|
US4783443A
(en)
|
1986-03-03 |
1988-11-08 |
The University Of Chicago |
Amino acyl cephalosporin derivatives
|
|
US5877016A
(en)
|
1994-03-18 |
1999-03-02 |
Genentech, Inc. |
Human trk receptors and neurotrophic factor inhibitors
|
|
US5844092A
(en)
|
1994-03-18 |
1998-12-01 |
Genentech, Inc. |
Human TRK receptors and neurotrophic factor inhibitors
|
|
US6677135B1
(en)
|
1996-05-08 |
2004-01-13 |
Biogen, Inc. |
Ret ligand (RetL) for stimulating neutral and renal growth
|
|
BR9710665A
(pt)
|
1996-05-08 |
1999-08-17 |
Biogen Inc |
Compostos que promovem o desenvolvimento do tecido
|
|
US6682921B1
(en)
|
1996-08-21 |
2004-01-27 |
New York University |
Crystals of the tyrosine kinase domain of non-insulin receptor tyrosine kinases
|
|
US6531152B1
(en)
|
1998-09-30 |
2003-03-11 |
Dexcel Pharma Technologies Ltd. |
Immediate release gastrointestinal drug delivery system
|
|
AU7103900A
(en)
|
1999-09-01 |
2001-03-26 |
Biogen, Inc. |
Ret ligand 5 (retl5) compositions and uses thereof
|
|
FI20000403A0
(fi)
|
2000-02-22 |
2000-02-22 |
Hannu Sariola |
GDNF perhesukuisten yhdisteiden käyttö kivessyövän hoitoon tarkoitettujen tuotteiden valmistamiseksi
|
|
DK1292680T3
(da)
|
2000-06-22 |
2010-03-08 |
Genentech Inc |
Agonist-anti-TrkC monoklonale antistoffer
|
|
WO2003020698A2
(fr)
|
2001-09-06 |
2003-03-13 |
Prochon Biotech Ltd. |
Inhibiteurs de la tyrosine kinase
|
|
US7466344B2
(en)
|
2002-06-07 |
2008-12-16 |
Scimeasure Analytical Systems, Inc. |
High-speed low noise CCD controller
|
|
ITMI20021620A1
(it)
|
2002-07-23 |
2004-01-23 |
Novuspharma Spa |
Composto ad ativita' antitumorale
|
|
JP2005535675A
(ja)
|
2002-07-24 |
2005-11-24 |
ユニバーシティ・オブ・シンシナティ |
変異型retキナーゼ関連疾患を処置するための4−(4−メチルピペラジン−1−イルメチル)−n−[4−メチル−3−(4−ピリジン−3−イル)ピリミジン−2−イルアミノ]フェニル]−ベンズアミド
|
|
EP1597251B1
(fr)
|
2003-02-20 |
2009-06-10 |
SmithKline Beecham Corporation |
Composes de pyrimidine
|
|
JP2005106669A
(ja)
|
2003-09-30 |
2005-04-21 |
Olympus Corp |
生体関連物質の反応・測定システム
|
|
US20090143399A1
(en)
|
2003-10-14 |
2009-06-04 |
Arizona Board Of Regents On Behalf Of The University Of Arizona |
Protein Kinase Inhibitors
|
|
WO2005044835A1
(fr)
|
2003-10-27 |
2005-05-19 |
Genelabs Technologies, Inc. |
Procedes de preparation de derives 7-(2'-$g(b)-d-ribofuranosyl substitue)-4-(nr2r3)-5-(ethyn-1-yl substitue)-pyrrolo[2,3-d]pyrimidine
|
|
MY141220A
(en)
|
2003-11-17 |
2010-03-31 |
Astrazeneca Ab |
Pyrazole derivatives as inhibitors of receptor tyrosine kinases
|
|
WO2005054237A1
(fr)
|
2003-11-21 |
2005-06-16 |
Novartis Ag |
Derives d'1h-imidazoquinoline en tant qu'inhibiteurs de la proteine kinase
|
|
AR047496A1
(es)
|
2003-11-28 |
2006-01-25 |
Novartis Ag |
Derivados de diaril-urea en el tratamiento de enfermedades dependientes de la quinasa de proteina
|
|
ES2527118T3
(es)
|
2003-12-19 |
2015-01-20 |
Plexxikon Inc. |
Compuestos y procedimientos de desarrollo de moduladores de Ret
|
|
GB0330042D0
(en)
|
2003-12-24 |
2004-01-28 |
Pharmacia Italia Spa |
Pyrrolo [2,3-b] pyridine derivatives active as kinase inhibitors process for their preparation and pharmaceutical compositions them
|
|
GB0330043D0
(en)
|
2003-12-24 |
2004-01-28 |
Pharmacia Italia Spa |
Pyrrolo [2,3-b] pyridine derivatives active as kinase inhibitors process for their preparation and pharmaceutical compositions comprising them
|
|
WO2005068424A1
(fr)
|
2004-01-20 |
2005-07-28 |
Cell Therapeutics Europe S.R.L. |
Derives d'indolinone en tant qu'inhibiteurs de tyrosine kinase de recepteurs
|
|
AR049769A1
(es)
|
2004-01-22 |
2006-09-06 |
Novartis Ag |
Derivados de pirazolo(1,5-a)pirimidin 7-il-amina para utilizarse en el tratamiento de enfermedades dependientes de la quinasa de proteina
|
|
US20050222171A1
(en)
|
2004-01-22 |
2005-10-06 |
Guido Bold |
Organic compounds
|
|
WO2005099363A2
(fr)
|
2004-03-26 |
2005-10-27 |
Whitehead Institute For Biomedical Research |
Methodes de diagnostic, de prevention et de traitement de metastases cancereuses
|
|
GB0512324D0
(en)
|
2005-06-16 |
2005-07-27 |
Novartis Ag |
Organic compounds
|
|
US7465726B2
(en)
|
2004-08-02 |
2008-12-16 |
Osi Pharmaceuticals, Inc. |
Substituted pyrrolo[2.3-B]pyridines
|
|
PE20060664A1
(es)
|
2004-09-15 |
2006-08-04 |
Novartis Ag |
Amidas biciclicas como inhibidores de cinasa
|
|
US7855205B2
(en)
|
2004-10-29 |
2010-12-21 |
Janssen Pharmaceutica Nv |
Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders
|
|
DE102005003687A1
(de)
|
2005-01-26 |
2006-07-27 |
Sphingo Tec Gmbh |
Immunoassay zur Bestimmung der Freisetzung von Neurotensin in die Zirkulation
|
|
GB0501999D0
(en)
|
2005-02-01 |
2005-03-09 |
Sentinel Oncology Ltd |
Pharmaceutical compounds
|
|
EP1848506A2
(fr)
|
2005-02-18 |
2007-10-31 |
Attenuon, LLC |
Derives de diazepine fusionnes pyrimidine et pteridines fusionnees indole
|
|
GB0507575D0
(en)
*
|
2005-04-14 |
2005-05-18 |
Novartis Ag |
Organic compounds
|
|
US7402579B2
(en)
|
2005-04-15 |
2008-07-22 |
Cylene Pharmaceuticals, Inc. |
Quinobenzoxazine analogs and compositions
|
|
WO2006123113A2
(fr)
|
2005-05-16 |
2006-11-23 |
Astrazeneca Ab |
Composes chimiques
|
|
WO2006128042A2
(fr)
|
2005-05-26 |
2006-11-30 |
The Johns Hopkins University |
Procedes d'identification de mutations dans un acide nucleique
|
|
US7541367B2
(en)
|
2005-05-31 |
2009-06-02 |
Janssen Pharmaceutica, N.V. |
3-benzoimidazolyl-pyrazolopyridines useful in treating kinase disorders
|
|
WO2006130613A2
(fr)
|
2005-05-31 |
2006-12-07 |
The Pfahl Family Trust (Dated 9 July 1996) |
Derives de biarylheterocycle substitues utilises comme inhibiteurs de la proteine kinase pour le traitement du cancer et d'autres maladies
|
|
ITRM20050290A1
(it)
|
2005-06-07 |
2006-12-08 |
Lay Line Genomics Spa |
Uso di molecole in grado di inibire il legame tra ngf e il suo recettore trka come analgesici ad effetto prolungato.
|
|
PT1893612E
(pt)
*
|
2005-06-22 |
2011-11-21 |
Plexxikon Inc |
Derivados de pirrolo [2,3-b]piridina como inibidores de proteína quinase
|
|
GB0515026D0
(en)
|
2005-07-21 |
2005-08-31 |
Novartis Ag |
Organic compounds
|
|
MX2008002524A
(es)
|
2005-08-25 |
2008-03-14 |
Creabilis Therapeutics Spa |
Conjugados polimericos de k-252a y sus derivados.
|
|
EP1948647A1
(fr)
|
2005-11-03 |
2008-07-30 |
SGX Pharmaceuticals, Inc. |
Modulateurs de kinase de type pyrimidinylthiophène
|
|
US20070149523A1
(en)
|
2005-11-14 |
2007-06-28 |
Jan Ehlert |
Thiazole Analogues and Uses Thereof
|
|
EP1785420A1
(fr)
|
2005-11-14 |
2007-05-16 |
4Sc Ag |
Analogues de thiazole et leurs utilisation
|
|
WO2007057397A1
(fr)
|
2005-11-15 |
2007-05-24 |
Boehringer Ingelheim International Gmbh |
Traitement du cancer
|
|
WO2007057399A2
(fr)
|
2005-11-15 |
2007-05-24 |
Boehringer Ingelheim International Gmbh |
Traitement du cancer
|
|
GB0524436D0
(en)
|
2005-11-30 |
2006-01-11 |
Novartis Ag |
Organic compounds
|
|
AU2006322187A1
(en)
|
2005-12-08 |
2007-06-14 |
Novartis Ag |
Pyrazolo[1,5-a]pyridine-3-carboxylic acids as EphB and VEGFR2 kinase inhibitors
|
|
EP1968579A1
(fr)
|
2005-12-30 |
2008-09-17 |
Astex Therapeutics Limited |
Composes pharmaceutiques
|
|
EP1978958A4
(fr)
|
2006-01-24 |
2009-12-02 |
Merck & Co Inc |
Inhibition de la tyrosine kinase ret
|
|
PL1973910T3
(pl)
|
2006-01-27 |
2013-11-29 |
Shanghai hengrui pharmaceutical co ltd |
Pirolo[3,2-c]pirydyn-4-onowo-2-indolinonowe inhibitory kinazy białkowej
|
|
EP2001864A1
(fr)
|
2006-03-16 |
2008-12-17 |
Novartis Pharma AG |
Composes organiques
|
|
BRPI0708823B1
(pt)
|
2006-03-17 |
2022-01-18 |
Ambit Biosciences Corporation |
Composto, e, composição
|
|
ZA200808966B
(en)
|
2006-03-27 |
2010-03-31 |
Nerviano Medical Sciences Srl |
Pyridyl- and pyrimidinyl-substituted pyrrole-, thiophene- and furane-derivatives as kinase inhibitors
|
|
MX2008014618A
(es)
|
2006-05-15 |
2008-11-28 |
Irm Llc |
Composiciones y metodos para inhibidores de cinasas del receptor fgf.
|
|
CA2652442C
(fr)
|
2006-05-18 |
2014-12-09 |
Eisai R & D Management Co., Ltd. |
Agent antitumoral destine au cancer de la thyroide
|
|
US8063225B2
(en)
|
2006-08-14 |
2011-11-22 |
Chembridge Corporation |
Tricyclic compound derivatives useful in the treatment of neoplastic diseases, inflammatory disorders and immunomodulatory disorders
|
|
WO2008031551A2
(fr)
|
2006-09-12 |
2008-03-20 |
Novartis Forschungsstiftung, Zweigniederlassung |
Traitement du cancer non neuroendocrinien
|
|
KR101507375B1
(ko)
|
2006-09-15 |
2015-04-07 |
엑스커버리 홀딩 컴퍼니 엘엘씨 |
키나아제 억제제 화합물
|
|
US20120225057A1
(en)
|
2006-10-11 |
2012-09-06 |
Deciphera Pharmaceuticals, Llc |
Methods and compositions for the treatment of myeloproliferative diseases and other proliferative diseases
|
|
EP1918291A1
(fr)
|
2006-10-30 |
2008-05-07 |
Novartis AG |
Dérives de pyrazole fusionnes substitués de 3-aminocarbonyle comme modulateurs de protéine kinase
|
|
HUE035868T2
(en)
|
2006-11-15 |
2018-05-28 |
Ym Biosciences Australia Pty |
Inhibitors of kinase activity
|
|
PE20121126A1
(es)
|
2006-12-21 |
2012-08-24 |
Plexxikon Inc |
Compuestos pirrolo [2,3-b] piridinas como moduladores de quinasa
|
|
CA2673736A1
(fr)
|
2006-12-21 |
2008-07-03 |
Plexxikon, Inc. |
Composes et procedes pour la modulation de kinases et indications pour celle-ci
|
|
WO2008079909A1
(fr)
|
2006-12-21 |
2008-07-03 |
Plexxikon, Inc. |
Composés et méthodes de modulation des kinases, et indications connexes
|
|
US20080199426A1
(en)
|
2007-01-11 |
2008-08-21 |
Sukhatme Vikas P |
Methods and compositions for the treatment and diagnosis of vascular inflammatory disorders or endothelial cell disorders
|
|
WO2008089388A2
(fr)
|
2007-01-19 |
2008-07-24 |
Bayer Healthcare Llc |
Traitement de cancers présentant une résistance à des agents chimiothérapeutiques
|
|
US20080234267A1
(en)
|
2007-03-20 |
2008-09-25 |
Karen Elizabeth Lackey |
Compounds and Methods of Treatment
|
|
US20110189167A1
(en)
|
2007-04-20 |
2011-08-04 |
Flynn Daniel L |
Methods and Compositions for the Treatment of Myeloproliferative Diseases and other Proliferative Diseases
|
|
CN101720322A
(zh)
|
2007-05-04 |
2010-06-02 |
Irm责任有限公司 |
作为c-kit和pdgfr激酶抑制剂的化合物和组合物
|
|
WO2008138184A1
(fr)
|
2007-05-14 |
2008-11-20 |
Shanghai Hengrui Pharmaceutical Co.Ltd. |
Dérivés de pyrrolo-azacycles, leur procédé de fabrication et leur utilisation en tant qu'inhibiteurs de protéine kinases
|
|
US20090012045A1
(en)
|
2007-06-26 |
2009-01-08 |
Rigel Pharmaceuticals, Inc. |
Methods of Treating Cell Proliferative Disorders
|
|
AR067478A1
(es)
|
2007-07-09 |
2009-10-14 |
Astrazeneca Ab |
Compuestos derivados de morfolina pirimidina
|
|
US20100209488A1
(en)
|
2007-07-16 |
2010-08-19 |
The Regents Of The University Of California |
Protein kinase modulating compounds and methods for making and using them
|
|
AU2008276063B2
(en)
|
2007-07-17 |
2013-11-28 |
Plexxikon Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
|
EP2178861B1
(fr)
|
2007-07-19 |
2014-08-20 |
Merck Sharp & Dohme Corp. |
Composés hétérocycliques d'amide en tant qu'inhibiteurs de protéine kinase
|
|
JP5506674B2
(ja)
|
2007-07-20 |
2014-05-28 |
ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ |
キナーゼ阻害剤として活性な置換インダゾール誘導体
|
|
WO2009017838A2
(fr)
|
2007-08-01 |
2009-02-05 |
Exelixis, Inc. |
Combinaisons d'inhibiteurs jak-2 et d'autres agents
|
|
DK2185698T3
(en)
|
2007-08-07 |
2015-07-27 |
Purdue Research Foundation |
Kinase Inhibitors and Uses thereof
|
|
EP2025678A1
(fr)
|
2007-08-17 |
2009-02-18 |
Oncalis AG |
Composés pyrazolo[3,4-d]pyrimidine et leur utilisation comme modulateur de protein kinase
|
|
WO2009042646A1
(fr)
|
2007-09-24 |
2009-04-02 |
Curis, Inc. |
Agents antiprolifératifs
|
|
MX2010004494A
(es)
|
2007-10-23 |
2010-08-30 |
Novartis Ag |
Uso de anticuerpos de trkb para el tratamiento de trastornos respiratorios.
|
|
JP5400791B2
(ja)
|
2007-12-04 |
2014-01-29 |
ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ |
置換ジヒドロプテリジン−6−オン誘導体、その製造方法及びキナーゼ阻害剤としてのその使用
|
|
CN101459004B
(zh)
|
2007-12-14 |
2011-02-09 |
深圳富泰宏精密工业有限公司 |
电子装置的按键面板结构及制造该按键面板结构的方法
|
|
EP2235062A1
(fr)
|
2008-01-17 |
2010-10-06 |
Irm Llc |
Anticorps anti-trkb améliorés
|
|
US20090227556A1
(en)
|
2008-01-31 |
2009-09-10 |
Eisai R&D Management Co., Ltd. |
Receptor tyrosine kinase inhibitors comprising pyridine and pyrimidine derivatives
|
|
TW200938542A
(en)
|
2008-02-01 |
2009-09-16 |
Irm Llc |
Compounds and compositions as kinase inhibitors
|
|
WO2009103076A1
(fr)
|
2008-02-15 |
2009-08-20 |
Oxigene, Inc. |
Méthodes et compositions pour améliorer l'efficacité des inhibiteurs des récepteurs tyrosine kinases (rtk)
|
|
US8822500B2
(en)
|
2008-03-19 |
2014-09-02 |
Chembridge Corporation |
Tyrosine kinase inhibitors
|
|
CN102036990B
(zh)
|
2008-03-19 |
2015-09-30 |
凯姆桥公司 |
新型酪氨酸激酶抑制剂
|
|
US8207165B2
(en)
|
2008-03-28 |
2012-06-26 |
Nerviano Medical Sciences S.R.L. |
3,4-dihydro-2H-pyrazino[1,2-A]indol-1-one derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them
|
|
WO2009143018A2
(fr)
|
2008-05-19 |
2009-11-26 |
Plexxikon, Inc. |
Composés et procédés de modulation des kinases, et indications associées
|
|
PE20091846A1
(es)
|
2008-05-19 |
2009-12-16 |
Plexxikon Inc |
DERIVADOS DE PIRROLO[2,3-d]-PIRIMIDINA COMO MODULADORES DE CINASAS
|
|
GEP20125502B
(en)
|
2008-05-23 |
2012-04-25 |
Novartis Ag |
Derivatives of quinolines and quinoxalines as protein tyrosine kinase inhibitors
|
|
US20090298820A1
(en)
*
|
2008-05-28 |
2009-12-03 |
Wyeth |
3-substituted-1h-pyrrolo[2,3-b]pyridine and 3-substituted-1h-pyrrolo[3,2-b]pyridine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses
|
|
CA2727389A1
(fr)
|
2008-06-10 |
2009-12-17 |
Prabha N. Ibrahim |
Derives 5h-pyrrolo-[2,3-b]-pyrazine destines a la modulation de kinases, et des indications pour ceux-ci
|
|
US20110212053A1
(en)
|
2008-06-19 |
2011-09-01 |
Dapeng Qian |
Phosphatidylinositol 3 kinase inhibitors
|
|
US8629135B2
(en)
|
2008-07-14 |
2014-01-14 |
Queen's University At Kingston |
Pharmaceutical compositions comprising RET inhibitors and methods for the treatment of cancer
|
|
US8946226B2
(en)
|
2008-07-29 |
2015-02-03 |
Nerviano Medical Sciences S.R.L. |
Use of CDK inhibitor for the treatment of glioma
|
|
US8410685B2
(en)
|
2008-09-01 |
2013-04-02 |
Sharp Kabushiki Kaisha |
Organic electroluminescent panel, organic electroluminescent display, organic electroluminescent lighting device, and production methods thereof
|
|
WO2010028254A2
(fr)
|
2008-09-05 |
2010-03-11 |
Auspek Pharmaceuticals, Inc. |
Inhibiteurs de tyrosine kinases de récepteur de facteur de croissance de type quinazoline substituée
|
|
EP2161271A1
(fr)
|
2008-09-08 |
2010-03-10 |
Università Degli Studi Di Milano - Bicocca |
Inhibiteurs d'alpha-carboline de NMP-ALK, RET, et Bcr-Abl
|
|
EP2376492B1
(fr)
|
2008-09-19 |
2015-04-08 |
Nerviano Medical Sciences S.r.l. |
Dérivés de 3,4-dihydro-2h-pyrrolo[1,2-a]pyrazine-1-one
|
|
PT2350075E
(pt)
|
2008-09-22 |
2014-06-09 |
Array Biopharma Inc |
Compostos imidazo[1,2b]piridazina substituídos como inibidores da trk cinase
|
|
DK2331530T3
(da)
|
2008-09-26 |
2013-11-11 |
Nat Health Research Institutes |
Kondenserede multicycliske forbindelser som proteinkinaseinhibitorer
|
|
ME03010B
(fr)
|
2008-10-22 |
2018-10-20 |
Array Biopharma Inc |
Pyrazolo [1,5-] pyrimidine en tant qu'inhibiteurs de kinases trk
|
|
US8551963B2
(en)
|
2008-11-06 |
2013-10-08 |
Ambit Biosciences Corporation |
Imidazolothiazole compounds and methods of use thereof
|
|
JP2012509859A
(ja)
|
2008-11-24 |
2012-04-26 |
ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ |
中皮腫の治療のためのcdk阻害物質
|
|
KR101061599B1
(ko)
|
2008-12-05 |
2011-09-02 |
한국과학기술연구원 |
비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물
|
|
JO3265B1
(ar)
|
2008-12-09 |
2018-09-16 |
Novartis Ag |
مثبطات بيريديلوكسى اندولات vegf-r2 واستخدامها لعلاج المرض
|
|
WO2010111527A1
(fr)
|
2009-03-26 |
2010-09-30 |
Plexxikon, Inc. |
Pyrazolo [ 3, 4 -b] pyridines en tant qu'inhibiteurs de la kinase et leur utilisation médicale
|
|
TWI410418B
(zh)
|
2009-04-29 |
2013-10-01 |
Ind Tech Res Inst |
氮雜薁化合物、藥學組合物與抑制一細胞中蛋白質激酶之活性的方法
|
|
HUE026647T2
(en)
|
2009-05-08 |
2016-07-28 |
Astellas Pharma Inc |
Diamino heterocyclic carboxamide compound
|
|
CN102480966B
(zh)
|
2009-06-12 |
2015-09-16 |
达娜-法勃肿瘤研究所公司 |
融合的杂环化合物及其用途
|
|
EP3045457B1
(fr)
|
2009-06-15 |
2018-05-09 |
Nerviano Medical Sciences S.r.l. |
Dérivés de pyrimidinylpyrrolopyridinone substitués, leur procédé de préparation et leur utilisation en tant qu'inhibiteurs de kinase
|
|
AR077468A1
(es)
|
2009-07-09 |
2011-08-31 |
Array Biopharma Inc |
Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa
|
|
JP5819831B2
(ja)
|
2009-08-17 |
2015-11-24 |
インテリカイン, エルエルシー |
複素環式化合物およびそれらの使用
|
|
KR101256018B1
(ko)
|
2009-08-20 |
2013-04-18 |
한국과학기술연구원 |
단백질 키나아제 저해활성을 갖는 1,3,6-치환된 인돌 화합물
|
|
FR2951172B1
(fr)
|
2009-10-13 |
2014-09-26 |
Pf Medicament |
Derives pyrazolopyridines en tant qu'agent anticancereux
|
|
KR101147550B1
(ko)
|
2009-10-22 |
2012-05-17 |
한국과학기술연구원 |
단백질 키나아제 저해활성을 가지는 2,7-치환된 티에노[3,2-d]피리미딘 화합물
|
|
KR101116756B1
(ko)
|
2009-10-27 |
2012-03-13 |
한국과학기술연구원 |
단백질 키나아제 저해활성을 갖는 신규의 1,6-치환된 인돌 화합물
|
|
EA029273B1
(ru)
|
2009-10-29 |
2018-03-30 |
Джиноско |
Киназные ингибиторы
|
|
CA2780892C
(fr)
|
2009-11-13 |
2017-02-14 |
Genosco |
Inhibiteurs de kinases
|
|
KR101094446B1
(ko)
|
2009-11-19 |
2011-12-15 |
한국과학기술연구원 |
단백질 키나아제 저해활성을 가지는 2,4,7-치환된 티에노[3,2-d]피리미딘 화합물
|
|
US9180127B2
(en)
|
2009-12-29 |
2015-11-10 |
Dana-Farber Cancer Institute, Inc. |
Type II Raf kinase inhibitors
|
|
SG182361A1
(en)
|
2010-01-29 |
2012-08-30 |
Hanmi Science Co Ltd |
THIENO[3,2-d]PYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY ON PROTEIN KINASES
|
|
WO2011092120A1
(fr)
|
2010-01-29 |
2011-08-04 |
Nerviano Medical Sciences S.R.L. |
Dérivés de 6,7-dihydroimidazo[1,5-a]pyrazin-8(5h)-one comme modulateurs de protéines kinases
|
|
KR101483215B1
(ko)
|
2010-01-29 |
2015-01-16 |
한미약품 주식회사 |
단백질 키나아제 저해활성을 갖는 비시클릭 헤테로아릴 유도체
|
|
ES2594927T3
(es)
|
2010-02-18 |
2016-12-23 |
INSERM (Institut National de la Santé et de la Recherche Médicale) |
Métodos para prevenir las metástasis cancerosas
|
|
TWI619713B
(zh)
|
2010-04-21 |
2018-04-01 |
普雷辛肯公司 |
用於激酶調節的化合物和方法及其適應症
|
|
PL2918588T3
(pl)
|
2010-05-20 |
2017-10-31 |
Array Biopharma Inc |
Związki makrocykliczne jako inhibitory kinazy TRK
|
|
WO2012034095A1
(fr)
|
2010-09-09 |
2012-03-15 |
Irm Llc |
Composés et compositions comme inhibiteurs de trk
|
|
US8637516B2
(en)
|
2010-09-09 |
2014-01-28 |
Irm Llc |
Compounds and compositions as TRK inhibitors
|
|
WO2012047017A2
(fr)
|
2010-10-05 |
2012-04-12 |
크리스탈지노믹스(주) |
Dérivé 2,3-dihydro-isoindol-1-one et composition le comprenant
|
|
JP2014005206A
(ja)
|
2010-10-22 |
2014-01-16 |
Astellas Pharma Inc |
アリールアミノヘテロ環カルボキサミド化合物
|
|
ES2586588T3
(es)
|
2011-01-26 |
2016-10-17 |
Nerviano Medical Sciences S.R.L. |
Derivados tricíclicos, procedimiento para su preparación y su uso como inhibidores de quinasa
|
|
CN103339134B
(zh)
|
2011-01-26 |
2015-12-23 |
内尔维阿诺医学科学有限公司 |
三环吡咯并衍生物、它们的制备方法和它们作为激酶抑制剂的应用
|
|
CN102093421B
(zh)
|
2011-01-28 |
2014-07-02 |
北京康辰药业有限公司 |
一种含磷取代基的喹啉类化合物及其制备方法、以及含有该化合物的药物组合物及其应用
|
|
SI2672967T1
(sl)
|
2011-02-07 |
2018-12-31 |
Plexxikon Inc. |
Spojine in postopki za kinazno modulacijo in indikacije zanjo
|
|
EP2678336B1
(fr)
|
2011-02-24 |
2016-04-20 |
Nerviano Medical Sciences S.r.l. |
Dérivés de thiazolylphényl-benzènesulfonamido en tant qu'inhibiteurs de la kinase
|
|
MX2013009767A
(es)
|
2011-02-25 |
2013-10-01 |
Irm Llc |
Compuestos y composiciones como inhibidores de trk.
|
|
US8791112B2
(en)
|
2011-03-30 |
2014-07-29 |
Arrien Pharmaceuticals Llc |
Substituted 5-(pyrazin-2-yl)-1H-pyrazolo [3, 4-B] pyridine and pyrazolo [3, 4-B] pyridine derivatives as protein kinase inhibitors
|
|
ES2759615T3
(es)
|
2011-04-01 |
2020-05-11 |
Univ Utah Res Found |
Análogos de N-fenilpirimidina-2-amina sustituidos como inhibidores de la quinasa AXL
|
|
US9284298B2
(en)
|
2011-04-11 |
2016-03-15 |
Nerviano Medical Sciences S.R.L. |
Pyrazolyl-pyrimidine derivatives as kinase inhibitors
|
|
EP2699564B1
(fr)
|
2011-04-19 |
2016-12-14 |
Nerviano Medical Sciences S.r.l. |
Pyrimidinylpyrroles substitués actifs en tant qu'inhibiteurs de kinases
|
|
AR086042A1
(es)
*
|
2011-04-28 |
2013-11-13 |
Galapagos Nv |
Compuesto util para el tratamiento de enfermedades degenerativas e inflamatorias y composicion farmaceutica
|
|
EP2707359B1
(fr)
|
2011-05-12 |
2016-11-30 |
Nerviano Medical Sciences S.r.l. |
Dérivés d'indazole substitués actifs en tant qu'inhibiteurs de kinases
|
|
KR102001364B1
(ko)
|
2011-05-13 |
2019-07-22 |
어레이 바이오파마 인크. |
Trka 키나제 저해제로서의 피롤리디닐 유레아 및 피롤리디닐 티오유레아 화합물
|
|
RU2477723C2
(ru)
|
2011-06-16 |
2013-03-20 |
Общество С Ограниченной Ответственностью "Фьюжн Фарма" |
Ингибиторы протеинкиназ (варианты), их применение для лечения онкологических заболеваний и фармацевтическая композиция на их основе
|
|
CN102827073A
(zh)
|
2011-06-17 |
2012-12-19 |
安吉奥斯医药品有限公司 |
治疗活性组合物和它们的使用方法
|
|
WO2013014039A1
(fr)
|
2011-07-28 |
2013-01-31 |
Nerviano Medical Sciences S.R.L. |
Pyrimidinyl-pyrroles substitués alcynyle agissant comme inhibiteurs de kinase
|
|
WO2013016720A2
(fr)
|
2011-07-28 |
2013-01-31 |
Gerinda Therapeutics, Inc. |
Nouveaux dérivés biaryl-hétérocycliques substitués en tant qu'inhibiteurs de protéine kinase pour le traitement du cancer et d'autres maladies
|
|
KR20140047138A
(ko)
|
2011-08-04 |
2014-04-21 |
도쿠리츠교세이호진 고쿠리츠간켄큐센터 |
Kif5b 유전자와 ret 유전자와의 융합 유전자, 및 당해 융합 유전자를 표적으로 한 암 치료의 유효성을 판정하는 방법
|
|
WO2013028817A1
(fr)
|
2011-08-23 |
2013-02-28 |
Foundation Medicine , Inc. |
Molécules de fusion kif5b-ret inédites et leurs utilisations
|
|
AU2012341028C1
(en)
|
2011-09-02 |
2017-10-19 |
Mount Sinai School Of Medicine |
Substituted pyrazolo[3,4-D]pyrimidines and uses thereof
|
|
WO2013036232A2
(fr)
|
2011-09-08 |
2013-03-14 |
Deciphera Pharmaceuticals, Llc |
Méthodes et compositions pouvant être utilisées en vue du traitement de maladies myéloprolifératives et d'autres maladies prolifératives
|
|
US8846712B2
(en)
*
|
2011-09-12 |
2014-09-30 |
Sanofi |
6-(4-hydroxy-phenyl)-3-styryl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
|
|
WO2013042137A1
(fr)
|
2011-09-19 |
2013-03-28 |
Aurigene Discovery Technologies Limited |
Hétérocycles bicycliques convenant comme inhibiteurs de l'irak4
|
|
CN102408411B
(zh)
|
2011-09-19 |
2014-10-22 |
北京康辰药业股份有限公司 |
一种含喹啉基的羟肟酸类化合物及其制备方法、以及含有该化合物的药物组合物及其应用
|
|
JP6063945B2
(ja)
|
2011-10-07 |
2017-01-18 |
ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ |
キナーゼ阻害剤としての4−アルキル置換3,4−ジヒドロピロロ[1,2−a]ピラジン−1(2H)−オン誘導体
|
|
EP2788351B1
(fr)
|
2011-10-07 |
2017-06-28 |
Nerviano Medical Sciences S.r.l. |
DÉRIVÉS DE LA 3,4-DIHYDROPYRROLO[1,2-a]PYRAZIN-1(2H)-ONE EN TANT QU'INHIBITEURS DE KINASES
|
|
BR112014011465A2
(pt)
|
2011-11-14 |
2017-05-09 |
Tesaro Inc |
modulação de determinadas quinases de tirosina
|
|
CN104080907A
(zh)
|
2011-11-30 |
2014-10-01 |
日本国立癌症研究中心 |
诱导恶性干细胞
|
|
US8377946B1
(en)
|
2011-12-30 |
2013-02-19 |
Pharmacyclics, Inc. |
Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors
|
|
ES2751608T3
(es)
|
2011-12-30 |
2020-04-01 |
Hanmi Pharm Ind Co Ltd |
Derivados de tieno[3,2-d]pirimidina que tienen actividad inhibitoria para las proteínas quinasas
|
|
JP2015109806A
(ja)
|
2012-03-22 |
2015-06-18 |
アステラス製薬株式会社 |
新規ret融合体の検出法
|
|
US9242977B2
(en)
|
2012-04-26 |
2016-01-26 |
Ono Pharmaceutical Co., Ltd. |
Trk-inhibiting compound
|
|
US20150099721A1
(en)
|
2012-05-10 |
2015-04-09 |
Synta Pharmaceuticals Corp. |
Treating cancer with hsp90 inhibitory compounds
|
|
PL3333166T3
(pl)
|
2012-05-23 |
2020-09-07 |
Nerviano Medical Sciences S.R.L. |
Proces otrzymywania n-[5-(3,5-difluorobenzylo)-1h-indazol-3-ilo]- 4-(4-metylopiperazyn-1-ylo)-2-(tetrahydropiran- 4-yloamino)benzamidu
|
|
TWI585088B
(zh)
|
2012-06-04 |
2017-06-01 |
第一三共股份有限公司 |
作爲激酶抑制劑之咪唑并[1,2-b]嗒衍生物
|
|
NZ703495A
(en)
|
2012-07-11 |
2018-02-23 |
Blueprint Medicines Corp |
Inhibitors of the fibroblast growth factor receptor
|
|
JPWO2014017491A1
(ja)
|
2012-07-26 |
2016-07-11 |
国立研究開発法人国立がん研究センター |
Cep55遺伝子とret遺伝子との融合遺伝子
|
|
WO2014019908A2
(fr)
|
2012-08-02 |
2014-02-06 |
Nerviano Medical Sciences S.R.L. |
Pyrroles substitués actifs en tant qu'inhibiteurs de kinase
|
|
JP6513567B2
(ja)
|
2012-09-07 |
2019-05-15 |
エクセリクシス, インク. |
肺腺癌の治療で使用するためのmet、vegfr、およびretの阻害剤
|
|
TWI603733B
(zh)
|
2012-09-25 |
2017-11-01 |
中外製藥股份有限公司 |
Ret抑制劑
|
|
ES2755772T3
(es)
|
2012-11-07 |
2020-04-23 |
Nerviano Medical Sciences Srl |
Pirimidinil y piridinilpirrolopiridinonas sustituidas, proceso para su preparación y su uso como inhibidores de cinasas
|
|
EP2917183A1
(fr)
|
2012-11-12 |
2015-09-16 |
Ignyta, Inc. |
Dérivés de bendamustine et leurs procédés d'utilisation
|
|
US9809578B2
(en)
|
2012-11-13 |
2017-11-07 |
Array Biopharma Inc. |
Pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trkA kinase inhibitors
|
|
US9828360B2
(en)
|
2012-11-13 |
2017-11-28 |
Array Biopharma Inc. |
Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
|
|
US9896435B2
(en)
|
2012-11-13 |
2018-02-20 |
Array Biopharma Inc. |
N-pyrrolidinyl,N′-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
|
|
WO2014078322A1
(fr)
|
2012-11-13 |
2014-05-22 |
Array Biopharma Inc. |
Composés de thiazolyl-urée, oxazolyl-urée, thio-urée, guanidine et cyanoguanidine en tant qu'inhibiteurs de la kinase trka
|
|
WO2014078325A1
(fr)
|
2012-11-13 |
2014-05-22 |
Array Biopharma Inc. |
Composés de n-aryle monocycliques, n'-pyrazolyl-urée, thiourée, guanidine et cyanoguanidine utiles comme inhibiteurs de trka kinase
|
|
US9969694B2
(en)
|
2012-11-13 |
2018-05-15 |
Array Biopharma Inc. |
N-(arylalkyl)-N′-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
|
|
ME02879B
(fr)
|
2012-11-13 |
2018-04-20 |
Array Biopharma Inc |
Composes bicycliques a base d' uree, thiouree, guanidine ou cyanoguanidine utiles dans le traitement de la douleur
|
|
US9822118B2
(en)
|
2012-11-13 |
2017-11-21 |
Array Biopharma Inc. |
Bicyclic heteroaryl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
|
|
WO2014078328A1
(fr)
|
2012-11-13 |
2014-05-22 |
Array Biopharma Inc. |
Composés de n-pyrrolidinyle, n'-pyrazolyl-urée, thio-urée,guanidine et cyanoguanidine en tant qu'inhibiteurs de la kinase trka
|
|
WO2014078372A1
(fr)
|
2012-11-13 |
2014-05-22 |
Array Biopharma Inc. |
Composés de n-pyrrolidinyle urée, thio-urée,guanidine et cyanoguanidine en tant qu'inhibiteurs de la kinase trka
|
|
HK1213189A1
(zh)
|
2012-11-29 |
2016-06-30 |
耶达研究及发展有限公司 |
预防肿瘤转移、癌症治疗和预後及鉴定为推定转移抑制剂的试剂的方法
|
|
CN103848785B
(zh)
|
2012-12-04 |
2016-07-13 |
上海医药集团股份有限公司 |
一类氘代3-氰基喹啉类化合物、其药用组合物、制备方法及其用途
|
|
FR3000493A1
(fr)
|
2012-12-28 |
2014-07-04 |
Oribase Pharma |
Nouveaux inhibiteurs de proteines kinases
|
|
MX386542B
(es)
|
2012-12-28 |
2025-03-18 |
Crystalgenomics Inc |
Derivados de la 2,3-dihidro-isoindol-1-ona, como inhibidores de la btk quinasa y composiciones farmacéuticas que los incluyen.
|
|
FR3000492B1
(fr)
|
2012-12-28 |
2015-09-11 |
Oribase Pharma |
Nouveaux derives azaindole en tant qu'inhibiteurs multikinases
|
|
FR3000494B1
(fr)
|
2012-12-28 |
2015-08-21 |
Oribase Pharma |
Nouveaux derives d'azaindoles en tant qu'inhibiteurs de proteines kinases
|
|
TW201443037A
(zh)
*
|
2013-01-09 |
2014-11-16 |
Gilead Sciences Inc |
治療用化合物
|
|
SG11201506514QA
(en)
|
2013-02-19 |
2015-09-29 |
Ono Pharmaceutical Co |
Trk-INHIBITING COMPOUND
|
|
US20160151461A1
(en)
|
2013-03-14 |
2016-06-02 |
The Trustees Of The University Of Pennsylvania |
Cardio-Metabolic and Vascular Effects of GLP-1 Metabolites
|
|
EP3521284B1
(fr)
*
|
2013-03-15 |
2020-12-02 |
The Trustees of Columbia University in the City of New York |
Composés de pyrazine comme modulateurs de map kinase et leurs utilisations
|
|
EP2970191B1
(fr)
|
2013-03-15 |
2016-12-21 |
GlaxoSmithKline Intellectual Property Development Limited |
Dérivés des pyridines comme inhibiteurs de la kinase arrangé pendant transfection (ret)
|
|
US8937071B2
(en)
|
2013-03-15 |
2015-01-20 |
Glaxosmithkline Intellectual Property Development Limited |
Compounds as rearranged during transfection (RET) inhibitors
|
|
EP2970231A1
(fr)
|
2013-03-15 |
2016-01-20 |
Blueprint Medicines Corporation |
Dérivés de pipérazine et leur utilisation comme modulateurs de kit
|
|
JP6397897B2
(ja)
|
2013-05-14 |
2018-09-26 |
ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ |
ピロロ[2,3−d]ピリミジン誘導体、その製造方法及びキナーゼ阻害剤としてのその使用
|
|
MX2015015966A
(es)
|
2013-05-30 |
2016-04-13 |
Plexxikon Inc |
Compuestos para la modulacion de cinasas e indicaciones para los mismos.
|
|
WO2015017528A1
(fr)
|
2013-07-30 |
2015-02-05 |
Blueprint Medicines Corporation |
Fusions de pik3c2g
|
|
WO2015017533A1
(fr)
|
2013-07-30 |
2015-02-05 |
Blueprint Medicines Corporation |
Fusions de ntrk2
|
|
CN105658814A
(zh)
|
2013-08-20 |
2016-06-08 |
日本国立癌症研究中心 |
在肺癌中检测出的新型融合基因
|
|
RU2016111675A
(ru)
|
2013-08-30 |
2017-10-04 |
Эмбит Байосайенсиз Корпорейшн |
Соединения биарилацетамида и способы их применения
|
|
US9200002B2
(en)
|
2013-10-17 |
2015-12-01 |
Blueprint Medicines Corporation |
Compositions useful for treating disorders related to KIT
|
|
US9334263B2
(en)
|
2013-10-17 |
2016-05-10 |
Blueprint Medicines Corporation |
Compositions useful for treating disorders related to kit
|
|
HUE059037T2
(hu)
|
2013-10-25 |
2022-10-28 |
Blueprint Medicines Corp |
Fibroblaszt növekedési faktor receptor gátlók
|
|
GB201321146D0
(en)
|
2013-11-29 |
2014-01-15 |
Cancer Rec Tech Ltd |
Quinazoline compounds
|
|
WO2015082887A2
(fr)
|
2013-12-02 |
2015-06-11 |
Bergenbio As |
Utilisation d'inhibiteurs de kinases
|
|
WO2015108992A1
(fr)
|
2014-01-15 |
2015-07-23 |
Blueprint Medicines Corporation |
Composés hétérobicycliques et leur utilisation en tant qu'inhibiteurs du récepteur fgfr4
|
|
DK3636649T3
(da)
|
2014-01-24 |
2024-05-21 |
Turning Point Therapeutics Inc |
Diarylmakrocykler som modulatorer af proteinkinaser
|
|
WO2015123639A1
(fr)
|
2014-02-14 |
2015-08-20 |
Exelixis, Inc. |
Formes solides cristallines du n-{4-[(6,7-diméthoxyquinolin-4-yl)oxy]phényl}-n'-(4-fluorophényl)cyclopropane-1,1-dicarboxamide, procédés de préparation, et méthodes d'utilisation
|
|
TWI672141B
(zh)
|
2014-02-20 |
2019-09-21 |
美商醫科泰生技 |
投予ros1突變癌細胞之分子
|
|
US20170044622A1
(en)
|
2014-04-18 |
2017-02-16 |
Blueprint Medicines Corporation |
Pik3ca fusions
|
|
WO2015161277A1
(fr)
|
2014-04-18 |
2015-10-22 |
Blueprint Medicines Corporation |
Fusions de met
|
|
HRP20191593T1
(hr)
|
2014-05-15 |
2019-11-29 |
Array Biopharma Inc |
1-((3s,4r)-4-(3-fluorfenil)-1-(2-metoksietil)pirolidin-3-il)-3-(4-metil-3-(2-metilpirimidin-5-il)-1-fenil-1h-pirazol-5-il)urea kao inhibitor trka kinaze
|
|
EP3155118A1
(fr)
|
2014-06-10 |
2017-04-19 |
Blueprint Medicines Corporation |
Fusions de pkn1
|
|
EP3155131B1
(fr)
|
2014-06-10 |
2020-02-12 |
Blueprint Medicines Corporation |
Fusions de raf1
|
|
HUE046008T2
(hu)
|
2014-07-17 |
2020-02-28 |
Sunshine Lake Pharma Co Ltd |
I-(5-terc-butil)-izoxazol-3-il)-3-(4-((feniI)-etinil)-fenil)-kabamid származékok, valamint az ezekkel rokon vegyületek FLT-3 inhibitorokként rák kezelésére
|
|
EP3169809B1
(fr)
|
2014-07-17 |
2020-04-29 |
Blueprint Medicines Corporation |
Fusions de prkc
|
|
EP3169808B1
(fr)
|
2014-07-17 |
2019-05-22 |
Blueprint Medicines Corporation |
Fusion trio:tert dans le cancer
|
|
WO2016011141A1
(fr)
|
2014-07-17 |
2016-01-21 |
Blueprint Medicines Corporation |
Fusions de fgr
|
|
US9688680B2
(en)
|
2014-08-04 |
2017-06-27 |
Blueprint Medicines Corporation |
Compositions useful for treating disorders related to kit
|
|
AU2015304438B2
(en)
|
2014-08-18 |
2019-06-20 |
Ono Pharmaceutical Co., Ltd. |
Acid-addition salt of Trk-inhibiting compound
|
|
EP3191480A1
(fr)
|
2014-09-08 |
2017-07-19 |
GlaxoSmithKline Intellectual Property Development Limited |
Formes cristallines de 2-(4-(4-éthoxy-6-oxo-1,6-dihydropyridin-3-yl)-2-fluorophényl)-n-(5-(1,1,1-trifluoro-2-méthylpropan-2-yl)isoxazol-3-yl)acétamide
|
|
WO2016037578A1
(fr)
|
2014-09-10 |
2016-03-17 |
Glaxosmithkline Intellectual Property Development Limited |
Nouveaux composés utilisés comme inhibiteurs de la kinase réarrangée au cours de la transfection (ret)
|
|
CA2960768A1
(fr)
|
2014-09-10 |
2016-03-17 |
Glaxosmithkline Intellectual Property Development Limited |
Derives de pyridone a titre d'inhibiteurs de la kinase rearrangee au cours de la transfection (ret)
|
|
TWI538914B
(zh)
|
2014-10-03 |
2016-06-21 |
國立交通大學 |
蛋白質激酶之選擇性抑制劑、其醫藥組成物及其用途
|
|
PL3218378T3
(pl)
*
|
2014-11-14 |
2020-10-19 |
Nerviano Medical Sciences S.R.L. |
Pochodne 6-amino-7-bicyklo-7-deazapuryny jako inhibitory kinaz białkowych
|
|
TWI767858B
(zh)
|
2014-11-16 |
2022-06-11 |
美商亞雷生物製藥股份有限公司 |
(S)-N-(5-((R)-2-(2,5-二氟苯基)-吡咯啶-1-基)-吡唑并[1,5-a]嘧啶-3-基)-3-羥基吡咯啶-1-甲醯胺硫酸氫鹽結晶型
|
|
US20170356052A1
(en)
|
2014-11-18 |
2017-12-14 |
Blueprint Medicines Corporation |
Prkacb fusions
|
|
US10336707B2
(en)
|
2014-12-16 |
2019-07-02 |
Eudendron S.R.L. |
Heterocyclic derivatives modulating activity of certain protein kinases
|
|
US10202365B2
(en)
|
2015-02-06 |
2019-02-12 |
Blueprint Medicines Corporation |
2-(pyridin-3-yl)-pyrimidine derivatives as RET inhibitors
|
|
KR101675984B1
(ko)
|
2015-02-23 |
2016-11-14 |
한양대학교 에리카산학협력단 |
티에노디아제핀 유도체 또는 이의 약학적으로 허용가능한 염, 및 이를 유효성분으로 포함하는 약학적 조성물
|
|
EP3265079A4
(fr)
|
2015-03-03 |
2019-01-02 |
Caris MPI, Inc. |
Profilage moléculaire du cancer
|
|
CN108137593B
(zh)
|
2015-04-21 |
2021-01-05 |
上海交通大学医学院附属瑞金医院 |
蛋白激酶抑制剂的制备和用途
|
|
GB201512365D0
(en)
|
2015-07-15 |
2015-08-19 |
King S College London |
Novel therapy
|
|
WO2017011776A1
(fr)
|
2015-07-16 |
2017-01-19 |
Array Biopharma, Inc. |
Composés substitués de pyrazolo[1,5-a]pyridines comme inhibiteurs de la kinase ret
|
|
EP3120851A1
(fr)
|
2015-07-21 |
2017-01-25 |
Pangaea Biotech S.L. |
4-amino-6- (2,6-dichlorophényl) -8-methyl-2-(phénylamino) -pyrido[2,3-d]pyrimidin-7-(8h)-one pour le traitement de cancers solides
|
|
KR101766194B1
(ko)
|
2015-08-07 |
2017-08-10 |
한국과학기술연구원 |
RET 키나아제 저해제인 신규 3-(이속사졸-3-일)-피라졸로[3,4-d]피리미딘-4-아민 화합물
|
|
WO2017027883A1
(fr)
|
2015-08-13 |
2017-02-16 |
San Diego State University Research Foundation |
Atropisomérisme pour une sélectivité accrue des inhibiteurs de kinase
|
|
MA41559A
(fr)
|
2015-09-08 |
2017-12-26 |
Taiho Pharmaceutical Co Ltd |
Composé de pyrimidine condensé ou un sel de celui-ci
|
|
WO2017049462A1
(fr)
|
2015-09-22 |
2017-03-30 |
合肥中科普瑞昇生物医药科技有限公司 |
Nouvel inhibiteur de la kinase flt3 et ses utilisations
|
|
CN105255927B
(zh)
|
2015-09-30 |
2018-07-27 |
温州医科大学附属第一医院 |
一种kiaa1217-ret融合基因
|
|
MX384884B
(es)
|
2015-11-02 |
2025-03-14 |
Blueprint Medicines Corp |
Inhibidores de ret.
|
|
US20190002988A1
(en)
|
2015-12-08 |
2019-01-03 |
Boehringer Ingelheim International Gmbh |
Method of using a ret fusion gene as a biomarker to select non small cell lung cancer (nsclc) and thyroid cancer patients for a cancer treatment
|
|
JP6871869B2
(ja)
|
2016-01-15 |
2021-05-19 |
公益財団法人がん研究会 |
新規融合体及びその検出法
|
|
TWI620748B
(zh)
|
2016-02-05 |
2018-04-11 |
National Health Research Institutes |
氨基噻唑化合物及其用途
|
|
ES2775751T3
(es)
|
2016-02-23 |
2020-07-28 |
Taiho Pharmaceutical Co Ltd |
Nuevo compuesto de pirimidina condensada o sal del mismo
|
|
WO2017145050A1
(fr)
|
2016-02-23 |
2017-08-31 |
Glaxosmithkline Intellectual Property Development Limited |
Dérivé de pyridylpyridone utile comme inhibiteur de la kinase ret dans le traitement du sci et du cancer
|
|
WO2017161269A1
(fr)
|
2016-03-17 |
2017-09-21 |
Blueprint Medicines Corporation |
Inhibiteurs des tyrosine kinases du récepteur ret
|
|
US10045991B2
(en)
|
2016-04-04 |
2018-08-14 |
Loxo Oncology, Inc. |
Methods of treating pediatric cancers
|
|
CA3020778A1
(fr)
|
2016-04-15 |
2017-10-19 |
Cancer Research Technology Limited |
Composes heterocycliques utilises en tant qu'inhibiteurs de kinase ret
|
|
SMT202200348T1
(it)
*
|
2016-04-15 |
2022-11-18 |
Cancer Research Tech Ltd |
Composti eterociclici come inibitori della chinasi ret
|
|
TWI704148B
(zh)
|
2016-10-10 |
2020-09-11 |
美商亞雷生物製藥股份有限公司 |
作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物
|
|
JOP20190077A1
(ar)
|
2016-10-10 |
2019-04-09 |
Array Biopharma Inc |
مركبات بيرازولو [1، 5-a]بيريدين بها استبدال كمثبطات كيناز ret
|