DE280853C
(en)
|
|
|
|
|
US850370A
(en)
|
1906-06-05 |
1907-04-16 |
William L Hynes |
Water-automobile.
|
DE2156720A1
(en)
|
1971-11-16 |
1973-05-24 |
Bayer Ag |
Pyrimido(4,5-d) pyrimidines - prepd from polychloroalkylimino acid chloride and 4-amino uracils, are starting materials for plant
|
US3894021A
(en)
|
1974-01-28 |
1975-07-08 |
Squibb & Sons Inc |
Derivatives of 1,7-dihydro-2H-pyrazolo{8 4{40 ,3{40 :5,6{9 pyrido{8 4,3-D{9 pyrimidine-2,4-(3H)-diones
|
JPS5120580B2
(en)
|
1974-06-19 |
1976-06-25 |
|
|
JPS522706Y2
(en)
|
1974-07-31 |
1977-01-21 |
|
|
US4347348A
(en)
|
1978-06-05 |
1982-08-31 |
Chernikhov Alexei Y |
Heat-resistant heterocyclic polymers and methods for producing same
|
FR2428654A1
(en)
|
1978-06-13 |
1980-01-11 |
Chernikhov Alexei |
Heat-stable heterocyclic polymer prepn. - by reacting polyfunctional nitrile with polyfunctional isocyanate opt. contg. silicon, halogen, nitrogen, phosphorus and/or boron atoms
|
CH635828A5
(en)
|
1978-08-30 |
1983-04-29 |
Ciba Geigy Ag |
N-SUBSTITUTED IMIDES AND BISIMIDS.
|
CH641470A5
(en)
|
1978-08-30 |
1984-02-29 |
Ciba Geigy Ag |
SILANES CONTAINING IMID GROUPS.
|
US4339267A
(en)
|
1980-01-18 |
1982-07-13 |
E. I. Du Pont De Nemours And Company |
Herbicidal sulfonamides
|
US4402878A
(en)
|
1980-10-22 |
1983-09-06 |
Plastics Engineering Company |
Addition products of di-acetylene-terminated polyimide derivatives with a polyimide having terminal non-conjugated acetylene groups
|
US4405519A
(en)
|
1980-10-22 |
1983-09-20 |
Plastics Engineering Company |
Di-Acetylene-terminated polyimide derivatives
|
US4405520A
(en)
|
1980-10-22 |
1983-09-20 |
Plastics Engineering Company |
Addition products of di-acetylene-terminated polymide derivatives and dienophiles having terminal maleimide grops
|
US4405786A
(en)
|
1980-10-22 |
1983-09-20 |
Plastics Engineering Company |
Addition products of di-acetylene-terminated polyimide derivatives and an dienophile having ethylene groups
|
US4460773A
(en)
|
1982-02-05 |
1984-07-17 |
Lion Corporation |
1-Phenyl-1H-pyrazolo [3,4-b]pyrazine derivatives and process for preparing same
|
DE3432983A1
(en)
|
1983-09-07 |
1985-04-18 |
Lion Corp., Tokio/Tokyo |
1,5-disubstituted 1H-pyrazolo[3,4-b]pyrazine derivatives and antitumour agents which contain them
|
JPS62273979A
(en)
|
1986-05-21 |
1987-11-28 |
Lion Corp |
1,5-substituted-1h-pyrazolo(3,4-b)pyrazine derivative and antitumor agent containing said compound
|
JPS6310630A
(en)
|
1986-06-23 |
1988-01-18 |
Teijin Ltd |
Production of aromatic polyamide-imide ether
|
JPS6317882A
(en)
|
1986-07-09 |
1988-01-25 |
Lion Corp |
5-substituted-1h-pyrazolo(3,4-b)pyrazine derivative and antitumor agent containing said compound
|
JPS6336665U
(en)
|
1986-08-27 |
1988-03-09 |
|
|
US4859672A
(en)
|
1986-10-29 |
1989-08-22 |
Rorer Pharmaceutical Corporation |
Pyrido[2,3-d]pyrimidinone and imidazo[4,5-b]pyrimidinone
|
US4874803A
(en)
|
1987-09-21 |
1989-10-17 |
Pennwalt Corporation |
Dianhydride coupled polymer stabilizers
|
DE3814549A1
(en)
|
1987-10-30 |
1989-05-18 |
Bayer Ag |
N-SUBSTITUTED DERIVATIVES OF 1-DESOXYNOJIRIMYCIN AND 1-DESOXYMANNONOJIRIMYCIN, METHOD FOR THE PRODUCTION AND USE THEREOF IN MEDICINAL PRODUCTS
|
JPH029895A
(en)
|
1988-06-28 |
1990-01-12 |
Lion Corp |
Nucleoside analog compound and antitumor agent
|
DD280853A1
(en)
|
1989-03-21 |
1990-07-18 |
Akad Nauk Sssr |
BINDER FOR ELECTRODES, PREFERABLY FOR POLYMER ELECTRODES
|
US5159054A
(en)
|
1989-05-16 |
1992-10-27 |
The United States Of America As Represented By The Secretary Of The Navy |
Synthesis of phthalonitrile resins containing ether and imide linkages
|
JP2845957B2
(en)
|
1989-07-17 |
1999-01-13 |
三井化学株式会社 |
Novel diphenols having imide ring and process for producing the same
|
US5726302A
(en)
|
1989-09-15 |
1998-03-10 |
Gensia Inc. |
Water soluble adenosine kinase inhibitors
|
DE3937633A1
(en)
|
1989-11-11 |
1991-05-16 |
Bayer Ag |
HETEROCYCLIC COMPOUNDS AND THEIR USE AS PIGMENTS AND DYES
|
US5329046A
(en)
|
1989-12-28 |
1994-07-12 |
Hoechst Aktiengesellschaft |
Biscationic acid amide and imide derivatives and processes for their preparation
|
JP2723670B2
(en)
|
1989-12-28 |
1998-03-09 |
ヘキスト・アクチェンゲゼルシャフト |
Acid amide- and -imide derivatives of biscations as charge control agents
|
JP2883670B2
(en)
|
1990-03-23 |
1999-04-19 |
三井化学株式会社 |
Novel bisphenol having imide ring and method for producing the same
|
GB9113137D0
(en)
|
1990-07-13 |
1991-08-07 |
Ici Plc |
Thioxo heterocycles
|
NZ240089A
(en)
|
1990-10-03 |
1993-04-28 |
Commw Scient Ind Res Org |
Diaminobisimide compounds and compositions comprising such compounds for curing epoxy resins
|
JPH04158084A
(en)
|
1990-10-22 |
1992-06-01 |
Fuji Photo Film Co Ltd |
Recording material
|
JPH04179576A
(en)
|
1990-11-14 |
1992-06-26 |
Fuji Photo Film Co Ltd |
Recording material
|
JPH04328121A
(en)
|
1991-04-26 |
1992-11-17 |
Sumitomo Bakelite Co Ltd |
Epoxy resin composition for sealing semiconductor
|
KR100207360B1
(en)
|
1991-06-14 |
1999-07-15 |
돈 더블유. 슈미츠 |
Imidazon (1,5-a) quinoxalines
|
DE4119767A1
(en)
|
1991-06-15 |
1992-12-17 |
Dresden Arzneimittel |
Prepn. of (pyrimid-2-yl-thio- or seleno-) acetic acid derivs. - by reacting the corresp. chloro:alkanoyl-amino cpd. with a rhodanide and water or an alcohol
|
US5521184A
(en)
|
1992-04-03 |
1996-05-28 |
Ciba-Geigy Corporation |
Pyrimidine derivatives and processes for the preparation thereof
|
JP3279635B2
(en)
|
1992-05-18 |
2002-04-30 |
鐘淵化学工業株式会社 |
Hydrosilyl group-containing imide compound
|
JP3232123B2
(en)
|
1992-05-20 |
2001-11-26 |
鐘淵化学工業株式会社 |
Curable composition
|
CA2136606A1
(en)
|
1992-05-28 |
1993-11-29 |
Trevor C. Morton |
Bismaleimide compounds
|
JPH08504196A
(en)
|
1992-12-07 |
1996-05-07 |
コモンウェルス・サイエンティフィック・アンド・インダストリアル・リサーチ・オーガニゼイション |
Bisnadimide
|
CA2153595A1
(en)
|
1993-01-11 |
1994-07-21 |
Anthony F. Garito |
Polycyclic aromatic compounds having nonlinear optical properties
|
WO1994025438A1
(en)
|
1993-04-28 |
1994-11-10 |
The Du Pont Merck Pharmaceutical Company |
Novel trisubstituted aromatic amines useful for the treatment of cognitive deficits
|
US5536725A
(en)
|
1993-08-25 |
1996-07-16 |
Fmc Corporation |
Insecticidal substituted-2,4-diamino-5,6,7,8-tetrahydroquinazolines
|
RO118291B1
(en)
|
1993-11-30 |
2003-04-30 |
Searle & Co |
1, 3, 4, 5-tetrasubstituted pyrazol derivatives and pharmaceutical composition containing the same
|
US5480887A
(en)
|
1994-02-02 |
1996-01-02 |
Eli Lilly And Company |
Protease inhibitors
|
ES2153434T3
(en)
|
1994-02-02 |
2001-03-01 |
Lilly Co Eli |
INHIBITORS OF HIV PROTEASA AND ITS INTERMEDIATES.
|
ATE190978T1
(en)
|
1994-11-14 |
2000-04-15 |
Warner Lambert Co |
6-ARYL-PYRIDO(2,3-D)PYRIMIDINES AND NAPHTHYRIDINES FOR INHIBITING CELL PRODUCTION CAUSED BY PROTEIN TYROSINE KINASE
|
US7125880B1
(en)
|
1995-06-06 |
2006-10-24 |
Pfizer Inc. |
Corticotropin releasing factor antagonists
|
US5783577A
(en)
|
1995-09-15 |
1998-07-21 |
Trega Biosciences, Inc. |
Synthesis of quinazolinone libraries and derivatives thereof
|
JPH09188812A
(en)
|
1996-01-11 |
1997-07-22 |
Mitsui Toatsu Chem Inc |
Crystallization accelerator
|
AU2980797A
(en)
|
1996-06-11 |
1998-01-07 |
Yoshitomi Pharmaceutical Industries, Ltd. |
Fused heterocyclic compounds and medicinal uses thereof
|
CN1093130C
(en)
|
1996-08-06 |
2002-10-23 |
辉瑞大药厂 |
Substituted pyrido- or pyrimido-containing 6,6- or 6,7-bicyclic derivatives
|
US6184235B1
(en)
|
1996-08-14 |
2001-02-06 |
Warner-Lambert Company |
2-phenyl benzimidazole derivatives as MCP-1 antagonists
|
JP3669783B2
(en)
|
1996-08-21 |
2005-07-13 |
三井化学株式会社 |
Organic electroluminescence device
|
US5994364A
(en)
|
1996-09-13 |
1999-11-30 |
Schering Corporation |
Tricyclic antitumor farnesyl protein transferase inhibitors
|
AU6908398A
(en)
|
1996-10-28 |
1998-05-22 |
Versicor Inc |
Fused 2,4-pyrimidinedione combinatorial libraries and biologically active fused 2,4-pyramidinediones
|
AU5330698A
(en)
|
1996-12-23 |
1998-07-17 |
Celltech Therapeutics Limited |
Fused polycyclic 2-aminopyrimidine derivatives, their preparation and their use as protein tyrosine kinase inhibitors
|
KR20000070751A
(en)
|
1997-02-05 |
2000-11-25 |
로즈 암스트롱, 크리스틴 에이. 트러트웨인 |
Pyrido[2,3-D]pyrimidines and 4-Aminopyrimidines as Inhibitors of Cellular Proliferation
|
WO1998046609A1
(en)
|
1997-04-11 |
1998-10-22 |
Abbott Laboratories |
Furopyridine, thienopyridine, pyrrolopyridine and related pyrimidine, pyridazine and triazine compounds useful in controlling chemical synaptic transmission
|
IL133007A
(en)
|
1997-05-28 |
2005-06-19 |
Aventis Pharma Inc |
Quinoline and quinoxaline compounds which inhibit platelet-derived growth factor and/or p56lck tyrosine kinases
|
GB9716231D0
(en)
|
1997-07-31 |
1997-10-08 |
Amersham Int Ltd |
Base analogues
|
WO1999007732A1
(en)
|
1997-08-11 |
1999-02-18 |
Cor Therapeutics, Inc. |
SELECTIVE FACTOR Xa INHIBITORS
|
WO1999009030A1
(en)
|
1997-08-20 |
1999-02-25 |
Warner-Lambert Company |
Naphthyridinones for inhibiting protein tyrosine kinase and cell cycle kinase mediated cellular proliferation
|
US6465484B1
(en)
|
1997-09-26 |
2002-10-15 |
Merck & Co., Inc. |
Angiogenesis inhibitors
|
JPH11171865A
(en)
|
1997-12-04 |
1999-06-29 |
Yoshitomi Pharmaceut Ind Ltd |
Condensed heterocyclic compound
|
AU4481899A
(en)
|
1998-02-20 |
1999-09-06 |
Takeda Chemical Industries Ltd. |
Aminoguanidine hydrazone derivatives, process for producing the same and drugs thereof
|
EP1077946A1
(en)
|
1998-05-15 |
2001-02-28 |
Guilford Pharmaceuticals Inc. |
Fused tricyclic compounds which inhibit parp activity
|
US20040044012A1
(en)
|
1998-05-26 |
2004-03-04 |
Dobrusin Ellen Myra |
Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation
|
DE69939168D1
(en)
|
1998-05-26 |
2008-09-04 |
Warner Lambert Co |
BICYCLIC PYRIMIDINES AND BICYCLIC 3,4-DIHYDROPYRIMIDINES AS INHIBITORS OF CELL REPRODUCTION
|
JP2002517486A
(en)
|
1998-06-12 |
2002-06-18 |
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 |
inhibitors of p38
|
AU5620299A
(en)
|
1998-08-11 |
2000-03-06 |
Novartis Ag |
Isoquinoline derivatives with angiogenesis inhibiting activity
|
JP2000123973A
(en)
|
1998-10-09 |
2000-04-28 |
Canon Inc |
Organic light emitting element
|
GB9823103D0
(en)
|
1998-10-23 |
1998-12-16 |
Pfizer Ltd |
Pharmaceutically active compounds
|
ES2228123T3
(en)
|
1998-10-23 |
2005-04-01 |
F. Hoffmann-La Roche Ag |
BICYCLE NITROGEN HETEROCICLES.
|
US6133031A
(en)
|
1999-08-19 |
2000-10-17 |
Isis Pharmaceuticals Inc. |
Antisense inhibition of focal adhesion kinase expression
|
GB9905075D0
(en)
|
1999-03-06 |
1999-04-28 |
Zeneca Ltd |
Chemical compounds
|
DE19912638A1
(en)
|
1999-03-20 |
2000-09-21 |
Bayer Ag |
Naphthylcarboxamide substituted sulfonamides
|
DE19920790A1
(en)
|
1999-05-06 |
2000-11-09 |
Bayer Ag |
Bis-sulfonamides with anti-HCMV activity
|
PE20010306A1
(en)
|
1999-07-02 |
2001-03-29 |
Agouron Pharma |
INDAZOLE COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM USEFUL FOR THE INHIBITION OF PROTEIN KINASE
|
JP4041624B2
(en)
|
1999-07-21 |
2008-01-30 |
三井化学株式会社 |
Organic electroluminescence device
|
BRPI0014271B1
(en)
|
1999-09-24 |
2021-06-22 |
Janssen Pharmaceutica N.V. |
PARTICLE CONSISTING OF A DISPERSION OF SOLIDS, USE OF SUCH PARTICLE, DISPERSION OF SOLIDS, PHARMACEUTICAL DOSAGE FORM, AS WELL AS PROCESSES FOR THE PREPARATION OF SUCH PARTICLE, DISPERSION AND DOSAGE FORM
|
DE19946289A1
(en)
|
1999-09-28 |
2001-03-29 |
Basf Ag |
Benzodiazepine derivatives, their production and use
|
WO2001029042A1
(en)
|
1999-10-21 |
2001-04-26 |
F. Hoffmann-La Roche Ag |
Heteroalkylamino-substituted bicyclic nitrogen heterocycles as inhibitors of p38 protein kinase
|
KR100537241B1
(en)
|
1999-10-21 |
2005-12-19 |
에프. 호프만-라 로슈 아게 |
Alkylamino substituted bicyclic nitrogen heterocycles as inhibitors of p38 protein kinase
|
TWI271406B
(en)
|
1999-12-13 |
2007-01-21 |
Eisai Co Ltd |
Tricyclic condensed heterocyclic compounds, preparation method of the same and pharmaceuticals comprising the same
|
CN1262541C
(en)
|
1999-12-29 |
2006-07-05 |
惠氏公司 |
Tricyclic protein kinase inhibitors
|
SK10572002A3
(en)
|
2000-01-24 |
2003-10-07 |
Warner-Lambert Company |
3-Aminoquinazolin-2,4-dione antibacterial agents
|
CN1433417A
(en)
|
2000-01-27 |
2003-07-30 |
沃尼尔·朗伯公司 |
Pyridopyrimidinone derivatives for treatment of neurodegenerative disease
|
ES2290115T3
(en)
|
2000-02-01 |
2008-02-16 |
ABBOTT GMBH & CO. KG |
HETEROCICLICAL COMPOUNDS AND ITS APPLICATION AS PARP INHIBITORS.
|
US20020025961A1
(en)
|
2000-02-04 |
2002-02-28 |
Scarborough Robert M. |
Platelet ADP receptor inhibitors
|
AU2001231710A1
(en)
|
2000-02-09 |
2001-08-20 |
Novartis Ag |
Pyridine derivatives inhibiting angiogenesis and/or vegf receptor tyrosine kinase
|
GB0004890D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
JP2003525897A
(en)
|
2000-03-06 |
2003-09-02 |
アストラゼネカ アクチボラグ |
Treatment
|
DE10012549A1
(en)
|
2000-03-15 |
2001-09-20 |
Bayer Ag |
New heterocyclic-substituted dihydropyrimidine derivatives useful for treatment of viral infections, especially hepatitis B infections
|
JP2001265031A
(en)
|
2000-03-15 |
2001-09-28 |
Fuji Xerox Co Ltd |
Electrophotographic photoreceptor, process cartridge and electrophotographic device
|
JP4119126B2
(en)
|
2000-04-28 |
2008-07-16 |
アカディア ファーマシューティカルズ,インコーポレーテッド |
Muscarinic agonist
|
CA2408156A1
(en)
|
2000-05-05 |
2001-11-15 |
Millennium Pharmaceuticals, Inc. |
Heterobicyclic sulfonamides and their use as platelet adp receptor inhibitors
|
EP1296982B1
(en)
|
2000-06-23 |
2007-09-19 |
Bristol-Myers Squibb Pharma Company |
1-(heteroaryl-phenyl)-condensed pyrazol derivatives as factor xa inhibitors
|
CA2413330A1
(en)
|
2000-06-28 |
2002-01-03 |
Smithkline Beecham P.L.C. |
Wet milling process
|
US20050009876A1
(en)
|
2000-07-31 |
2005-01-13 |
Bhagwat Shripad S. |
Indazole compounds, compositions thereof and methods of treatment therewith
|
IL154310A0
(en)
|
2000-08-07 |
2003-09-17 |
Neurogen Corp |
Heterocyclic compounds as ligands of the gabaa receptor
|
US6953793B2
(en)
|
2000-08-14 |
2005-10-11 |
Ortho-Mcneil Pharmaceutical, Inc. |
Substituted pyrazoles
|
NZ524681A
(en)
|
2000-09-06 |
2005-09-30 |
Ortho Mcneil Pharm Inc |
A method for treating allergies using substituted pyrazoles
|
GB0025782D0
(en)
|
2000-10-20 |
2000-12-06 |
Pfizer Ltd |
Use of inhibitors
|
EP1217000A1
(en)
|
2000-12-23 |
2002-06-26 |
Aventis Pharma Deutschland GmbH |
Inhibitors of factor Xa and factor VIIa
|
GB0100621D0
(en)
|
2001-01-10 |
2001-02-21 |
Vernalis Res Ltd |
Chemical compounds VI
|
GB0103926D0
(en)
|
2001-02-17 |
2001-04-04 |
Astrazeneca Ab |
Chemical compounds
|
AP1699A
(en)
|
2001-03-21 |
2006-12-26 |
Warner Lambert Co |
New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors
|
US6998408B2
(en)
|
2001-03-23 |
2006-02-14 |
Bristol-Myers Squibb Pharma Company |
6-5, 6-6, or 6-7 Heterobicycles as factor Xa inhibitors
|
JP2002296731A
(en)
|
2001-03-30 |
2002-10-09 |
Fuji Photo Film Co Ltd |
Heat developable color image recording material
|
EP1380576B1
(en)
|
2001-04-16 |
2009-11-25 |
Eisai R&D Management Co., Ltd. |
1h-indazole compounds inhibiting jnk
|
ES2310202T3
(en)
|
2001-04-26 |
2009-01-01 |
EISAI R&D MANAGEMENT CO., LTD. |
CONDENSED CYCLING COMPOUND CONTAINING NITROGEN THAT HAS A PIRAZOLIL GROUP AS A SUBSTITUTING GROUP AND PHARMACEUTICAL COMPOSITION OF THE SAME.
|
EP1383747B1
(en)
|
2001-04-30 |
2008-02-20 |
Glaxo Group Limited |
Fused pyrimidines as antagonists of the corticotropin releasing factor (crf)
|
WO2002094825A1
(en)
|
2001-05-22 |
2002-11-28 |
Banyu Pharmaceutical Co., Ltd. |
Novel spiropiperidine derivative
|
US20030114448A1
(en)
|
2001-05-31 |
2003-06-19 |
Millennium Pharmaceuticals, Inc. |
Inhibitors of factor Xa
|
CA2446963A1
(en)
|
2001-06-19 |
2002-12-27 |
Warner-Lambert Company Llc |
Quinazolinediones as antibacterial agents
|
EP1463742A4
(en)
|
2001-06-21 |
2006-05-10 |
Ariad Pharma Inc |
Novel pyrazolo-and pyrrolo-pyrimidines and uses thereof
|
GB0115109D0
(en)
|
2001-06-21 |
2001-08-15 |
Aventis Pharma Ltd |
Chemical compounds
|
WO2003000690A1
(en)
|
2001-06-25 |
2003-01-03 |
Aventis Pharmaceuticals Inc. |
Synthesis of heterocyclic compounds employing microwave technology
|
WO2003009852A1
(en)
|
2001-07-24 |
2003-02-06 |
Merck & Co., Inc. |
Tyrosine kinase inhibitors
|
US7205417B2
(en)
|
2001-08-07 |
2007-04-17 |
Banyu Pharmaceutical Co., Ltd. |
Spiro compounds
|
IL160915A0
(en)
|
2001-09-19 |
2004-08-31 |
Aventis Pharma Sa |
Indolizines inhibiting kinase proteins
|
TWI302836B
(en)
|
2001-10-30 |
2008-11-11 |
Novartis Ag |
Staurosporine derivatives as inhibitors of flt3 receptor tyrosine kinase activity
|
MXPA04004178A
(en)
|
2001-11-01 |
2004-09-06 |
Janssen Pharmaceutica Nv |
Heteroaryl amines as glycogen synthase kinase 3beta inhibitors (gsk3 inhibitors).
|
CN1582284A
(en)
|
2001-11-07 |
2005-02-16 |
霍夫曼-拉罗奇有限公司 |
Aminopyrimidines and pyridines
|
EP1456652A4
(en)
|
2001-11-13 |
2005-11-02 |
Dana Farber Cancer Inst Inc |
Agents that modulate immune cell activation and methods of use thereof
|
GB0129476D0
(en)
|
2001-12-10 |
2002-01-30 |
Syngenta Participations Ag |
Organic compounds
|
DK1470124T3
(en)
|
2002-01-22 |
2006-04-18 |
Warner Lambert Co |
2- (Pyridin-2-yl amino) pyrido [2,3] pyrimidin-7-one
|
ATE395911T1
(en)
|
2002-03-05 |
2008-06-15 |
Merck Frosst Canada Ltd |
CATHEPSIN-CYSTEIN PROTEASE INHIBITORS
|
US6815519B2
(en)
|
2002-03-22 |
2004-11-09 |
Chung-Shan Institute Of Science & Technology |
Acidic fluorine-containing poly (siloxane amideimide) silica hybrids
|
PL374544A1
(en)
|
2002-04-03 |
2005-10-31 |
F.Hoffmann-La Roche Ag |
Imidazo fused compounds
|
JP2006502097A
(en)
|
2002-05-15 |
2006-01-19 |
ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ |
N-substituted tricyclic 3-aminopyrazoles as PDGF receptor inhibitors
|
JP4499342B2
(en)
|
2002-05-16 |
2010-07-07 |
株式会社カネカ |
Method for producing nitrogen-containing organic compound containing SiH group
|
WO2003099818A1
(en)
|
2002-05-23 |
2003-12-04 |
Chiron Corporation |
Substituted quinazolinone compounds
|
US7119111B2
(en)
|
2002-05-29 |
2006-10-10 |
Amgen, Inc. |
2-oxo-1,3,4-trihydroquinazolinyl derivatives and methods of use
|
TW200406374A
(en)
|
2002-05-29 |
2004-05-01 |
Novartis Ag |
Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases
|
US7105526B2
(en)
|
2002-06-28 |
2006-09-12 |
Banyu Pharmaceuticals Co., Ltd. |
Benzimidazole derivatives
|
GB0215676D0
(en)
|
2002-07-05 |
2002-08-14 |
Novartis Ag |
Organic compounds
|
US7196090B2
(en)
|
2002-07-25 |
2007-03-27 |
Warner-Lambert Company |
Kinase inhibitors
|
EP1534286B1
(en)
|
2002-07-29 |
2009-12-09 |
Rigel Pharmaceuticals, Inc. |
Methods of treating or preventing autoimmune diseases with 2,4-pyrimidinediamine compounds
|
EP1539755B1
(en)
|
2002-08-06 |
2007-09-26 |
F. Hoffmann-La Roche Ag |
6-alkoxy-pyrido-pyrimidines as p-38 map kinase inhibitors
|
EP1388541A1
(en)
|
2002-08-09 |
2004-02-11 |
Centre National De La Recherche Scientifique (Cnrs) |
Pyrrolopyrazines as kinase inhibitors
|
US7084270B2
(en)
|
2002-08-14 |
2006-08-01 |
Hoffman-La Roche Inc. |
Pyrimido compounds having antiproliferative activity
|
GB0220187D0
(en)
|
2002-08-30 |
2002-10-09 |
Novartis Ag |
Organic compounds
|
GB0223349D0
(en)
|
2002-10-08 |
2002-11-13 |
Merck Sharp & Dohme |
Therapeutic agents
|
TW200413381A
(en)
|
2002-11-04 |
2004-08-01 |
Hoffmann La Roche |
Novel amino-substituted dihydropyrimido [4,5-d]pyrimidinone derivatives, their manufacture and use as pharmaceutical agents
|
US7129351B2
(en)
|
2002-11-04 |
2006-10-31 |
Hoffmann-La Roche Inc. |
Pyrimido compounds having antiproliferative activity
|
WO2004043367A2
(en)
|
2002-11-06 |
2004-05-27 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds and use thereof
|
TWI335913B
(en)
|
2002-11-15 |
2011-01-11 |
Vertex Pharma |
Diaminotriazoles useful as inhibitors of protein kinases
|
JP2006514624A
(en)
|
2002-11-18 |
2006-05-11 |
エフ.ホフマン−ラ ロシュ アーゲー |
Diazinopyrimidines
|
NZ539823A
(en)
|
2002-11-28 |
2008-04-30 |
Schering Aktiengessellschaft |
Chk-, Pdk- and Akt-inhibitory pyrimidines, their production and use as pharmaceutical agents
|
CA2508165C
(en)
|
2002-12-06 |
2014-05-06 |
Purdue Research Foundation |
Pyridines for treating injured mammalian nerve tissue
|
AU2003288994A1
(en)
|
2002-12-10 |
2004-06-30 |
Ono Pharmaceutical Co., Ltd. |
Nitrogen-containing heterocyclic compounds and medicinal use thereof
|
UA80171C2
(en)
|
2002-12-19 |
2007-08-27 |
Pfizer Prod Inc |
Pyrrolopyrimidine derivatives
|
UA80767C2
(en)
|
2002-12-20 |
2007-10-25 |
Pfizer Prod Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
US7098332B2
(en)
|
2002-12-20 |
2006-08-29 |
Hoffmann-La Roche Inc. |
5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones
|
ES2367430T3
(en)
|
2002-12-23 |
2011-11-03 |
Wyeth Llc |
ANTIBODIES AGAINST PD-1 AND ITS USES.
|
JP2004203749A
(en)
|
2002-12-24 |
2004-07-22 |
Kanegafuchi Chem Ind Co Ltd |
METHOD FOR PRODUCING NITROGEN-CONTAINING ORGANIC COMPOUND CONTAINING SiH GROUP
|
ATE433967T1
(en)
|
2003-01-17 |
2009-07-15 |
Warner Lambert Co |
2-AMINOPYRIDINE SUBSTITUTED HETEROCYCLES AS INHIBITORS OF CELLULAR PROLIFERATION
|
GB0305929D0
(en)
|
2003-03-14 |
2003-04-23 |
Novartis Ag |
Organic compounds
|
US7135469B2
(en)
|
2003-03-18 |
2006-11-14 |
Bristol Myers Squibb, Co. |
Linear chain substituted monocyclic and bicyclic derivatives as factor Xa inhibitors
|
CN1894234A
(en)
|
2003-03-25 |
2007-01-10 |
武田药品工业株式会社 |
Dipeptidyl peptidase inhibitors
|
GB0308208D0
(en)
|
2003-04-09 |
2003-05-14 |
Glaxo Group Ltd |
Chemical compounds
|
MXPA05010765A
(en)
|
2003-04-10 |
2005-12-12 |
Hoffmann La Roche |
Pyrimido compounds.
|
MXPA05011710A
(en)
|
2003-05-05 |
2006-01-23 |
Hoffmann La Roche |
Fused pyrimidine derivatives with crf activity.
|
JP2004346145A
(en)
|
2003-05-21 |
2004-12-09 |
Teijin Ltd |
Imide composition, resin composition comprising the same and its manufacturing method
|
WO2004112793A1
(en)
|
2003-05-23 |
2004-12-29 |
Chiron Corporation |
Guanidino-substituted quinazolinone compounds as mc4-r agonists
|
KR101205257B1
(en)
|
2003-06-06 |
2012-11-27 |
아렉시스 악티에볼라그 |
Use of fused heterocyclic compounds as scce inhibitors for the treatment of skin conditions or cancer
|
IL156495A0
(en)
|
2003-06-17 |
2004-01-04 |
Prochon Biotech Ltd |
Use of fgfr3 antagonists for treating t cell mediated diseases
|
US20060270849A1
(en)
|
2003-06-18 |
2006-11-30 |
Shigeyoshi Nishino |
Process for producing pyrimidin-4-one compound
|
JP2005015395A
(en)
|
2003-06-26 |
2005-01-20 |
Japan Science & Technology Agency |
New pyrimidopyrimidine nucleoside and its structural analog
|
EP1660092A2
(en)
|
2003-07-03 |
2006-05-31 |
Myriad Genetics, Inc. |
4-arylamino-quinazolines as activators of caspases and inducers of apoptosis
|
AR045037A1
(en)
|
2003-07-10 |
2005-10-12 |
Aventis Pharma Sa |
TETRAHIDRO-1H-PIRAZOLO [3,4-C] SUBSTITUTED PYRIDINS, COMPOSITIONS THAT CONTAIN THEM AND ITS USE.
|
CN1860118A
(en)
|
2003-07-29 |
2006-11-08 |
Irm责任有限公司 |
Compounds and compositions as protein kinase inhibitors
|
US7390820B2
(en)
|
2003-08-25 |
2008-06-24 |
Amgen Inc. |
Substituted quinolinone derivatives and methods of use
|
AU2004274403A1
(en)
|
2003-09-03 |
2005-03-31 |
Aventis Pharmaceuticals Inc. |
5-aryl-Pyrazolo(4,3-d)pyrimidines, pyridines, and pyrazines and related compounds
|
WO2005028434A2
(en)
|
2003-09-18 |
2005-03-31 |
Conforma Therapeutics Corporation |
Novel heterocyclic compounds as hsp90-inhibitors
|
ATE433974T1
(en)
|
2003-09-19 |
2009-07-15 |
Gilead Sciences Inc |
AZACHINOLINOL PHOSPHONATE COMPOUNDS AS INTEGRAS INHIBITORS
|
AR045944A1
(en)
|
2003-09-24 |
2005-11-16 |
Novartis Ag |
ISOQUINOLINE DERIVATIVES 1.4-DISPOSED
|
DE602004019294D1
(en)
|
2003-10-01 |
2009-03-19 |
Xention Ltd |
TETRAHYDRONAPHTHALIN AND UREA DERIVATIVES
|
MXPA06003996A
(en)
|
2003-10-08 |
2006-07-05 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors.
|
CN1897950A
(en)
|
2003-10-14 |
2007-01-17 |
惠氏公司 |
Fused-aryl and heteroaryl derivatives and methods of their use
|
US20090099165A1
(en)
|
2003-10-14 |
2009-04-16 |
Arizona Board Of Regents On Behalf Of The University Of Arizona |
Protein Kinase Inhibitors
|
CA2546192C
(en)
|
2003-11-17 |
2010-04-06 |
Pfizer Products Inc. |
Pyrrolopyrimidine compounds useful in treatment of cancer
|
WO2005056524A2
(en)
|
2003-12-09 |
2005-06-23 |
Euro-Celtique S.A. |
Therapeutic agents useful for treating pain
|
US20080188527A1
(en)
|
2003-12-23 |
2008-08-07 |
Cashman John R |
Synthetic Compounds and Derivatives as Modulators of Smoking or Nicotine Ingestion and Lung Cancer
|
KR100703068B1
(en)
|
2003-12-30 |
2007-04-05 |
에스케이케미칼주식회사 |
Novel pyridine derivatives, process for preparing thereof and pharmaceutical compositions containing them
|
US20050222171A1
(en)
|
2004-01-22 |
2005-10-06 |
Guido Bold |
Organic compounds
|
BRPI0507065B8
(en)
|
2004-01-23 |
2021-05-25 |
Janssen Pharmaceutica Nv |
quinoline derivatives, composition comprising them, their preparation process and their use as mycobacterial inhibitors
|
JP2007524673A
(en)
|
2004-01-23 |
2007-08-30 |
アムジエン・インコーポレーテツド |
Vanilloid receptor ligands and their use in therapy
|
JP2007529422A
(en)
|
2004-01-29 |
2007-10-25 |
エリクシアー ファーマシューティカルズ, インコーポレイテッド |
Antiviral treatment
|
GB0402137D0
(en)
|
2004-01-30 |
2004-03-03 |
Smithkline Beecham Corp |
Novel compounds
|
JP4989233B2
(en)
|
2004-02-14 |
2012-08-01 |
アイアールエム・リミテッド・ライアビリティ・カンパニー |
Compounds and compositions as protein kinase inhibitors
|
WO2005082903A1
(en)
|
2004-02-18 |
2005-09-09 |
Warner-Lambert Company Llc |
2-(pyridin-3-ylamino)-pyrido[2,3-d]pyrimidin-7-ones
|
AU2005219517A1
(en)
|
2004-02-27 |
2005-09-15 |
F.Hoffmann-La Roche Ag |
Heteroaryl-fused pyrazolo derivatives
|
CA2557575A1
(en)
|
2004-02-27 |
2005-09-15 |
F. Hoffmann-La Roche Ag |
Fused derivatives of pyrazole
|
US20080004263A1
(en)
|
2004-03-04 |
2008-01-03 |
Santora Vincent J |
Ligands of Follicle Stimulating Hormone Receptor and Methods of Use Thereof
|
WO2005085210A1
(en)
|
2004-03-10 |
2005-09-15 |
Ono Pharmaceutical Co., Ltd. |
Nitriles and medicinal compositions containing the same as the active ingredient
|
JP4627528B2
(en)
|
2004-03-29 |
2011-02-09 |
三井化学株式会社 |
Novel compound and organic electronic device using the compound
|
WO2005105097A2
(en)
|
2004-04-28 |
2005-11-10 |
Gpc Biotech Ag |
Pyridopyrimidines for treating inflammatory and other diseases
|
JP2005320288A
(en)
|
2004-05-10 |
2005-11-17 |
Mitsui Chemicals Inc |
Tetracarboxylic acid derivative, electrophotographic photoreceptor given by using the compound, and electrophotographic device
|
US20050256309A1
(en)
|
2004-05-12 |
2005-11-17 |
Altenbach Robert J |
Tri-and bi-cyclic heteroaryl histamine-3 receptor ligands
|
MXPA06013805A
(en)
|
2004-05-27 |
2007-02-02 |
Pfizer Prod Inc |
Pyrrolopyrimidine derivatives useful in cancer treatment.
|
PE20060426A1
(en)
|
2004-06-02 |
2006-06-28 |
Schering Corp |
TARTARIC ACID DERIVATIVES AS INHIBITORS OF MMPs, ADAMs, TACE AND TNF-alpha
|
WO2005118587A1
(en)
*
|
2004-06-02 |
2005-12-15 |
Takeda Pharmaceutical Company Limited |
Indole derivative and use for treatment of cancer
|
MXPA06014247A
(en)
|
2004-06-10 |
2007-03-12 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors.
|
CN101006086B
(en)
|
2004-06-11 |
2010-09-29 |
日本烟草产业株式会社 |
5-amino-2,4,7-trioxo-3,4,7,8-tetrahydro-2h-pyrido'2,3-d! pyrimidine derivatives and related compounds for the treatment of cancer
|
GB0512324D0
(en)
|
2005-06-16 |
2005-07-27 |
Novartis Ag |
Organic compounds
|
JP2006028027A
(en)
|
2004-07-12 |
2006-02-02 |
Mitsui Chemicals Inc |
Tetracarboxylic acid derivative, electrophotographic photoconductor using the compound and electrohptographic apparatus
|
US7494993B2
(en)
|
2004-08-31 |
2009-02-24 |
Hoffmann-La Roche Inc. |
Amide derivatives of 7-amino-3-phenyl-dihydropyrimido[4,5-d]pyrimidinones, their manufacture and use as pharmaceutical agents
|
WO2006024834A1
(en)
|
2004-08-31 |
2006-03-09 |
Astrazeneca Ab |
Quinazolinone derivatives and their use as b-raf inhibitors
|
WO2006024486A2
(en)
|
2004-08-31 |
2006-03-09 |
F. Hoffmann-La Roche Ag |
Amide derivatives of 3-phenyl dihydropyrimido[4,5-d]pyrimidinones, their manufacture and use as pharmaceutical agents
|
DE102004042667A1
(en)
|
2004-09-01 |
2006-03-30 |
Ewald Dörken Ag |
Multilayered building wall
|
TWI370147B
(en)
|
2004-09-10 |
2012-08-11 |
Ube Industries |
Modified polyimide resin and curable resin composition
|
JP5635726B2
(en)
|
2004-09-14 |
2014-12-03 |
ミネルバ バイオテクノロジーズ コーポレーション |
Cancer diagnosis and treatment method
|
GB0420719D0
(en)
|
2004-09-17 |
2004-10-20 |
Addex Pharmaceuticals Sa |
Novel allosteric modulators
|
WO2006038112A1
(en)
|
2004-10-01 |
2006-04-13 |
Warner-Lambert Company Llc |
Use of kinase inhibitors to promote neochondrogenesis
|
FR2876582B1
(en)
|
2004-10-15 |
2007-01-05 |
Centre Nat Rech Scient Cnrse |
USE OF PYRROLO-PYRAZINE DERIVATIVES FOR THE MANUFACTURE OF MEDICAMENTS FOR THE TREATMENT OF MUCOVISCIDOSIS AND DISEASES ASSOCIATED WITH A DEFECT OF ADDRESSING PROTEINS IN CELLS
|
WO2006050162A2
(en)
|
2004-10-28 |
2006-05-11 |
Phenomix Corporation |
Imidazole derivatives
|
US7855205B2
(en)
|
2004-10-29 |
2010-12-21 |
Janssen Pharmaceutica Nv |
Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders
|
WO2006052712A1
(en)
|
2004-11-08 |
2006-05-18 |
Baxter International Inc. |
Nanoparticulate compositions of tubulin inhibitor
|
BRPI0518281A2
(en)
|
2004-11-18 |
2008-11-18 |
Incyte Corp |
11-beta hydroxylesterase dehydrogenase type i inhibitors and methods of using them
|
MX2007006103A
(en)
|
2004-11-22 |
2007-07-20 |
Vertex Pharma |
Pyrrolopyrazines and pyrazolopyrazines useful as inhibitors of protein kinases.
|
CN101106983A
(en)
|
2004-11-24 |
2008-01-16 |
诺瓦提斯公司 |
Combinations comprising JAK inhibitors and at least one of Bcr-Abl, Flt-3, FAK or RAF kinase inhibitors
|
MY140748A
(en)
|
2004-12-06 |
2010-01-15 |
Astrazeneca Ab |
Novel pyrrolo [3,2-d] pyrimidin-4-one derivatives and their use in therapy
|
CA2590294A1
(en)
|
2004-12-13 |
2006-06-22 |
Sunesis Pharmaceuticals, Inc. |
Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as raf kinase inhibitors
|
US20100152206A1
(en)
|
2005-01-07 |
2010-06-17 |
Ralph Mazitschek |
Bicyclic Dihydropyrimidines and Uses Thereof
|
DE102005008310A1
(en)
|
2005-02-17 |
2006-08-24 |
Schering Ag |
Use of CDKII inhibitors for fertility control
|
CA2599662A1
(en)
|
2005-03-01 |
2006-09-08 |
Pfizer Limited |
Use of pde7 inhibitors for the treatment of neuropathic pain
|
US7402596B2
(en)
|
2005-03-24 |
2008-07-22 |
Renovis, Inc. |
Bicycloheteroaryl compounds as P2X7 modulators and uses thereof
|
CA2610292C
(en)
|
2005-03-30 |
2015-06-02 |
Minerva Biotechnologies Corporation |
Proliferation of muc1 expressing cells
|
JP2006284843A
(en)
|
2005-03-31 |
2006-10-19 |
Mitsui Chemicals Inc |
Electrophotographic photoreceptor using tetracarboxylic acid derivative and electrophotographing device
|
US20060223993A1
(en)
|
2005-04-01 |
2006-10-05 |
Connor Daniel M |
Colorant compounds, intermediates, and compositions
|
JP2006316054A
(en)
|
2005-04-15 |
2006-11-24 |
Tanabe Seiyaku Co Ltd |
High-conductance type calcium-sensitive k channel opening agent
|
KR100781704B1
(en)
|
2005-04-20 |
2007-12-03 |
에스케이케미칼주식회사 |
Novel pyridine derivatives, process for preparing thereof and pharmaceutical compositions containing them
|
MX2007013595A
(en)
|
2005-05-04 |
2008-01-24 |
Renovis Inc |
Fused heterocyclic compounds, and compositions and uses thereof.
|
ES2427646T5
(en)
|
2005-05-09 |
2017-08-22 |
Ono Pharmaceutical Co., Ltd. |
Human monoclonal antibodies against programmed death 1 (PD1) and methods for the treatment of cancer through the use of anti-PD-1 antibodies alone or in combination with other immunotherapeutic agents
|
WO2006124731A2
(en)
|
2005-05-12 |
2006-11-23 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
DE602006019088D1
(en)
|
2005-05-13 |
2011-02-03 |
Irm Llc |
COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS
|
US20060279115A1
(en)
|
2005-06-09 |
2006-12-14 |
Ash Tisdelle |
Vehicular head and neck safety system and method
|
GB0512844D0
(en)
|
2005-06-23 |
2005-08-03 |
Novartis Ag |
Organic compounds
|
MX2007015942A
(en)
|
2005-07-01 |
2008-03-07 |
Medarex Inc |
Human monoclonal antibodies to programmed death ligand 1 (pd-l1).
|
WO2007013964A1
(en)
|
2005-07-22 |
2007-02-01 |
Sunesis Pharmaceuticals, Inc. |
Pyrazolo pyrimidines useful as aurora kinase inhibitors
|
ES2270715B1
(en)
|
2005-07-29 |
2008-04-01 |
Laboratorios Almirall S.A. |
NEW DERIVATIVES OF PIRAZINA.
|
US20100216798A1
(en)
|
2005-07-29 |
2010-08-26 |
Astellas Pharma Inc |
Fused heterocycles as lck inhibitors
|
US7868018B2
(en)
|
2005-08-09 |
2011-01-11 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
WO2007022268A2
(en)
|
2005-08-16 |
2007-02-22 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
KR101011958B1
(en)
|
2005-08-25 |
2011-01-31 |
에프. 호프만-라 로슈 아게 |
Fused pyrazole as ?38 map kinase inhibitors
|
US7678917B2
(en)
|
2005-09-01 |
2010-03-16 |
Hoffman-La Roche Inc. |
Factor Xa inhibitors
|
WO2007030366A1
(en)
|
2005-09-06 |
2007-03-15 |
Smithkline Beecham Corporation |
Regioselective process for preparing benzimidazole thiophenes
|
CN101268073B
(en)
|
2005-09-15 |
2011-10-19 |
Aska制药株式会社 |
Heterocyclic compound, and production process and use thereof
|
US20070116984A1
(en)
|
2005-09-21 |
2007-05-24 |
Doosan Corporation |
Spiro-compound for electroluminescent display device and electroluminescent display device comprising the same
|
EP1940850A2
(en)
|
2005-09-23 |
2008-07-09 |
Schering Corporation |
Fused tetracyclic mglur1 antagonists as therapeutic agents
|
DE102005048072A1
(en)
|
2005-09-24 |
2007-04-05 |
Bayer Cropscience Ag |
Thiazoles as fungicides
|
US8247408B2
(en)
|
2005-10-07 |
2012-08-21 |
Exelixis, Inc. |
Pyridopyrimidinone inhibitors of PI3Kα for the treatment of cancer
|
KR101504994B1
(en)
|
2005-10-07 |
2015-03-23 |
엑셀리시스, 인코포레이티드 |
Phosphatidylinositol 3-kinase inhibitors and methods of their use
|
WO2007061554A2
(en)
|
2005-10-21 |
2007-05-31 |
Purdue Research Foundation |
Dosage of 4-aminopyridine derivatives for treatment of central nervous system injuries
|
EP1943231A1
(en)
|
2005-10-26 |
2008-07-16 |
Boehringer Ingelheim International Gmbh |
(hetero)aryl compounds with mch antagonistic activity and medicaments comprising these compounds
|
US8067457B2
(en)
|
2005-11-01 |
2011-11-29 |
Millennium Pharmaceuticals, Inc. |
Compounds useful as antagonists of CCR2
|
US8604042B2
(en)
|
2005-11-01 |
2013-12-10 |
Targegen, Inc. |
Bi-aryl meta-pyrimidine inhibitors of kinases
|
EP1951684B1
(en)
|
2005-11-01 |
2016-07-13 |
TargeGen, Inc. |
Bi-aryl meta-pyrimidine inhibitors of kinases
|
CA2627839C
(en)
|
2005-11-02 |
2014-08-19 |
Bayer Healthcare Ag |
Pyrrolo[2,1-f] [1,2,4] triazin-4-ylamines igf-1r kinase inhibitors for the treatment of cancer and other hyperproliferative diseases
|
WO2007056075A2
(en)
|
2005-11-02 |
2007-05-18 |
Targegen, Inc. |
Six membered heteroaromatic inhibitors targeting resistant kinase mutations
|
AU2006312557B2
(en)
|
2005-11-10 |
2011-12-08 |
Msd K.K. |
Aza-substituted spiro derivative
|
WO2007059108A2
(en)
|
2005-11-10 |
2007-05-24 |
Chemocentryx, Inc. |
Substituted quinolones and methods of use
|
WO2007058626A1
(en)
|
2005-11-16 |
2007-05-24 |
S*Bio Pte Ltd |
Indazole compounds
|
AR057986A1
(en)
|
2005-11-21 |
2008-01-09 |
Japan Tobacco Inc |
HETEROCICLICAL COMPOUND AND ITS PHARMACEUTICAL USE
|
KR20130141706A
(en)
|
2005-12-02 |
2013-12-26 |
바이엘 헬스케어 엘엘씨 |
Substituted 4-amino-pyrrolotriazine derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis
|
PE20070855A1
(en)
|
2005-12-02 |
2007-10-14 |
Bayer Pharmaceuticals Corp |
DERIVATIVES OF 4-AMINO-PYRROLOTRIAZINE SUBSTITUTE AS KINASE INHIBITORS
|
ZA200804679B
(en)
|
2005-12-08 |
2010-02-24 |
Millenium Pharmaceuticals Inc |
Bicyclic compounds with kinase inhibitory activity
|
WO2007066189A2
(en)
|
2005-12-09 |
2007-06-14 |
Pfizer Products Inc. |
Salts, prodrugs and formulations of 1-[5-(4-amino-7-isopropyl-7h-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-2-methoxy-phenyl]-3-(2,4-dichloro-phenyl)-urea
|
WO2007120339A1
(en)
|
2005-12-19 |
2007-10-25 |
Genentech, Inc. |
Pyrimidine kinase inhibitors
|
ME00011A
(en)
|
2005-12-21 |
2009-02-10 |
Novartis Ag |
Pyrimidinyl aryl urea derivatives being fgf inhibitors
|
WO2007084314A2
(en)
|
2006-01-12 |
2007-07-26 |
Incyte Corporation |
MODULATORS OF 11-ß HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME
|
PE20071025A1
(en)
|
2006-01-31 |
2007-10-17 |
Mitsubishi Tanabe Pharma Corp |
TRISUSTITUTED AMINE COMPOUND
|
WO2007092879A2
(en)
|
2006-02-08 |
2007-08-16 |
Janssen Pharmaceutica, N.V. |
Substituted thiatriazaacenaphthylene-6-carbonitrile kinase inhibitors
|
EP1987030B1
(en)
|
2006-02-17 |
2011-11-09 |
Pfizer Limited |
3 -deazapurine derivatives as tlr7 modulators
|
WO2007112347A1
(en)
|
2006-03-28 |
2007-10-04 |
Takeda Pharmaceutical Company Limited |
Dipeptidyl peptidase inhibitors
|
EP2233472B1
(en)
|
2006-03-28 |
2014-01-15 |
Atir Holding S.A. |
Heterocyclic compounds and uses thereof in the treatment of sexual disorders
|
AU2007245129A1
(en)
|
2006-03-29 |
2007-11-08 |
Foldrx Pharmaceuticals, Inc. |
Inhibition of alpha-synuclein toxicity
|
EP2046737B1
(en)
|
2006-04-06 |
2011-09-07 |
Wisconsin Alumni Research Foundation |
2-methylene-1 alpha,25-dihydroxy-19,21-dinorvitamin d3 analogs and uses thereof
|
US20090286813A1
(en)
|
2006-04-13 |
2009-11-19 |
Astrazeneca Ab |
Thioxanthine Derivatives and Their Use as Inhibitors of MPO
|
GB0608386D0
(en)
|
2006-04-27 |
2006-06-07 |
Senexis Ltd |
Compounds
|
US7998978B2
(en)
|
2006-05-01 |
2011-08-16 |
Pfizer Inc. |
Substituted 2-amino-fused heterocyclic compounds
|
AU2007249249A1
(en)
|
2006-05-11 |
2007-11-22 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
AU2007254491A1
(en)
|
2006-05-15 |
2007-11-29 |
Irm Llc |
Compositions and methods for FGF receptor kinases inhibitors
|
WO2007143600A2
(en)
|
2006-06-05 |
2007-12-13 |
Incyte Corporation |
Sheddase inhibitors combined with cd30-binding immunotherapeutics for the treatment of cd30 positive diseases
|
DE102006027156A1
(en)
|
2006-06-08 |
2007-12-13 |
Bayer Schering Pharma Ag |
New sulfimide compounds are protein kinase inhibitors useful to treat e.g. cancer, Hodgkin's lymphoma, Kaposi's sarcoma, cardiovascular disease, Crohn's disease, endometriosis and hemangioma
|
CN101589026B
(en)
|
2006-06-22 |
2013-10-16 |
普拉纳生物技术有限公司 |
Method of treatment of glioma brain tumour
|
WO2008005877A2
(en)
|
2006-06-30 |
2008-01-10 |
Board Of Regents, The University Of Texas System |
Inhibitors of c-kit and uses thereof
|
AU2007263655A1
(en)
|
2006-06-30 |
2008-01-03 |
Astrazeneca Ab |
Pyrimidine derivatives useful in the treatment of cancer
|
US8258129B2
(en)
|
2006-07-06 |
2012-09-04 |
Boehringer Ingelheim International Gmbh |
4-heterocycloalkylpyri(mi)dines, process for the preparation thereof and their use as medicaments
|
US8030487B2
(en)
|
2006-07-07 |
2011-10-04 |
Targegen, Inc. |
2-amino—5-substituted pyrimidine inhibitors
|
TW200811134A
(en)
|
2006-07-12 |
2008-03-01 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
WO2008012635A2
(en)
|
2006-07-26 |
2008-01-31 |
Pfizer Products Inc. |
Amine derivatives useful as anticancer agents
|
WO2008021851A2
(en)
|
2006-08-09 |
2008-02-21 |
Smithkline Beecham Corporation |
Novel compounds as antagonists or inverse agonists for opioid receptors
|
EP2056829B9
(en)
|
2006-08-16 |
2012-09-26 |
Exelixis, Inc. |
Using pi3k and mek modulators in treatments of cancer
|
DE102006041382A1
(en)
|
2006-08-29 |
2008-03-20 |
Bayer Schering Pharma Ag |
Carbamoyl sulfoximides as protein kinase inhibitors
|
EP2061765B1
(en)
|
2006-09-01 |
2014-10-22 |
Senhwa Biosciences, Inc. |
Serine-threonine protein kinase and PARP modulators
|
JP5600004B2
(en)
|
2006-09-05 |
2014-10-01 |
エモリー ユニバーシティー |
Tyrosine kinase inhibitors for the prevention or treatment of infection
|
EP2270200A3
(en)
|
2006-09-11 |
2011-07-13 |
CGI Pharmaceuticals, Inc. |
Kinase inhibitors, and methods of using and identifying kinase inhibitors
|
US7897762B2
(en)
|
2006-09-14 |
2011-03-01 |
Deciphera Pharmaceuticals, Llc |
Kinase inhibitors useful for the treatment of proliferative diseases
|
CA2664095A1
(en)
|
2006-09-21 |
2008-03-27 |
Boehringer Ingelheim International Gmbh |
Glucopyranosyl-substituted difluorobenzyl-benzene derivatives, medicaments containing such compounds, their use and process for their manufacture
|
ATE493411T1
(en)
|
2006-09-22 |
2011-01-15 |
Glaxo Group Ltd |
PYRROLOÄ2, 3-BÜPYRIDINE-4-YL-BENZENESULFONAMIDE COMPOUNDS AS IKK2 INHIBITORS
|
MX2009002995A
(en)
|
2006-09-28 |
2009-04-01 |
Novartis Ag |
Pyrazolo [1, 5-a] pyrimidine derivatives and their therapeutic use.
|
KR101101675B1
(en)
|
2006-10-02 |
2011-12-30 |
노파르티스 아게 |
Compounds and compositions as protein kinase inhibitors
|
EP2077841A1
(en)
|
2006-10-30 |
2009-07-15 |
Glaxo Group Limited |
Novel substituted pyrimidines as cysteine protease inhibitors
|
US7858645B2
(en)
|
2006-11-01 |
2010-12-28 |
Hoffmann-La Roche Inc. |
Indazole derivatives
|
WO2008060907A2
(en)
|
2006-11-10 |
2008-05-22 |
Bristol-Myers Squibb Company |
Pyrrolo-pyridine kinase inhibitors
|
US7902363B2
(en)
|
2006-11-17 |
2011-03-08 |
Polyera Corporation |
Diimide-based semiconductor materials and methods of preparing and using the same
|
US7892454B2
(en)
|
2006-11-17 |
2011-02-22 |
Polyera Corporation |
Acene-based organic semiconductor materials and methods of preparing and using the same
|
KR20080045536A
(en)
|
2006-11-20 |
2008-05-23 |
에스케이케미칼주식회사 |
A pharmaceutical compositions containing pyridine derivatives as an effective ingredient for the prevention and treatment of hepatitis or the liver protection
|
AU2007334456A1
(en)
|
2006-12-13 |
2008-06-26 |
Merck Sharp & Dohme Corp. |
Methods of cancer treatment with IGF1R inhibitors
|
WO2008071455A1
(en)
|
2006-12-15 |
2008-06-19 |
Bayer Schering Pharma Aktiengesellschaft |
Bicyclic acyltryptophanols
|
WO2008074068A1
(en)
|
2006-12-20 |
2008-06-26 |
Prana Biotechnology Limited |
Substituted quinoline derivatives as antiamyloidogeneic agents
|
US7737149B2
(en)
|
2006-12-21 |
2010-06-15 |
Astrazeneca Ab |
N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]-4-(3,5-dimethylpiperazin-1-yl)benzamide and salts thereof
|
AU2007337895C1
(en)
|
2006-12-22 |
2014-07-31 |
Astex Therapeutics Limited |
Tricyclic amine derivatives as protein tyrosine kinase inhibitors
|
BRPI0720635A2
(en)
|
2006-12-22 |
2014-01-07 |
Novartis Ag |
ORGANIC COMPOUNDS AND THEIR USES
|
CA2672172C
(en)
|
2006-12-22 |
2016-05-03 |
Astex Therapeutics Limited |
Bicyclic heterocyclic compounds as fgfr inhibitors
|
FR2911140B1
(en)
|
2007-01-05 |
2009-02-20 |
Sanofi Aventis Sa |
NOVEL 2-ANILINO 4-HETEROARYL PYRIMIDES DERIVATIVES, THEIR PREPARATION AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS, AND IN PARTICULAR AS INHIBITORS OF IKK
|
WO2008085942A2
(en)
|
2007-01-08 |
2008-07-17 |
Polyera Corporation |
Methods for preparing arene-bis(dicarboximide)-based semiconducting materials and related intermediates for preparing same
|
CN101007778A
(en)
|
2007-01-10 |
2007-08-01 |
复旦大学 |
Chain-prolonged type fluorenyl bimaleimide and its preparation method
|
CN101578285A
(en)
|
2007-01-12 |
2009-11-11 |
安斯泰来制药株式会社 |
Condensed pyridine compound
|
JP2010515760A
(en)
|
2007-01-12 |
2010-05-13 |
バイオクライスト ファーマシューティカルズ, インコーポレイテッド |
Antiviral nucleoside analogues
|
FR2911604B1
(en)
|
2007-01-19 |
2009-04-17 |
Sanofi Aventis Sa |
N- (HETEROARYL-1H-INDOLE-2-CARBOXAMIDE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE
|
JP5358962B2
(en)
|
2007-02-06 |
2013-12-04 |
住友化学株式会社 |
Composition and light-emitting device using the composition
|
JP2008198769A
(en)
|
2007-02-13 |
2008-08-28 |
Nippon Steel Chem Co Ltd |
Organic electroluminescence (el) element
|
JP5390407B2
(en)
|
2007-03-06 |
2014-01-15 |
ノバルティス アーゲー |
Bicyclic organic compounds suitable for the treatment of inflammation or allergic symptoms
|
CA2680173A1
(en)
|
2007-03-07 |
2008-09-12 |
Alantos Pharmaceuticals Holding, Inc. |
Metalloprotease inhibitors containing a heterocyclic moiety
|
KR101737753B1
(en)
|
2007-03-12 |
2017-05-18 |
와이엠 바이오사이언시즈 오스트레일리아 피티와이 엘티디 |
Phenyl amino pyrimidine compounds and uses thereof
|
CA2679980A1
(en)
|
2007-03-21 |
2007-09-27 |
Epix Pharmaceuticals, Inc. |
S1p receptor modulating compounds and use thereof
|
US20080234262A1
(en)
|
2007-03-21 |
2008-09-25 |
Wyeth |
Pyrazolopyrimidine analogs and their use as mtor kinase and pi3 kinase inhibitors
|
CA2680783C
(en)
|
2007-03-23 |
2012-04-24 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
EP2896624B1
(en)
|
2007-03-28 |
2016-07-13 |
Atir Holding S.A. |
Heterotricyclic compounds as serotonergic and/or dopaminergic agents and uses thereof
|
KR20080091948A
(en)
|
2007-04-10 |
2008-10-15 |
에스케이케미칼주식회사 |
A pharmaceutical compositions containing lactam type pyridine derivatives as an effective ingredient for the prevention and treatment of ischemia
|
WO2008128141A2
(en)
|
2007-04-12 |
2008-10-23 |
Advanced Technology Materials, Inc. |
Zirconium, hafnuim, titanium, and silicon precursors for ald/cvd
|
US8318751B2
(en)
|
2007-04-20 |
2012-11-27 |
Merck Sharp & Dohme Corp. |
Pyrimidinone derivatives and methods of use thereof
|
EP1985612A1
(en)
|
2007-04-26 |
2008-10-29 |
Bayer Schering Pharma Aktiengesellschaft |
Arymethylen substituted N-Acyl-gamma-aminoalcohols
|
EP1990342A1
(en)
|
2007-05-10 |
2008-11-12 |
AEterna Zentaris GmbH |
Pyridopyrazine Derivatives, Process of Manufacturing and Uses thereof
|
TW200902008A
(en)
|
2007-05-10 |
2009-01-16 |
Smithkline Beecham Corp |
Quinoxaline derivatives as PI3 kinase inhibitors
|
WO2008144253A1
(en)
|
2007-05-14 |
2008-11-27 |
Irm Llc |
Protein kinase inhibitors and methods for using thereof
|
GB2449293A
(en)
|
2007-05-17 |
2008-11-19 |
Evotec |
Compounds having Hsp90 inhibitory activity
|
WO2008151184A1
(en)
|
2007-06-03 |
2008-12-11 |
Vanderbilt University |
Benzamide mglur5 positive allosteric modulators and methods of making and using same
|
AU2008262406A1
(en)
|
2007-06-07 |
2008-12-18 |
Merck Sharp & Dohme Corp. |
Tricyclic anilide heterocyclic CGRP receptor antagonists
|
US7928111B2
(en)
|
2007-06-08 |
2011-04-19 |
Senomyx, Inc. |
Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
|
US8633186B2
(en)
|
2007-06-08 |
2014-01-21 |
Senomyx Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
PT2168966T
(en)
|
2007-06-15 |
2017-01-02 |
Msd Kk |
Bicycloaniline derivative
|
RS53072B
(en)
|
2007-06-18 |
2014-04-30 |
Merck Sharp & Dohme B.V. |
Antibodies to human programmed death receptor pd-1
|
EP2018859A1
(en)
|
2007-07-26 |
2009-01-28 |
Bayer Schering Pharma Aktiengesellschaft |
Arylmethylene substituted N-acyl-beta-amino alcohols
|
KR101150581B1
(en)
|
2007-07-26 |
2012-06-11 |
노파르티스 아게 |
Organic Compounds
|
EP2020404A1
(en)
|
2007-08-01 |
2009-02-04 |
Bayer Schering Pharma Aktiengesellschaft |
Cyanomethyl substituted N-Acyl Tryptamines
|
WO2009019518A1
(en)
|
2007-08-09 |
2009-02-12 |
Astrazeneca Ab |
Pyrimidine compounds having a fgfr inhibitory effect
|
JP2010535804A
(en)
|
2007-08-09 |
2010-11-25 |
グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー |
Quinoxaline derivatives as PI3 kinase inhibitors
|
US7960400B2
(en)
|
2007-08-27 |
2011-06-14 |
Duquesne University Of The Holy Ghost |
Tricyclic compounds having cytostatic and/or cytotoxic activity and methods of use thereof
|
WO2009029625A1
(en)
|
2007-08-27 |
2009-03-05 |
Kalypsys, Inc. |
4- [heterocyclyl-methyl] -8-fluoro-quinolin-2-ones useful as nitric oxide synthase inhibitors
|
PT2200436E
(en)
|
2007-09-04 |
2015-04-29 |
Scripps Research Inst |
Substituted pyrimidinyl-amines as protein kinase inhibitors
|
WO2009030871A1
(en)
|
2007-09-07 |
2009-03-12 |
Vernalis R & D Ltd |
Pyrrolopyrimidine derivatives having hsp90 inhibitory activity
|
TW200920357A
(en)
|
2007-09-10 |
2009-05-16 |
Curis Inc |
HSP90 inhibitors containing a zinc binding moiety
|
US8486904B2
(en)
|
2007-10-01 |
2013-07-16 |
Isis Pharmaceuticals, Inc. |
Antisense modulation of fibroblast growth factor receptor 4 expression
|
US8314094B2
(en)
|
2007-10-05 |
2012-11-20 |
Msd K.K |
Benzoxazinone derivative
|
WO2009047255A1
(en)
|
2007-10-09 |
2009-04-16 |
Ucb Pharma, S.A. |
Heterobicyclic compounds as histamine h4-receptor antagonists
|
WO2009049018A1
(en)
|
2007-10-10 |
2009-04-16 |
Syndax Pharmaceuticals, Inc. |
Novel compounds and methods of using them
|
US8513233B2
(en)
|
2007-10-11 |
2013-08-20 |
Shanghai Institute Of Materia Medica, Cas |
Pyrimidinyl-propionic acid derivatives and their use as PPAR agonists
|
GB0720038D0
(en)
|
2007-10-12 |
2007-11-21 |
Astex Therapeutics Ltd |
New compounds
|
GB0720041D0
(en)
|
2007-10-12 |
2007-11-21 |
Astex Therapeutics Ltd |
New Compounds
|
JP5273052B2
(en)
|
2007-10-13 |
2013-08-28 |
コニカミノルタ株式会社 |
Organic electroluminescence element, display device and lighting device
|
EP2212333A1
(en)
|
2007-10-16 |
2010-08-04 |
Wyeth LLC |
Thienopyrimidine and pyrazolopyrimidine compounds and their use as mtor kinase and pi3 kinase inhibitors
|
BRPI0817434A2
(en)
|
2007-10-17 |
2015-06-16 |
Novartis Ag |
Organic compounds
|
RU2007139634A
(en)
|
2007-10-25 |
2009-04-27 |
Сергей Олегович Бачурин (RU) |
NEW THIAZOLE-, TRIAZOLE- OR OXADIAZOLE-CONTAINING TETRACYCLIC COMPOUNDS
|
AU2008315746A1
(en)
|
2007-10-25 |
2009-04-30 |
Astrazeneca Ab |
Pyridine and pyrazine derivatives useful in the treatment of cell proliferative disorders
|
WO2009056886A1
(en)
|
2007-11-01 |
2009-05-07 |
Astrazeneca Ab |
Pyrimidine derivatives and their use as modulators of fgfr activity
|
BRPI0819453A2
(en)
|
2007-11-28 |
2014-10-07 |
Dana Farber Cancer Inst Inc |
COMPOUND, METHODS TO TREAT A KINASE ACTIVITY DISORDER, TO TREAT CANCER IN A PATIENT, TO INHIBIT KINASE ACTIVITY AND TO IDENTIFY A COMPOUND THAT MODULATES BCR-ABL KINASE ACTIVITY, PHARMACEUTICAL COMPOSITION, KARMACEUTICAL COMPOSITION
|
CA2707653A1
(en)
|
2007-12-03 |
2009-06-11 |
Boehringer Ingelheim International Gmbh |
Diaminopyridines for the treatment of diseases which are characterised by excessive or anomal cell proliferation
|
BRPI0821209A2
(en)
|
2007-12-19 |
2019-09-24 |
Amgen Inc |
compound, pharmaceutical composition, methods of treating cancer, reducing tumor size, treating disorders, and reducing metastasis in a tumor.
|
WO2009086130A1
(en)
|
2007-12-21 |
2009-07-09 |
Wyeth |
Imidazo [1,2-b] pyridazine compounds as modulators of liver x receptors
|
EP2219646A4
(en)
|
2007-12-21 |
2010-12-22 |
Univ Rochester |
Method for altering the lifespan of eukaryotic organisms
|
US8153827B2
(en)
|
2007-12-27 |
2012-04-10 |
Purdue Research Foundation |
Reagents for biomolecular labeling, detection and quantification employing Raman spectroscopy
|
FR2926297B1
(en)
|
2008-01-10 |
2013-03-08 |
Centre Nat Rech Scient |
INHIBITORY CHEMICAL MOLECULES IN THE SPLICE MECHANISM FOR TREATING DISEASES RESULTING FROM SPLICE ANOMALIES.
|
KR20100119776A
(en)
|
2008-01-24 |
2010-11-10 |
알라 캠, 엘엘씨 |
2-alkylamino-3-arylsulfonyl-cycloalcano[e or d]pyrazolo[1,5-a]pyrimidines/antagonists of serotonin 5-ht6 receptors, methods for the production and the use thereof
|
WO2009093210A2
(en)
|
2008-01-24 |
2009-07-30 |
Alla Chem, Llc |
SUBSTITUTED CYCLOALCANO[e AND d] PYRAZOLO [1,5-a]PYRIMIDINES/ANTAGONISTS OF SEROTONIN 5-HT6 RECEPTORS AND METHODS FOR PRODUCTION AND THE USE THEREOF
|
CN101925606A
(en)
|
2008-01-24 |
2010-12-22 |
Ucb医药有限公司 |
The compound that comprises cyclobutoxy group
|
CA2711576C
(en)
|
2008-01-25 |
2016-06-21 |
High Point Pharmaceuticals, Llc |
Tricyclic compounds as inhibitors of tnf-.alpha. synthesis and as pde4 inhibitors
|
EP2252616B1
(en)
|
2008-01-30 |
2014-07-23 |
Genentech, Inc. |
Pyrazolopyrimidine pi3k inhibitor compounds and methods of use
|
EP2265270A1
(en)
|
2008-02-04 |
2010-12-29 |
OSI Pharmaceuticals, Inc. |
2-aminopyridine kinase inhibitors
|
CN102007126A
(en)
|
2008-02-22 |
2011-04-06 |
Irm责任有限公司 |
Compounds and compositions as modulators of gpr119 activity
|
BRPI0907577A2
(en)
|
2008-02-22 |
2015-07-21 |
Hoffmann La Roche |
Beta Amyloid Modulators
|
US8383629B2
(en)
|
2008-02-27 |
2013-02-26 |
Vitae Pharmaceuticals, Inc. |
Inhibitors of 11β-hydroxysteroid dehydrogenase type 1
|
WO2009108827A1
(en)
|
2008-02-29 |
2009-09-03 |
Wyeth |
Fused tricyclic pyrazolo[1, 5-a]pyrimidines, methods for preparation and uses thereof
|
EP2262837A4
(en)
|
2008-03-12 |
2011-04-06 |
Merck Sharp & Dohme |
Pd-1 binding proteins
|
GB0804701D0
(en)
|
2008-03-13 |
2008-04-16 |
Amura Therapeutics Ltd |
Compounds
|
US8993580B2
(en)
|
2008-03-14 |
2015-03-31 |
Intellikine Llc |
Benzothiazole kinase inhibitors and methods of use
|
JP5547099B2
(en)
|
2008-03-14 |
2014-07-09 |
インテリカイン, エルエルシー |
Kinase inhibitors and methods of use
|
US20090246198A1
(en)
|
2008-03-31 |
2009-10-01 |
Takeda Pharmaceutical Company Limited |
Mapk/erk kinase inhibitors and methods of use thereof
|
WO2009122180A1
(en)
|
2008-04-02 |
2009-10-08 |
Medical Research Council |
Pyrimidine derivatives capable of inhibiting one or more kinases
|
US8436005B2
(en)
|
2008-04-03 |
2013-05-07 |
Abbott Laboratories |
Macrocyclic pyrimidine derivatives
|
MX2010010975A
(en)
|
2008-04-07 |
2010-11-01 |
Amgen Inc |
Gem-disubstituted and spirocyclic amino pyridines/pyrimidines as cell cycle inhibitors.
|
WO2009124755A1
(en)
|
2008-04-08 |
2009-10-15 |
European Molecular Biology Laboratory (Embl) |
Compounds with novel medical uses and method of identifying such compounds
|
WO2009125808A1
(en)
|
2008-04-11 |
2009-10-15 |
第一三共株式会社 |
Aminocyclohexyl derivative
|
WO2009125809A1
(en)
|
2008-04-11 |
2009-10-15 |
第一三共株式会社 |
Piperidine derivatives
|
US20110105457A1
(en)
|
2008-04-18 |
2011-05-05 |
Shionogi & Co., Ltd. |
Heterocyclic compound having inhibitory activity on pi3k
|
WO2009131687A2
(en)
|
2008-04-22 |
2009-10-29 |
Portola Pharmaceuticals, Inc. |
Inhibitors of protein kinases
|
US8309577B2
(en)
|
2008-04-23 |
2012-11-13 |
Bristol-Myers Squibb Company |
Quinuclidine compounds as α-7 nicotinic acetylcholine receptor ligands
|
US7863291B2
(en)
|
2008-04-23 |
2011-01-04 |
Bristol-Myers Squibb Company |
Quinuclidine compounds as alpha-7 nicotinic acetylcholine receptor ligands
|
CN102016592A
(en)
|
2008-04-29 |
2011-04-13 |
诺瓦提斯公司 |
Methods of monitoring the modulation of the kinase activity of fibroblast growth factor receptor and uses of said methods
|
JP5302389B2
(en)
|
2008-04-29 |
2013-10-02 |
エフ.ホフマン−ラ ロシュ アーゲー |
JNK's pyrimidinyl pyridone inhibitor
|
WO2009133127A1
(en)
|
2008-04-30 |
2009-11-05 |
Merck Serono S.A. |
Fused bicyclic compounds and use thereof as pi3k inhibitors
|
US9315449B2
(en)
|
2008-05-15 |
2016-04-19 |
Duke University |
Substituted pyrazoles as heat shock transcription factor activators
|
ES2554513T3
(en)
|
2008-05-23 |
2015-12-21 |
Novartis Ag |
Quinoline and quinoxaline derivatives as protein tyrosine kinase inhibitors
|
WO2009144205A1
(en)
|
2008-05-30 |
2009-12-03 |
Basf Se |
Rylene-based semiconductor materials and methods of preparation and use thereof
|
US8207169B2
(en)
|
2008-06-03 |
2012-06-26 |
Msd K.K. |
Substituted [1,2,4]triazolo[4′,3′:1,6]pyrido[2,3-b]pyrazines of the formula D
|
WO2009150150A1
(en)
|
2008-06-10 |
2009-12-17 |
Basf Se |
Novel transition metal complex and use thereof in organic light-emitting diodes - iii
|
US8507504B2
(en)
|
2008-06-12 |
2013-08-13 |
Merck Sharp & Dohme Corp. |
Process for producing bicycloaniline derivatives
|
GB0810902D0
(en)
|
2008-06-13 |
2008-07-23 |
Astex Therapeutics Ltd |
New compounds
|
MX2010014234A
(en)
|
2008-06-19 |
2011-03-25 |
Astrazeneca Ab |
Pyrazole compounds 436.
|
CN102131811A
(en)
|
2008-06-24 |
2011-07-20 |
财团法人乙卯研究所 |
Oxazolidinone derivative having fused ring
|
US8338439B2
(en)
|
2008-06-27 |
2012-12-25 |
Celgene Avilomics Research, Inc. |
2,4-disubstituted pyrimidines useful as kinase inhibitors
|
NZ602832A
(en)
|
2008-07-14 |
2014-04-30 |
Gilead Sciences Inc |
Fused heterocyclic hdac inhibitor compounds
|
EP2307413B1
(en)
|
2008-07-15 |
2015-09-09 |
F. Hoffmann-La Roche AG |
Novel phenyl-imidazopyridines and pyridazines
|
WO2010007099A1
(en)
|
2008-07-15 |
2010-01-21 |
Cellzome Limited |
2-aminoimidazo[1,2-b]pyridazine derivatives as pi3k inhibitors
|
CA2730610A1
(en)
|
2008-07-16 |
2010-01-21 |
Schering Corporation |
Bicyclic heterocycle derivatives and their use as gpcr modulators
|
UY31982A
(en)
|
2008-07-16 |
2010-02-26 |
Boehringer Ingelheim Int |
DERIVATIVES OF 1,2-DIHYDROPIRIDIN-3-CARBOXAMIDS N-SUBSTITUTED
|
EP2318404B1
(en)
|
2008-07-16 |
2013-08-21 |
Merck Sharp & Dohme Corp. |
Bicyclic heterocycle derivatives and use thereof as gpr119 modulators
|
WO2010009735A2
(en)
|
2008-07-23 |
2010-01-28 |
Dako Denmark A/S |
Combinatorial analysis and repair
|
AU2009279936A1
(en)
|
2008-08-05 |
2010-02-11 |
Banyu Pharmaceutical Co., Ltd. |
Therapeutic compounds
|
AR072906A1
(en)
|
2008-08-06 |
2010-09-29 |
Novartis Ag |
MODIFIED NUCLEOSIDS USEFUL AS ANTIVIRAL
|
CN102177152A
(en)
|
2008-08-11 |
2011-09-07 |
哈佛大学校长及研究员协会 |
Halofuginone analogs for inhibition of tRNA synthetases and uses thereof
|
UY32049A
(en)
|
2008-08-14 |
2010-03-26 |
Takeda Pharmaceutical |
CMET INHIBITORS
|
US20110166135A1
(en)
|
2008-09-10 |
2011-07-07 |
Hiroshi Morimoto |
Aromatic nitrogen-containing 6-membered ring compounds and their use
|
PL2342226T3
(en)
|
2008-09-26 |
2017-01-31 |
Dana-Farber Cancer Institute, Inc. |
Human anti-pd-1, pd-l1, and pd-l2 antibodies and uses thereof
|
TW201016676A
(en)
|
2008-10-03 |
2010-05-01 |
Astrazeneca Ab |
Heterocyclic derivatives and methods of use thereof
|
US20100267748A1
(en)
|
2008-10-15 |
2010-10-21 |
Gilead Palo Alto, Inc. |
HETEROCYCLIC COMPOUNDS USEFUL AS STEAROYL CoA DESATURASE INHIBITORS
|
US8110578B2
(en)
|
2008-10-27 |
2012-02-07 |
Signal Pharmaceuticals, Llc |
Pyrazino[2,3-b]pyrazine mTOR kinase inhibitors for oncology indications and diseases associated with the mTOR/PI3K/Akt pathway
|
US20100105655A1
(en)
|
2008-10-29 |
2010-04-29 |
Astrazeneca Ab |
Novel compounds 515
|
US8476282B2
(en)
|
2008-11-03 |
2013-07-02 |
Intellikine Llc |
Benzoxazole kinase inhibitors and methods of use
|
WO2010052448A2
(en)
|
2008-11-05 |
2010-05-14 |
Ucb Pharma S.A. |
Fused pyrazine derivatives as kinase inhibitors
|
WO2010059552A1
(en)
|
2008-11-18 |
2010-05-27 |
Glaxosmithkline Llc |
Prolyl hydroxylase inhibitors
|
WO2010059658A1
(en)
|
2008-11-20 |
2010-05-27 |
Glaxosmithkline Llc |
Chemical compounds
|
WO2010064621A1
(en)
|
2008-12-03 |
2010-06-10 |
コニカミノルタホールディングス株式会社 |
Organic electroluminescent element, organic electroluminescent element material, display device, and illuminating device
|
KR101061599B1
(en)
|
2008-12-05 |
2011-09-02 |
한국과학기술연구원 |
Novel indazole derivatives that are protein kinase inhibitors for the treatment of abnormal cell growth diseases, pharmaceutically acceptable salts thereof, and pharmaceutical compositions containing the same as active ingredients
|
CN102292338B
(en)
|
2008-12-08 |
2016-09-28 |
萌蒂制药国际有限公司 |
Compositions of protein receptor tyrosine kinase inhibitors
|
US8110265B2
(en)
|
2008-12-09 |
2012-02-07 |
The Coca-Cola Company |
Pet container and compositions having enhanced mechanical properties and gas barrier properties
|
HUE034832T2
(en)
|
2008-12-09 |
2021-12-28 |
Hoffmann La Roche |
Anti-pd-l1 antibodies and their use to enhance t-cell function
|
JP2012511502A
(en)
|
2008-12-12 |
2012-05-24 |
Msd株式会社 |
Dihydropyrimidopyrimidine derivatives
|
AU2009325400A1
(en)
|
2008-12-12 |
2010-06-17 |
Msd K.K. |
Dihydropyrimidopyrimidine derivatives
|
JP5770102B2
(en)
|
2008-12-19 |
2015-08-26 |
ジェネンテック, インコーポレイテッド |
Heterocyclic compounds and methods of use
|
JO2885B1
(en)
|
2008-12-22 |
2015-03-15 |
ايلي ليلي اند كومباني |
Protein kinase inhibitors
|
CN102325755B
(en)
|
2008-12-30 |
2015-07-01 |
艾科尔公司 |
Substituted 5,6-dihydro-6-phenylbenzo[f] isoquinolin-2-amine compounds
|
AU2009335016A1
(en)
|
2008-12-30 |
2011-08-18 |
Arqule, Inc. |
Substituted pyrazolo [3, 4-b] pyridine compounds
|
EP2379559B1
(en)
|
2009-01-06 |
2017-10-25 |
Dana-Farber Cancer Institute, Inc. |
Pyrimido-diazepinone kinase scaffold compounds and methods of treating disorders
|
JOP20190230A1
(en)
|
2009-01-15 |
2017-06-16 |
Incyte Corp |
Processes for preparing jak inhibitors and related intermediate compounds
|
EP2387315B1
(en)
|
2009-01-16 |
2015-07-15 |
Merck Sharp & Dohme Corp. |
IMIDAZO[1,2-a]PYRIDINES AND IMIDAZO[1,2-b]PYRIDAZINES AS MARK INHIBITORS
|
DE102009007038A1
(en)
|
2009-02-02 |
2010-08-05 |
Merck Patent Gmbh |
metal complexes
|
JP2010180147A
(en)
|
2009-02-04 |
2010-08-19 |
Mitsubishi Gas Chemical Co Inc |
Cyanic acid ester compound and cured product thereof
|
US8741295B2
(en)
|
2009-02-09 |
2014-06-03 |
Universite De La Mediterranee |
PD-1 antibodies and PD-L1 antibodies and uses thereof
|
TW201038569A
(en)
|
2009-02-16 |
2010-11-01 |
Abbott Gmbh & Co Kg |
Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy
|
TW201035102A
(en)
|
2009-03-04 |
2010-10-01 |
Gruenethal Gmbh |
Sulfonylated tetrahydroazolopyrazines and their use as medicinal products
|
US20100278835A1
(en)
|
2009-03-10 |
2010-11-04 |
Astrazeneca Uk Limited |
Novel compounds 660
|
JP5615261B2
(en)
|
2009-03-11 |
2014-10-29 |
学校法人関西学院 |
Polycyclic aromatic compounds
|
CA2755253A1
(en)
|
2009-03-18 |
2010-09-23 |
Schering Corporation |
Bicyclic compounds as inhibitors of diacylglycerol acyltransferase
|
CA2756137C
(en)
|
2009-03-23 |
2015-11-24 |
Siemens Medical Solutions Usa, Inc. |
Imaging agents for detecting neurological disorders
|
WO2010111573A1
(en)
|
2009-03-27 |
2010-09-30 |
Abbott Laboratories |
Compounds as cannabinoid receptor ligands
|
WO2010117425A1
(en)
|
2009-03-31 |
2010-10-14 |
Biogen Idec Ma Inc. |
Certain substituted pyrimidines, pharmaceutical compositions thereof, and methods for their use
|
EP2417127B1
(en)
|
2009-04-06 |
2014-02-26 |
University Health Network |
Kinase inhibitors and method of treating cancer with same
|
JP5711723B2
(en)
|
2009-04-07 |
2015-05-07 |
エメリティ・ファーマ・アクチボラグ |
Isoxazol-3 (2H) -one analogs as therapeutic agents
|
GB0906470D0
(en)
|
2009-04-15 |
2009-05-20 |
Astex Therapeutics Ltd |
New compounds
|
GB0906472D0
(en)
|
2009-04-15 |
2009-05-20 |
Astex Therapeutics Ltd |
New compounds
|
JP5531446B2
(en)
|
2009-04-20 |
2014-06-25 |
コニカミノルタ株式会社 |
ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT MATERIAL, DISPLAY DEVICE AND LIGHTING DEVICE
|
ES2347630B1
(en)
|
2009-04-29 |
2011-09-08 |
Universitat Ramon Llull |
SYNTHESIS AND USES OF 4-CIANOPENTANOATOS AND 4-CIANOPENTENOATS SUBSTITUTED.
|
US8765754B2
(en)
|
2009-04-29 |
2014-07-01 |
Locus Pharmaceuticals, Inc. |
Pyrrolotriazine compounds
|
WO2010127212A1
(en)
|
2009-04-30 |
2010-11-04 |
Forest Laboratories Holdings Limited |
Inhibitors of acetyl-coa carboxylase
|
JO2860B1
(en)
|
2009-05-07 |
2015-03-15 |
ايلي ليلي اند كومباني |
Vinyl indazolyl compounds
|
JP5600891B2
(en)
|
2009-05-15 |
2014-10-08 |
コニカミノルタ株式会社 |
Organic electroluminescence element, display device and lighting device
|
JP5604808B2
(en)
|
2009-05-20 |
2014-10-15 |
コニカミノルタ株式会社 |
Organic electroluminescence element, display device and lighting device
|
JP5568889B2
(en)
|
2009-05-22 |
2014-08-13 |
コニカミノルタ株式会社 |
ORGANIC ELECTROLUMINESCENT ELEMENT, DISPLAY DEVICE, LIGHTING DEVICE, AND ORGANIC ELECTROLUMINESCENT ELEMENT MATERIAL
|
JP5629980B2
(en)
|
2009-05-22 |
2014-11-26 |
コニカミノルタ株式会社 |
Organic electroluminescence element, display device and lighting device
|
JP2012528083A
(en)
|
2009-05-27 |
2012-11-12 |
コーベンハブンス ウニベルシテト |
Fibroblast growth factor receptor-derived peptide that binds to NCAM
|
JP5499519B2
(en)
|
2009-05-27 |
2014-05-21 |
コニカミノルタ株式会社 |
Organic electroluminescence element, display device and lighting device
|
GB0910003D0
(en)
|
2009-06-11 |
2009-07-22 |
Univ Leuven Kath |
Novel compounds for the treatment of neurodegenerative diseases
|
JP5600894B2
(en)
|
2009-06-24 |
2014-10-08 |
コニカミノルタ株式会社 |
White organic electroluminescence element, display device and lighting device
|
RS56352B2
(en)
|
2009-06-25 |
2023-02-28 |
Alkermes Pharma Ireland Ltd |
Heterocyclic compounds for the treatment of neurological and psychological disorders
|
US8883888B2
(en)
|
2009-06-30 |
2014-11-11 |
Zeon Corporation |
Diarylamine compounds, aging inhibitor, polymer composition, crosslinked rubber product and molded article of the crosslinked product, and method of producing diarylamine compound
|
US20120135997A1
(en)
|
2009-07-17 |
2012-05-31 |
Shionogi & Co., Ltd. |
Pharmaceutical composition comprising a lactam or benzenesulfonamide compound
|
US8680077B2
(en)
|
2009-07-24 |
2014-03-25 |
Duke University |
Prochelators useful for inhibiting metal-associated toxicity
|
FR2948568B1
(en)
|
2009-07-30 |
2012-08-24 |
Sanofi Aventis |
PHARMACEUTICAL FORMULATION
|
TWI468402B
(en)
|
2009-07-31 |
2015-01-11 |
必治妥美雅史谷比公司 |
Compounds for the reduction of β-amyloid production
|
CN102596946B
(en)
|
2009-08-05 |
2015-06-17 |
港大科桥有限公司 |
Antiviral compounds and methods of making and using thereof
|
JP2012197231A
(en)
|
2009-08-06 |
2012-10-18 |
Oncotherapy Science Ltd |
Pyridine and pyrimidine derivative having ttk-inhibiting action
|
BR112012008094A2
(en)
|
2009-08-07 |
2020-08-18 |
Chugai Seiyaku Kabushiki Kaisha |
aminopyrazole derivative, its use, pharmaceutical composition comprising it, agents to inhibit fgfr activity and to prevent or treat cancer
|
WO2011018894A1
(en)
|
2009-08-10 |
2011-02-17 |
Raqualia Pharma Inc. |
Pyrrolopyrimidine derivatives as potassium channel modulators
|
MY162604A
(en)
|
2009-08-17 |
2017-06-30 |
Intellikine Llc |
Heterocyclic compounds and uses thereof
|
JP5577650B2
(en)
|
2009-08-24 |
2014-08-27 |
コニカミノルタ株式会社 |
ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT MATERIAL, DISPLAY DEVICE AND LIGHTING DEVICE
|
KR101184115B1
(en)
|
2009-08-31 |
2012-09-18 |
일동제약주식회사 |
New peptide deformylase inhibitor compounds and the manufacturing process thereof
|
NZ598294A
(en)
|
2009-09-03 |
2013-07-26 |
Bioenergenix |
Heterocyclic compounds for the inhibition of pask
|
CN102596932A
(en)
|
2009-09-04 |
2012-07-18 |
拜耳医药股份有限公司 |
Substituted aminoquinoxalines as tyrosine threonine kinase inhibitors
|
WO2011031740A1
(en)
|
2009-09-09 |
2011-03-17 |
Achaogen, Inc. |
Antibacterial fluoroquinolone analogs
|
US9481675B2
(en)
|
2009-09-11 |
2016-11-01 |
Merck Sharp & Dohme Corp. |
Gyrase inhibitors
|
WO2011041143A1
(en)
|
2009-10-01 |
2011-04-07 |
Merck Sharp & Dohme Corp. |
HETEROCYCLIC-FUSED PYRAZOLO[4,3-c]PYRIDIN-3-ONE M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS
|
US8466155B2
(en)
|
2009-10-02 |
2013-06-18 |
Boehringer Ingelheim International Gmbh |
Pyrimidines
|
GB0917571D0
(en)
|
2009-10-07 |
2009-11-25 |
Karobio Ab |
Novel estrogen receptor ligands
|
EP2308866A1
(en)
|
2009-10-09 |
2011-04-13 |
Bayer CropScience AG |
Phenylpyri(mi)dinylpyrazoles and their use as fungicides
|
FR2951172B1
(en)
|
2009-10-13 |
2014-09-26 |
Pf Medicament |
PYRAZOLOPYRIDINE DERIVATIVES AS ANTI-CANCER AGENT
|
US20120232062A1
(en)
|
2009-10-20 |
2012-09-13 |
Eiger Biopharmaceuticals, Inc. |
Azaindazoles to treat flaviviridae virus infection
|
KR20110043270A
(en)
|
2009-10-21 |
2011-04-27 |
(주)씨에스엘쏠라 |
Organic light emitting compound and organic light emitting device comprising the same
|
US8507507B2
(en)
|
2009-10-22 |
2013-08-13 |
Gilead Sciences, Inc. |
Modulators of toll-like receptors
|
WO2011050245A1
(en)
|
2009-10-23 |
2011-04-28 |
Yangbo Feng |
Bicyclic heteroaryls as kinase inhibitors
|
WO2011053518A1
(en)
|
2009-10-26 |
2011-05-05 |
Signal Pharmaceuticals, Llc |
Methods of synthesis and purification of heteroaryl compounds
|
ES2524548T3
(en)
|
2009-10-30 |
2014-12-10 |
Novartis Ag |
3- (2,6-Dichloro-3,5-dimethoxy-phenyl) -1- {6- [4- (4-ethyl-piperazin-1-yl) -phenylamino] -pyrimidin-4-yl N-oxide } -1-methyl-urea
|
KR20110049217A
(en)
|
2009-11-04 |
2011-05-12 |
다우어드밴스드디스플레이머티리얼 유한회사 |
Novel organic electroluminescent compounds and organic electroluminescent device using the same
|
GB0919432D0
(en)
|
2009-11-05 |
2009-12-23 |
Glaxosmithkline Llc |
Use
|
CA2780190C
(en)
|
2009-11-06 |
2020-05-05 |
Plexxikon, Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
EP2498607B1
(en)
|
2009-11-13 |
2016-02-17 |
Genosco |
Kinase inhibitors
|
CN105906631A
(en)
|
2009-11-18 |
2016-08-31 |
普莱希科公司 |
Compounds and methods for kinase modulation, and indications therefor
|
JP2013032290A
(en)
|
2009-11-20 |
2013-02-14 |
Dainippon Sumitomo Pharma Co Ltd |
Novel fused pyrimidine derivative
|
US20120232073A1
(en)
|
2009-11-23 |
2012-09-13 |
Santhosh Francis Neelamkavil |
Fused bicyclic pyrimidine derivatives and methods of use thereof
|
US20130017199A1
(en)
|
2009-11-24 |
2013-01-17 |
AMPLIMMUNE ,Inc. a corporation |
Simultaneous inhibition of pd-l1/pd-l2
|
EP2332939A1
(en)
|
2009-11-26 |
2011-06-15 |
Æterna Zentaris GmbH |
Novel Naphthyridine derivatives and the use thereof as kinase inhibitors
|
KR20120102724A
(en)
|
2009-12-01 |
2012-09-18 |
아보트 러보러터리즈 |
Novel tricyclic compounds
|
JP2011116840A
(en)
|
2009-12-02 |
2011-06-16 |
Fujifilm Corp |
Pigment fine particle dispersion, photocurable composition using the same, and color filter
|
AR079257A1
(en)
|
2009-12-07 |
2012-01-04 |
Novartis Ag |
CRYSTAL FORMS OF 3- (2,6-DICLORO-3-5-DIMETOXI-PHENYL) -1- {6- [4- (4-ETIL-PIPERAZIN-1-IL) -PENYL-AMINO] -PIRIMIDIN-4- IL} -1-METHYL-UREA AND SALTS OF THE SAME
|
WO2011075517A1
(en)
|
2009-12-17 |
2011-06-23 |
Merck Sharp & Dohme Corp. |
Aminopyrimidines as syk inhibitors
|
US20120258940A1
(en)
|
2009-12-18 |
2012-10-11 |
Giordano Caponigro |
Method for treating haematological cancers
|
JP5721187B2
(en)
|
2009-12-22 |
2015-05-20 |
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Vertex Pharmaceuticals Incorporated |
Isoindolinone inhibitor of phosphatidylinositol 3-kinase
|
FR2954315B1
(en)
|
2009-12-23 |
2012-02-24 |
Galderma Res & Dev |
NOVEL PHENOLIC DERIVATIVES, AND THEIR PHARMACEUTICAL OR COSMETIC USE
|
US20110207736A1
(en)
|
2009-12-23 |
2011-08-25 |
Gatekeeper Pharmaceuticals, Inc. |
Compounds that modulate egfr activity and methods for treating or preventing conditions therewith
|
FR2954317B1
(en)
|
2009-12-23 |
2012-01-27 |
Galderma Res & Dev |
NOVEL PHENOLIC DERIVATIVES, AND THEIR PHARMACEUTICAL OR COSMETIC USE
|
WO2011090666A2
(en)
|
2009-12-28 |
2011-07-28 |
Afraxis, Inc. |
Methods for treating autism
|
WO2011080755A1
(en)
|
2009-12-29 |
2011-07-07 |
Advinus Therapeutics Private Limited |
Fused nitrogen heterocyclic compounds, process of preparation and uses thereof
|
AU2010343102B2
(en)
|
2009-12-29 |
2016-03-24 |
Dana-Farber Cancer Institute, Inc. |
Type II Raf kinase inhibitors
|
US8440828B2
(en)
|
2009-12-29 |
2013-05-14 |
Polyera Corporation |
Organic semiconductors and devices incorporating same
|
US8580803B2
(en)
|
2009-12-30 |
2013-11-12 |
Arqule, Inc. |
Substituted pyrrolo-aminopyrimidine compounds
|
US8329705B2
(en)
|
2009-12-30 |
2012-12-11 |
Arqule, Inc. |
Substituted triazolo-pyrazine compounds
|
US8563567B2
(en)
|
2009-12-30 |
2013-10-22 |
Arqule, Inc. |
Substituted heterocyclic compounds
|
CN102115026A
(en)
|
2009-12-31 |
2011-07-06 |
清华大学 |
One-dimensional nano-structure, preparation method thereof and method for marking by using one-dimensional nano-structure
|
US20130022629A1
(en)
|
2010-01-04 |
2013-01-24 |
Sharpe Arlene H |
Modulators of Immunoinhibitory Receptor PD-1, and Methods of Use Thereof
|
AR079975A1
(en)
|
2010-01-06 |
2012-03-07 |
British Columbia Cancer Agency |
THERAPEUTIC AGENTS DERIVED FROM BISPHENOL OR METHODS FOR USE, PHARMACEUTICAL COMPOSITIONS AND USE OF THE SAME
|
KR101483215B1
(en)
|
2010-01-29 |
2015-01-16 |
한미약품 주식회사 |
Bicyclic heteroaryl derivatives having inhibitory activity for protein kinases
|
WO2011094890A1
(en)
|
2010-02-02 |
2011-08-11 |
Argusina Inc. |
Phenylalanine derivatives and their use as non-peptide glp-1 receptor modulators
|
CA2789344A1
(en)
|
2010-02-15 |
2011-08-18 |
Jeremy Earle Wulff |
Synthesis of bicyclic compounds and method for their use as therapeutic agents
|
SA111320200B1
(en)
|
2010-02-17 |
2014-02-16 |
ديبيوفارم اس ايه |
Bicyclic Compounds and their Uses as Dual C-SRC / JAK Inhibitors
|
JP2013519732A
(en)
|
2010-02-17 |
2013-05-30 |
アムジエン・インコーポレーテツド |
Arylcarboxamide derivatives as sodium channel inhibitors for the treatment of pain
|
CN102782101B
(en)
|
2010-02-18 |
2015-10-07 |
Ntn株式会社 |
Thickening material, lubricating grease and their manufacture method and grease filled bearing
|
US9193728B2
(en)
|
2010-02-18 |
2015-11-24 |
Medivation Technologies, Inc. |
Fused tetracyclic pyrido [4,3-B] indole and pyrido [3,4-B] indole derivatives and methods of use
|
WO2011103441A1
(en)
|
2010-02-18 |
2011-08-25 |
Schering Corporation |
Substituted pyridine and pyrimidine derivatives and their use in treating viral infections
|
UY33227A
(en)
|
2010-02-19 |
2011-09-30 |
Novartis Ag |
PIRROLOPIRIMIDINE COMPOUNDS AS INHIBITORS OF THE CDK4 / 6
|
WO2011103557A1
(en)
|
2010-02-22 |
2011-08-25 |
Advanced Cancer Therapeutics, Llc |
Small molecule inhibitors of pfkfb3 and glycolytic flux and their methods of use as anti-cancer therapeutics
|
JP5662994B2
(en)
|
2010-02-26 |
2015-02-04 |
新日鉄住金化学株式会社 |
Organic electroluminescence device
|
WO2011109237A2
(en)
|
2010-03-02 |
2011-09-09 |
Emory University |
Uses of noscapine and derivatives in subjects diagnosed with fap
|
WO2011111880A1
(en)
|
2010-03-08 |
2011-09-15 |
주식회사 메디젠텍 |
Pharmaceutical composition for treating or preventing diseases caused by the nuclear export of gsk3, including a compound for inhibiting the nuclear export of gsk3
|
US20110237599A1
(en)
|
2010-03-10 |
2011-09-29 |
Kalypsys, Inc. |
Heterocyclic inhibitors of histamine receptors for the treatment of disease
|
PT2545052E
(en)
|
2010-03-11 |
2015-02-18 |
Gilead Connecticut Inc |
Imidazopyridines syk inhibitors
|
US8987275B2
(en)
|
2010-03-16 |
2015-03-24 |
Dana-Farber Cancer Institute, Inc. |
Indazole compounds and their uses
|
KR20180032686A
(en)
|
2010-03-24 |
2018-03-30 |
아미텍 테러퓨틱 솔루션즈 인크 |
Heterocyclic compounds useful for kinase inhibition
|
US8791257B2
(en)
|
2010-03-31 |
2014-07-29 |
Bristol-Myers Squibb Company |
Substituted pyrrolotriazines as protein kinase inhibitors
|
CN102153551B
(en)
|
2010-04-02 |
2012-04-25 |
济南海乐医药技术开发有限公司 |
Indazole/azaindazole-based diarylcarbamide/thiocarbamide-structure antineoplastic drug
|
JP5724204B2
(en)
|
2010-04-07 |
2015-05-27 |
コニカミノルタ株式会社 |
Organic electroluminescence element, display device, and lighting device
|
JP6067550B2
(en)
|
2010-04-13 |
2017-01-25 |
ライジェル ファーマシューティカルズ, インコーポレイテッド |
2,4-pyrimidinediamine compounds and prodrugs thereof and uses thereof
|
PL2558095T3
(en)
|
2010-04-16 |
2019-06-28 |
Novartis Ag |
Organic compound for use in the treatment of liver cancer
|
US8822447B2
(en)
|
2010-04-22 |
2014-09-02 |
Janssen Pharmaceutica Nv |
Indazole compounds useful as ketohexokinase inhibitors
|
MX2012012353A
(en)
|
2010-04-23 |
2013-02-07 |
Kineta Inc |
Anti-viral compounds.
|
AR081331A1
(en)
|
2010-04-23 |
2012-08-08 |
Cytokinetics Inc |
AMINO- PYRIMIDINES COMPOSITIONS OF THE SAME AND METHODS FOR THE USE OF THE SAME
|
WO2011137313A1
(en)
|
2010-04-30 |
2011-11-03 |
Bristol-Myers Squibb Company |
Aza-bicyclic amine n-oxide compounds as alpha-7 nicotinic acetylcholine receptor ligand pro-drugs
|
GB201007286D0
(en)
|
2010-04-30 |
2010-06-16 |
Astex Therapeutics Ltd |
New compounds
|
US8759398B2
(en)
|
2010-05-03 |
2014-06-24 |
Biolink Life Sciences, Inc. |
Phosphorus binder composition for treatment of hyperphosphatemia
|
US20130137709A1
(en)
|
2010-05-05 |
2013-05-30 |
Nathanael S. Gray |
Compounds that modulate EGFR activity and methods for treating or preventing conditions therewith
|
US8481688B2
(en)
|
2010-05-11 |
2013-07-09 |
Aveo Pharmaceuticals, Inc. |
Anti-FGFR2 antibodies
|
TWI513694B
(en)
|
2010-05-11 |
2015-12-21 |
Amgen Inc |
Pyrimidine compounds that inhibit anaplastic lymphoma kinase
|
WO2011141848A1
(en)
|
2010-05-11 |
2011-11-17 |
Pfizer Inc. |
Morpholine compounds as mineralocorticoid receptor antagonists
|
WO2011143430A1
(en)
|
2010-05-12 |
2011-11-17 |
Abbott Laboratories |
Indazole inhibitors of kinase
|
TWI446916B
(en)
|
2010-05-12 |
2014-08-01 |
Spectrum Pharmaceuticals Inc |
Lanthanum carbonate hydroxide, lanthanum oxycarbonate and methods of their manufacture and use
|
GB201008134D0
(en)
|
2010-05-14 |
2010-06-30 |
Medical Res Council Technology |
Compounds
|
WO2011147198A1
(en)
|
2010-05-28 |
2011-12-01 |
Versitech Limited |
Compounds and methods for treatment of proliferative diseases
|
WO2011147199A1
(en)
|
2010-05-28 |
2011-12-01 |
Versitech Limited |
Compounds and methods for treating viral infections
|
EP3075730B1
(en)
|
2010-06-04 |
2018-10-24 |
Genentech, Inc. |
Aminopyrimidine derivatives as lrrk2 modulators
|
WO2011153553A2
(en)
|
2010-06-04 |
2011-12-08 |
The Regents Of The University Of California |
Methods and compositions for kinase inhibition
|
WO2011155983A1
(en)
|
2010-06-07 |
2011-12-15 |
Bikam Pharmaceuticals Inc. |
Opsin-binding ligands, compositions and methods of use
|
TW201210597A
(en)
|
2010-06-09 |
2012-03-16 |
Gilead Sciences Inc |
Inhibitors of hepatitis C virus
|
US8299117B2
(en)
|
2010-06-16 |
2012-10-30 |
Metabolex Inc. |
GPR120 receptor agonists and uses thereof
|
US9163087B2
(en)
|
2010-06-18 |
2015-10-20 |
The Brigham And Women's Hospital, Inc. |
Bi-specific antibodies against TIM-3 and PD-1 for immunotherapy in chronic immune conditions
|
EP2584903B1
(en)
|
2010-06-24 |
2018-10-24 |
Merck Sharp & Dohme Corp. |
Novel heterocyclic compounds as erk inhibitors
|
US8907053B2
(en)
|
2010-06-25 |
2014-12-09 |
Aurigene Discovery Technologies Limited |
Immunosuppression modulating compounds
|
US8683564B2
(en)
|
2010-06-27 |
2014-03-25 |
King Saud University |
One-time password authentication with infinite nested hash claims
|
US8933070B2
(en)
|
2010-07-02 |
2015-01-13 |
University Health Network |
Methods of targeting PTEN mutant diseases and compositions therefor
|
CN103080106A
(en)
|
2010-07-06 |
2013-05-01 |
诺瓦提斯公司 |
Cyclic ether compounds useful as kinase inhibitors
|
FR2962437B1
(en)
|
2010-07-06 |
2012-08-17 |
Sanofi Aventis |
IMIDAZOPYRIDINE DERIVATIVES, PROCESS FOR PREPARING THEM AND THEIR THERAPEUTIC APPLICATION
|
FR2962438B1
(en)
|
2010-07-06 |
2012-08-17 |
Sanofi Aventis |
INDOLIZINE DERIVATIVES, PREPARATION METHODS AND THERAPEUTIC APPLICATION
|
EP2590982B1
(en)
|
2010-07-09 |
2017-08-23 |
The Walter and Eliza Hall Institute of Medical Research |
Protein kinase inhibitors and methods of treatment
|
WO2012009258A2
(en)
|
2010-07-13 |
2012-01-19 |
Edward Roberts |
Peptidomimetic galanin receptor modulators
|
WO2012008999A2
(en)
|
2010-07-14 |
2012-01-19 |
Merck Sharp & Dohme Corp. |
Tricyclic compounds as allosteric modulators of metabotropic glutamate receptors
|
TW201206946A
(en)
|
2010-07-15 |
2012-02-16 |
Bristol Myers Squibb Co |
Compounds for the reduction of beta-amyloid production
|
WO2012008563A1
(en)
|
2010-07-16 |
2012-01-19 |
協和発酵キリン株式会社 |
Nitrogenated aromatic heterocyclic ring derivative
|
WO2012008564A1
(en)
|
2010-07-16 |
2012-01-19 |
協和発酵キリン株式会社 |
Nitrogenated aromatic heterocyclic ring derivative
|
JP5926727B2
(en)
|
2010-07-28 |
2016-05-25 |
バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH |
Substituted imidazo [1,2-b] pyridazine
|
EP2413140A1
(en)
|
2010-07-29 |
2012-02-01 |
Sanofi |
Method for identifying a compound having an antiarrhythmic effect as well as uses relating thereto
|
TW201300501A
(en)
|
2010-07-30 |
2013-01-01 |
羅門哈斯電子材料韓國公司 |
Electroluminescent device using electroluminescent compound as luminescent material
|
WO2012019093A1
(en)
|
2010-08-05 |
2012-02-09 |
Human Biomolecular Research Institute |
Synthetic compounds and methods to decrease nicotine self-administration
|
US9051280B2
(en)
|
2010-08-13 |
2015-06-09 |
AbbVie Deutschland GmbH & Co. KG |
Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy
|
US8883839B2
(en)
|
2010-08-13 |
2014-11-11 |
Abbott Laboratories |
Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy
|
WO2012027239A1
(en)
|
2010-08-23 |
2012-03-01 |
Schering Corporation |
NOVEL PYRAZOLO[1,5-a]PYRROLO[3,2-e]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
EP2608669B1
(en)
|
2010-08-23 |
2016-06-22 |
Merck Sharp & Dohme Corp. |
NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
US9249123B2
(en)
|
2010-09-01 |
2016-02-02 |
Genentech, Inc. |
Pyridinones/pyrazinones, method of making, and method of use thereof
|
CA2809662C
(en)
|
2010-09-01 |
2019-04-16 |
Gilead Connecticut, Inc. |
Pyridazinones, method of making, and method of use thereof
|
AR082799A1
(en)
|
2010-09-08 |
2013-01-09 |
Ucb Pharma Sa |
DERIVATIVES OF QUINOLINE AND QUINOXALINE AS QUINASE INHIBITORS
|
JP5965402B2
(en)
|
2010-09-08 |
2016-08-03 |
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 |
N- [5- [4- (5-{[(2R, 6S) -2,6-dimethyl-4-morpholinyl] methyl} -1,3-oxazol-2-yl) -1H-indazol-6-yl ] -2- (Methyloxy) -3-pyridinyl] methanesulfonamide polymorphs and salts
|
EP2613781B1
(en)
|
2010-09-08 |
2016-08-24 |
GlaxoSmithKline Intellectual Property Development Limited |
Indazole derivatives for use in the treatment of influenza virus infection
|
TWI541243B
(en)
|
2010-09-10 |
2016-07-11 |
拜耳知識產權公司 |
Substituted imidazopyridazines
|
WO2012035996A1
(en)
|
2010-09-14 |
2012-03-22 |
保土谷化学工業株式会社 |
Charge control agent and toner using same
|
CN102399220A
(en)
|
2010-09-15 |
2012-04-04 |
黄振华 |
Tricyclic dual PI3K and mTOR inhibitors
|
CN102399233B
(en)
|
2010-09-15 |
2014-08-13 |
山东轩竹医药科技有限公司 |
Dual PI3K and mTOR inhibitor compounds
|
WO2012036233A1
(en)
|
2010-09-17 |
2012-03-22 |
塩野義製薬株式会社 |
Condensed heterocyclic derivative having melanine-concentrating hormone receptor antagonistic activity
|
GB201015949D0
(en)
|
2010-09-22 |
2010-11-03 |
Medical Res Council Technology |
Compounds
|
JO3062B1
(en)
|
2010-10-05 |
2017-03-15 |
Lilly Co Eli |
Crystalline (r)-(e)-2-(4-(2-(5-(1-(3,5-dichloropyridin-4-yl)ethoxy)-1h-indazol-3-yl)vinyl)-1h-pyrazol-1-yl)ethanol
|
EP2629777B1
(en)
|
2010-10-22 |
2018-12-19 |
Merck Sharp & Dohme Corp. |
Bicyclic diamines as janus kinase inhibitors
|
CA2961937C
(en)
|
2010-10-25 |
2018-09-25 |
G1 Therapeutics, Inc. |
Cdk inhibitors
|
JP2012092049A
(en)
|
2010-10-27 |
2012-05-17 |
Sumitomo Chemical Co Ltd |
Pest control composition and method for controlling pest
|
CA2816022C
(en)
|
2010-10-29 |
2019-09-10 |
Emory University |
Quinazoline derivatives, compositions, and uses related thereto
|
WO2012061337A1
(en)
|
2010-11-02 |
2012-05-10 |
Exelixis, Inc. |
Fgfr2 modulators
|
BR112013010768A2
(en)
|
2010-11-10 |
2016-07-12 |
Gruenenthal Gmbh |
heteroaromatic substituted urea and carboxamide derivatives as vanilloid receptor ligands
|
EP2638008B1
(en)
|
2010-11-10 |
2015-07-01 |
Actelion Pharmaceuticals Ltd |
Lactam derivatives useful as orexin receptor antagonists
|
JP2012116825A
(en)
|
2010-11-11 |
2012-06-21 |
Ehime Univ |
Method for producing acene diimide compound
|
KR101171232B1
(en)
|
2010-11-15 |
2012-08-06 |
단국대학교 산학협력단 |
Spiro Compound and Organic Light Emitting Device Including the Same
|
WO2012065297A1
(en)
|
2010-11-16 |
2012-05-24 |
Impact Therapeutics, Inc. |
3-ARYL-6-ARYL-[1,2,4]TRIAZOLO[4,3-a]PYRIDINES AS INHIBITORS OF CELL PROLIFERATION AND THE USE THEREOF
|
EP2640715A1
(en)
|
2010-11-17 |
2013-09-25 |
Amgen Inc. |
Quinoline derivatives as pik3 inhibitors
|
EP2640392B1
(en)
|
2010-11-18 |
2015-01-07 |
Kasina Laila Innova Pharmaceuticals Private Ltd. |
Substituted 4-(selenophen-2(or 3)-ylamino)pyrimidine compounds and methods of use thereof
|
GB201020179D0
(en)
|
2010-11-29 |
2011-01-12 |
Astex Therapeutics Ltd |
New compounds
|
WO2012078777A1
(en)
|
2010-12-09 |
2012-06-14 |
Amgen Inc. |
Bicyclic compounds as pim inhibitors
|
ES2553610T3
(en)
|
2010-12-14 |
2015-12-10 |
Electrophoretics Limited |
Casein kinase 1 delta inhibitors (CK1delta)
|
PT2655357T
(en)
|
2010-12-20 |
2016-09-28 |
Merck Serono Sa |
Indazolyl triazole derivatives as irak inhibitors
|
WO2012083866A1
(en)
|
2010-12-22 |
2012-06-28 |
The Hong Kong Polytechnic University |
Quinoline derivatives as anti-cancer agents
|
NZ710133A
(en)
|
2010-12-22 |
2016-08-26 |
Leo Lab Ltd |
Ingenol-3-acylates iii and ingenol-3-carbamates
|
AU2011348638B2
(en)
|
2010-12-22 |
2015-05-21 |
Leo Laboratories Limited |
3-acyl-ingenols II
|
EP2468258A1
(en)
|
2010-12-22 |
2012-06-27 |
LEK Pharmaceuticals d.d. |
Process for the preparation of a pharmaceutical composition comprising a low soluble pharmaceutically active ingredient
|
US8754114B2
(en)
|
2010-12-22 |
2014-06-17 |
Incyte Corporation |
Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
|
MX2013007261A
(en)
|
2010-12-23 |
2013-11-04 |
Amgen Inc |
Heterocyclic compounds and their uses.
|
JP5691508B2
(en)
|
2010-12-27 |
2015-04-01 |
Jnc株式会社 |
Diimide compound and inkjet ink and use thereof
|
KR101466150B1
(en)
|
2010-12-31 |
2014-11-27 |
제일모직 주식회사 |
Compound for organic photoelectric device and organic photoelectric device including the same
|
WO2012093731A1
(en)
|
2011-01-06 |
2012-07-12 |
Jx日鉱日石エネルギー株式会社 |
Imide compound, method for producing same, thickening agent for grease, and grease composition
|
US8362023B2
(en)
|
2011-01-19 |
2013-01-29 |
Hoffmann-La Roche Inc. |
Pyrazolo pyrimidines
|
FR2970967B1
(en)
|
2011-01-27 |
2013-02-15 |
Pf Medicament |
AZAINDAZOLE OR DIAZAINDAZOLE DERIVATIVES AS A MEDICINAL PRODUCT
|
EP2487159A1
(en)
|
2011-02-11 |
2012-08-15 |
MSD Oss B.V. |
RorgammaT inhibitors
|
WO2012112965A1
(en)
|
2011-02-18 |
2012-08-23 |
Medivation Technologies, Inc. |
Compounds and methods of treating diabetes
|
US9127000B2
(en)
|
2011-02-23 |
2015-09-08 |
Intellikine, LLC. |
Heterocyclic compounds and uses thereof
|
TWI532742B
(en)
|
2011-02-28 |
2016-05-11 |
艾伯維有限公司 |
Tricyclic inhibitors of kinases
|
CA2829988A1
(en)
|
2011-03-17 |
2012-09-20 |
Novartis Ag |
Fgfr and ligands thereof as biomarkers for breast cancer in hr positive subjects
|
CA2830516C
(en)
|
2011-03-23 |
2017-01-24 |
Amgen Inc. |
Fused tricyclic dual inhibitors of cdk 4/6 and flt3
|
ITPD20110091A1
(en)
|
2011-03-24 |
2012-09-25 |
Univ Padova |
USEFUL INHIBITORS FOR RELATED PATHOLOGIES: PHARMACOFORIC MODELS, IDENTIFIED COMPOUNDS BY THESE MODELS, METHODS FOR THEIR PREPARATION, THEIR FORMULATION AND THEIR THERAPEUTIC USE.
|
MX351165B
(en)
|
2011-03-25 |
2017-10-04 |
Abbvie Inc |
Trpv1 antagonists.
|
BR112013024717A2
(en)
|
2011-04-07 |
2017-08-08 |
Genentech Inc |
isolated antibody, isolated nucleic acid, host cell, immunoconjugate, pharmaceutical formulation, method of treating an individual who has cancer and method of inhibiting cell proliferation in an individual
|
FR2974088A1
(en)
|
2011-04-12 |
2012-10-19 |
Pf Medicament |
TRI- AND TETRACYCLIC PYRAZOLO [3,4-B] PYRIDINE COMPOUNDS AS ANTI-CANCER AGENTS
|
MY175338A
(en)
|
2011-05-16 |
2020-06-19 |
Genentech Inc |
Fgfr1 agonists and methods of use
|
WO2012158795A1
(en)
|
2011-05-17 |
2012-11-22 |
Principia Biopharma Inc. |
Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors
|
EP2710004A1
(en)
|
2011-05-17 |
2014-03-26 |
Bayer Intellectual Property GmbH |
Amino-substituted imidazopyridazines as mknk1 kinase inhibitors
|
US20150182525A1
(en)
|
2011-05-19 |
2015-07-02 |
Novartis Ag |
4-Amino-5-Fluoro-3-[6-(4-Methylpiperazin-1-YL)-1H-Benzimidazol-2-YL]-1H-Quinolin-2-one for use in the Treatment of Adenoid Cystic Carcinoma
|
WO2012163942A1
(en)
|
2011-06-01 |
2012-12-06 |
Bayer Intellectual Property Gmbh |
Substituted aminoimidazopyridazines
|
AR086656A1
(en)
|
2011-06-03 |
2014-01-15 |
Millennium Pharm Inc |
COMBINATION OF MEK INHIBITORS AND SELECTIVE INHIBITORS OF QUINASA AURORA A
|
WO2012173371A2
(en)
|
2011-06-13 |
2012-12-20 |
주식회사 엘지화학 |
Novel compounds and organic electronic device using same
|
US9284319B2
(en)
|
2011-06-22 |
2016-03-15 |
Bayer Intellectual Property Gmbh |
Heterocyclyl aminoimidazopyridazines
|
US8846656B2
(en)
|
2011-07-22 |
2014-09-30 |
Novartis Ag |
Tetrahydropyrido-pyridine and tetrahydropyrido-pyrimidine compounds and use thereof as C5a receptor modulators
|
IN2014MN00228A
(en)
|
2011-08-12 |
2015-09-25 |
Nissan Chemical Ind Ltd |
|
RU2638116C2
(en)
|
2011-08-12 |
2017-12-15 |
Ф. Хоффманн-Ля Рош Аг |
Pyrazolo [3,4-c] pyridines and methods of application thereof
|
JP2013049251A
(en)
|
2011-08-31 |
2013-03-14 |
Fujifilm Corp |
Relief printing plate original plate for laser engraving, and, relief printing plate and method for producing the same
|
WO2013033981A1
(en)
|
2011-09-06 |
2013-03-14 |
江苏先声药物研究有限公司 |
2,7-naphthyridine derivative, preparation method therefor and use thereof
|
EP2755482B1
(en)
|
2011-09-15 |
2016-06-01 |
Merck Sharp & Dohme Corp. |
Combination of mk-1775 and mk-8776 for treating cancer
|
US9376435B2
(en)
|
2011-09-23 |
2016-06-28 |
Jawaharlal Nehru Centre For Advanced Scientific Research |
Chromophores for the detection of volatile organic compounds
|
EP2758400A1
(en)
|
2011-09-23 |
2014-07-30 |
Bayer Intellectual Property GmbH |
Substituted imidazopyridazines
|
AU2012315988A1
(en)
|
2011-09-30 |
2014-04-10 |
Kineta, Inc. |
Anti-viral compounds
|
UA111382C2
(en)
|
2011-10-10 |
2016-04-25 |
Оріон Корпорейшн |
Protein kinase inhibitors
|
EP2766352B1
(en)
|
2011-10-12 |
2018-06-06 |
University Health Network (UHN) |
Indazole compounds as kinase inhibitors and method of treating cancer with same
|
KR101897044B1
(en)
|
2011-10-20 |
2018-10-23 |
에스에프씨 주식회사 |
Organic metal compounds and organic light emitting diodes comprising the same
|
JP2014532647A
(en)
|
2011-10-28 |
2014-12-08 |
ノバルティス アーゲー |
How to treat gastrointestinal stromal tumors
|
WO2013063003A1
(en)
|
2011-10-28 |
2013-05-02 |
Novartis Ag |
Method of treating gastrointestinal stromal tumors
|
WO2013088191A1
(en)
|
2011-12-12 |
2013-06-20 |
Institut National De La Sante Et De La Recherche Medicale (Inserm) |
Antagonist of the fibroblast growth factor receptor 3 (fgfr3) for use in the treatment or the prevention of skeletal disorders linked with abnormal activation of fgfr3
|
FR2985257B1
(en)
|
2011-12-28 |
2014-02-14 |
Sanofi Sa |
FGFS RECEPTOR AGONISTIC DIMERS (FGFRS), PREPARATION METHOD AND THERAPEUTIC USE THEREOF
|
FR2985258A1
(en)
|
2011-12-28 |
2013-07-05 |
Sanofi Sa |
FGFS RECEPTOR AGONISTIC DIMERS (FGFRS), PREPARATION METHOD AND THERAPEUTIC USE THEREOF
|
US10026905B2
(en)
|
2012-01-18 |
2018-07-17 |
Duk San Neolux Co., Ltd. |
Compound, organic electric element using the same, and an electronic device thereof
|
WO2013109027A1
(en)
|
2012-01-18 |
2013-07-25 |
덕산하이메탈(주) |
Compound, organic electronic element using same and electronic device thereof
|
PL2657233T3
(en)
|
2012-01-19 |
2015-01-30 |
Taiho Pharmaceutical Co Ltd |
3,5-disubstituted alkynylbenzene compound and salt thereof
|
US9475815B2
(en)
|
2012-02-23 |
2016-10-25 |
Bayer Intelletual Property Gmbh |
Substituted benzothienyl-pyrrolotriazines and uses thereof
|
JP2013179181A
(en)
|
2012-02-28 |
2013-09-09 |
Sumitomo Chemical Co Ltd |
Organic photoelectric conversion element
|
EP2834236B1
(en)
|
2012-03-14 |
2019-05-22 |
Lupin Limited |
Heterocyclyl compounds
|
JP6190871B2
(en)
|
2012-03-30 |
2017-08-30 |
ノバルティス アーゲー |
FGFR inhibitors for use in the treatment of hypophosphatemic disorders
|
JP5120580B1
(en)
|
2012-05-14 |
2013-01-16 |
Jsr株式会社 |
Liquid crystal alignment agent
|
AU2013264730B2
(en)
|
2012-05-20 |
2018-02-01 |
Tel Hashomer Medical Research Infrastructure And Services Ltd. |
Prosthetic mitral valve
|
CN107383009B
(en)
|
2012-06-13 |
2020-06-09 |
因塞特控股公司 |
Substituted tricyclic compounds as FGFR inhibitors
|
AU2013289175A1
(en)
|
2012-07-11 |
2015-01-22 |
Novartis Ag |
Method of treating gastrointestinal stromal tumors
|
PT2872491T
(en)
|
2012-07-11 |
2021-08-05 |
Blueprint Medicines Corp |
Inhibitors of the fibroblast growth factor receptor
|
BR112015002080A2
(en)
|
2012-08-02 |
2017-07-04 |
Merck Sharp & Dohme |
compound, pharmaceutical composition, use of a compound, and method of treating or preventing a disorder, condition or disease
|
WO2014019186A1
(en)
|
2012-08-02 |
2014-02-06 |
Merck Sharp & Dohme Corp. |
Antidiabetic tricyclic compounds
|
US9388185B2
(en)
|
2012-08-10 |
2016-07-12 |
Incyte Holdings Corporation |
Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
|
KR101985259B1
(en)
|
2012-08-10 |
2019-06-03 |
제이에스알 가부시끼가이샤 |
Liquid crystal aligning agent and compound
|
WO2014044846A1
(en)
|
2012-09-24 |
2014-03-27 |
Evotec (Uk) Ltd. |
3-(aryl- or heteroaryl-amino)-7-(3,5-dimethoxyphenyl)isoquinoline derivatives as fgfr inhibitors useful for the treatment of proliferative disorders or dysplasia
|
WO2014048878A1
(en)
|
2012-09-26 |
2014-04-03 |
Evotec (Uk) Ltd. |
Phenyl- or pyridyl- pyrrolo[2,3b]pyrazine derivatives useful in the treatment or prevention of proliferative disorders or dysplasia
|
WO2014062454A1
(en)
|
2012-10-15 |
2014-04-24 |
Merck Sharp & Dohme Corp. |
Compositions and methods for treating cancer
|
KR102000211B1
(en)
|
2012-10-29 |
2019-09-30 |
삼성디스플레이 주식회사 |
Organometallic compound and organic light emitting diode comprising the same
|
RU2660349C2
(en)
|
2012-11-28 |
2018-07-05 |
Мерк Шарп И Доум Корп. |
Compositions and methods for treatment of malignant tumour
|
US20140148548A1
(en)
|
2012-11-28 |
2014-05-29 |
Central Glass Company, Limited |
Fluorine-Containing Polymerizable Monomer And Polymer Compound Using Same
|
CN104968664A
(en)
|
2012-12-12 |
2015-10-07 |
山东亨利医药科技有限责任公司 |
Bicyclic compound functioning as tyrosine kinase inhibitor
|
US9266892B2
(en)
|
2012-12-19 |
2016-02-23 |
Incyte Holdings Corporation |
Fused pyrazoles as FGFR inhibitors
|
TWI629266B
(en)
|
2012-12-28 |
2018-07-11 |
藍印藥品公司 |
Inhibitors of the fibroblast growth factor receptor
|
WO2014105849A1
(en)
|
2012-12-28 |
2014-07-03 |
Xoma (Us) Llc |
Antibodies specific for fgfr4 and methods of use
|
KR102030587B1
(en)
|
2013-01-09 |
2019-10-10 |
에스에프씨주식회사 |
Asymmetric antracene derivatives having two naphthyl groups and organic light-emitting diode including the same
|
CN103694236B
(en)
|
2013-01-15 |
2017-05-31 |
苏州开拓药业股份有限公司 |
A kind of pyrimidine scaffold has the antitumoral compounds of activity of hedgehog path antagonist
|
WO2014113191A1
(en)
|
2013-01-15 |
2014-07-24 |
Xiaohu Zhang |
Hedgehog pathway signaling inhibitors and therapeutic applications thereof
|
KR101456626B1
(en)
|
2013-02-01 |
2014-11-03 |
대영이앤비 주식회사 |
Apparatus for protecting negative pressure of refrigerator
|
JP6311093B2
(en)
|
2013-03-07 |
2018-04-18 |
国立大学法人九州大学 |
Sensor elements for detecting supramolecular complexes, light emitters, and organic compounds
|
WO2014138485A1
(en)
|
2013-03-08 |
2014-09-12 |
Irm Llc |
Ex vivo production of platelets from hematopoietic stem cells and the product thereof
|
WO2014160478A1
(en)
|
2013-03-13 |
2014-10-02 |
Flatley Discovery Lab |
Compounds and methods for the treatment of cystic fibrosis
|
US9498532B2
(en)
|
2013-03-13 |
2016-11-22 |
Novartis Ag |
Antibody drug conjugates
|
CA2902655A1
(en)
|
2013-03-14 |
2014-09-18 |
AbbVie Deutschland GmbH & Co. KG |
Novel inhibitor compounds of phosphodiesterase type 10a
|
ES2892423T3
(en)
|
2013-03-15 |
2022-02-04 |
Celgene Car Llc |
Heteroaryl compounds and uses thereof
|
BR112015022191A8
(en)
|
2013-03-15 |
2018-01-23 |
Celgene Avilomics Res Inc |
heteroaryl compounds and uses thereof
|
TWI647220B
(en)
*
|
2013-03-15 |
2019-01-11 |
美商西建卡爾有限責任公司 |
Heteroaryl compound and its use
|
WO2014160521A1
(en)
|
2013-03-15 |
2014-10-02 |
Blueprint Medicines Corporation |
Piperazine derivatives and their use as kit modulators
|
TWI628176B
(en)
|
2013-04-04 |
2018-07-01 |
奧利安公司 |
Protein kinase inhibitors
|
KR101573611B1
(en)
|
2013-04-17 |
2015-12-01 |
주식회사 엘지화학 |
Fullerene derivatives, organic solar cell using the same and fabricating method thereof
|
CN105263931B
(en)
|
2013-04-19 |
2019-01-25 |
因赛特公司 |
Bicyclic heterocycle as FGFR inhibitor
|
KR20160002882A
(en)
|
2013-04-19 |
2016-01-08 |
코바겐 아게 |
Novel bispecific binding molecules with antitumoral activity
|
GB201307577D0
(en)
|
2013-04-26 |
2013-06-12 |
Astex Therapeutics Ltd |
New compounds
|
WO2014182829A1
(en)
|
2013-05-09 |
2014-11-13 |
Principia Biopharma Inc. |
Quinolone derivatives as fibroblast growth factor inhibitors
|
ES2691923T3
(en)
|
2013-06-14 |
2018-11-29 |
Sanofi |
Pyrazolopyridine derivatives for use in the treatment of bladder cancer
|
JP6380861B2
(en)
|
2013-06-28 |
2018-08-29 |
ベイジーン リミテッド |
Condensed tricyclic urea compounds as Raf kinase and / or dimer inhibitors of Raf kinase
|
JP6380862B2
(en)
|
2013-06-28 |
2018-08-29 |
ベイジーン リミテッド |
Condensed tricyclic amide compounds as inhibitors of multiple kinases
|
BR112016000059B1
(en)
|
2013-07-02 |
2020-12-29 |
Syngenta Participations Ag |
bi or tricyclic heterocycles compounds, composition comprising said compounds, method for combating and controlling pests, method for protecting plant propagation material from attack by pests and plant propagation material coated with said composition
|
JP6018547B2
(en)
|
2013-07-09 |
2016-11-02 |
大成ロテック株式会社 |
Paving machine
|
EP3019491A4
(en)
|
2013-07-09 |
2016-12-21 |
Dana Farber Cancer Inst Inc |
Kinase inhibitors for the treatment of disease
|
CA2917364C
(en)
|
2013-07-11 |
2020-09-29 |
Acea Biosciences Inc. |
Heterocyclic compounds and uses thereof
|
AR097455A1
(en)
|
2013-08-28 |
2016-03-16 |
Astellas Pharma Inc |
PHARMACEUTICAL COMPOSITION CONTAINING PYRIMIDINE COMPOSITE AS AN ACTIVE INGREDIENT
|
ES2679521T3
(en)
|
2013-10-18 |
2018-08-28 |
Eisai R&D Management Co., Ltd. |
FGFR4 pyrimidine inhibitors
|
AU2014338549B2
(en)
|
2013-10-25 |
2017-05-25 |
Novartis Ag |
Ring-fused bicyclic pyridyl derivatives as FGFR4 inhibitors
|
EP3060560A1
(en)
|
2013-10-25 |
2016-08-31 |
Blueprint Medicines Corporation |
Inhibitors of the fibroblast growth factor receptor
|
FR3012330B1
(en)
|
2013-10-29 |
2015-10-23 |
Oreal |
BIPHASE COMPOSITION COMPRISING AN ESTER OF FATTY ACID AND SUGAR OR A LIQUID ALKYLPOLYGLUCOSIDE OF HLB <8, AND A C8-C18 BRANCHED ALKANE
|
WO2015066452A2
(en)
|
2013-11-01 |
2015-05-07 |
Foundation Medicine, Inc. |
Methods of treating pediatric cancers
|
WO2015108992A1
(en)
*
|
2014-01-15 |
2015-07-23 |
Blueprint Medicines Corporation |
Heterobicyclic compounds and their use as fgfr4 receptor inhibitors
|
MX2017002206A
(en)
|
2014-08-19 |
2018-01-23 |
Shanghai Haihe Pharmaceutical Co Ltd |
Indazole compounds as fgfr kinase inhibitor, preparation and use thereof.
|
CN104262330B
(en)
|
2014-08-27 |
2016-09-14 |
广东东阳光药业有限公司 |
A kind of urea substituted biphenyl compounds and combinations thereof thing and purposes
|
US10350206B2
(en)
|
2014-09-19 |
2019-07-16 |
Bayer Pharma Aktiengesellschaft |
Benzyl substituted indazoles as BUB1 inhibitors
|
US20160115164A1
(en)
|
2014-10-22 |
2016-04-28 |
Incyte Corporation |
Bicyclic heterocycles as fgfr4 inhibitors
|
US10851105B2
(en)
|
2014-10-22 |
2020-12-01 |
Incyte Corporation |
Bicyclic heterocycles as FGFR4 inhibitors
|
WO2016134294A1
(en)
|
2015-02-20 |
2016-08-25 |
Incyte Corporation |
Bicyclic heterocycles as fgfr4 inhibitors
|
MA41551A
(en)
|
2015-02-20 |
2017-12-26 |
Incyte Corp |
BICYCLIC HETEROCYCLES USED AS FGFR4 INHIBITORS
|
MX2017010638A
(en)
|
2015-02-20 |
2018-05-07 |
Univ Oregon Health & Science |
Derivatives of sobetirome.
|
EP3617205B1
(en)
|
2015-02-20 |
2021-08-04 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
AU2016272089B2
(en)
|
2015-06-03 |
2021-02-18 |
Triastek, Inc. |
Dosage forms and use thereof
|
CA2992269C
(en)
|
2015-07-15 |
2020-06-02 |
Cabot Corporation |
Methods of making an elastomer composite reinforced with silica and carbon black and products containing same
|
MX2018000592A
(en)
|
2015-07-15 |
2018-04-24 |
Hoffmann La Roche |
Ethynyl derivatives as metabotropic glutamate receptor modulators.
|
AU2016293619B2
(en)
|
2015-07-15 |
2021-02-25 |
Protagonist Therapeutics, Inc. |
Peptide inhibitors of interleukin-23 receptor and their use to treat inflammatory diseases
|
MY189596A
(en)
|
2015-07-15 |
2022-02-18 |
Immatics Biotechnologies Gmbh |
A novel peptides for use in immunotherapy against epithelial ovarian cancer and other cancers
|
DK3328419T3
(en)
|
2015-07-30 |
2021-10-11 |
Macrogenics Inc |
PD-1 BINDING MOLECULES AND METHODS FOR USING IT
|
US10329309B2
(en)
|
2015-08-03 |
2019-06-25 |
Samumed, Llc |
3-(3H-imidazo[4,5-B]pyridin-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
US10195185B2
(en)
|
2015-08-03 |
2019-02-05 |
Samumed, Llc |
3-(1H-imidazo[4,5-C]pyridin-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
US10231956B2
(en)
|
2015-08-03 |
2019-03-19 |
Samumed, Llc |
3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
WO2017024025A1
(en)
|
2015-08-03 |
2017-02-09 |
Sunil Kumar Kc |
3-(1h-pyrrolo[2,3-c]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
WO2017023989A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(1h-benzo[d]imidazol-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
US10206909B2
(en)
|
2015-08-03 |
2019-02-19 |
Samumed, Llc |
3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
US10188634B2
(en)
|
2015-08-03 |
2019-01-29 |
Samumed, Llc |
3-(3H-imidazo[4,5-C]pyridin-2-yl)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
EP3337787B1
(en)
|
2015-08-20 |
2021-03-03 |
JS InnoPharm (Shanghai) Ltd. |
1h-pyrazolo[3,4-b]pyridine, 1h-thieno[2,3-c]pyrazole and 1h-indazole carboxamide derivatives and related compounds as extracellular signal-regulated kinases (erk) inhibitors for treating cancer
|
WO2017058915A1
(en)
|
2015-09-28 |
2017-04-06 |
Araxes Pharma Llc |
Inhibitors of kras g12c mutant proteins
|
TW201718581A
(en)
|
2015-10-19 |
2017-06-01 |
英塞特公司 |
Heterocyclic compounds as immunomodulators
|
CA3002560A1
(en)
|
2015-10-23 |
2017-04-27 |
Array Biopharma, Inc. |
2-aryl- and 2-heteroaryl-substituted 2-pyridazin-3(2h)-one compounds as inhibitors of fgfr tyrosine kinases
|
ES2928856T3
(en)
|
2015-11-19 |
2022-11-23 |
Incyte Corp |
Heterocyclic compounds as immunomodulators
|
MA44075A
(en)
|
2015-12-17 |
2021-05-19 |
Incyte Corp |
N-PHENYL-PYRIDINE-2-CARBOXAMIDE DERIVATIVES AND THEIR USE AS MODULATORS OF PROTEIN / PROTEIN PD-1 / PD-L1 INTERACTIONS
|
UA126113C2
(en)
|
2015-12-22 |
2022-08-17 |
Інсайт Корпорейшн |
Heterocyclic compounds as immunomodulators
|
WO2017192961A1
(en)
|
2016-05-06 |
2017-11-09 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
EP3464279B1
(en)
|
2016-05-26 |
2021-11-24 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
WO2017222976A1
(en)
|
2016-06-20 |
2017-12-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
US10138248B2
(en)
|
2016-06-24 |
2018-11-27 |
Incyte Corporation |
Substituted imidazo[2,1-f][1,2,4]triazines, substituted imidazo[1,2-a]pyridines, substituted imidazo[1,2-b]pyridazines and substituted imidazo[1,2-a]pyrazines as PI3K-γ inhibitors
|
WO2018013789A1
(en)
|
2016-07-14 |
2018-01-18 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
MA46045A
(en)
|
2016-08-29 |
2021-04-28 |
Incyte Corp |
HETEROCYCLIC COMPOUNDS USED AS IMMUNOMODULATORS
|
US10647693B2
(en)
|
2016-08-30 |
2020-05-12 |
North & South Brother Pharmacy Investment Company Limited |
Inhibitors of influenza virus replication, application methods and uses thereof
|
US20180072718A1
(en)
|
2016-09-09 |
2018-03-15 |
Incyte Corporation |
Pyrazolopyridine compounds and uses thereof
|
CA3037064A1
(en)
|
2016-10-05 |
2018-04-12 |
Zeno Royalties & Milestones, LLC |
Spirocyclic compounds
|
KR101755556B1
(en)
|
2016-11-18 |
2017-07-07 |
주식회사 케마스 |
Pharmaceutical composition for prevention or treatment of brain cancer comprising polymorphic form of tetraarsenic oxide and preparation method thereof
|
KR101834366B1
(en)
|
2016-11-21 |
2018-03-05 |
주식회사 케마스 |
Pharmaceutical composition for prevention or treatment of breast cancer comprising polymorphic form of tetraarsenic oxide and preparation method thereof
|
KR101844049B1
(en)
|
2016-12-05 |
2018-03-30 |
주식회사 케마스 |
Pharmaceutical composition for prevention or treatment of liver cancer comprising polymorphic form of tetraarsenic oxide
|
KR101844050B1
(en)
|
2016-12-09 |
2018-05-14 |
주식회사 케마스 |
Pharmaceutical composition for prevention or treatment of cancer comprising polymorphic form of tetraarsenic oxide
|
WO2018119286A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Bicyclic heteroaromatic compounds as immunomodulators
|
ES2874756T3
(en)
|
2016-12-22 |
2021-11-05 |
Incyte Corp |
Triazolo [1,5-A] pyridine derivatives as immunomodulators
|
US20180177784A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
BR112019012957A2
(en)
|
2016-12-22 |
2019-11-26 |
Incyte Corp |
tetrahydroimidazo [4,5-c] pyridine derivatives as inducers of internalization of pd-11
|
US20180179179A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
AU2017382870B2
(en)
|
2016-12-22 |
2022-03-24 |
Incyte Corporation |
Benzooxazole derivatives as immunomodulators
|
AR111960A1
(en)
|
2017-05-26 |
2019-09-04 |
Incyte Corp |
CRYSTALLINE FORMS OF A FGFR INHIBITOR AND PROCESSES FOR ITS PREPARATION
|
WO2018234354A1
(en)
|
2017-06-20 |
2018-12-27 |
Grünenthal GmbH |
Novel substituted 3-indole and 3-indazole compounds as phosphodiesterase inhibitors
|
WO2019037640A1
(en)
|
2017-08-22 |
2019-02-28 |
Js Innopharm (Shanghai) Ltd |
Heterocyclic compounds as kinase inhibitors, compositions comprising the heterocyclic compound, and methods of use thereof
|
EP3697777A1
(en)
|
2017-10-19 |
2020-08-26 |
eFFECTOR Therapeutics, Inc. |
Benzimidazole-indole inhibitors of mnk1 and mnk2
|
ES2908283T3
(en)
|
2017-12-02 |
2022-04-28 |
Galapagos Nv |
New compounds and pharmaceutical compositions thereof for the treatment of diseases
|
SI3774791T1
(en)
|
2018-03-30 |
2023-04-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
JP2021523118A
(en)
|
2018-05-04 |
2021-09-02 |
インサイト・コーポレイションIncyte Corporation |
FGFR inhibitor salt
|
US11466004B2
(en)
|
2018-05-04 |
2022-10-11 |
Incyte Corporation |
Solid forms of an FGFR inhibitor and processes for preparing the same
|
DK3790877T3
(en)
|
2018-05-11 |
2023-04-24 |
Incyte Corp |
TETRAHYDRO-IMIDAZO[4,5-C]PYRIDINE DERIVATIVES AS PD-L1 IMMUNE MODULATORS
|
KR20210075071A
(en)
|
2018-08-14 |
2021-06-22 |
오스테오큐씨 인코포레이티드 |
pyrrolo-dipyridine compounds
|
ES2954572T3
(en)
|
2018-09-07 |
2023-11-23 |
Merck Patent Gmbh |
5-morpholin-4-yl-pyrazolo[4,3-b]pyridine derivatives
|
WO2020081898A1
(en)
|
2018-10-20 |
2020-04-23 |
The Johns Hopkins University |
Non-invasive urinary biomarkers for the detection of urothelial carcinoma of the bladder
|
EP3898626A1
(en)
|
2018-12-19 |
2021-10-27 |
Array Biopharma, Inc. |
Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases
|
JP2022515197A
(en)
|
2018-12-19 |
2022-02-17 |
アレイ バイオファーマ インコーポレイテッド |
7-((3,5-dimethoxyphenyl) amino) quinoxaline derivative as an FGFR inhibitor for treating cancer
|
JP7148802B2
(en)
|
2019-01-25 |
2022-10-06 |
富士通株式会社 |
Analysis program, analysis method and analysis device
|
US11591329B2
(en)
|
2019-07-09 |
2023-02-28 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
US20210094935A1
(en)
|
2019-10-01 |
2021-04-01 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
AU2020366006A1
(en)
|
2019-10-14 |
2022-04-21 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
US11566028B2
(en)
|
2019-10-16 |
2023-01-31 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
BR112022010664A2
(en)
|
2019-12-04 |
2022-08-16 |
Incyte Corp |
DERIVATIVES OF A FGFR INHIBITOR
|
EP4069696A1
(en)
|
2019-12-04 |
2022-10-12 |
Incyte Corporation |
Tricyclic heterocycles as fgfr inhibitors
|
WO2021146424A1
(en)
|
2020-01-15 |
2021-07-22 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
CA3215903A1
(en)
|
2021-04-12 |
2022-10-20 |
Incyte Corporation |
Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent
|