GB812366A
(en)
|
1955-08-18 |
1959-04-22 |
Wellcome Found |
Improvements in and relating to derivatives of pyrimidine and the preparation thereof
|
GB937725A
(en)
|
1960-05-11 |
1963-09-25 |
Ciba Ltd |
Pyrazolo[3:4-d]pyrimidines
|
JPS4834699B1
(en)
|
1968-07-03 |
1973-10-23 |
|
|
DE2139107A1
(en)
|
1971-08-04 |
1973-02-15 |
Merck Patent Gmbh |
N(6)-subst adenosine derivs - with coronary circulatory etc activity
|
IT1153216B
(en)
|
1981-10-16 |
1987-01-14 |
Schering Ag |
PROCEDURE FOR THE PREPARATION OF CYANETHEROCYCLIC COMPOUNDS
|
GB2116183B
(en)
|
1982-03-03 |
1985-06-05 |
Genentech Inc |
Human antithrombin iii dna sequences therefore expression vehicles and cloning vectors containing such sequences and cell cultures transformed thereby a process for expressing human antithrombin iii and pharmaceutical compositions comprising it
|
DE3244594A1
(en)
|
1982-12-02 |
1984-06-07 |
Hoechst Ag, 6230 Frankfurt |
1-PHENYLISOCHINOLINE DERIVATIVES AND METHOD FOR THE PRODUCTION THEREOF, PHARMACEUTICAL PREPARATIONS CONTAINING THIS COMPOUND AND THE USE THEREOF
|
DE3406533A1
(en)
|
1984-02-23 |
1985-08-29 |
Boehringer Mannheim Gmbh, 6800 Mannheim |
USE OF ADENOSINE DERIVATIVES AS ANTIALLERGICA AND MEDICINAL PRODUCTS CONTAINING THEM
|
US5310731A
(en)
|
1984-06-28 |
1994-05-10 |
Whitby Research, Inc. |
N-6 substituted-5'-(N-substitutedcarboxamido)adenosines as cardiac vasodilators and antihypertensive agents
|
US4795627A
(en)
|
1984-10-18 |
1989-01-03 |
University Of Pittsburgh |
Tritium labelled N-mustard type compounds and a process for their production
|
US4656159A
(en)
|
1984-10-31 |
1987-04-07 |
Georgetown University |
Galactose-C-6 nitrogen mustard compounds and their uses
|
JPS61109797A
(en)
|
1984-11-01 |
1986-05-28 |
Yuki Gosei Yakuhin Kogyo Kk |
Labeled nucleotide and labeled polynucleotide
|
WO1990003370A1
(en)
|
1988-09-28 |
1990-04-05 |
Microprobe Corporation |
DERIVATIVES OF PYRAZOLO[3,4-d]PYRIMIDINE
|
US5428125A
(en)
|
1989-07-17 |
1995-06-27 |
The Dow Chemical Company |
Mesogenic polycyanates and thermosets thereof
|
US5442039A
(en)
|
1989-07-17 |
1995-08-15 |
The Dow Chemical Company |
Mesogenic polycyanates and thermosets thereof
|
US5721356A
(en)
|
1989-09-15 |
1998-02-24 |
Gensia, Inc. |
Orally active adenosine kinase inhibitors
|
US5674998A
(en)
|
1989-09-15 |
1997-10-07 |
Gensia Inc. |
C-4' modified adenosine kinase inhibitors
|
US5763596A
(en)
|
1989-09-15 |
1998-06-09 |
Metabasis Therapeutics, Inc. |
C-4' modified adenosine kinase inhibitors
|
US5646128A
(en)
|
1989-09-15 |
1997-07-08 |
Gensia, Inc. |
Methods for treating adenosine kinase related conditions
|
US5795977A
(en)
|
1989-09-15 |
1998-08-18 |
Metabasis Therapeutics, Inc. |
Water soluble adenosine kinase inhibitors
|
US5763597A
(en)
|
1989-09-15 |
1998-06-09 |
Metabasis Therapeutics, Inc. |
Orally active adenosine kinase inhibitors
|
WO1991009594A1
(en)
|
1989-12-28 |
1991-07-11 |
Virginia Commonwealth University |
Sigma receptor ligands and the use thereof
|
JPH04211063A
(en)
|
1990-03-05 |
1992-08-03 |
Takeda Chem Ind Ltd |
Condensed tricyclic heterocyclic compound, its production, use and intermediate
|
GB9009542D0
(en)
|
1990-04-27 |
1990-06-20 |
Beecham Group Plc |
Novel compounds
|
GB9113137D0
(en)
|
1990-07-13 |
1991-08-07 |
Ici Plc |
Thioxo heterocycles
|
DE4026265A1
(en)
|
1990-08-20 |
1992-02-27 |
Boehringer Mannheim Gmbh |
NEW PHOSPHOLIPID DERIVATIVES OF NUCLEOSIDES, THEIR PRODUCTION AND THEIR USE AS ANTIVIRAL MEDICINAL PRODUCTS
|
US5563257A
(en)
|
1990-08-20 |
1996-10-08 |
Boehringer Mannheim Gmbh |
Phospholipid derivatives of nucleosides
|
ES2095960T3
(en)
|
1990-09-25 |
1997-03-01 |
Rhone Poulenc Rorer Int |
COMPOUNDS THAT HAVE ANTI-HYPERTENSIVE AND ANTI-ISCHEMICAL PROPERTIES.
|
US5652366A
(en)
|
1990-09-25 |
1997-07-29 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
DI (1R)-(-)camphosulfonic acid) salt, preparation thereof and use thereof
|
US5561134A
(en)
|
1990-09-25 |
1996-10-01 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties
|
GB9103839D0
(en)
|
1991-02-23 |
1991-04-10 |
Smithkline Beecham Plc |
Pharmaceuticals
|
WO1992020642A1
(en)
|
1991-05-10 |
1992-11-26 |
Rhone-Poulenc Rorer International (Holdings) Inc. |
Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit egf and/or pdgf receptor tyrosine kinase
|
US6645969B1
(en)
|
1991-05-10 |
2003-11-11 |
Aventis Pharmaceuticals Inc. |
Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase
|
US5710158A
(en)
|
1991-05-10 |
1998-01-20 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
|
US5721237A
(en)
|
1991-05-10 |
1998-02-24 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Protein tyrosine kinase aryl and heteroaryl quinazoline compounds having selective inhibition of HER-2 autophosphorylation properties
|
USRE37650E1
(en)
|
1991-05-10 |
2002-04-09 |
Aventis Pharmacetical Products, Inc. |
Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase
|
US5714493A
(en)
|
1991-05-10 |
1998-02-03 |
Rhone-Poulenc Rorer Pharmaceuticals, Inc. |
Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase
|
US5480883A
(en)
|
1991-05-10 |
1996-01-02 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
|
IL104369A0
(en)
|
1992-01-13 |
1993-05-13 |
Smithkline Beecham Corp |
Novel compounds and compositions
|
US5916891A
(en)
|
1992-01-13 |
1999-06-29 |
Smithkline Beecham Corporation |
Pyrimidinyl imidazoles
|
DE4204032A1
(en)
|
1992-02-12 |
1993-08-19 |
Boehringer Mannheim Gmbh |
NEW LIPONUCLEOTIDES, THEIR PRODUCTION AND THEIR USE AS ANTIVIRAL MEDICINAL PRODUCTS
|
DE4204031A1
(en)
|
1992-02-12 |
1993-08-19 |
Boehringer Mannheim Gmbh |
NEW LIPID PHOSPHONIC ACID-NUCLEOSIDE CONJUGATES AND THEIR USE AS ANTIVIRAL MEDICINAL PRODUCTS
|
WO1993018035A1
(en)
|
1992-03-04 |
1993-09-16 |
Abbott Laboratories |
Angiotensin ii receptor antagonists
|
JP2737518B2
(en)
|
1992-03-16 |
1998-04-08 |
富士通株式会社 |
Cooling structure of infrared detector
|
US5294612A
(en)
|
1992-03-30 |
1994-03-15 |
Sterling Winthrop Inc. |
6-heterocyclyl pyrazolo [3,4-d]pyrimidin-4-ones and compositions and method of use thereof
|
CA2133075A1
(en)
|
1992-04-07 |
1993-10-14 |
Craig B. Thompson |
CD28 Pathway Immunoregulation
|
GB9208135D0
(en)
|
1992-04-13 |
1992-05-27 |
Ludwig Inst Cancer Res |
Polypeptides having kinase activity,their preparation and use
|
AU4115693A
(en)
|
1992-04-24 |
1993-11-29 |
Sri International |
In vivo homologous sequence targeting in eukaryotic cells
|
JP3261617B2
(en)
|
1992-06-19 |
2002-03-04 |
ハネウエル・インコーポレーテッド |
Infrared camera
|
US6057305A
(en)
|
1992-08-05 |
2000-05-02 |
Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic |
Antiretroviral enantiomeric nucleotide analogs
|
TW370529B
(en)
|
1992-12-17 |
1999-09-21 |
Pfizer |
Pyrazolopyrimidines
|
IL108523A0
(en)
|
1993-02-03 |
1994-05-30 |
Gensia Inc |
Pharmaceutical compositions containing adenosine kinase inhibitors for preventing or treating conditions involving inflammatory responses and pain
|
EP0684953A4
(en)
|
1993-02-03 |
1999-12-22 |
Gensia Inc |
Adenosine kinase inhibitors comprising lyxofuranosyl derivatives.
|
GB9308957D0
(en)
|
1993-04-30 |
1993-06-16 |
Cancer Res Campaign Tech |
Novel produgs
|
ES2240962T3
(en)
|
1993-06-04 |
2005-10-16 |
The United States Of America As Represented By The Secretary Of The Navy |
METHOD FOR SELECTIVELY STIMULATING THE PROLIFERATION OF CELLS T.
|
US5504103A
(en)
|
1993-08-25 |
1996-04-02 |
Eli Lilly And Company |
Inhibition of phosphatidylinositol 3-kinase with 17 β-hydroxywortmannin and analogs thereof
|
US5525503A
(en)
|
1993-09-28 |
1996-06-11 |
Dana-Farber Cancer Institute, Inc. |
Signal transduction via CD28
|
AU6672794A
(en)
|
1993-11-05 |
1995-05-23 |
Biochem Pharma Inc. |
Antineoplastic heteronaphthoquinones
|
US5656643A
(en)
|
1993-11-08 |
1997-08-12 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
|
US5679683A
(en)
|
1994-01-25 |
1997-10-21 |
Warner-Lambert Company |
Tricyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family
|
IL112249A
(en)
|
1994-01-25 |
2001-11-25 |
Warner Lambert Co |
Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds
|
US6632789B1
(en)
|
1994-04-29 |
2003-10-14 |
The United States Of America As Represented By The Secretary Of The Navy |
Methods for modulating T cell responses by manipulating intracellular signal transduction
|
DE4418690A1
(en)
|
1994-05-28 |
1996-01-11 |
Boehringer Mannheim Gmbh |
Nucleoside 5'-mono-phosphate ester(s) of glyceryl di:ether derivs.
|
US6323201B1
(en)
|
1994-12-29 |
2001-11-27 |
The Regents Of The University Of California |
Compounds for inhibition of ceramide-mediated signal transduction
|
WO1996031510A1
(en)
|
1995-04-03 |
1996-10-10 |
Novartis Ag |
Pyrazole derivatives and processes for the preparation thereof
|
US6312894B1
(en)
|
1995-04-03 |
2001-11-06 |
Epoch Pharmaceuticals, Inc. |
Hybridization and mismatch discrimination using oligonucleotides conjugated to minor groove binders
|
US5977061A
(en)
|
1995-04-21 |
1999-11-02 |
Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic |
N6 - substituted nucleotide analagues and their use
|
JPH08295667A
(en)
|
1995-04-27 |
1996-11-12 |
Takeda Chem Ind Ltd |
Heterocyclic compound, its production and pharmaceutical preparation
|
WO1996037777A1
(en)
|
1995-05-23 |
1996-11-28 |
Nelson Randall W |
Mass spectrometric immunoassay
|
US5593997A
(en)
|
1995-05-23 |
1997-01-14 |
Pfizer Inc. |
4-aminopyrazolo(3-,4-D)pyrimidine and 4-aminopyrazolo-(3,4-D)pyridine tyrosine kinase inhibitors
|
US6403599B1
(en)
|
1995-11-08 |
2002-06-11 |
Pfizer Inc |
Corticotropin releasing factor antagonists
|
EP0831911B1
(en)
|
1995-06-07 |
2002-04-17 |
G.D. Searle & Co. |
Spironolactone and angiotensin ii antagonist combination therapy for treatment of congestive heart failure
|
DE69617235T2
(en)
|
1995-06-07 |
2002-07-25 |
G.D. Searle & Co., Chicago |
EPOXYSTEROIDE ALDOSTERONANTAGONIST AND ANGIOTENSIN II RECEPTOR ANTAGONIST COMBINATION THERAPY FOR TREATING CONGESTIVE HEART FAILURE
|
US5665721A
(en)
|
1995-06-07 |
1997-09-09 |
Abbott Laboratories |
Heterocyclic substituted cyclopentane compounds
|
AU5982296A
(en)
|
1995-06-07 |
1996-12-30 |
G.D. Searle & Co. |
Method to treat cardiofibrosis with a combination of an angi otensin ii antagonist and spironolactone
|
US5811097A
(en)
|
1995-07-25 |
1998-09-22 |
The Regents Of The University Of California |
Blockade of T lymphocyte down-regulation associated with CTLA-4 signaling
|
US5855887A
(en)
|
1995-07-25 |
1999-01-05 |
The Regents Of The University Of California |
Blockade of lymphocyte down-regulation associated with CTLA-4 signaling
|
US6051227A
(en)
|
1995-07-25 |
2000-04-18 |
The Regents Of The University Of California, Office Of Technology Transfer |
Blockade of T lymphocyte down-regulation associated with CTLA-4 signaling
|
US5763885A
(en)
|
1995-12-19 |
1998-06-09 |
Loral Infrared & Imaging Systems, Inc. |
Method and apparatus for thermal gradient stabilization of microbolometer focal plane arrays
|
JPH09143163A
(en)
|
1995-11-29 |
1997-06-03 |
Fuji Photo Film Co Ltd |
Production of nitrogen-containing heteroaromatic amides
|
US5747235A
(en)
|
1996-01-26 |
1998-05-05 |
Eastman Kodak Company |
Silver halide light sensitive emulsion layer having enhanced photographic sensitivity
|
CH690773A5
(en)
|
1996-02-01 |
2001-01-15 |
Novartis Ag |
Pyrrolo (2,3-d) pyrimides and their use.
|
DE19603576A1
(en)
|
1996-02-01 |
1997-08-07 |
Bayer Ag |
Acylated 4-amino and 4-hydrazinopyrimidines
|
GB2310952B
(en)
|
1996-03-05 |
1998-08-19 |
Mitsubishi Electric Corp |
Infrared detector
|
US6207157B1
(en)
|
1996-04-23 |
2001-03-27 |
The United States Of America As Represented By The Department Of Health And Human Services |
Conjugate vaccine for nontypeable Haemophilus influenzae
|
EP0807633B1
(en)
|
1996-05-15 |
2002-11-06 |
Pfizer Inc. |
Novel 2,3-disubstituted-(5,6)- heteroarylfused-pyrimidine-4-ones
|
GB9611460D0
(en)
|
1996-06-01 |
1996-08-07 |
Ludwig Inst Cancer Res |
Novel lipid kinase
|
CA2258822A1
(en)
|
1996-06-20 |
1997-12-24 |
Sean Kerwin |
Compounds and methods for providing pharmacologically active preparations and uses thereof
|
EP1947183B1
(en)
|
1996-08-16 |
2013-07-17 |
Merck Sharp & Dohme Corp. |
Mammalian cell surface antigens; related reagents
|
US6111090A
(en)
|
1996-08-16 |
2000-08-29 |
Schering Corporation |
Mammalian cell surface antigens; related reagents
|
US6153631A
(en)
|
1996-10-23 |
2000-11-28 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5994358A
(en)
|
1996-10-23 |
1999-11-30 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US6251901B1
(en)
|
1996-10-23 |
2001-06-26 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5919808A
(en)
|
1996-10-23 |
1999-07-06 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5922753A
(en)
|
1996-10-23 |
1999-07-13 |
Zymogenetics, Inc. |
Methods for treating bone deficit conditions with benzothiazole
|
US6342514B1
(en)
|
1996-10-23 |
2002-01-29 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5948776A
(en)
|
1996-10-23 |
1999-09-07 |
Zymogenetic, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5990169A
(en)
|
1996-10-23 |
1999-11-23 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5965573A
(en)
|
1996-10-23 |
1999-10-12 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5858753A
(en)
|
1996-11-25 |
1999-01-12 |
Icos Corporation |
Lipid kinase
|
AU7624798A
(en)
|
1996-12-06 |
1998-06-29 |
Vertex Pharmaceuticals Incorporated |
Inhibitors of interleukin-1 beta converting enzyme
|
US6093737A
(en)
|
1996-12-30 |
2000-07-25 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
JPH10206995A
(en)
|
1997-01-21 |
1998-08-07 |
Konica Corp |
Silver halide photographic sensitive material
|
CA2279846C
(en)
|
1997-02-07 |
2008-06-03 |
Princeton University |
Engineered protein kinases which can utilize modified nucleotide triphosphate substrates
|
US7863444B2
(en)
|
1997-03-19 |
2011-01-04 |
Abbott Laboratories |
4-aminopyrrolopyrimidines as kinase inhibitors
|
KR20000076426A
(en)
|
1997-03-19 |
2000-12-26 |
스타르크, 카르크 |
Pyrrolo[2,3-D]Pyrimidines and Their Use as Tyrosine Kinase Inhibitors
|
AU7449598A
(en)
|
1997-05-23 |
1998-12-11 |
Nippon Shinyaku Co. Ltd. |
Medicinal composition for prevention or treatment of hepatopathy
|
US6207679B1
(en)
|
1997-06-19 |
2001-03-27 |
Sepracor, Inc. |
Antimicrobial agents uses and compositions related thereto
|
ATE404539T1
(en)
|
1997-10-02 |
2008-08-15 |
Eisai R&D Man Co Ltd |
CONDENSED PYRIDINE DERIVATIVES
|
EP1025228A4
(en)
|
1997-10-21 |
2002-09-18 |
Human Genome Sciences Inc |
Human tumor necrosis factor receptor-like proteins tr11, tr11sv1, and tr11sv2
|
US6649631B1
(en)
|
1997-10-23 |
2003-11-18 |
The Board Of Regents Of The University Of Texas System |
Compositions and methods for treating bone deficit conditions
|
ES2222614T3
(en)
|
1997-11-12 |
2005-02-01 |
Mitsubishi Chemical Corporation |
DERIVATIVES OF PURINE AND MEDICINE THAT CONTAINS THEM AS ACTIVE INGREDIENT.
|
US6191170B1
(en)
|
1998-01-13 |
2001-02-20 |
Tularik Inc. |
Benzenesulfonamides and benzamides as therapeutic agents
|
JP2002502607A
(en)
|
1998-02-09 |
2002-01-29 |
ジェネンテク・インコーポレイテッド |
Novel tumor necrosis factor receptor homologs and nucleic acids encoding the same
|
DE69940808D1
(en)
|
1998-03-04 |
2009-06-10 |
Bristol Myers Squibb Co |
HETEROCYCLES SUBSTITUTED IMIDAZOPYRAZINES AS PROTEIN TYROSINE KINASE INHIBITORS
|
US6127121A
(en)
|
1998-04-03 |
2000-10-03 |
Epoch Pharmaceuticals, Inc. |
Oligonucleotides containing pyrazolo[3,4-D]pyrimidines for hybridization and mismatch discrimination
|
US7715989B2
(en)
|
1998-04-03 |
2010-05-11 |
Elitech Holding B.V. |
Systems and methods for predicting oligonucleotide melting temperature (TmS)
|
US6432970B2
(en)
|
1998-04-09 |
2002-08-13 |
Johns Hopkins University School Of Medicine |
Inhibitors of hedgehog signaling pathways, compositions and uses related thereto
|
JP2000072773A
(en)
|
1998-08-28 |
2000-03-07 |
Zeria Pharmaceut Co Ltd |
Purine derivative
|
PL347138A1
(en)
|
1998-09-18 |
2002-03-25 |
Basf Ag |
4-aminopyrrolopyrimidines as kinase inhibitors
|
US6362216B1
(en)
|
1998-10-27 |
2002-03-26 |
Array Biopharma Inc. |
Compounds which inhibit tryptase activity
|
EE05627B1
(en)
|
1998-12-23 |
2013-02-15 |
Pfizer Inc. |
Human monoclonal antibodies to CTLA-4
|
EP1140938B1
(en)
|
1999-01-11 |
2003-08-27 |
Princeton University |
High affinity inhibitors for target validation and uses thereof
|
CZ27399A3
(en)
|
1999-01-26 |
2000-08-16 |
Ústav Experimentální Botaniky Av Čr |
Substituted nitrogen heterocyclic derivatives process of their preparation, the derivatives employed as medicaments, pharmaceutical composition and a compound pharmaceutical preparation in which these derivatives are comprised as well as use of these derivatives for preparing medicaments
|
EP1157026A1
(en)
|
1999-02-22 |
2001-11-28 |
Boehringer Ingelheim Pharmaceuticals Inc. |
Polycyclo heterocyclic derivatives as antiinflammatory agents
|
WO2000055139A2
(en)
|
1999-03-12 |
2000-09-21 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Heterocyclic urea and related compounds useful as anti-inflammatory agents
|
EP1040831A3
(en)
|
1999-04-02 |
2003-05-02 |
Pfizer Products Inc. |
Use of corticotropin releasing factor (CRF) antagonists to prevent sudden death
|
SE515856C2
(en)
|
1999-05-19 |
2001-10-22 |
Ericsson Telefon Ab L M |
Carrier for electronic components
|
US7049312B1
(en)
|
1999-06-03 |
2006-05-23 |
Abbott Gmbh & Co. Kg |
Benzothiazinone and benzoxazinone compounds
|
US6387894B1
(en)
|
1999-06-11 |
2002-05-14 |
Pfizer Inc. |
Use of CRF antagonists and renin-angiotensin system inhibitors
|
TWI262914B
(en)
|
1999-07-02 |
2006-10-01 |
Agouron Pharma |
Compounds and pharmaceutical compositions for inhibiting protein kinases
|
PE20010306A1
(en)
|
1999-07-02 |
2001-03-29 |
Agouron Pharma |
INDAZOLE COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM USEFUL FOR THE INHIBITION OF PROTEIN KINASE
|
EP1196186B1
(en)
|
1999-07-12 |
2007-10-31 |
Genentech, Inc. |
Promotion or inhibition of angiogenesis and cardiovascularization by tumor necrosis factor ligand/receptor homologs
|
GB9919588D0
(en)
|
1999-08-18 |
1999-10-20 |
Hoechst Schering Agrevo Gmbh |
Fungicidal compounds
|
EP3214175A1
(en)
|
1999-08-24 |
2017-09-06 |
E. R. Squibb & Sons, L.L.C. |
Human ctla-4 antibodies and their uses
|
US7605238B2
(en)
|
1999-08-24 |
2009-10-20 |
Medarex, Inc. |
Human CTLA-4 antibodies and their uses
|
ATE342257T1
(en)
|
1999-08-27 |
2006-11-15 |
Chemocentryx Inc |
HETEROCYCLIC COMPOUNDS AND METHODS FOR MODULATING CXCR3 FUNCTION
|
US20070021493A1
(en)
|
1999-09-16 |
2007-01-25 |
Curis, Inc. |
Mediators of hedgehog signaling pathways, compositions and uses related thereto
|
WO2001019800A2
(en)
|
1999-09-16 |
2001-03-22 |
Curis, Inc. |
Mediators of hedgehog signaling pathways, compositions and uses related thereto
|
US6921763B2
(en)
|
1999-09-17 |
2005-07-26 |
Abbott Laboratories |
Pyrazolopyrimidines as therapeutic agents
|
KR20020088406A
(en)
|
1999-09-17 |
2002-11-27 |
애보트 게엠베하 운트 콤파니 카게 |
Pyrazolopyrimidines as therapeutic agents
|
WO2001021160A2
(en)
|
1999-09-23 |
2001-03-29 |
Axxima Pharmaceuticals Aktiengesellschaft |
Carboxymide and aniline derivatives as selective inhibitors of pathogens
|
ATE277044T1
(en)
|
1999-10-06 |
2004-10-15 |
Boehringer Ingelheim Pharma |
HETEROCYCLIC COMPOUNDS USABLE AS TYROSINE KINASE INHIBITORS
|
US6506769B2
(en)
|
1999-10-06 |
2003-01-14 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Heterocyclic compounds useful as inhibitors of tyrosine kinases
|
US7087597B1
(en)
|
1999-10-12 |
2006-08-08 |
Takeda Pharmaceutical Company Limited |
Pyrimidine 5-carboxamide compounds, process for producing the same and use thereof
|
CA2386190C
(en)
|
1999-10-13 |
2009-04-14 |
Johns Hopkins University School Of Medicine |
Regulators of the hedgehog pathway, compositions and uses related thereto
|
ATE324876T1
(en)
|
1999-10-14 |
2006-06-15 |
Curis Inc |
AGENTS OF ßHEDGEHOGß TRANSMITTING RAILWAYS, ASSOCIATED INTERLINGS AND USE
|
US6472153B1
(en)
|
1999-10-26 |
2002-10-29 |
Epoch Biosciences, Inc. |
Hybridization-triggered fluorescent detection of nucleic acids
|
EP1095933A1
(en)
|
1999-10-30 |
2001-05-02 |
Aventis Pharma Deutschland GmbH |
Novel N-guanidinoalkylamides, their preparation, their use, and pharmaceutical preparations comprising them
|
US6660845B1
(en)
|
1999-11-23 |
2003-12-09 |
Epoch Biosciences, Inc. |
Non-aggregating, non-quenching oligomers comprising nucleotide analogues; methods of synthesis and use thereof
|
IL133809A0
(en)
|
1999-12-30 |
2001-04-30 |
Yeda Res & Dev |
Steroidal alkaloids and pharmaceutical compositions comprising them
|
GB0002032D0
(en)
|
2000-01-28 |
2000-03-22 |
Zeneca Ltd |
Chemical compounds
|
US7217722B2
(en)
|
2000-02-01 |
2007-05-15 |
Kirin Beer Kabushiki Kaisha |
Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same
|
FR2804958B1
(en)
|
2000-02-15 |
2005-07-08 |
Hoechst Marion Roussel Inc |
XANTHINE DERIVATIVES, PREPARATION METHOD AND INTERMEDIATES THEREOF, THEIR APPLICATION AS MEDICAMENT AND PHARMACEUTICAL COMPOSITIONS COMPRISING THE SAME
|
JP4808895B2
(en)
|
2000-03-30 |
2011-11-02 |
キュリス,インコーポレイテッド |
Small organic molecular regulator of cell proliferation
|
US7115653B2
(en)
|
2000-03-30 |
2006-10-03 |
Curis, Inc. |
Small organic molecule regulators of cell proliferation
|
US6613798B1
(en)
|
2000-03-30 |
2003-09-02 |
Curis, Inc. |
Small organic molecule regulators of cell proliferation
|
US20020127625A1
(en)
|
2000-03-31 |
2002-09-12 |
Forskarpatent Is Syd Ab |
Methods of diagnosing immune related diseases
|
US6667300B2
(en)
|
2000-04-25 |
2003-12-23 |
Icos Corporation |
Inhibitors of human phosphatidylinositol 3-kinase delta
|
SI2223922T1
(en)
|
2000-04-25 |
2016-04-29 |
Icos Corporation |
Inhibitors of human phosphatidyl-inositol 3-kinase delta
|
EP1289472A4
(en)
|
2000-05-30 |
2004-09-08 |
Advanced Res & Tech Inst |
Compositions and methods for identifying agents which modulate pten function and pi-3 kinase pathways
|
US6667398B2
(en)
|
2000-06-22 |
2003-12-23 |
Pfizer Inc |
Process for the preparation of pyrazolopyrimidinones
|
EP1294713A2
(en)
|
2000-06-27 |
2003-03-26 |
Genelabs Technologies, Inc. |
Compounds possessing antibacterial, antifungal or antitumor activity
|
US6534691B2
(en)
|
2000-07-18 |
2003-03-18 |
E. I. Du Pont De Nemours And Company |
Manufacturing process for α-olefins
|
AU2001292320A1
(en)
|
2000-10-02 |
2002-04-15 |
Tanabe Seiyaku Co., Ltd. |
Benzylamine compound, process for producing the same, and intermediate therefor
|
ATE431355T1
(en)
|
2000-10-11 |
2009-05-15 |
Applera Corp |
FLUORESCENT NUCLEOBASECONJUGATES WITH ANIONIC LINKERS
|
AU2002213467A1
(en)
|
2000-10-11 |
2002-04-22 |
Chemocentryx, Inc. |
Modulation of ccr4 function
|
FR2815346B1
(en)
|
2000-10-13 |
2004-02-20 |
Servier Lab |
NOVEL AMINOTRIAZOLONE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME
|
JP2002131859A
(en)
|
2000-10-19 |
2002-05-09 |
Konica Corp |
Infrared sensitive silver halide photographic sensitive material for photographing and infrared sensitive silver halide emulsion
|
US6890747B2
(en)
|
2000-10-23 |
2005-05-10 |
Warner-Lambert Company |
Phosphoinositide 3-kinases
|
AU2001297717B2
(en)
|
2000-12-11 |
2006-02-23 |
Amgen Inc. |
CXCR3 antagonists
|
IL156064A0
(en)
|
2000-12-28 |
2003-12-23 |
Daiichi Seiyaku Co |
Vla-4 inhibitors
|
EP1353674A1
(en)
|
2000-12-29 |
2003-10-22 |
Alteon, Inc. |
Method for treating glaucoma ivb
|
EP1359911A2
(en)
|
2000-12-29 |
2003-11-12 |
Alteon, Inc. |
Method for treating fibrotic diseases or other indications ivc
|
US7105499B2
(en)
|
2001-01-22 |
2006-09-12 |
Merck & Co., Inc. |
Nucleoside derivatives as inhibitors of RNA-dependent RNA viral polymerase
|
EP1539188B1
(en)
|
2001-01-22 |
2015-01-07 |
Merck Sharp & Dohme Corp. |
Nucleoside derivatives as inhibitors of rna-dependent rna viral polymerase
|
GB0102239D0
(en)
|
2001-01-29 |
2001-03-14 |
Cancer Res Ventures Ltd |
Methods of chemical synthisis
|
PA8539501A1
(en)
|
2001-02-14 |
2002-09-30 |
Warner Lambert Co |
TRIAZOLO COMPOUNDS AS MMP INHIBITORS
|
PA8539401A1
(en)
|
2001-02-14 |
2002-10-28 |
Warner Lambert Co |
QUINAZOLINAS AS INHIBITORS OF MMP-13
|
MXPA03008560A
(en)
|
2001-03-22 |
2004-06-30 |
Abbot Gmbh & Co Kg |
Single-stage pfc + ballast control circuit/general purpose power converter.
|
US7250569B2
(en)
|
2001-04-26 |
2007-07-31 |
New York University School Of Medicine |
Method for dissolving nanostructural materials
|
ATE355278T1
(en)
|
2001-05-08 |
2006-03-15 |
Kudos Pharm Ltd |
ISOQUINOLINONE DERIVATIVES AS PARP INHIBITORS
|
NZ518726A
(en)
|
2001-05-09 |
2004-06-25 |
Warner Lambert Co |
Method of treating or inhibiting neutrophil chemotaxis by administering a mek inhibitor
|
WO2002094264A1
(en)
|
2001-05-23 |
2002-11-28 |
Tularik Inc. |
Ccr4 antagonists
|
CA2450625A1
(en)
|
2001-06-13 |
2002-12-19 |
Genesoft Pharmaceuticals, Inc. |
Isoquinoline compounds having antiinfective activity
|
WO2002101007A2
(en)
|
2001-06-13 |
2002-12-19 |
Genesoft Pharmaceuticals, Inc |
Antipathogenic benzamide compounds
|
US6825228B2
(en)
|
2001-06-13 |
2004-11-30 |
Genesoft Pharmaceuticals, Inc. |
Benzothiophene compounds having antiinfective activity
|
US20030114467A1
(en)
|
2001-06-21 |
2003-06-19 |
Shakespeare William C. |
Novel pyrazolo- and pyrrolo-pyrimidines and uses thereof
|
DE10134721A1
(en)
|
2001-07-17 |
2003-02-06 |
Bayer Ag |
tetrahydroquinoxalines
|
US8354397B2
(en)
|
2001-07-27 |
2013-01-15 |
Curis, Inc. |
Mediators of hedgehog signaling pathways, compositions and uses related thereto
|
WO2003011285A1
(en)
|
2001-08-01 |
2003-02-13 |
Merck & Co., Inc. |
BENZIMIDAZO[4,5-f]ISOQUINOLINONE DERIVATIVES
|
AU2002327422A1
(en)
|
2001-08-03 |
2003-03-18 |
Abbott Laboratories |
Method of identifying inhibitors of lck
|
DK3042894T1
(en)
|
2001-08-10 |
2016-11-07 |
Shionogi & Co |
ANTIVIRAL AGENT
|
JP2003073357A
(en)
|
2001-09-03 |
2003-03-12 |
Mitsubishi Pharma Corp |
Rho KINASE INHIBITOR COMPRISING AMIDE COMPOUND
|
WO2004043335A2
(en)
|
2001-09-13 |
2004-05-27 |
Genesoft, Inc. |
Methods of treating infection by drug resistant bacteria
|
US7101884B2
(en)
|
2001-09-14 |
2006-09-05 |
Merck & Co., Inc. |
Tyrosine kinase inhibitors
|
US8124625B2
(en)
|
2001-09-14 |
2012-02-28 |
Shionogi & Co., Ltd. |
Method of enhancing the expression of apolipoprotein AI using olefin derivatives
|
AUPR769501A0
(en)
|
2001-09-14 |
2001-10-11 |
Biomolecular Research Institute Limited |
Cytokine receptor 1
|
US7269663B2
(en)
|
2001-09-28 |
2007-09-11 |
Intel Corporation |
Tagging packets with a lookup key to facilitate usage of a unified packet forwarding cache
|
TWI330183B
(en)
|
2001-10-22 |
2010-09-11 |
Eisai R&D Man Co Ltd |
|
NZ531853A
(en)
|
2001-11-01 |
2006-02-24 |
Janssen Pharmaceutica Nv |
Heteroaryl amines as glycogen synthase kinase 3beta inhibitors (gsk3 inhibitors)
|
CA2464419A1
(en)
|
2001-11-09 |
2003-05-22 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Benzimidazoles useful as protein kinase inhibitors
|
US20030113828A1
(en)
|
2001-11-09 |
2003-06-19 |
Ginsberg Mark H. |
Compositions and methods for modulating Syk function
|
EP1456652A4
(en)
|
2001-11-13 |
2005-11-02 |
Dana Farber Cancer Inst Inc |
Agents that modulate immune cell activation and methods of use thereof
|
DE10159269A1
(en)
|
2001-12-03 |
2003-06-18 |
Bayer Ag |
Arylation of olefins
|
DE10159270A1
(en)
|
2001-12-03 |
2003-06-12 |
Bayer Ag |
Process for the arylation of olefins
|
WO2003048081A2
(en)
|
2001-12-04 |
2003-06-12 |
Bristol-Myers Squibb Company |
Glycinamides as factor xa inhibitors
|
ES2421511T3
(en)
|
2001-12-21 |
2013-09-03 |
X Ceptor Therapeutics Inc |
LXR modulators
|
US20030158195A1
(en)
|
2001-12-21 |
2003-08-21 |
Cywin Charles L. |
1,6 naphthyridines useful as inhibitors of SYK kinase
|
JP4085237B2
(en)
|
2001-12-21 |
2008-05-14 |
日本電気株式会社 |
Mobile phone usage contract system and communication method
|
US7064218B2
(en)
|
2001-12-26 |
2006-06-20 |
Genelabs Technologies, Inc. |
Aromatic compounds and poly(oxyalkylene) containing aromatic compounds possessing antibacterial, antifungal or antitumor activity
|
US7414036B2
(en)
|
2002-01-25 |
2008-08-19 |
Muscagen Limited |
Compounds useful as A3 adenosine receptor agonists
|
US20040043959A1
(en)
|
2002-03-04 |
2004-03-04 |
Bloom Laura A. |
Combination therapies for treating methylthioadenosine phosphorylase deficient cells
|
WO2003082341A1
(en)
|
2002-03-22 |
2003-10-09 |
Cellular Genomics, Inc. |
AN IMPROVED FORMULATION OF CERTAIN PYRAZOLO[3,4-d] PYRIMIDINES AS KINASE MODULATORS
|
CA2480468C
(en)
|
2002-03-26 |
2012-03-13 |
Biofrontera Discovery Gmbh |
Fredericamycin derivatives
|
US7166293B2
(en)
|
2002-03-29 |
2007-01-23 |
Carlsbad Technology, Inc. |
Angiogenesis inhibitors
|
DE10217046A1
(en)
|
2002-04-17 |
2003-11-06 |
Bioleads Gmbh |
Fredericamycin derivatives
|
EP1496905B1
(en)
|
2002-04-22 |
2008-08-13 |
Johns Hopkins University School of Medicine |
Modulators of hedgehog signaling pathways, compositions and uses related thereto
|
WO2003090751A1
(en)
|
2002-04-26 |
2003-11-06 |
Pfizer Products Inc. |
Pyrimidine-2, 4, 6-trione metallo-proteinase inhibitors
|
US6794562B2
(en)
|
2002-05-01 |
2004-09-21 |
Stine Seed Farm, Inc. |
Soybean cultivar 0332143
|
US20050203110A1
(en)
|
2002-05-23 |
2005-09-15 |
Coleman Paul J. |
Mitotic kinesin inhibitors
|
AU2003236527A1
(en)
|
2002-06-14 |
2003-12-31 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
US7265111B2
(en)
|
2002-06-27 |
2007-09-04 |
Sanofi-Aventis Deutschland Gmbh |
Adenosine analogues and their use as pharmaceutical agents
|
MXPA05000130A
(en)
|
2002-06-27 |
2005-02-17 |
Novo Nordisk As |
Aryl carbonyl derivatives as therapeutic agents.
|
CN1678311A
(en)
|
2002-06-27 |
2005-10-05 |
诺沃挪第克公司 |
Aryl carbonyl derivatives as therapeutic agents
|
DE10230917A1
(en)
|
2002-07-09 |
2004-02-05 |
Bioleads Gmbh |
Fredericamycin derivatives
|
WO2004006906A2
(en)
|
2002-07-15 |
2004-01-22 |
Combinatorx, Incorporated |
Methods for the treatment of neoplasms
|
EP1394159A1
(en)
|
2002-08-13 |
2004-03-03 |
Warner-Lambert Company LLC |
New thiophene derivatives, process for their preparation and pharmaceutical compositions containing them
|
JP2006503008A
(en)
|
2002-08-13 |
2006-01-26 |
ワーナー−ランバート カンパニー リミティド ライアビリティー カンパニー |
4-Hydroxyquinoline derivatives as matrix metalloproteinase inhibitors
|
JP4646626B2
(en)
|
2002-08-16 |
2011-03-09 |
アストラゼネカ アクチボラグ |
Inhibition of phosphoinositide 3-kinase β
|
JP2005536553A
(en)
|
2002-08-21 |
2005-12-02 |
サイトキネティクス・インコーポレーテッド |
Compounds, compositions and methods
|
US20030139427A1
(en)
|
2002-08-23 |
2003-07-24 |
Osi Pharmaceuticals Inc. |
Bicyclic pyrimidinyl derivatives and methods of use thereof
|
WO2004020599A2
(en)
|
2002-08-29 |
2004-03-11 |
Curis, Inc. |
Hedgehog antagonists, methods and uses related thereto
|
GB0220319D0
(en)
|
2002-09-02 |
2002-10-09 |
Cancer Res Campaign Tech |
Enzyme activated self-immolative nitrogen mustard drugs
|
WO2004031177A1
(en)
|
2002-09-30 |
2004-04-15 |
Banyu Pharmaceutical Co., Ltd. |
2-aminobenzimidazole derivative
|
KR20110050745A
(en)
|
2002-10-03 |
2011-05-16 |
탈자진 인코포레이티드 |
Vasculostatic agents and methods of use thereof
|
US20050282814A1
(en)
|
2002-10-03 |
2005-12-22 |
Targegen, Inc. |
Vasculostatic agents and methods of use thereof
|
US20040146941A1
(en)
|
2002-11-04 |
2004-07-29 |
Biliang Zhang |
Chemical encoding technology for combinatorial synthesis
|
JP2004161716A
(en)
|
2002-11-15 |
2004-06-10 |
Takeda Chem Ind Ltd |
Jnk inhibitor
|
AU2003286251A1
(en)
|
2002-11-21 |
2004-06-15 |
Vicore Pharma Ab |
New bicyclic angiotensin ii agonists
|
EP1572660B1
(en)
|
2002-12-20 |
2011-01-26 |
X-Ceptor Therapeutics, Inc. |
Isoquinolinone derivatives and their use as therapeutic agents
|
WO2004056746A1
(en)
|
2002-12-23 |
2004-07-08 |
4Sc Ag |
Cycloalkene dicarboxylic acid compounds as anti-inflammatory, immunomodulatory and anti-proliferatory agents
|
ATE514713T1
(en)
|
2002-12-23 |
2011-07-15 |
Wyeth Llc |
ANTIBODIES TO PD-1 AND THEIR USE
|
US7365094B2
(en)
|
2002-12-23 |
2008-04-29 |
4Sc Ag |
Compounds as anti-inflammatory, immunomodulatory and anti-proliferatory agents
|
US7247736B2
(en)
|
2002-12-23 |
2007-07-24 |
4Sc Ag |
Method of identifying inhibitors of DHODH
|
FR2850022B1
(en)
|
2003-01-22 |
2006-09-08 |
Centre Nat Rech Scient |
NOVEL USE OF MIFEPRISTONE AND ITS DERIVATIVES AS MODULATORS OF THE HEDGEHOG PROTEIN SIGNALING PATH AND ITS APPLICATIONS
|
WO2004075917A1
(en)
|
2003-02-28 |
2004-09-10 |
Toudai Tlo, Ltd. |
Organ or tissue fibrosis inhibitor
|
EP1599441A1
(en)
|
2003-03-06 |
2005-11-30 |
DSM IP Assets B.V. |
Process for the preparation of an alpha-amino carbonyl compound
|
AR043633A1
(en)
|
2003-03-20 |
2005-08-03 |
Schering Corp |
CANABINOID RECEIVERS LINKS
|
US7550590B2
(en)
|
2003-03-25 |
2009-06-23 |
Takeda Pharmaceutical Company Limited |
Dipeptidyl peptidase inhibitors
|
GB0306907D0
(en)
|
2003-03-26 |
2003-04-30 |
Angiogene Pharm Ltd |
Boireductively-activated prodrugs
|
EP1644338A1
(en)
|
2003-04-01 |
2006-04-12 |
Aponetics AG |
2, 4, 6-trisubstituted pyrimidine derivatives useful for the treatment of neoplastic and autoimmune diseases
|
US7217794B2
(en)
|
2003-04-02 |
2007-05-15 |
Daiamed, Inc. |
Compounds and methods for treatment of thrombosis
|
WO2004089881A1
(en)
|
2003-04-14 |
2004-10-21 |
Astrazeneca Ab |
New sulfonyl derivatives of aminonaphtols
|
EP1479675A1
(en)
|
2003-05-19 |
2004-11-24 |
Aventis Pharma Deutschland GmbH |
Indazole-derivatives as factor Xa inhibitors
|
US7317027B2
(en)
|
2003-05-19 |
2008-01-08 |
Sanofi-Aventis Deutschland Gmbh |
Azaindole-derivatives as factor Xa inhibitors
|
US7223780B2
(en)
|
2003-05-19 |
2007-05-29 |
Sanofi-Aventis Deutschland Gmbh |
Triazole-derivatives as blood clotting enzyme factor Xa inhibitors
|
BRPI0410785A
(en)
|
2003-05-23 |
2006-06-20 |
Wyeth Corp |
isolated nucleic acid molecule, host cell, non-human transgenic animal, isolated protein, antisense oligonucleotide, sirna molecule, isolated antibody, screening methods for test compounds capable of inhibiting, enhancing or mimicking gitrl interaction with gitr, to diagnose disease, to treat a patient at risk or diagnosed with a disease, to induce and to inhibit the proliferation of a cell population containing effector cells, to block the suppression and suppression of a cell population that includes t cells. effectors in the presence of cd4 + cd25 + regulatory t cells, and to treat a disease, pharmaceutical composition, and vaccine adjuvant
|
DE602004022819D1
(en)
|
2003-06-06 |
2009-10-08 |
Vertex Pharma |
TRANSPORTER OF ATP-BINDING CASSETTE
|
US7429596B2
(en)
|
2003-06-20 |
2008-09-30 |
The Regents Of The University Of California |
1H-pyrrolo [2,3-D] pyrimidine derivatives and methods of use thereof
|
WO2005002585A1
(en)
|
2003-07-02 |
2005-01-13 |
Warner-Lambert Company Llc |
Combination of an allosteric inhibitor of matrix metalloproteinase-13 and a ligand to an alpha-2-delta receptor
|
EP2371835A1
(en)
|
2003-07-03 |
2011-10-05 |
The Trustees Of The University Of Pennsylvania |
Inhibition of syk kinase expression
|
US20050048054A1
(en)
|
2003-07-11 |
2005-03-03 |
Shino Hanabuchi |
Lymphocytes; methods
|
US20080118493A1
(en)
|
2003-07-15 |
2008-05-22 |
Beachy Philip A |
Elevated Hedgehog Pathway Activity In Digestive System Tumors, And Methods Of Treating Digestive Sytem Tumors Having Elevated Hedgehog Pathway Activity
|
GB0317951D0
(en)
|
2003-07-31 |
2003-09-03 |
Trigen Ltd |
Compounds
|
US7208601B2
(en)
|
2003-08-08 |
2007-04-24 |
Mjalli Adnan M M |
Aryl and heteroaryl compounds, compositions, and methods of use
|
US7501538B2
(en)
|
2003-08-08 |
2009-03-10 |
Transtech Pharma, Inc. |
Aryl and heteroaryl compounds, compositions and methods of use
|
US20050054614A1
(en)
|
2003-08-14 |
2005-03-10 |
Diacovo Thomas G. |
Methods of inhibiting leukocyte accumulation
|
WO2005016348A1
(en)
|
2003-08-14 |
2005-02-24 |
Icos Corporation |
Method of inhibiting immune responses stimulated by an endogenous factor
|
AU2004264419B2
(en)
|
2003-08-15 |
2009-01-15 |
Irm Llc |
6-substituted anilino purines as RTK inhibitors
|
US7390820B2
(en)
|
2003-08-25 |
2008-06-24 |
Amgen Inc. |
Substituted quinolinone derivatives and methods of use
|
WO2005044181A2
(en)
|
2003-09-09 |
2005-05-19 |
Temple University-Of The Commonwealth System Of Higher Education |
Protection of tissues and cells from cytotoxic effects of ionizing radiation by abl inhibitors
|
GB0321710D0
(en)
|
2003-09-16 |
2003-10-15 |
Novartis Ag |
Organic compounds
|
GB0322409D0
(en)
|
2003-09-25 |
2003-10-29 |
Astrazeneca Ab |
Quinazoline derivatives
|
WO2005033288A2
(en)
|
2003-09-29 |
2005-04-14 |
The Johns Hopkins University |
Hedgehog pathway antagonists
|
WO2005032343A2
(en)
|
2003-10-01 |
2005-04-14 |
The Johns Hopkins University |
Hedgehog signaling in prostate regeneration neoplasia and metastasis
|
US20080057071A1
(en)
|
2003-10-20 |
2008-03-06 |
Watkins David N |
Use Of Hedgehog Pathway Inhibitors In Small-Cell Lung Cancer
|
EP1687002A4
(en)
|
2003-11-10 |
2008-07-23 |
Synta Pharmaceuticals Corp |
Fused heterocyclic compounds
|
WO2005049838A2
(en)
|
2003-11-14 |
2005-06-02 |
Yale University |
Syk-targeted nucleic acid interference
|
WO2005047289A1
(en)
|
2003-11-17 |
2005-05-26 |
Pfizer Products Inc. |
Pyrrolopyrimidine compounds useful in treatment of cancer
|
EP1689719A1
(en)
|
2003-11-25 |
2006-08-16 |
Eli Lilly And Company |
7-phenyl-isoquinoline-5-sulfonylamino derivatives as inhibitors of akt (proteinkinase b)
|
JP2007518399A
(en)
|
2003-12-02 |
2007-07-12 |
ジェンザイム コーポレイション |
Compositions and methods for diagnosing and treating lung cancer
|
US7439254B2
(en)
|
2003-12-08 |
2008-10-21 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
MXPA06007095A
(en)
|
2003-12-22 |
2006-09-04 |
Gilead Sciences Inc |
Kinase inhibitor phosphonate conjugates.
|
JP2007517052A
(en)
|
2003-12-23 |
2007-06-28 |
ノバルティス アクチエンゲゼルシャフト |
Bicyclic heterocyclic P-38 kinase inhibitor
|
WO2005067901A2
(en)
|
2004-01-08 |
2005-07-28 |
Michigan State University |
Methods for treating and preventing hypertension and hypertension-related disorders
|
US20050214310A1
(en)
|
2004-01-23 |
2005-09-29 |
Seattle Genetics, Inc. |
Melphalan prodrugs
|
EP1730148A4
(en)
|
2004-02-03 |
2009-08-19 |
Abbott Lab |
Aminobenzoxazoles as therapeutic agents
|
EP1717230B1
(en)
|
2004-02-13 |
2014-08-06 |
Msd K.K. |
Fused-ring 4-oxopyrimidine derivative
|
US20050187418A1
(en)
|
2004-02-19 |
2005-08-25 |
Small Brooke L. |
Olefin oligomerization
|
WO2005080394A1
(en)
|
2004-02-24 |
2005-09-01 |
Bioaxone Therapeutique Inc. |
4-substituted piperidine derivatives
|
EP1737865A1
(en)
|
2004-02-27 |
2007-01-03 |
F.Hoffmann-La Roche Ag |
Fused derivatives of pyrazole
|
EP1568698A1
(en)
|
2004-02-27 |
2005-08-31 |
Aventis Pharma Deutschland GmbH |
Pyrrole-derivatives as factor Xa inhibitors
|
EP1571154A1
(en)
|
2004-03-03 |
2005-09-07 |
Aventis Pharma Deutschland GmbH |
Beta-aminoacid-derivatives as factor Xa inhibitors
|
DK1740591T3
(en)
|
2004-04-02 |
2009-10-26 |
Osi Pharm Inc |
Heterobicyclic protein kinase inhibitors substituted with a 6,6-biocyclic ring
|
US8057815B2
(en)
|
2004-04-19 |
2011-11-15 |
Portola Pharmaceuticals, Inc. |
Methods of treatment with Syk inhibitors
|
GB0409799D0
(en)
|
2004-04-30 |
2004-06-09 |
Isis Innovation |
Method of generating improved immune response
|
BRPI0510305A
(en)
|
2004-04-30 |
2007-10-02 |
Takeda Pharmaceutical |
compound or a salt thereof, prodrug or a salt thereof, pharmaceutical agent, method of producing the compound or a salt thereof, matrix metalloproteinase inhibitor or a salt thereof or a prodrug thereof, method of inhibiting a metalloproteinase matrix, and use of a compound or salt thereof or a prodrug thereof
|
US8273743B2
(en)
|
2004-04-30 |
2012-09-25 |
Curis, Inc. |
Quinoxaline inhibitors of the hedgehog signalling
|
DE102004022897A1
(en)
|
2004-05-10 |
2005-12-08 |
Bayer Cropscience Ag |
Azinyl-imidazoazines
|
HUE030950T2
(en)
|
2004-05-13 |
2017-06-28 |
Icos Corp |
Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta
|
CA2566436C
(en)
|
2004-05-13 |
2011-05-10 |
Vanderbilt University |
Phosphoinositide 3-kinase delta selective inhibitors for inhibiting angiogenesis
|
CA2567883A1
(en)
|
2004-05-25 |
2005-12-15 |
Icos Corporation |
Methods for treating and/or preventing aberrant proliferation of hematopoietic cells
|
WO2006083289A2
(en)
|
2004-06-04 |
2006-08-10 |
Duke University |
Methods and compositions for enhancement of immunity by in vivo depletion of immunosuppressive cell activity
|
CN101123968A
(en)
|
2004-06-04 |
2008-02-13 |
艾科斯有限公司 |
Methods for treating mast cell disorders
|
GB0413605D0
(en)
|
2004-06-17 |
2004-07-21 |
Addex Pharmaceuticals Sa |
Novel compounds
|
US20060019967A1
(en)
|
2004-07-21 |
2006-01-26 |
Su-Ying Wu |
SARS CoV main protease inhibitors
|
WO2006015279A1
(en)
|
2004-07-28 |
2006-02-09 |
Neurogen Corporation |
Heterocyclic diamine compounds as ligands of the melanin concentrating hormone receptor useful for the treatment of obesity, diabetes, eating and sexual disorders
|
JP5204486B2
(en)
|
2004-08-27 |
2013-06-05 |
インフィニティ ファーマスーティカルズ、インク. |
Cyclopamine analogs and methods of use thereof
|
KR20140048343A
(en)
|
2004-09-02 |
2014-04-23 |
제넨테크, 인크. |
Pyridyl inhibitors of hedgehog signalling
|
GB0420722D0
(en)
|
2004-09-17 |
2004-10-20 |
Addex Pharmaceuticals Sa |
Novel allosteric modulators
|
WO2006038865A1
(en)
|
2004-10-01 |
2006-04-13 |
Betagenon Ab |
Nucleotide derivatives for the treatment of type 2 diabetes and other disorders
|
CA2583812A1
(en)
|
2004-10-28 |
2006-05-11 |
Irm Llc |
Compounds and compositions as hedgehog pathway modulators
|
US8212011B2
(en)
|
2004-11-03 |
2012-07-03 |
University Of Kansas |
Novobiocin analogues
|
US7622451B2
(en)
|
2004-11-03 |
2009-11-24 |
University Of Kansas |
Novobiocin analogues as neuroprotective agents and in the treatment of autoimmune disorders
|
US8212012B2
(en)
|
2004-11-03 |
2012-07-03 |
University Of Kansas |
Novobiocin analogues having modified sugar moieties
|
WO2006050501A2
(en)
|
2004-11-03 |
2006-05-11 |
University Of Kansas |
Novobiocin analogues as anticancer agents
|
GB0425035D0
(en)
|
2004-11-12 |
2004-12-15 |
Novartis Ag |
Organic compounds
|
US9512125B2
(en)
|
2004-11-19 |
2016-12-06 |
The Regents Of The University Of California |
Substituted pyrazolo[3.4-D] pyrimidines as anti-inflammatory agents
|
US8143257B2
(en)
|
2004-11-23 |
2012-03-27 |
Ptc Therapeutics, Inc. |
Substituted phenols as active agents inhibiting VEGF production
|
AU2005311251A1
(en)
|
2004-12-01 |
2006-06-08 |
Devgen Nv |
5-carboxamido substituted thiazole derivatives that interact with ion channels, in particular with ion channels from the Kv family
|
US20060156485A1
(en)
|
2005-01-14 |
2006-07-20 |
The Procter & Gamble Company |
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
|
GB0501999D0
(en)
|
2005-02-01 |
2005-03-09 |
Sentinel Oncology Ltd |
Pharmaceutical compounds
|
WO2006089106A2
(en)
|
2005-02-17 |
2006-08-24 |
Icos Corporation |
Phosphoinositide 3-kinase inhibitors for inhibiting leukocyte accumulation
|
WO2006091897A2
(en)
|
2005-02-25 |
2006-08-31 |
Adenosine Therapeutics, Llc |
Derivatives of 8-substituted xanthines
|
EP1854793A4
(en)
|
2005-02-28 |
2011-01-26 |
Japan Tobacco Inc |
NOVEL AMINOPYRIDINE COMPOUND WITH Syk INHIBITORY ACTIVITY
|
US20090124654A1
(en)
|
2005-03-01 |
2009-05-14 |
Mjalli Adnan M M |
Aryl and Heteroaryl Compounds, Compositions, Methods of Use
|
US7872050B2
(en)
|
2005-03-14 |
2011-01-18 |
Yaupon Therapeutics Inc. |
Stabilized compositions of volatile alkylating agents and methods of using thereof
|
DK1866339T3
(en)
|
2005-03-25 |
2013-09-02 |
Gitr Inc |
GTR-binding molecules and their applications
|
AU2006232109A1
(en)
|
2005-04-06 |
2006-10-12 |
Irm Llc |
Diarylamine-containing compounds and compositions, and their use as modulators of steroid hormone nuclear receptors
|
KR100781704B1
(en)
|
2005-04-20 |
2007-12-03 |
에스케이케미칼주식회사 |
Novel pyridine derivatives, process for preparing thereof and pharmaceutical compositions containing them
|
AU2006239677A1
(en)
|
2005-04-25 |
2006-11-02 |
Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic |
Use of compounds to enhance processivity of telomerase
|
NZ563193A
(en)
|
2005-05-09 |
2010-05-28 |
Ono Pharmaceutical Co |
Human monoclonal antibodies to programmed death 1(PD-1) and methods for treating cancer using anti-PD-1 antibodies alone or in combination with other immunotherapeutics
|
CN100526315C
(en)
|
2005-06-16 |
2009-08-12 |
浙江医药股份有限公司新昌制药厂 |
N2-quinoline or isoquinoline substituted purine derivative and its preparation method and uses
|
WO2007002667A2
(en)
|
2005-06-22 |
2007-01-04 |
Chemocentryx, Inc. |
Azaindazole compounds and methods of use
|
US7799795B2
(en)
|
2005-06-27 |
2010-09-21 |
Amgen Inc. |
Aryl nitrile compounds and compositions and their uses in treating inflammatory and related disorders
|
DK1907424T3
(en)
|
2005-07-01 |
2015-11-09 |
Squibb & Sons Llc |
HUMAN MONOCLONAL ANTIBODIES TO PROGRAMMED death ligand 1 (PD-L1)
|
JP2009500437A
(en)
|
2005-07-11 |
2009-01-08 |
デブジェン エヌブイ |
Amide derivatives as kinase inhibitors
|
JP2009505948A
(en)
|
2005-07-11 |
2009-02-12 |
デブジェン エヌブイ |
Amide derivatives as kinase inhibitors
|
WO2007029121A2
(en)
|
2005-07-21 |
2007-03-15 |
Galderma Research & Development |
Novel cyclopent-2-en-1-one derivatives which are ppar receptor modulators, and use thereof in pharmaceutical or cosmetic compositions
|
US20070017915A1
(en)
|
2005-07-22 |
2007-01-25 |
Weder Donald E |
Collapsible and/or erectable substantially egg-shaped container
|
CN101273038A
(en)
|
2005-07-29 |
2008-09-24 |
美迪维尔公司 |
Macrocylic inhibitors of hepatitis C virus
|
GB0516723D0
(en)
|
2005-08-15 |
2005-09-21 |
Novartis Ag |
Organic compounds
|
WO2007025090A2
(en)
|
2005-08-25 |
2007-03-01 |
Kalypsys, Inc. |
Heterobicyclic and - tricyclic inhibitors of mapk/erk kinase
|
JP2009506006A
(en)
|
2005-08-25 |
2009-02-12 |
エフ.ホフマン−ラ ロシュ アーゲー |
p38 MAP kinase inhibitor and method of using the same
|
WO2007025534A1
(en)
|
2005-09-01 |
2007-03-08 |
Bioagency Ag |
Fredericamycin derivatives
|
WO2007028022A2
(en)
|
2005-09-01 |
2007-03-08 |
Renovis, Inc. |
Novel compounds as p2x7 modulators and uses thereof
|
CA2624220A1
(en)
|
2005-09-29 |
2007-04-12 |
Wyeth |
1- (1h- indol- 1-yl) -3- (methylamino) -1- phenylpropan-2-ol derivatives and related compounds as modulators of the monoamine reuptake for the treatment of vasomotor symptoms (vms)
|
FR2892859B1
(en)
|
2005-10-27 |
2008-06-06 |
Commissariat Energie Atomique |
METHOD OF GRAFTING MOLECULES OF INTEREST ON INORGANIC SURFACES, SURFACES OBTAINED AND APPLICATIONS
|
EP1945202A2
(en)
|
2005-11-11 |
2008-07-23 |
Licentia OY |
Mammalian hedgehog signaling inhiabitors
|
US8101610B2
(en)
|
2005-11-14 |
2012-01-24 |
Genentech, Inc. |
Bisamide inhibitors of hedgehog signaling
|
EP1951724B1
(en)
|
2005-11-17 |
2011-04-27 |
OSI Pharmaceuticals, Inc. |
FUSED BICYCLIC mTOR INHIBITORS
|
US8642278B2
(en)
|
2005-11-22 |
2014-02-04 |
University Of South Florida |
Inhibition of cell proliferation
|
EP1954276A2
(en)
|
2005-11-22 |
2008-08-13 |
Merck & Co., Inc. |
Indole orexin receptor antagonists
|
US20080299113A1
(en)
|
2005-12-19 |
2008-12-04 |
Arnold Lee D |
Combined treatment with and composition of 6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitor and anti-cancer agents
|
US7572809B2
(en)
|
2005-12-19 |
2009-08-11 |
Hoffmann-La Roche Inc. |
Isoquinoline aminopyrazole derivatives
|
CA2635231C
(en)
|
2005-12-29 |
2014-07-15 |
Abbott Laboratories |
Protein kinase inhibitors
|
US8053603B2
(en)
|
2006-01-06 |
2011-11-08 |
Sunovion Pharmaceuticals Inc. |
Tetralone-based monoamine reuptake inhibitors
|
WO2007094912A2
(en)
|
2006-01-13 |
2007-08-23 |
University Of Kentucky |
Bis-quaternary ammonium salts and methods for modulating neuronal nicotinic acetylcholine receptors
|
WO2007133822A1
(en)
|
2006-01-19 |
2007-11-22 |
Genzyme Corporation |
Gitr antibodies for the treatment of cancer
|
WO2007089669A2
(en)
|
2006-01-26 |
2007-08-09 |
Wyeth |
Processes for the preparation of compounds which modulate cell proliferation
|
PE20071025A1
(en)
|
2006-01-31 |
2007-10-17 |
Mitsubishi Tanabe Pharma Corp |
TRISUSTITUTED AMINE COMPOUND
|
JP2009529047A
(en)
|
2006-03-07 |
2009-08-13 |
アレイ バイオファーマ、インコーポレイテッド |
Heterobicyclic pyrazole compounds and uses thereof
|
CN101405001A
(en)
|
2006-03-20 |
2009-04-08 |
霍夫曼-拉罗奇有限公司 |
Methods of inhibiting BTK and SYK protein kinases
|
TWI428448B
(en)
|
2006-03-24 |
2014-03-01 |
Syntonix Pharmaceuticals Inc |
Pc5 as a factor ix propeptide processing enzyme
|
US20100273776A1
(en)
|
2006-03-29 |
2010-10-28 |
FOLDRx PHARMACEUTICALS, INC |
Inhibition of alpha-synuclein toxicity
|
DK2004654T3
(en)
|
2006-04-04 |
2013-07-22 |
Univ California |
Pyrazolopyrimidine derivatives for use as kinase antagonists
|
EP2007757B1
(en)
|
2006-04-13 |
2012-10-03 |
Vertex Pharmceuticals Incorporated |
Thiophene-carboxamides useful as inhibitors of protein kinases
|
KR20090006089A
(en)
|
2006-04-14 |
2009-01-14 |
노파르티스 아게 |
Use of biarylcarboxamides in the treatment of hedgehog pathway-related disorders
|
WO2007121453A2
(en)
|
2006-04-17 |
2007-10-25 |
The Regents Of The University Of California |
2-hydroxy-1-oxo 1,2 dihydro isoquinoline chelating agents
|
GB0607950D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
GB0607948D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
ES2440317T3
(en)
|
2006-04-21 |
2014-01-28 |
Novartis Ag |
Purine derivatives for use as adenosine A2A receptor agonists
|
WO2007125315A2
(en)
|
2006-04-25 |
2007-11-08 |
Astex Therapeutics Limited |
Pharmaceutical compounds
|
US20090082370A1
(en)
|
2006-04-25 |
2009-03-26 |
Neil Thomas Thompson |
Pharmaceutical Combinations of PK Inhibitors and Other Active Agents
|
DE102006020327A1
(en)
|
2006-04-27 |
2007-12-27 |
Bayer Healthcare Ag |
Heterocyclic substituted, fused pyrazole derivatives and their use
|
UA93548C2
(en)
|
2006-05-05 |
2011-02-25 |
Айерем Елелсі |
Compounds and compositions as hedgehog pathway modulators
|
US20090306214A1
(en)
|
2006-05-09 |
2009-12-10 |
Eliahu Kaplan |
Use of Syk Tyrosine Kinase Inhibitors for the Treatment of Cell Proliferative Disorders
|
WO2007135398A1
(en)
|
2006-05-22 |
2007-11-29 |
Astrazeneca Ab |
Indole derivatives
|
GB0610242D0
(en)
|
2006-05-23 |
2006-07-05 |
Novartis Ag |
Organic compounds
|
GB0610317D0
(en)
|
2006-05-24 |
2006-07-05 |
Medical Res Council |
Antiparasitic compounds and compositions
|
EP1859772B1
(en)
|
2006-05-24 |
2010-12-15 |
Guardant S.r.l. |
Alkalized local anesthetic in bag
|
EP2079724B1
(en)
|
2006-07-20 |
2010-05-26 |
Amgen Inc. |
Substituted pyridone compounds and methods of use
|
CA2657200A1
(en)
|
2006-07-28 |
2008-01-31 |
Novartis Ag |
2,4-substituted quinazolines as lipid kinase inhibitors
|
US20100216791A1
(en)
|
2006-08-17 |
2010-08-26 |
Astrazeneca |
Pyridinylquinazolinamine derivatives and their use as b-raf inhibitors
|
WO2008023357A1
(en)
|
2006-08-22 |
2008-02-28 |
Technion Research And Development Foundation Ltd. |
Heterocyclic derivatives binding to the peripheral-type benzodiazepine receptor (pbr)
|
EP2069325A2
(en)
|
2006-08-24 |
2009-06-17 |
Serenex, Inc. |
Isoquinoline, quinazoline and phthalazine derivatives
|
WO2008025755A1
(en)
|
2006-09-01 |
2008-03-06 |
Basf Se |
Use of n-containing heterocycles in dermocosmetics
|
PT2061765E
(en)
|
2006-09-01 |
2015-02-06 |
Senhwa Biosciences Inc |
Serine-threonine protein kinase and parp modulators
|
EP1903044A1
(en)
|
2006-09-14 |
2008-03-26 |
Novartis AG |
Adenosine Derivatives as A2A Receptor Agonists
|
AU2007357448B2
(en)
|
2006-09-18 |
2012-09-06 |
Compugen Ltd |
Bioactive peptides and method of using same
|
JP5306818B2
(en)
|
2006-10-18 |
2013-10-02 |
武田薬品工業株式会社 |
Fused heterocyclic compounds
|
SG178743A1
(en)
|
2006-10-31 |
2012-03-29 |
Us Gov Health & Human Serv |
Smoothened polypeptides and methods of use
|
US7772180B2
(en)
|
2006-11-09 |
2010-08-10 |
Bristol-Myers Squibb Company |
Hepatitis C virus inhibitors
|
KR20090087027A
(en)
|
2006-11-13 |
2009-08-14 |
일라이 릴리 앤드 캄파니 |
Thienopyrimidinones for treatment of inflammatory disorders and cancers
|
WO2008063625A2
(en)
|
2006-11-20 |
2008-05-29 |
Adolor Corporation |
Pyridine compounds and methods of their use
|
EA015677B1
(en)
|
2006-11-20 |
2011-10-31 |
Новартис Аг |
SALTS AND CRYSTAL FORMS OF 2-METHYL-2-[4-(3-METHYL-2-OXO-8-QUINOLIN-3-YL-2,3-DIHYDROIMIDAZO[4,5-c]QUINOLIN-1-YL)PHENYL]PROPIONITRILE
|
BRPI0720131A2
(en)
|
2006-12-06 |
2014-02-04 |
Boehringer Ingelheim Int |
MIMETIC GLYCORTICOIDS, METHODS FOR MAKING THEM, PHARMACEUTICAL COMPOSITIONS AND USES OF THE SAME.
|
MX2009006397A
(en)
|
2006-12-14 |
2009-08-13 |
Daiichi Sankyo Co Ltd |
Imidazothiazole derivatives.
|
WO2008082487A2
(en)
|
2006-12-20 |
2008-07-10 |
Schering Corporation |
Novel jnk inhibitors
|
CN101600711A
(en)
|
2006-12-22 |
2009-12-09 |
工业研究有限公司 |
The azetidine analogues of nucleosidase and phosphorglase inhibitor
|
TWI433674B
(en)
|
2006-12-28 |
2014-04-11 |
Infinity Discovery Inc |
Cyclopamine analogs
|
CN101622001A
(en)
|
2007-01-26 |
2010-01-06 |
Irm责任有限公司 |
The purine compound and the compositions that are used for the treatment of plasmodium related diseases as inhibitors of kinases
|
US20080200461A1
(en)
|
2007-02-20 |
2008-08-21 |
Cropsolution, Inc. |
Modulators of acetyl-coenzyme a carboxylase and methods of use thereof
|
WO2008109829A1
(en)
|
2007-03-07 |
2008-09-12 |
Infinity Pharmaceuticals, Inc. |
Cyclopamine lactam analogs and methods of use thereof
|
JP2010520295A
(en)
|
2007-03-07 |
2010-06-10 |
インフィニティ・ディスカバリー・インコーポレイテッド |
Heterocyclic cyclopamine analogues and methods of use
|
US8586619B2
(en)
|
2007-03-12 |
2013-11-19 |
Vm Therapeutics Llc |
Agents of calcium ion channel modulators
|
BRPI0808772A2
(en)
|
2007-03-14 |
2014-08-12 |
Exelixis Inc |
HEDGEHOG INHIBITORS
|
PE20090188A1
(en)
|
2007-03-15 |
2009-03-20 |
Novartis Ag |
HETEROCYCLIC COMPOUNDS AS MODULATORS OF THE HEDGEHOG PATH
|
EP2132207A2
(en)
|
2007-03-23 |
2009-12-16 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
HUE028954T2
(en)
|
2007-03-23 |
2017-01-30 |
Amgen Inc |
Heterocyclic compounds and their uses
|
AU2008231385B2
(en)
|
2007-03-23 |
2012-02-02 |
Amgen Inc. |
Delta3- substituted quinoline or quinoxaline derivatives and their use as phosphatidylinositol 3-kinase ( PI3K) inhibitors
|
WO2008117050A1
(en)
|
2007-03-27 |
2008-10-02 |
Astrazeneca Ab |
Pyrazolyl-amino-substituted pyrazines and their use for the treatment of cancer
|
WO2008156513A2
(en)
|
2007-03-29 |
2008-12-24 |
University Of Connecticut |
Methods to protect skeletal muscle against injury
|
CN101636397B
(en)
|
2007-04-13 |
2012-06-13 |
中国人民解放军军事医学科学院毒物药物研究所 |
Urea compounds, preparation methods and pharmaceutical uses thereof
|
AU2008238379A1
(en)
|
2007-04-13 |
2008-10-23 |
Sanofi-Aventis |
A transition metal catalyzed synthesis of N-aminoindoles
|
US20090054517A1
(en)
|
2007-04-20 |
2009-02-26 |
Lubahn Dennis B |
Phytoestrogens As Regulators Of Hedgehog Signaling And Methods Of Their Use In Cancer Treatment
|
JP2010163361A
(en)
|
2007-04-27 |
2010-07-29 |
Dainippon Sumitomo Pharma Co Ltd |
Quinoline derivative
|
US7960353B2
(en)
|
2007-05-10 |
2011-06-14 |
University Of Kansas |
Novobiocin analogues as neuroprotective agents and in the treatment of autoimmune disorders
|
US20090214529A9
(en)
|
2007-05-22 |
2009-08-27 |
Taigen Biotechnology Co., Ltd. |
Kinesin inhibitors
|
US9603848B2
(en)
|
2007-06-08 |
2017-03-28 |
Senomyx, Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
US7928111B2
(en)
|
2007-06-08 |
2011-04-19 |
Senomyx, Inc. |
Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
|
US8557823B2
(en)
|
2007-06-18 |
2013-10-15 |
Advanced Cancer Therapeutics, Llc |
Family of PFKFB3 inhibitors with anti-neoplastic activities
|
WO2008156783A2
(en)
|
2007-06-18 |
2008-12-24 |
University Of Louisville Research Foundation, Inc. |
Family of pfkfb3 inhibitors with anti-neoplastic activities
|
EP2170959B1
(en)
|
2007-06-18 |
2013-10-02 |
Merck Sharp & Dohme B.V. |
Antibodies to human programmed death receptor pd-1
|
CA2692128A1
(en)
|
2007-06-21 |
2008-12-31 |
Amgen Inc. |
Process for making substituted 2-amino-thiazolones
|
KR20100033484A
(en)
|
2007-06-26 |
2010-03-30 |
사노피-아벤티스 |
A regioselective metal catalyzed synthesis of annelated benzimidazoles and azabenzimidazoles
|
US8685962B2
(en)
|
2007-07-02 |
2014-04-01 |
Technion Research & Development Foundation Limited |
Compositions, articles and methods comprising TSPO ligands for preventing or reducing tobacco-associated damage
|
US20090012031A1
(en)
|
2007-07-03 |
2009-01-08 |
The Regents Of The University Of Michigan |
EZH2 Cancer Markers
|
CN101801413A
(en)
|
2007-07-12 |
2010-08-11 |
托勒克斯股份有限公司 |
Combination therapies employing GITR binding molecules
|
RU2345996C1
(en)
|
2007-07-17 |
2009-02-10 |
Андрей Александрович Иващенко |
Annelated azaheterocyclic amides, which include pyrimidine fragment, method of obtaining and their application
|
JP4834699B2
(en)
|
2007-07-30 |
2011-12-14 |
田辺三菱製薬株式会社 |
Pharmaceutical composition
|
JP4846769B2
(en)
|
2007-07-30 |
2011-12-28 |
田辺三菱製薬株式会社 |
Pharmaceutical composition
|
CA2696113A1
(en)
|
2007-08-10 |
2009-04-02 |
Burnham Institute For Medical Research |
Tissue-nonspecific alkaline phosphatase (tnap) activators and uses thereof
|
MX2010001784A
(en)
|
2007-08-13 |
2010-03-15 |
Metabasis Therapeutics Inc |
Novel activators of glucokinase.
|
WO2009029617A1
(en)
|
2007-08-27 |
2009-03-05 |
Kalypsys, Inc. |
Diarylamine-substituted quinolones useful as inducible nitric oxide synthase inhibitors
|
JP5227965B2
(en)
|
2007-10-03 |
2013-07-03 |
独立行政法人理化学研究所 |
Nitrotriazole derivative and method for producing compound using the same
|
EP2217234A2
(en)
|
2007-10-15 |
2010-08-18 |
AstraZeneca AB |
Combinations of mek inhibitors with mtor inhibitors
|
GEP20125635B
(en)
|
2007-11-13 |
2012-09-10 |
Icos Corp |
Inhibitors of human phosphatidyl-inositol 3-kinase delta
|
AU2008338963A1
(en)
|
2007-12-13 |
2009-06-25 |
Sri International |
PPAR-delta ligands and methods of their use
|
CN101896472A
(en)
|
2007-12-13 |
2010-11-24 |
锡耶纳生物技术股份公司 |
HEDGEHOG pathway antagonists and treatment thereof are used
|
US8399483B2
(en)
|
2007-12-21 |
2013-03-19 |
Ucb Pharma S.A. |
Quinoxaline and quinoline derivatives as kinase inhibitors
|
US7960397B2
(en)
|
2007-12-28 |
2011-06-14 |
Institute Of Experimental Botany, Academy Of Sciences Of The Czech Republic |
6,9-disubstituted purine derivatives and their use as cosmetics and cosmetic compositions
|
US8703777B2
(en)
|
2008-01-04 |
2014-04-22 |
Intellikine Llc |
Certain chemical entities, compositions and methods
|
US8193182B2
(en)
|
2008-01-04 |
2012-06-05 |
Intellikine, Inc. |
Substituted isoquinolin-1(2H)-ones, and methods of use thereof
|
EA201001135A1
(en)
|
2008-01-09 |
2011-02-28 |
ПиДжиИксХЭЛС ЭлЭлСи |
INTRATECAL TREATMENT OF NEUROPATHIC PAIN BY AR AGONISTS
|
EP2228350A4
(en)
|
2008-01-10 |
2010-12-29 |
Asahi Glass Co Ltd |
Glass, coating material for light-emitting device, and light-emitting device
|
WO2009089598A2
(en)
|
2008-01-18 |
2009-07-23 |
Katholieke Universiteit Leuven |
Msmb-gene methylation based diagnosis, staging and prognosis of prostate cancer
|
KR20100117105A
(en)
|
2008-02-07 |
2010-11-02 |
질레드 팔로 알토 인코포레이티드 |
Abca-1 elevating compounds and the use thereof
|
WO2009100406A2
(en)
|
2008-02-07 |
2009-08-13 |
Synta Pharmaceuticals Corp. |
Topical formulations for the treatment of psoriasis
|
CN101970499B
(en)
|
2008-02-11 |
2014-12-31 |
治疗科技公司 |
Monoclonal antibodies for tumor treatment
|
WO2009103022A1
(en)
|
2008-02-13 |
2009-08-20 |
Itherx Pharmaceuticals, Inc. |
Derivatives of substituted fused ring cycloindoles and methods of their use
|
TWI444384B
(en)
|
2008-02-20 |
2014-07-11 |
Gilead Sciences Inc |
Nucleotide analogues and their use in the treatment of malignancies
|
US8673970B2
(en)
|
2008-02-21 |
2014-03-18 |
Sequoia Pharmaceuticals, Inc. |
HIV protease inhibitor and cytochrome p450 inhibitor combinations
|
US8168757B2
(en)
|
2008-03-12 |
2012-05-01 |
Merck Sharp & Dohme Corp. |
PD-1 binding proteins
|
WO2009114874A2
(en)
|
2008-03-14 |
2009-09-17 |
Intellikine, Inc. |
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
|
WO2009117157A1
(en)
|
2008-03-20 |
2009-09-24 |
Amgen Inc. |
Aurora kinase modulators and method of use
|
WO2009118765A2
(en)
|
2008-03-28 |
2009-10-01 |
Panacea Biotec Limited |
Novel monoamine re-uptake inhibitor
|
FR2929851B1
(en)
|
2008-04-09 |
2012-11-30 |
Centre Nat Rech Scient |
MOLECULES INHIBITING A METABOLIC PATHWAY INVOLVING THE TYROSINE KINASE SYK PROTEIN AND METHOD OF IDENTIFYING SAID MOLECULES
|
NZ589315A
(en)
|
2008-04-16 |
2012-11-30 |
Portola Pharm Inc |
2,6-diamino-pyrimidin-5-yl-carboxamides as Spleen tryosine kinase (syk) or Janus kinase (JAK) inhibitors
|
WO2009146406A1
(en)
|
2008-05-30 |
2009-12-03 |
Genentech, Inc. |
Purine pi3k inhibitor compounds and methods of use
|
US20090312406A1
(en)
|
2008-06-12 |
2009-12-17 |
Hsing-Pang Hsieh |
Coumarin compounds and their use for treating viral infection
|
BRPI0915177A2
(en)
|
2008-06-20 |
2016-04-26 |
Amgen Inc |
process for making substituted 2-amino thiazolones
|
CN102203258A
(en)
|
2008-07-02 |
2011-09-28 |
新兴产品开发西雅图有限公司 |
TGF-b antagonist multi-target binding proteins
|
AU2009268611B2
(en)
|
2008-07-08 |
2015-04-09 |
Intellikine, Llc |
Kinase inhibitors and methods of use
|
US20110224223A1
(en)
|
2008-07-08 |
2011-09-15 |
The Regents Of The University Of California, A California Corporation |
MTOR Modulators and Uses Thereof
|
EP2328897A1
(en)
|
2008-07-16 |
2011-06-08 |
Schering Corporation |
Bicyclic heterocycle derivatives and their use as gpcr modulators
|
US8450344B2
(en)
|
2008-07-25 |
2013-05-28 |
Aerie Pharmaceuticals, Inc. |
Beta- and gamma-amino-isoquinoline amide compounds and substituted benzamide compounds
|
US9284297B2
(en)
|
2008-08-11 |
2016-03-15 |
President And Fellows Of Harvard College |
Halofuginone analogs for inhibition of tRNA synthetases and uses thereof
|
AR072999A1
(en)
|
2008-08-11 |
2010-10-06 |
Medarex Inc |
HUMAN ANTIBODIES THAT JOIN GEN 3 OF LYMPHOCYTARY ACTIVATION (LAG-3) AND THE USES OF THESE
|
US20110190157A1
(en)
|
2008-08-15 |
2011-08-04 |
The Regents Of The University Of California |
Biomarkers for Diagnosis and Treatment of Chronic Lymphocytic Leukemia
|
SI2350129T1
(en)
|
2008-08-25 |
2015-11-30 |
Amplimmune, Inc. |
Compositions of pd-1 antagonists and methods of use
|
KR20110092267A
(en)
|
2008-09-10 |
2011-08-17 |
칼립시스, 인코포레이티드 |
Aminopyrimidine inhibitors of histamine receptors for the treatment of disease
|
WO2010030002A1
(en)
|
2008-09-12 |
2010-03-18 |
国立大学法人三重大学 |
Cell capable of expressing exogenous gitr ligand
|
EP2344481B9
(en)
|
2008-09-23 |
2014-12-31 |
Georgetown University |
Viral and fungal inhibitors
|
JP5731978B2
(en)
|
2008-09-26 |
2015-06-10 |
インテリカイン, エルエルシー |
Heterocyclic kinase inhibitor
|
CA2998281C
(en)
|
2008-09-26 |
2022-08-16 |
Dana-Farber Cancer Institute, Inc. |
Human anti-pd-1 antobodies and uses therefor
|
EP2177510A1
(en)
|
2008-10-17 |
2010-04-21 |
Universität des Saarlandes |
Allosteric protein kinase modulators
|
WO2010051550A1
(en)
|
2008-10-31 |
2010-05-06 |
University Of Rochester |
Methods of diagnosing and treating fibrosis
|
US8476282B2
(en)
|
2008-11-03 |
2013-07-02 |
Intellikine Llc |
Benzoxazole kinase inhibitors and methods of use
|
WO2010053998A1
(en)
|
2008-11-05 |
2010-05-14 |
Xenon Pharmaceuticals, Inc. |
Spiro-condensed indole derivatives as sodium channel inhibitors
|
CA3092449A1
(en)
|
2008-11-13 |
2010-05-20 |
Gilead Calistoga Llc |
Therapies for hematologic malignancies
|
WO2010059593A1
(en)
|
2008-11-18 |
2010-05-27 |
Intellikine, Inc. |
Methods and compositions for treatment of ophthalmic conditions
|
WO2010065923A2
(en)
|
2008-12-04 |
2010-06-10 |
The United States Of America, As Represented By The Secretary, Department Of Health And Human Services |
Phosphatidylinositol-3-kinase p110 delta-targeted drugs in the treatment of cns disorders
|
US8450321B2
(en)
|
2008-12-08 |
2013-05-28 |
Gilead Connecticut, Inc. |
6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor
|
CN102307581B
(en)
|
2008-12-08 |
2016-08-17 |
吉利德康涅狄格股份有限公司 |
Imidazopyrazine SYK inhibitors
|
CN108997498A
(en)
|
2008-12-09 |
2018-12-14 |
霍夫曼-拉罗奇有限公司 |
Anti- PD-L1 antibody and they be used to enhance the purposes of T cell function
|
EA020548B1
(en)
|
2008-12-19 |
2014-12-30 |
Бёрингер Ингельхайм Интернациональ Гмбх |
Cyclic pyrimidin-4-carboxamides as ccr2 receptor antagonists for treatment of inflammation, asthma and copd
|
US20110135655A1
(en)
|
2009-01-13 |
2011-06-09 |
PHILADELPHIA HEALTH AND EDUCATION CORPORATION d/b/a Drexel University College of Medicine; |
Role of PI3K p110 delta Signaling in Retroviral Infection and Replication
|
EA201190062A1
(en)
|
2009-01-13 |
2012-02-28 |
Глаксо Груп Лимитед |
DERIVATIVES OF PYRIMIDINCARBOXAMIDE AS SYK-KINASE INHIBITORS
|
US8173670B2
(en)
|
2009-01-13 |
2012-05-08 |
Van Andel Research Institute |
Methods of using substituted isoxazolo pyridinones as dissociated glucocorticoids
|
US8642602B2
(en)
|
2009-02-04 |
2014-02-04 |
University Of Georgia Research Foundation, Inc. |
Method of inhibiting fibrogenesis and treating fibrotic disease
|
JP5844159B2
(en)
|
2009-02-09 |
2016-01-13 |
ユニヴェルシテ デクス−マルセイユUniversite D’Aix−Marseille |
PD-1 antibody and PD-L1 antibody and use thereof
|
WO2010092340A1
(en)
|
2009-02-13 |
2010-08-19 |
Ucb Pharma S.A. |
Fused pyridine and pyrazine derivatives as kinase inhibitors
|
TW201038569A
(en)
|
2009-02-16 |
2010-11-01 |
Abbott Gmbh & Co Kg |
Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy
|
US20100280067A1
(en)
|
2009-04-30 |
2010-11-04 |
Pakala Kumara Savithru Sarma |
Inhibitors of acetyl-coa carboxylase
|
JP5789252B2
(en)
|
2009-05-07 |
2015-10-07 |
インテリカイン, エルエルシー |
Heterocyclic compounds and uses thereof
|
JP2012527474A
(en)
|
2009-05-22 |
2012-11-08 |
エクセリクシス, インク. |
Benzoxazepine-based PI3K / MT0R inhibitors for proliferative diseases
|
GB0908957D0
(en)
|
2009-05-22 |
2009-07-01 |
Ucb Pharma Sa |
Therapeutic agents
|
ES2425091T3
(en)
|
2009-05-26 |
2013-10-11 |
Exelixis, Inc. |
Benzoxazepines as PI3K / mTOR inhibitors and their methods of use and manufacture
|
CA2765534C
(en)
|
2009-06-15 |
2018-09-18 |
Rigel Pharmaceuticals, Inc. |
Small molecule inhibitors of spleen tyrosine kinase (syk)
|
CN101602768B
(en)
|
2009-07-17 |
2012-05-30 |
河南省农科院农副产品加工研究所 |
Method for purifying sesamin and sesamolin
|
TW201105669A
(en)
|
2009-07-30 |
2011-02-16 |
Irm Llc |
Compounds and compositions as Syk kinase inhibitors
|
US8722692B2
(en)
|
2009-07-30 |
2014-05-13 |
Jianwei Che |
Compounds and compositions as Syk kinase inhibitors
|
US9212177B2
(en)
|
2009-08-05 |
2015-12-15 |
Versitech Limited |
Antiviral compounds and methods of making and using thereof
|
US8709424B2
(en)
|
2009-09-03 |
2014-04-29 |
Merck Sharp & Dohme Corp. |
Anti-GITR antibodies
|
US8106146B2
(en)
|
2009-10-06 |
2012-01-31 |
Medtronic, Inc. |
Therapeutic polymers and methods of generation
|
GB0919054D0
(en)
|
2009-10-30 |
2009-12-16 |
Isis Innovation |
Treatment of obesity
|
WO2011058109A1
(en)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Fused bicyclic pyrrole and imidazole derivatives as kinase inhibitors
|
EP2499129B1
(en)
|
2009-11-12 |
2014-07-30 |
UCB Pharma, S.A. |
Quinoline and quinoxaline derivatives as kinase inhibitors
|
WO2011058110A1
(en)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Quinoline and quinoxaline derivatives as kinase inhibitors
|
CA2780749A1
(en)
|
2009-11-13 |
2011-05-19 |
Constar International, Inc. |
Oxygen scavengers, compositions comprising the scavengers, and artcles made from the compositions
|
US20130017199A1
(en)
|
2009-11-24 |
2013-01-17 |
AMPLIMMUNE ,Inc. a corporation |
Simultaneous inhibition of pd-l1/pd-l2
|
EP2507226A1
(en)
|
2009-12-03 |
2012-10-10 |
Glaxo Group Limited |
Novel compounds
|
AU2010327936B2
(en)
|
2009-12-11 |
2015-08-20 |
Nono Inc. |
Agents and methods for treating ischemic and other diseases
|
MA33926B1
(en)
|
2009-12-17 |
2013-01-02 |
Merck Sharp & Dohme |
AMINOPYRIMIDINES AS INHIBITORS OF SYK
|
EP2512246B1
(en)
|
2009-12-17 |
2015-09-30 |
Merck Sharp & Dohme Corp. |
Aminopyrimidines as syk inhibitors
|
EP2513109A1
(en)
|
2009-12-18 |
2012-10-24 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
AU2010341573B2
(en)
|
2009-12-22 |
2016-10-13 |
Vertex Pharmaceuticals Incorporated |
Isoindolinone inhibitors of phosphatidylinositol 3-kinase
|
PT2516434E
(en)
|
2009-12-23 |
2015-10-05 |
Takeda Pharmaceutical |
Fused heteroaromatic pyrrolidinones as syk inhibitors
|
ME02505B
(en)
|
2009-12-29 |
2017-02-20 |
Aptevo Res & Development Llc |
Heterodimer binding proteins and uses thereof
|
WO2011082400A2
(en)
|
2010-01-04 |
2011-07-07 |
President And Fellows Of Harvard College |
Modulators of immunoinhibitory receptor pd-1, and methods of use thereof
|
WO2011094890A1
(en)
|
2010-02-02 |
2011-08-11 |
Argusina Inc. |
Phenylalanine derivatives and their use as non-peptide glp-1 receptor modulators
|
EP2536275A1
(en)
|
2010-02-16 |
2012-12-26 |
UWM Research Foundation, Inc. |
Methods of reducing virulence in bacteria
|
US20110251216A1
(en)
|
2010-02-19 |
2011-10-13 |
The Regents Of The University Of Michigan |
Compositions and methods for inhibiting ezh2
|
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
|
CN102206172B
(en)
|
2010-03-30 |
2015-02-25 |
中国医学科学院医药生物技术研究所 |
Substituted diaryl compound and preparation method and antiviral application thereof
|
CA2812043A1
(en)
|
2010-04-23 |
2011-10-27 |
Kineta, Inc. |
Pyrimidinedione anti-viral compounds
|
JP2013525368A
(en)
|
2010-04-23 |
2013-06-20 |
キネタ・インコーポレイテツド |
Antiviral compounds
|
GB201007203D0
(en)
|
2010-04-29 |
2010-06-16 |
Glaxo Group Ltd |
Novel compounds
|
WO2011140183A1
(en)
|
2010-05-04 |
2011-11-10 |
Alkermes, Inc. |
Process for synthesizing oxidized lactam compounds
|
AU2011255218B2
(en)
|
2010-05-21 |
2015-03-12 |
Infinity Pharmaceuticals, Inc. |
Chemical compounds, compositions and methods for kinase modulation
|
JP5911476B2
(en)
|
2010-05-26 |
2016-04-27 |
スノビオン プハルマセウトイカルス インコーポレイテッド |
Heteroaryl compounds and methods of use thereof
|
US20120142701A1
(en)
|
2010-05-28 |
2012-06-07 |
The University Of Hong Kong |
Compounds and methods for the treatment of proliferative diseases
|
CA3113343A1
(en)
|
2010-06-03 |
2011-12-08 |
Pharmacyclics Llc |
Use of inhibitors of bruton's tyrosine kinase (btk) in the treatment of follicular lymphoma
|
CA2802484A1
(en)
|
2010-06-11 |
2011-12-15 |
Gilead Calistoga Llc |
Methods of treating hematological disorders with quinazolinone compounds in selected patients
|
CA2802344C
(en)
|
2010-06-18 |
2023-06-13 |
The Brigham And Women's Hospital, Inc. |
Bi-specific antibodies against tim-3 and pd-1 for immunotherapy in chronic immune conditions
|
US20130195843A1
(en)
|
2010-06-23 |
2013-08-01 |
British Columbia Cancer Agency Branch |
Biomarkers for Non-Hodgkin Lymphomas and Uses Thereof
|
WO2011163610A2
(en)
|
2010-06-25 |
2011-12-29 |
Rutgers, The State University Of New Jersey |
Antimicrobial agents
|
US8907053B2
(en)
|
2010-06-25 |
2014-12-09 |
Aurigene Discovery Technologies Limited |
Immunosuppression modulating compounds
|
JP5886842B2
(en)
|
2010-07-05 |
2016-03-16 |
メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung |
Bipyridyl derivatives useful for the treatment of kinase-induced diseases
|
WO2012019093A1
(en)
|
2010-08-05 |
2012-02-09 |
Human Biomolecular Research Institute |
Synthetic compounds and methods to decrease nicotine self-administration
|
AR082799A1
(en)
|
2010-09-08 |
2013-01-09 |
Ucb Pharma Sa |
DERIVATIVES OF QUINOLINE AND QUINOXALINE AS QUINASE INHIBITORS
|
US9175331B2
(en)
|
2010-09-10 |
2015-11-03 |
Epizyme, Inc. |
Inhibitors of human EZH2, and methods of use thereof
|
RU2765155C2
(en)
|
2010-09-10 |
2022-01-26 |
Эпизайм, Инк. |
Human ezh2 inhibitors and methods for application thereof
|
AU2011302196B2
(en)
|
2010-09-14 |
2016-04-28 |
Exelixis, Inc. |
Inhibitors of PI3K-delta and methods of their use and manufacture
|
US8765773B2
(en)
|
2010-10-18 |
2014-07-01 |
Millennium Pharmaceuticals, Inc. |
Substituted hydroxamic acids and uses thereof
|
US9394290B2
(en)
|
2010-10-21 |
2016-07-19 |
Universitaet Des Saarlandes Campus Saarbruecken |
Selective CYP11B1 inhibitors for the treatment of cortisol dependent diseases
|
CN103282352B
(en)
|
2010-11-01 |
2016-08-10 |
波托拉医药品公司 |
Benzamides and nicotinamide as SYK regulator
|
US20140031355A1
(en)
|
2010-11-04 |
2014-01-30 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
EP2637669A4
(en)
|
2010-11-10 |
2014-04-02 |
Infinity Pharmaceuticals Inc |
Heterocyclic compounds and uses thereof
|
WO2012068096A2
(en)
|
2010-11-15 |
2012-05-24 |
Exelixis, Inc. |
Benzoxazepines as inhibitors of pi3k/mtor and methods of their use and manufacture
|
WO2012068106A2
(en)
|
2010-11-15 |
2012-05-24 |
Exelixis, Inc. |
Benzoxazepines as inhibitors of pi3k/mtor and methods of their use and manufacture
|
KR20130119950A
(en)
|
2010-11-24 |
2013-11-01 |
엑셀리시스, 인코포레이티드 |
Benzoxaepines as inhibitors of pi3k/mtor and methods of their use and manufacutre
|
WO2012071509A2
(en)
|
2010-11-24 |
2012-05-31 |
Exelixis, Inc. |
Benzoxazepines as inhibitors of p13k/mtor and methods of their use and manufacture
|
CA2818903C
(en)
|
2010-12-14 |
2021-03-23 |
Electrophoretics Limited |
5-(1,3-benzoxazol-2-yl)-4-(pyridin-4-yl)pyrimidin-2-amine and its use as a casein kinase 1delta inhibitor
|
US8765978B2
(en)
|
2010-12-16 |
2014-07-01 |
Transitions Optical, Inc. |
Method of making indeno-fused naphthol materials
|
EP2655334B1
(en)
|
2010-12-22 |
2018-10-03 |
Eutropics Pharmaceuticals, Inc. |
Compositions and methods useful for treating diseases
|
JP2014501790A
(en)
|
2011-01-10 |
2014-01-23 |
インフィニティー ファーマシューティカルズ, インコーポレイテッド |
Process for the preparation of isoquinolinone and solid form of isoquinolinone
|
JP5931933B2
(en)
|
2011-02-25 |
2016-06-08 |
武田薬品工業株式会社 |
N-substituted oxazinopteridines and oxazinopteridinones
|
US20140213630A1
(en)
|
2011-03-08 |
2014-07-31 |
Thomas Diacovo |
Methods and pharmaceutical compositions for treating lymphoid malignancy
|
AP2013007158A0
(en)
|
2011-03-11 |
2013-10-31 |
Gilead Calistoga Llc |
Combination therapies for hematologic malignancies
|
CA2830234A1
(en)
|
2011-03-15 |
2012-09-20 |
Abbvie Inc. |
Nuclear hormone receptor modulators
|
US9464065B2
(en)
|
2011-03-24 |
2016-10-11 |
The Scripps Research Institute |
Compounds and methods for inducing chondrogenesis
|
CN102731492B
(en)
|
2011-03-30 |
2016-06-29 |
江苏恒瑞医药股份有限公司 |
Cyclohexanes derivant, its preparation method and in application pharmaceutically
|
SG194045A1
(en)
|
2011-04-01 |
2013-11-29 |
Genentech Inc |
Combinations of akt inhibitor compounds and abiraterone, and methods of use
|
JO3733B1
(en)
|
2011-04-05 |
2021-01-31 |
Bayer Ip Gmbh |
Use of substituted 2,3-dihydroimidazo[1,2-c] quinazolines
|
CN103619170B
(en)
|
2011-05-04 |
2016-07-06 |
默沙东公司 |
Spleen tyrosine kinase (SYK) inhibitor containing amino-pyridine
|
KR101644051B1
(en)
|
2011-05-20 |
2016-08-01 |
삼성전자 주식회사 |
Optoelectronic device and laminated structure
|
EA030465B1
(en)
|
2011-07-01 |
2018-08-31 |
Новартис Аг |
Combination therapy comprising a cdk4/6 inhibitor and a pi3k inhibitor for use in the treatment of cancer
|
AR088218A1
(en)
|
2011-07-19 |
2014-05-21 |
Infinity Pharmaceuticals Inc |
USEFUL HETEROCICLICAL COMPOUNDS AS PI3K INHIBITORS
|
EP2734520B1
(en)
|
2011-07-19 |
2016-09-14 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
CN103635456B
(en)
|
2011-07-26 |
2016-03-09 |
山东亨利医药科技有限责任公司 |
Tigecycline derivative
|
WO2013013505A1
(en)
|
2011-07-26 |
2013-01-31 |
山东亨利医药科技有限责任公司 |
9-aminomethyl substituted tetracycline compound
|
EP2741609A4
(en)
|
2011-08-12 |
2015-04-08 |
Salk Inst For Biological Studi |
Neuroprotective polyphenol analogs
|
RU2014111823A
(en)
|
2011-08-29 |
2015-10-10 |
Инфинити Фармасьютикалз, Инк. |
HETEROCYCLIC COMPOUNDS AND THEIR APPLICATIONS
|
WO2013066483A1
(en)
|
2011-08-31 |
2013-05-10 |
Novartis Ag |
Synergistic combinations of pi3k- and mek-inhibitors
|
US20130108641A1
(en)
|
2011-09-14 |
2013-05-02 |
Sanofi |
Anti-gitr antibodies
|
WO2013044169A1
(en)
|
2011-09-21 |
2013-03-28 |
Nestec S.A. |
Methods for determining combination therapy with il-2 for the treatment of cancer
|
MX361772B
(en)
|
2011-10-19 |
2018-12-17 |
Pharmacyclics Llc |
Use of inhibitors of bruton's tyrosine kinase (btk).
|
WO2013074583A1
(en)
|
2011-11-14 |
2013-05-23 |
The Broad Institute, Inc. |
Treatment and prognosis of lymphangioleiomyomatosis
|
SI2785375T1
(en)
|
2011-11-28 |
2020-11-30 |
Merck Patent Gmbh |
Anti-pd-l1 antibodies and uses thereof
|
WO2013086131A1
(en)
|
2011-12-06 |
2013-06-13 |
The Trustees Of The University Of Pennsylvania |
Inhibitors targeting drug-resistant influenza a
|
US8772541B2
(en)
|
2011-12-15 |
2014-07-08 |
University of Pittsburgh—of the Commonwealth System of Higher Education |
Cannabinoid receptor 2 (CB2) inverse agonists and therapeutic potential for multiple myeloma and osteoporosis bone diseases
|
WO2013090725A1
(en)
|
2011-12-15 |
2013-06-20 |
Philadelphia Health & Education Corporation |
NOVEL PI3K p110 INHIBITORS AND METHODS OF USE THEREOF
|
EP3330288A1
(en)
|
2011-12-21 |
2018-06-06 |
Novartis AG |
Compositions and methods for antibodies targeting factor p
|
TWI573792B
(en)
|
2012-02-01 |
2017-03-11 |
歐陸斯迪公司 |
Novel therapeutic agents
|
CN104582732A
(en)
|
2012-06-15 |
2015-04-29 |
布里格姆及妇女医院股份有限公司 |
Compositions for treating cancer and methods for making the same
|
US8828998B2
(en)
|
2012-06-25 |
2014-09-09 |
Infinity Pharmaceuticals, Inc. |
Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors
|
UY34887A
(en)
|
2012-07-02 |
2013-12-31 |
Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware |
OPTIMIZATION OF ANTIBODIES THAT FIX THE LYMPHOCYTE ACTIVATION GEN 3 (LAG-3) AND ITS USES
|
DK3260455T3
(en)
|
2012-07-04 |
2019-06-11 |
Rhizen Pharmaceuticals S A |
SELECTIVE PI3K DELTA REQUESTS
|
EP3550031A1
(en)
|
2012-07-24 |
2019-10-09 |
Pharmacyclics, LLC |
Mutations associated with resistance to inhibitors of bruton's tyrosine kinase (btk)
|
CA3163776A1
(en)
|
2012-08-03 |
2014-02-06 |
Foundation Medicine, Inc. |
Human papilloma virus as predictor of cancer prognosis
|
WO2014046617A1
(en)
|
2012-09-19 |
2014-03-27 |
Agency For Science, Technology And Research |
Compositions and methods for treating cancer
|
US20140120083A1
(en)
|
2012-11-01 |
2014-05-01 |
Infinity Pharmaceuticals, Inc. |
Treatment of cancers using pi3 kinase isoform modulators
|
DK2914296T4
(en)
|
2012-11-01 |
2022-01-03 |
Infinity Pharmaceuticals Inc |
Treatment of cancers using PI3 kinase isoform modulators
|
US20140120060A1
(en)
|
2012-11-01 |
2014-05-01 |
Infinity Pharmaceuticals, Inc. |
Treatment of rheumatoid arthritis and asthma using pi3 kinase inhibitors
|
US9694071B2
(en)
|
2012-11-02 |
2017-07-04 |
Tg Therapeutics, Inc. |
Combination of anti-CD20 antibody and PI3 kinase selective inhibitor
|
EA035391B1
(en)
|
2012-11-08 |
2020-06-05 |
Ризен Фармасьютикалз Са |
Pharmaceutical compositions containing a pde4 inhibitor and a pi3 delta or dual pi3 delta-gamma kinase inhibitor
|
MX2015006192A
(en)
|
2012-11-16 |
2015-08-10 |
Merck Sharp & Dohme |
Purine inhibitors of human phosphatidylinositol 3-kinase delta.
|
WO2014124458A1
(en)
|
2013-02-11 |
2014-08-14 |
The Regents Of The University Of California |
Compositions and methods for treating neurodegenerative diseases
|
US20160067212A1
(en)
|
2013-03-15 |
2016-03-10 |
Universite De Geneve |
Use of insulin signaling antagonists, optionally in combination of transfection of non-beta cells, for inducing insulin production
|
EP2983670A4
(en)
|
2013-04-08 |
2017-03-08 |
Pharmacyclics LLC |
Ibrutinib combination therapy
|
JP6227889B2
(en)
|
2013-04-23 |
2017-11-08 |
関東化學株式会社 |
Novel organometallic complex and method for producing amine compound
|
AU2014273946B2
(en)
|
2013-05-30 |
2020-03-12 |
Infinity Pharmaceuticals, Inc. |
Treatment of cancers using PI3 kinase isoform modulators
|
EP3632208A1
(en)
|
2013-06-13 |
2020-04-08 |
Biomatrica, INC. |
Cell stabilization
|
JP6030783B2
(en)
|
2013-06-14 |
2016-11-24 |
ギリアード サイエンシーズ, インコーポレイテッド |
Phosphatidylinositol 3-kinase inhibitor
|
WO2014203959A1
(en)
|
2013-06-20 |
2014-12-24 |
大鵬薬品工業株式会社 |
METHOD FOR PREDICTING THERAPEUTIC EFFICACY OF PI3K/AKT/mTOR INHIBITOR ON BASIS OF PHLDA1 OR PIK3C2B EXPRESSION
|
UY35675A
(en)
|
2013-07-24 |
2015-02-27 |
Novartis Ag |
SUBSTITUTED DERIVATIVES OF QUINAZOLIN-4-ONA
|
US20150065431A1
(en)
|
2013-08-27 |
2015-03-05 |
Northwestern University |
Reducing cutaneous scar formation and treating skin conditions
|
EP3043819A4
(en)
|
2013-09-11 |
2017-04-05 |
Compugen Ltd. |
Anti-vstm5 antibodies and the use thereof in therapy and diagnosis
|
US10111897B2
(en)
|
2013-10-03 |
2018-10-30 |
Duke University |
Compositions and methods for treating cancer with JAK2 activity
|
EP3054952B1
(en)
|
2013-10-08 |
2022-10-26 |
Acetylon Pharmaceuticals, Inc. |
Combinations of histone deacetylase 6 inhibitors and the her2 inhibitor lapatinib for use in the treatment of breast cancer
|
ES2818933T3
(en)
|
2013-10-10 |
2021-04-14 |
Acetylon Pharmaceuticals Inc |
HDAC inhibitors in combination with pi3k inhibitors, for the treatment of non-Hodgkin lymphoma
|
EP3060251A4
(en)
*
|
2013-10-25 |
2017-12-06 |
Pharmacyclics LLC |
Treatment using bruton's tyrosine kinase inhibitors and immunotherapy
|
AU2014354769A1
(en)
|
2013-11-26 |
2016-05-26 |
Gilead Sciences, Inc. |
Therapies for treating myeloproliferative disorders
|
WO2015083008A1
(en)
|
2013-12-05 |
2015-06-11 |
Acerta Pharma B.V. |
Therapeutic combination of a pi3k inhibitor and a btk inhibitor
|
EP3082779B1
(en)
|
2013-12-20 |
2023-06-07 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of type 2 mek and erk inhibitors
|
AU2014368925A1
(en)
|
2013-12-20 |
2016-07-21 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of MEK type I and ERK inhibitors
|
ES2918375T3
(en)
|
2013-12-20 |
2022-07-15 |
Biomed Valley Discoveries Inc |
Cancer Treatments Using Combinations of PI3K/Akt and ERK Pathway Inhibitors
|
WO2015095840A1
(en)
|
2013-12-20 |
2015-06-25 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of cdk and erk inhibitors
|
WO2015095834A2
(en)
|
2013-12-20 |
2015-06-25 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using erk1/2 and bcl-2 family inhibitors
|
US10668055B2
(en)
|
2013-12-20 |
2020-06-02 |
Biomed Valley Discoveries, Inc. |
Cancer treatment using combinations of ERK and RAF inhibitors
|
WO2015095842A2
(en)
|
2013-12-20 |
2015-06-25 |
Biomed Valley Discoveries, Inc. |
Methods and compositions for treating non-erk mapk pathway inhibitor-resistant cancers
|
WO2015095831A1
(en)
|
2013-12-20 |
2015-06-25 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of mtor and erk inhibitors
|
WO2015095807A1
(en)
|
2013-12-20 |
2015-06-25 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of egfr and erk inhibitors
|
US20160331754A1
(en)
|
2014-01-20 |
2016-11-17 |
Gilead Sciences, Inc. |
Therapies for treating cancers
|
KR20160138177A
(en)
|
2014-03-21 |
2016-12-02 |
애브비 인코포레이티드 |
Anti-egfr antibodies and antibody drug conjugates
|
US20150320754A1
(en)
|
2014-04-16 |
2015-11-12 |
Infinity Pharmaceuticals, Inc. |
Combination therapies
|
US20150320755A1
(en)
*
|
2014-04-16 |
2015-11-12 |
Infinity Pharmaceuticals, Inc. |
Combination therapies
|
WO2015175966A1
(en)
|
2014-05-16 |
2015-11-19 |
Memorial Sloan Kettering Cancer Center |
Platelet-derived growth factor receptor mutations and compositions and methods relating thereto
|
WO2015179772A1
(en)
|
2014-05-23 |
2015-11-26 |
Concert Pharmaceuticals, Inc. |
Deuterated phenylquinazolinone and phenylisoquinolinone compounds
|
MA39827A
(en)
|
2014-05-27 |
2015-12-03 |
Almirall Sa |
Addition salts of (s)-2-(1-(6-amino-5-cyanopyrimidin-4-ylamino)ethyl)-4-oxo-3-phenyl-3,4-dihydropyrrolo[1,2-f][1,2,4]triazine-5-carbonitrile
|
US10479975B2
(en)
|
2014-06-06 |
2019-11-19 |
Bluebird Bio, Inc. |
Methods of making T cell compositions
|
TW201618775A
(en)
*
|
2014-08-11 |
2016-06-01 |
艾森塔製藥公司 |
Therapeutic combinations of a BTK inhibitor, a PI3K inhibitor, a JAK-2 inhibitor, a PD-1 inhibitor and/or a PD-L1 inhibitor
|
AU2015327868A1
(en)
*
|
2014-10-03 |
2017-04-20 |
Novartis Ag |
Combination therapies
|
SG10201912456RA
(en)
*
|
2016-06-24 |
2020-02-27 |
Infinity Pharmaceuticals Inc |
Combination therapies
|