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
|
DE3486009T2
(de)
|
1983-09-09 |
1993-04-15 |
Takeda Chemical Industries Ltd |
5-pyridyl-1,3-thiazol-derivate, ihre herstellung und anwendung.
|
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
|
EP1014953B1
(en)
|
1997-03-05 |
2012-04-25 |
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
|
US6465493B1
(en)
|
1999-04-09 |
2002-10-15 |
Smithkline Beecham Corporation |
Triarylimidazoles
|
WO2000062778A1
(en)
|
1999-04-15 |
2000-10-26 |
Bristol-Myers Squibb Co. |
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
|
DE60037597T2
(de)
|
1999-11-22 |
2008-12-11 |
Smithkline Beecham P.L.C., Brentford |
Imidazol- Derivate
|
AU2001232809A1
(en)
|
2000-01-18 |
2001-07-31 |
Vertex Pharmaceuticals Incorporated |
Gyrase inhibitors and uses thereof
|
NZ520628A
(en)
|
2000-01-18 |
2004-05-28 |
Vertex Pharma |
thiazole, oxazole, imdazole or pyrazole substituted pyrazole derivatives useful as treating bacterial infections
|
AR029803A1
(es)
|
2000-02-21 |
2003-07-16 |
Smithkline Beecham Plc |
Imidazoles sustituidos con piridilo y composiciones farmaceuticas que las comprenden
|
EP1263753B1
(en)
|
2000-03-06 |
2004-05-06 |
SmithKline Beecham plc |
Imidazol derivatives as raf kinase inhibitors
|
GB0005357D0
(en)
|
2000-03-06 |
2000-04-26 |
Smithkline Beecham Plc |
Compounds
|
GB0007405D0
(en)
|
2000-03-27 |
2000-05-17 |
Smithkline Beecham Corp |
Compounds
|
AU2001244618A1
(en)
|
2000-03-30 |
2001-10-15 |
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
|
KR100850728B1
(ko)
|
2000-06-12 |
2008-08-06 |
에자이 알앤드디 매니지먼트 가부시키가이샤 |
1,2-디하이드로피리딘 화합물, 그의 제조 방법 및 그의 용도
|
HU230251B1
(hu)
|
2000-07-19 |
2015-11-30 |
Warner-Lambert Co. |
4-Jód-fenil-amino-benzhidroxámsav-észter-származékok és ezeket tartalmazó gyógyászati készítmények
|
EP1332131A2
(en)
|
2000-11-07 |
2003-08-06 |
Bristol-Myers Squibb Company |
Acid derivatives useful as serine protease inhibitors
|
WO2002039954A2
(en)
|
2000-11-20 |
2002-05-23 |
Smithkline Beecham Corporation |
Novel compounds
|
US7238813B2
(en)
|
2000-11-29 |
2007-07-03 |
Smithkline Beecham Corporation |
Chemical compounds
|
WO2002064136A2
(en)
|
2001-01-26 |
2002-08-22 |
Chugai Seiyaku Kabushiki Kaisha |
Malonyl-coa decarboxylase inhibitors useful as metabolic modulators
|
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
|
CA2480638C
(en)
|
2002-03-29 |
2013-02-12 |
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
|
DE60328028D1
(de)
|
2002-09-18 |
2009-07-30 |
Pfizer Prod Inc |
Imidazolverbindungen als inhibitoren des transformierenden wachstumsfaktors (twf)
|
CA2499429C
(en)
|
2002-09-18 |
2010-09-21 |
Pfizer Products Inc. |
Novel oxazole and thiazole compounds as transforming growth factor (tgf) inhibitors
|
US7531553B2
(en)
|
2003-03-21 |
2009-05-12 |
Amgen Inc. |
Heterocyclic compounds and methods of use
|
PE20050952A1
(es)
|
2003-09-24 |
2005-12-19 |
Novartis Ag |
Derivados de isoquinolina como inhibidores de b-raf
|
EP1673343A4
(en)
|
2003-10-08 |
2008-09-10 |
Irm Llc |
COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS
|
US7423150B2
(en)
|
2003-10-16 |
2008-09-09 |
Novartis Ag |
Substituted benzazoles and methods of their use as inhibitors of Raf kinase
|
DK1692113T3
(en)
|
2003-11-14 |
2018-01-08 |
Lorus Therapeutics Inc |
ARYLIMIDAZOLES AND USE THEREOF AS ANTICANCES
|
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
|
ES2397825T3
(es)
|
2004-06-11 |
2013-03-11 |
Japan Tobacco, Inc. |
Derivados de 5-amino-2,4,7-trioxo-3,4,7,8-tetrahidro-2H-pirido[2,3-d]pirimidina y compuestos relacionados para el tratamiento del cáncer
|
US7453002B2
(en)
|
2004-06-15 |
2008-11-18 |
Bristol-Myers Squibb Company |
Five-membered heterocycles useful as serine protease inhibitors
|
GB0415365D0
(en)
|
2004-07-09 |
2004-08-11 |
Astrazeneca Ab |
Pyrimidine derivatives
|
GB0415367D0
(en)
|
2004-07-09 |
2004-08-11 |
Astrazeneca Ab |
Pyrimidine derivatives
|
GB0415364D0
(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
|
EP1804801A2
(en)
|
2004-10-15 |
2007-07-11 |
Biogen Idec MA, Inc. |
Methods of treating vascular injuries
|
JP2007246520A
(ja)
|
2006-02-15 |
2007-09-27 |
Takeda Yuichiro |
Rage阻害剤
|
CA2682189C
(en)
|
2006-04-07 |
2015-12-08 |
Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College |
Thiazole and thiophene analogues, and their use in treating autoimmune diseases and cancers
|
JP4450857B2
(ja)
|
2006-08-08 |
2010-04-14 |
中外製薬株式会社 |
Pi3k阻害剤としてのピリミジン誘導体およびその用途
|
WO2008071605A2
(en)
|
2006-12-15 |
2008-06-19 |
F. Hoffmann-La Roche Ag |
Methods of treating inflammatory diseases
|
DK2170848T3
(en)
|
2007-06-27 |
2015-01-05 |
Astrazeneca Ab |
Pyrazinonderivater and their use to treat lung diseases
|
TWI444379B
(zh)
|
2007-06-29 |
2014-07-11 |
Sunesis Pharmaceuticals Inc |
有用於作為Raf激酶抑制劑之化合物
|
CN101743242A
(zh)
|
2007-06-29 |
2010-06-16 |
苏尼西斯制药有限公司 |
用作raf激酶抑制剂的杂环化合物
|
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
|
EP2170830B1
(en)
|
2007-07-17 |
2014-10-15 |
Plexxikon, Inc. |
2-FLUORO-BENZENESULFONAMIDE COMPOUNDS AS Raf KINASE MODULATORS
|
RU2474580C2
(ru)
|
2007-07-19 |
2013-02-10 |
Шеринг Корпорейшн |
Гетероциклические амидные соединения как ингибиторы протеинкиназ
|
US20110190280A1
(en)
|
2007-08-29 |
2011-08-04 |
George Adjabeng |
Thiazole And Oxazole Kinase Inhibitors
|
TW200916458A
(en)
|
2007-09-05 |
2009-04-16 |
Astrazeneca Ab |
Heterocyclic compounds and methods of use thereof
|
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
|
US8865732B2
(en)
|
2008-03-21 |
2014-10-21 |
Novartis Ag |
Heterocyclic compounds and uses thereof
|
CN102015686B
(zh)
|
2008-03-21 |
2014-07-02 |
诺华股份有限公司 |
杂环化合物及其用途
|
UA103319C2
(en)
|
2008-05-06 |
2013-10-10 |
Глаксосмитклайн Ллк |
Thiazole- and oxazole-benzene sulfonamide compounds
|
WO2009152356A2
(en)
|
2008-06-11 |
2009-12-17 |
Irm Llc |
Compounds and compositions useful for the treatment of malaria
|
EA019722B1
(ru)
|
2008-07-24 |
2014-05-30 |
НЕРВИАНО МЕДИКАЛ САЙЕНСИЗ С.р.л. |
3,4-диарилпиразолы в качестве ингибиторов протеинкиназ
|
US8685980B2
(en)
|
2008-08-22 |
2014-04-01 |
Novartis Ag |
Pyrrolopyrimidine compounds and their uses
|
WO2010048149A2
(en)
|
2008-10-20 |
2010-04-29 |
Kalypsys, Inc. |
Heterocyclic modulators of gpr119 for treatment of disease
|
CN102300862B
(zh)
|
2008-12-19 |
2016-11-23 |
沃泰克斯药物股份有限公司 |
用作atr激酶抑制剂的化合物
|
US8242260B2
(en)
|
2009-08-28 |
2012-08-14 |
Novartis Ag |
Compounds and compositions as protein kinase inhibitors
|
MX2012002761A
(es)
|
2009-09-04 |
2012-04-19 |
Novartis Ag |
Bipiridinas utiles para el tratamiento de enfermedades proliferativas.
|
EP2498608A4
(en)
|
2009-11-10 |
2013-04-24 |
Glaxosmithkline Llc |
BENZOLSULFONAMIDE THIAZOL AND OXAZOLE COMPOUNDS
|
US8796320B2
(en)
|
2009-12-28 |
2014-08-05 |
General Incorporated Association Pharma Valley Project Supporting Organization |
1,3,4-Oxadiazole-2-carboxamide compound
|
US9315491B2
(en)
|
2009-12-28 |
2016-04-19 |
Development Center For Biotechnology |
Pyrimidine compounds as mTOR and PI3K inhibitors
|
KR20110123657A
(ko)
|
2010-05-07 |
2011-11-15 |
에스케이케미칼주식회사 |
피콜린아마이드 및 피리미딘-4-카복사미드 화합물, 이의 제조방법 및 이를 함유하는 약제학적 조성물
|
AU2011268906A1
(en)
|
2010-06-25 |
2013-01-31 |
Novartis Ag |
Heteroaryl compounds and compositions as protein kinase inhibitors
|
WO2012027438A1
(en)
|
2010-08-26 |
2012-03-01 |
Glaxosmithkline Llc |
Pharmaceutical combination of a vegfr inhibitor and a mek inhibitor useful for treating cancer
|
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
|
AR083797A1
(es)
|
2010-11-10 |
2013-03-20 |
Novartis Ag |
Succinato de dimetil-amida del acido 7-ciclopentil-2-(5-piperazin-1-il-piridin-2-il-amino)-7h-pirrolo-[2,3-d]pirimidin-6-carboxilico, proceso para prepararla, intermediarios de dicha sintesis y proceso de preparacion de los mismos
|
PL2672967T3
(pl)
|
2011-02-07 |
2019-04-30 |
Plexxikon Inc |
Związki i sposoby modulacji kinaz i wskazania ku temu
|
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
|
PL2751104T3
(pl)
|
2011-09-01 |
2020-04-30 |
Novartis Ag |
Związki i kompozycje jako inhibitory kinazy c-kit
|
EP2758379B1
(en)
|
2011-09-21 |
2016-10-19 |
Cellzome Limited |
Urea and carbamate derivatives of 2-morpholino-1,3,5-triazine as mTOR inhibitors for the treatment of immunological or proliferative diseases
|
WO2013164769A1
(en)
|
2012-05-02 |
2013-11-07 |
Lupin Limited |
Substituted pyridine compounds as crac modulators
|
JP6078640B2
(ja)
|
2012-05-15 |
2017-02-08 |
ノバルティス アーゲー |
Abl1、abl2およびbcr−abl1の活性を阻害するためのベンズアミド誘導体
|
WO2014008214A1
(en)
|
2012-07-02 |
2014-01-09 |
Biogen Idec Ma Inc. |
Biaryl-containing compounds as inverse agonists of ror-gamma receptors
|
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
|
PL2892535T3
(pl)
|
2012-09-04 |
2022-01-31 |
Novartis Ag |
Sposób leczenia adjuwantowego raka
|
EA030253B1
(ru)
|
2012-09-28 |
2018-07-31 |
Кэнсэр Ресерч Текнолоджи Лимитед |
Азахиназолиновые ингибиторы атипичной протеинкиназы c
|
WO2014058691A1
(en)
|
2012-10-08 |
2014-04-17 |
Merck Sharp & Dohme Corp. |
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
|
WO2014147573A2
(en)
*
|
2013-03-21 |
2014-09-25 |
Novartis Ag |
Combination therapy
|
PL3063143T3
(pl)
*
|
2013-11-01 |
2018-10-31 |
Novartis Ag |
Aminoheteroarylowe benzamidy jako inhibitory kinaz
|
CN106211755B
(zh)
*
|
2013-12-20 |
2021-06-22 |
生物医学谷探索股份有限公司 |
使用erk和raf抑制剂的组合的癌症治疗
|
CN107001329B
(zh)
|
2014-09-12 |
2020-09-01 |
诺华股份有限公司 |
作为激酶抑制剂的化合物和组合物
|
UY36294A
(es)
*
|
2014-09-12 |
2016-04-29 |
Novartis Ag |
Compuestos y composiciones como inhibidores de quinasa
|
JP6636014B2
(ja)
|
2014-09-12 |
2020-01-29 |
ノバルティス アーゲー |
Rafキナーゼ阻害剤としての化合物および組成物
|
WO2016115376A1
(en)
*
|
2015-01-14 |
2016-07-21 |
The Regents Of The University Of California |
Detection and treatment of double drug resistant melanomas
|
ME03772B
(me)
|
2015-07-10 |
2021-04-20 |
Genmab As |
Konjugati antitijela specifičnog za axl i lijeka za liječenje kancera
|
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
|
US20180250302A1
(en)
|
2015-08-28 |
2018-09-06 |
Giordano Caponigro |
Combination of ribociclib and dabrafenib for treating or preventing cancer
|
RU2759669C2
(ru)
*
|
2016-06-03 |
2021-11-16 |
Аррэй Байофарма Инк. |
Фармацевтические комбинации
|
KR20190017767A
(ko)
*
|
2016-06-10 |
2019-02-20 |
노파르티스 아게 |
C-raf 억제제의 치료적 용도
|
CN109715163B
(zh)
|
2016-09-19 |
2022-11-22 |
诺华股份有限公司 |
包含raf抑制剂和erk抑制剂的治疗组合
|
US11590133B2
(en)
|
2016-12-11 |
2023-02-28 |
Memorial Sloan Kettering Cancer Center |
Methods and compositions for treatment of BRAF mutant cancers
|
JP7309614B2
(ja)
|
2017-05-02 |
2023-07-18 |
ノバルティス アーゲー |
組み合わせ療法
|
EP3624896A4
(en)
|
2017-05-16 |
2021-03-31 |
Biomed Valley Discoveries, Inc. |
COMPOSITIONS AND METHODS FOR THE TREATMENT OF CANCER WITH ATYPICAL BRAF MUTATIONS
|
WO2020046966A1
(en)
|
2018-08-27 |
2020-03-05 |
Kura Oncology, Inc. |
Treatment of adenocarcinomas with mapk pathway inhibitors
|
WO2020128878A1
(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
|
BR112021022335A2
(pt)
|
2019-05-13 |
2021-12-28 |
Novartis Ag |
Formas cristalinas de n-(3-(2-(2-hidroxietoxi)-6-morfolinopiridin-4-il)-4-metilfenil)-2 (trifluorome-til)isonicotinamida como inibidores raf para o tratamento de câncer
|
WO2021165849A1
(en)
|
2020-02-18 |
2021-08-26 |
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
|