15 |
Southern Methodist University |
Compounds and derivatives of 2H-pyrido (3,2-b)(1, 4) oxazin 3)4H)-ones as raf kinase and LRRK2 inhibitors
|
|
GB201105137D0
(en)
|
2011-03-28 |
2011-05-11 |
Isis Innovation |
Therapeutic molecules for use in the suppression of Parkinson's disease
|
|
WO2012135631A1
(en)
|
2011-03-30 |
2012-10-04 |
Arrien Pharmaeuticals Llc |
Substituted 5-(pyrazin-2-yl)-1h-pyrazolo [3, 4-b] pyridine and pyrazolo [3, 4-b] pyridine derivatives as protein kinase inhibitors
|
|
CN103492389B
(zh)
|
2011-04-21 |
2016-09-14 |
原真股份有限公司 |
用作激酶抑制剂的吡唑并[4,3-d]嘧啶
|
|
WO2012143143A1
(en)
|
2011-04-21 |
2012-10-26 |
Origenis Gmbh |
Heterocyclic compounds as kinase inhibitors
|
|
WO2012159079A1
(en)
|
2011-05-18 |
2012-11-22 |
The Parkinson's Institute |
Assay to determine lrrk2 activity in parkinson's disease
|
|
JP6047556B2
(ja)
|
2011-05-23 |
2016-12-21 |
エラン ファーマシューティカルズ,リミテッド・ライアビリティ・カンパニー |
Lrrk2キナーゼ活性の阻害剤
|
|
US20140205537A1
(en)
|
2011-06-24 |
2014-07-24 |
Zenobia Therapeutics, Inc. |
Lrrk2 inhibitors
|
|
WO2013007768A1
(en)
|
2011-07-13 |
2013-01-17 |
F. Hoffmann-La Roche Ag |
Tricyclic heterocyclic compounds, compositions and methods of use thereof as jak inhibitors
|
|
US9096609B2
(en)
|
2011-09-30 |
2015-08-04 |
Ipsen Pharma S.A.S. |
Macrocyclic LRRK2 kinase inhibitors
|
|
GB201204985D0
(en)
|
2012-03-21 |
2012-05-02 |
Genentech Inc |
Compounds
|
|
WO2013166276A1
(en)
|
2012-05-02 |
2013-11-07 |
Southern Research Institute |
Triazolopyridazine compounds, use as inhibitors of the kinase lrrk2, and methods for preparation thereof
|
|
WO2013164321A1
(en)
|
2012-05-03 |
2013-11-07 |
F. Hoffmann-La Roche Ag |
Pyrazole aminopyrimidine derivatives as lrrk2 modulators
|
|
EP2867236B1
(en)
|
2012-06-29 |
2017-06-14 |
Pfizer Inc |
Novel 4-(substituted-amino)-7h-pyrrolo[2,3-d]pyrimidines as lrrk2 inhibitors
|
|
US10000482B2
(en)
|
2012-10-19 |
2018-06-19 |
Origenis Gmbh |
Kinase inhibitors
|
|
US9260426B2
(en)
|
2012-12-14 |
2016-02-16 |
Arrien Pharmaceuticals Llc |
Substituted 1H-pyrrolo [2, 3-b] pyridine and 1H-pyrazolo [3, 4-b] pyridine derivatives as salt inducible kinase 2 (SIK2) inhibitors
|
|
JP6116239B2
(ja)
|
2012-12-28 |
2017-04-19 |
キヤノン株式会社 |
被検体情報取得装置および被検体情報取得方法
|
|
JP6041114B2
(ja)
|
2013-03-21 |
2016-12-07 |
▲華▼▲為▼▲終▼端有限公司 |
データ送信方法、基地局、及びユーザ装置
|
|
WO2015022664A1
(en)
|
2013-08-14 |
2015-02-19 |
Novartis Ag |
Compounds and compositions as inhibitors of mek
|
|
EP3083618B1
(en)
|
2013-12-17 |
2018-02-21 |
Pfizer Inc |
Novel 3,4-disubstituted-1h-pyrrolo[2,3-b]pyridines and 4,5-disubstituted-7h-pyrrolo[2,3-c]pyridazines as lrrk2 inhibitors
|
|
EP3119347B1
(en)
|
2014-03-21 |
2023-06-07 |
Align Technology, Inc. |
Segmented orthodontic appliance with elastics
|