GB812366A
(en)
|
1955-08-18 |
1959-04-22 |
Wellcome Found |
Improvements in and relating to derivatives of pyrimidine and the preparation thereof
|
US135A
(en)
|
|
1837-03-03 |
|
Jesse j |
US5458A
(en)
|
|
1848-02-22 |
|
Bench-vise |
US2517482A
(en)
|
1949-04-09 |
1950-08-01 |
Sharp & Dohme Inc |
Inhaler
|
GB937725A
(en)
|
1960-05-11 |
1963-09-25 |
Ciba Ltd |
Pyrazolo[3:4-d]pyrimidines
|
GB1182779A
(en)
|
1966-09-17 |
1970-03-04 |
Fisons Pharmaceuticals Ltd |
Inhalation Device
|
US3507277A
(en)
|
1966-09-17 |
1970-04-21 |
Fisons Pharmaceuticals Ltd |
Inhalation device
|
GB1268051A
(en)
|
1968-06-07 |
1972-03-22 |
Fisons Pharmaceuticals Ltd |
Inhalation device
|
US3536809A
(en)
|
1969-02-17 |
1970-10-27 |
Alza Corp |
Medication method
|
US3598123A
(en)
|
1969-04-01 |
1971-08-10 |
Alza Corp |
Bandage for administering drugs
|
US3831606A
(en)
|
1971-02-19 |
1974-08-27 |
Alza Corp |
Auto inhaler
|
IT941426B
(it)
|
1971-07-17 |
1973-03-01 |
Isf Spa |
Inalatore a camera di turbinio per sostanze medicamentose polveriformi
|
DE2139107A1
(de)
|
1971-08-04 |
1973-02-15 |
Merck Patent Gmbh |
Heterocyclisch substituierte adenosinverbindungen
|
US3845770A
(en)
|
1972-06-05 |
1974-11-05 |
Alza Corp |
Osmatic dispensing device for releasing beneficial agent
|
US3795244A
(en)
|
1973-02-02 |
1974-03-05 |
Syntex Corp |
Inhalation device
|
US3916899A
(en)
|
1973-04-25 |
1975-11-04 |
Alza Corp |
Osmotic dispensing device with maximum and minimum sizes for the passageway
|
US3948264A
(en)
|
1975-05-21 |
1976-04-06 |
Mead Johnson & Company |
Inhalation device
|
US4008719A
(en)
|
1976-02-02 |
1977-02-22 |
Alza Corporation |
Osmotic system having laminar arrangement for programming delivery of active agent
|
US4270537A
(en)
|
1979-11-19 |
1981-06-02 |
Romaine Richard A |
Automatic hypodermic syringe
|
IT1153216B
(it)
|
1981-10-16 |
1987-01-14 |
Schering Ag |
Procedimento per la preparazione di composti cianoeterociclici
|
DE3244594A1
(de)
|
1982-12-02 |
1984-06-07 |
Hoechst Ag, 6230 Frankfurt |
1-phenylisochinolinderivate und verfahren zu ihrer herstellung, diese verbindung enthaltende pharmazeutische praeparate und deren anwendung
|
DE3406533A1
(de)
|
1984-02-23 |
1985-08-29 |
Boehringer Mannheim Gmbh, 6800 Mannheim |
Verwendung von adenosin-derivaten als antiallergica und arzneimittel, die diese enthalten
|
US5310731A
(en)
|
1984-06-28 |
1994-05-10 |
Whitby Research, Inc. |
N-6 substituted-5'-(N-substitutedcarboxamido)adenosines as cardiac vasodilators and antihypertensive agents
|
ES8702440A1
(es)
|
1984-10-04 |
1986-12-16 |
Monsanto Co |
Un procedimiento para la preparacion de una composicion de polipeptido inyectable sustancialmente no acuosa.
|
US4795627A
(en)
|
1984-10-18 |
1989-01-03 |
University Of Pittsburgh |
Tritium labelled N-mustard type compounds and a process for their production
|
IE58110B1
(en)
|
1984-10-30 |
1993-07-14 |
Elan Corp Plc |
Controlled release powder and process for its preparation
|
US4656159A
(en)
|
1984-10-31 |
1987-04-07 |
Georgetown University |
Galactose-C-6 nitrogen mustard compounds and their uses
|
JPS61109797A
(ja)
|
1984-11-01 |
1986-05-28 |
Yuki Gosei Yakuhin Kogyo Kk |
標識化ヌクレオチドおよび標識化ポリヌクレオチド
|
US4596556A
(en)
|
1985-03-25 |
1986-06-24 |
Bioject, Inc. |
Hypodermic injection apparatus
|
US5023252A
(en)
|
1985-12-04 |
1991-06-11 |
Conrex Pharmaceutical Corporation |
Transdermal and trans-membrane delivery of drugs
|
US4886499A
(en)
|
1986-12-18 |
1989-12-12 |
Hoffmann-La Roche Inc. |
Portable injection appliance
|
GB8704027D0
(en)
|
1987-02-20 |
1987-03-25 |
Owen Mumford Ltd |
Syringe needle combination
|
GB8707053D0
(en)
|
1987-03-25 |
1987-04-29 |
Ici Plc |
Anti-tumour agents
|
US5001139A
(en)
|
1987-06-12 |
1991-03-19 |
American Cyanamid Company |
Enchancers for the transdermal flux of nivadipine
|
US4992445A
(en)
|
1987-06-12 |
1991-02-12 |
American Cyanamid Co. |
Transdermal delivery of pharmaceuticals
|
US4941880A
(en)
|
1987-06-19 |
1990-07-17 |
Bioject, Inc. |
Pre-filled ampule and non-invasive hypodermic injection device assembly
|
US4790824A
(en)
|
1987-06-19 |
1988-12-13 |
Bioject, Inc. |
Non-invasive hypodermic injection device
|
US4940460A
(en)
|
1987-06-19 |
1990-07-10 |
Bioject, Inc. |
Patient-fillable and non-invasive hypodermic injection device assembly
|
US5339163A
(en)
|
1988-03-16 |
1994-08-16 |
Canon Kabushiki Kaisha |
Automatic exposure control device using plural image plane detection areas
|
US5073543A
(en)
|
1988-07-21 |
1991-12-17 |
G. D. Searle & Co. |
Controlled release formulations of trophic factors in ganglioside-lipsome vehicle
|
WO1990003370A1
(en)
|
1988-09-28 |
1990-04-05 |
Microprobe Corporation |
DERIVATIVES OF PYRAZOLO[3,4-d]PYRIMIDINE
|
FR2638359A1
(fr)
|
1988-11-03 |
1990-05-04 |
Tino Dalto |
Guide de seringue avec reglage de la profondeur de penetration de l'aiguille dans la peau
|
IT1229203B
(it)
|
1989-03-22 |
1991-07-25 |
Bioresearch Spa |
Impiego di acido 5 metiltetraidrofolico, di acido 5 formiltetraidrofolico e dei loro sali farmaceuticamente accettabili per la preparazione di composizioni farmaceutiche in forma a rilascio controllato attive nella terapia dei disturbi mentali organici e composizioni farmaceutiche relative.
|
PH30995A
(en)
|
1989-07-07 |
1997-12-23 |
Novartis Inc |
Sustained release formulations of water soluble peptides.
|
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
|
US5795977A
(en)
|
1989-09-15 |
1998-08-18 |
Metabasis Therapeutics, Inc. |
Water soluble 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
|
US5763597A
(en)
|
1989-09-15 |
1998-06-09 |
Metabasis Therapeutics, Inc. |
Orally active adenosine kinase inhibitors
|
US5120548A
(en)
|
1989-11-07 |
1992-06-09 |
Merck & Co., Inc. |
Swelling modulated polymeric drug delivery device
|
US5312335A
(en)
|
1989-11-09 |
1994-05-17 |
Bioject Inc. |
Needleless hypodermic injection device
|
US5064413A
(en)
|
1989-11-09 |
1991-11-12 |
Bioject, Inc. |
Needleless hypodermic injection device
|
GB9009542D0
(en)
|
1990-04-27 |
1990-06-20 |
Beecham Group Plc |
Novel compounds
|
US5733566A
(en)
|
1990-05-15 |
1998-03-31 |
Alkermes Controlled Therapeutics Inc. Ii |
Controlled release of antiparasitic agents in animals
|
GB9113137D0
(en)
|
1990-07-13 |
1991-08-07 |
Ici Plc |
Thioxo heterocycles
|
US5563257A
(en)
|
1990-08-20 |
1996-10-08 |
Boehringer Mannheim Gmbh |
Phospholipid derivatives of nucleosides
|
DE4026265A1
(de)
|
1990-08-20 |
1992-02-27 |
Boehringer Mannheim Gmbh |
Neue phospholipid-derivate von nucleosiden, deren herstellung sowie deren verwendung als antivirale arzneimittel
|
US5190521A
(en)
|
1990-08-22 |
1993-03-02 |
Tecnol Medical Products, Inc. |
Apparatus and method for raising a skin wheal and anesthetizing skin
|
US5561134A
(en)
|
1990-09-25 |
1996-10-01 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties
|
US5652366A
(en)
|
1990-09-25 |
1997-07-29 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
DI (1R)-(-)camphosulfonic acid) salt, preparation thereof and use thereof
|
ES2095960T3
(es)
|
1990-09-25 |
1997-03-01 |
Rhone Poulenc Rorer Int |
Compuestos que tienen propiedades antihipertensivas y antiisquemicas.
|
US5527288A
(en)
|
1990-12-13 |
1996-06-18 |
Elan Medical Technologies Limited |
Intradermal drug delivery device and method for intradermal delivery of drugs
|
GB9103839D0
(en)
|
1991-02-23 |
1991-04-10 |
Smithkline Beecham Plc |
Pharmaceuticals
|
SG64322A1
(en)
|
1991-05-10 |
1999-04-27 |
Rhone Poulenc Rorer Int |
Bis mono and bicyclic aryl and heteroaryl compounds which inhibit egf and/or pdgf receptor tyrosine kinase
|
ATE359842T1
(de)
|
1991-07-02 |
2007-05-15 |
Nektar Therapeutics |
Abgabevorrichtung für nebelförmige medikamente
|
GB9118204D0
(en)
|
1991-08-23 |
1991-10-09 |
Weston Terence E |
Needle-less injector
|
SE9102652D0
(sv)
|
1991-09-13 |
1991-09-13 |
Kabi Pharmacia Ab |
Injection needle arrangement
|
US5272158A
(en)
|
1991-10-29 |
1993-12-21 |
Merck & Co., Inc. |
Fibrinogen receptor antagonists
|
US5580578A
(en)
|
1992-01-27 |
1996-12-03 |
Euro-Celtique, S.A. |
Controlled release formulations coated with aqueous dispersions of acrylic polymers
|
US5916891A
(en)
|
1992-01-13 |
1999-06-29 |
Smithkline Beecham Corporation |
Pyrimidinyl imidazoles
|
MX9300141A
(es)
|
1992-01-13 |
1994-07-29 |
Smithkline Beecham Corp |
Compuestos de imidazol novedosos, procedimiento para su preparacion y composiciones farmaceuticas que lo contienen.
|
DE4204031A1
(de)
|
1992-02-12 |
1993-08-19 |
Boehringer Mannheim Gmbh |
Neue lipidphosphonsaeure-nucleosid-konjugate sowie deren verwendung als antivirale arzneimittel
|
DE4204032A1
(de)
|
1992-02-12 |
1993-08-19 |
Boehringer Mannheim Gmbh |
Neue liponucleotide, deren herstellunmg sowie deren verwendung als antivirale arzneimittel
|
US5328483A
(en)
|
1992-02-27 |
1994-07-12 |
Jacoby Richard M |
Intradermal injection device with medication and needle guard
|
JPH05239036A
(ja)
|
1992-02-27 |
1993-09-17 |
Nissan Chem Ind Ltd |
含窒素複素環化合物の製造方法
|
WO1993018035A1
(en)
|
1992-03-04 |
1993-09-16 |
Abbott Laboratories |
Angiotensin ii receptor antagonists
|
JP2737518B2
(ja)
|
1992-03-16 |
1998-04-08 |
富士通株式会社 |
赤外線検知器の冷却構造
|
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
|
DE69333580D1
(de)
|
1992-04-07 |
2004-09-09 |
Univ Michigan |
Immunregulation über die cd28-route
|
GB9208135D0
(en)
|
1992-04-13 |
1992-05-27 |
Ludwig Inst Cancer Res |
Polypeptides having kinase activity,their preparation and use
|
WO1993022443A1
(en)
|
1992-04-24 |
1993-11-11 |
Sri International |
In vivo homologous sequence targeting in eukaryotic cells
|
DE69328440T3
(de)
|
1992-06-19 |
2009-05-07 |
Honeywell, Inc., Minneapolis |
Infrarot kamera mit thermoelektrischer temperaturstabilisierung
|
US5383851A
(en)
|
1992-07-24 |
1995-01-24 |
Bioject Inc. |
Needleless hypodermic injection device
|
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
|
US5569189A
(en)
|
1992-09-28 |
1996-10-29 |
Equidyne Systems, Inc. |
hypodermic jet injector
|
US5334144A
(en)
|
1992-10-30 |
1994-08-02 |
Becton, Dickinson And Company |
Single use disposable needleless injector
|
TW333456B
(en)
|
1992-12-07 |
1998-06-11 |
Takeda Pharm Ind Co Ltd |
A pharmaceutical composition of sustained-release preparation the invention relates to a pharmaceutical composition of sustained-release preparation which comprises a physiologically active peptide.
|
TW370529B
(en)
|
1992-12-17 |
1999-09-21 |
Pfizer |
Pyrazolopyrimidines
|
US5591767A
(en)
|
1993-01-25 |
1997-01-07 |
Pharmetrix Corporation |
Liquid reservoir transdermal patch for the administration of ketorolac
|
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
|
WO1994018215A1
(en)
|
1993-02-03 |
1994-08-18 |
Gensia, Inc. |
Adenosine kinase inhibitors comprising lyxofuranosyl derivatives
|
GB9308957D0
(en)
|
1993-04-30 |
1993-06-16 |
Cancer Res Campaign Tech |
Novel produgs
|
ATE293686T1
(de)
|
1993-06-04 |
2005-05-15 |
Us Navy |
Verfahren zur selektiven stimulierung der t- zellproliferation.
|
US6087324A
(en)
|
1993-06-24 |
2000-07-11 |
Takeda Chemical Industries, Ltd. |
Sustained-release preparation
|
EP0634402A1
(en)
|
1993-07-14 |
1995-01-18 |
Takeda Chemical Industries, Ltd. |
Isochinolinone derivatives, their production and use
|
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
|
DE4333761A1
(de)
|
1993-10-04 |
1995-04-06 |
Luitpold Pharma Gmbh |
Heterocyclische Carbamate, Verfahren zu ihrer Herstellung und Arzneimittel
|
WO1995012588A1
(en)
|
1993-11-05 |
1995-05-11 |
Biochem Pharma Inc. |
Antineoplastic heteronaphthoquinones
|
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
|
US5654307A
(en)
|
1994-01-25 |
1997-08-05 |
Warner-Lambert Company |
Bicyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family
|
WO1995024176A1
(en)
|
1994-03-07 |
1995-09-14 |
Bioject, Inc. |
Ampule filling device
|
US5466220A
(en)
|
1994-03-08 |
1995-11-14 |
Bioject, Inc. |
Drug vial mixing and transfer device
|
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
(de)
|
1994-05-28 |
1996-01-11 |
Boehringer Mannheim Gmbh |
Neue Lipidester von Nucleosid-Monophosphaten und deren Verwendung als immunsuppressive Arzneimittel
|
IT1270594B
(it)
|
1994-07-07 |
1997-05-07 |
Recordati Chem Pharm |
Composizione farmaceutica a rilascio controllato di moguisteina in sospensione liquida
|
US5756502A
(en)
|
1994-08-08 |
1998-05-26 |
Warner-Lambert Company |
Quinazolinone derivatives as cholyecystokinin (CCK) ligands
|
US6323201B1
(en)
|
1994-12-29 |
2001-11-27 |
The Regents Of The University Of California |
Compounds for inhibition of ceramide-mediated signal transduction
|
US5599302A
(en)
|
1995-01-09 |
1997-02-04 |
Medi-Ject Corporation |
Medical injection system and method, gas spring thereof and launching device using gas spring
|
GB9501841D0
(en)
|
1995-01-31 |
1995-03-22 |
Co Ordinated Drug Dev |
Improvements in and relating to carrier particles for use in dry powder inhalers
|
EP0819129B1
(en)
|
1995-04-03 |
2000-08-02 |
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
(ja)
|
1995-04-27 |
1996-11-12 |
Takeda Chem Ind Ltd |
複素環化合物、その製造法および剤
|
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
|
WO1996037777A1
(en)
|
1995-05-23 |
1996-11-28 |
Nelson Randall W |
Mass spectrometric immunoassay
|
US5730723A
(en)
|
1995-10-10 |
1998-03-24 |
Visionary Medical Products Corporation, Inc. |
Gas pressured needle-less injection device and method
|
US6403599B1
(en)
|
1995-11-08 |
2002-06-11 |
Pfizer Inc |
Corticotropin releasing factor antagonists
|
WO1996040256A1
(en)
|
1995-06-07 |
1996-12-19 |
G.D. Searle & Co. |
Method to treat cardiofibrosis with a combination of an angiotensin ii antagonist and spironolactone
|
US5665721A
(en)
|
1995-06-07 |
1997-09-09 |
Abbott Laboratories |
Heterocyclic substituted cyclopentane compounds
|
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
|
RO118046B1
(ro)
|
1995-06-07 |
2003-01-30 |
Gd Searle & Co Chicago |
Asociere farmaceutica
|
ATE268591T1
(de)
|
1995-06-27 |
2004-06-15 |
Takeda Chemical Industries Ltd |
Verfahren zur herstellung von zubereitungen mit verzögerter freisetzung
|
GB9515182D0
(en)
|
1995-07-24 |
1995-09-20 |
Co Ordinated Drug Dev |
Improvements in and relating to powders for use in dry powder inhalers
|
TW448055B
(en)
|
1995-09-04 |
2001-08-01 |
Takeda Chemical Industries Ltd |
Method of production of sustained-release preparation
|
WO1997010221A1
(en)
|
1995-09-15 |
1997-03-20 |
Torrey Pines Institute For Molecular Studies |
Synthesis of quinazolinone libraries
|
JP2909418B2
(ja)
|
1995-09-18 |
1999-06-23 |
株式会社資生堂 |
薬物の遅延放出型マイクロスフイア
|
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
(ja)
|
1995-11-29 |
1997-06-03 |
Fuji Photo Film Co Ltd |
含窒素ヘテロ芳香族アミド類の製造方法
|
US5893397A
(en)
|
1996-01-12 |
1999-04-13 |
Bioject Inc. |
Medication vial/syringe liquid-transfer apparatus
|
US5980945A
(en)
|
1996-01-16 |
1999-11-09 |
Societe De Conseils De Recherches Et D'applications Scientifique S.A. |
Sustained release drug formulations
|
US5747235A
(en)
|
1996-01-26 |
1998-05-05 |
Eastman Kodak Company |
Silver halide light sensitive emulsion layer having enhanced photographic sensitivity
|
DE19603576A1
(de)
|
1996-02-01 |
1997-08-07 |
Bayer Ag |
Acylierte 4-Amino und 4-Hydrazinopyrimidine
|
CH690773A5
(de)
|
1996-02-01 |
2001-01-15 |
Novartis Ag |
Pyrrolo(2,3-d)pyrimide und ihre Verwendung.
|
US5763608A
(en)
|
1996-02-05 |
1998-06-09 |
Hoechst Celanese Corporation |
Process for preparing pyrimidine derivatives
|
US5914488A
(en)
|
1996-03-05 |
1999-06-22 |
Mitsubishi Denki Kabushiki Kaisha |
Infrared detector
|
JP2000507590A
(ja)
|
1996-04-03 |
2000-06-20 |
メルク エンド カンパニー インコーポレーテッド |
ファルネシル―タンパク質トランスフェラーゼ阻害剤
|
US5872136A
(en)
|
1996-04-03 |
1999-02-16 |
Merck & Co., Inc. |
Arylheteroaryl inhibitors of farnesyl-protein transferase
|
GB9607549D0
(en)
|
1996-04-11 |
1996-06-12 |
Weston Medical Ltd |
Spring-powered dispensing device
|
GB9611460D0
(en)
|
1996-06-01 |
1996-08-07 |
Ludwig Inst Cancer Res |
Novel lipid kinase
|
AU727708B2
(en)
|
1996-06-20 |
2000-12-21 |
Board Of Regents, The University Of Texas System |
Compounds and methods for providing pharmacologically active preparations and uses thereof
|
US6264970B1
(en)
|
1996-06-26 |
2001-07-24 |
Takeda Chemical Industries, Ltd. |
Sustained-release preparation
|
FR2750862B1
(fr)
|
1996-07-12 |
1998-10-16 |
Dupin Jean Pierre |
Utilisation d'heterocycles diazotes fusionnes avec un systeme aromatique ou heteroaromatique pour le traitement des maladies thrombo-emboliques
|
US6419961B1
(en)
|
1996-08-29 |
2002-07-16 |
Takeda Chemical Industries, Ltd. |
Sustained release microcapsules of a bioactive substance and a biodegradable polymer
|
CA2217134A1
(en)
|
1996-10-09 |
1998-04-09 |
Sumitomo Pharmaceuticals Co., Ltd. |
Sustained release formulation
|
US5948776A
(en)
|
1996-10-23 |
1999-09-07 |
Zymogenetic, Inc. |
Compositions and methods for treating bone deficit conditions
|
US6342514B1
(en)
|
1996-10-23 |
2002-01-29 |
Zymogenetics, 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
|
US5994358A
(en)
|
1996-10-23 |
1999-11-30 |
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
|
US5965573A
(en)
|
1996-10-23 |
1999-10-12 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US6153631A
(en)
|
1996-10-23 |
2000-11-28 |
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
|
US6251901B1
(en)
|
1996-10-23 |
2001-06-26 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
EP0839525B1
(en)
|
1996-10-31 |
2004-08-04 |
Takeda Chemical Industries, Ltd. |
Sustained-release preparation
|
US5858753A
(en)
|
1996-11-25 |
1999-01-12 |
Icos Corporation |
Lipid kinase
|
US5977134A
(en)
|
1996-12-05 |
1999-11-02 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
JP4094066B2
(ja)
|
1996-12-06 |
2008-06-04 |
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 |
インターロイキン−1β変換酵素のインヒビター
|
EP0946169B1
(en)
|
1996-12-20 |
2003-02-26 |
Takeda Chemical Industries, Ltd. |
Method of producing a sustained-release preparation
|
US6093737A
(en)
|
1996-12-30 |
2000-07-25 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
JPH10206995A
(ja)
|
1997-01-21 |
1998-08-07 |
Konica Corp |
ハロゲン化銀写真感光材料
|
US5891474A
(en)
|
1997-01-29 |
1999-04-06 |
Poli Industria Chimica, S.P.A. |
Time-specific controlled release dosage formulations and method of preparing same
|
DE69825066T2
(de)
|
1997-02-07 |
2005-08-25 |
Princeton University |
Gentechnisch hergestellte Proteinkinasen, welche modifizierte Nukleotidtriphosphatsubstrate verwenden können
|
CA2283961A1
(en)
|
1997-03-19 |
1998-09-24 |
Basf Aktiengesellschaft |
Pyrrolo[2,3d]pyrimidines and their use as tyrosine kinase inhibitors
|
US7863444B2
(en)
|
1997-03-19 |
2011-01-04 |
Abbott Laboratories |
4-aminopyrrolopyrimidines as kinase inhibitors
|
US5993412A
(en)
|
1997-05-19 |
1999-11-30 |
Bioject, Inc. |
Injection apparatus
|
WO1998052611A1
(fr)
|
1997-05-23 |
1998-11-26 |
Nippon Shinyaku Co., Ltd. |
Preparation medicamenteuse aux fins de la prevention et du traitement des hepatopathies
|
US6207679B1
(en)
|
1997-06-19 |
2001-03-27 |
Sepracor, Inc. |
Antimicrobial agents uses and compositions related thereto
|
AU9309898A
(en)
|
1997-09-09 |
1999-03-29 |
Du Pont Pharmaceuticals Company |
Benzimidazolinones, benzoxazolinones, benzopiperazinones, indanones, and derivatives thereof as inhibitors of factor xa
|
WO1999018077A1
(fr)
|
1997-10-02 |
1999-04-15 |
Eisai Co., Ltd. |
Derives de pyridine condenses
|
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
|
CN1130363C
(zh)
|
1997-11-12 |
2003-12-10 |
三菱化学株式会社 |
嘌呤衍生物以及含有其作为有效成分的药物
|
US6040321A
(en)
|
1997-11-12 |
2000-03-21 |
Bristol-Myers Squibb Company |
Aminothiazole inhibitors of cyclin dependent kinases
|
US6184377B1
(en)
|
1997-12-15 |
2001-02-06 |
Sepracor Inc. |
Compositions containing N-amino- and N-hydroxy-quinazolinones and methods for preparing libraries thereof
|
IT1298087B1
(it)
|
1998-01-08 |
1999-12-20 |
Fiderm S R L |
Dispositivo per il controllo della profondita' di penetrazione di un ago, in particolare applicabile ad una siringa per iniezioni
|
US6191170B1
(en)
|
1998-01-13 |
2001-02-20 |
Tularik Inc. |
Benzenesulfonamides and benzamides as therapeutic agents
|
US6613358B2
(en)
|
1998-03-18 |
2003-09-02 |
Theodore W. Randolph |
Sustained-release composition including amorphous polymer
|
DE19912383A1
(de)
|
1998-03-27 |
1999-09-30 |
Degussa |
Verfahren zur Herstellung von cyclischen 4-Oxoamidinen
|
US7715989B2
(en)
|
1998-04-03 |
2010-05-11 |
Elitech Holding B.V. |
Systems and methods for predicting oligonucleotide melting temperature (TmS)
|
US6127121A
(en)
|
1998-04-03 |
2000-10-03 |
Epoch Pharmaceuticals, Inc. |
Oligonucleotides containing pyrazolo[3,4-D]pyrimidines for hybridization and mismatch discrimination
|
US6432970B2
(en)
|
1998-04-09 |
2002-08-13 |
Johns Hopkins University School Of Medicine |
Inhibitors of hedgehog signaling pathways, compositions and uses related thereto
|
KR19990085365A
(ko)
|
1998-05-16 |
1999-12-06 |
허영섭 |
지속적으로 약물 조절방출이 가능한 생분해성 고분자 미립구 및그 제조방법
|
JP2000072773A
(ja)
|
1998-08-28 |
2000-03-07 |
Zeria Pharmaceut Co Ltd |
プリン誘導体
|
CZ2001959A3
(cs)
|
1998-09-18 |
2001-12-12 |
Basf Aktiengesellschaft |
4-Aminopyrrolopyrimidiny jako inhibitory kinasy
|
PT1144411E
(pt)
|
1998-12-19 |
2005-09-30 |
Janssen Pharmaceutica Nv |
Compostos espiro anti-histaminicos
|
JP4876239B2
(ja)
|
1999-01-11 |
2012-02-15 |
プリンストン ユニバーシティー |
標的確認のための高親和性阻害剤およびその使用
|
CZ27399A3
(cs)
|
1999-01-26 |
2000-08-16 |
Ústav Experimentální Botaniky Av Čr |
Substituované dusíkaté heterocyklické deriváty, způsob jejich přípravy, tyto deriváty pro použití jako léčiva, farmaceutická kompozice a kombinovaný farmaceutický přípravek tyto deriváty obsahující a použití těchto derivátů pro výrobu léčiv
|
US6248363B1
(en)
|
1999-11-23 |
2001-06-19 |
Lipocine, Inc. |
Solid carriers for improved delivery of active ingredients in pharmaceutical compositions
|
US6596497B1
(en)
|
1999-03-17 |
2003-07-22 |
New York Blood Center, Inc. |
Screening of antiviral compounds targeted to the HIV-1 gp41 core structure
|
EP1040831A3
(en)
|
1999-04-02 |
2003-05-02 |
Pfizer Products Inc. |
Use of corticotropin releasing factor (CRF) antagonists to prevent sudden death
|
SE515856C2
(sv)
|
1999-05-19 |
2001-10-22 |
Ericsson Telefon Ab L M |
Bärare för elektronikkomponenter
|
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
(es)
|
1999-07-02 |
2001-03-29 |
Agouron Pharma |
Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa
|
GB9919588D0
(en)
|
1999-08-18 |
1999-10-20 |
Hoechst Schering Agrevo Gmbh |
Fungicidal compounds
|
DE19940859A1
(de)
|
1999-08-27 |
2001-03-01 |
Bayer Ag |
Selektive Herbizide auf Basis eines substituierten Phenylsulfonylaminocarbonyltriazolinons und Safenern
|
DE19940860A1
(de)
|
1999-08-27 |
2001-03-01 |
Bayer Ag |
Selektive Herbizide auf Basis eines substituierten Phenylsulfonyl aminocarbonyltriazolinons und Safenern II
|
DE60031285T2
(de)
|
1999-08-27 |
2007-08-30 |
Chemocentryx Inc., Mountain View |
Heterozyclische verbindungen und verfahren zur modulierung von cxcr3 funktion
|
US20070021493A1
(en)
|
1999-09-16 |
2007-01-25 |
Curis, Inc. |
Mediators of hedgehog signaling pathways, compositions and uses related thereto
|
US20050080138A1
(en)
|
1999-09-16 |
2005-04-14 |
Curis, Inc. |
Mediators of hedgehog signaling pathways, compositions and uses related thereto
|
EP1216234B1
(en)
|
1999-09-16 |
2004-12-29 |
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
|
IL148718A0
(en)
|
1999-09-17 |
2002-09-12 |
Abbott Gmbh & Co Kg |
Pyrazolopyrimidines as therapeutic agents
|
EP1222187B1
(en)
|
1999-10-06 |
2004-09-22 |
Boehringer Ingelheim Pharmaceuticals Inc. |
Heterocyclic compounds useful as inhibitors of tyrosine kinases
|
US6506769B2
(en)
|
1999-10-06 |
2003-01-14 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Heterocyclic compounds useful as inhibitors of tyrosine kinases
|
EP1728797A3
(en)
|
1999-10-13 |
2011-03-02 |
Johns Hopkins University School of Medicine |
Regulators of the hedgehog pathway, compositions and uses related thereto
|
JP4898044B2
(ja)
|
1999-10-14 |
2012-03-14 |
キュリス,インコーポレイテッド |
ヘッジホッグシグナル伝達経路のメディエーター、それらと関連する組成物及び利用
|
US6472153B1
(en)
|
1999-10-26 |
2002-10-29 |
Epoch Biosciences, Inc. |
Hybridization-triggered fluorescent detection of nucleic acids
|
US6545004B1
(en)
|
1999-10-27 |
2003-04-08 |
Cytokinetics, Inc. |
Methods and compositions utilizing quinazolinones
|
US7671200B2
(en)
|
1999-10-27 |
2010-03-02 |
Cytokinetics, Inc. |
Quinazolinone KSP inhibitors
|
US7230000B1
(en)
|
1999-10-27 |
2007-06-12 |
Cytokinetics, Incorporated |
Methods and compositions utilizing quinazolinones
|
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
|
JP2001250689A
(ja)
|
2000-03-07 |
2001-09-14 |
Toray Ind Inc |
発光素子
|
US6469026B2
(en)
|
2000-03-24 |
2002-10-22 |
Millennium Pharmaceuticals, Inc. |
Isoquinolone inhibitors of factor Xa
|
AU2001249664C1
(en)
|
2000-03-30 |
2008-08-14 |
Curis, Inc. |
Small organic molecule regulators of cell proliferation
|
US20050070578A1
(en)
|
2000-03-30 |
2005-03-31 |
Baxter Anthony David |
Small organic molecule regulators of cell proliferation
|
US6683192B2
(en)
|
2000-03-30 |
2004-01-27 |
Curis, Inc. |
Small organic molecule regulators of cell proliferation
|
US6683108B1
(en)
|
2000-03-30 |
2004-01-27 |
Curis, Inc. |
Agonists of hedgehog signaling pathways and uses related thereto
|
US6613798B1
(en)
|
2000-03-30 |
2003-09-02 |
Curis, Inc. |
Small organic molecule regulators of cell proliferation
|
US7115653B2
(en)
|
2000-03-30 |
2006-10-03 |
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
|
SI2223922T1
(sl)
|
2000-04-25 |
2016-04-29 |
Icos Corporation |
Inhibitorji humane fosfatidil-inositol 3-kinazne delta izoforme
|
US6667300B2
(en)
|
2000-04-25 |
2003-12-23 |
Icos Corporation |
Inhibitors of human phosphatidylinositol 3-kinase delta
|
GB0010709D0
(en)
|
2000-05-03 |
2000-06-28 |
Vectura Ltd |
Powders for use a in dry powder inhaler
|
AU6513701A
(en)
|
2000-05-30 |
2001-12-11 |
Advanced Res & Tech Inst |
Compositions and methods for identifying agents which modulate pten function andpi-3 kinase pathways
|
US6849713B2
(en)
|
2000-06-27 |
2005-02-01 |
Genelabs Technologies, Inc. |
Compounds possessing antibacterial, antifungal or antitumor activity
|
US7080644B2
(en)
|
2000-06-28 |
2006-07-25 |
Microdose Technologies, Inc. |
Packaging and delivery of pharmaceuticals and drugs
|
US6534691B2
(en)
|
2000-07-18 |
2003-03-18 |
E. I. Du Pont De Nemours And Company |
Manufacturing process for α-olefins
|
AU2002212969B2
(en)
|
2000-09-20 |
2006-07-06 |
Merck Sharp & Dohme Corp. |
Isoquinolinone potassium channel inhibitors
|
US6811979B2
(en)
|
2000-10-11 |
2004-11-02 |
Applera Corporation |
Fluorescent nucleobase conjugates having anionic linkers
|
WO2002030358A2
(en)
|
2000-10-11 |
2002-04-18 |
Tularik Inc. |
Modulation of ccr4 function
|
JP2002131859A
(ja)
|
2000-10-19 |
2002-05-09 |
Konica Corp |
撮影用赤外感光性ハロゲン化銀写真感光材料及び赤外感光性ハロゲン化銀乳剤
|
US6890747B2
(en)
|
2000-10-23 |
2005-05-10 |
Warner-Lambert Company |
Phosphoinositide 3-kinases
|
EP1343505A1
(en)
|
2000-12-11 |
2003-09-17 |
Tularik Inc. |
Cxcr3 antagonists
|
AU2002217277B2
(en)
|
2000-12-21 |
2005-06-16 |
Glaxo Group Limited |
Macrolide antibiotics
|
KR100884877B1
(ko)
|
2000-12-28 |
2009-02-23 |
다이이찌 세이야꾸 가부시기가이샤 |
Vla-4 저해제
|
RS50236B
(sr)
|
2001-01-22 |
2009-07-15 |
Merck & Co.Inc., |
Nukleozidni derivati kao inhibitori rnk-zavisne rnk virusne polimeraze
|
US7105499B2
(en)
|
2001-01-22 |
2006-09-12 |
Merck & Co., Inc. |
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
|
GB2373186A
(en)
|
2001-02-23 |
2002-09-18 |
Astrazeneca Ab |
Pharmaceutical combinations of a CCR3 antagonist and a compound which is usefulreatment of asthma, allergic disease or inflammation
|
MXPA03008560A
(es)
|
2001-03-22 |
2004-06-30 |
Abbot Gmbh & Co Kg |
Pirazolopirimidinas como agentes terapeuticos.
|
DE10118698A1
(de)
|
2001-04-17 |
2002-11-07 |
Jerini Ag |
Verfahren zur Immobilisierung und damit hergestellte Anordnungen von Verbindungen auf einer planaren Oberfläche
|
US7250569B2
(en)
|
2001-04-26 |
2007-07-31 |
New York University School Of Medicine |
Method for dissolving nanostructural materials
|
US7405235B2
(en)
|
2001-05-04 |
2008-07-29 |
Paratek Pharmaceuticals, Inc. |
Transcription factor modulating compounds and methods of use thereof
|
US6664269B2
(en)
|
2001-05-08 |
2003-12-16 |
Maybridge Plc |
Isoquinolinone derivatives
|
US7144903B2
(en)
|
2001-05-23 |
2006-12-05 |
Amgen Inc. |
CCR4 antagonists
|
US6794379B2
(en)
|
2001-06-06 |
2004-09-21 |
Tularik Inc. |
CXCR3 antagonists
|
EP1470119A4
(en)
|
2001-06-13 |
2005-10-19 |
Genesoft Pharmaceuticals Inc |
BENZOTHIOPHENE COMPOUNDS WITH ANTI-INFECTIOUS ACTIVITY
|
US6777425B2
(en)
|
2001-06-13 |
2004-08-17 |
Genesoft Pharmaceuticals, Inc. |
Isoquinoline compounds having antiinfective activity
|
WO2002101007A2
(en)
|
2001-06-13 |
2002-12-19 |
Genesoft Pharmaceuticals, Inc |
Antipathogenic benzamide compounds
|
US20030114467A1
(en)
|
2001-06-21 |
2003-06-19 |
Shakespeare William C. |
Novel pyrazolo- and pyrrolo-pyrimidines and uses thereof
|
US6596723B1
(en)
|
2001-07-16 |
2003-07-22 |
Essential Therapeutics, Inc. |
Fungal efflux pump inhibitors
|
US20030220338A1
(en)
|
2001-07-16 |
2003-11-27 |
Watkins Will J. |
Fungal efflux pump inhibitors
|
US6689782B2
(en)
|
2001-07-16 |
2004-02-10 |
Essential Therapeutics, Inc. |
Fungal efflux pump inhibitors
|
AU2002322585A1
(en)
|
2001-07-20 |
2003-03-03 |
Adipogenix, Inc. |
Fat accumulation-modulating compounds
|
BR0211513A
(pt)
|
2001-07-27 |
2005-08-30 |
Curis Inc |
Mediadores de caminhos sinalizantes de hedgehog, composições e usos relacionados ao mesmo
|
US6852727B2
(en)
|
2001-08-01 |
2005-02-08 |
Merck & Co., Inc. |
Benzimisazo[4,5-f]isoquinolinone derivatives
|
AU2002327422A1
(en)
|
2001-08-03 |
2003-03-18 |
Abbott Laboratories |
Method of identifying inhibitors of lck
|
CN100491349C
(zh)
|
2001-08-10 |
2009-05-27 |
盐野义制药株式会社 |
抗病毒药
|
JP2003073357A
(ja)
|
2001-09-03 |
2003-03-12 |
Mitsubishi Pharma Corp |
アミド化合物を含有するRhoキナーゼ阻害剤
|
DE60236605D1
(de)
|
2001-09-05 |
2010-07-15 |
Minerva Biotechnologies Corp |
Zusammensetzungen und deren verwendung zur behandlung von krebs
|
WO2003024969A1
(en)
|
2001-09-14 |
2003-03-27 |
Merck & Co., Inc. |
Tyrosine kinase inhibitors
|
AU2002368274A1
(en)
|
2001-09-13 |
2004-06-03 |
Genesoft, Inc. |
Methods of treating infection by drug resistant bacteria
|
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
(ru)
|
2001-10-22 |
2010-09-11 |
Eisai R&D Man Co Ltd |
|
EP1448556A1
(en)
|
2001-11-01 |
2004-08-25 |
Janssen Pharmaceutica N.V. |
Heteroaryl amines as glycogen synthase kinase 3beta inhibitors (gsk3 inhibitors)
|
US20030113828A1
(en)
|
2001-11-09 |
2003-06-19 |
Ginsberg Mark H. |
Compositions and methods for modulating Syk function
|
WO2003043961A2
(en)
|
2001-11-19 |
2003-05-30 |
Iconix Pharmaceuticals, Inc. |
Modulators of rho c activity
|
AU2002346471A1
(en)
|
2001-11-20 |
2003-06-10 |
Cytokinetics, Inc. |
Process for the racemization of chiral quinazolinones
|
EP1450796B1
(en)
|
2001-11-27 |
2008-04-09 |
F. Hoffmann-La Roche Ag |
Benzothiazole derivatives
|
AU2002350217A1
(en)
|
2001-12-04 |
2003-06-17 |
Bristol-Myers Squibb Company |
Glycinamides as factor xa inhibitors
|
DE60231439D1
(de)
|
2001-12-06 |
2009-04-16 |
Merck & Co Inc |
Mitotische kinesinhemmer
|
AU2002351183B2
(en)
|
2001-12-06 |
2008-05-08 |
Merck Sharp & Dohme Corp. |
Mitotic kinesin inhibitors
|
EP1465869B1
(en)
|
2001-12-21 |
2013-05-15 |
Exelixis Patent Company LLC |
Modulators of lxr
|
JP4085237B2
(ja)
|
2001-12-21 |
2008-05-14 |
日本電気株式会社 |
携帯電話の利用契約システムと通信方法
|
US20030158195A1
(en)
|
2001-12-21 |
2003-08-21 |
Cywin Charles L. |
1,6 naphthyridines useful as inhibitors of SYK kinase
|
AU2002364209A1
(en)
|
2001-12-26 |
2003-07-24 |
Genelabs Technologies, Inc. |
Polyamide derivatives possessing antibacterial, antifungal or antitumor activity
|
US7414036B2
(en)
|
2002-01-25 |
2008-08-19 |
Muscagen Limited |
Compounds useful as A3 adenosine receptor agonists
|
US7009049B2
(en)
|
2002-02-15 |
2006-03-07 |
Cytokinetics, Inc. |
Syntheses of quinazolinones
|
US20040043959A1
(en)
|
2002-03-04 |
2004-03-04 |
Bloom Laura A. |
Combination therapies for treating methylthioadenosine phosphorylase deficient cells
|
WO2003076418A1
(en)
|
2002-03-07 |
2003-09-18 |
X-Ceptor Therapeutics, Inc. |
Quinazolinone modulators of nuclear receptors
|
US6995144B2
(en)
|
2002-03-14 |
2006-02-07 |
Eisai Co., Ltd. |
Nitrogen containing heterocyclic compounds and medicines containing the same
|
WO2003082341A1
(en)
|
2002-03-22 |
2003-10-09 |
Cellular Genomics, Inc. |
AN IMPROVED FORMULATION OF CERTAIN PYRAZOLO[3,4-d] PYRIMIDINES AS KINASE MODULATORS
|
EP1503988B1
(de)
|
2002-03-26 |
2009-07-22 |
Biofrontera Discovery Gmbh |
Fredericamycin-derivate
|
US7166293B2
(en)
|
2002-03-29 |
2007-01-23 |
Carlsbad Technology, Inc. |
Angiogenesis inhibitors
|
US6900219B2
(en)
|
2002-04-04 |
2005-05-31 |
Cv Therapeutics, Inc. |
ABCA-1 elevating compounds
|
DE10217046A1
(de)
|
2002-04-17 |
2003-11-06 |
Bioleads Gmbh |
Fredericamycin-Derivate
|
EP1496905B1
(en)
|
2002-04-22 |
2008-08-13 |
Johns Hopkins University School of Medicine |
Modulators of hedgehog signaling pathways, compositions and uses related thereto
|
JP2005529889A
(ja)
|
2002-04-26 |
2005-10-06 |
ファイザー・プロダクツ・インク |
ピリミジン−2,4,6−トリオンメタロ−プロテイナーゼ阻害剤
|
US6794562B2
(en)
|
2002-05-01 |
2004-09-21 |
Stine Seed Farm, Inc. |
Soybean cultivar 0332143
|
US7166595B2
(en)
|
2002-05-09 |
2007-01-23 |
Cytokinetics, Inc. |
Compounds, methods and compositions
|
EP1553931A4
(en)
|
2002-05-09 |
2006-08-30 |
Cytokinetics Inc |
COMPOUNDS, COMPOSITIONS AND METHODS
|
TW200407143A
(en)
|
2002-05-21 |
2004-05-16 |
Bristol Myers Squibb Co |
Pyrrolotriazinone compounds and their use to treat diseases
|
AU2003299517A1
(en)
|
2002-05-23 |
2004-05-25 |
Merck & Co., Inc. |
Mitotic kinesin inhibitors
|
AU2003265242A1
(en)
|
2002-05-23 |
2003-12-22 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
EP1556357A4
(en)
|
2002-06-14 |
2006-09-13 |
Cytokinetics Inc |
COMPOUNDS, COMPOSITIONS AND METHODS
|
JP4881559B2
(ja)
|
2002-06-27 |
2012-02-22 |
ノボ・ノルデイスク・エー/エス |
治療薬としてのアリールカルボニル誘導体
|
RU2340605C2
(ru)
|
2002-06-27 |
2008-12-10 |
Ново Нордиск А/С |
Арилкарбонильные производные в качестве терапевтических средств
|
US7265111B2
(en)
|
2002-06-27 |
2007-09-04 |
Sanofi-Aventis Deutschland Gmbh |
Adenosine analogues and their use as pharmaceutical agents
|
DE10230917A1
(de)
|
2002-07-09 |
2004-02-05 |
Bioleads Gmbh |
Fredericamycin-Derivate
|
CN1681811B
(zh)
|
2002-07-10 |
2010-05-26 |
默克雪兰诺有限公司 |
唑烷酮-乙烯基稠合的-苯衍生物
|
AU2003249244A1
(en)
|
2002-07-15 |
2004-02-02 |
Combinatorx, Incorporated |
Methods for the treatment of neoplasms
|
CA2494048A1
(en)
|
2002-08-13 |
2004-02-19 |
Warner-Lambert Company Llc |
4-hydroxyquinoline derivatives as matrix metalloproteinase inhibitors
|
CA2495661C
(en)
|
2002-08-16 |
2011-06-14 |
Kinacia Pty Ltd. |
Inhibition of phosphoinositide 3-kinase beta
|
EP1539180A4
(en)
|
2002-08-21 |
2006-08-30 |
Cytokinetics Inc |
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
|
JP4487774B2
(ja)
|
2002-09-30 |
2010-06-23 |
萬有製薬株式会社 |
2−アミノベンズイミダゾール誘導体
|
WO2004037176A2
(en)
|
2002-10-21 |
2004-05-06 |
Bristol-Myers Squibb Company |
Quinazolinones and derivatives thereof as factor xa inhibitors
|
JP2004161716A
(ja)
|
2002-11-15 |
2004-06-10 |
Takeda Chem Ind Ltd |
Jnk阻害剤
|
CN1281590C
(zh)
|
2002-11-27 |
2006-10-25 |
南京凯衡科贸有限公司 |
具有抑制血管生成活性的六员氨基酰胺类衍生物
|
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
|
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
|
EP1583562B1
(en)
*
|
2003-01-06 |
2011-06-15 |
Angiochem Inc. |
Angiopep-1, related compounds, and uses thereof
|
FR2850022B1
(fr)
|
2003-01-22 |
2006-09-08 |
Centre Nat Rech Scient |
Nouvelle utilisation de la mifepristone et de ses derives comme modulateurs de la voie de signalisation des proteines hedgehog et ses applications
|
WO2004069145A2
(en)
|
2003-02-07 |
2004-08-19 |
Dr. Reddy's Laboratories Ltd. |
Anticancer compounds, process for their preparation and pharmaceutical compositions containing them
|
JP2006521373A
(ja)
|
2003-03-06 |
2006-09-21 |
デーエスエム アイピー アセッツ ベー. ヴェー. |
α−アミノカルボニル化合物の調製方法
|
WO2006018628A1
(en)
|
2003-03-07 |
2006-02-23 |
Astrazeneca Ab |
Enantiomers of selected fused pyrimidones and uses in the treatment and preventi on of cancer
|
CN1894234A
(zh)
|
2003-03-25 |
2007-01-10 |
武田药品工业株式会社 |
二肽基肽酶抑制剂
|
GB0306907D0
(en)
|
2003-03-26 |
2003-04-30 |
Angiogene Pharm Ltd |
Boireductively-activated prodrugs
|
WO2004103270A2
(en)
|
2003-04-02 |
2004-12-02 |
Suntory Pharmaceutical Research Laboratories Llc |
Compounds and methods for treatment of thrombosis
|
WO2004092123A2
(en)
|
2003-04-10 |
2004-10-28 |
Microbia, Inc. |
Inhibitors of fungal invasion
|
CA2525764C
(en)
|
2003-05-20 |
2012-07-17 |
Novartis Ag |
N-acyl nitrogen heterocycles as ligands of peroxisome proliferator-activated receptors
|
US7022850B2
(en)
|
2003-05-22 |
2006-04-04 |
Bristol-Myers Squibb Co. |
Bicyclicpyrimidones and their use to treat diseases
|
US7345046B2
(en)
|
2003-05-30 |
2008-03-18 |
Chiron Corporation |
Heteroaryl-fused pyrimidinyl compounds as anticancer agents
|
WO2004111014A1
(en)
|
2003-06-06 |
2004-12-23 |
Vertex Pharmaceuticals Incorporated |
Pyrimidine derivatives as modulators of atp-binding cassette transporters
|
WO2004113307A1
(ja)
|
2003-06-18 |
2004-12-29 |
Ube Industries, Ltd. |
ピリミジン−4−オン化合物の製造方法
|
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
|
EP1680125A1
(en)
|
2003-07-02 |
2006-07-19 |
Warner-Lambert Company LLC |
Combination of an allosteric inhibitor of matrix metalloproteinase-13 and a ligand to an alpha-2-delta receptor
|
CN100577680C
(zh)
|
2003-07-03 |
2010-01-06 |
宾夕法尼亚大学理事会 |
对Syk激酶表达的抑制
|
WO2005005421A1
(en)
|
2003-07-08 |
2005-01-20 |
Novartis Ag |
Benzenesulfonylamino compounds and pharmaceutical compositions containing these compounds
|
JP2005035933A
(ja)
|
2003-07-15 |
2005-02-10 |
Takeda Chem Ind Ltd |
含窒素縮合複素環化合物の製造方法
|
WO2005013800A2
(en)
|
2003-07-15 |
2005-02-17 |
The Johns Hopkins University |
Elevated hedgehog pathway activity in digestive system tumors, and methods of treating digestive system 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
|
WO2005014532A1
(en)
|
2003-08-08 |
2005-02-17 |
Transtech Pharma, Inc. |
Aryl and heteroaryl compounds, compositions and methods of use
|
WO2005016349A1
(en)
|
2003-08-14 |
2005-02-24 |
Icos Corporation |
Methods of inhibiting leukocyte accumulation
|
US20050043239A1
(en)
|
2003-08-14 |
2005-02-24 |
Jason Douangpanya |
Methods of inhibiting immune responses stimulated by an endogenous factor
|
MXPA06001758A
(es)
|
2003-08-15 |
2006-08-11 |
Irm Llc |
Anilino purinas sustituidas en la posicion 6 utiles como inhibidores de rtk.
|
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
|
US8067608B2
(en)
|
2003-09-29 |
2011-11-29 |
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
|
WO2005042700A2
(en)
|
2003-10-20 |
2005-05-12 |
The Johns Hopkins University |
Use of hedgehog pathway inhibitors in small-cell lung cancer
|
CA2545340A1
(en)
|
2003-11-10 |
2005-05-26 |
Synta Pharmaceuticals, Corp. |
Fused heterocyclic compounds
|
WO2005049838A2
(en)
|
2003-11-14 |
2005-06-02 |
Yale University |
Syk-targeted nucleic acid interference
|
US20070135454A1
(en)
|
2003-11-14 |
2007-06-14 |
Tracy Bayliss |
Bicyclic pyrimidin-4(3h)-ones and analogues and derivatives thereof which modulate the function of the vanilloid-1-receptor(vr1)
|
EP1687309A1
(en)
|
2003-11-17 |
2006-08-09 |
Pfizer Products Inc. |
Pyrrolopyrimidine compounds useful in treatment of cancer
|
US7449477B2
(en)
|
2003-11-25 |
2008-11-11 |
Eli Lilly And Company |
7-phenyl-isoquinoline-5-sulfonylamino derivatives as inhibitors of akt (protein kinase B)
|
DK1689724T3
(da)
|
2003-11-25 |
2012-02-27 |
Novartis Ag |
Quinazolinonforbindelser som anticancermidler
|
EP1692112A4
(en)
|
2003-12-08 |
2008-09-24 |
Cytokinetics Inc |
COMPOUNDS, COMPOSITIONS, AND METHODS
|
EP1715871A1
(en)
|
2003-12-22 |
2006-11-02 |
Gilead Sciences, Inc. |
Kinase inhibitor phosphonate conjugates
|
ES2339670T3
(es)
|
2003-12-23 |
2010-05-24 |
Novartis Ag |
Inhibidores heterociclicos biciclicos de la quinasa p-38.
|
US20050152940A1
(en)
|
2003-12-23 |
2005-07-14 |
Medtronic Vascular, Inc. |
Medical devices to treat or inhibit restenosis
|
JPWO2005061707A1
(ja)
|
2003-12-24 |
2007-07-12 |
協和醗酵工業株式会社 |
癌細胞のEg5阻害剤に対する感受性を判定する方法
|
US20050239809A1
(en)
|
2004-01-08 |
2005-10-27 |
Watts Stephanie W |
Methods for treating and preventing hypertension and hypertension-related disorders
|
WO2005070457A1
(en)
|
2004-01-23 |
2005-08-04 |
Seattle Genetics, Inc. |
Melphalan prodrugs
|
CA2553724A1
(en)
|
2004-02-03 |
2005-08-18 |
Abbott Laboratories |
Aminobenzoxazoles as therapeutic agents
|
CA2555824C
(en)
|
2004-02-13 |
2011-06-07 |
Banyu Pharmaceutical Co., Ltd. |
Fused-ring 4-oxopyrimidine derivative
|
US7650848B2
(en)
|
2004-02-17 |
2010-01-26 |
University Of Florida Research Foundation, Inc. |
Surface topographies for non-toxic bioadhesion control
|
US7117807B2
(en)
|
2004-02-17 |
2006-10-10 |
University Of Florida Research Foundation, Inc. |
Dynamically modifiable polymer coatings and devices
|
US9016221B2
(en)
|
2004-02-17 |
2015-04-28 |
University Of Florida Research Foundation, Inc. |
Surface topographies for non-toxic bioadhesion control
|
US20050187418A1
(en)
|
2004-02-19 |
2005-08-25 |
Small Brooke L. |
Olefin oligomerization
|
CN1980929A
(zh)
|
2004-02-24 |
2007-06-13 |
比奥阿克松医疗技术股份有限公司 |
4-取代哌啶衍生物
|
US20070049593A1
(en)
|
2004-02-24 |
2007-03-01 |
Japan Tobacco Inc. |
Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor
|
CA2554136C
(en)
|
2004-02-24 |
2013-05-28 |
Microdose Technologies, Inc. |
Synthetic jet based medicament delivery method and apparatus
|
CA2557575A1
(en)
|
2004-02-27 |
2005-09-15 |
F. Hoffmann-La Roche Ag |
Fused derivatives of pyrazole
|
WO2005097800A1
(en)
|
2004-04-02 |
2005-10-20 |
Osi Pharmaceuticals, Inc. |
6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors
|
US8057815B2
(en)
|
2004-04-19 |
2011-11-15 |
Portola Pharmaceuticals, Inc. |
Methods of treatment with Syk inhibitors
|
WO2005105760A1
(en)
|
2004-04-30 |
2005-11-10 |
Takeda Pharmaceutical Company Limited |
Heterocyclic amide compound and use thereof as an mmp-13 inhibitor
|
AU2005325267B2
(en)
|
2004-04-30 |
2010-11-04 |
Curis Inc. |
Quinoxaline inhibitors of the hedgehog signalling pathway
|
DE102004022897A1
(de)
|
2004-05-10 |
2005-12-08 |
Bayer Cropscience Ag |
Azinyl-imidazoazine
|
DK1761540T3
(en)
|
2004-05-13 |
2016-11-21 |
Icos Corp |
Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase DELTA
|
CA2730540A1
(en)
|
2004-05-13 |
2005-12-01 |
Vanderbilt University |
Phosphoinositide 3-kinase delta selective inhibitors for inhibiting angiogenesis
|
EP1755609A1
(en)
|
2004-05-25 |
2007-02-28 |
Icos Corporation |
Methods for treating and/or preventing aberrant proliferation of hematopoietic cells
|
GB0412467D0
(en)
|
2004-06-04 |
2004-07-07 |
Astrazeneca Ab |
Chemical compounds
|
JP2008501707A
(ja)
|
2004-06-04 |
2008-01-24 |
アイコス、コーポレーション |
マスト細胞障害を処置するための方法
|
WO2005123083A1
(en)
|
2004-06-09 |
2005-12-29 |
Cytokinetics, Inc. |
Compositions, devices and methods for treating cardiovascular disease
|
US7375102B2
(en)
|
2004-06-28 |
2008-05-20 |
Amgen Sf, Llc |
Tetrahydroquinazolin-4(3H)-one-related and tetrahydropyrido[2,3-D]pyrimidin-4(3H)-one-related compounds, compositions and methods for their use
|
US7939538B2
(en)
|
2004-06-28 |
2011-05-10 |
Amgen Inc. |
Compounds, compositions and methods for prevention and treatment of inflammatory and immunoregulatory disorders and diseases
|
WO2006023381A1
(en)
|
2004-08-16 |
2006-03-02 |
Taigen Biotechnology |
Pyrimidinone compounds
|
UY29070A1
(es)
|
2004-08-18 |
2006-03-31 |
Astrazeneca Ab |
Enantiómeros de heterocíclicos fusionados y sus usos
|
US20060041128A1
(en)
|
2004-08-18 |
2006-02-23 |
Astrazeneca Ab |
Selected fused heterocyclics and uses thereof
|
CN102241727B
(zh)
|
2004-08-27 |
2015-03-25 |
无限药品股份有限公司 |
环杷明类似物及其使用方法
|
WO2006026597A2
(en)
|
2004-08-30 |
2006-03-09 |
Smithkline Beecham Corporation |
Novel compositions and methods of treatment
|
CN101048388A
(zh)
|
2004-08-31 |
2007-10-03 |
阿斯利康(瑞典)有限公司 |
喹唑啉酮衍生物及其作为B-Raf抑制剂的用途
|
KR20150090263A
(ko)
|
2004-09-02 |
2015-08-05 |
제넨테크, 인크. |
헤지호그 신호전달에 대한 피리딜 억제제
|
US7825126B2
(en)
|
2004-09-09 |
2010-11-02 |
The United States Of America As Represented By The Department Of Health And Human Services |
Purine derivatives as A3 and A1 adenosine receptor agonists
|
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
|
RU2007119637A
(ru)
|
2004-10-28 |
2008-12-10 |
Айрм Ллк (Bm) |
Соединения и композиции в качестве модуляторов hedgehog-пути
|
EP1807440B1
(en)
|
2004-11-03 |
2020-02-19 |
The University of Kansas |
Novobiocin analogues as anticancer agents
|
US7622451B2
(en)
|
2004-11-03 |
2009-11-24 |
University Of Kansas |
Novobiocin analogues as neuroprotective agents and in the treatment of autoimmune disorders
|
US8212011B2
(en)
|
2004-11-03 |
2012-07-03 |
University Of Kansas |
Novobiocin analogues
|
US8212012B2
(en)
|
2004-11-03 |
2012-07-03 |
University Of Kansas |
Novobiocin analogues having modified sugar moieties
|
GB0425035D0
(en)
|
2004-11-12 |
2004-12-15 |
Novartis Ag |
Organic compounds
|
JP2008520744A
(ja)
|
2004-11-19 |
2008-06-19 |
ザ・レジェンツ・オブ・ザ・ユニバーシティ・オブ・カリフォルニア |
抗炎症性ピラゾロピリミジン
|
CA2588389A1
(en)
|
2004-11-23 |
2006-06-22 |
Ptc Therapeutics, Inc. |
Substituted phenols as active agents inhibiting vegf production
|
US20060156485A1
(en)
|
2005-01-14 |
2006-07-20 |
The Procter & Gamble Company |
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
|
EP1855685A4
(en)
|
2005-01-19 |
2009-12-23 |
Merck & Co Inc |
INHIBITORS OF MITOTIC KINESINE
|
CA2595130A1
(en)
|
2005-01-19 |
2006-07-27 |
Paul J. Coleman |
Mitotic kinesin inhibitors
|
EP1848698B1
(en)
|
2005-01-25 |
2013-03-13 |
Prolexys Pharmaceuticals, Inc. |
Quinoxaline derivatives as antitumor agents
|
US20070161644A1
(en)
|
2005-01-25 |
2007-07-12 |
Stockwell Brent R |
Erastin analogs and uses 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
|
US7579348B2
(en)
|
2005-02-25 |
2009-08-25 |
Pgxhealth, Llc |
Derivatives of 8-substituted xanthines
|
BRPI0607062A2
(pt)
|
2005-02-28 |
2009-08-04 |
Japan Tobacco Inc |
composto de aminopiridina com atividade inibidora de syk, composição farmacêutica e agente terapêutico compreendendo os mesmos
|
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
|
JP2006265107A
(ja)
|
2005-03-22 |
2006-10-05 |
Kyowa Hakko Kogyo Co Ltd |
緑内障治療剤
|
GB0506147D0
(en)
|
2005-03-24 |
2005-05-04 |
Merck Sharp & Dohme |
Therapeutic agents
|
CN101189234B
(zh)
|
2005-03-25 |
2011-08-17 |
泰博特克药品有限公司 |
Hcv的杂二环抑制剂
|
MX2007011850A
(es)
|
2005-03-25 |
2007-10-03 |
Tibotec Pharm Ltd |
Inhibidores heterobiciclicos de virus de hepatitis c.
|
JP2008534565A
(ja)
|
2005-03-31 |
2008-08-28 |
アストラゼネカ アクチボラグ |
Tie2阻害活性のあるアミノピリミジン誘導体
|
MX2007012449A
(es)
|
2005-04-06 |
2007-12-05 |
Irm Llc |
Compuestos y composiciones que contienen diaril-amina, y su uso como moduladores de los receptores nucleares de hormonas esteroideas.
|
KR100781704B1
(ko)
|
2005-04-20 |
2007-12-03 |
에스케이케미칼주식회사 |
피리딘 유도체와 이의 제조방법, 및 이를 포함하는약제조성물
|
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
|
WO2006121518A2
(en)
|
2005-05-10 |
2006-11-16 |
Angiotech International Ag |
Electrical devices, anti-scarring agents, and therapeutic compositions
|
WO2006135479A2
(en)
|
2005-05-10 |
2006-12-21 |
Angiotech International Ag |
Anti-scarring agents, therapeutic compositions, and use thereof
|
WO2006121522A2
(en)
|
2005-05-10 |
2006-11-16 |
Angiotech International Ag |
Implantable sensors and pumps, anti-scarring agents, and therapeutic compositions
|
CA2607929A1
(en)
|
2005-05-11 |
2006-11-16 |
Merck Sharp & Dohme Limited |
2,3-substituted fused bicyclic pyrimidin-4(3h)-ones modulating the function of the vanilloid-1 receptor (vr1)
|
GB0509573D0
(en)
|
2005-05-11 |
2005-06-15 |
Merck Sharp & Dohme |
Therapeutic compounds
|
DE102005024017A1
(de)
|
2005-05-25 |
2006-11-30 |
Merck Patent Gmbh |
Chinazolinone
|
CN100526315C
(zh)
|
2005-06-16 |
2009-08-12 |
浙江医药股份有限公司新昌制药厂 |
N2-喹啉或异喹啉取代的嘌呤衍生物及其制备方法和其用途
|
SG10201504801VA
(en)
|
2005-06-22 |
2015-07-30 |
Chemocentryx Inc |
Azaindazole compounds and methods of use
|
EP1917250B1
(en)
|
2005-06-27 |
2010-07-21 |
Amgen, Inc |
Anti-inflammatory aryl nitrile compounds
|
WO2007008541A2
(en)
|
2005-07-08 |
2007-01-18 |
Kalypsys, Inc. |
Cellular cholesterol absorption modifiers
|
WO2007006547A1
(en)
|
2005-07-11 |
2007-01-18 |
Devgen N.V. |
Amide derivatives as kinase inhibitors
|
WO2007006546A1
(en)
|
2005-07-11 |
2007-01-18 |
Devgen N.V. |
Amide derivatives as kinase inhibitors
|
WO2007015877A2
(en)
|
2005-07-20 |
2007-02-08 |
Kalypsys, Inc. |
Inhibitors of p38 kinase and methods of treating inflammatory disorders
|
US20070017915A1
(en)
|
2005-07-22 |
2007-01-25 |
Weder Donald E |
Collapsible and/or erectable substantially egg-shaped container
|
GB0516723D0
(en)
|
2005-08-15 |
2005-09-21 |
Novartis Ag |
Organic compounds
|
WO2007023110A2
(en)
|
2005-08-25 |
2007-03-01 |
F. Hoffmann-La Roche Ag |
P38 map kinase inhibitors and methods for using the same
|
US20070049591A1
(en)
|
2005-08-25 |
2007-03-01 |
Kalypsys, Inc. |
Inhibitors of MAPK/Erk Kinase
|
CA2620414A1
(en)
|
2005-08-26 |
2007-03-01 |
Methylgene Inc. |
Benzodiazepine and benzopiperazine analog inhibitors of histone deacetylase
|
US20080318942A1
(en)
|
2005-09-01 |
2008-12-25 |
Bioagency Ag |
Fredericamycin Derivatives
|
WO2007041023A1
(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)
|
WO2007056155A1
(en)
|
2005-11-03 |
2007-05-18 |
Chembridge Research Laboratories, Inc. |
Heterocyclic compounds as tyrosine kinase modulators
|
JP2009514954A
(ja)
|
2005-11-04 |
2009-04-09 |
ハイドラ バイオサイエンシズ インコーポレイテッド |
Trpv3機能を変調するための化合物
|
EP1945202A2
(en)
|
2005-11-11 |
2008-07-23 |
Licentia OY |
Mammalian hedgehog signaling inhiabitors
|
JP5225857B2
(ja)
|
2005-11-14 |
2013-07-03 |
ジェネンテック,インコーポレイティド |
ヘッジホッグシグナル伝達のビスアミド阻害剤
|
JP5335432B2
(ja)
|
2005-11-17 |
2013-11-06 |
オーエスアイ・フアーマシユーテイカルズ・エル・エル・シー |
縮合2環系mTOR阻害剤
|
EP1954276A2
(en)
|
2005-11-22 |
2008-08-13 |
Merck & Co., Inc. |
Indole orexin receptor antagonists
|
US20070265231A1
(en)
|
2005-11-30 |
2007-11-15 |
Michael Hofmann |
Hydrazide Compounds for Combating Animal Pests
|
EP1956908A2
(en)
|
2005-12-08 |
2008-08-20 |
Cytokinetics, Inc. |
Certain compositions and methods of treatment
|
EP1979002A2
(en)
|
2005-12-19 |
2008-10-15 |
OSI Pharmaceuticals, Inc. |
Combination of igfr inhibitor and anti-cancer agent
|
US7572809B2
(en)
|
2005-12-19 |
2009-08-11 |
Hoffmann-La Roche Inc. |
Isoquinoline aminopyrazole derivatives
|
WO2007076055A2
(en)
|
2005-12-22 |
2007-07-05 |
Entremed, Inc. |
Compositions and methods comprising proteinase activated receptor antagonists
|
US20090170834A1
(en)
|
2005-12-22 |
2009-07-02 |
Prolexys Pharmaceuticals, Inc. |
Fused Pyrimidones and Thiopyrimidones, and Uses Thereof
|
CN101389630A
(zh)
|
2005-12-29 |
2009-03-18 |
艾博特公司 |
蛋白激酶抑制剂
|
EP1984376A4
(en)
|
2006-01-25 |
2009-04-08 |
Smithkline Beecham Corp |
CHEMICAL COMPOUNDS
|
WO2007089669A2
(en)
|
2006-01-26 |
2007-08-09 |
Wyeth |
Processes for the preparation of compounds which modulate cell proliferation
|
AU2007224020A1
(en)
|
2006-03-07 |
2007-09-13 |
Array Biopharma Inc. |
Heterobicyclic pyrazole compounds and methods of use
|
JP2009530342A
(ja)
|
2006-03-20 |
2009-08-27 |
エフ.ホフマン−ラ ロシュ アーゲー |
Btkおよびsyk蛋白キナーゼを阻害する方法
|
TW200800997A
(en)
|
2006-03-22 |
2008-01-01 |
Astrazeneca Ab |
Chemical compounds
|
SI2004683T1
(sl)
|
2006-03-24 |
2016-09-30 |
Biogen Hemophilia Inc. |
Pc5 kot encim za obdelavo propeptida faktorja ix
|
BRPI0709699A2
(pt)
|
2006-03-29 |
2011-07-26 |
Foldrx Pharmaceuticals Inc |
inibiÇço da toxidez da alfa-sinucleina
|
CA2647391C
(en)
|
2006-04-04 |
2015-12-29 |
The Regents Of The University Of California |
Kinase antagonists
|
EP2007737A2
(en)
|
2006-04-05 |
2008-12-31 |
AstraZeneca AB |
Chemical compounds
|
US20090163525A1
(en)
|
2006-04-05 |
2009-06-25 |
Astrazeneca Ab |
Substituted quinazolines with anti-cancer activity
|
JP2009536156A
(ja)
|
2006-04-14 |
2009-10-08 |
ノバルティス アクチエンゲゼルシャフト |
ヘッジホッグ経路関連障害の処置におけるビアリールカルボキサミドの使用
|
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
|
US20090149484A1
(en)
|
2006-04-18 |
2009-06-11 |
Astrazeneca Ab |
Quinazolin-4-one derivatives, process for their preparation and pharmaceutical compositions containing them
|
JP5331681B2
(ja)
|
2006-04-20 |
2013-10-30 |
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 |
c−fmsキナーゼの阻害剤
|
GB0607950D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
GB0607948D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
KR20080110925A
(ko)
|
2006-04-21 |
2008-12-19 |
노파르티스 아게 |
아데노신 a2a 수용체 효능제로서 사용하기 위한 퓨린 유도체
|
EP2016077A2
(en)
|
2006-04-25 |
2009-01-21 |
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
(de)
|
2006-04-27 |
2007-12-27 |
Bayer Healthcare Ag |
Heterocyclisch substituierte, anellierte Pyrazol-Derivate und ihre Verwendung
|
UA93548C2
(ru)
|
2006-05-05 |
2011-02-25 |
Айерем Елелсі |
Соединения и композиции kak модуляторы хеджхоговского сигнального пути
|
KR100722686B1
(ko)
|
2006-05-09 |
2007-05-30 |
주식회사 비에스이 |
부가적인 백 챔버를 갖고 기판에 음향홀이 형성된 실리콘콘덴서 마이크로폰
|
HUE026820T2
(en)
|
2006-05-09 |
2016-07-28 |
Novaremed Ltd |
The use of Syk tyrosine kinase inhibitors for the treatment of cell proliferative disorders
|
US20090306126A1
(en)
|
2006-05-22 |
2009-12-10 |
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
|
DE602006018877D1
(de)
|
2006-05-24 |
2011-01-27 |
Guardant S R L |
Alkalisiertes Lokalanästhetikum im Beutel
|
EP2044086A2
(en)
|
2006-06-30 |
2009-04-08 |
Janssen Pharmaceutica N.V. |
Thiazolopyrimidine modulators of trpv1
|
EP2079724B1
(en)
|
2006-07-20 |
2010-05-26 |
Amgen Inc. |
Substituted pyridone compounds and methods of use
|
WO2008014373A2
(en)
|
2006-07-27 |
2008-01-31 |
Smithkline Beecham Corporation |
Hspa1a as a marker for sensitivity to ksp inhibitors
|
WO2008013987A2
(en)
|
2006-07-27 |
2008-01-31 |
Prolexys Pharmaceuticals, Inc. |
N-alkyl substituted piperazinylmethylquinazolinones and azepanylmethylquinazolinones
|
KR20090033371A
(ko)
|
2006-07-28 |
2009-04-02 |
노파르티스 아게 |
지질 키나제 억제제로서의 2,4-치환된 퀴나졸린
|
EP2589597B1
(en)
|
2006-08-22 |
2019-03-06 |
Technion Research & Development Foundation |
Heterocyclic derivatives binding to the peripheral-type benzodiazepine receptor (PBR)
|
WO2008024977A2
(en)
|
2006-08-24 |
2008-02-28 |
Serenex, Inc. |
Isoquinoline, quinazoline and phthalazine derivatives
|
WO2008025755A1
(de)
|
2006-09-01 |
2008-03-06 |
Basf Se |
Verwendung von n-haltigen heterozyklen in dermokosmetika
|
DK2061765T3
(en)
|
2006-09-01 |
2015-01-26 |
Senhwa Biosciences Inc |
Serine-threonine protein kinase AND PARP-MODULATOR
|
EP1903044A1
(en)
|
2006-09-14 |
2008-03-26 |
Novartis AG |
Adenosine Derivatives as A2A Receptor Agonists
|
EP2298772A1
(en)
|
2006-10-18 |
2011-03-23 |
Takeda Pharmaceutical Company Limited |
Fused heterocyclic compounds
|
WO2008070357A2
(en)
|
2006-10-31 |
2008-06-12 |
Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services |
Smoothened polypeptides and methods of use
|
RU2333211C1
(ru)
|
2006-11-01 |
2008-09-10 |
Институт физиологически активных веществ Российской Академии наук |
N,n`-замещенные 3, 7-диазабицикло[3.3.1]нонаны, обладающие фармакологической активностью, фармацевтические композиции на их основе и способ их применения
|
US7772180B2
(en)
|
2006-11-09 |
2010-08-10 |
Bristol-Myers Squibb Company |
Hepatitis C virus inhibitors
|
CN101605797A
(zh)
|
2006-11-13 |
2009-12-16 |
伊莱利利公司 |
治疗炎症疾病和癌症的噻吩并嘧啶酮
|
WO2008063625A2
(en)
|
2006-11-20 |
2008-05-29 |
Adolor Corporation |
Pyridine compounds and methods of their use
|
CN109970735A
(zh)
|
2006-11-20 |
2019-07-05 |
诺华公司 |
化合物的盐和晶型
|
KR20090097908A
(ko)
|
2006-12-06 |
2009-09-16 |
베링거 인겔하임 인터내셔날 게엠베하 |
글루코코르티코이드 모사물, 이의 제조 방법, 이의 약제학적 조성물 및 용도
|
CN101605798A
(zh)
|
2006-12-14 |
2009-12-16 |
第一三共株式会社 |
咪唑并噻唑衍生物
|
WO2008082487A2
(en)
|
2006-12-20 |
2008-07-10 |
Schering Corporation |
Novel jnk inhibitors
|
CA2674525A1
(en)
|
2006-12-22 |
2008-07-03 |
Albert Einstein College Of Medicine Of Yeshiva University |
Azetidine analogues of nucleosidase and phosphorylase inhibitors
|
TWI433674B
(zh)
|
2006-12-28 |
2014-04-11 |
Infinity Discovery Inc |
環杷明(cyclopamine)類似物類
|
CN101583601B
(zh)
|
2007-01-17 |
2013-06-05 |
香港科技大学 |
作为褪黑素受体mt1和mt2的亚型选择性激动剂的异喹诺酮化合物
|
CN101641013B
(zh)
|
2007-01-22 |
2014-07-30 |
Gtx公司 |
核受体结合剂
|
US20130116277A1
(en)
|
2007-01-22 |
2013-05-09 |
James T. Dalton |
Aldo-keto reductase subfamily 1c3 (akr1c3) inhibitors
|
US20170014401A1
(en)
|
2007-01-22 |
2017-01-19 |
Gtx, Inc. |
Nuclear receptor binding agents
|
EA200900983A1
(ru)
|
2007-01-26 |
2010-02-26 |
Айрм Ллк |
Соединения и композиции в качестве ингибиторов киназы
|
TW200836743A
(en)
|
2007-01-29 |
2008-09-16 |
Xenon Pharmaceuticals Inc |
Quinazolinone and fused pyrimidinone compounds and their use in treating sodium channel-mediated diseases or conditions
|
JP2010520295A
(ja)
|
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 |
へテロ環状シクロパミン類似体及びその使用方法
|
CA2679845A1
(en)
|
2007-03-07 |
2008-09-12 |
Infinity Discovery, Inc. |
Cyclopamine lactam analogs and methods of use thereof
|
US20090306625A1
(en)
|
2007-03-09 |
2009-12-10 |
Angiodynamics, Inc. |
Treatment systems and methods for renal-related diseases
|
EP2073799A4
(en)
|
2007-03-12 |
2009-08-19 |
Vm Discovery Inc |
NOVEL ACTIVE SUBSTANCES FROM CALCIUMIONAL CHANNEL MODULATORS
|
EA018441B1
(ru)
|
2007-03-14 |
2013-08-30 |
ЭКСЕЛИКСИС ПАТЕНТ КОМПАНИ ЭлЭлСи |
Ингибиторы пути хеджхога
|
PE20090188A1
(es)
|
2007-03-15 |
2009-03-20 |
Novartis Ag |
Compuestos heterociclicos como moduladores de la senda de hedgehog
|
PT2137186E
(pt)
|
2007-03-23 |
2016-03-30 |
Amgen Inc |
Compostos heterocíclicos e suas utilizações
|
EP2139882B1
(en)
|
2007-03-23 |
2013-12-25 |
Amgen Inc. |
3- substituted quinoline or quinoxaline derivatives and their use as phosphatidylinositol 3-kinase (pi3k) inhibitors
|
CA2680783C
(en)
|
2007-03-23 |
2012-04-24 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
WO2008156513A2
(en)
|
2007-03-29 |
2008-12-24 |
University Of Connecticut |
Methods to protect skeletal muscle against injury
|
EP1977765A1
(en)
|
2007-04-03 |
2008-10-08 |
Diatos |
Peptide prodrugs
|
WO2008125014A1
(fr)
|
2007-04-13 |
2008-10-23 |
Institute Of Pharmacology And Toxicology Academy Of Military Medical Sciences P.L.A. |
Composés d'urée, leurs procédés de préparation et leurs utilisations pharmaceutiques
|
EP2134682B1
(en)
|
2007-04-13 |
2011-12-14 |
Sanofi |
A transition metal catalyzed synthesis of n-aminoindoles
|
WO2008131354A2
(en)
|
2007-04-20 |
2008-10-30 |
The Curators Of The University Of Missouri |
Phytoestrogens as regulators of hedgehog signaling and methods of their use in cancer treatment
|
JP2010163361A
(ja)
|
2007-04-27 |
2010-07-29 |
Dainippon Sumitomo Pharma Co Ltd |
キノリン誘導体
|
CA2685753A1
(en)
|
2007-05-09 |
2008-11-20 |
Neuromed Pharmaceuticals Ltd. |
Bicyclic pyrimidine derivatives as calcium channel blockers
|
US7960353B2
(en)
|
2007-05-10 |
2011-06-14 |
University Of Kansas |
Novobiocin analogues as neuroprotective agents and in the treatment of autoimmune disorders
|
AU2008254960B2
(en)
|
2007-05-17 |
2014-11-27 |
Cortex Pharmaceuticals, Inc. |
Di-substituted amides for enhancing glutamatergic synaptic responses
|
US20090214529A9
(en)
|
2007-05-22 |
2009-08-27 |
Taigen Biotechnology Co., Ltd. |
Kinesin inhibitors
|
WO2008147962A1
(en)
|
2007-05-23 |
2008-12-04 |
Siga Technologies, Inc. |
Antiviral drugs for treatment or prevention of dengue infection
|
WO2008153701A1
(en)
|
2007-05-24 |
2008-12-18 |
Schering Corporation |
Compounds for inhibiting ksp kinesin activity
|
US7928111B2
(en)
|
2007-06-08 |
2011-04-19 |
Senomyx, Inc. |
Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
|
US9603848B2
(en)
|
2007-06-08 |
2017-03-28 |
Senomyx, Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
MX2009013815A
(es)
|
2007-06-22 |
2010-03-01 |
Arqule Inc |
Compuestos de quinazolinona y metodos de uso para los mismos.
|
US20110217300A1
(en)
|
2007-06-22 |
2011-09-08 |
Arqule, Inc. |
Quinazolinone Compounds and Methods of Use Thereof
|
US20110123486A1
(en)
|
2007-06-25 |
2011-05-26 |
Prolexys Pharmaceuticals, Inc. |
Methods of treating multiple myeloma and resistant cancers
|
RU2523909C2
(ru)
|
2007-06-25 |
2014-07-27 |
Эндосайт, Инк. |
Конъюгаты, содержащие гидрофильные спейсеры линкеров
|
JP5492769B2
(ja)
|
2007-06-26 |
2014-05-14 |
サノフイ |
縮環されたベンゾイミダゾール及びアザベンゾイミダゾールの位置選択的金属触媒合成
|
WO2009004621A1
(en)
|
2007-07-02 |
2009-01-08 |
Technion Research & Development Foundation Ltd. |
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
|
RU2345996C1
(ru)
|
2007-07-17 |
2009-02-10 |
Андрей Александрович Иващенко |
Аннелированные азагетероциклические амиды, включающие пиримидиновый фрагмент, способ их получения и применения
|
CA2694218A1
(en)
|
2007-07-31 |
2009-02-05 |
Schering Corporation |
Anti-mitotic agent and aurora kinase inhibitor combination as anti-cancer treatment
|
WO2009018811A1
(de)
|
2007-08-06 |
2009-02-12 |
Schebo Biotech Ag |
Neue pharmazeutika, verfahren zu ihrer herstellung und ihre verwendung in der medizinischen therapie
|
US20110081317A1
(en)
|
2007-08-08 |
2011-04-07 |
University Of Rochester |
Enhancing Gene Transfer
|
US20090053192A1
(en)
|
2007-08-10 |
2009-02-26 |
Burnham Institute For Medical Research |
Tissue-nonspecific alkaline phosphatase (tnap) activators and uses thereof
|
JP5572549B2
(ja)
|
2007-08-13 |
2014-08-13 |
リガンド・ファーマシューティカルズ・インコーポレイテッド |
グルコキナーゼの新規な活性化剤
|
WO2009029617A1
(en)
|
2007-08-27 |
2009-03-05 |
Kalypsys, Inc. |
Diarylamine-substituted quinolones useful as inducible nitric oxide synthase inhibitors
|
WO2009036059A2
(en)
|
2007-09-10 |
2009-03-19 |
Boston Biomedical, Inc. |
Novel stat3 pathway inhibitors and cancer stem cell inhibitors
|
JP5227965B2
(ja)
|
2007-10-03 |
2013-07-03 |
独立行政法人理化学研究所 |
ニトロトリアゾール誘導体、およびそれを用いる化合物の製造方法
|
BRPI0818426A2
(pt)
|
2007-10-15 |
2017-06-13 |
Astrazeneca Ab |
produto de combinação, uso de um produto de combinação, e, método para tratar câncer
|
SG185996A1
(en)
|
2007-11-13 |
2012-12-28 |
Icos Corp |
Inhibitors of human phosphatidyl-inositol 3-kinase delta
|
JP5385297B2
(ja)
|
2007-11-22 |
2014-01-08 |
ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング |
新規化合物
|
EP2070932A1
(en)
|
2007-12-13 |
2009-06-17 |
4Sc Ag |
Pyrazolotriazines
|
BRPI0820856A2
(pt)
|
2007-12-13 |
2019-05-14 |
Siena Bhiotech.S.P.A. |
anatagonista da série de reação de hedgehog e aplicações terapêuticas dos mesmos
|
AU2008338963A1
(en)
|
2007-12-13 |
2009-06-25 |
Sri International |
PPAR-delta ligands and methods of their use
|
WO2009086303A2
(en)
|
2007-12-21 |
2009-07-09 |
University Of Rochester |
Method for altering the lifespan of eukaryotic organisms
|
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
|
US7894450B2
(en)
|
2007-12-31 |
2011-02-22 |
Nortel Network, Ltd. |
Implementation of VPNs over a link state protocol controlled ethernet network
|
US8193182B2
(en)
|
2008-01-04 |
2012-06-05 |
Intellikine, Inc. |
Substituted isoquinolin-1(2H)-ones, and methods of use thereof
|
US8703777B2
(en)
|
2008-01-04 |
2014-04-22 |
Intellikine Llc |
Certain chemical entities, compositions and methods
|
EP2240020A4
(en)
|
2008-01-09 |
2011-05-11 |
Trovis Pharmaceuticals Llc |
INTRATHEAL TREATMENT OF NEUROPATHIC PAIN WITH A2AR AGONISTS
|
JP5458893B2
(ja)
|
2008-01-10 |
2014-04-02 |
旭硝子株式会社 |
ガラス、発光装置用の被覆材および発光装置
|
WO2009089598A2
(en)
|
2008-01-18 |
2009-07-23 |
Katholieke Universiteit Leuven |
Msmb-gene methylation based diagnosis, staging and prognosis of prostate cancer
|
NZ586399A
(en)
|
2008-01-24 |
2011-12-22 |
Ucb Pharma Sa |
Compounds comprising a cyclobutoxy group
|
CA2710929A1
(en)
|
2008-01-28 |
2009-08-06 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
US20110098267A1
(en)
|
2008-02-07 |
2011-04-28 |
Synta Pharmaceuticals Corporation |
Topical formulations for the treatment of psoriasis
|
KR20100117105A
(ko)
|
2008-02-07 |
2010-11-02 |
질레드 팔로 알토 인코포레이티드 |
Abca-1 상승 화합물 및 이의 용도
|
TWI444384B
(zh)
|
2008-02-20 |
2014-07-11 |
Gilead Sciences Inc |
核苷酸類似物及其在治療惡性腫瘤上的用途
|
CN101531638B
(zh)
|
2008-03-13 |
2011-12-28 |
中国科学院广州生物医药与健康研究院 |
用作雌激素相关受体调节剂的化合物及其应用
|
US8993580B2
(en)
|
2008-03-14 |
2015-03-31 |
Intellikine Llc |
Benzothiazole kinase inhibitors and methods of use
|
US8637542B2
(en)
|
2008-03-14 |
2014-01-28 |
Intellikine, Inc. |
Kinase inhibitors and methods of use
|
JP2011515401A
(ja)
|
2008-03-20 |
2011-05-19 |
アムジエン・インコーポレーテツド |
オーロラキナーゼモジュレーターおよび使用方法
|
MX2010010525A
(es)
|
2008-03-24 |
2010-10-25 |
Novartis Ag |
Inhibidores de metaloproteasa de matriz basados en aril-sulfonamida.
|
JP5511786B2
(ja)
|
2008-03-31 |
2014-06-04 |
ジェネンテック, インコーポレイテッド |
ベンゾピランおよびベンゾキセピンpi3k阻害剤化合物および使用方法
|
FR2929851B1
(fr)
|
2008-04-09 |
2012-11-30 |
Centre Nat Rech Scient |
Molecules inhibant une voie metabolique impliquant la proteine tyrosine kinase syk et procede d'identification de ces 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
|
GB0808282D0
(en)
|
2008-05-07 |
2008-06-11 |
Medical Res Council |
Compounds for use in stabilizing p53 mutants
|
US8148408B2
(en)
|
2008-05-09 |
2012-04-03 |
Abbott Laboratories |
Selective substituted pyridine ligands for neuronal nicotinic receptors
|
KR20110042153A
(ko)
|
2008-05-30 |
2011-04-25 |
제넨테크, 인크. |
퓨린 pi3k 억제 화합물 및 사용 방법
|
WO2009150137A2
(en)
|
2008-06-10 |
2009-12-17 |
Novartis Ag |
Organic compounds
|
US20090312406A1
(en)
|
2008-06-12 |
2009-12-17 |
Hsing-Pang Hsieh |
Coumarin compounds and their use for treating viral infection
|
WO2010006072A2
(en)
|
2008-07-08 |
2010-01-14 |
The Regents Of The University Of California |
Mtor modulators and uses thereof
|
WO2010006086A2
(en)
|
2008-07-08 |
2010-01-14 |
Intellikine, Inc. |
Kinase inhibitors and methods of use
|
WO2010009207A1
(en)
|
2008-07-16 |
2010-01-21 |
Schering Corporation |
Bicyclic heterocycle derivatives and their use as gpcr modulators
|
UY31984A
(es)
|
2008-07-16 |
2010-02-26 |
Boehringer Ingelheim Int |
DERIVADOS DE 1-(3,4-difluorobencil)-6-oxo-1,6-dihidropirimidin-5-carboxamidas N-sustituidas y de 2-(3,4-difluorobencil)-3-oxo-2,3-dihidro-1H-pirazol-4-carboxamidas N-sustituidas.
|
US8450344B2
(en)
|
2008-07-25 |
2013-05-28 |
Aerie Pharmaceuticals, Inc. |
Beta- and gamma-amino-isoquinoline amide compounds and substituted benzamide compounds
|
WO2010014739A2
(en)
|
2008-07-29 |
2010-02-04 |
Kalypsys, Inc. |
Heterocyclic modulators of tgr5
|
WO2010019210A2
(en)
|
2008-08-11 |
2010-02-18 |
President And Fellows Of Harvard College |
Halofuginone analogs for inhibition of trna synthetases and uses thereof
|
US20100099871A1
(en)
|
2008-08-15 |
2010-04-22 |
Miller Dwight W |
Anti-psychotic compounds and pharmaceutical compositions
thereof
|
US8513295B2
(en)
|
2008-09-23 |
2013-08-20 |
Georgetown University |
Viral and fungal inhibitors
|
CA2738429C
(en)
|
2008-09-26 |
2016-10-25 |
Intellikine, Inc. |
Heterocyclic kinase inhibitors
|
WO2010046780A2
(en)
|
2008-10-22 |
2010-04-29 |
Institut Pasteur Korea |
Anti viral compounds
|
WO2010051550A1
(en)
|
2008-10-31 |
2010-05-06 |
University Of Rochester |
Methods of diagnosing and treating fibrosis
|
EP2361263A1
(en)
|
2008-10-31 |
2011-08-31 |
Abbott Biotherapeutics Corp. |
Use of anti-cs1 antibodies for treatment of rare lymphomas
|
US8476431B2
(en)
|
2008-11-03 |
2013-07-02 |
Itellikine LLC |
Benzoxazole kinase inhibitors and methods of use
|
WO2010056758A1
(en)
|
2008-11-12 |
2010-05-20 |
Yangbo Feng |
Quinazoline derivatives as kinase inhibitors
|
US20110269779A1
(en)
|
2008-11-18 |
2011-11-03 |
Intellikine, Inc. |
Methods and compositions for treatment of ophthalmic conditions
|
EP2752189B1
(en)
*
|
2008-11-22 |
2016-10-26 |
F. Hoffmann-La Roche AG |
Use of anti-vegf antibody in combination with chemotherapy for treating breast cancer
|
AU2009322187B2
(en)
|
2008-12-04 |
2015-02-19 |
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
|
SG10201707798SA
(en)
|
2008-12-08 |
2017-10-30 |
Gilead Connecticut Inc |
Imidazopyrazine syk inhibitors
|
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
|
CA2746220A1
(en)
|
2008-12-08 |
2010-07-08 |
Vm Pharma Llc |
Compositions of protein receptor tyrosine kinase inhibitors
|
MA33085B1
(fr)
|
2008-12-19 |
2012-03-01 |
Boehringer Ingelheim Int |
Pyrimidine-4 carboxamides cycliques en tant qu'antagonistes du recepteur ccr2 pour le traitement d'inflammations, de l'asthme et des broncho-pneumopathies chroniques obstructives
|
US20120046242A1
(en)
|
2008-12-24 |
2012-02-23 |
Massachusetts Institute Of Technology |
Molecular activators of the wnt/beta-catenin pathway
|
CA2749585A1
(en)
|
2009-01-13 |
2010-07-22 |
Van Andel Research Institute |
Methods of using substituted isoxazolo pyridinones as dissociated glucocorticoids
|
JP2012515148A
(ja)
|
2009-01-13 |
2012-07-05 |
グラクソ グループ リミテッド |
Sykキナーゼ阻害剤としてのピリミジンカルボキサミド誘導体
|
KR20120046099A
(ko)
|
2009-02-04 |
2012-05-09 |
유니버시티 오브 조지아 리서치 파운데이션 인코퍼레이티드 |
섬유화를 억제하고 섬유화 질병을 치료하는 방법
|
US8513284B2
(en)
|
2009-02-13 |
2013-08-20 |
Ucb Pharma, S.A. |
Fused pyridine and pyrazine derivatives as kinase inhibitors
|
WO2010094695A1
(en)
|
2009-02-17 |
2010-08-26 |
Boehringer Ingelheim International Gmbh |
Pyrimido [5,4-d] pyrimidine derivatives for the inhibition of tyrosine kinases
|
AU2010215874B2
(en)
|
2009-02-20 |
2016-02-11 |
Sunyoung Kim |
Protein structural biomarkers to guide targeted chemotherapies
|
US8591943B2
(en)
|
2009-04-09 |
2013-11-26 |
Merck Sharp & Dohme Corp. |
Pyrazolo[1,5-a]pyrimidine derivatives as mTOR inhibitors
|
WO2010127208A1
(en)
|
2009-04-30 |
2010-11-04 |
Forest Laboratories Holdings Limited |
Inhibitors of acetyl-coa carboxylase
|
JP5789252B2
(ja)
|
2009-05-07 |
2015-10-07 |
インテリカイン, エルエルシー |
複素環式化合物およびその使用
|
GB0908957D0
(en)
|
2009-05-22 |
2009-07-01 |
Ucb Pharma Sa |
Therapeutic agents
|
SG175708A1
(en)
|
2009-05-27 |
2011-12-29 |
Genentech Inc |
Bicyclic pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use
|
CA2772371A1
(en)
|
2009-05-27 |
2010-12-02 |
F. Hoffmann-La Roche Ag |
Bicyclic indole-pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use
|
US20120065205A1
(en)
|
2009-06-01 |
2012-03-15 |
Mercer Swati P |
Pyrazine carboxamide orexin receptor antagonists
|
US8377945B2
(en)
|
2009-06-15 |
2013-02-19 |
Rigel Pharmaceuticals Inc. |
Small molecule inhibitors of spleen tyrosine kinase (SYK)
|
UA110324C2
(en)
|
2009-07-02 |
2015-12-25 |
Genentech Inc |
Jak inhibitory compounds based on pyrazolo pyrimidine
|
CN101602768B
(zh)
|
2009-07-17 |
2012-05-30 |
河南省农科院农副产品加工研究所 |
一种芝麻素和芝麻林素的提纯方法
|
TW201105669A
(en)
|
2009-07-30 |
2011-02-16 |
Irm Llc |
Compounds and compositions as Syk kinase inhibitors
|
CN102574847A
(zh)
|
2009-07-30 |
2012-07-11 |
Irm责任有限公司 |
作为syk激酶抑制剂的化合物和组合物
|
EP2286808A1
(en)
|
2009-08-18 |
2011-02-23 |
Rheinische Friedrich-Wilhelms Universität |
Cytohesin inhibitors
|
TWI481601B
(zh)
|
2009-08-21 |
2015-04-21 |
Otsuka Pharma Co Ltd |
含氮化合物及藥學組成物
|
JP5671538B2
(ja)
|
2009-08-27 |
2015-02-18 |
メルク・シャープ・エンド・ドーム・コーポレイション |
新規なピロリジン誘導体型β3−アドレナリン作動性受容体アゴニスト
|
US20130005802A1
(en)
|
2009-09-21 |
2013-01-03 |
Wei Chen |
Treatment of wnt/frizzled-related diseases
|
CA2775133A1
(en)
|
2009-09-23 |
2011-03-31 |
Medivation Technologies, Inc. |
Pyrido[3,4-b]indoles and methods of use
|
AU2010298190A1
(en)
|
2009-09-25 |
2012-05-03 |
Vertex Pharmaceuticals Incorporated |
Methods for preparing pyrimidine derivatives useful as protein kinase inhibitors
|
EP2483272A4
(en)
|
2009-09-29 |
2013-09-18 |
Xcovery Holding Co Llc |
SELECTIVE PI3K (DELTA) INHIBITOR
|
US8106146B2
(en)
|
2009-10-06 |
2012-01-31 |
Medtronic, Inc. |
Therapeutic polymers and methods of generation
|
US9095596B2
(en)
|
2009-10-15 |
2015-08-04 |
Southern Research Institute |
Treatment of neurodegenerative diseases, causation of memory enhancement, and assay for screening compounds for such
|
GB0918249D0
(en)
|
2009-10-19 |
2009-12-02 |
Respivert Ltd |
Compounds
|
US9062076B2
(en)
|
2009-10-22 |
2015-06-23 |
Fibrotech Therapeutics Pty Ltd |
Fused ring analogues of anti-fibrotic agents
|
WO2011058108A1
(en)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Quinoline and quinoxaline derivatives as kinase inhibitors
|
ES2442369T3
(es)
|
2009-11-12 |
2014-02-11 |
Ucb Pharma, S.A. |
Derivados de quinolina y quinoxalina como inhibidores de cinasa
|
WO2011058109A1
(en)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Fused bicyclic pyrrole and imidazole derivatives as kinase inhibitors
|
EP2512246B1
(en)
|
2009-12-17 |
2015-09-30 |
Merck Sharp & Dohme Corp. |
Aminopyrimidines as syk inhibitors
|
MA33926B1
(fr)
|
2009-12-17 |
2013-01-02 |
Merck Sharp & Dohme |
Aminopyrimidines en tant qu'inhibiteurs de la syk
|
AU2010330875B2
(en)
|
2009-12-18 |
2013-08-01 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
KR101758046B1
(ko)
|
2009-12-22 |
2017-07-14 |
버텍스 파마슈티칼스 인코포레이티드 |
포스파티딜이노시톨 3-키나제의 이소인돌리논 억제제
|
ME02186B
(me)
|
2009-12-23 |
2016-02-20 |
Takeda Pharmaceuticals Co |
Fuzionisani heteroaromatski pirolidinoni kao syk inhibitori
|
US20110251216A1
(en)
|
2010-02-19 |
2011-10-13 |
The Regents Of The University Of Michigan |
Compositions and methods for inhibiting ezh2
|
US8440651B2
(en)
|
2010-02-22 |
2013-05-14 |
F. Hoffmann-La Roche Ag |
Pyrido[3,2-d]pyrimidine PI3K delta inhibitor compounds and methods of use
|
US8247436B2
(en)
|
2010-03-19 |
2012-08-21 |
Novartis Ag |
Pyridine and pyrazine derivative for the treatment of CF
|
DE102010013716A1
(de)
|
2010-03-31 |
2011-10-06 |
Rheinische Friedrich-Wilhelms-Universität Bonn Körperschaft des öffentlichen Rechts |
Verwendung von Cytohesin-Inhibitoren
|
CA2796272C
(en)
|
2010-04-29 |
2019-10-01 |
The Regents Of The University Of California |
Pathway recognition algorithm using data integration on genomic models (paradigm)
|
GB201007203D0
(en)
|
2010-04-29 |
2010-06-16 |
Glaxo Group Ltd |
Novel compounds
|
JP5951600B2
(ja)
|
2010-05-21 |
2016-07-13 |
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 |
キナーゼ調節のための、化合物、組成物および方法
|
WO2011150201A2
(en)
|
2010-05-27 |
2011-12-01 |
Ambit Biosciences Corporation |
Azolyl amide compounds and methods of use thereof
|
EP2582682B1
(en)
|
2010-06-17 |
2015-01-14 |
Cytokinetics, Inc. |
Mitotic kinesin inhibitors for use in the treatmetnof pulmonary arterial hypertension
|
US20130195843A1
(en)
|
2010-06-23 |
2013-08-01 |
British Columbia Cancer Agency Branch |
Biomarkers for Non-Hodgkin Lymphomas and Uses Thereof
|
WO2012028578A1
(de)
|
2010-09-03 |
2012-03-08 |
Bayer Cropscience Ag |
Substituierte anellierte pyrimidinone und dihydropyrimidinone
|
AR082799A1
(es)
|
2010-09-08 |
2013-01-09 |
Ucb Pharma Sa |
Derivados de quinolina y quinoxalina como inhibidores de quinasa
|
RU2618475C2
(ru)
|
2010-09-10 |
2017-05-03 |
Эпизайм, Инк. |
Ингибиторы ezh2 человека и способы их применения
|
US9175331B2
(en)
|
2010-09-10 |
2015-11-03 |
Epizyme, Inc. |
Inhibitors of human EZH2, and methods of use thereof
|
US9670212B2
(en)
|
2010-09-14 |
2017-06-06 |
Exelixis, Inc. |
Inhibitors of PI3K-delta and methods of their use and manufacture
|
CA2812091C
(en)
|
2010-09-14 |
2020-03-24 |
Exelixis, Inc. |
Inhibitors of pi3k-delta and methods of their use and manufacture
|
EP2619209A1
(en)
|
2010-09-24 |
2013-07-31 |
Gilead Calistoga LLC |
Atropisomers of pi3k-inhibiting compounds
|
US8765773B2
(en)
|
2010-10-18 |
2014-07-01 |
Millennium Pharmaceuticals, Inc. |
Substituted hydroxamic acids and uses thereof
|
UY33337A
(es)
|
2010-10-18 |
2011-10-31 |
Respivert Ltd |
DERIVADOS SUSTITUIDOS DE 1H-PIRAZOL[ 3,4-d]PIRIMIDINA COMO INHIBIDORES DE LAS FOSFOINOSITIDA 3-QUINASAS
|
US8846928B2
(en)
|
2010-11-01 |
2014-09-30 |
Portola Pharmaceuticals, Inc. |
Benzamides and nicotinamides as Syk modulators
|
AU2011323243A1
(en)
|
2010-11-04 |
2013-05-23 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
CA2817577A1
(en)
|
2010-11-10 |
2012-05-18 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
WO2012065057A2
(en)
|
2010-11-12 |
2012-05-18 |
Exelixis, Inc. |
Phosphatidylinositol 3-kinase inhibitors and methods of their use
|
WO2012065019A2
(en)
|
2010-11-12 |
2012-05-18 |
Exelixis, Inc. |
Pyridopyrimidinone inhibitors of p13k alpha
|
JP6154746B2
(ja)
|
2010-12-08 |
2017-06-28 |
ザ ユナイテッド ステイツ オブ アメリカ, アズ リプレゼンテッド バイ ザ セクレタリー, デパートメント オブ ヘルス アンド ヒューマン サービシーズ |
グルコセレブロシダーゼ活性剤としての置換ピラゾロピリミジン類
|
GB201021104D0
(en)
|
2010-12-13 |
2011-01-26 |
Univ Leuven Kath |
Novel compounds for the treatment of neurodegenerative diseases
|
US8809349B2
(en)
|
2011-01-10 |
2014-08-19 |
Infinity Pharmaceuticals, Inc. |
Processes for preparing isoquinolinones and solid forms of isoquinolinones
|
CA2827311A1
(en)
|
2011-02-18 |
2012-08-23 |
Vertex Pharmaceuticals Incorporated |
Chroman-spirocyclic piperidine amides as modulators of ion channels
|
JP2012184225A
(ja)
|
2011-02-18 |
2012-09-27 |
Otsuka Pharmaceut Co Ltd |
医薬組成物
|
WO2012148548A1
(en)
|
2011-02-25 |
2012-11-01 |
Takeda Pharmaceutical Company Limited |
N-substituted oxazinopteridines and oxazinopteridinones
|
JP5569437B2
(ja)
|
2011-03-09 |
2014-08-13 |
コニカミノルタ株式会社 |
光学フィルム及びそれを用いた偏光板、液晶表示装置
|
US9090628B2
(en)
|
2011-03-21 |
2015-07-28 |
Genentech, Inc. |
Benzoxazepin compounds selective for PI3K P110 delta and methods of use
|
US9029389B2
(en)
|
2011-04-21 |
2015-05-12 |
Institut Pasteur Korea |
Anti-inflammation compounds
|
WO2012151137A1
(en)
|
2011-05-04 |
2012-11-08 |
Merck Sharp & Dohme Corp. |
Amino-pyridine-containing spleen tyrosine kinase (syk) inhibitors
|
US9115096B2
(en)
|
2011-05-10 |
2015-08-25 |
Gilead Sciences, Inc. |
Fused heterocyclic compounds as ion channel modulators
|
JP2013010734A
(ja)
|
2011-06-03 |
2013-01-17 |
Sumitomo Chemical Co Ltd |
N−置換ラクタム化合物の製造方法
|
CA2840224C
(en)
|
2011-06-22 |
2019-08-13 |
The General Hospital Corporation |
Treatment of proteinopathies
|
EP2731953A1
(en)
|
2011-07-15 |
2014-05-21 |
Abbvie Inc. |
Tricyclic inhibitors of kinases useful for the treatment of proliferative diseases
|
AR088218A1
(es)
|
2011-07-19 |
2014-05-21 |
Infinity Pharmaceuticals Inc |
Compuestos heterociclicos utiles como inhibidores de pi3k
|
AU2012284088B2
(en)
*
|
2011-07-19 |
2015-10-08 |
Infinity Pharmaceuticals Inc. |
Heterocyclic compounds and uses thereof
|
EP2751093A1
(en)
|
2011-08-29 |
2014-07-09 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
WO2013038381A1
(en)
|
2011-09-16 |
2013-03-21 |
Novartis Ag |
Pyridine/pyrazine amide derivatives
|
CA2862895A1
(en)
|
2011-09-30 |
2013-04-04 |
Kineta, Inc. |
Anti-viral compounds
|
JP2015027951A
(ja)
|
2011-11-02 |
2015-02-12 |
日本農薬株式会社 |
フタルアミド誘導体及び該誘導体を含有する農園芸用殺虫剤並びにその使用方法
|
PE20150159A1
(es)
|
2011-12-21 |
2015-02-08 |
Novartis Ag |
Composiciones y metodos para anticuerpos que actuan sobre el factor p
|
NZ628072A
(en)
|
2012-03-13 |
2015-08-28 |
Respivert Ltd |
Crystalline pi3 kinase inhibitors
|
US8940742B2
(en)
*
|
2012-04-10 |
2015-01-27 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
RU2629947C2
(ru)
|
2012-04-10 |
2017-09-05 |
Аннцзи Фармасьютикал Ко., Лтд. |
Ингибиторы деацетилаз гистонов (hdacs)
|
US9221744B2
(en)
|
2012-06-11 |
2015-12-29 |
New York University |
Asymmetric catalysts
|
WO2013190555A1
(en)
*
|
2012-06-21 |
2013-12-27 |
Compugen Ltd. |
Lsr antibodies, and uses thereof for treatment of cancer
|
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
|
EP2870157B1
(en)
|
2012-07-04 |
2017-08-30 |
Rhizen Pharmaceuticals S.A. |
Selective pi3k delta inhibitors
|
CN104582702B
(zh)
|
2012-08-30 |
2018-07-10 |
国立大学法人东京大学 |
体内寄生虫防治剂
|
US20140120060A1
(en)
|
2012-11-01 |
2014-05-01 |
Infinity Pharmaceuticals, Inc. |
Treatment of rheumatoid arthritis and asthma using pi3 kinase inhibitors
|
US20140120083A1
(en)
|
2012-11-01 |
2014-05-01 |
Infinity Pharmaceuticals, Inc. |
Treatment of cancers using pi3 kinase isoform modulators
|
BR112015014034A2
(pt)
|
2013-01-10 |
2017-07-11 |
Nimbus Iris Inc |
inibidores de irak e usos dos mesmos
|
US20140275082A1
(en)
|
2013-03-14 |
2014-09-18 |
Abbvie Inc. |
Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
|
EP2981522A4
(en)
|
2013-04-05 |
2016-08-31 |
Salk Inst For Biological Studi |
ANTAGONISTS OF PPAR
|
UY35675A
(es)
|
2013-07-24 |
2015-02-27 |
Novartis Ag |
Derivados sustituidos de quinazolin-4-ona
|
JP6340416B2
(ja)
|
2013-09-25 |
2018-06-06 |
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 |
ホスファチジルイノシトール3−キナーゼ−ガンマの選択的インヒビター
|
PE20160685A1
(es)
|
2013-10-04 |
2016-07-23 |
Infinity Pharmaceuticals Inc |
Compuestos heterociclicos y usos de los mismos
|
US9751888B2
(en)
|
2013-10-04 |
2017-09-05 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
US10328080B2
(en)
|
2013-12-05 |
2019-06-25 |
Acerta Pharma, B.V. |
Therapeutic combination of PI3K inhibitor and a BTK inhibitor
|
TWI672297B
(zh)
|
2013-12-18 |
2019-09-21 |
義大利商吉斯藥品公司 |
作為磷脂肌醇-3-激酶抑制劑之異唏衍生物
|
NZ736970A
(en)
|
2013-12-20 |
2018-11-30 |
Gilead Calistoga Llc |
Process methods for phosphatidylinositol 3-kinase inhibitors
|
SG10201808053XA
(en)
|
2014-03-19 |
2018-10-30 |
Infinity Pharmaceuticals Inc |
Heterocyclic compounds for use in the treatment of pi3k-gamma mediated disorders
|
KR20210132233A
(ko)
|
2014-04-14 |
2021-11-03 |
아비나스 오퍼레이션스, 인코포레이티드 |
단백질분해의 이미드-기초된 조절인자 및 연관된 이용 방법
|
JP6752780B2
(ja)
|
2014-09-24 |
2020-09-09 |
メルク パテント ゲーエムベーハー |
有機エレクトロルミネッセンス素子のための材料
|
US9708348B2
(en)
|
2014-10-03 |
2017-07-18 |
Infinity Pharmaceuticals, Inc. |
Trisubstituted bicyclic heterocyclic compounds with kinase activities and uses thereof
|
WO2016057322A1
(en)
|
2014-10-08 |
2016-04-14 |
Salk Institute For Biological Studies |
Ppar agonists and methods of use thereof
|
US10144724B2
(en)
|
2015-07-22 |
2018-12-04 |
Araxes Pharma Llc |
Substituted quinazoline compounds and methods of use thereof
|
GB201513614D0
(en)
|
2015-07-31 |
2015-09-16 |
Univ College Cork Nat Univ Ie |
Compositions, compounds and methods and uses relating thereto
|
WO2017048702A1
(en)
|
2015-09-14 |
2017-03-23 |
Infinity Pharmaceuticals, Inc. |
Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same
|
CN106632243B
(zh)
|
2015-10-28 |
2019-03-15 |
华领医药技术(上海)有限公司 |
吡咯烷衍生物
|
SG11201804901WA
(en)
|
2015-12-22 |
2018-07-30 |
SHY Therapeutics LLC |
Compounds for the treatment of cancer and inflammatory disease
|
WO2017161116A1
(en)
|
2016-03-17 |
2017-09-21 |
Infinity Pharmaceuticals, Inc. |
Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as pi3k kinase inhibitors
|
HRP20220577T1
(hr)
|
2016-05-06 |
2022-06-24 |
Shanghai De Novo Pharmatech Co., Ltd. |
Derivat benzazepina, metoda pripreme, farmaceutski sastav i njegova upotreba
|
WO2017214269A1
(en)
|
2016-06-08 |
2017-12-14 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
US10179787B2
(en)
|
2016-07-29 |
2019-01-15 |
Flx Bio, Inc. |
Chemokine receptor modulators and uses thereof
|
KR102497742B1
(ko)
|
2016-08-30 |
2023-02-10 |
다나-파버 캔서 인스티튜트 인크. |
약물 전달 조성물 및 그의 용도
|
US10246462B2
(en)
|
2016-09-09 |
2019-04-02 |
Flx Bio, Inc. |
Chemokine receptor modulators and uses thereof
|
US20180154142A1
(en)
|
2016-12-05 |
2018-06-07 |
Old Dominion University Research Foundation |
Methods and devices for treatment of tumors with nano-pulse stimulation
|
CA3045041A1
(en)
|
2016-12-14 |
2018-06-21 |
Tarveda Therapeutics, Inc. |
Hsp90-targeting conjugates and formulations thereof
|
US20190070166A1
(en)
|
2017-09-02 |
2019-03-07 |
Richard Postrel |
Optimized Method for Treating and Curing Arthritis, Diabetes, Multiple Sclerosis and Other Autoimmune Disease
|
CN108658937A
(zh)
|
2017-03-28 |
2018-10-16 |
中国海洋大学 |
一种双环生物碱类化合物及其制备方法和应用
|
EA201992780A1
(ru)
|
2017-06-21 |
2020-06-02 |
ШАЙ ТЕРАПЬЮТИКС ЭлЭлСи |
Соединения, которые взаимодействуют с суперсемейством ras, для лечения рака, воспалительных заболеваний, ras-опатий и фиброзного заболевания
|
WO2018237007A1
(en)
|
2017-06-22 |
2018-12-27 |
The United States Of America, As Represented By The Secretary, Department Of Health And Human Services |
INHIBITORS OF PHOSPHOINOSITIDE 3-KINASE AND HISTONE DEACETYLASE FOR THE TREATMENT OF CANCER
|
US11459306B2
(en)
|
2017-07-31 |
2022-10-04 |
The Trustees Of Columbia University In The City Of New York |
Compounds, compositions, and methods for treating T-cell acute lymphoblastic leukemia
|
US20190074458A1
(en)
|
2017-09-05 |
2019-03-07 |
Samsung Electronics Co., Ltd. |
Organometallic compound, organic light-emitting device including the organometallic compound, and diagnostic composition including the organometallic compound
|
KR20240017986A
(ko)
|
2017-09-26 |
2024-02-08 |
더 리전트 오브 더 유니버시티 오브 캘리포니아 |
암 치료를 위한 조성물 및 방법
|
JP2021506797A
(ja)
|
2017-12-14 |
2021-02-22 |
ターベダ セラピューティクス インコーポレイテッドTarveda Therapeutics,Inc. |
Hsp90標的化コンジュゲート及びその製剤
|
CN108310384B
(zh)
|
2018-02-05 |
2021-06-15 |
苏州大学 |
Pi3k抑制剂在制备治疗血小板数量减少相关疾病药物中的用途
|
WO2019200224A1
(en)
|
2018-04-13 |
2019-10-17 |
The Broad Institute, Inc. |
Synergistic drug combinations predicted from genomic features and single-agent response profiles
|
WO2019228404A1
(zh)
|
2018-05-31 |
2019-12-05 |
信达生物制药(苏州)有限公司 |
一种新型磷酸肌醇3-激酶抑制剂及其制备方法和用途
|
JP2021527655A
(ja)
|
2018-06-19 |
2021-10-14 |
ビオンテック ユーエス インコーポレイテッド |
ネオ抗原およびそれらの使用
|
US20200085925A1
(en)
|
2018-07-26 |
2020-03-19 |
Atyr Pharma Inc. |
Compositions and methods for treating nrp2-associated diseases
|
EP3836929A1
(en)
|
2018-08-14 |
2021-06-23 |
Camp4 Therapeutics Corporation |
Methods of treating liver diseases
|
CN110833546B
(zh)
|
2018-08-17 |
2022-06-28 |
中国科学院分子细胞科学卓越创新中心 |
通佐溴胺在治疗胃癌中的用途
|
CN113166255A
(zh)
|
2018-09-28 |
2021-07-23 |
伊麦吉纳博公司 |
Cd8成像构建体及其使用方法
|
US20210338681A1
(en)
|
2018-10-01 |
2021-11-04 |
Secura Bio, Inc. |
Combination therapies
|
US20210355545A1
(en)
|
2018-10-15 |
2021-11-18 |
The Johns Hopkins University |
Methods and materials for assessing and treating cancer
|
EP3873608A1
(en)
|
2018-10-31 |
2021-09-08 |
Gilead Sciences, Inc. |
Substituted 6-azabenzimidazole compounds having hpk1 inhibitory activity
|
CA3117556A1
(en)
|
2018-10-31 |
2020-05-07 |
Gilead Sciences, Inc. |
Substituted 6-azabenzimidazole compounds as hpk1 inhibitors
|
BR112021011894A2
(pt)
|
2018-12-21 |
2021-09-08 |
Daiichi Sankyo Company, Limited |
Composição farmacêutica
|
EP3923969A4
(en)
|
2019-02-13 |
2022-10-19 |
Vasgene Therapeutics Inc. |
EPHB4-EPHRIN B2 RECEPTOR LIGAND PAIR AS A NEW MARKER FOR THE TREATMENT OF PROSTATE CANCER
|
US20220362381A1
(en)
|
2019-02-21 |
2022-11-17 |
Bambu Vault Llc |
Remotely triggered therapy
|
WO2020176501A1
(en)
|
2019-02-25 |
2020-09-03 |
Albert Einstein College Of Medicine |
Compounds useful for inhibiting raf dimers
|
US20230227446A9
(en)
|
2019-04-10 |
2023-07-20 |
Nanjing Zhengxiang Pharmaceuticals Co., Ltd. |
Phosphatidylinositol 3-kinase inhibitors
|
TWI826690B
(zh)
|
2019-05-23 |
2023-12-21 |
美商基利科學股份有限公司 |
經取代之烯吲哚酮化物及其用途
|
US20220324880A1
(en)
|
2019-06-10 |
2022-10-13 |
Kymara Therapeutics, Inc. |
Smarca inhibitors and uses thereof
|
US20220249609A1
(en)
|
2019-06-19 |
2022-08-11 |
Orionis Biosciences, Inc. |
Combination therapy with cd13-targeted chimeric proteins or chimeric protein complexes
|
CN112194659A
(zh)
|
2019-07-08 |
2021-01-08 |
浙江海正药业股份有限公司 |
炔类衍生物及其制备方法和用途
|
US20210017607A1
(en)
|
2019-07-18 |
2021-01-21 |
The University Of Chicago |
Methods of Predicting Responsiveness to Cancer Therapies
|