GB812366A
(en)
|
1955-08-18 |
1959-04-22 |
Wellcome Found |
Improvements in and relating to derivatives of pyrimidine and the preparation thereof
|
GB937725A
(en)
|
1960-05-11 |
1963-09-25 |
Ciba Ltd |
Pyrazolo[3:4-d]pyrimidines
|
JPS4834699B1
(el)
|
1968-07-03 |
1973-10-23 |
|
|
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
|
US3657744A
(en)
|
1970-05-08 |
1972-04-25 |
Univ Minnesota |
Method for fixing prosthetic implants in a living body
|
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
|
US3916899A
(en)
|
1973-04-25 |
1975-11-04 |
Alza Corp |
Osmotic dispensing device with maximum and minimum sizes for the passageway
|
US3939161A
(en)
|
1973-10-29 |
1976-02-17 |
Abbott Laboratories |
1,3-Dimethyl- 1H-pyrazolo(4,3-D) pyrimidine-7 (6H)-ones
|
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
|
HU196714B
(en)
|
1984-10-04 |
1989-01-30 |
Monsanto Co |
Process for producing non-aqueous composition comprising somatotropin
|
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
|
US4733665C2
(en)
|
1985-11-07 |
2002-01-29 |
Expandable Grafts Partnership |
Expandable intraluminal graft and method and apparatus for implanting an expandable intraluminal graft
|
US5023252A
(en)
|
1985-12-04 |
1991-06-11 |
Conrex Pharmaceutical Corporation |
Transdermal and trans-membrane delivery of drugs
|
US5061273A
(en)
|
1989-06-01 |
1991-10-29 |
Yock Paul G |
Angioplasty apparatus facilitating rapid exchanges
|
US5040548A
(en)
|
1989-06-01 |
1991-08-20 |
Yock Paul G |
Angioplasty mehtod
|
US5350395A
(en)
|
1986-04-15 |
1994-09-27 |
Yock Paul G |
Angioplasty apparatus facilitating rapid exchanges
|
US4886499A
(en)
|
1986-12-18 |
1989-12-12 |
Hoffmann-La Roche Inc. |
Portable injection appliance
|
US4748982A
(en)
|
1987-01-06 |
1988-06-07 |
Advanced Cardiovascular Systems, Inc. |
Reinforced balloon dilatation catheter with slitted exchange sleeve and method
|
GB8704027D0
(en)
|
1987-02-20 |
1987-03-25 |
Owen Mumford Ltd |
Syringe needle combination
|
US4992445A
(en)
|
1987-06-12 |
1991-02-12 |
American Cyanamid Co. |
Transdermal delivery of pharmaceuticals
|
US5001139A
(en)
|
1987-06-12 |
1991-03-19 |
American Cyanamid Company |
Enchancers for the transdermal flux of nivadipine
|
US4941880A
(en)
|
1987-06-19 |
1990-07-17 |
Bioject, Inc. |
Pre-filled ampule and non-invasive hypodermic injection device assembly
|
US4940460A
(en)
|
1987-06-19 |
1990-07-10 |
Bioject, Inc. |
Patient-fillable and non-invasive hypodermic injection device assembly
|
US4790824A
(en)
|
1987-06-19 |
1988-12-13 |
Bioject, Inc. |
Non-invasive hypodermic injection device
|
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
|
CA1322628C
(en)
|
1988-10-04 |
1993-10-05 |
Richard A. Schatz |
Expandable intraluminal graft
|
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
|
GB8827305D0
(en)
|
1988-11-23 |
1988-12-29 |
British Bio Technology |
Compounds
|
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.
|
US5442039A
(en)
|
1989-07-17 |
1995-08-15 |
The Dow Chemical Company |
Mesogenic polycyanates and thermosets thereof
|
US5428125A
(en)
|
1989-07-17 |
1995-06-27 |
The Dow Chemical Company |
Mesogenic polycyanates and thermosets thereof
|
US5674278A
(en)
|
1989-08-24 |
1997-10-07 |
Arterial Vascular Engineering, Inc. |
Endovascular support device
|
US6344053B1
(en)
|
1993-12-22 |
2002-02-05 |
Medtronic Ave, Inc. |
Endovascular support device and method
|
US5292331A
(en)
|
1989-08-24 |
1994-03-08 |
Applied Vascular Engineering, Inc. |
Endovascular support device
|
US5763597A
(en)
|
1989-09-15 |
1998-06-09 |
Metabasis Therapeutics, Inc. |
Orally active adenosine kinase inhibitors
|
US5674998A
(en)
|
1989-09-15 |
1997-10-07 |
Gensia Inc. |
C-4' modified adenosine kinase inhibitors
|
US5721356A
(en)
|
1989-09-15 |
1998-02-24 |
Gensia, Inc. |
Orally active adenosine kinase inhibitors
|
US5646128A
(en)
|
1989-09-15 |
1997-07-08 |
Gensia, Inc. |
Methods for treating adenosine kinase related conditions
|
US5763596A
(en)
|
1989-09-15 |
1998-06-09 |
Metabasis Therapeutics, Inc. |
C-4' modified adenosine kinase inhibitors
|
US5795977A
(en)
|
1989-09-15 |
1998-08-18 |
Metabasis Therapeutics, Inc. |
Water soluble adenosine kinase inhibitors
|
US5120548A
(en)
|
1989-11-07 |
1992-06-09 |
Merck & Co., Inc. |
Swelling modulated polymeric drug delivery device
|
US5064413A
(en)
|
1989-11-09 |
1991-11-12 |
Bioject, Inc. |
Needleless hypodermic injection device
|
US5312335A
(en)
|
1989-11-09 |
1994-05-17 |
Bioject Inc. |
Needleless hypodermic injection device
|
JPH05503517A
(ja)
|
1989-12-18 |
1993-06-10 |
バージニア・コモンウェルス・ユニバーシティ |
シグマレセプターリガンド及びその用途
|
JPH04211063A
(ja)
|
1990-03-05 |
1992-08-03 |
Takeda Chem Ind Ltd |
縮合三環性複素環化合物、その製造法、用途及び中間体
|
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
|
DE69123974T2
(de)
|
1990-09-25 |
1997-05-07 |
Rhone-Poulenc Rorer International (Holdings) Inc., Greenville, Del. |
Verbindungen welche antihypertensive und antiischemische eigenschaften besitzen
|
US5652366A
(en)
|
1990-09-25 |
1997-07-29 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
DI (1R)-(-)camphosulfonic acid) salt, preparation thereof and use thereof
|
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
|
US5710158A
(en)
|
1991-05-10 |
1998-01-20 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
|
USRE37650E1
(en)
|
1991-05-10 |
2002-04-09 |
Aventis Pharmacetical Products, Inc. |
Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase
|
US5480883A
(en)
|
1991-05-10 |
1996-01-02 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
|
US6645969B1
(en)
|
1991-05-10 |
2003-11-11 |
Aventis Pharmaceuticals Inc. |
Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase
|
AU658646B2
(en)
|
1991-05-10 |
1995-04-27 |
Rhone-Poulenc Rorer International (Holdings) Inc. |
Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
|
US5721237A
(en)
|
1991-05-10 |
1998-02-24 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Protein tyrosine kinase aryl and heteroaryl quinazoline compounds having selective inhibition of HER-2 autophosphorylation properties
|
US5714493A
(en)
|
1991-05-10 |
1998-02-03 |
Rhone-Poulenc Rorer Pharmaceuticals, Inc. |
Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase
|
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
|
US5580578A
(en)
|
1992-01-27 |
1996-12-03 |
Euro-Celtique, S.A. |
Controlled release formulations coated with aqueous dispersions of acrylic polymers
|
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.
|
US5916891A
(en)
|
1992-01-13 |
1999-06-29 |
Smithkline Beecham Corporation |
Pyrimidinyl imidazoles
|
DE4204032A1
(de)
|
1992-02-12 |
1993-08-19 |
Boehringer Mannheim Gmbh |
Neue liponucleotide, deren herstellunmg sowie deren verwendung als antivirale arzneimittel
|
DE4204031A1
(de)
|
1992-02-12 |
1993-08-19 |
Boehringer Mannheim Gmbh |
Neue lipidphosphonsaeure-nucleosid-konjugate 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
|
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
|
AU684461B2
(en)
|
1992-04-07 |
1997-12-18 |
Regents Of The University Of Michigan, The |
CD28 pathway immunoregulation
|
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
|
AU669548B2
(en)
|
1992-06-19 |
1996-06-13 |
Honeywell Inc. |
Infrared camera with thermoelectric temperature stabilization
|
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.
|
TW444018B
(en)
*
|
1992-12-17 |
2001-07-01 |
Pfizer |
Pyrazolopyrimidines
|
US5455258A
(en)
|
1993-01-06 |
1995-10-03 |
Ciba-Geigy Corporation |
Arylsulfonamido-substituted hydroxamic acids
|
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
|
CA2154681A1
(en)
|
1993-02-03 |
1994-08-18 |
Mark David Erion |
Adenosine kinase inhibitors comprising lyxofuranosyl derivatives
|
GB9308957D0
(en)
|
1993-04-30 |
1993-06-16 |
Cancer Res Campaign Tech |
Novel produgs
|
WO1994029436A1
(en)
|
1993-06-04 |
1994-12-22 |
The United States Of America Represented By The Secretary Of The Navy |
Methods for selectively stimulating proliferation of t cells
|
US6087324A
(en)
|
1993-06-24 |
2000-07-11 |
Takeda Chemical Industries, Ltd. |
Sustained-release preparation
|
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
|
WO1995012588A1
(en)
|
1993-11-05 |
1995-05-11 |
Biochem Pharma Inc. |
Antineoplastic heteronaphthoquinones
|
US5656643A
(en)
|
1993-11-08 |
1997-08-12 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
|
US5679683A
(en)
|
1994-01-25 |
1997-10-21 |
Warner-Lambert Company |
Tricyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family
|
IL112249A
(en)
|
1994-01-25 |
2001-11-25 |
Warner Lambert Co |
Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds
|
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
|
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
|
US5863949A
(en)
|
1995-03-08 |
1999-01-26 |
Pfizer Inc |
Arylsulfonylamino hydroxamic acid derivatives
|
DK0819129T3
(da)
|
1995-04-03 |
2000-10-23 |
Novartis Ag |
Pyrazolderivater og fremgangsmåde til deres fremstilling
|
US6312894B1
(en)
|
1995-04-03 |
2001-11-06 |
Epoch Pharmaceuticals, Inc. |
Hybridization and mismatch discrimination using oligonucleotides conjugated to minor groove binders
|
WO1996033172A1
(en)
|
1995-04-20 |
1996-10-24 |
Pfizer Inc. |
Arylsulfonyl hydroxamic acid derivatives as mmp and tnf inhibitors
|
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
|
WO1996037777A1
(en)
|
1995-05-23 |
1996-11-28 |
Nelson Randall W |
Mass spectrometric immunoassay
|
US5593997A
(en)
|
1995-05-23 |
1997-01-14 |
Pfizer Inc. |
4-aminopyrazolo(3-,4-D)pyrimidine and 4-aminopyrazolo-(3,4-D)pyridine tyrosine kinase inhibitors
|
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
|
US5665721A
(en)
|
1995-06-07 |
1997-09-09 |
Abbott Laboratories |
Heterocyclic substituted cyclopentane compounds
|
AU5982296A
(en)
|
1995-06-07 |
1996-12-30 |
G.D. Searle & Co. |
Method to treat cardiofibrosis with a combination of an angi otensin ii antagonist and spironolactone
|
PL185150B1
(pl)
|
1995-06-07 |
2003-03-31 |
Searle & Co |
Kompozycja farmaceutyczna do leczenia zaburzeń sercowo-naczyniowych
|
CA2224222A1
(en)
|
1995-06-07 |
1996-12-19 |
G.D. Searle & Co. |
Spironolactone and angiotensin ii antagonist combination therapy for treatment of congestive heart failure
|
ATE268591T1
(de)
|
1995-06-27 |
2004-06-15 |
Takeda Chemical Industries Ltd |
Verfahren zur herstellung von zubereitungen mit verzögerter freisetzung
|
TW448055B
(en)
|
1995-09-04 |
2001-08-01 |
Takeda Chemical Industries Ltd |
Method of production of sustained-release preparation
|
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
|
ES2183905T3
(es)
|
1995-12-20 |
2003-04-01 |
Hoffmann La Roche |
Inhibidores de metaloproteasa de matriz.
|
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
|
CH690773A5
(de)
|
1996-02-01 |
2001-01-15 |
Novartis Ag |
Pyrrolo(2,3-d)pyrimide und ihre Verwendung.
|
DE19603576A1
(de)
|
1996-02-01 |
1997-08-07 |
Bayer Ag |
Acylierte 4-Amino und 4-Hydrazinopyrimidine
|
GB2310952B
(en)
|
1996-03-05 |
1998-08-19 |
Mitsubishi Electric Corp |
Infrared detector
|
GB9607549D0
(en)
|
1996-04-11 |
1996-06-12 |
Weston Medical Ltd |
Spring-powered dispensing device
|
ATE227293T1
(de)
|
1996-05-15 |
2002-11-15 |
Pfizer |
2,3-disubstituierte-(5,6)-heteroarylkondensiert - pyrimidin-4-one
|
GB9611460D0
(en)
|
1996-06-01 |
1996-08-07 |
Ludwig Inst Cancer Res |
Novel lipid kinase
|
PL330814A1
(en)
|
1996-06-20 |
1999-06-07 |
Regents Board Of |
Compounds for and methods of delivering pharmaceutical preparations and their application
|
US6264970B1
(en)
|
1996-06-26 |
2001-07-24 |
Takeda Chemical Industries, Ltd. |
Sustained-release preparation
|
EP0818442A3
(en)
|
1996-07-12 |
1998-12-30 |
Pfizer Inc. |
Cyclic sulphone derivatives as inhibitors of metalloproteinases and of the production of tumour necrosis factor
|
DK0923585T3
(da)
|
1996-07-18 |
2002-07-01 |
Pfizer |
Phosphinatbaserede inhibitorer af matrixmetalloproteinaser
|
JP2000501423A
(ja)
|
1996-08-23 |
2000-02-08 |
ファイザー インク. |
アリールスルホニルアミノヒドロキサム酸誘導体
|
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
|
US5922753A
(en)
|
1996-10-23 |
1999-07-13 |
Zymogenetics, Inc. |
Methods for treating bone deficit conditions with benzothiazole
|
US5990169A
(en)
|
1996-10-23 |
1999-11-23 |
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
|
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
|
US5994358A
(en)
|
1996-10-23 |
1999-11-30 |
Zymogenetics, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5948776A
(en)
|
1996-10-23 |
1999-09-07 |
Zymogenetic, Inc. |
Compositions and methods for treating bone deficit conditions
|
US5965573A
(en)
|
1996-10-23 |
1999-10-12 |
Zymogenetics, 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
|
ATE272394T1
(de)
|
1996-10-31 |
2004-08-15 |
Takeda Chemical Industries Ltd |
Zubereitung mit verzögerter freisetzung
|
US5858753A
(en)
|
1996-11-25 |
1999-01-12 |
Icos Corporation |
Lipid kinase
|
WO1998024804A2
(en)
|
1996-12-06 |
1998-06-11 |
Vertex Pharmaceuticals Incorporated |
INHIBITORS OF INTERLEUKIN-1β CONVERTING ENZYME
|
ZA9711385B
(en)
|
1996-12-20 |
1999-06-18 |
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
|
PT950059E
(pt)
|
1997-01-06 |
2004-10-29 |
Pfizer |
Derivados de sulfona ciclicos
|
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
|
DE69817801T2
(de)
|
1997-02-03 |
2004-03-11 |
Pfizer Products Inc., Groton |
Arylsulfonylhydroxamsäurederivate
|
EP1017823B1
(en)
|
1997-02-07 |
2004-07-14 |
Princeton University |
Engineered protein kinases which can utilize modified nucleotide triphosphate substrates
|
BR9807824A
(pt)
|
1997-02-07 |
2000-03-08 |
Pfizer |
Derivados de n-hidróxi-beta-sulfonil-propionamida e seu uso como inibidores de metaloproteinases de matriz
|
JP3710489B2
(ja)
|
1997-02-11 |
2005-10-26 |
ファイザー・インク |
アリールスルホニルヒドロキサム酸誘導体
|
US7863444B2
(en)
|
1997-03-19 |
2011-01-04 |
Abbott Laboratories |
4-aminopyrrolopyrimidines as kinase inhibitors
|
TR199902301T2
(xx)
|
1997-03-19 |
1999-12-21 |
Basf Aktiengesellschaft |
Pirilo $2,3D]pirimidinler ve onlar�n kullan�m�.
|
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
|
JP3448275B2
(ja)
|
1997-08-08 |
2003-09-22 |
ファイザー・プロダクツ・インク |
アリールオキシアリールスルホニルアミノヒドロキサム酸誘導体
|
US6340759B1
(en)
|
1997-10-02 |
2002-01-22 |
Eisai Co., Ltd. |
Fused pyridine derivatives
|
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
|
GB9725782D0
(en)
|
1997-12-05 |
1998-02-04 |
Pfizer Ltd |
Therapeutic agents
|
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
|
GB9801690D0
(en)
|
1998-01-27 |
1998-03-25 |
Pfizer Ltd |
Therapeutic agents
|
AU756838B2
(en)
|
1998-03-04 |
2003-01-23 |
Bristol-Myers Squibb Company |
Heterocyclo-substituted imidazopyrazine protein tyrosine kinase inhibitors
|
US6613358B2
(en)
|
1998-03-18 |
2003-09-02 |
Theodore W. Randolph |
Sustained-release composition including amorphous polymer
|
JP4462654B2
(ja)
|
1998-03-26 |
2010-05-12 |
ソニー株式会社 |
映像素材選択装置及び映像素材選択方法
|
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
|
PA8469501A1
(es)
|
1998-04-10 |
2000-09-29 |
Pfizer Prod Inc |
Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico
|
PA8469401A1
(es)
|
1998-04-10 |
2000-05-24 |
Pfizer Prod Inc |
Derivados biciclicos del acido hidroxamico
|
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
|
TR200101395T2
(tr)
|
1998-09-18 |
2001-11-21 |
Basf Ag. |
Kinaz engelleyiciler olarak 4-Aminopyrrolopyrimidin'ler
|
US6362216B1
(en)
|
1998-10-27 |
2002-03-26 |
Array Biopharma Inc. |
Compounds which inhibit tryptase activity
|
DK1004578T3
(da)
|
1998-11-05 |
2004-06-28 |
Pfizer Prod Inc |
5-oxo-pyrrolidin-2-carboxylsyrehydroxamidderivater
|
DE1140938T1
(de)
|
1999-01-11 |
2003-01-09 |
Princeton University, Princeton |
Kinase-inhibitoren mit hoher affinität zur ziel detektion und ihre verwendung
|
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
|
WO2000050425A1
(en)
|
1999-02-22 |
2000-08-31 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Polycyclo heterocyclic derivatives as antiinflammatory agents
|
US6248363B1
(en)
|
1999-11-23 |
2001-06-19 |
Lipocine, Inc. |
Solid carriers for improved delivery of active ingredients in pharmaceutical compositions
|
SK12832001A3
(sk)
|
1999-03-12 |
2002-01-07 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Protizápalové látky, spôsob ich výroby, farmaceutický prostriedok s ich obsahom a ich použitie
|
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
|
KR20020062808A
(ko)
|
1999-06-03 |
2002-07-31 |
크놀 게엠베하 |
벤조티아지논 및 벤족사지논 화합물
|
US6387894B1
(en)
|
1999-06-11 |
2002-05-14 |
Pfizer Inc. |
Use of CRF antagonists and renin-angiotensin system inhibitors
|
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
|
TWI262914B
(en)
|
1999-07-02 |
2006-10-01 |
Agouron Pharma |
Compounds and pharmaceutical compositions for inhibiting protein kinases
|
EP1081137A1
(en)
|
1999-08-12 |
2001-03-07 |
Pfizer Products Inc. |
Selective inhibitors of aggrecanase in osteoarthritis treatment
|
GB9919588D0
(en)
|
1999-08-18 |
1999-10-20 |
Hoechst Schering Agrevo Gmbh |
Fungicidal compounds
|
JP4831906B2
(ja)
|
1999-08-27 |
2011-12-07 |
ケモセントリックス, インコーポレイテッド |
Cxcr3機能を調節するための複素環式化合物および方法
|
US20070021493A1
(en)
|
1999-09-16 |
2007-01-25 |
Curis, Inc. |
Mediators of hedgehog signaling pathways, compositions and uses related thereto
|
US6545005B1
(en)
|
1999-09-16 |
2003-04-08 |
Curtis, 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
|
TR200201505T2
(tr)
|
1999-09-17 |
2003-01-21 |
Abbott Gmbh & Co.Kg |
Terapötik maddeler olarak pirazolopirimidinler
|
WO2001021160A2
(en)
|
1999-09-23 |
2001-03-29 |
Axxima Pharmaceuticals Aktiengesellschaft |
Carboxymide and aniline derivatives as selective inhibitors of pathogens
|
US6506769B2
(en)
|
1999-10-06 |
2003-01-14 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Heterocyclic compounds useful as inhibitors of tyrosine kinases
|
ATE277044T1
(de)
|
1999-10-06 |
2004-10-15 |
Boehringer Ingelheim Pharma |
Heterocyclische verbindungen verwendbar als tyrosinkinase inhibitoren
|
EP1223170B1
(en)
|
1999-10-12 |
2005-12-28 |
Takeda Pharmaceutical Company Limited |
Pyrimidine-5-carboxamide compounds, process for producing the same and use thereof
|
CA2386190C
(en)
|
1999-10-13 |
2009-04-14 |
Johns Hopkins University School Of Medicine |
Regulators of the hedgehog pathway, compositions and uses related thereto
|
CA2286451A1
(en)
|
1999-10-14 |
2001-04-14 |
Grant A. Mitchell |
Hormone-sensitive lipase mediated male infertility
|
US6472153B1
(en)
|
1999-10-26 |
2002-10-29 |
Epoch Biosciences, Inc. |
Hybridization-triggered fluorescent detection of nucleic acids
|
EP1095933A1
(en)
|
1999-10-30 |
2001-05-02 |
Aventis Pharma Deutschland GmbH |
Novel N-guanidinoalkylamides, their preparation, their use, and pharmaceutical preparations comprising them
|
US6660845B1
(en)
|
1999-11-23 |
2003-12-09 |
Epoch Biosciences, Inc. |
Non-aggregating, non-quenching oligomers comprising nucleotide analogues; methods of synthesis and use thereof
|
IL133809A0
(en)
|
1999-12-30 |
2001-04-30 |
Yeda Res & Dev |
Steroidal alkaloids and pharmaceutical compositions comprising them
|
GB0002032D0
(en)
|
2000-01-28 |
2000-03-22 |
Zeneca Ltd |
Chemical compounds
|
US7217722B2
(en)
|
2000-02-01 |
2007-05-15 |
Kirin Beer Kabushiki Kaisha |
Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same
|
FR2804958B1
(fr)
|
2000-02-15 |
2005-07-08 |
Hoechst Marion Roussel Inc |
Derives de xanthine, leur procede de preparation et les intermediaires de ce procede, leur application comme medicament et les compositions pharmaceutiques les renfermant
|
US7115653B2
(en)
|
2000-03-30 |
2006-10-03 |
Curis, Inc. |
Small organic molecule regulators of cell proliferation
|
US6613798B1
(en)
|
2000-03-30 |
2003-09-02 |
Curis, Inc. |
Small organic molecule regulators of cell proliferation
|
ES2250377T5
(es)
|
2000-03-30 |
2010-04-06 |
Curis, Inc. |
Moleculas organicas pequeñas reguladoras de la proliferacion celular.
|
US20020127625A1
(en)
|
2000-03-31 |
2002-09-12 |
Forskarpatent Is Syd Ab |
Methods of diagnosing immune related diseases
|
AU5566701A
(en)
*
|
2000-04-25 |
2001-11-07 |
Icos Corp |
Inhibitors of human phosphatidyl-inositol 3-kinase delta
|
US6667300B2
(en)
|
2000-04-25 |
2003-12-23 |
Icos Corporation |
Inhibitors of human phosphatidylinositol 3-kinase delta
|
WO2001091699A2
(en)
|
2000-05-30 |
2001-12-06 |
Advanced Research & Technology Institute |
Compositions and methods for identifying agents which modulate pten function and pi-3 kinase pathways
|
US6667398B2
(en)
|
2000-06-22 |
2003-12-23 |
Pfizer Inc |
Process for the preparation of pyrazolopyrimidinones
|
NZ522839A
(en)
|
2000-06-27 |
2004-11-26 |
Genelabs Tech Inc |
Novel compounds possessing antibacterial, antifungal or antitumor activity
|
US6534691B2
(en)
|
2000-07-18 |
2003-03-18 |
E. I. Du Pont De Nemours And Company |
Manufacturing process for α-olefins
|
AU2001292320A1
(en)
*
|
2000-10-02 |
2002-04-15 |
Tanabe Seiyaku Co., Ltd. |
Benzylamine compound, process for producing the same, and intermediate therefor
|
EP1578341A4
(en)
|
2000-10-11 |
2005-09-28 |
Tularik Inc |
MODULATION OF THE CCR4 FUNCTION
|
JP4741170B2
(ja)
|
2000-10-11 |
2011-08-03 |
アプライド バイオシステムズ リミテッド ライアビリティー カンパニー |
アニオン性リンカーを有する蛍光核酸塩基結合体
|
FR2815346B1
(fr)
|
2000-10-13 |
2004-02-20 |
Servier Lab |
Nouveaux composes aminotriazolones, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
|
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
|
CA2431553A1
(en)
|
2000-12-11 |
2002-10-24 |
Tularik Inc. |
Cxcr3 antagonists
|
CN100471838C
(zh)
|
2000-12-28 |
2009-03-25 |
第一制药株式会社 |
Vla-4抑制剂
|
EP1359911A2
(en)
|
2000-12-29 |
2003-11-12 |
Alteon, Inc. |
Method for treating fibrotic diseases or other indications ivc
|
WO2002053160A1
(en)
|
2000-12-29 |
2002-07-11 |
Alteon, Inc. |
Method for treating glaucoma ivb
|
US7105499B2
(en)
|
2001-01-22 |
2006-09-12 |
Merck & Co., Inc. |
Nucleoside derivatives as inhibitors of RNA-dependent RNA viral polymerase
|
CZ20032005A3
(en)
|
2001-01-22 |
2004-04-14 |
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
|
PA8539401A1
(es)
|
2001-02-14 |
2002-10-28 |
Warner Lambert Co |
Quinazolinas como inhibidores de mmp-13
|
PA8539501A1
(es)
|
2001-02-14 |
2002-09-30 |
Warner Lambert Co |
Compuestos triazolo como inhibidores de mmp
|
MXPA03008560A
(es)
|
2001-03-22 |
2004-06-30 |
Abbot Gmbh & Co Kg |
Pirazolopirimidinas como agentes terapeuticos.
|
US7250569B2
(en)
|
2001-04-26 |
2007-07-31 |
New York University School Of Medicine |
Method for dissolving nanostructural materials
|
US6664269B2
(en)
|
2001-05-08 |
2003-12-16 |
Maybridge Plc |
Isoquinolinone derivatives
|
NZ518726A
(en)
|
2001-05-09 |
2004-06-25 |
Warner Lambert Co |
Method of treating or inhibiting neutrophil chemotaxis by administering a mek inhibitor
|
WO2002094264A1
(en)
|
2001-05-23 |
2002-11-28 |
Tularik Inc. |
Ccr4 antagonists
|
US20030236198A1
(en)
|
2001-06-13 |
2003-12-25 |
Genesoft, Inc. |
Antipathogenic benzamide compounds
|
US6777425B2
(en)
|
2001-06-13 |
2004-08-17 |
Genesoft Pharmaceuticals, Inc. |
Isoquinoline compounds having antiinfective activity
|
US6825228B2
(en)
|
2001-06-13 |
2004-11-30 |
Genesoft Pharmaceuticals, Inc. |
Benzothiophene compounds having antiinfective activity
|
US20030114467A1
(en)
|
2001-06-21 |
2003-06-19 |
Shakespeare William C. |
Novel pyrazolo- and pyrrolo-pyrimidines and uses thereof
|
DE10134721A1
(de)
|
2001-07-17 |
2003-02-06 |
Bayer Ag |
Tetrahydrochinoxaline
|
DE60233823D1
(de)
|
2001-07-27 |
2009-11-05 |
Curis Inc |
N und relevante verwendungszwecke
|
JP4286134B2
(ja)
|
2001-08-01 |
2009-06-24 |
メルク エンド カムパニー インコーポレーテッド |
ベンズイミダゾ[4,5−f]イソキノリノン誘導体
|
AU2002327422A1
(en)
|
2001-08-03 |
2003-03-18 |
Abbott Laboratories |
Method of identifying inhibitors of lck
|
KR20100087209A
(ko)
|
2001-08-10 |
2010-08-03 |
시오노기세이야쿠가부시키가이샤 |
항바이러스제
|
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
|
WO2003024969A1
(en)
|
2001-09-14 |
2003-03-27 |
Merck & Co., Inc. |
Tyrosine kinase inhibitors
|
WO2004043335A2
(en)
|
2001-09-13 |
2004-05-27 |
Genesoft, Inc. |
Methods of treating infection by drug resistant bacteria
|
US8124625B2
(en)
|
2001-09-14 |
2012-02-28 |
Shionogi & Co., Ltd. |
Method of enhancing the expression of apolipoprotein AI using olefin derivatives
|
AUPR769501A0
(en)
|
2001-09-14 |
2001-10-11 |
Biomolecular Research Institute Limited |
Cytokine receptor 1
|
US7269663B2
(en)
|
2001-09-28 |
2007-09-11 |
Intel Corporation |
Tagging packets with a lookup key to facilitate usage of a unified packet forwarding cache
|
TWI330183B
(el)
|
2001-10-22 |
2010-09-11 |
Eisai R&D Man Co Ltd |
|
AU2002363176B2
(en)
|
2001-11-01 |
2008-09-25 |
Janssen Pharmaceutica N.V. |
Heteroaryl amines as glycogen synthase kinase 3Beta inhibitors (GSK3 inhibitors)
|
IL161516A0
(en)
|
2001-11-09 |
2004-09-27 |
Boehringer Ingelheim Pharma |
Benzimidazoles useful as protein kinase inhibitors
|
DE10159269A1
(de)
|
2001-12-03 |
2003-06-18 |
Bayer Ag |
Arylierung von Olefinen
|
DE10159270A1
(de)
|
2001-12-03 |
2003-06-12 |
Bayer Ag |
Verfahren zur Arylierung von Olefinen
|
WO2003048081A2
(en)
|
2001-12-04 |
2003-06-12 |
Bristol-Myers Squibb Company |
Glycinamides as factor xa inhibitors
|
WO2003059884A1
(en)
|
2001-12-21 |
2003-07-24 |
X-Ceptor Therapeutics, Inc. |
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
|
WO2003057212A1
(en)
|
2001-12-26 |
2003-07-17 |
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
|
US20040043959A1
(en)
|
2002-03-04 |
2004-03-04 |
Bloom Laura A. |
Combination therapies for treating methylthioadenosine phosphorylase deficient cells
|
AU2003225933A1
(en)
|
2002-03-22 |
2003-10-13 |
Cellular Genomics, Inc. |
AN IMPROVED FORMULATION OF CERTAIN PYRAZOLO(3,4-d) PYRIMIDINES AS KINASE MODULATORS
|
US8247424B2
(en)
|
2002-03-26 |
2012-08-21 |
Zentopharm Gmbh |
Fredericamycin derivatives
|
US7166293B2
(en)
|
2002-03-29 |
2007-01-23 |
Carlsbad Technology, Inc. |
Angiogenesis inhibitors
|
DE10217046A1
(de)
|
2002-04-17 |
2003-11-06 |
Bioleads Gmbh |
Fredericamycin-Derivate
|
DE60322869D1
(de)
|
2002-04-22 |
2008-09-25 |
Univ Johns Hopkins |
Modulatoren von hedgehog signalpfaden, zusammensetzungen und verwandte verwendungen
|
BR0309556A
(pt)
|
2002-04-26 |
2005-02-09 |
Pfizer Prod Inc |
Inibidores de metaloproteinase pirimidina-2,4,6-triona
|
US6794562B2
(en)
|
2002-05-01 |
2004-09-21 |
Stine Seed Farm, Inc. |
Soybean cultivar 0332143
|
CA2485343A1
(en)
|
2002-05-23 |
2004-05-13 |
Merck & Co., Inc. |
Mitotic kinesin inhibitors
|
WO2003106426A1
(en)
|
2002-06-14 |
2003-12-24 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
WO2004002481A1
(en)
|
2002-06-27 |
2004-01-08 |
Novo Nordisk A/S |
Aryl carbonyl derivatives as therapeutic agents
|
KR101124245B1
(ko)
|
2002-06-27 |
2012-07-02 |
노보 노르디스크 에이/에스 |
치료제로서 아릴 카르보닐 유도체
|
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
|
AU2003249244A1
(en)
|
2002-07-15 |
2004-02-02 |
Combinatorx, Incorporated |
Methods for the treatment of neoplasms
|
EP1539163A1
(en)
|
2002-08-13 |
2005-06-15 |
Warner-Lambert Company LLC |
4-hydroxyquinoline derivatives as matrix metalloproteinase inhibitors
|
EP1394159A1
(fr)
|
2002-08-13 |
2004-03-03 |
Warner-Lambert Company LLC |
Nouveaux dérivés de thiophène, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent
|
US7598377B2
(en)
*
|
2002-08-16 |
2009-10-06 |
Astrazeneca Ab |
Inhibition of phosphoinositide 3-kinase β
|
CN101260104A
(zh)
*
|
2002-08-16 |
2008-09-10 |
阿斯利康(瑞典)有限公司 |
抑制磷酸肌醇3-激酶β
|
US20040048853A1
(en)
|
2002-08-21 |
2004-03-11 |
Gustave Bergnes |
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
|
AU2003266668A1
(en)
|
2002-09-30 |
2004-04-23 |
Banyu Pharmaceutical Co., Ltd. |
2-aminobenzimidazole derivative
|
EP1549614A4
(en)
|
2002-10-03 |
2008-04-16 |
Targegen Inc |
VASCULATORY AGENTS AND METHODS FOR THEIR APPLICATION
|
US20050282814A1
(en)
|
2002-10-03 |
2005-12-22 |
Targegen, Inc. |
Vasculostatic agents and methods of use thereof
|
US20040146941A1
(en)
|
2002-11-04 |
2004-07-29 |
Biliang Zhang |
Chemical encoding technology for combinatorial synthesis
|
JP2004161716A
(ja)
|
2002-11-15 |
2004-06-10 |
Takeda Chem Ind Ltd |
Jnk阻害剤
|
AU2003286251A1
(en)
|
2002-11-21 |
2004-06-15 |
Vicore Pharma Ab |
New bicyclic angiotensin ii agonists
|
EP1572660B1
(en)
|
2002-12-20 |
2011-01-26 |
X-Ceptor Therapeutics, Inc. |
Isoquinolinone derivatives and their use as therapeutic agents
|
US7071355B2
(en)
|
2002-12-23 |
2006-07-04 |
4 Sc Ag |
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
|
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
|
WO2004075917A1
(ja)
|
2003-02-28 |
2004-09-10 |
Toudai Tlo, Ltd. |
器官または組織の線維化抑制剤
|
CA2517942A1
(en)
|
2003-03-06 |
2004-09-16 |
Dsm Ip Assets B.V. |
Process for the preparation of an .alpha.-amino carbonyl compound
|
TW200505902A
(en)
|
2003-03-20 |
2005-02-16 |
Schering Corp |
Cannabinoid receptor ligands
|
US20040242568A1
(en)
|
2003-03-25 |
2004-12-02 |
Syrrx, Inc. |
Dipeptidyl peptidase inhibitors
|
GB0306907D0
(en)
|
2003-03-26 |
2003-04-30 |
Angiogene Pharm Ltd |
Boireductively-activated prodrugs
|
WO2004087679A1
(en)
|
2003-04-01 |
2004-10-14 |
Aponetics Ag |
2, 4, 6-trisubstituted pyrimidine derivatives useful for the treatment of neoplastic and autoimmune diseases
|
WO2004089297A2
(en)
|
2003-04-02 |
2004-10-21 |
Suntory Pharmaceutical Research Laboratories, Llc |
Compounds and methods for treatment of thrombosis
|
WO2004089877A1
(en)
|
2003-04-14 |
2004-10-21 |
Astrazeneca Ab |
New hydroxynaphthyl amides
|
EP1479675A1
(en)
|
2003-05-19 |
2004-11-24 |
Aventis Pharma Deutschland GmbH |
Indazole-derivatives as factor Xa inhibitors
|
US7223780B2
(en)
|
2003-05-19 |
2007-05-29 |
Sanofi-Aventis Deutschland Gmbh |
Triazole-derivatives as blood clotting enzyme factor Xa inhibitors
|
US7317027B2
(en)
|
2003-05-19 |
2008-01-08 |
Sanofi-Aventis Deutschland Gmbh |
Azaindole-derivatives as factor Xa inhibitors
|
EP1646615B1
(en)
|
2003-06-06 |
2009-08-26 |
Vertex Pharmaceuticals Incorporated |
Pyrimidine derivatives as modulators of atp-binding cassette transporters
|
US7429596B2
(en)
|
2003-06-20 |
2008-09-30 |
The Regents Of The University Of California |
1H-pyrrolo [2,3-D] pyrimidine derivatives and methods of use thereof
|
WO2005002585A1
(en)
|
2003-07-02 |
2005-01-13 |
Warner-Lambert Company Llc |
Combination of an allosteric inhibitor of matrix metalloproteinase-13 and a ligand to an alpha-2-delta receptor
|
US20080118493A1
(en)
|
2003-07-15 |
2008-05-22 |
Beachy Philip A |
Elevated Hedgehog Pathway Activity In Digestive System Tumors, And Methods Of Treating Digestive Sytem Tumors Having Elevated Hedgehog Pathway Activity
|
GB0317951D0
(en)
|
2003-07-31 |
2003-09-03 |
Trigen Ltd |
Compounds
|
WO2005014532A1
(en)
|
2003-08-08 |
2005-02-17 |
Transtech Pharma, Inc. |
Aryl and heteroaryl compounds, compositions and methods of use
|
US7208601B2
(en)
|
2003-08-08 |
2007-04-24 |
Mjalli Adnan M M |
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
|
BRPI0413563A
(pt)
|
2003-08-15 |
2006-10-17 |
Irm Llc |
compostos e composições como inibidores de atividade do receptor de quìnase de tirosina
|
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
|
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
|
US20080095761A1
(en)
|
2003-10-01 |
2008-04-24 |
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
|
AU2004289303A1
(en)
|
2003-11-10 |
2005-05-26 |
Synta Pharmaceuticals, Corp. |
Fused heterocyclic compounds
|
JP2007511596A
(ja)
|
2003-11-17 |
2007-05-10 |
ファイザー・プロダクツ・インク |
癌の治療において有用なピロロピリミジン化合物
|
EP1689719A1
(en)
*
|
2003-11-25 |
2006-08-16 |
Eli Lilly And Company |
7-phenyl-isoquinoline-5-sulfonylamino derivatives as inhibitors of akt (proteinkinase b)
|
JP2007513154A
(ja)
|
2003-12-08 |
2007-05-24 |
サイトキネティクス・インコーポレーテッド |
化合物、組成物及び方法
|
EP1715871A1
(en)
|
2003-12-22 |
2006-11-02 |
Gilead Sciences, Inc. |
Kinase inhibitor phosphonate conjugates
|
DE602004025504D1
(de)
|
2003-12-23 |
2010-03-25 |
Novartis Ag |
Bicyclische heterocyclische p-38-kinase-inhibitoren
|
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
|
EP1723467A2
(en)
|
2004-02-03 |
2006-11-22 |
Rochester Institute of Technology |
Method of photolithography using a fluid and a system thereof
|
CA2553724A1
(en)
|
2004-02-03 |
2005-08-18 |
Abbott Laboratories |
Aminobenzoxazoles as therapeutic agents
|
KR20070026385A
(ko)
*
|
2004-02-13 |
2007-03-08 |
반유 세이야꾸 가부시끼가이샤 |
축합환 4-옥소피리미딘 유도체
|
US20050187418A1
(en)
|
2004-02-19 |
2005-08-25 |
Small Brooke L. |
Olefin oligomerization
|
WO2005080394A1
(en)
|
2004-02-24 |
2005-09-01 |
Bioaxone Therapeutique Inc. |
4-substituted piperidine derivatives
|
EP1737865A1
(en)
|
2004-02-27 |
2007-01-03 |
F.Hoffmann-La Roche Ag |
Fused derivatives of pyrazole
|
EP1568698A1
(en)
|
2004-02-27 |
2005-08-31 |
Aventis Pharma Deutschland GmbH |
Pyrrole-derivatives as factor Xa inhibitors
|
EP1571154A1
(en)
|
2004-03-03 |
2005-09-07 |
Aventis Pharma Deutschland GmbH |
Beta-aminoacid-derivatives as factor Xa inhibitors
|
EP1740591B1
(en)
|
2004-04-02 |
2009-06-17 |
OSI Pharmaceuticals, Inc. |
6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors
|
US9212149B2
(en)
|
2004-04-30 |
2015-12-15 |
Takeda Pharmaceutical Company Limited |
Substituted 2-amidoquinazol-4-ones as matrix metalloproteinase-13 inhibitors
|
PL1745041T3
(pl)
|
2004-04-30 |
2012-11-30 |
Genentech Inc |
Inhibitory chinoksalinowe szlaku sygnałowego hedgehog
|
DE102004022897A1
(de)
|
2004-05-10 |
2005-12-08 |
Bayer Cropscience Ag |
Azinyl-imidazoazine
|
SI3153514T1
(sl)
*
|
2004-05-13 |
2022-02-28 |
Icos Corporation |
Kinazolinoni kot zaviralci človeške fosfatidilinozitol 3-kinaze delta
|
EP1750714A1
(en)
|
2004-05-13 |
2007-02-14 |
Vanderbilt University |
Phosphoinositide 3-kinase delta selective inhibitors for inhibiting angiogenesis
|
JP2008500338A
(ja)
|
2004-05-25 |
2008-01-10 |
イコス・コーポレイション |
造血細胞の異常増殖を治療及び/又は予防する方法
|
WO2005120511A1
(en)
|
2004-06-04 |
2005-12-22 |
Icos Corporation |
Methods for treating mast cell disorders
|
GB0413605D0
(en)
|
2004-06-17 |
2004-07-21 |
Addex Pharmaceuticals Sa |
Novel compounds
|
CA2571824A1
(en)
|
2004-07-01 |
2006-01-19 |
Merck & Co., Inc. |
Mitotic kinesin inhibitors
|
US20060019967A1
(en)
|
2004-07-21 |
2006-01-26 |
Su-Ying Wu |
SARS CoV main protease inhibitors
|
WO2006015279A1
(en)
|
2004-07-28 |
2006-02-09 |
Neurogen Corporation |
Heterocyclic diamine compounds as ligands of the melanin concentrating hormone receptor useful for the treatment of obesity, diabetes, eating and sexual disorders
|
WO2006026430A2
(en)
|
2004-08-27 |
2006-03-09 |
Infinity Pharmaceuticals, Inc. |
Cyclopamine analogues and methods of use thereof
|
KR101366414B1
(ko)
|
2004-09-02 |
2014-03-18 |
쿠리스 인코퍼레이션 |
헤지호그 신호전달에 대한 피리딜 억제제
|
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
|
KR20070083836A
(ko)
|
2004-10-28 |
2007-08-24 |
아이알엠 엘엘씨 |
헷지혹 경로 조절제로서의 화합물 및 조성물
|
US7622451B2
(en)
|
2004-11-03 |
2009-11-24 |
University Of Kansas |
Novobiocin analogues as neuroprotective agents and in the treatment of autoimmune disorders
|
US8212012B2
(en)
|
2004-11-03 |
2012-07-03 |
University Of Kansas |
Novobiocin analogues having modified sugar moieties
|
US8212011B2
(en)
|
2004-11-03 |
2012-07-03 |
University Of Kansas |
Novobiocin analogues
|
EP1807440B1
(en)
|
2004-11-03 |
2020-02-19 |
The University of Kansas |
Novobiocin analogues as anticancer agents
|
GB0425035D0
(en)
|
2004-11-12 |
2004-12-15 |
Novartis Ag |
Organic compounds
|
EP1831225A2
(en)
|
2004-11-19 |
2007-09-12 |
The Regents of the University of California |
Anti-inflammatory pyrazolopyrimidines
|
WO2006058088A2
(en)
|
2004-11-23 |
2006-06-01 |
Ptc Therapeutics, Inc. |
Carbazole, carboline and indole derivatives useful in the inhibition of vegf production
|
JP2008521862A
(ja)
|
2004-12-01 |
2008-06-26 |
デブジェン エヌブイ |
イオンチャンネル、特にkvファミリーのイオンチャンネルと相互作用する5−カルボキサミド置換チアゾール誘導体
|
US20060156485A1
(en)
|
2005-01-14 |
2006-07-20 |
The Procter & Gamble Company |
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
|
GB0501999D0
(en)
|
2005-02-01 |
2005-03-09 |
Sentinel Oncology Ltd |
Pharmaceutical compounds
|
US20080287469A1
(en)
|
2005-02-17 |
2008-11-20 |
Diacovo Thomas G |
Phosphoinositide 3-Kinase Inhibitors for Inhibiting Leukocyte Accumulation
|
WO2006091897A2
(en)
|
2005-02-25 |
2006-08-31 |
Adenosine Therapeutics, Llc |
Derivatives of 8-substituted xanthines
|
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
|
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
|
WO2006114064A2
(en)
|
2005-04-25 |
2006-11-02 |
Institute Of Organic Chemistry And Biochemistry Ofthe Academy Of Sciences Of The Czech Republic |
Use of compounds to enhance processivity of telomerase
|
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
|
UA95777C2
(en)
|
2005-06-22 |
2011-09-12 |
Кемосентрикс, Инк. |
Azaindazole compounds and methods of use
|
ATE474829T1
(de)
|
2005-06-27 |
2010-08-15 |
Amgen Inc |
Entzündungshemmende arylnitrilverbindungen
|
BRPI0615524A2
(pt)
|
2005-07-11 |
2010-04-06 |
Devgen Nv |
derivados da amida como inibidores da quinase
|
BRPI0615522A2
(pt)
|
2005-07-11 |
2012-04-10 |
Devgen Nv |
derivados da amida como inibidores da quinase
|
WO2007029121A2
(en)
|
2005-07-21 |
2007-03-15 |
Galderma Research & Development |
Novel cyclopent-2-en-1-one derivatives which are ppar receptor modulators, and use thereof in pharmaceutical or cosmetic compositions
|
US20070017915A1
(en)
|
2005-07-22 |
2007-01-25 |
Weder Donald E |
Collapsible and/or erectable substantially egg-shaped container
|
CN101273038A
(zh)
|
2005-07-29 |
2008-09-24 |
美迪维尔公司 |
丙型肝炎病毒的大环化合物抑制剂
|
GB0516723D0
(en)
|
2005-08-15 |
2005-09-21 |
Novartis Ag |
Organic compounds
|
WO2007025090A2
(en)
|
2005-08-25 |
2007-03-01 |
Kalypsys, Inc. |
Heterobicyclic and - tricyclic inhibitors of mapk/erk kinase
|
CN101243090A
(zh)
|
2005-08-25 |
2008-08-13 |
霍夫曼-拉罗奇有限公司 |
p38 MAP激酶抑制剂及使用它的方法
|
WO2007025534A1
(de)
|
2005-09-01 |
2007-03-08 |
Bioagency Ag |
Fredericamycin-derivate
|
WO2007028022A2
(en)
|
2005-09-01 |
2007-03-08 |
Renovis, Inc. |
Novel compounds as p2x7 modulators and uses thereof
|
BRPI0616459A2
(pt)
|
2005-09-29 |
2011-06-21 |
Wyeth Corp |
compostos das fórmulas i, ii, e iii; processos para o tratamento ou para a prevenção de: um estado de saúde com melhora devido à recaptação de monoamina; pelo menos um sintoma vasomotor; pelo menos um distúrbio depressivo; pelo menos uma disfunção sexual; para a prevenção de dor; de distúrbio gastrointestinal ou genitourinário; de sìndrome de fadiga crÈnica; de sìndrome de fibromialgia; de esquizofrenia; e uso de um composto
|
FR2892859B1
(fr)
|
2005-10-27 |
2008-06-06 |
Commissariat Energie Atomique |
Procede de greffage de molecules d'interet sur des surfaces inorganiques, surfaces obtenues et applications
|
WO2007054623A2
(en)
|
2005-11-11 |
2007-05-18 |
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
|
EP2325186B1
(en)
|
2005-11-17 |
2014-10-08 |
OSI Pharmaceuticals, LLC |
Fused Bicyclic mTor Inhibitors
|
JP2009516742A
(ja)
|
2005-11-22 |
2009-04-23 |
メルク エンド カムパニー インコーポレーテッド |
インドールオレキシン受容体アンタゴニスト
|
CA2630920A1
(en)
|
2005-11-22 |
2007-05-31 |
University Of South Florida |
Inhibition of cell proliferation
|
JP2009520028A
(ja)
|
2005-12-19 |
2009-05-21 |
オーエスアイ・ファーマスーティカルズ・インコーポレーテッド |
Igfr抑制剤および抗癌剤の併用
|
US7572809B2
(en)
|
2005-12-19 |
2009-08-11 |
Hoffmann-La Roche Inc. |
Isoquinoline aminopyrazole derivatives
|
TW201307354A
(zh)
|
2005-12-29 |
2013-02-16 |
Abbott Lab |
蛋白質激酶抑制劑
|
ES2566479T3
(es)
|
2006-01-06 |
2016-04-13 |
Sunovion Pharmaceuticals Inc. |
Inhibidores de reabsorción de monoamina con base en tetralona
|
WO2007094912A2
(en)
|
2006-01-13 |
2007-08-23 |
University Of Kentucky |
Bis-quaternary ammonium salts and methods for modulating neuronal nicotinic acetylcholine receptors
|
US20080058521A1
(en)
|
2006-01-26 |
2008-03-06 |
Wyeth |
Processes for the preparation of compounds
|
PE20071025A1
(es)
|
2006-01-31 |
2007-10-17 |
Mitsubishi Tanabe Pharma Corp |
Compuesto amina trisustituido
|
AU2007224020A1
(en)
|
2006-03-07 |
2007-09-13 |
Array Biopharma Inc. |
Heterobicyclic pyrazole compounds and methods of use
|
US7566565B2
(en)
|
2006-03-24 |
2009-07-28 |
Syntonix Pharmaceuticals, Inc. |
PC5 as a factor IX propeptide processing enzyme
|
EP2007373A4
(en)
|
2006-03-29 |
2012-12-19 |
Foldrx Pharmaceuticals Inc |
INHIBITION OF ALPHA SYNUCLEINE TOXICITY
|
GB2453058A
(en)
*
|
2006-04-04 |
2009-03-25 |
Univ California |
Kinase antagonists
|
US7829590B2
(en)
|
2006-04-13 |
2010-11-09 |
Guy Brenchley |
Thiophene-carboxamides useful as inhibitors of protein kinases
|
US20090306149A1
(en)
|
2006-04-14 |
2009-12-10 |
Rishi Kumar Jain |
Use of biarylcarboxamies in the treatment of hedgehog pathway-related disorders
|
WO2007121453A2
(en)
|
2006-04-17 |
2007-10-25 |
The Regents Of The University Of California |
2-hydroxy-1-oxo 1,2 dihydro isoquinoline chelating agents
|
JP5373599B2
(ja)
|
2006-04-21 |
2013-12-18 |
ノバルティス アーゲー |
アデノシンa2a受容体アゴニストとして使用するためのプリン誘導体
|
GB0607948D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
GB0607950D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
JP2009536161A
(ja)
|
2006-04-25 |
2009-10-08 |
アステックス、セラピューティックス、リミテッド |
医薬化合物
|
EP2037931A2
(en)
|
2006-04-25 |
2009-03-25 |
Astex Therapeutics Limited |
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
(uk)
|
2006-05-05 |
2011-02-25 |
Айерем Елелсі |
Сполуки та композиції як модулятори хеджхогівського сигнального шляху
|
EP2029593A1
(en)
|
2006-05-22 |
2009-03-04 |
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
|
ATE491428T1
(de)
|
2006-05-24 |
2011-01-15 |
Guardant S R L |
Alkalisiertes lokalanästhetikum im beutel
|
DE602007006835D1
(de)
|
2006-07-20 |
2010-07-08 |
Amgen Inc |
Substituierte pyridonverbindungen und anwendungsverfahren
|
ATE540029T1
(de)
|
2006-07-28 |
2012-01-15 |
Novartis Ag |
2,4-substituierte chinazoline als lipidkinasehemmer
|
US20100216791A1
(en)
|
2006-08-17 |
2010-08-26 |
Astrazeneca |
Pyridinylquinazolinamine derivatives and their use as b-raf inhibitors
|
US8541428B2
(en)
|
2006-08-22 |
2013-09-24 |
Technion Research And Development Foundation Ltd. |
Heterocyclic derivatives, pharmaceutical compositions and methods of use thereof
|
CA2661436A1
(en)
|
2006-08-24 |
2008-02-28 |
Serenex, Inc. |
Isoquinoline, quinazoline and phthalazine derivatives
|
ES2528316T3
(es)
|
2006-09-01 |
2015-02-06 |
Senhwa Biosciences, Inc. |
Moduladores de la serina-treonina proteína quinasa y de PARP
|
WO2008025755A1
(de)
|
2006-09-01 |
2008-03-06 |
Basf Se |
Verwendung von n-haltigen heterozyklen in dermokosmetika
|
EP1903044A1
(en)
|
2006-09-14 |
2008-03-26 |
Novartis AG |
Adenosine Derivatives as A2A Receptor Agonists
|
US7884180B2
(en)
|
2006-09-18 |
2011-02-08 |
Compugen Ltd |
Peptides which bind to G protein-coupled receptors
|
US8492405B2
(en)
|
2006-10-18 |
2013-07-23 |
Takeda Pharmaceutical Company Limited |
Glucokinase-activating fused heterocyclic compounds and methods of treating diabetes and obesity
|
KR101563010B1
(ko)
|
2006-10-31 |
2015-10-26 |
더 가버먼트 오브 더 유나이티드 스테이츠 오브 어메리카 애즈 리프리젠티드 바이 더 디파트먼트 오브 헬스 앤 휴먼 서비씨즈 |
평활화 폴리펩티드 및 사용 방법
|
US7772180B2
(en)
|
2006-11-09 |
2010-08-10 |
Bristol-Myers Squibb Company |
Hepatitis C virus inhibitors
|
EP2097422A4
(en)
|
2006-11-13 |
2010-04-14 |
Lilly Co Eli |
THIENOPYRIMIDINONE FOR THE TREATMENT OF INFLAMMATORY DISEASES AND CARCINOMAS
|
WO2008063625A2
(en)
|
2006-11-20 |
2008-05-29 |
Adolor Corporation |
Pyridine compounds and methods of their use
|
KR20090080530A
(ko)
|
2006-11-20 |
2009-07-24 |
노파르티스 아게 |
2-메틸-2-[4-(3-메틸-2-옥소-8-퀴놀린-3-일-2,3-디히드로-이미다조[4,5-c]퀴놀린-1-일)-페닐]-프로피오니트릴의 염 및 결정 형태
|
JP2010512331A
(ja)
|
2006-12-06 |
2010-04-22 |
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 |
グルココルチコイド模倣薬、それらの製造方法、医薬組成物、及びこれらの使用
|
BRPI0720546A2
(pt)
|
2006-12-14 |
2015-06-23 |
Daiichi Sankyo Co Ltd |
Composto, inibidor, medicamento, agente antitumor, composição farmacêutica, método para tratar câncer, e, uso do composto
|
JP5178738B2
(ja)
|
2006-12-20 |
2013-04-10 |
メルク・シャープ・アンド・ドーム・コーポレーション |
新規なjnk阻害剤
|
US8283345B2
(en)
|
2006-12-22 |
2012-10-09 |
Industrial Research Limited |
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
|
WO2008094737A2
(en)
|
2007-01-26 |
2008-08-07 |
Irm Llc |
Purine compounds and compositions as kinase inhibitors for the treatment of plasmodium related diseases
|
WO2008103354A2
(en)
|
2007-02-20 |
2008-08-28 |
Cropsolution, Inc. |
Modulators of acetyl-coenzyme a carboxylase and methods of use thereof
|
CN101675054B
(zh)
|
2007-03-07 |
2014-05-14 |
无限发现股份有限公司 |
环杷明内酰胺类似物及其使用方法
|
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
|
US8586619B2
(en)
|
2007-03-12 |
2013-11-19 |
Vm Therapeutics Llc |
Agents of calcium ion channel modulators
|
AU2008224941C1
(en)
|
2007-03-14 |
2013-06-27 |
Exelixis Patent Company Llc |
Inhibitors of the hedgehog pathway
|
DK2137162T3
(en)
|
2007-03-15 |
2018-11-26 |
Novartis Ag |
Organic compounds and their applications
|
WO2008118455A1
(en)
|
2007-03-23 |
2008-10-02 |
Amgen Inc. |
δ3- SUBSTITUTED QUINOLINE OR QUINOXALINE DERIVATIVES AND THEIR USE AS PHOSPHATIDYLINOSITOL 3-KINASE ( PI3K) INHIBITORS
|
EP2132207A2
(en)
|
2007-03-23 |
2009-12-16 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
NZ579834A
(en)
|
2007-03-23 |
2012-03-30 |
Amgen Inc |
Heterocyclic compounds as selective inhibitors of PI3K activity
|
WO2008117050A1
(en)
|
2007-03-27 |
2008-10-02 |
Astrazeneca Ab |
Pyrazolyl-amino-substituted pyrazines and their use for the treatment of cancer
|
US7867983B2
(en)
|
2007-03-29 |
2011-01-11 |
The University Of Connecticut |
Methods to protect skeletal muscle against injury
|
CN101636397B
(zh)
|
2007-04-13 |
2012-06-13 |
中国人民解放军军事医学科学院毒物药物研究所 |
脲类化合物、其制备方法及其医药用途
|
AU2008238379A1
(en)
|
2007-04-13 |
2008-10-23 |
Sanofi-Aventis |
A transition metal catalyzed synthesis of N-aminoindoles
|
US20090054517A1
(en)
|
2007-04-20 |
2009-02-26 |
Lubahn Dennis B |
Phytoestrogens As Regulators Of Hedgehog Signaling And Methods Of Their Use In Cancer Treatment
|
JP2010163361A
(ja)
|
2007-04-27 |
2010-07-29 |
Dainippon Sumitomo Pharma Co Ltd |
キノリン誘導体
|
US7960353B2
(en)
|
2007-05-10 |
2011-06-14 |
University Of Kansas |
Novobiocin analogues as neuroprotective agents and in the treatment of autoimmune disorders
|
US20090214529A9
(en)
|
2007-05-22 |
2009-08-27 |
Taigen Biotechnology Co., Ltd. |
Kinesin inhibitors
|
US9603848B2
(en)
|
2007-06-08 |
2017-03-28 |
Senomyx, Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
US7928111B2
(en)
|
2007-06-08 |
2011-04-19 |
Senomyx, Inc. |
Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
|
AU2008266856A1
(en)
|
2007-06-18 |
2008-12-24 |
University Of Louisville Research Foundation, Inc. |
Family of PFKFB3 inhibitors with anti-neoplastic activities
|
US8557823B2
(en)
|
2007-06-18 |
2013-10-15 |
Advanced Cancer Therapeutics, Llc |
Family of PFKFB3 inhibitors with anti-neoplastic activities
|
US8541593B2
(en)
|
2007-06-21 |
2013-09-24 |
Amgen Inc. |
Process for making substituted 2-amino-thiazolones
|
CN101772479B
(zh)
|
2007-06-22 |
2014-07-23 |
北卡罗莱纳州立大学 |
利用二环丙烯化合物抑制植物中乙烯响应的方法
|
WO2009000412A1
(en)
|
2007-06-26 |
2008-12-31 |
Sanofi Aventis |
A regioselective metal catalyzed synthesis of annelated benzimidazoles and azabenzimidazoles
|
EP2170274A1
(en)
|
2007-07-02 |
2010-04-07 |
Technion Research and Development Foundation, Ltd. |
Compositions, articles and methods comprising tspo ligands for preventing or reducing tobacco-associated damage
|
RU2345996C1
(ru)
|
2007-07-17 |
2009-02-10 |
Андрей Александрович Иващенко |
Аннелированные азагетероциклические амиды, включающие пиримидиновый фрагмент, способ их получения и применения
|
JP4846769B2
(ja)
|
2007-07-30 |
2011-12-28 |
田辺三菱製薬株式会社 |
医薬組成物
|
JP4834699B2
(ja)
|
2007-07-30 |
2011-12-14 |
田辺三菱製薬株式会社 |
医薬組成物
|
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
|
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
|
CA2702315A1
(en)
|
2007-10-15 |
2009-04-23 |
Astrazeneca Ab |
Combination 059
|
EA201070611A1
(ru)
|
2007-11-13 |
2010-12-30 |
Айкос Корпорейшн |
Ингибиторы человеческой фосфатидилинозитол-3-киназы дельта
|
CA2708391A1
(en)
|
2007-12-13 |
2009-06-25 |
Sri International |
Ppar-delta ligands and methods of their use
|
AU2008335880B2
(en)
|
2007-12-13 |
2014-03-13 |
Siena Biotech S.P.A. |
Hedgehog pathway antagonists and therapeutic applications thereof
|
WO2009081105A2
(en)
*
|
2007-12-21 |
2009-07-02 |
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
|
SG187426A1
(en)
*
|
2008-01-04 |
2013-02-28 |
Intellikine Llc |
Certain chemical entities, compositions and methods
|
US8193182B2
(en)
|
2008-01-04 |
2012-06-05 |
Intellikine, Inc. |
Substituted isoquinolin-1(2H)-ones, and methods of use thereof
|
CN101938904A
(zh)
|
2008-01-09 |
2011-01-05 |
PGx健康有限责任公司 |
用a2ar激动剂鞘内治疗神经性疼痛
|
JP2011511802A
(ja)
|
2008-02-07 |
2011-04-14 |
ギリアード・パロ・アルト・インコーポレイテッド |
Abca−1を上昇させる化合物およびかかる化合物の使用方法
|
US20110098267A1
(en)
|
2008-02-07 |
2011-04-28 |
Synta Pharmaceuticals Corporation |
Topical formulations for the treatment of psoriasis
|
WO2009103022A1
(en)
|
2008-02-13 |
2009-08-20 |
Itherx Pharmaceuticals, Inc. |
Derivatives of substituted fused ring cycloindoles and methods of their use
|
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
|
WO2009105782A1
(en)
|
2008-02-21 |
2009-08-27 |
Sequoia Pharmaceuticals, Inc. |
Hiv protease inhibitor and cytochrome p450 inhibitor combinations
|
US8993580B2
(en)
|
2008-03-14 |
2015-03-31 |
Intellikine Llc |
Benzothiazole kinase inhibitors and methods of use
|
WO2009114870A2
(en)
|
2008-03-14 |
2009-09-17 |
Intellikine, Inc. |
Kinase inhibitors and methods of use
|
MX2010010151A
(es)
|
2008-03-20 |
2010-10-25 |
Amgen Inc |
Moduladores de cinasa aurora y metodo de uso.
|
WO2009118765A2
(en)
|
2008-03-28 |
2009-10-01 |
Panacea Biotec Limited |
Novel monoamine re-uptake inhibitor
|
KR20110042153A
(ko)
|
2008-05-30 |
2011-04-25 |
제넨테크, 인크. |
퓨린 pi3k 억제 화합물 및 사용 방법
|
US20090312406A1
(en)
|
2008-06-12 |
2009-12-17 |
Hsing-Pang Hsieh |
Coumarin compounds and their use for treating viral infection
|
JP2011524914A
(ja)
|
2008-06-20 |
2011-09-08 |
アムジエン・インコーポレーテツド |
置換2−アミノ−チアゾロンを作製するための方法
|
US20110224223A1
(en)
|
2008-07-08 |
2011-09-15 |
The Regents Of The University Of California, A California Corporation |
MTOR Modulators and Uses Thereof
|
CN102124009B
(zh)
|
2008-07-08 |
2014-07-23 |
因特利凯公司 |
激酶抑制剂及其使用方法
|
JP2011528368A
(ja)
|
2008-07-16 |
2011-11-17 |
シェーリング コーポレイション |
二環式ヘテロ環誘導体およびgpcrモジュレーターとしてのその使用
|
US8450344B2
(en)
|
2008-07-25 |
2013-05-28 |
Aerie Pharmaceuticals, Inc. |
Beta- and gamma-amino-isoquinoline amide compounds and substituted benzamide compounds
|
EP2331525A4
(en)
|
2008-08-11 |
2013-01-02 |
Harvard College |
HALOFUGINONE ANALOGUE FOR INHIBITING TRNA SYNTHETASES AND APPLICATIONS THEREOF
|
WO2010019921A2
(en)
|
2008-08-15 |
2010-02-18 |
The Regents Of The University Of California |
Biomarkers for diagnosis and treatment of chronic lymphocytic leukemia
|
CA2735368A1
(en)
|
2008-09-10 |
2010-03-18 |
Kalypsys Inc. |
Aminopyrimidine inhibitors of histamine receptors for the treatment of disease
|
US8513295B2
(en)
|
2008-09-23 |
2013-08-20 |
Georgetown University |
Viral and fungal inhibitors
|
US8703778B2
(en)
|
2008-09-26 |
2014-04-22 |
Intellikine Llc |
Heterocyclic kinase inhibitors
|
EP2177510A1
(en)
|
2008-10-17 |
2010-04-21 |
Universität des Saarlandes |
Allosteric protein kinase modulators
|
US8476282B2
(en)
|
2008-11-03 |
2013-07-02 |
Intellikine Llc |
Benzoxazole kinase inhibitors and methods of use
|
WO2010053998A1
(en)
|
2008-11-05 |
2010-05-14 |
Xenon Pharmaceuticals, Inc. |
Spiro-condensed indole derivatives as sodium channel inhibitors
|
KR20160091440A
(ko)
|
2008-11-13 |
2016-08-02 |
길리아드 칼리스토가 엘엘씨 |
혈액 종양에 대한 요법
|
US20110269779A1
(en)
|
2008-11-18 |
2011-11-03 |
Intellikine, Inc. |
Methods and compositions for treatment of ophthalmic conditions
|
WO2010065923A2
(en)
|
2008-12-04 |
2010-06-10 |
The United States Of America, As Represented By The Secretary, Department Of Health And Human Services |
Phosphatidylinositol-3-kinase p110 delta-targeted drugs in the treatment of cns disorders
|
SG172289A1
(en)
|
2008-12-19 |
2011-07-28 |
Boehringer Ingelheim Int |
Cyclic pyrimidin-4-carboxamides as ccr2 receptor antagonists for treatment of inflammation, asthma and copd
|
US20110135655A1
(en)
|
2009-01-13 |
2011-06-09 |
PHILADELPHIA HEALTH AND EDUCATION CORPORATION d/b/a Drexel University College of Medicine; |
Role of PI3K p110 delta Signaling in Retroviral Infection and Replication
|
WO2010083218A1
(en)
|
2009-01-13 |
2010-07-22 |
Van Andel Research Institute |
Methods of using substituted isoxazolo pyridinones as dissociated glucocorticoids
|
US8513284B2
(en)
|
2009-02-13 |
2013-08-20 |
Ucb Pharma, S.A. |
Fused pyridine and pyrazine derivatives as kinase inhibitors
|
TW201038569A
(en)
|
2009-02-16 |
2010-11-01 |
Abbott Gmbh & Co Kg |
Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy
|
US20100280067A1
(en)
|
2009-04-30 |
2010-11-04 |
Pakala Kumara Savithru Sarma |
Inhibitors of acetyl-coa carboxylase
|
WO2010129816A2
(en)
|
2009-05-07 |
2010-11-11 |
Intellikine, Inc. |
Heterocyclic compounds and uses thereof
|
GB0908957D0
(en)
|
2009-05-22 |
2009-07-01 |
Ucb Pharma Sa |
Therapeutic agents
|
US8648066B2
(en)
|
2009-05-22 |
2014-02-11 |
Exelixis, Inc. |
Benzoxazepines as inhibitors of PI3K/mTOR and methods of their use and manufacture
|
CN102459248A
(zh)
|
2009-05-26 |
2012-05-16 |
埃克塞里艾克西斯公司 |
作为PI3K/mTOR抑制剂的苯并氧杂环庚三烯以及它们使用与制造方法
|
WO2010136491A1
(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
|
EP2435438A1
(en)
|
2009-05-27 |
2012-04-04 |
Genentech, Inc. |
Bicyclic pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use
|
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
|
US20120209047A1
(en)
|
2009-07-29 |
2012-08-16 |
Wright Michael E |
Homogeneous metallocene ziegler-natta catalysts for the oligomerization of olefins in aliphatic-hydrocarbon solvents
|
US9212177B2
(en)
|
2009-08-05 |
2015-12-15 |
Versitech Limited |
Antiviral compounds and methods of making and using thereof
|
KR20120081164A
(ko)
|
2009-09-29 |
2012-07-18 |
엑스커버리 홀딩 컴퍼니 엘엘씨 |
Pi3k(델타) 선택적 억제제
|
US8106146B2
(en)
|
2009-10-06 |
2012-01-31 |
Medtronic, Inc. |
Therapeutic polymers and methods of generation
|
WO2011058109A1
(en)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Fused bicyclic pyrrole and imidazole derivatives as kinase inhibitors
|
WO2011058110A1
(en)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Quinoline and quinoxaline derivatives as kinase inhibitors
|
WO2011058108A1
(en)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Quinoline and quinoxaline derivatives as kinase inhibitors
|
EP2499195B1
(en)
|
2009-11-13 |
2020-12-09 |
Plastipak Packaging, Inc. |
Oxygen scavengers, compositions comprising the scavengers, and artcles made from the compositions
|
JP2013512878A
(ja)
|
2009-12-03 |
2013-04-18 |
グラクソ グループ リミテッド |
新規化合物
|
AU2010327936B2
(en)
|
2009-12-11 |
2015-08-20 |
Nono Inc. |
Agents and methods for treating ischemic and other diseases
|
MX2012006953A
(es)
|
2009-12-18 |
2012-10-09 |
Amgen Inc |
Compuestos heterociclicos y sus usos.
|
EP3309152B1
(en)
|
2009-12-22 |
2020-09-09 |
Vertex Pharmaceuticals Incorporated |
Isoindolinone inhibitors of phosphatidylinositol 3-kinase
|
WO2011094890A1
(en)
|
2010-02-02 |
2011-08-11 |
Argusina Inc. |
Phenylalanine derivatives and their use as non-peptide glp-1 receptor modulators
|
CN102883602B
(zh)
|
2010-02-16 |
2017-07-18 |
Uwm研究基金会有限公司 |
降低细菌的毒力的方法
|
WO2011111880A1
(ko)
|
2010-03-08 |
2011-09-15 |
주식회사 메디젠텍 |
세포핵에서 세포질로의 gsk3의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 gsk3 이동에 의해 발생되는 질환의 치료 또는 예방용 약학적 조성물
|
CN102206172B
(zh)
|
2010-03-30 |
2015-02-25 |
中国医学科学院医药生物技术研究所 |
一组取代双芳基化合物及其制备方法和抗病毒应用
|
BR112012026641A2
(pt)
|
2010-04-23 |
2016-07-12 |
Kineta Inc |
compostos antivirais
|
EP2560636A4
(en)
|
2010-04-23 |
2013-11-27 |
Kineta Inc |
ANTIVIRAL CONNECTIONS
|
JP5857040B2
(ja)
|
2010-05-04 |
2016-02-10 |
アルカーメス ファーマ アイルランド リミテッド |
酸化ラクタム化合物の合成方法
|
WO2011146882A1
(en)
*
|
2010-05-21 |
2011-11-24 |
Intellikine, Inc. |
Chemical compounds, compositions and methods for kinase modulation
|
WO2011150156A2
(en)
|
2010-05-26 |
2011-12-01 |
Sunovion Pharmaceuticals Inc. |
Heteroaryl compounds and methods of use thereof
|
US20120142701A1
(en)
|
2010-05-28 |
2012-06-07 |
The University Of Hong Kong |
Compounds and methods for the treatment of proliferative diseases
|
WO2011153514A2
(en)
|
2010-06-03 |
2011-12-08 |
Pharmacyclics, Inc. |
The use of inhibitors of bruton's tyrosine kinase (btk)
|
WO2011156759A1
(en)
|
2010-06-11 |
2011-12-15 |
Calistoga Pharmaceuticals, Inc. |
Methods of treating hematological disorders with quinazolinone compounds in selected patients
|
US9102617B2
(en)
|
2010-06-25 |
2015-08-11 |
Rutgers, The State University Of New Jersey |
Antimicrobial agents
|
MX2012014537A
(es)
|
2010-07-05 |
2013-02-21 |
Merck Patent Gmbh |
Derivados de bipiridilo utiles para el tratamiento de enfermedades inducidas por cinasa.
|
US8906943B2
(en)
|
2010-08-05 |
2014-12-09 |
John R. Cashman |
Synthetic compounds and methods to decrease nicotine self-administration
|
AR082799A1
(es)
|
2010-09-08 |
2013-01-09 |
Ucb Pharma Sa |
Derivados de quinolina y quinoxalina como inhibidores de quinasa
|
WO2012037204A1
(en)
|
2010-09-14 |
2012-03-22 |
Exelixis, Inc. |
Inhibitors of pi3k-delta and methods of their use and manufacture
|
US8765773B2
(en)
|
2010-10-18 |
2014-07-01 |
Millennium Pharmaceuticals, Inc. |
Substituted hydroxamic acids and uses thereof
|
US9394290B2
(en)
|
2010-10-21 |
2016-07-19 |
Universitaet Des Saarlandes Campus Saarbruecken |
Selective CYP11B1 inhibitors for the treatment of cortisol dependent diseases
|
US20140031355A1
(en)
|
2010-11-04 |
2014-01-30 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
JP2013545749A
(ja)
|
2010-11-10 |
2013-12-26 |
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 |
複素環化合物及びその使用
|
WO2012068096A2
(en)
|
2010-11-15 |
2012-05-24 |
Exelixis, Inc. |
Benzoxazepines as inhibitors of pi3k/mtor and methods of their use and manufacture
|
WO2012068106A2
(en)
|
2010-11-15 |
2012-05-24 |
Exelixis, Inc. |
Benzoxazepines as inhibitors of pi3k/mtor and methods of their use and manufacture
|
WO2012071509A2
(en)
|
2010-11-24 |
2012-05-31 |
Exelixis, Inc. |
Benzoxazepines as inhibitors of p13k/mtor and methods of their use and manufacture
|
MX2013005826A
(es)
|
2010-11-24 |
2013-08-27 |
Exelixis Inc |
Benzoxazepinas como inhibidores de fosfatidilinositol 3-cinasa/objetivo de rapamicina en mamiferos (p13k/mtor) y metodos de uso y fabricacion.
|
EP2651404B1
(en)
|
2010-12-14 |
2015-10-14 |
Electrophoretics Limited |
Casein kinase 1delta (ck1delta) inhibitors
|
US8765978B2
(en)
|
2010-12-16 |
2014-07-01 |
Transitions Optical, Inc. |
Method of making indeno-fused naphthol materials
|
US8987271B2
(en)
|
2010-12-22 |
2015-03-24 |
Eutropics Pharmaceuticals, Inc. |
2,2′-biphenazine compounds and methods useful for treating disease
|
PH12013501465A1
(en)
|
2011-01-10 |
2013-09-09 |
Infinity Pharmaceuticals Inc |
Processes for preparing isoquinolinones and solid forms of isoquinolinones
|
US8791107B2
(en)
|
2011-02-25 |
2014-07-29 |
Takeda Pharmaceutical Company Limited |
N-substituted oxazinopteridines and oxazinopteridinones
|
WO2012121953A1
(en)
|
2011-03-08 |
2012-09-13 |
The Trustees Of Columbia University In The City Of New York |
Methods and pharmaceutical compositions for treating lymphoid malignancy
|
AP2013007158A0
(en)
|
2011-03-11 |
2013-10-31 |
Gilead Calistoga Llc |
Combination therapies for hematologic malignancies
|
TW201247610A
(en)
|
2011-03-15 |
2012-12-01 |
Abbott Lab |
Nuclear hormone receptor modulators
|
US9464065B2
(en)
|
2011-03-24 |
2016-10-11 |
The Scripps Research Institute |
Compounds and methods for inducing chondrogenesis
|
CN102731492B
(zh)
|
2011-03-30 |
2016-06-29 |
江苏恒瑞医药股份有限公司 |
环己烷类衍生物、其制备方法及其在医药上的应用
|
BR112013025386B1
(pt)
|
2011-04-01 |
2023-03-07 |
Genentech, Inc |
Uso de um composto, combinação, medicamento, produto e sistema
|
JO3733B1
(ar)
|
2011-04-05 |
2021-01-31 |
Bayer Ip Gmbh |
استخدام 3,2-دايهيدروايميدازو[1, 2 -c]كوينازولينات مستبدلة
|
KR101644051B1
(ko)
|
2011-05-20 |
2016-08-01 |
삼성전자 주식회사 |
광전자 소자 및 적층 구조
|
KR20140040770A
(ko)
|
2011-07-01 |
2014-04-03 |
노파르티스 아게 |
암 치료에 사용하기 위한 cdk4/6 억제제 및 pi3k 억제제를 포함하는 조합 요법
|
AU2012284088B2
(en)
|
2011-07-19 |
2015-10-08 |
Infinity Pharmaceuticals Inc. |
Heterocyclic compounds and uses thereof
|
JP6027611B2
(ja)
|
2011-07-19 |
2016-11-16 |
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 |
複素環式化合物及びその使用
|
CA2842838C
(en)
|
2011-07-26 |
2017-04-25 |
Kbp Biosciences Co., Ltd. |
9-aminomethyl substituted tetracycline compounds
|
WO2013013504A1
(zh)
|
2011-07-26 |
2013-01-31 |
山东亨利医药科技有限责任公司 |
替加环素衍生物
|
WO2013025498A1
(en)
|
2011-08-12 |
2013-02-21 |
Schubert David R |
Neuroprotective polyphenol analogs
|
TW201311663A
(zh)
|
2011-08-29 |
2013-03-16 |
Infinity Pharmaceuticals Inc |
雜環化合物及其用途
|
US9675595B2
(en)
|
2011-08-31 |
2017-06-13 |
Novartis Ag |
Synergistic combinations of PI3K- and MEK-inhibitors
|
WO2013044169A1
(en)
|
2011-09-21 |
2013-03-28 |
Nestec S.A. |
Methods for determining combination therapy with il-2 for the treatment of cancer
|
CA3110966A1
(en)
|
2011-10-19 |
2013-04-25 |
Pharmacyclics Llc |
Use of inhibitors of bruton's tyrosine kinase (btk)
|
US20150338425A1
(en)
|
2011-11-14 |
2015-11-26 |
The Brigham And Women's Hospital, Inc. |
Treatment and prognosis of lymphangioleiomyomatosis
|
WO2013086131A1
(en)
|
2011-12-06 |
2013-06-13 |
The Trustees Of The University Of Pennsylvania |
Inhibitors targeting drug-resistant influenza a
|
US20150011569A1
(en)
|
2011-12-15 |
2015-01-08 |
Philadelphia Health & Education Corporation D/B/A Drexel University College Of Medicine |
NOVEL P13K p110 INHIBITORS AND METHODS OF USE THEREOF
|
US8772541B2
(en)
|
2011-12-15 |
2014-07-08 |
University of Pittsburgh—of the Commonwealth System of Higher Education |
Cannabinoid receptor 2 (CB2) inverse agonists and therapeutic potential for multiple myeloma and osteoporosis bone diseases
|
TWI573792B
(zh)
|
2012-02-01 |
2017-03-11 |
歐陸斯迪公司 |
新穎治療劑
|
US8940742B2
(en)
|
2012-04-10 |
2015-01-27 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
CN104582732A
(zh)
|
2012-06-15 |
2015-04-29 |
布里格姆及妇女医院股份有限公司 |
治疗癌症的组合物及其制造方法
|
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
|
AU2013293087B2
(en)
|
2012-07-24 |
2017-08-31 |
Pharmacyclics Llc |
Mutations associated with resistance to inhibitors of Bruton's tyrosine kinase (BTK)
|
EP4119676A1
(en)
|
2012-08-03 |
2023-01-18 |
Foundation Medicine, Inc. |
Human papilloma virus as predictor of cancer prognosis
|
WO2014046617A1
(en)
|
2012-09-19 |
2014-03-27 |
Agency For Science, Technology And Research |
Compositions and methods for treating cancer
|
US20140120083A1
(en)
|
2012-11-01 |
2014-05-01 |
Infinity Pharmaceuticals, Inc. |
Treatment of cancers using pi3 kinase isoform modulators
|
NZ708563A
(en)
|
2012-11-01 |
2019-02-22 |
Infinity Pharmaceuticals Inc |
Treatment of cancers using pi3 kinase isoform modulators
|
US20150283142A1
(en)
|
2013-03-15 |
2015-10-08 |
Infinity Pharmaceuticals, Inc. |
Treatment of cancers using pi3 kinase isoform modulators
|
US20140120060A1
(en)
|
2012-11-01 |
2014-05-01 |
Infinity Pharmaceuticals, Inc. |
Treatment of rheumatoid arthritis and asthma using pi3 kinase inhibitors
|
KR102185175B1
(ko)
|
2012-11-02 |
2020-12-02 |
티지 쎄라퓨틱스, 인코포레이티드 |
항cd20 항체와 pi3 키나아제 선택적 억제제의 조합물
|
KR20150079745A
(ko)
|
2012-11-08 |
2015-07-08 |
리젠 파마슈티컬스 소시에떼 아노님 |
Pde4 억제제 및 pi3 델타 또는 이중 pi3 델타-감마 키나아제 억제제를 함유하는 약제학적 조성물
|
US9938281B2
(en)
|
2012-11-16 |
2018-04-10 |
Merck Sharp & Dohme Corp. |
Purine inhibitors of human phosphatidylinositol 3-kinase delta
|
EP2953950B1
(en)
|
2013-02-11 |
2021-01-13 |
The Regents of The University of California |
Compositions and methods for treating neurodegenerative diseases
|
US9481667B2
(en)
|
2013-03-15 |
2016-11-01 |
Infinity Pharmaceuticals, Inc. |
Salts and solid forms of isoquinolinones and composition comprising and methods of using the same
|
WO2014151386A1
(en)
|
2013-03-15 |
2014-09-25 |
Infinity Pharmaceuticals, Inc. |
Salts and solid forms of isoquinolinones and composition comprising and methods of using the same
|
EP2968472A1
(en)
|
2013-03-15 |
2016-01-20 |
Université de Genève |
Use of insulin signaling antagonists, optionally in combination of transfection of non-beta cells, for inducing insulin production
|
EP2983670A4
(en)
|
2013-04-08 |
2017-03-08 |
Pharmacyclics LLC |
Ibrutinib combination therapy
|
JP6227889B2
(ja)
|
2013-04-23 |
2017-11-08 |
関東化學株式会社 |
新規な有機金属錯体およびアミン化合物の製造方法
|
AU2014273946B2
(en)
|
2013-05-30 |
2020-03-12 |
Infinity Pharmaceuticals, Inc. |
Treatment of cancers using PI3 kinase isoform modulators
|
US20160135446A1
(en)
|
2013-06-13 |
2016-05-19 |
Biomatrica, Inc. |
Cell stabilization
|
ES2667173T3
(es)
|
2013-06-14 |
2018-05-09 |
Gilead Calistoga Llc |
Inhibidores de fosfatidilinositol 3-quinasa
|
PT3543355T
(pt)
|
2013-06-20 |
2021-02-19 |
Taiho Pharmaceutical Co Ltd |
Método para prever a eficácia terapêutica do inibidor de pi3k/akt/mtor com base na expressão de phlda1 ou pik3c2b
|
UY35675A
(es)
|
2013-07-24 |
2015-02-27 |
Novartis Ag |
Derivados sustituidos de quinazolin-4-ona
|
US20150065431A1
(en)
|
2013-08-27 |
2015-03-05 |
Northwestern University |
Reducing cutaneous scar formation and treating skin conditions
|
EP3043819A4
(en)
|
2013-09-11 |
2017-04-05 |
Compugen Ltd. |
Anti-vstm5 antibodies and the use thereof in therapy and diagnosis
|
US10111897B2
(en)
|
2013-10-03 |
2018-10-30 |
Duke University |
Compositions and methods for treating cancer with JAK2 activity
|
PT3052485T
(pt)
|
2013-10-04 |
2021-10-22 |
Infinity Pharmaceuticals Inc |
Compostos heterocíclicos e suas utilizações
|
WO2015051241A1
(en)
|
2013-10-04 |
2015-04-09 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
US9403779B2
(en)
|
2013-10-08 |
2016-08-02 |
Acetylon Pharmaceuticals, Inc. |
Combinations of histone deacetylase inhibitors and either Her2 inhibitors or PI3K inhibitors
|
EP3054953B1
(en)
|
2013-10-10 |
2020-07-01 |
Acetylon Pharmaceuticals, Inc. |
Hdac inhibitors in combination with pi3k inhibitors, for treating non-hodgkin's lymphoma
|
WO2015061204A1
(en)
|
2013-10-21 |
2015-04-30 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
AU2014354769A1
(en)
|
2013-11-26 |
2016-05-26 |
Gilead Sciences, Inc. |
Therapies for treating myeloproliferative disorders
|
US10328080B2
(en)
|
2013-12-05 |
2019-06-25 |
Acerta Pharma, B.V. |
Therapeutic combination of PI3K inhibitor and a BTK inhibitor
|
WO2015095842A2
(en)
|
2013-12-20 |
2015-06-25 |
Biomed Valley Discoveries, Inc. |
Methods and compositions for treating non-erk mapk pathway inhibitor-resistant cancers
|
WO2015095831A1
(en)
|
2013-12-20 |
2015-06-25 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of mtor and erk inhibitors
|
WO2015095834A2
(en)
|
2013-12-20 |
2015-06-25 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using erk1/2 and bcl-2 family inhibitors
|
US11007183B2
(en)
|
2013-12-20 |
2021-05-18 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of PI3K/Akt pathway and ERK inhibitors
|
EP4512480A2
(en)
|
2013-12-20 |
2025-02-26 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of cdk and erk inhibitors
|
WO2015095807A1
(en)
|
2013-12-20 |
2015-06-25 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of egfr and erk inhibitors
|
EP3082422A4
(en)
|
2013-12-20 |
2017-07-05 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of mek type i and erk inhibitors
|
EP4389225A3
(en)
|
2013-12-20 |
2024-10-09 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of type 2 mek and erk inhibitors
|
WO2015095819A2
(en)
|
2013-12-20 |
2015-06-25 |
Biomed Valley Discoveries, Inc. |
Cancer treatment using combinations of erk and raf inhibitors
|
JP2017503001A
(ja)
|
2014-01-20 |
2017-01-26 |
ギリアード サイエンシーズ, インコーポレイテッド |
がんを処置するための療法
|
AU2015231413B2
(en)
|
2014-03-19 |
2020-04-23 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds for use in the treatment of PI3K-gamma mediated disorders
|
SG11201607746QA
(en)
|
2014-03-21 |
2016-10-28 |
Abbvie Inc |
Anti-egfr antibodies and antibody drug conjugates
|
WO2015160986A2
(en)
|
2014-04-16 |
2015-10-22 |
Infinity Pharmaceuticals, Inc. |
Combination therapies
|
WO2015160975A2
(en)
|
2014-04-16 |
2015-10-22 |
Infinity Pharmaceuticals, Inc. |
Combination therapies
|
US10632121B2
(en)
|
2014-05-16 |
2020-04-28 |
Memorial Sloan Kettering Cancer Center |
Platelet-derived growth factor receptor mutations and compositions and methods relating thereto
|
WO2015179772A1
(en)
|
2014-05-23 |
2015-11-26 |
Concert Pharmaceuticals, Inc. |
Deuterated phenylquinazolinone and phenylisoquinolinone compounds
|
CN106414449A
(zh)
|
2014-05-27 |
2017-02-15 |
阿尔米雷尔有限公司 |
医药用途
|
SMT202100049T1
(it)
|
2014-06-06 |
2021-03-15 |
Bluebird Bio Inc |
Composizioni di cellule t migliorate
|
BR112017006664A2
(pt)
|
2014-10-03 |
2017-12-26 |
Novartis Ag |
terapias de combinação
|
WO2016054491A1
(en)
|
2014-10-03 |
2016-04-07 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
AU2016322552B2
(en)
|
2015-09-14 |
2021-03-25 |
Infinity Pharmaceuticals, Inc. |
Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same
|
US10759806B2
(en)
|
2016-03-17 |
2020-09-01 |
Infinity Pharmaceuticals, Inc. |
Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as PI3K kinase inhibitors
|