|
AU616564B2
(en)
*
|
1988-09-29 |
1991-10-31 |
Sumitomo Chemical Company, Limited |
Novel pyrazole compounds, method for production thereof, use thereof and intermediates for production thereof
|
|
DE4039733A1
(de)
*
|
1990-12-13 |
1992-06-17 |
Basf Ag |
Substituierte 5-aminopyrazole
|
|
NO179282C
(no)
*
|
1991-01-18 |
1996-09-11 |
Rhone Poulenc Agrochimie |
Nye 1-(2-pyridyl)pyrazolforbindelser til kontroll av skadeinsekter
|
|
WO1992019615A2
(en)
*
|
1991-04-24 |
1992-11-12 |
E.I. Du Pont De Nemours And Company |
Fungicidal pyrazoles, pyrazolines and tetrahydropyridazines
|
|
FR2682379B1
(fr)
*
|
1991-10-09 |
1994-02-11 |
Rhone Poulenc Agrochimie |
Nouveaux phenylpyrazoles fongicides.
|
|
US5550147A
(en)
*
|
1992-02-05 |
1996-08-27 |
Fujisawa Pharmaceutical Co., Ltd. |
Pyrazole derivatives, processes for preparation thereof and pharmaceutical composition comprising the same
|
|
IL104311A
(en)
*
|
1992-02-05 |
1997-07-13 |
Fujisawa Pharmaceutical Co |
Pyrazole derivatives, processes for the preparation thereof and pharmaceutical compositions containing the same
|
|
FR2690440B1
(fr)
*
|
1992-04-27 |
1995-05-19 |
Rhone Poulenc Agrochimie |
Arylpyrazoles fongicides.
|
|
FR2692575B1
(fr)
*
|
1992-06-23 |
1995-06-30 |
Sanofi Elf |
Nouveaux derives du pyrazole, procede pour leur preparation et compositions pharmaceutiques les contenant.
|
|
FR2713225B1
(fr)
*
|
1993-12-02 |
1996-03-01 |
Sanofi Sa |
N-pipéridino-3-pyrazolecarboxamide substitué.
|
|
US6492413B2
(en)
|
1993-01-15 |
2002-12-10 |
G.D. Searle & Co. |
3.4-diaryl thiophenes and analogs thereof having use as antiinflammatory agents
|
|
GB9420616D0
(en)
*
|
1994-10-12 |
1994-11-30 |
Merck Sharp & Dohme |
Method, compositions and use
|
|
US5380738A
(en)
*
|
1993-05-21 |
1995-01-10 |
Monsanto Company |
2-substituted oxazoles further substituted by 4-fluorophenyl and 4-methylsulfonylphenyl as antiinflammatory agents
|
|
US5474995A
(en)
*
|
1993-06-24 |
1995-12-12 |
Merck Frosst Canada, Inc. |
Phenyl heterocycles as cox-2 inhibitors
|
|
US5840746A
(en)
*
|
1993-06-24 |
1998-11-24 |
Merck Frosst Canada, Inc. |
Use of inhibitors of cyclooxygenase in the treatment of neurodegenerative diseases
|
|
US5387602A
(en)
*
|
1993-08-30 |
1995-02-07 |
Ortho Pharmaceutical Corporation |
1.5-diphenyl-3-(N-hydroxycarbamoyloxyalkyl)pyrazoles
|
|
FR2711140B1
(fr)
*
|
1993-10-12 |
1996-01-05 |
Sanofi Sa |
1-Naphtylpyrazole-3-carboxamides substitués actifs sur la neurotensine, leur préparation, les compositions pharmaceutiques en contenant.
|
|
US5475018A
(en)
*
|
1993-11-30 |
1995-12-12 |
G. D. Searle & Co. |
1,5-diphenyl pyrazole compounds for treatment of inflammation
|
|
US5401765A
(en)
*
|
1993-11-30 |
1995-03-28 |
G. D. Searle |
1,4,5-triphenyl pyrazolyl compounds for the treatment of inflammation and inflammation-related disorders
|
|
NZ276885A
(en)
*
|
1993-11-30 |
1999-08-30 |
Searle & Co |
Substituted pyrazolyl-benzenesulphonamide derivatives, preparation and pharmaceutical compositions thereof
|
|
US5434178A
(en)
|
1993-11-30 |
1995-07-18 |
G.D. Searle & Co. |
1,3,5 trisubstituted pyrazole compounds for treatment of inflammation
|
|
US6716991B1
(en)
|
1993-11-30 |
2004-04-06 |
G. D. Searle & Co. |
Process for preparing a substituted pyrazolyl benzenesulfonamide for the treatment of inflammation
|
|
US6492411B1
(en)
|
1993-11-30 |
2002-12-10 |
G. D. Searle & Co. |
Substituted pyrazolyl benzenesulfonamides for the treatment of inflammation
|
|
US5466823A
(en)
*
|
1993-11-30 |
1995-11-14 |
G.D. Searle & Co. |
Substituted pyrazolyl benzenesulfonamides
|
|
US5500439A
(en)
*
|
1993-12-09 |
1996-03-19 |
Alteon Inc. |
Aminopyrazoles
|
|
US5486534A
(en)
*
|
1994-07-21 |
1996-01-23 |
G. D. Searle & Co. |
3,4-substituted pyrazoles for the treatment of inflammation
|
|
US5908852A
(en)
*
|
1994-11-14 |
1999-06-01 |
G. D. Searle & Co. |
1,3,5 trisubstituted pyrazole compounds for treatment of inflammation
|
|
JP2636819B2
(ja)
|
1994-12-20 |
1997-07-30 |
日本たばこ産業株式会社 |
オキサゾール系複素環式芳香族化合物
|
|
CZ292320B6
(cs)
*
|
1995-05-25 |
2003-09-17 |
G. D. Searle & Co. |
Způsob přípravy pyrazolů
|
|
US6515014B2
(en)
|
1995-06-02 |
2003-02-04 |
G. D. Searle & Co. |
Thiophene substituted hydroxamic acid derivatives as cyclooxygenase-2 and 5-lipoxygenase inhibitors
|
|
US6512121B2
(en)
|
1998-09-14 |
2003-01-28 |
G.D. Searle & Co. |
Heterocyclo substituted hydroxamic acid derivatives as cyclooxygenase-2 and 5-lipoxygenase inhibitors
|
|
EP0828718A1
(en)
|
1995-06-02 |
1998-03-18 |
G.D. SEARLE & CO. |
Heterocyclo substituted hydroxamic acid derivatives as cyclooxygenase-2 and 5-lipoxygenase inhibitors
|
|
US5756529A
(en)
*
|
1995-09-29 |
1998-05-26 |
G.D. Searle & Co. |
Substituted pyrazolyl benzenesulfonamides for use in veterinary therapies
|
|
GB9520584D0
(en)
*
|
1995-10-09 |
1995-12-13 |
Fujisawa Pharmaceutical Co |
Pyrazole derivatives,processes for preparation thereof and pharmaceutical composition comprising the same
|
|
FR2742148B1
(fr)
*
|
1995-12-08 |
1999-10-22 |
Sanofi Sa |
Nouveaux derives du pyrazole-3-carboxamide, procede pour leur preparation et compositions pharmaceutiques les contenant
|
|
US5908858A
(en)
*
|
1996-04-05 |
1999-06-01 |
Sankyo Company, Limited |
1,2-diphenylpyrrole derivatives, their preparation and their therapeutic uses
|
|
US6677364B2
(en)
*
|
1998-04-20 |
2004-01-13 |
G.D. Searle & Co. |
Substituted sulfonylphenylheterocycles as cyclooxygenase-2 and 5-lipoxygenase inhibitors
|
|
ES2331860T3
(es)
*
|
1996-12-23 |
2010-01-18 |
Bristol-Myers Squibb Pharma Company |
Compuestos heteroaromaticos que contienen nitrogeno como inhibidores del factor xa.
|
|
DK2011514T3
(da)
|
1997-03-21 |
2012-03-26 |
Chugai Pharmaceutical Co Ltd |
Forebyggende eller terapeutisk middel til sensibiliserede-T-celle-medierede sygdomme omfattende IL-6-antagonist som en aktiv bestanddel
|
|
AU7726898A
(en)
*
|
1997-05-22 |
1998-12-11 |
G.D. Searle & Co. |
Pyrazole derivatives as p38 kinase inhibitors
|
|
US6514977B1
(en)
*
|
1997-05-22 |
2003-02-04 |
G.D. Searle & Company |
Substituted pyrazoles as p38 kinase inhibitors
|
|
CA2288741A1
(en)
*
|
1997-05-22 |
1998-11-26 |
G.D. Searle And Co. |
4-aryl-3(5)-heteroaryl substituted pyrazoles as p38 kinase inhibitors
|
|
US6979686B1
(en)
|
2001-12-07 |
2005-12-27 |
Pharmacia Corporation |
Substituted pyrazoles as p38 kinase inhibitors
|
|
US6087496A
(en)
|
1998-05-22 |
2000-07-11 |
G. D. Searle & Co. |
Substituted pyrazoles suitable as p38 kinase inhibitors
|
|
JP2002507968A
(ja)
*
|
1997-06-19 |
2002-03-12 |
デュポン ファーマシューティカルズ カンパニー |
中性のP1特異性基を有するXa因子阻害剤
|
|
US5998424A
(en)
|
1997-06-19 |
1999-12-07 |
Dupont Pharmaceuticals Company |
Inhibitors of factor Xa with a neutral P1 specificity group
|
|
AUPO941497A0
(en)
|
1997-09-24 |
1997-10-16 |
Fujisawa Pharmaceutical Co., Ltd. |
Novel compounds
|
|
AU750356B2
(en)
*
|
1997-09-24 |
2002-07-18 |
Fujisawa Pharmaceutical Co., Ltd. |
1,5-diphenylpyrazole derivatives
|
|
AU751139B2
(en)
|
1997-10-13 |
2002-08-08 |
Astellas Pharma Inc. |
Amide derivative
|
|
AUPP042397A0
(en)
*
|
1997-11-18 |
1997-12-11 |
Fujisawa Pharmaceutical Co., Ltd. |
5-arylpyrazole compounds
|
|
ES2137138B1
(es)
*
|
1998-05-29 |
2000-09-16 |
Esteve Labor Dr |
Derivados de pirazolinas, su preparacion y su aplicacion como medicamentos.
|
|
EP1082121A4
(en)
*
|
1998-06-03 |
2003-02-05 |
Merck & Co Inc |
HIV integrase
|
|
US6380249B1
(en)
|
1998-06-03 |
2002-04-30 |
Merck & Co., Inc. |
HIV integrase inhibitors
|
|
US6306891B1
(en)
|
1998-06-03 |
2001-10-23 |
Merck & Co., Inc. |
HIV integrase inhibitors
|
|
US6262055B1
(en)
*
|
1998-06-03 |
2001-07-17 |
Merck & Co., Inc. |
HIV integrase inhibitors
|
|
WO1999062885A1
(en)
*
|
1998-06-05 |
1999-12-09 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Substituted 1-(4-aminophenyl)pyrazoles and their use as anti-inflammatory agents
|
|
US6727238B2
(en)
|
1998-06-11 |
2004-04-27 |
Pfizer Inc. |
Sulfonylbenzene compounds as anti-inflammatory/analgesic agents
|
|
TNSN99111A1
(fr)
*
|
1998-06-11 |
2005-11-10 |
Pfizer |
Derives de sulfonylbenzene nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant.
|
|
US6294558B1
(en)
|
1999-05-31 |
2001-09-25 |
Pfizer Inc. |
Sulfonylbenzene compounds as anti-inflammatory/analgesic agents
|
|
DE19831656A1
(de)
*
|
1998-07-15 |
2000-01-20 |
Basf Ag |
Verfahren zur Herstellung von Pyrazolen
|
|
GB9816358D0
(en)
*
|
1998-07-27 |
1998-09-23 |
Angeletti P Ist Richerche Bio |
Enzyme inhibitors
|
|
ES2244204T3
(es)
|
1998-07-27 |
2005-12-01 |
Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. |
Derivados de dicetoacidos como inhibidores de polimerasas.
|
|
USRE39708E1
(en)
|
1998-08-07 |
2007-06-26 |
Chiron Corporation |
Estrogen receptor modulators
|
|
US6291190B1
(en)
*
|
1998-08-25 |
2001-09-18 |
The Board Of Trustees Of The Leland Stanford Junior University |
Molecular differences between species of the M. tuberculosis complex
|
|
US6191147B1
(en)
*
|
1998-12-24 |
2001-02-20 |
Ppd Discovery, Inc. |
Pyrazole compounds and uses thereof
|
|
PL348596A1
(en)
|
1998-12-25 |
2002-06-03 |
Shionogi & Co |
Aromatic heterocycle compounds having hiv integrase inhibiting activities
|
|
DE19904397A1
(de)
*
|
1999-02-04 |
2000-08-10 |
Bayer Ag |
Verwendung von Pyrazol-Carbonsäureamiden
|
|
ES2345921T3
(es)
*
|
1999-03-26 |
2010-10-06 |
Euro-Celtique S.A. |
Pirazoles, imidazoles, oxazoles, tiazoles y pirroles sustituidos con arilo y su uso.
|
|
PT1206474E
(pt)
*
|
1999-08-27 |
2004-10-29 |
Abbott Lab |
Compostos de sulfonilfenilpirazole uteis como inibidores de cox-2
|
|
ES2208227T3
(es)
|
1999-12-03 |
2004-06-16 |
Pfizer Products Inc. |
Compuestos de heteroarilfenilpirazol como agentes antiinflamatorios/analgesicos.
|
|
EP1104758B1
(en)
|
1999-12-03 |
2003-07-23 |
Pfizer Products Inc. |
Acetylene derivatives as anti-inflammatory/analgesic agents
|
|
ATE291019T1
(de)
|
1999-12-03 |
2005-04-15 |
Pfizer Prod Inc |
Heterocyclo-alkylsulfonylpyrazolderivate zur verwendung als anti-imflammatorische oder analgetische verbindungen
|
|
PT1104760E
(pt)
|
1999-12-03 |
2003-06-30 |
Pfizer Prod Inc |
Compostos de sulfamoil-heteroarilpirazole como agentes analgesicos e anti-inflamatorios
|
|
US6569885B1
(en)
*
|
1999-12-23 |
2003-05-27 |
Icos Corporation |
Cyclic AMP-specific phosphodiesterase inhibitors
|
|
US6372752B1
(en)
*
|
2000-02-07 |
2002-04-16 |
Genzyme Corporation |
Inha inhibitors and methods of use thereof
|
|
MXPA02008627A
(es)
*
|
2000-03-03 |
2003-02-24 |
Pfizer Prod Inc |
Derivados de eteres de pirazol como agentes antiinflamatorios/analgesicos.
|
|
NZ520875A
(en)
|
2000-03-24 |
2005-04-29 |
Euro Celtique S |
Aryl substituted pyrazoles, triazoles and tetrazoles as sodium channel blocker
|
|
JP2004517870A
(ja)
*
|
2001-01-02 |
2004-06-17 |
藤沢薬品工業株式会社 |
シクロオキシゲナーゼ阻害剤
|
|
US20030105144A1
(en)
|
2001-04-17 |
2003-06-05 |
Ping Gao |
Stabilized oral pharmaceutical composition
|
|
US6673818B2
(en)
|
2001-04-20 |
2004-01-06 |
Pharmacia Corporation |
Fluoro-substituted benzenesulfonyl compounds for the treatment of inflammation
|
|
AU2002313633B2
(en)
*
|
2001-06-08 |
2007-03-01 |
Cytovia, Inc. |
Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs
|
|
ATE298749T1
(de)
|
2001-07-05 |
2005-07-15 |
Pfizer Prod Inc |
Heterocyclo-alkylsulfonyl pyrazole als entzündungshemmende/analgetische mittel
|
|
US7076539B2
(en)
*
|
2001-07-30 |
2006-07-11 |
Hewlett-Packard Development Company, L.P. |
Network connectivity establishment at user log-in
|
|
BR0212661A
(pt)
*
|
2001-09-19 |
2004-08-24 |
Pharmacia Corp |
Compostos de pirazolil benzenossulfamida substituìdos para o tratamento de inflamação
|
|
AU2002341729A1
(en)
*
|
2001-09-19 |
2003-04-01 |
Pharmacia Corporation |
Substituted pyrazolyl compounds for the treatment of inflammation
|
|
RU2277534C2
(ru)
*
|
2001-09-25 |
2006-06-10 |
Фармация Корпорейшн |
Способ получения замещенных пиразолов
|
|
US7057049B2
(en)
*
|
2001-09-25 |
2006-06-06 |
Pharmacia Corporation |
Process for making substituted pyrazoles
|
|
IL161009A0
(en)
|
2001-09-25 |
2004-08-31 |
Pharmacia Corp |
Process for making substituted pyrazoles
|
|
GT200200183A
(es)
|
2001-09-28 |
2003-05-23 |
|
Procedimiento para preparar derivados de heterocicloalquilsulfonil pirazol
|
|
WO2003037336A1
(en)
|
2001-11-02 |
2003-05-08 |
Pfizer Products Inc. |
1-(5-sulfonyl-pyridin-2-yl)-5-(methylidene-cycloalkylmethoxy)-1h-pyrazole-4-carbonitrile derivatives and other compounds as cyclooxygenase inhibitors for the treatment of arthritis, neurodegeneration and colon cancer
|
|
US20050107404A1
(en)
|
2001-12-06 |
2005-05-19 |
Fraley Mark E. |
Mitotic kinesin inhibitors
|
|
SI1480955T1
(sl)
*
|
2002-03-05 |
2007-12-31 |
Syngenta Participations Ag |
O-ciklopropil-karboksanilidi in njihova uporaba kot fungicidi
|
|
JP4399269B2
(ja)
*
|
2002-03-08 |
2010-01-13 |
メルク エンド カムパニー インコーポレーテッド |
有糸分裂性キネシン阻害薬
|
|
AR038967A1
(es)
*
|
2002-03-18 |
2005-02-02 |
Solvay Pharm Bv |
Derivados de 2,3 - diaril - pirazolidinas como inhibidores de enzimas que degradan la neurotensina
|
|
US7329401B2
(en)
*
|
2002-04-15 |
2008-02-12 |
The Regents Of The University Of California |
Cyclooxygenase-2 selective agents useful as imaging probes and related methods
|
|
EP1507766A4
(en)
|
2002-05-24 |
2006-06-14 |
Pharmacia Corp |
SYNTHESIS OF DIARYLPYRAZOLENE
|
|
US7348440B2
(en)
|
2002-06-14 |
2008-03-25 |
Merck & Co., Inc. |
Mitotic kinesin inhibitors
|
|
WO2004002420A2
(en)
*
|
2002-06-28 |
2004-01-08 |
Nitromed, Inc. |
Oxime and/or hydrazone containing nitrosated and/or nitrosylated cyclooxigenase-2 selective inhibitors, compositions and methods of use
|
|
WO2004016741A2
(en)
*
|
2002-08-14 |
2004-02-26 |
Ppd Discovery, Inc. |
Prenylation inhibitors containing dimethyl-cyclobutane and methods of their synthesis and use
|
|
US6649638B1
(en)
|
2002-08-14 |
2003-11-18 |
Ppd Discovery, Inc. |
Prenylation inhibitors and methods of their synthesis and use
|
|
WO2004016592A1
(en)
*
|
2002-08-14 |
2004-02-26 |
Ppd Discovery, Inc. |
Prenylation inhibitors and methods of their synthesis and use
|
|
EP1556373A1
(en)
*
|
2002-10-18 |
2005-07-27 |
Pfizer Products Inc. |
Cannabinoid receptor ligands and uses thereof
|
|
US7129239B2
(en)
*
|
2002-10-28 |
2006-10-31 |
Pfizer Inc. |
Purine compounds and uses thereof
|
|
CA2505945A1
(en)
*
|
2002-12-02 |
2004-06-17 |
Fujisawa Pharmaceutical Co., Ltd. |
Pyrazole derivatives useful as cox-i inhibitors
|
|
US7247628B2
(en)
*
|
2002-12-12 |
2007-07-24 |
Pfizer, Inc. |
Cannabinoid receptor ligands and uses thereof
|
|
CN100364531C
(zh)
*
|
2002-12-18 |
2008-01-30 |
西托维亚公司 |
3,5-二取代-[1,2,4]-二唑及类似物和其用途
|
|
US7329658B2
(en)
*
|
2003-02-06 |
2008-02-12 |
Pfizer Inc |
Cannabinoid receptor ligands and uses thereof
|
|
ZA200505734B
(en)
*
|
2003-02-07 |
2006-12-27 |
Daiichi Seiyaku Co |
Pyrazole Derivative
|
|
KR20050096956A
(ko)
*
|
2003-02-07 |
2005-10-06 |
다이이찌 세이야꾸 가부시기가이샤 |
피라졸 유도체
|
|
US7176210B2
(en)
*
|
2003-02-10 |
2007-02-13 |
Pfizer Inc. |
Cannabinoid receptor ligands and uses thereof
|
|
US7268133B2
(en)
*
|
2003-04-23 |
2007-09-11 |
Pfizer, Inc. Patent Department |
Cannabinoid receptor ligands and uses thereof
|
|
US7141669B2
(en)
*
|
2003-04-23 |
2006-11-28 |
Pfizer Inc. |
Cannabiniod receptor ligands and uses thereof
|
|
US20040214856A1
(en)
*
|
2003-04-23 |
2004-10-28 |
Pfizer Inc |
Cannabinoid receptor ligands and uses thereof
|
|
US7145012B2
(en)
*
|
2003-04-23 |
2006-12-05 |
Pfizer Inc. |
Cannabinoid receptor ligands and uses thereof
|
|
WO2004099157A1
(en)
*
|
2003-05-07 |
2004-11-18 |
Pfizer Products Inc. |
Cannabinoid receptor ligands and uses thereof
|
|
US7232823B2
(en)
|
2003-06-09 |
2007-06-19 |
Pfizer, Inc. |
Cannabinoid receptor ligands and uses thereof
|
|
US20040259887A1
(en)
*
|
2003-06-18 |
2004-12-23 |
Pfizer Inc |
Cannabinoid receptor ligands and uses thereof
|
|
EP1656146A4
(en)
|
2003-08-15 |
2009-04-15 |
Merck & Co Inc |
INHIBITORS OF MITOTIC KINESINE
|
|
EP1656133A4
(en)
|
2003-08-15 |
2008-10-29 |
Merck & Co Inc |
INHIBITORS OF MITOTIC KINESINE
|
|
US20060079566A1
(en)
*
|
2003-10-03 |
2006-04-13 |
Ching-Shih Chen |
PDK-1/Akt signaling inhibitors
|
|
JP2007084437A
(ja)
*
|
2003-12-26 |
2007-04-05 |
Dai Ichi Seiyaku Co Ltd |
アミノアルキルピラゾール誘導体
|
|
TW200526641A
(en)
*
|
2003-12-26 |
2005-08-16 |
Daiichi Seiyaku Co |
Amidopyrazole derivatives
|
|
US7718687B2
(en)
*
|
2004-07-01 |
2010-05-18 |
Merck Sharp & Dohme Corp., |
Prodrugs of mitotic kinesin inhibitors
|
|
JP2008505089A
(ja)
*
|
2004-07-01 |
2008-02-21 |
メルク エンド カムパニー インコーポレーテッド |
有糸分裂キネシン阻害剤
|
|
US7632833B2
(en)
|
2004-07-01 |
2009-12-15 |
Merck & Co., Inc. |
Mitotic kinesin inhibitors
|
|
JP2008505094A
(ja)
*
|
2004-07-01 |
2008-02-21 |
メルク エンド カムパニー インコーポレーテッド |
有糸分裂キネシン阻害剤
|
|
CN101001852A
(zh)
*
|
2004-08-06 |
2007-07-18 |
第一制药株式会社 |
吡唑衍生物
|
|
CN101072769A
(zh)
*
|
2004-08-06 |
2007-11-14 |
第一制药株式会社 |
抗血小板药及其制造方法
|
|
CA2602146A1
(en)
*
|
2005-04-07 |
2006-10-19 |
Merck & Co., Inc. |
Mitotic kinesin inhibitors
|
|
US8362075B2
(en)
|
2005-05-17 |
2013-01-29 |
Merck Sharp & Dohme Corp. |
Cyclohexyl sulphones for treatment of cancer
|
|
EP1928859A1
(en)
*
|
2005-06-17 |
2008-06-11 |
Carex SA |
Pyrazole derivates as cannabinoid receptor modulators
|
|
WO2007002559A1
(en)
|
2005-06-27 |
2007-01-04 |
Exelixis, Inc. |
Pyrazole based lxr modulators
|
|
TWI387592B
(zh)
*
|
2005-08-30 |
2013-03-01 |
Novartis Ag |
經取代之苯并咪唑及其作為與腫瘤形成相關激酶之抑制劑之方法
|
|
US20090062302A1
(en)
|
2006-01-24 |
2009-03-05 |
Buser-Doepner Carolyn A |
Jak2 Tyrosine Kinase Inhibition
|
|
GB0603041D0
(en)
|
2006-02-15 |
2006-03-29 |
Angeletti P Ist Richerche Bio |
Therapeutic compounds
|
|
MX2008013427A
(es)
|
2006-04-19 |
2008-11-04 |
Novartis Ag |
Compuestos de benzoxazole y benzotiazole sustituidos-6-0 y metodos para inhibir la señalizacion csf-1r.
|
|
EP2698157B1
(en)
|
2006-09-22 |
2015-05-20 |
Merck Sharp & Dohme Corp. |
Method of treatment using fatty acid synthesis inhibitors
|
|
KR101100028B1
(ko)
*
|
2006-09-29 |
2011-12-29 |
주식회사 녹십자 |
칸나비노이드 cb1 수용체 길항제로서의 헤테로아릴-피라졸 유도체
|
|
US20110218176A1
(en)
|
2006-11-01 |
2011-09-08 |
Barbara Brooke Jennings-Spring |
Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development
|
|
MX2009007200A
(es)
|
2007-01-10 |
2009-07-15 |
Angeletti P Ist Richerche Bio |
Indazoles sustituidos con amida como inhibidores de poli(adp-ribosa)polimerasa (parp).
|
|
JP2010516679A
(ja)
*
|
2007-01-19 |
2010-05-20 |
マリンクロット インコーポレイテッド |
診断用および治療用シクロオキシゲナーゼ−2結合リガンド
|
|
US20080207704A1
(en)
*
|
2007-02-27 |
2008-08-28 |
The Green Cross Corporation |
Heteroaryl-imidazole derivatives as cannabinoid cb1 receptor antagonists
|
|
US8822497B2
(en)
|
2007-03-01 |
2014-09-02 |
Novartis Ag |
PIM kinase inhibitors and methods of their use
|
|
WO2008129280A1
(en)
*
|
2007-04-20 |
2008-10-30 |
Biolipox Ab |
Pyrazoles useful in the treatment of inflammation
|
|
US8293769B2
(en)
|
2007-05-21 |
2012-10-23 |
Novartis Ag |
CSF-1R inhibitors, compositions, and methods of use
|
|
RU2459807C2
(ru)
*
|
2007-05-31 |
2012-08-27 |
Зингента Партисипейшнс Аг |
Способ получения пиразолов
|
|
EP3103791B1
(en)
|
2007-06-27 |
2018-01-31 |
Merck Sharp & Dohme Corp. |
4-carboxybenzylamino derivatives as histone deacetylase inhibitors
|
|
US8039502B2
(en)
|
2007-07-24 |
2011-10-18 |
The Ohio State University Research Foundation |
Anti-infective agents against intracellular pathogens
|
|
US7977358B2
(en)
*
|
2007-07-26 |
2011-07-12 |
Hoffmann-La Roche Inc. |
Pyrazol derivatives
|
|
KR101257550B1
(ko)
|
2007-09-10 |
2013-04-24 |
칼시메디카, 인크 |
세포내 칼슘을 조절하는 화합물
|
|
WO2009051772A1
(en)
*
|
2007-10-17 |
2009-04-23 |
Duke University |
Geranylgeranyl transferase inhibitors and methods of making and using the same
|
|
WO2009078498A1
(en)
*
|
2007-12-17 |
2009-06-25 |
Green Cross Corporation |
Biarylpyrazole 4-carboxamides as cannabinoid cb1 receptor ligands
|
|
US9029411B2
(en)
|
2008-01-25 |
2015-05-12 |
Millennium Pharmaceuticals, Inc. |
Thiophenes and uses thereof
|
|
JP2011515343A
(ja)
|
2008-03-03 |
2011-05-19 |
タイガー ファーマテック |
チロシンキナーゼ阻害薬
|
|
DE102008015033A1
(de)
|
2008-03-17 |
2009-09-24 |
Aicuris Gmbh & Co. Kg |
Substituierte (Pyrazolyl-carbonyl)imidazolidinone und ihre Verwendung
|
|
DE102008015032A1
(de)
|
2008-03-17 |
2009-09-24 |
Aicuris Gmbh & Co. Kg |
Substituierte Pyrazolamide und ihre Verwendung
|
|
CA2726999C
(en)
*
|
2008-06-09 |
2017-05-02 |
Ludwig-Maximilians-Universitaet Muenchen |
New drugs for inhibiting aggregation of proteins involved in diseases linked to protein aggregation and/or neurodegenerative diseases
|
|
CA2727242A1
(en)
*
|
2008-06-11 |
2009-12-17 |
Merck Sharp & Dohme Corp. |
Pyrazole derivatives useful as inhibitors of faah
|
|
CN102256969A
(zh)
|
2008-08-27 |
2011-11-23 |
钙医学公司 |
调节胞内钙的化合物
|
|
DE102008062863A1
(de)
|
2008-12-17 |
2010-06-24 |
Aicuris Gmbh & Co. Kg |
Substituierte (Thiophenyl-carbonyl)imidazolidinone und ihre Verwendung
|
|
DE102008062878A1
(de)
|
2008-12-17 |
2010-06-24 |
Aicuris Gmbh & Co. Kg |
Substituierte Furancarboxamide und ihre Verwendung
|
|
CN102395585A
(zh)
|
2009-01-30 |
2012-03-28 |
米伦纽姆医药公司 |
杂芳基化合物和其作为pi3k抑制剂的用途
|
|
US9090601B2
(en)
|
2009-01-30 |
2015-07-28 |
Millennium Pharmaceuticals, Inc. |
Thiazole derivatives
|
|
US8796314B2
(en)
|
2009-01-30 |
2014-08-05 |
Millennium Pharmaceuticals, Inc. |
Heteroaryls and uses thereof
|
|
US20120108823A1
(en)
|
2009-04-22 |
2012-05-03 |
The Ohio State University Research Foundation |
Anti-francisella agents
|
|
DE102009036604A1
(de)
|
2009-07-30 |
2011-02-03 |
Aicuris Gmbh & Co. Kg |
Substituierte Bis-Arylpyrazolamide mit terminaler primärer Amidfunktionalisierung und ihre Verwendung
|
|
JP5099731B1
(ja)
|
2009-10-14 |
2012-12-19 |
メルク・シャープ・アンド・ドーム・コーポレーション |
p53活性を増大する置換ピペリジン及びその使用
|
|
PT2563776T
(pt)
|
2010-04-27 |
2016-09-19 |
Calcimedica Inc |
Compostos que modulam o cálcio intracelular
|
|
CA2797533A1
(en)
|
2010-04-27 |
2011-11-10 |
Calcimedica, Inc. |
Compounds that modulate intracellular calcium
|
|
EP2584903B1
(en)
|
2010-06-24 |
2018-10-24 |
Merck Sharp & Dohme Corp. |
Novel heterocyclic compounds as erk inhibitors
|
|
CN107090456B
(zh)
|
2010-08-02 |
2022-01-18 |
瑟纳治疗公司 |
使用短干扰核酸的RNA干扰介导的联蛋白(钙粘蛋白关联蛋白质),β1基因表达的抑制
|
|
PH12013500274A1
(en)
|
2010-08-11 |
2013-03-04 |
Millennium Pharm Inc |
Heteroaryls and uses thereof
|
|
US8859768B2
(en)
|
2010-08-11 |
2014-10-14 |
Millennium Pharmaceuticals, Inc. |
Heteroaryls and uses thereof
|
|
WO2012021611A1
(en)
|
2010-08-11 |
2012-02-16 |
Millennium Pharmaceuticals, Inc. |
Heteroaryls and uses thereof
|
|
LT2606134T
(lt)
|
2010-08-17 |
2019-07-25 |
Sirna Therapeutics, Inc. |
Hepatito b viruso (hbv) geno raiškos slopinimas, tarpininkaujant rnr interferencijai naudojant mažą interferuojančią nukleorūgštį (sina)
|
|
EP2608669B1
(en)
|
2010-08-23 |
2016-06-22 |
Merck Sharp & Dohme Corp. |
NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
|
US9079891B2
(en)
|
2010-08-27 |
2015-07-14 |
Calcimedica, Inc. |
Compounds that modulate intracellular calcium
|
|
US8580805B2
(en)
*
|
2010-08-31 |
2013-11-12 |
Hubert Maehr |
Pyrimidine carboxamide derivatives
|
|
WO2012030685A2
(en)
|
2010-09-01 |
2012-03-08 |
Schering Corporation |
Indazole derivatives useful as erk inhibitors
|
|
EP2615916B1
(en)
|
2010-09-16 |
2017-01-04 |
Merck Sharp & Dohme Corp. |
Fused pyrazole derivatives as novel erk inhibitors
|
|
EP2627181A4
(en)
|
2010-10-13 |
2014-03-19 |
Millennium Pharm Inc |
HETEROARYLE AND USES THEREOF
|
|
ES2663009T3
(es)
|
2010-10-29 |
2018-04-10 |
Sirna Therapeutics, Inc. |
Inhibición de la expresión génica mediada por interferencia por ARN utilizando ácidos nucleicos de interferencia cortos (ANic)
|
|
US9351965B2
(en)
|
2010-12-21 |
2016-05-31 |
Merck Sharp & Dohme Corp. |
Indazole derivatives useful as ERK inhibitors
|
|
JP2014514321A
(ja)
|
2011-04-21 |
2014-06-19 |
メルク・シャープ・アンド・ドーム・コーポレーション |
インスリン様増殖因子1受容体阻害剤
|
|
EP2770987B1
(en)
|
2011-10-27 |
2018-04-04 |
Merck Sharp & Dohme Corp. |
Novel compounds that are erk inhibitors
|
|
EP2773207B1
(en)
|
2011-10-31 |
2018-03-07 |
Merck Sharp & Dohme Corp. |
Aminopyrimidinones as interleukin receptor-associated kinase inhibitors
|
|
DE102011055815A1
(de)
|
2011-11-29 |
2013-05-29 |
Aicuris Gmbh & Co. Kg |
Carboxamid-substituierte Heteroaryl-Pyrazole und ihre Verwendung
|
|
WO2013096637A1
(en)
*
|
2011-12-23 |
2013-06-27 |
Millennium Pharmaceuticals, Inc. |
Heteroaryls and uses thereof
|
|
EP3358013B1
(en)
|
2012-05-02 |
2020-06-24 |
Sirna Therapeutics, Inc. |
Short interfering nucleic acid (sina) compositions
|
|
CA2880542C
(en)
*
|
2012-07-30 |
2018-01-02 |
The Ohio State University |
Antibacterial protein kinase inhibitors
|
|
DE102012016908A1
(de)
|
2012-08-17 |
2014-02-20 |
Aicuris Gmbh & Co. Kg |
Tris-(Hetero)Aryl-Pyrazole und ihre Verwendung
|
|
US9233979B2
(en)
|
2012-09-28 |
2016-01-12 |
Merck Sharp & Dohme Corp. |
Compounds that are ERK inhibitors
|
|
US9512116B2
(en)
|
2012-10-12 |
2016-12-06 |
Calcimedica, Inc. |
Compounds that modulate intracellular calcium
|
|
RU2660349C2
(ru)
|
2012-11-28 |
2018-07-05 |
Мерк Шарп И Доум Корп. |
Композиции и способы для лечения злокачественной опухоли
|
|
BR112015013611A2
(pt)
|
2012-12-20 |
2017-11-14 |
Merck Sharp & Dohme |
composto, e, composição farmacêutica
|
|
WO2014120748A1
(en)
|
2013-01-30 |
2014-08-07 |
Merck Sharp & Dohme Corp. |
2,6,7,8 substituted purines as hdm2 inhibitors
|
|
CN103265537B
(zh)
*
|
2013-05-14 |
2015-05-27 |
浙江医药高等专科学校 |
抗肿瘤化合物、其制备方法和用途
|
|
EP3019171B1
(en)
|
2013-07-11 |
2018-09-05 |
Merck Sharp & Dohme Corp. |
Substituted amidopyrazole inhibitors of interleukin receptor-associated kinases (irak-4)
|
|
EA201690240A1
(ru)
|
2013-07-31 |
2016-10-31 |
Каунсел Оф Сайентифик Энд Индастриал Рисёч |
Новые соединения индазола и способ их получения
|
|
WO2015034925A1
(en)
|
2013-09-03 |
2015-03-12 |
Moderna Therapeutics, Inc. |
Circular polynucleotides
|
|
WO2015054283A1
(en)
|
2013-10-08 |
2015-04-16 |
Calcimedica, Inc. |
Compounds that modulate intracellular calcium
|
|
JO3589B1
(ar)
|
2014-08-06 |
2020-07-05 |
Novartis Ag |
مثبطات كيناز البروتين c وطرق استخداماتها
|
|
KR101650476B1
(ko)
*
|
2015-02-06 |
2016-08-23 |
한국건설기술연구원 |
중공슬래브를 위한 중공체의 부력방지장치
|
|
US10329294B2
(en)
|
2015-03-12 |
2019-06-25 |
Merck Sharp & Dohme Corp. |
Pyrazolopyrimidine inhibitors of IRAK4 activity
|
|
WO2016144849A1
(en)
|
2015-03-12 |
2016-09-15 |
Merck Sharp & Dohme Corp. |
Thienopyrazine inhibitors of irak4 activity
|
|
EP3268367B8
(en)
|
2015-03-12 |
2022-11-16 |
Merck Sharp & Dohme LLC |
Carboxamide inhibitors of irak4 activity
|
|
WO2018071283A1
(en)
|
2016-10-12 |
2018-04-19 |
Merck Sharp & Dohme Corp. |
Kdm5 inhibitors
|
|
AR112900A1
(es)
|
2017-09-13 |
2019-12-26 |
Hanmi Pharm Ind Co Ltd |
Compuesto derivado de pirazol y uso de este
|
|
WO2019094312A1
(en)
|
2017-11-08 |
2019-05-16 |
Merck Sharp & Dohme Corp. |
Prmt5 inhibitors
|
|
US10947234B2
(en)
|
2017-11-08 |
2021-03-16 |
Merck Sharp & Dohme Corp. |
PRMT5 inhibitors
|
|
EP3833668B1
(en)
|
2018-08-07 |
2025-03-19 |
Merck Sharp & Dohme LLC |
Prmt5 inhibitors
|
|
WO2020033284A1
(en)
|
2018-08-07 |
2020-02-13 |
Merck Sharp & Dohme Corp. |
Prmt5 inhibitors
|
|
MA53287A
(fr)
|
2018-08-07 |
2022-05-11 |
Merck Sharp & Dohme |
Inhibiteurs de prmt5
|
|
WO2020163689A1
(en)
|
2019-02-08 |
2020-08-13 |
University Of Pittsburgh - Of The Commonwealth System Of Higher Education |
20-hete formation inhibitors
|
|
US12441730B2
(en)
|
2019-12-17 |
2025-10-14 |
Merck Sharp & Dohme Llc |
PRMT5 inhibitors
|
|
WO2021126731A1
(en)
|
2019-12-17 |
2021-06-24 |
Merck Sharp & Dohme Corp. |
Prmt5 inhibitors
|
|
US20230108114A1
(en)
|
2019-12-17 |
2023-04-06 |
Merck Sharp & Dohme Llc |
Prmt5 inhibitors
|
|
CN112961109B
(zh)
*
|
2021-01-27 |
2022-05-17 |
台州学院 |
一种1,4-双磺酰化的全取代吡唑类化合物及其制备和应用
|