PT72878B
(en)
|
1980-04-24 |
1983-03-29 |
Merck & Co Inc |
Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents
|
GB2116183B
(en)
|
1982-03-03 |
1985-06-05 |
Genentech Inc |
Human antithrombin iii dna sequences therefore expression vehicles and cloning vectors containing such sequences and cell cultures transformed thereby a process for expressing human antithrombin iii and pharmaceutical compositions comprising it
|
GB8827305D0
(en)
|
1988-11-23 |
1988-12-29 |
British Bio Technology |
Compounds
|
JP2762522B2
(ja)
|
1989-03-06 |
1998-06-04 |
藤沢薬品工業株式会社 |
血管新生阻害剤
|
US5112946A
(en)
|
1989-07-06 |
1992-05-12 |
Repligen Corporation |
Modified pf4 compositions and methods of use
|
PT98990A
(pt)
|
1990-09-19 |
1992-08-31 |
American Home Prod |
Processo para a preparacao de esteres de acidos carboxilicos de rapamicina
|
US5892112A
(en)
|
1990-11-21 |
1999-04-06 |
Glycomed Incorporated |
Process for preparing synthetic matrix metalloprotease inhibitors
|
US5120842A
(en)
|
1991-04-01 |
1992-06-09 |
American Home Products Corporation |
Silyl ethers of rapamycin
|
US5100883A
(en)
|
1991-04-08 |
1992-03-31 |
American Home Products Corporation |
Fluorinated esters of rapamycin
|
US5118678A
(en)
|
1991-04-17 |
1992-06-02 |
American Home Products Corporation |
Carbamates of rapamycin
|
DK0584222T3
(da)
|
1991-05-10 |
1998-02-23 |
Rhone Poulenc Rorer Int |
Bis-mono- og bicycliske aryl- og heteroarylforbindelser, som inhiberer EGF- og/eller PDGF-receptor-tyrosinkinase
|
US5118677A
(en)
|
1991-05-20 |
1992-06-02 |
American Home Products Corporation |
Amide esters of rapamycin
|
NZ243082A
(en)
|
1991-06-28 |
1995-02-24 |
Ici Plc |
4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof
|
US5151413A
(en)
|
1991-11-06 |
1992-09-29 |
American Home Products Corporation |
Rapamycin acetals as immunosuppressant and antifungal agents
|
GB9125660D0
(en)
|
1991-12-03 |
1992-01-29 |
Smithkline Beecham Plc |
Novel compound
|
GB9300059D0
(en)
|
1992-01-20 |
1993-03-03 |
Zeneca Ltd |
Quinazoline derivatives
|
US5521184A
(en)
|
1992-04-03 |
1996-05-28 |
Ciba-Geigy Corporation |
Pyrimidine derivatives and processes for the preparation thereof
|
ZA935111B
(en)
|
1992-07-17 |
1994-02-04 |
Smithkline Beecham Corp |
Rapamycin derivatives
|
ZA935112B
(en)
|
1992-07-17 |
1994-02-08 |
Smithkline Beecham Corp |
Rapamycin derivatives
|
US5256790A
(en)
|
1992-08-13 |
1993-10-26 |
American Home Products Corporation |
27-hydroxyrapamycin and derivatives thereof
|
GB9221220D0
(en)
|
1992-10-09 |
1992-11-25 |
Sandoz Ag |
Organic componds
|
US5258389A
(en)
|
1992-11-09 |
1993-11-02 |
Merck & Co., Inc. |
O-aryl, O-alkyl, O-alkenyl and O-alkynylrapamycin derivatives
|
NZ258697A
(en)
|
1992-11-13 |
1996-03-26 |
Immunex Corp |
Elk-l polypeptide, coding sequence and vector therefor
|
US5455258A
(en)
|
1993-01-06 |
1995-10-03 |
Ciba-Geigy Corporation |
Arylsulfonamido-substituted hydroxamic acids
|
US5629327A
(en)
|
1993-03-01 |
1997-05-13 |
Childrens Hospital Medical Center Corp. |
Methods and compositions for inhibition of angiogenesis
|
US5516658A
(en)
|
1993-08-20 |
1996-05-14 |
Immunex Corporation |
DNA encoding cytokines that bind the cell surface receptor hek
|
CA2148931A1
(fr)
|
1993-10-01 |
1995-04-13 |
Jurg Zimmermann |
Derives pyrimidineamine et leurs procedes de preparation
|
US5656643A
(en)
|
1993-11-08 |
1997-08-12 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
|
JP4105761B2
(ja)
|
1993-11-19 |
2008-06-25 |
アボット・ラボラトリーズ |
ラパミシン(マクロライド)の半合成類似体免疫調節剤
|
ES2146741T3
(es)
|
1993-12-17 |
2000-08-16 |
Novartis Ag |
Derivados de rapamicina utiles como inmunosupresores.
|
US5700823A
(en)
|
1994-01-07 |
1997-12-23 |
Sugen, Inc. |
Treatment of platelet derived growth factor related disorders such as cancers
|
IL112249A
(en)
|
1994-01-25 |
2001-11-25 |
Warner Lambert Co |
Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds
|
IL112248A0
(en)
|
1994-01-25 |
1995-03-30 |
Warner Lambert Co |
Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them
|
WO1995024190A2
(fr)
|
1994-03-07 |
1995-09-14 |
Sugen, Inc. |
Inhibiteurs de tyrosine-kinase receptrice destines a inhiber les troubles lies a la proliferation cellulaire et compositions les contenant
|
EP0756627A1
(fr)
|
1994-04-15 |
1997-02-05 |
Amgen Inc. |
Nouvelles proteines tyrosine kinases receptrices analogues a l'eph, du type hek5, hek7, hek8, hek11
|
DK0682027T3
(da)
|
1994-05-03 |
1998-05-04 |
Ciba Geigy Ag |
Pyrrolopyrimidinderivater med antiproliferativ virkning
|
US6303769B1
(en)
|
1994-07-08 |
2001-10-16 |
Immunex Corporation |
Lerk-5 dna
|
US5919905A
(en)
|
1994-10-05 |
1999-07-06 |
Immunex Corporation |
Cytokine designated LERK-6
|
US6057124A
(en)
|
1995-01-27 |
2000-05-02 |
Amgen Inc. |
Nucleic acids encoding ligands for HEK4 receptors
|
US5863949A
(en)
|
1995-03-08 |
1999-01-26 |
Pfizer Inc |
Arylsulfonylamino hydroxamic acid derivatives
|
WO1996030347A1
(fr)
|
1995-03-30 |
1996-10-03 |
Pfizer Inc. |
Derives de quinazoline
|
NZ304859A
(en)
|
1995-04-03 |
2000-01-28 |
Novartis Ag |
4-amino-1H-pyrazolo[3,4-d]pyrimidine derivatives, medicaments and processes for the preparation thereof
|
JP3053222B2
(ja)
|
1995-04-20 |
2000-06-19 |
ファイザー・インコーポレーテッド |
Mmpおよびtnf抑制剤としてのアリールスルホニルヒドロキサム酸誘導体
|
GB9508538D0
(en)
|
1995-04-27 |
1995-06-14 |
Zeneca Ltd |
Quinazoline derivatives
|
US5747498A
(en)
|
1996-05-28 |
1998-05-05 |
Pfizer Inc. |
Alkynyl and azido-substituted 4-anilinoquinazolines
|
US5880141A
(en)
|
1995-06-07 |
1999-03-09 |
Sugen, Inc. |
Benzylidene-Z-indoline compounds for the treatment of disease
|
US5650415A
(en)
|
1995-06-07 |
1997-07-22 |
Sugen, Inc. |
Quinoline compounds
|
DE69624921T2
(de)
|
1995-06-09 |
2003-09-11 |
Novartis Ag, Basel |
Rapamycinderivate
|
WO1997002266A1
(fr)
|
1995-07-06 |
1997-01-23 |
Novartis Ag |
Pyrrolopyrimidines et leurs procedes de preparation
|
DE19534177A1
(de)
|
1995-09-15 |
1997-03-20 |
Merck Patent Gmbh |
Cyclische Adhäsionsinhibitoren
|
AR004010A1
(es)
|
1995-10-11 |
1998-09-30 |
Glaxo Group Ltd |
Compuestos heterociclicos
|
GB9523675D0
(en)
|
1995-11-20 |
1996-01-24 |
Celltech Therapeutics Ltd |
Chemical compounds
|
PT780386E
(pt)
|
1995-12-20 |
2003-02-28 |
Hoffmann La Roche |
Inibidores de metaloprotease de matriz
|
JP4275733B2
(ja)
|
1996-01-23 |
2009-06-10 |
ノバルティス アクチエンゲゼルシャフト |
ピロロピリミジンおよびその製造法
|
JP3406763B2
(ja)
|
1996-01-30 |
2003-05-12 |
東レ・ダウコーニング・シリコーン株式会社 |
シリコーンゴム組成物
|
GB9603097D0
(en)
|
1996-02-14 |
1996-04-10 |
Zeneca Ltd |
Quinazoline compounds
|
GB9603095D0
(en)
|
1996-02-14 |
1996-04-10 |
Zeneca Ltd |
Quinazoline derivatives
|
DE19608588A1
(de)
|
1996-03-06 |
1997-09-11 |
Thomae Gmbh Dr K |
Pyrimido [5,4-d]pyrimidine, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung
|
DE19629652A1
(de)
|
1996-03-06 |
1998-01-29 |
Thomae Gmbh Dr K |
4-Amino-pyrimidin-Derivate, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung
|
ATE244719T1
(de)
|
1996-03-15 |
2003-07-15 |
Novartis Pharma Gmbh |
N-7 heterocyclyl-pyrrolo( 2,3-d)pyrimidine und ihre verwendung
|
WO1997038983A1
(fr)
|
1996-04-12 |
1997-10-23 |
Warner-Lambert Company |
Inhibiteurs irreversibles de tyrosine kinases
|
GB9607729D0
(en)
|
1996-04-13 |
1996-06-19 |
Zeneca Ltd |
Quinazoline derivatives
|
JP2000512990A
(ja)
|
1996-06-24 |
2000-10-03 |
ファイザー・インク |
過増殖性疾患を処置するためのフェニルアミノ置換三環式誘導体
|
US6258823B1
(en)
|
1996-07-12 |
2001-07-10 |
Ariad Pharmaceuticals, Inc. |
Materials and method for treating or preventing pathogenic fungal infection
|
EP0818442A3
(fr)
|
1996-07-12 |
1998-12-30 |
Pfizer Inc. |
Dérivés cycliques de sulfones comme inhibiteurs de métalloprotéinase et de la production du facteur de nécrose des tumeurs
|
ES2186908T3
(es)
|
1996-07-13 |
2003-05-16 |
Glaxo Group Ltd |
Compuestos heterociciclos condensados como inhibidores de pproteina-tirosina-quinasas.
|
HRP970371A2
(en)
|
1996-07-13 |
1998-08-31 |
Kathryn Jane Smith |
Heterocyclic compounds
|
EP0912572B1
(fr)
|
1996-07-13 |
2003-01-15 |
Glaxo Group Limited |
Composes heteroaromatiques bicycliques en tant qu'inhibiteurs de la proteine tyrosine kinase
|
EA199900036A1
(ru)
|
1996-07-18 |
1999-06-24 |
Пфайзер Инк |
Ингибиторы металлопротеаз матрикса на основе фосфинатов, фармацевтическая композиция, способ лечения
|
DK0920505T3
(da)
|
1996-08-16 |
2008-09-08 |
Schering Corp |
Pattedyrcelleoverfladeantigener og tilhörende reagenser
|
US6111090A
(en)
|
1996-08-16 |
2000-08-29 |
Schering Corporation |
Mammalian cell surface antigens; related reagents
|
JP4242928B2
(ja)
|
1996-08-23 |
2009-03-25 |
ノバルティス アクチエンゲゼルシャフト |
置換ピロロピリミジンおよびその製造方法
|
BR9711223A
(pt)
|
1996-08-23 |
1999-08-17 |
Pfizer |
Derivados de cido arilsulfonilamino-hidrox mico
|
ID18494A
(id)
|
1996-10-02 |
1998-04-16 |
Novartis Ag |
Turunan pirazola leburan dan proses pembuatannya
|
JP4205168B2
(ja)
|
1996-10-02 |
2009-01-07 |
ノバルティス アクチエンゲゼルシヤフト |
ピリミジン誘導体およびその製造法
|
AU4779897A
(en)
|
1996-10-02 |
1998-04-24 |
Novartis Ag |
Fused pyrazole derivatives and processes for their preparation
|
EP0837063A1
(fr)
|
1996-10-17 |
1998-04-22 |
Pfizer Inc. |
Dérivés de 4-aminoquinazoline
|
GB9621757D0
(en)
|
1996-10-18 |
1996-12-11 |
Ciba Geigy Ag |
Phenyl-substituted bicyclic heterocyclyl derivatives and their use
|
ATE272640T1
(de)
|
1997-01-06 |
2004-08-15 |
Pfizer |
Cyclische sulfonderivate
|
PL335027A1
(en)
|
1997-02-03 |
2000-03-27 |
Pfizer Prod Inc |
Derivatives of arylsulphonylamino hydroxamic acid
|
ATE391719T1
(de)
|
1997-02-05 |
2008-04-15 |
Warner Lambert Co |
Pyrido (2,3-d) pyrimidine und 4-amino-primidine als inhibitoren der zellulären proliferation
|
AU5493598A
(en)
|
1997-02-07 |
1998-08-26 |
Pfizer Inc. |
N-hydroxy-beta-sulfonyl-propionamide derivatives and their use as inhibitors of matrix metalloproteinases
|
AU722784B2
(en)
|
1997-02-11 |
2000-08-10 |
Pfizer Inc. |
Arylsulfonyl hydroxamic acid derivatives
|
CO4950519A1
(es)
|
1997-02-13 |
2000-09-01 |
Novartis Ag |
Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion
|
US6150395A
(en)
|
1997-05-30 |
2000-11-21 |
The Regents Of The University Of California |
Indole-3-carbinol (I3C) derivatives and methods
|
AU8689298A
(en)
|
1997-08-05 |
1999-03-01 |
Sugen, Inc. |
Tricyclic quinoxaline derivatives as protein tyrosine kinase inhibitors
|
DE69822839T2
(de)
|
1997-08-08 |
2004-08-19 |
Pfizer Products Inc., Groton |
Derivate von aryloxyarylsulfonylamino hydroxyaminsäuren
|
US6509173B1
(en)
|
1997-10-21 |
2003-01-21 |
Human Genome Sciences, Inc. |
Human tumor necrosis factor receptor-like proteins TR11, TR11SV1, and TR11SV2
|
GB9725782D0
(en)
|
1997-12-05 |
1998-02-04 |
Pfizer Ltd |
Therapeutic agents
|
GB9800575D0
(en)
|
1998-01-12 |
1998-03-11 |
Glaxo Group Ltd |
Heterocyclic compounds
|
GB9800569D0
(en)
|
1998-01-12 |
1998-03-11 |
Glaxo Group Ltd |
Heterocyclic compounds
|
GB9801690D0
(en)
|
1998-01-27 |
1998-03-25 |
Pfizer Ltd |
Therapeutic agents
|
WO1999040196A1
(fr)
|
1998-02-09 |
1999-08-12 |
Genentech, Inc. |
Nouveaux homologues recepteurs du facteur necrosant des tumeurs et acides nucleiques codant ceux-ci
|
AU756838B2
(en)
|
1998-03-04 |
2003-01-23 |
Bristol-Myers Squibb Company |
Heterocyclo-substituted imidazopyrazine protein tyrosine kinase inhibitors
|
PA8469501A1
(es)
|
1998-04-10 |
2000-09-29 |
Pfizer Prod Inc |
Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico
|
PA8469401A1
(es)
|
1998-04-10 |
2000-05-24 |
Pfizer Prod Inc |
Derivados biciclicos del acido hidroxamico
|
DK2020408T3
(da)
|
1998-05-29 |
2013-09-30 |
Sugen Inc |
Pyrrol-substitueret 2-indolinon som proteinkinaseinhibitor
|
UA60365C2
(uk)
|
1998-06-04 |
2003-10-15 |
Пфайзер Продактс Інк. |
Похідні ізотіазолу, спосіб їх одержання, фармацевтична композиція та спосіб лікування гіперпроліферативного захворювання у ссавця
|
AU747427B2
(en)
|
1998-07-10 |
2002-05-16 |
Merck & Co., Inc. |
Novel angiogenesis inhibitors
|
CA2341409A1
(fr)
|
1998-08-31 |
2000-03-09 |
Merck And Co., Inc. |
Nouveaux inhibiteurs d'angiogenese
|
PT1004578E
(pt)
|
1998-11-05 |
2004-06-30 |
Pfizer Prod Inc |
Derivados hidroxamida do acido 5-oxo-pirrolidino-2-carboxilico
|
ATE556713T1
(de)
|
1999-01-13 |
2012-05-15 |
Bayer Healthcare Llc |
Omega-carboxyarylsubstituierte-diphenyl- harnstoffe als p38-kinasehemmer
|
PT1165085E
(pt)
|
1999-03-30 |
2006-10-31 |
Novartis Ag |
Derivados de ftalazina para tratar doencas inflamatorias
|
GB9912961D0
(en)
|
1999-06-03 |
1999-08-04 |
Pfizer Ltd |
Metalloprotease inhibitors
|
ATE324444T1
(de)
|
1999-06-07 |
2006-05-15 |
Immunex Corp |
Tek-antagonisten
|
US6521424B2
(en)
|
1999-06-07 |
2003-02-18 |
Immunex Corporation |
Recombinant expression of Tek antagonists
|
PT1196186E
(pt)
|
1999-07-12 |
2008-02-14 |
Genentech Inc |
Promoção ou inibição da angiogénese e da cardiovascularização com homólogos de ligandos/receptores do factor de necrose tumoral.
|
WO2001014387A1
(fr)
|
1999-08-24 |
2001-03-01 |
Ariad Gene Therapeutics, Inc. |
Analogues d'epirapamycine-28
|
EP1244647B1
(fr)
|
1999-11-05 |
2006-06-21 |
AstraZeneca AB |
Derives de quinazoline utilises en tant qu'inhibiteurs du facteur de croissance endotheliale vasculaire (vegf)
|
ES2367007T3
(es)
|
1999-11-24 |
2011-10-27 |
Sugen, Inc. |
Derivados de indolinona ionizables y su uso como ligandos de ptk.
|
US6515004B1
(en)
|
1999-12-15 |
2003-02-04 |
Bristol-Myers Squibb Company |
N-[5-[[[5-alkyl-2-oxazolyl]methyl]thio]-2-thiazolyl]-carboxamide inhibitors of cyclin dependent kinases
|
US6727225B2
(en)
|
1999-12-20 |
2004-04-27 |
Immunex Corporation |
TWEAK receptor
|
CA2400040A1
(fr)
|
2000-02-25 |
2001-08-30 |
Immunex Corporation |
Antagonistes des integrines
|
US6651123B1
(en)
|
2000-03-30 |
2003-11-18 |
International Business Machines Corporation |
File system locking
|
US6534309B1
(en)
|
2000-08-03 |
2003-03-18 |
Cytokinetics, Inc. |
Motor proteins and methods for their use
|
US6630500B2
(en)
|
2000-08-25 |
2003-10-07 |
Cephalon, Inc. |
Selected fused pyrrolocarbazoles
|
EP1343782B1
(fr)
|
2000-12-21 |
2009-05-06 |
SmithKline Beecham Corporation |
Composes chimiques
|
US20020147198A1
(en)
|
2001-01-12 |
2002-10-10 |
Guoqing Chen |
Substituted arylamine derivatives and methods of use
|
US7102009B2
(en)
|
2001-01-12 |
2006-09-05 |
Amgen Inc. |
Substituted amine derivatives and methods of use
|
US7105682B2
(en)
|
2001-01-12 |
2006-09-12 |
Amgen Inc. |
Substituted amine derivatives and methods of use
|
US6878714B2
(en)
|
2001-01-12 |
2005-04-12 |
Amgen Inc. |
Substituted alkylamine derivatives and methods of use
|
US6995162B2
(en)
|
2001-01-12 |
2006-02-07 |
Amgen Inc. |
Substituted alkylamine derivatives and methods of use
|
AU2003299517A1
(en)
|
2002-05-23 |
2004-05-25 |
Merck & Co., Inc. |
Mitotic kinesin inhibitors
|
US7307088B2
(en)
|
2002-07-09 |
2007-12-11 |
Amgen Inc. |
Substituted anthranilic amide derivatives and methods of use
|
TWI329112B
(en)
|
2002-07-19 |
2010-08-21 |
Bristol Myers Squibb Co |
Novel inhibitors of kinases
|
EP2305813A3
(fr)
|
2002-11-14 |
2012-03-28 |
Dharmacon, Inc. |
SIRNA fonctionnel et hyperfonctionnel
|
US7423018B2
(en)
|
2002-12-13 |
2008-09-09 |
University Of Massachusetts |
Kinesin-like proteins and methods of use
|
US7618632B2
(en)
|
2003-05-23 |
2009-11-17 |
Wyeth |
Method of treating or ameliorating an immune cell associated pathology using GITR ligand antibodies
|
US20060173033A1
(en)
|
2003-07-08 |
2006-08-03 |
Michaela Kneissel |
Use of rapamycin and rapamycin derivatives for the treatment of bone loss
|
EP1660126A1
(fr)
|
2003-07-11 |
2006-05-31 |
Schering Corporation |
Agonistes ou antagonistes du recepteur du facteur de necrose tumorale induit par les glucocorticoides (gitr) ou de son ligand utilises dans le traitement des troubles immuns, des infections et du cancer
|
WO2005016252A2
(fr)
|
2003-07-11 |
2005-02-24 |
Ariad Gene Therapeutics, Inc. |
Macrocycles contenant du phosphore
|
AR045134A1
(es)
|
2003-07-29 |
2005-10-19 |
Smithkline Beecham Plc |
Compuesto de 1h - imidazo [4,5-c] piridin-ilo, composicion farmaceutica que lo comprende, proceso para prepararla, su uso para preparar dicha composicion farmaceutica, combinacion farmaceutica, uso de la combinacion farmaceutica para la preparacion de un medicamento, procedimientos para preparar dic
|
AU2004264533B2
(en)
|
2003-08-15 |
2009-01-22 |
Merck Sharp & Dohme Corp. |
Mitotic kinesin inhibitors
|
EP1692318A4
(fr)
|
2003-12-02 |
2008-04-02 |
Genzyme Corp |
Compositions et methodes pour le diagnostic et le traitement du cancer du poumon
|
BRPI0417498A
(pt)
|
2003-12-09 |
2007-05-29 |
Us Gov Health & Human Serv |
método para suprimir uma resposta imune em um indivìduo; método de inibição da proliferação de um célula; método de tratamento de um distúrbio proliferativo em um indivìduo; método para selecionar um agente imunossupressor ou anti-proliferativo; composição farmacêutica e estente vascular
|
GB0409799D0
(en)
|
2004-04-30 |
2004-06-09 |
Isis Innovation |
Method of generating improved immune response
|
US7504413B2
(en)
|
2004-05-06 |
2009-03-17 |
Cytokinetics, Inc. |
N-(4-(imidazo[1,2A]pyridin-YL)phenethyl)benzamide inhibitors of the mitotic kinesin CENP-E for treating certain cellular proliferation diseases
|
WO2006083289A2
(fr)
|
2004-06-04 |
2006-08-10 |
Duke University |
Methodes et compositions ameliorant l'immunite par depletion in vivo de l'activite cellulaire immunosuppressive
|
MXPA06014909A
(es)
|
2004-06-18 |
2007-02-28 |
Chiron Corp |
Derivados de n-(1-(1-bencil -4-fenil-1h -imidazol -2-il)-2, 2-dimetilpropil) benzamida y compuestos relacionados como inhibidores de proteina de huso de cinesina (ksp) para el tratamiento del cancer.
|
CA2576619A1
(fr)
|
2004-08-18 |
2006-02-23 |
Altana Pharma Ag |
Benzothienopyridines destinees a etre utilisees en tant qu'inhibiteurs de la kinesine eg5
|
KR100859891B1
(ko)
|
2004-08-26 |
2008-09-23 |
화이자 인코포레이티드 |
단백질 키나제 억제제로서 거울상이성질체적으로 순수한아미노헤테로아릴 화합물
|
CA2582163A1
(fr)
|
2004-10-13 |
2006-04-27 |
Wyeth |
Analogues de la 17-hydroxywortmannine employes en tant qu'inhibiteurs de pi3k
|
WO2006105021A2
(fr)
|
2005-03-25 |
2006-10-05 |
Tolerrx, Inc. |
Molecules de liaison gitr et leurs utilisations
|
WO2006114788A1
(fr)
|
2005-04-25 |
2006-11-02 |
Ramot At Tel Aviv University Ltd. |
Polypeptides de kinesine, polynucleotides codant pour ceux-ci et compositions et leurs methodes d'utilisation
|
DK2439273T3
(da)
|
2005-05-09 |
2019-06-03 |
Ono Pharmaceutical Co |
Humane monoklonale antistoffer til programmeret død-1(pd-1) og fremgangsmåder til behandling af cancer ved anvendelse af anti-pd-1- antistoffer alene eller i kombination med andre immunterapeutika
|
GB0510390D0
(en)
|
2005-05-20 |
2005-06-29 |
Novartis Ag |
Organic compounds
|
US20090012085A1
(en)
|
2005-09-20 |
2009-01-08 |
Charles Michael Baum |
Dosage forms and methods of treatment using a tyrosine kinase inhibitor
|
JP2009514866A
(ja)
|
2005-11-02 |
2009-04-09 |
サイトキネティクス・インコーポレーテッド |
ある種の化学物質、組成物、および方法
|
WO2007133822A1
(fr)
|
2006-01-19 |
2007-11-22 |
Genzyme Corporation |
Anticorps anti-gitr destinés au traitement du cancer
|
JP2009543770A
(ja)
|
2006-07-14 |
2009-12-10 |
アステックス・セラピューティクス・リミテッド |
Cdk及びgskの阻害のためのピラゾール誘導体の組合せ剤
|
AR062200A1
(es)
|
2006-08-04 |
2008-10-22 |
Aeterna Zentaris Gmbh |
Derivados de antraceno y su uso para el tratamiento de emfermedades tumorales bengnas y malingnas
|
TWI499420B
(zh)
|
2006-12-07 |
2015-09-11 |
Hoffmann La Roche |
肌醇磷脂3-激酶抑制劑化合物及使用方法
|
ES2776406T3
(es)
|
2007-07-12 |
2020-07-30 |
Gitr Inc |
Terapias de combinación que emplean moléculas de enlazamiento a GITR
|
KR101584823B1
(ko)
|
2007-09-12 |
2016-01-22 |
제넨테크, 인크. |
포스포이노시타이드 3-키나제 저해제 화합물과 화학치료제의 배합물 및 이의 사용방법
|
JP5348725B2
(ja)
|
2007-10-25 |
2013-11-20 |
ジェネンテック, インコーポレイテッド |
チエノピリミジン化合物の製造方法
|
WO2010003118A1
(fr)
|
2008-07-02 |
2010-01-07 |
Trubion Pharmaceuticals, Inc. |
Protéines de liaison multi-cibles antagonistes du tgf-b
|
CN102149820B
(zh)
|
2008-09-12 |
2014-07-23 |
国立大学法人三重大学 |
能够表达外源gitr配体的细胞
|
TW201103904A
(en)
|
2009-06-11 |
2011-02-01 |
Hoffmann La Roche |
Janus kinase inhibitor compounds and methods
|
DK3023438T3
(en)
|
2009-09-03 |
2020-05-11 |
Merck Sharp & Dohme |
Anti-gitr-antistoffer
|
EP2295543A1
(fr)
|
2009-09-11 |
2011-03-16 |
Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. |
Procédé de préparation de virus de la grippe
|
GB0919054D0
(en)
|
2009-10-30 |
2009-12-16 |
Isis Innovation |
Treatment of obesity
|
EA023674B1
(ru)
|
2009-12-29 |
2016-06-30 |
Эмерджент Продакт Дивелопмент Сиэтл, Ллс |
Гетеродимерные связывающие белки и их применение
|
WO2011085261A1
(fr)
*
|
2010-01-08 |
2011-07-14 |
Selexagen Therapeutics, Inc. |
Inhibiteurs de hedgehog
|
CN102796103A
(zh)
*
|
2011-05-23 |
2012-11-28 |
南京英派药业有限公司 |
6-(芳基甲酰)咪唑并[1,2-a]嘧啶和6-(芳基甲酰)[1,2,4]三唑并[4,3-a]嘧啶作为Hedgehog抑制剂及其应用
|
US20130108641A1
(en)
|
2011-09-14 |
2013-05-02 |
Sanofi |
Anti-gitr antibodies
|
ES2672992T3
(es)
|
2013-08-09 |
2018-06-19 |
Takeda Pharmaceutical Company Limited |
Compuesto aromático
|
US20170095479A1
(en)
|
2014-05-29 |
2017-04-06 |
Merck Sharp & Dohme Corp. |
Methods for Treating Cancer with a WEE1 Inhibitor
|
EP3233918A1
(fr)
|
2014-12-19 |
2017-10-25 |
Novartis AG |
Polythérapies
|
TW201643138A
(zh)
|
2015-04-17 |
2016-12-16 |
佛瑪治療公司 |
作為組蛋白脫乙醯基酶(hdac)抑制劑之3-螺-7-異羥肟酸四氫萘
|
AU2016264623B2
(en)
|
2015-05-20 |
2022-06-30 |
Dana-Farber Cancer Institute, Inc. |
Shared neoantigens
|
SG11201808167VA
(en)
|
2016-03-24 |
2018-10-30 |
Bayer Pharma AG |
Prodrugs of cytotoxic active agents having enzymatically cleavable groups
|
US11485743B2
(en)
|
2018-01-12 |
2022-11-01 |
Kymera Therapeutics, Inc. |
Protein degraders and uses thereof
|
CN108768023B
(zh)
|
2018-08-13 |
2020-01-07 |
珠海格力电器股份有限公司 |
转子组件及交替极电机
|
DE102018213662A1
(de)
|
2018-08-14 |
2020-02-20 |
Robert Bosch Gmbh |
Lautsprecher mit einem darin enthaltenen Leuchtelement
|
CN109039072B
(zh)
|
2018-08-21 |
2020-09-08 |
南京南瑞继保电气有限公司 |
一种双极双向直流变换器及其控制方法和控制装置
|
IL283639B2
(en)
|
2018-12-20 |
2024-06-01 |
Amgen Inc |
KIF18A inhibitors
|
JP2022513967A
(ja)
|
2018-12-20 |
2022-02-09 |
アムジエン・インコーポレーテツド |
Kif18a阻害剤として有用なヘテロアリールアミド
|
MA54550A
(fr)
|
2018-12-20 |
2022-03-30 |
Amgen Inc |
Inhibiteurs de kif18a
|
CA3123044A1
(fr)
|
2018-12-20 |
2020-06-25 |
Amgen Inc. |
Amides d'heteroaryle utiles en tant qu'inhibiteurs de kif18a
|
GB2617512B
(en)
|
2019-04-05 |
2023-12-27 |
Earli Inc |
Improved methods and compositions for synthetic biomarkers
|
WO2020226333A1
(fr)
|
2019-05-03 |
2020-11-12 |
주식회사 디시젠 |
Méthode de prédiction et de pronostic du cancer et composition à cet effet
|
WO2021011634A1
(fr)
|
2019-07-15 |
2021-01-21 |
Kymera Therapeutics, Inc. |
Agents de dégradation de protéines et leurs utilisations
|
EP4007756A1
(fr)
|
2019-08-02 |
2022-06-08 |
Amgen Inc. |
Inhibiteurs de kif18a
|
CN114391012A
(zh)
|
2019-08-02 |
2022-04-22 |
美国安进公司 |
作为kif18a抑制剂的吡啶衍生物
|
EP4007753A1
(fr)
|
2019-08-02 |
2022-06-08 |
Amgen Inc. |
Inhibiteurs de kif18a
|
JP2022542967A
(ja)
|
2019-08-02 |
2022-10-07 |
アムジエン・インコーポレーテツド |
Kif18a阻害剤
|
WO2021161323A1
(fr)
|
2020-02-16 |
2021-08-19 |
Genetikaplus Ltd. |
Procédés de pronostic thérapeutique
|
US12187992B2
(en)
|
2020-02-19 |
2025-01-07 |
The Regents Of The University Of California |
Method and device for early cancer screening
|
JP2023521802A
(ja)
|
2020-04-14 |
2023-05-25 |
アムジエン・インコーポレーテツド |
新生物疾患の処置のためのkif18a阻害剤
|
WO2021231413A1
(fr)
|
2020-05-11 |
2021-11-18 |
University Of Vermont |
Approche de traitement impliquant l'inhibition de kif18a pour des tumeurs instables du point de vue chromosomique
|
MX2023004802A
(es)
|
2020-10-27 |
2023-06-22 |
Amgen Inc |
Compuestos espiro heterocíclicos y métodos de uso.
|
US20240261425A1
(en)
|
2021-04-09 |
2024-08-08 |
Nanjing University |
Conjugate and the preparing method and use thereof
|
WO2022268230A1
(fr)
|
2021-06-25 |
2022-12-29 |
杭州英创医药科技有限公司 |
Composé destiné à être utilisé en tant qu'inhibiteur de kif18a
|
TW202321213A
(zh)
|
2021-07-21 |
2023-06-01 |
美商安進公司 |
Kif18a抑制劑化合物之鹽和固態形式
|
KR20240109977A
(ko)
|
2021-08-26 |
2024-07-12 |
볼라스트라 쎄라퓨틱스, 인코포레이티드 |
Kif18a의 스피로 인돌린 억제제
|
WO2023041055A1
(fr)
|
2021-09-16 |
2023-03-23 |
微境生物医药科技(上海)有限公司 |
Inhibiteur de kif18a
|
CN118201923A
(zh)
|
2021-10-15 |
2024-06-14 |
海南先声再明医药股份有限公司 |
三环类化合物
|
CN118215657A
(zh)
|
2021-11-19 |
2024-06-18 |
微境生物医药科技(上海)有限公司 |
Kif18a抑制剂
|
WO2023146979A1
(fr)
|
2022-01-27 |
2023-08-03 |
The Board Of Trustees Of The Leland Stanford Junior University |
Plateforme de cytométrie de masse à cellule unique pour cartographier les effets d'agents candidats sur le cartilage
|
AU2023254325A1
(en)
|
2022-04-15 |
2024-10-17 |
Wuhan Humanwell Innovative Drug Research and Development Center Limited Company |
Kif18a inhibitor and use thereof
|
TW202346288A
(zh)
|
2022-04-28 |
2023-12-01 |
美商佛拉斯托醫療公司 |
用於抑制kif18a之化合物
|
WO2023212714A1
(fr)
|
2022-04-29 |
2023-11-02 |
Amgen Inc. |
Inhibition de kif18a pour le traitement du cancer
|