|
US5559137A
(en)
*
|
1994-05-16 |
1996-09-24 |
Smithkline Beecham Corp. |
Compounds
|
|
US6087496A
(en)
|
1998-05-22 |
2000-07-11 |
G. D. Searle & Co. |
Substituted pyrazoles suitable as p38 kinase inhibitors
|
|
US6979686B1
(en)
|
2001-12-07 |
2005-12-27 |
Pharmacia Corporation |
Substituted pyrazoles as p38 kinase inhibitors
|
|
CA2288787A1
(en)
|
1997-05-22 |
1998-11-26 |
G.D. Searle And 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
|
|
AU7966198A
(en)
|
1997-06-13 |
1998-12-30 |
Smithkline Beecham Corporation |
Novel pyrazole and pyrazoline substituted compounds
|
|
US6339099B1
(en)
*
|
1997-06-20 |
2002-01-15 |
Dupont Pharmaceuticals Company |
Guanidine mimics as factor Xa inhibitors
|
|
US7301021B2
(en)
|
1997-07-02 |
2007-11-27 |
Smithkline Beecham Corporation |
Substituted imidazole compounds
|
|
ATE529109T1
(de)
*
|
1997-12-22 |
2011-11-15 |
Bayer Healthcare Llc |
Hemmung der p38 kinase aktivität durch substituierte heterocyclische harnstoffe
|
|
MY132496A
(en)
*
|
1998-05-11 |
2007-10-31 |
Vertex Pharma |
Inhibitors of p38
|
|
US6858617B2
(en)
|
1998-05-26 |
2005-02-22 |
Smithkline Beecham Corporation |
Substituted imidazole compounds
|
|
WO2000002561A1
(en)
*
|
1998-07-13 |
2000-01-20 |
University Of South Florida |
Modulation of the phospholipase a2 pathway as a therapeutic
|
|
CA2346665A1
(en)
|
1998-10-07 |
2000-04-13 |
Smithkline Beecham Corporation |
Novel treatment for stroke management
|
|
JP2002528506A
(ja)
|
1998-11-04 |
2002-09-03 |
スミスクライン・ビーチャム・コーポレイション |
ピリジン−4−イルまたはピリミジン−4−イル置換ピラジン
|
|
SA99191255B1
(ar)
|
1998-11-30 |
2006-11-25 |
جي دي سيرل اند كو |
مركبات سيليكوكسيب celecoxib
|
|
DE69903976T2
(de)
|
1998-12-16 |
2003-07-24 |
Aventis Pharma Ltd |
Heteroaryl-zyklische acetale
|
|
CA2356263C
(en)
*
|
1998-12-25 |
2009-04-21 |
Teikoku Hormone Mfg. Co., Ltd. |
Aminopyrazole derivatives
|
|
US8124630B2
(en)
|
1999-01-13 |
2012-02-28 |
Bayer Healthcare Llc |
ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
|
|
ATE538794T1
(de)
|
1999-01-13 |
2012-01-15 |
Bayer Healthcare Llc |
Gamma carboxyarylsubstituierte diphenylharnstoffverbindungen als p38 kinasehemmer
|
|
JP2000281588A
(ja)
*
|
1999-03-30 |
2000-10-10 |
Sankyo Co Ltd |
ガンの予防又は治療薬及びそのスクリーニング方法
|
|
US7122666B2
(en)
|
1999-07-21 |
2006-10-17 |
Sankyo Company, Limited |
Heteroaryl-substituted pyrrole derivatives, their preparation and their therapeutic uses
|
|
US6808902B1
(en)
|
1999-11-12 |
2004-10-26 |
Amgen Inc. |
Process for correction of a disulfide misfold in IL-1Ra Fc fusion molecules
|
|
AU1783201A
(en)
|
1999-11-23 |
2001-06-04 |
Smithkline Beecham Corporation |
3,4-dihydro-(1h)quinazolin-2-one compounds as csbp/p38 kinase inhibitors
|
|
JP2003514899A
(ja)
|
1999-11-23 |
2003-04-22 |
スミスクライン・ビーチャム・コーポレイション |
CSBP/p38キナーゼ阻害剤としての3,4‐ジヒドロ−(1H)−キナゾリン−2−オン化合物
|
|
DE60023025T2
(de)
|
1999-11-23 |
2006-07-13 |
Smithkline Beecham Corp. |
3,4-dihydro-(1h)chinazolin-2-on-verbindungen als csbp/p39-kinase-inhibitoren
|
|
CZ20013540A3
(cs)
*
|
2000-02-05 |
2002-03-13 |
Vertex Pharmaceuticals Incorporated |
Deriváty pyrazolu jako inhibitory ERK a farmaceutický prostředek, který je obsahuje
|
|
AU2001236720A1
(en)
*
|
2000-02-05 |
2001-08-14 |
Bemis, Guy |
Compositions useful as inhibitors of erk
|
|
WO2003018008A1
(en)
*
|
2000-02-25 |
2003-03-06 |
Shionogi & Co., Ltd. |
Apo ai expression accelerating agent
|
|
US7235551B2
(en)
|
2000-03-02 |
2007-06-26 |
Smithkline Beecham Corporation |
1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases
|
|
GB0016787D0
(en)
|
2000-07-07 |
2000-08-30 |
Pfizer Ltd |
Compounds useful in therapy
|
|
PE20020506A1
(es)
*
|
2000-08-22 |
2002-07-09 |
Glaxo Group Ltd |
Derivados de pirazol fusionados como inhibidores de la proteina cinasa
|
|
US6670357B2
(en)
*
|
2000-11-17 |
2003-12-30 |
Bristol-Myers Squibb Company |
Methods of treating p38 kinase-associated conditions and pyrrolotriazine compounds useful as kinase inhibitors
|
|
US6867300B2
(en)
*
|
2000-11-17 |
2005-03-15 |
Bristol-Myers Squibb Company |
Methods for the preparation of pyrrolotriazine compounds useful as kinase inhibitors
|
|
DE60203263T2
(de)
*
|
2001-02-02 |
2006-02-09 |
Smithkline Beecham Corp. |
Pyrazolderivate gegen tgf überexprimierung
|
|
JP2004535381A
(ja)
|
2001-04-13 |
2004-11-25 |
バーテックス ファーマシューティカルズ インコーポレイテッド |
c−JunN末端キナーゼ(JNK)および他のプロテインキナーゼのインヒビター
|
|
EP1382603B1
(en)
*
|
2001-04-26 |
2008-07-23 |
Eisai R&D Management Co., Ltd. |
Nitrogenous fused-ring compound having pyrazolyl group as substituent and medicinal composition thereof
|
|
GB0112348D0
(en)
*
|
2001-05-19 |
2001-07-11 |
Smithkline Beecham Plc |
Compounds
|
|
ES2706902T3
(es)
|
2001-06-26 |
2019-04-01 |
Amgen Inc |
Anticuerpos para OPGL
|
|
CA2456187A1
(en)
*
|
2001-08-03 |
2003-02-13 |
Qing Tang |
Pyrazole-derived kinase inhibitors and uses thereof
|
|
BR0212812A
(pt)
|
2001-09-25 |
2004-08-03 |
Pharmacia Corp |
Processos para a fabricação de pirazóis substituìdos e composição farmacêutica compreendendo os mesmos
|
|
US7057049B2
(en)
|
2001-09-25 |
2006-06-06 |
Pharmacia Corporation |
Process for making substituted pyrazoles
|
|
GB0124932D0
(en)
*
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
|
GB0124934D0
(en)
*
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
|
GB0124933D0
(en)
*
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
|
GB0124941D0
(en)
*
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
|
GB0124936D0
(en)
*
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
|
GB0124938D0
(en)
*
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
|
GB0124931D0
(en)
*
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
|
GB0124939D0
(en)
*
|
2001-10-17 |
2001-12-05 |
Glaxo Group Ltd |
Chemical compounds
|
|
DK1439863T3
(da)
|
2001-10-29 |
2011-03-14 |
Boehringer Ingelheim Int |
MNK-kinase-homologe proteiner, som er involveret i reguleringen af energihomeostase og organelmetabolisme
|
|
JP4399265B2
(ja)
*
|
2001-12-21 |
2010-01-13 |
ヴァーナリス(ケンブリッジ)リミテッド |
3,4−ジアリールピラゾール、および癌の治療におけるそれらの使用
|
|
MXPA04007832A
(es)
|
2002-02-11 |
2005-09-08 |
Bayer Pharmaceuticals Corp |
Aril-ureas con actividad inhibitoria de angiogenesis.
|
|
KR101058292B1
(ko)
*
|
2002-02-12 |
2011-08-22 |
글락소스미스클라인 엘엘씨 |
P38 억제제로 유용한 니코틴아미드 유도체
|
|
AR039241A1
(es)
*
|
2002-04-04 |
2005-02-16 |
Biogen Inc |
Heteroarilos trisustituidos y metodos para su produccion y uso de los mismos
|
|
US20050124620A1
(en)
*
|
2002-04-09 |
2005-06-09 |
Martyn Frederickson |
Pharmaceutical compounds
|
|
HRP20040988A2
(en)
|
2002-04-23 |
2005-06-30 |
Bristol-Myers Squibb Company A Delaware (Usa) Corp |
Pyrrolo-triazine aniline compounds useful as kinas
|
|
ATE365740T1
(de)
|
2002-05-10 |
2007-07-15 |
Smithkline Beecham Corp |
Substituierte pyrazolopyrimidine
|
|
DE60310730T2
(de)
|
2002-07-09 |
2007-05-16 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Pharmazeutische zusammensetzungen aus anticholinergica und p38 kinase hemmern zur behandlung von erkrankungen der atemwege
|
|
GB0217757D0
(en)
|
2002-07-31 |
2002-09-11 |
Glaxo Group Ltd |
Novel compounds
|
|
UA80295C2
(en)
*
|
2002-09-06 |
2007-09-10 |
Biogen Inc |
Pyrazolopyridines and using the same
|
|
US6967254B2
(en)
|
2002-09-09 |
2005-11-22 |
Amgen Inc. |
Substituted heterocyclic compounds and methods of use
|
|
BR0314302A
(pt)
|
2002-09-18 |
2005-07-05 |
Pfizer Producs Inc |
Compostos de pirazol como inibidores do fator de crescimento trnasformante (tgf)
|
|
AU2003256003A1
(en)
|
2002-09-18 |
2004-04-08 |
Pfizer Products Inc. |
Novel oxazole and thiazole compounds as transforming growth factor (TGF) inhibitors
|
|
WO2004026859A1
(en)
|
2002-09-18 |
2004-04-01 |
Pfizer Products Inc. |
Novel imidazole compounds as transforming growth factor (tgf) inhibitors
|
|
EA200500286A1
(ru)
|
2002-09-18 |
2005-08-25 |
Пфайзер Продактс Инк. |
Новые изотиазольные и изоксазольные соединения в качестве ингибиторов трансформирующего фактора роста (тфр)
|
|
KR20050057393A
(ko)
|
2002-09-18 |
2005-06-16 |
화이자 프로덕츠 인크. |
전환 성장 인자 (tgf) 억제제로서 트리아졸 유도체
|
|
EP1553096B1
(en)
|
2002-09-25 |
2012-10-31 |
Ube Industries, Ltd. |
Pyrazole compounds
|
|
CA2515119A1
(en)
|
2003-02-07 |
2004-08-19 |
Daiichi Pharmaceutical Co., Ltd. |
Pyrazole derivative
|
|
CL2004000234A1
(es)
*
|
2003-02-12 |
2005-04-15 |
Biogen Idec Inc |
Compuestos derivados 3-(piridin-2-il)-4-heteroaril-pirazol sustituidos, antagonistas de aik5 y/o aik4; composicion farmaceutica y uso del compuesto en el tratamiento de desordenes fibroticos como esclerodermia, lupus nefritico, cicatrizacion de herid
|
|
CL2004000366A1
(es)
*
|
2003-02-26 |
2005-01-07 |
Pharmacia Corp Sa Organizada B |
USO DE UNA COMBINACION DE UN COMPUESTO DERIVADO DE PIRAZOL INHIBIDOR DE QUINASA p38, Y UN INHIBIDOR DE ACE PARA TRATAR DISFUNCION RENAL, ENFERMEDAD CARDIOVASCULAR Y VASCULAR, RETINOPATIA, NEUROPATIA, EDEMA, DISFUNCION ENDOTELIAL O INSULINOPATIA.
|
|
PA8595001A1
(es)
|
2003-03-04 |
2004-09-28 |
Pfizer Prod Inc |
Nuevos compuestos heteroaromaticos condensados que son inhibidores del factor de crecimiento transforante (tgf)
|
|
EP1606019A1
(en)
*
|
2003-03-07 |
2005-12-21 |
The University Court of The University of Aberdeen |
Cannabinoid receptor inverse agonists and neutral antagonists as therapeutic agents for the treatment of bone disorders
|
|
GB0308201D0
(en)
*
|
2003-04-09 |
2003-05-14 |
Smithkline Beecham Corp |
Novel compounds
|
|
GB0308185D0
(en)
*
|
2003-04-09 |
2003-05-14 |
Smithkline Beecham Corp |
Novel compounds
|
|
GB0308186D0
(en)
*
|
2003-04-09 |
2003-05-14 |
Smithkline Beecham Corp |
Novel compounds
|
|
ES2275218T3
(es)
|
2003-05-07 |
2007-06-01 |
Osteologix A/S |
Sales de estroncio hidrosolubles para el tratamiento de afecciones de cartilagos y/o huesos.
|
|
EP1636585B2
(en)
|
2003-05-20 |
2012-06-13 |
Bayer HealthCare LLC |
Diaryl ureas with kinase inhibiting activity
|
|
ES2332135T3
(es)
*
|
2003-06-03 |
2010-01-27 |
Novartis Ag |
Inhibidores p-38 basados en heterociclo de 5 miembros.
|
|
WO2005009973A1
(en)
|
2003-06-26 |
2005-02-03 |
Novartis Ag |
5-membered heterocycle-based p38 kinase inhibitors
|
|
HRP20060073B1
(hr)
|
2003-07-23 |
2014-03-14 |
Bayer Healthcare Llc |
Fluoro supstituirana omega-karboksiaril difenil urea za lijeäśenje i prevenciju bolesti i stanja
|
|
AU2004261589B2
(en)
|
2003-07-25 |
2008-05-22 |
Novartis Ag |
p-38 kinase inhibitors
|
|
GB0318814D0
(en)
*
|
2003-08-11 |
2003-09-10 |
Smithkline Beecham Corp |
Novel compounds
|
|
US7419978B2
(en)
*
|
2003-10-22 |
2008-09-02 |
Bristol-Myers Squibb Company |
Phenyl-aniline substituted bicyclic compounds useful as kinase inhibitors
|
|
GB0402143D0
(en)
*
|
2004-01-30 |
2004-03-03 |
Smithkline Beecham Corp |
Novel compounds
|
|
US7504521B2
(en)
*
|
2004-08-05 |
2009-03-17 |
Bristol-Myers Squibb Co. |
Methods for the preparation of pyrrolotriazine compounds
|
|
US20060035893A1
(en)
|
2004-08-07 |
2006-02-16 |
Boehringer Ingelheim International Gmbh |
Pharmaceutical compositions for treatment of respiratory and gastrointestinal disorders
|
|
US7148348B2
(en)
|
2004-08-12 |
2006-12-12 |
Bristol-Myers Squibb Company |
Process for preparing pyrrolotriazine aniline compounds useful as kinase inhibitors
|
|
PL1778686T3
(pl)
|
2004-08-12 |
2009-04-30 |
Pfizer |
Pochodne triazolopirydynylosulfanylowe jako inhibitory kinazy MAP P38
|
|
US20080051416A1
(en)
*
|
2004-10-05 |
2008-02-28 |
Smithkline Beecham Corporation |
Novel Compounds
|
|
PE20060777A1
(es)
|
2004-12-24 |
2006-10-06 |
Boehringer Ingelheim Int |
Derivados de indolinona para el tratamiento o la prevencion de enfermedades fibroticas
|
|
TW200639163A
(en)
|
2005-02-04 |
2006-11-16 |
Genentech Inc |
RAF inhibitor compounds and methods
|
|
US20060178388A1
(en)
*
|
2005-02-04 |
2006-08-10 |
Wrobleski Stephen T |
Phenyl-substituted pyrimidine compounds useful as kinase inhibitors
|
|
US20060235020A1
(en)
*
|
2005-04-18 |
2006-10-19 |
Soojin Kim |
Process for preparing salts of 4-[[5-[(cyclopropylamino)carbonyl]-2-methylphenyl]amino]-5-methyl-N-propylpyrrolo[2,1-f][1,2,4]triazine-6-carboxamide and novel stable forms produced therein
|
|
US20060252807A1
(en)
*
|
2005-04-22 |
2006-11-09 |
Kalypsys, Inc. |
Novel ortho-terphenyl inhibitors of p38 kinase and methods of treating inflammatory disorders
|
|
GB0512429D0
(en)
*
|
2005-06-17 |
2005-07-27 |
Smithkline Beecham Corp |
Novel compound
|
|
US7473784B2
(en)
|
2005-08-01 |
2009-01-06 |
Bristol-Myers Squibb Company |
Benzothiazole and azabenzothiazole compounds useful as kinase inhibitors
|
|
US20070054884A1
(en)
*
|
2005-08-31 |
2007-03-08 |
Emergent Product Development Gaithersburg Inc. |
4-substituted 2-aryloxyphenol derivatives as antibacterial agents
|
|
WO2007049041A1
(en)
*
|
2005-10-28 |
2007-05-03 |
Astrazeneca Ab |
4- (3-aminopyrazole) pyrimidine derivatives for use as tyrosine kinase inhibitors in the treatment of cancer
|
|
CN101341128A
(zh)
*
|
2005-12-23 |
2009-01-07 |
阿斯利康(瑞典)有限公司 |
用于治疗gerd和ibs的吡唑
|
|
EA200801945A1
(ru)
*
|
2006-03-07 |
2009-02-27 |
Бристол-Маерс Сквибб Компани |
Пирролотриазинанилиновые пролекарственные соединения, полезные в качестве ингибиторов киназы
|
|
JP2007205153A
(ja)
*
|
2006-08-07 |
2007-08-16 |
Seiki Hanbai Co Ltd |
網戸用ネットの押さえ部材
|
|
US8128460B2
(en)
*
|
2006-09-14 |
2012-03-06 |
The Material Works, Ltd. |
Method of producing rust inhibitive sheet metal through scale removal with a slurry blasting descaling cell
|
|
US7935696B2
(en)
*
|
2006-10-27 |
2011-05-03 |
Bristol-Myers Squibb Company |
Heterocyclic amide compounds useful as kinase inhibitors
|
|
US7943617B2
(en)
*
|
2006-11-27 |
2011-05-17 |
Bristol-Myers Squibb Company |
Heterobicyclic compounds useful as kinase inhibitors
|
|
GB0702862D0
(en)
*
|
2007-02-14 |
2007-03-28 |
Univ Aberdeen |
Therapeutic compounds
|
|
US20080254029A1
(en)
*
|
2007-04-11 |
2008-10-16 |
Alcon Research, Ltd. |
Use of an Inhibitor of TNFa Plus an Antihistamine to Treat Allergic Rhinitis and Allergic Conjunctivitis
|
|
US20090182035A1
(en)
*
|
2007-04-11 |
2009-07-16 |
Alcon Research, Ltd. |
Use of a combination of olopatadine and cilomilast to treat non-infectious rhinitis and allergic conjunctivitis
|
|
EP1992344A1
(en)
|
2007-05-18 |
2008-11-19 |
Institut Curie |
P38 alpha as a therapeutic target in pathologies linked to FGFR3 mutation
|
|
KR20100080514A
(ko)
*
|
2007-08-29 |
2010-07-08 |
센주 세이야꾸 가부시키가이샤 |
각막 내피 세포 접착 촉진제
|
|
AU2009235634B8
(en)
*
|
2008-04-08 |
2013-05-23 |
Grunenthal Gmbh |
Substituted sulfonamide derivatives
|
|
JP2011525184A
(ja)
*
|
2008-06-20 |
2011-09-15 |
ブリストル−マイヤーズ スクイブ カンパニー |
キナーゼ阻害剤として有用なトリアゾロピリジン化合物
|
|
CN102131805A
(zh)
|
2008-06-20 |
2011-07-20 |
百时美施贵宝公司 |
用作激酶抑制剂的咪唑并吡啶和咪唑并吡嗪化合物
|
|
CN102177138A
(zh)
*
|
2008-10-23 |
2011-09-07 |
隆萨有限公司 |
合成取代的吡唑类的方法
|
|
CN102548536A
(zh)
*
|
2009-10-01 |
2012-07-04 |
爱尔康研究有限公司 |
奥洛他定组合物及其用途
|
|
EP2308866A1
(de)
|
2009-10-09 |
2011-04-13 |
Bayer CropScience AG |
Phenylpyri(mi)dinylpyrazole und ihre Verwendung als Fungizide
|
|
AR079545A1
(es)
|
2009-12-21 |
2012-02-01 |
Bayer Cropscience Ag |
Tienilpiri(mi)dinilazol
|
|
AR081810A1
(es)
|
2010-04-07 |
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|
|
WO2012031057A1
(en)
|
2010-09-01 |
2012-03-08 |
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|
|
AR086992A1
(es)
|
2011-06-20 |
2014-02-05 |
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|
|
US9314026B2
(en)
|
2011-10-06 |
2016-04-19 |
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|
|
PL2763987T3
(pl)
|
2011-10-06 |
2019-01-31 |
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|
|
CN103360315B
(zh)
*
|
2013-07-22 |
2015-03-04 |
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|
|
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(en)
|
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|