|
US3707475A
(en)
|
1970-11-16 |
1972-12-26 |
Pfizer |
Antiinflammatory imidazoles
|
|
DE3029376A1
(de)
|
1980-07-31 |
1982-03-18 |
Nepera Chemical Co. Inc., Harriman, N.Y. |
Verfahren zur herstellung von 2,4,5-tris-pyridylimidazolen
|
|
EP0149884B1
(en)
|
1983-09-09 |
1992-12-16 |
Takeda Chemical Industries, Ltd. |
5-pyridyl-1,3-thiazole derivatives, their production and use
|
|
JP2722586B2
(ja)
|
1989-01-13 |
1998-03-04 |
大正製薬株式会社 |
インドリルイミダゾール誘導体
|
|
JP2808460B2
(ja)
|
1989-11-16 |
1998-10-08 |
大正製薬株式会社 |
イミダゾール誘導体
|
|
US6358932B1
(en)
|
1994-05-31 |
2002-03-19 |
Isis Pharmaceticals, Inc. |
Antisense oligonucleotide inhibition of raf gene expression
|
|
US5717100A
(en)
|
1995-10-06 |
1998-02-10 |
Merck & Co., Inc. |
Substituted imidazoles having anti-cancer and cytokine inhibitory activity
|
|
GB2306108A
(en)
|
1995-10-13 |
1997-04-30 |
Merck & Co Inc |
Treatment of Raf-mediated cancers with imidazole derivatives
|
|
US6268308B1
(en)
|
1996-08-27 |
2001-07-31 |
Syngenta Crop Protection, Inc. |
Herbicidal S-substituted 1,2,4,6-thiatriazines
|
|
AU743024B2
(en)
|
1997-03-05 |
2002-01-17 |
Sugen, Inc. |
Formulations for hydrophobic pharmaceutical agents
|
|
AR012634A1
(es)
|
1997-05-02 |
2000-11-08 |
Sugen Inc |
Compuesto basado en quinazolina, composicion famaceutica que lo comprende, metodo para sintetizarlo, su uso, metodos de modulacion de la funcion deserina/treonina proteinaquinasa con dicho compuesto y metodo in vitro para identificar compuestos que modulan dicha funcion
|
|
GB9711650D0
(en)
|
1997-06-05 |
1997-07-30 |
Pfizer Ltd |
Compounds useful in therapy
|
|
GB9716557D0
(en)
|
1997-08-06 |
1997-10-08 |
Glaxo Group Ltd |
Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity
|
|
US6022884A
(en)
|
1997-11-07 |
2000-02-08 |
Amgen Inc. |
Substituted pyridine compounds and methods of use
|
|
US6211177B1
(en)
|
1998-11-24 |
2001-04-03 |
Cell Pathways, Inc. |
Method for treating neoplasia by exposure to substituted 2-aryl-benzimidazole derivatives
|
|
EP1140840B1
(en)
|
1999-01-13 |
2006-03-22 |
Bayer Pharmaceuticals Corp. |
-g(v)-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
|
|
US6548529B1
(en)
|
1999-04-05 |
2003-04-15 |
Bristol-Myers Squibb Company |
Heterocyclic containing biphenyl aP2 inhibitors and method
|
|
DE60001229T2
(de)
|
1999-04-09 |
2003-10-30 |
Smithkline Beecham Corp., Philadelphia |
Triarylimidazole
|
|
EP1169038B9
(en)
|
1999-04-15 |
2013-07-10 |
Bristol-Myers Squibb Company |
Cyclic protein tyrosine kinase inhibitors
|
|
JP2000302680A
(ja)
|
1999-04-23 |
2000-10-31 |
Takeda Chem Ind Ltd |
脳保護剤
|
|
AU7031500A
(en)
|
1999-09-23 |
2001-04-24 |
Astrazeneca Ab |
Therapeutic quinazoline compounds
|
|
AU1529901A
(en)
|
1999-11-22 |
2001-06-04 |
Smithkline Beecham Plc |
Compounds
|
|
JP2003520233A
(ja)
|
2000-01-18 |
2003-07-02 |
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 |
ジャイレースインヒビターおよびそれらの使用
|
|
AU2001232809A1
(en)
|
2000-01-18 |
2001-07-31 |
Vertex Pharmaceuticals Incorporated |
Gyrase inhibitors and uses thereof
|
|
CO5271680A1
(es)
|
2000-02-21 |
2003-04-30 |
Smithkline Beecham Corp |
Compuestos
|
|
ATE266022T1
(de)
|
2000-03-06 |
2004-05-15 |
Smithkline Beecham Plc |
Imidazol derivate als raf kinase inhibitoren
|
|
GB0005357D0
(en)
|
2000-03-06 |
2000-04-26 |
Smithkline Beecham Plc |
Compounds
|
|
GB0007405D0
(en)
|
2000-03-27 |
2000-05-17 |
Smithkline Beecham Corp |
Compounds
|
|
WO2001074811A2
(en)
|
2000-03-30 |
2001-10-11 |
Takeda Chemical Industries, Ltd. |
Substituted 1,3-thiazole compounds, their production and use
|
|
US6608053B2
(en)
|
2000-04-27 |
2003-08-19 |
Yamanouchi Pharmaceutical Co., Ltd. |
Fused heteroaryl derivatives
|
|
ES2320973T3
(es)
|
2000-06-12 |
2009-06-01 |
EISAI R&D MANAGEMENT CO., LTD. |
Compuestos de 1,2-dihidropiridina, procedimiento para su preparacion y uso de los mismos.
|
|
JP3811775B2
(ja)
|
2000-07-19 |
2006-08-23 |
ワーナー−ランバート カンパニー リミティド ライアビリティー カンパニー |
4−ヨードフェニルアミノベンズヒドロキサム酸の酸素化エステル
|
|
EP1332131A2
(en)
|
2000-11-07 |
2003-08-06 |
Bristol-Myers Squibb Company |
Acid derivatives useful as serine protease inhibitors
|
|
ATE365730T1
(de)
|
2000-11-20 |
2007-07-15 |
Smithkline Beecham Corp |
Neuartige verbindungen
|
|
JP2004517080A
(ja)
|
2000-11-29 |
2004-06-10 |
グラクソ グループ リミテッド |
Tie−2および/またはvegfr−2の阻害剤として有用なベンゾイミダゾール誘導体
|
|
ES2274005T3
(es)
|
2001-01-26 |
2007-05-16 |
Chugai Seiyaku Kabushiki Kaisha |
Inhibidores de malonyl-coa decarboxilasa usados como moduladores metabolicos.
|
|
US7199124B2
(en)
|
2001-02-02 |
2007-04-03 |
Takeda Pharmaceutical Company Limited |
JNK inhibitor
|
|
US20030009034A1
(en)
|
2001-03-22 |
2003-01-09 |
Neil Wishart |
Transition metal mediated process
|
|
JP2002338537A
(ja)
|
2001-05-16 |
2002-11-27 |
Mitsubishi Pharma Corp |
アミド化合物およびその医薬用途
|
|
GB0112348D0
(en)
|
2001-05-19 |
2001-07-11 |
Smithkline Beecham Plc |
Compounds
|
|
GB0129260D0
(en)
|
2001-12-06 |
2002-01-23 |
Eisai London Res Lab Ltd |
Pharmaceutical compositions and their uses
|
|
US8299108B2
(en)
|
2002-03-29 |
2012-10-30 |
Novartis Ag |
Substituted benzazoles and methods of their use as inhibitors of raf kinase
|
|
WO2003082272A1
(en)
|
2002-03-29 |
2003-10-09 |
Chiron Corporation |
Substituted benzazoles and use thereof as raf kinase inhibitors
|
|
AR039241A1
(es)
|
2002-04-04 |
2005-02-16 |
Biogen Inc |
Heteroarilos trisustituidos y metodos para su produccion y uso de los mismos
|
|
AU2003256003A1
(en)
|
2002-09-18 |
2004-04-08 |
Pfizer Products Inc. |
Novel oxazole and thiazole compounds as transforming growth factor (TGF) inhibitors
|
|
MXPA05002981A
(es)
|
2002-09-18 |
2005-06-22 |
Pfizer Prod Inc |
Nuevos compuestos de imidazol como inhibidores del factor de crecimiento transformante (tgf).
|
|
US7531553B2
(en)
|
2003-03-21 |
2009-05-12 |
Amgen Inc. |
Heterocyclic compounds and methods of use
|
|
AR045944A1
(es)
|
2003-09-24 |
2005-11-16 |
Novartis Ag |
Derivados de isoquinolina 1.4-disustituidas
|
|
AU2004279427B2
(en)
|
2003-10-08 |
2008-07-03 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
|
KR20060118472A
(ko)
|
2003-10-16 |
2006-11-23 |
카이론 코포레이션 |
치환 벤자졸 및 raf 키나아제의 저해제로서 그것의 사용
|
|
CA2545942C
(en)
|
2003-11-14 |
2012-07-10 |
Lorus Therapeutics Inc. |
Aryl imidazoles and their use as anti-cancer agents
|
|
RU2367661C2
(ru)
|
2004-03-05 |
2009-09-20 |
Тайсо Фармасьютикал Ко., Лтд. |
Производные тиазола
|
|
KR100749566B1
(ko)
|
2004-04-21 |
2007-08-16 |
이화여자대학교 산학협력단 |
Alk5 및/또는 alk4 억제제로 유효한 2-피리딜이치환된 이미다졸 유도체
|
|
US20060106020A1
(en)
|
2004-04-28 |
2006-05-18 |
Rodgers James D |
Tetracyclic inhibitors of Janus kinases
|
|
PE20060315A1
(es)
|
2004-05-24 |
2006-05-15 |
Irm Llc |
Compuestos de tiazol como moduladores de ppar
|
|
SI1761528T1
(sl)
|
2004-06-11 |
2008-06-30 |
Japan Tobacco Inc |
5-amino-2,4,7-triokso-3,4,7,8-tetrahidro-2H-pirido(2,3-D)pirimidinski derivati in sorodne spojine za zdravljenje raka
|
|
US7453002B2
(en)
|
2004-06-15 |
2008-11-18 |
Bristol-Myers Squibb Company |
Five-membered heterocycles useful as serine protease inhibitors
|
|
GB0415367D0
(en)
|
2004-07-09 |
2004-08-11 |
Astrazeneca Ab |
Pyrimidine derivatives
|
|
GB0415364D0
(en)
|
2004-07-09 |
2004-08-11 |
Astrazeneca Ab |
Pyrimidine derivatives
|
|
GB0415365D0
(en)
|
2004-07-09 |
2004-08-11 |
Astrazeneca Ab |
Pyrimidine derivatives
|
|
AU2005280168A1
(en)
|
2004-08-31 |
2006-03-09 |
Biogen Idec Ma Inc. |
Pyrimidinylimidazoles as TGF-beta inhibitors
|
|
WO2006038734A1
(en)
|
2004-10-08 |
2006-04-13 |
Astellas Pharma Inc. |
Pyridazinone derivatives cytokines inhibitors
|
|
AU2005295734A1
(en)
|
2004-10-15 |
2006-04-27 |
Biogen Idec Ma Inc. |
Methods of treating vascular injuries
|
|
JP2007246520A
(ja)
|
2006-02-15 |
2007-09-27 |
Takeda Yuichiro |
Rage阻害剤
|
|
WO2007118149A2
(en)
|
2006-04-07 |
2007-10-18 |
Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical Lollege |
Thiazole and thiophene analogues, and their use in treating autoimmune diseases and cancers
|
|
EP2050749B1
(en)
|
2006-08-08 |
2017-11-22 |
Chugai Seiyaku Kabushiki Kaisha |
Pyrimidine derivative as pi3k inhibitor and use thereof
|
|
WO2008071605A2
(en)
|
2006-12-15 |
2008-06-19 |
F. Hoffmann-La Roche Ag |
Methods of treating inflammatory diseases
|
|
JP5140154B2
(ja)
|
2007-06-27 |
2013-02-06 |
アストラゼネカ・アクチエボラーグ |
ピラジノン誘導体および肺疾患の処置におけるそれらの使用
|
|
US7968536B2
(en)
|
2007-06-29 |
2011-06-28 |
Millennium Pharmaceuticals, Inc. |
Heterocyclic compounds useful as RAF kinase inhibitors
|
|
CL2008001933A1
(es)
|
2007-06-29 |
2009-09-25 |
Millennium Pharm Inc |
Compuestos derivados de pirimidina, inhibidores de la raf quinasa; compuestos intermediarios; procedimiento de preparacion; composicion farmaceutica; y su uso para tratar trastornos proliferativos, cardiacos, neurodegenerativos, inflamatorios, oseos, inmunologicos enfermedad viral, entre otros.
|
|
CA2692379A1
(en)
|
2007-07-02 |
2009-01-08 |
Boehringer Ingelheim International Gmbh |
Antiproliferative compounds based on 5-membered heterocycles
|
|
US20100261723A1
(en)
|
2007-07-09 |
2010-10-14 |
Astrazeneca Ab |
Trisubstituted pyrimidine derivatives for the treatment of proliferative diseases
|
|
WO2009012283A1
(en)
|
2007-07-17 |
2009-01-22 |
Plexxikon Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
|
MY150032A
(en)
|
2007-07-19 |
2013-11-29 |
Merck Sharp & Dohme |
Heterocyclic amide compounds as protein kinase inhibitors
|
|
WO2009032667A1
(en)
|
2007-08-29 |
2009-03-12 |
Smithkline Beecham Corporation |
Thiazole and oxazole kinase inhibitors
|
|
WO2009030952A2
(en)
|
2007-09-05 |
2009-03-12 |
Astrazeneca Ab |
Phenylcarboxamide derivatives as inhibitors and effectors of the hedgehog pathway
|
|
WO2009047163A1
(en)
|
2007-10-10 |
2009-04-16 |
F. Hoffmann-La Roche Ag |
Methods of treating inflammatory diseases
|
|
TW200940537A
(en)
|
2008-02-26 |
2009-10-01 |
Astrazeneca Ab |
Heterocyclic urea derivatives and methods of use thereof
|
|
WO2009115572A2
(en)
|
2008-03-21 |
2009-09-24 |
Novartis Ag |
Novel heterocyclic compounds and uses therof
|
|
US8865732B2
(en)
|
2008-03-21 |
2014-10-21 |
Novartis Ag |
Heterocyclic compounds and uses thereof
|
|
UA103319C2
(en)
|
2008-05-06 |
2013-10-10 |
Глаксосмитклайн Ллк |
Thiazole- and oxazole-benzene sulfonamide compounds
|
|
CN102089278A
(zh)
|
2008-06-11 |
2011-06-08 |
Irm责任有限公司 |
用于治疗疟疾的化合物和组合物
|
|
PT2324008E
(pt)
|
2008-07-24 |
2012-06-25 |
Nerviano Medical Sciences Srl |
3,4-diarilpirazoles como inibidores da proteína quinase
|
|
ES2522346T3
(es)
|
2008-08-22 |
2014-11-14 |
Novartis Ag |
Compuestos de pirrolopirimidina como inhibidores de CDK
|
|
WO2010048149A2
(en)
|
2008-10-20 |
2010-04-29 |
Kalypsys, Inc. |
Heterocyclic modulators of gpr119 for treatment of disease
|
|
ES2921576T3
(es)
|
2008-12-19 |
2022-08-29 |
Vertex Pharma |
Compuestos útiles como inhibidores de la quinasa ATR
|
|
US8242260B2
(en)
|
2009-08-28 |
2012-08-14 |
Novartis Ag |
Compounds and compositions as protein kinase inhibitors
|
|
WO2011026911A1
(en)
|
2009-09-04 |
2011-03-10 |
Novartis Ag |
Bipyridines useful for the treatment of proliferative diseases
|
|
EP2498608A4
(en)
|
2009-11-10 |
2013-04-24 |
Glaxosmithkline Llc |
BENZOLSULFONAMIDE THIAZOL AND OXAZOLE COMPOUNDS
|
|
US9315491B2
(en)
|
2009-12-28 |
2016-04-19 |
Development Center For Biotechnology |
Pyrimidine compounds as mTOR and PI3K inhibitors
|
|
PL2520575T3
(pl)
|
2009-12-28 |
2017-05-31 |
General Incorporated Association Pharma Valley Project Supporting Organization |
Związek 1,3,4-oksadiazolo-2-karboksyamidowy
|
|
KR20110123657A
(ko)
|
2010-05-07 |
2011-11-15 |
에스케이케미칼주식회사 |
피콜린아마이드 및 피리미딘-4-카복사미드 화합물, 이의 제조방법 및 이를 함유하는 약제학적 조성물
|
|
JP2013529619A
(ja)
|
2010-06-25 |
2013-07-22 |
ノバルティス アーゲー |
タンパク質キナーゼ阻害剤としてのヘテロアリール化合物および組成物
|
|
JP5903433B2
(ja)
|
2010-08-26 |
2016-04-13 |
ノバルティス アーゲー |
癌の治療に有用なvegfr阻害剤およびmek阻害剤の医薬的組み合わせ
|
|
CN101993415B
(zh)
|
2010-09-15 |
2013-08-14 |
北京韩美药品有限公司 |
作为Hedgehog通路抑制剂的化合物以及包含该化合物的药物组合物及其应用
|
|
US20120115878A1
(en)
|
2010-11-10 |
2012-05-10 |
John Vincent Calienni |
Salt(s) of 7-cyclopentyl-2-(5-piperazin-1-yl-pyridin-2-ylamino)-7h-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide and processes of making thereof
|
|
US9624213B2
(en)
|
2011-02-07 |
2017-04-18 |
Plexxikon Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
|
EP2739143B1
(en)
|
2011-08-05 |
2018-07-11 |
Gary A. Flynn |
Preparation and methods of use for ortho-aryl 5- membered heteroaryl-carboxamide containing multi-targeted kinase inhibitors
|
|
EP2751104B1
(en)
|
2011-09-01 |
2019-09-25 |
Novartis AG |
Compounds and compositions as c-kit kinase inhibitors
|
|
WO2013041652A1
(en)
|
2011-09-21 |
2013-03-28 |
Cellzome Limited |
Morpholino substituted urea or carbamate derivatives as mtor inhibitors
|
|
CA2871270A1
(en)
|
2012-05-02 |
2013-11-07 |
Lupin Limited |
Substituted pyridine compounds as crac modulators
|
|
CN104379574B
(zh)
|
2012-05-15 |
2017-03-01 |
诺华股份有限公司 |
用于抑制abl1、abl2和bcr‑abl1的活性的苯甲酰胺衍生物
|
|
AR091654A1
(es)
|
2012-07-02 |
2015-02-18 |
Biogen Idec Inc |
COMPUESTOS QUE CONTIENEN BIARILO COMO AGONISTAS INVERSOS DE RECEPTORES ROR-g
|
|
AR091876A1
(es)
*
|
2012-07-26 |
2015-03-04 |
Novartis Ag |
Combinaciones farmaceuticas para el tratamiento de enfermedades proliferativas
|
|
JP6342396B2
(ja)
*
|
2012-08-07 |
2018-06-13 |
ノバルティス アーゲー |
B−Raf阻害薬、EGFR阻害薬及び場合によってはPI3K−α阻害薬を含む組合せ医薬
|
|
CN104582706A
(zh)
|
2012-09-04 |
2015-04-29 |
葛兰素史克有限责任公司 |
辅助癌症治疗的方法
|
|
KR102215272B1
(ko)
|
2012-09-28 |
2021-02-15 |
이그니타, 인코포레이티드 |
비정형 단백질 키나제 c의 아자퀴나졸린 억제제
|
|
EP2903613B1
(en)
|
2012-10-08 |
2017-11-22 |
Merck Sharp & Dohme Corp. |
Pyrazole derivatives useful as inhibitors of irak4 activity
|
|
US9867825B2
(en)
*
|
2012-12-20 |
2018-01-16 |
Novartis Ag |
Pharmaceutical combination comprising binimetinib
|
|
US9242969B2
(en)
|
2013-03-14 |
2016-01-26 |
Novartis Ag |
Biaryl amide compounds as kinase inhibitors
|
|
MA38522A1
(fr)
*
|
2013-03-21 |
2017-10-31 |
Novartis Ag |
Thérapie de combinaison comprenant un inhibiteur de b-raf et un second inhibiteur.
|
|
AP2016009099A0
(en)
*
|
2013-11-01 |
2016-03-31 |
Novartis Ag |
Aminoheteroaryl benzamides as kinase inhibitors
|
|
US10668055B2
(en)
|
2013-12-20 |
2020-06-02 |
Biomed Valley Discoveries, Inc. |
Cancer treatment using combinations of ERK and RAF inhibitors
|
|
CN107074828B
(zh)
|
2014-09-12 |
2020-05-19 |
诺华股份有限公司 |
用作raf激酶抑制剂的化合物和组合物
|
|
EP3191467B1
(en)
|
2014-09-12 |
2020-10-21 |
Novartis AG |
Compounds and compositions as kinase inhibitors
|
|
UY36294A
(es)
|
2014-09-12 |
2016-04-29 |
Novartis Ag |
Compuestos y composiciones como inhibidores de quinasa
|
|
WO2016115376A1
(en)
|
2015-01-14 |
2016-07-21 |
The Regents Of The University Of California |
Detection and treatment of double drug resistant melanomas
|
|
PL3319993T3
(pl)
|
2015-07-10 |
2020-07-27 |
Genmab A/S |
Specyficzne wobec AXL koniugaty przeciwciało-lek do leczenia raka
|
|
WO2017037575A1
(en)
*
|
2015-08-28 |
2017-03-09 |
Novartis Ag |
A pharmaceutical combination comprising the pi3k inhibitor alpelisib and the cdk4/6 inhibitor ribociclib, and the use thereof in the treatment/prevention of cancer
|
|
EP3340987A1
(en)
|
2015-08-28 |
2018-07-04 |
Novartis AG |
Combination of ribociclib and dabrafenib for treating or preventing cancer
|
|
FI3463345T3
(fi)
*
|
2016-06-03 |
2023-01-31 |
|
Farmaseuttisia yhdistelmiä
|
|
CA3026876A1
(en)
*
|
2016-06-10 |
2017-12-14 |
Novartis Ag |
Therapeutic uses of a c-raf inhibitor
|
|
AU2017329090B9
(en)
*
|
2016-09-19 |
2019-09-05 |
Novartis Ag |
Therapeutic combinations comprising a RAF inhibitor and a ERK inhibitor
|
|
WO2018107146A1
(en)
|
2016-12-11 |
2018-06-14 |
Memorial Sloan Kettering Cancer Center |
Methods and compositions for treatment of braf mutant cancers
|
|
CA3057969A1
(en)
|
2017-05-02 |
2018-11-08 |
Novartis Ag |
Combination therapy
|
|
EP3624896A4
(en)
|
2017-05-16 |
2021-03-31 |
Biomed Valley Discoveries, Inc. |
COMPOSITIONS AND METHODS OF TREATMENT OF CANCER WITH ATYPICAL BRAF MUTATIONS
|
|
TW202023556A
(zh)
|
2018-08-27 |
2020-07-01 |
美商庫拉腫瘤技術股份有限公司 |
以mapk路徑抑制劑治療腺癌
|
|
CA3123510A1
(en)
|
2018-12-20 |
2020-06-25 |
Novartis Ag |
Combination therapy with a raf inhibitor and a cdk4/6 inhibitor for use in the treatment of cancer
|
|
EP3969449B1
(en)
|
2019-05-13 |
2025-02-12 |
Novartis AG |
New crystalline forms of n-(3-(2-(2-hydroxyethoxy)-6-morpholinopyridin-4-yl)-4-methvlphenyl)-2(trifluoromethyl)isonicotinamide as raf inhibitors for the treatment of cancer
|
|
EP4106756A1
(en)
|
2020-02-18 |
2022-12-28 |
Novartis AG |
Therapeutic combinations comprising a raf inhibitor for use in treating braf mutant nsclc
|
|
US20240000789A1
(en)
|
2020-05-12 |
2024-01-04 |
Novartis Ag |
Therapeutic combinations comprising a craf inhibitor
|