|
US4783443A
(en)
|
1986-03-03 |
1988-11-08 |
The University Of Chicago |
Amino acyl cephalosporin derivatives
|
|
US5844092A
(en)
|
1994-03-18 |
1998-12-01 |
Genentech, Inc. |
Human TRK receptors and neurotrophic factor inhibitors
|
|
US5877016A
(en)
|
1994-03-18 |
1999-03-02 |
Genentech, Inc. |
Human trk receptors and neurotrophic factor inhibitors
|
|
DE69736428T2
(de)
|
1996-05-08 |
2007-08-30 |
Biogen Idec Ma Inc., Cambridge |
RET-LIGAND 3 (RetL3), UM NEURALES UND RENALES WACHSTUM ZU STIMULIEREN
|
|
US6677135B1
(en)
|
1996-05-08 |
2004-01-13 |
Biogen, Inc. |
Ret ligand (RetL) for stimulating neutral and renal growth
|
|
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
|
|
WO2001016169A2
(fr)
|
1999-09-01 |
2001-03-08 |
Biogen, Inc. |
COMPOSITIONS A BASE DE LIGAND 5 (RetL5) ET SES UTILISATIONS
|
|
FI20000403A0
(fi)
|
2000-02-22 |
2000-02-22 |
Hannu Sariola |
GDNF perhesukuisten yhdisteiden käyttö kivessyövän hoitoon tarkoitettujen tuotteiden valmistamiseksi
|
|
IL153375A0
(en)
|
2000-06-22 |
2003-07-06 |
Genentech Inc |
Agonist anti-trk-c monoclonal antibodies
|
|
AU2002334355A1
(en)
|
2001-09-06 |
2003-03-18 |
Prochon Biotech Ltd. |
Protein tyrosine kinase inhibitors
|
|
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
|
|
US20060116381A1
(en)
|
2002-07-24 |
2006-06-01 |
Fagin James A |
4-4(methylpiperazin-1-ylmethyl)-n-[4-methyl-3-(pyridin-3-yl)pyrimidin-2-ylamino)phenyl]-ben-zamide for treating mutated-ret kinase associated diseases
|
|
DE602004021472D1
(en)
|
2003-02-20 |
2009-07-23 |
Smithkline Beecham Corp |
Pyrimiidinverbindungen
|
|
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
|
|
JP2007511575A
(ja)
|
2003-11-21 |
2007-05-10 |
ノバルティス アクチエンゲゼルシャフト |
タンパク質キナーゼ阻害剤としての1h−イミダゾキノリン誘導体
|
|
TW200529849A
(en)
|
2003-11-28 |
2005-09-16 |
Novartis Ag |
Diaryl urea derivatives in the treatment of protein kinase dependent diseases
|
|
PL1696920T3
(pl)
|
2003-12-19 |
2015-03-31 |
Plexxikon Inc |
Związki i sposoby opracowywania modulatorów 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
|
|
US20050222171A1
(en)
|
2004-01-22 |
2005-10-06 |
Guido Bold |
Organic compounds
|
|
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
|
|
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
|
|
EP1874731A4
(fr)
|
2005-04-15 |
2009-08-05 |
Cylene Pharmaceuticals Inc |
Analogues de quinobenzoxazines et procedes d'utilisation de ceux-ci
|
|
JP2008540622A
(ja)
|
2005-05-16 |
2008-11-20 |
アストラゼネカ アクチボラグ |
化合物
|
|
US20100047777A1
(en)
|
2005-05-26 |
2010-02-25 |
The Johns Hopkins University |
Methods for identifying mutations in coding and non-coding dna
|
|
EP1896462A2
(fr)
|
2005-05-31 |
2008-03-12 |
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
|
|
WO2006130673A1
(fr)
|
2005-05-31 |
2006-12-07 |
Janssen Pharmaceutica, N.V. |
3-benzoimidazolyl-pyrazolopyridines utilisees pour traiter des troubles dont la mediation est assuree par des kinases
|
|
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.
|
|
DK2395004T3
(en)
*
|
2005-06-22 |
2016-03-21 |
Plexxikon Inc |
Pyrrolo [2,3-b] pyridine derivatives as protein kinase inhibitors
|
|
GB0515026D0
(en)
|
2005-07-21 |
2005-08-31 |
Novartis Ag |
Organic compounds
|
|
HRP20140218T4
(hr)
|
2005-08-25 |
2017-06-16 |
Creabilis Therapeutics S.P.A. |
Polimerni konjugati k-252a i njihovi derivati
|
|
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
|
|
WO2007065664A2
(fr)
|
2005-12-08 |
2007-06-14 |
Novartis Ag |
Acides pyrazolo[1,5-a]pyridine-3-carboxyliques utilises en tant qu’inhibiteurs de la ephb et vegfr2 kinase
|
|
WO2007077435A1
(fr)
|
2005-12-30 |
2007-07-12 |
Astex Therapeutics Limited |
Composes pharmaceutiques
|
|
WO2007087245A2
(fr)
|
2006-01-24 |
2007-08-02 |
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
|
|
BRPI0710181A2
(pt)
|
2006-03-16 |
2011-08-09 |
Novartis Ag |
compostos orgánicos
|
|
WO2007109120A2
(fr)
|
2006-03-17 |
2007-09-27 |
Ambit Biosciences Corporation |
Composés d'imidazolothiazole pour le traitement de maladies
|
|
UA94097C2
(ru)
|
2006-03-27 |
2011-04-11 |
НЕРВИАНО МЕДИКАЛ САЙЕНСИЗ С.р.л. |
Пиридил- и пиримидинилзамещенные производной пиррола, тиофена и фурана как ингибиторы киназ
|
|
MX2008014618A
(es)
|
2006-05-15 |
2008-11-28 |
Irm Llc |
Composiciones y metodos para inhibidores de cinasas del receptor fgf.
|
|
WO2007136103A1
(fr)
|
2006-05-18 |
2007-11-29 |
Eisai R & D Management Co., Ltd. |
Agent antitumoral destiné au cancer de la thyroïde
|
|
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
|
|
EP2067039A2
(fr)
|
2006-09-12 |
2009-06-10 |
Novartis Forschungsstiftung, Zweigniederlassung Friedrich Miescher Institute for Biomedical Research |
Traitement du cancer non neuroendocrinien
|
|
WO2008033562A2
(fr)
|
2006-09-15 |
2008-03-20 |
Xcovery, Inc. |
Composés inhibiteurs de kinases
|
|
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
|
|
LT2848610T
(lt)
|
2006-11-15 |
2017-11-10 |
Ym Biosciences Australia Pty Ltd |
Kinazės aktyvumo inhibitoriai
|
|
PE20081581A1
(es)
|
2006-12-21 |
2008-11-12 |
Plexxikon Inc |
COMPUESTOS PIRROLO[2,3-b]PIRIDINAS COMO MODULADORES DE QUINASA
|
|
WO2008080015A2
(fr)
|
2006-12-21 |
2008-07-03 |
Plexxikon, Inc. |
Composés et procédés pour la modulation des kinases, et indications correspondantes
|
|
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
|
|
JP2010516692A
(ja)
|
2007-01-19 |
2010-05-20 |
バイエル・ヘルスケア・エルエルシー |
化学療法剤に対し抵抗性を有する癌の処置
|
|
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
|
|
EP2152688A1
(fr)
|
2007-05-04 |
2010-02-17 |
Irm Llc |
Composés et compositions utiles en tant qu'inhibiteurs des kinases c-kit et pdgfr
|
|
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
|
|
WO2009003136A1
(fr)
|
2007-06-26 |
2008-12-31 |
Rigel Pharmaceuticals, Inc. |
Pyrimidine-2,4-diamines substituées destinées au traitement de troubles de prolifération cellulaire
|
|
BRPI0814818A2
(pt)
|
2007-07-09 |
2019-09-10 |
Astrazeneca Ab |
composto, uso de um composto, métodos para produzir um efeito anti-proliferativo e um efeito inibitório de mtor quinase em uma animal de sangue quente, método para tratar doenças, e, composição farmacêutica
|
|
WO2009012262A1
(fr)
|
2007-07-16 |
2009-01-22 |
The Regents Of The University Of California |
Composés modulant les protéine kinases et leurs procédés de préparation et d'utilisation
|
|
US20100190777A1
(en)
|
2007-07-17 |
2010-07-29 |
Plexxikon Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
|
WO2009014637A2
(fr)
|
2007-07-19 |
2009-01-29 |
Schering Corporation |
Composés hétérocycliques d'amide en tant qu'inhibiteurs de protéine kinase
|
|
US8299057B2
(en)
|
2007-07-20 |
2012-10-30 |
Nerviano Medical Sciences S.R.L. |
Substituted indazole derivatives active as kinase inhibitors
|
|
WO2009017838A2
(fr)
|
2007-08-01 |
2009-02-05 |
Exelixis, Inc. |
Combinaisons d'inhibiteurs jak-2 et d'autres agents
|
|
JP5703466B2
(ja)
|
2007-08-07 |
2015-04-22 |
パーデュー・リサーチ・ファウンデーションPurdue Research Foundation |
キナーゼ阻害薬およびその使用
|
|
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
|
|
EA201000603A1
(ru)
|
2007-10-23 |
2010-12-30 |
Новартис Аг |
ПРИМЕНЕНИЕ АНТИТЕЛ К TrkB ДЛЯ ЛЕЧЕНИЯ РЕСПИРАТОРНЫХ НАРУШЕНИЙ
|
|
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
|
|
CL2009000090A1
(es)
|
2008-01-17 |
2009-07-24 |
Irm Llc |
Anticuerpo que se une al receptor de tirosina quinasa b (trkb); composicion que comprende el anticuerpo; metodo para reducir los niveles de glucosa en la sangre y/o el peso corporal en un individuo.
|
|
US20090227556A1
(en)
|
2008-01-31 |
2009-09-10 |
Eisai R&D Management Co., Ltd. |
Receptor tyrosine kinase inhibitors comprising pyridine and pyrimidine derivatives
|
|
TW200942537A
(en)
|
2008-02-01 |
2009-10-16 |
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)
|
|
DK2262807T3
(en)
|
2008-03-19 |
2015-11-30 |
Chembridge Corp |
NOVEL tyrosine kinase inhibitors
|
|
WO2009118411A2
(fr)
|
2008-03-28 |
2009-10-01 |
Nerviano Medical Sciences S.R.L. |
Dérivés actifs de 3,4-dihydro-2h-pyrazino[1,2-a]indol-1-one en tant qu’inhibiteurs de kinase, procédé pour leur préparation et compositions pharmaceutiques les contenant
|
|
PE20091846A1
(es)
|
2008-05-19 |
2009-12-16 |
Plexxikon Inc |
DERIVADOS DE PIRROLO[2,3-d]-PIRIMIDINA COMO MODULADORES DE CINASAS
|
|
US8158636B2
(en)
|
2008-05-19 |
2012-04-17 |
Plexxikon Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
|
JP5351254B2
(ja)
|
2008-05-23 |
2013-11-27 |
ノバルティス アーゲー |
キノキサリン−およびキノリン−カルボキシアミド誘導体
|
|
WO2009155052A1
(fr)
*
|
2008-05-28 |
2009-12-23 |
Wyeth |
Composés de 1h-pyrrolo[2,3-b]pyridine substituée en position 3 et composés de 1h-pyrrolo[3,2-b]pyridine substituée en position 3, leur utilisation en tant qu’inhibiteurs de kinase mtor et pi3 kinase, et leur synthèses
|
|
US8119637B2
(en)
|
2008-06-10 |
2012-02-21 |
Plexxikon Inc. |
Substituted pyrrolo[2,3-b]pyrazines and methods for kinase modulation, and indications therefor
|
|
EP2303890A4
(fr)
|
2008-06-19 |
2012-04-11 |
Progenics Pharm Inc |
Inhibiteurs de phosphatidylinositol 3 kinase
|
|
WO2010006432A1
(fr)
|
2008-07-14 |
2010-01-21 |
Queen's University At Kingston |
Compositions pharmaceutiques contenant des inhibiteurs de ret et procédés de traitement du cancer
|
|
WO2010012733A1
(fr)
|
2008-07-29 |
2010-02-04 |
Nerviano Medical Sciences S.R.L. |
Utilisation d'un inhibiteur de cdk pour le traitement d'un gliome
|
|
BRPI0917178A2
(pt)
|
2008-09-01 |
2015-11-10 |
Sharp Kk |
painel eletroluminescente orgânico, visor eletroluminescente orgânico e métodos de produção dos mesmos
|
|
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
|
|
RS53350B
(sr)
|
2008-09-22 |
2014-10-31 |
Array Biopharma, Inc. |
Supstituisana jedinjenja imidazo[1,2-b]piridazina kao inhibitori trk kinaze
|
|
EP2331530B8
(fr)
|
2008-09-26 |
2013-12-25 |
National Health Research Institutes |
Composés multicycliques fusionnés en tant qu inhibiteurs des protéines kinases
|
|
HRP20140309T1
(hr)
|
2008-10-22 |
2014-05-09 |
Array Biopharma, Inc. |
SUPSTITUIRANI SPOJEVI PIRAZOLO[1,5-a]PIRIMIDINA KAO INHIBITORI TRK KINAZE
|
|
JP5686736B2
(ja)
|
2008-11-06 |
2015-03-18 |
アムビト ビオスシエンセス コルポラチオン |
プロテインキナーゼモジュレーターとしてのイミダゾロチアゾール化合物
|
|
WO2010058006A1
(fr)
|
2008-11-24 |
2010-05-27 |
Nerviano Medical Sciences S.R.L. |
Inhibiteur de cdk (kinase cycline-dépendante) pour le traitement d'un mésothéliome
|
|
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
|
|
JP5364159B2
(ja)
|
2009-05-08 |
2013-12-11 |
アステラス製薬株式会社 |
ジアミノへテロ環カルボキサミド化合物
|
|
EP2440058A4
(fr)
|
2009-06-12 |
2012-11-21 |
Dana Farber Cancer Inst Inc |
Composés hétérocycliques fondus et leurs utilisations
|
|
WO2010145998A1
(fr)
|
2009-06-15 |
2010-12-23 |
Nerviano Medical Sciences S.R.L. |
Dérivés de pyrimidinylpyrrolopyridinone substitués, procédé pour leur 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
|
|
MY162604A
(en)
|
2009-08-17 |
2017-06-30 |
Intellikine Llc |
Heterocyclic compounds and uses thereof
|
|
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
|
|
MX2012004846A
(es)
|
2009-10-29 |
2012-10-05 |
Genosco |
Inhibidores de cinasa.
|
|
US8629132B2
(en)
|
2009-11-13 |
2014-01-14 |
Genosco |
Kinase inhibitors
|
|
KR101094446B1
(ko)
|
2009-11-19 |
2011-12-15 |
한국과학기술연구원 |
단백질 키나아제 저해활성을 가지는 2,4,7-치환된 티에노[3,2-d]피리미딘 화합물
|
|
EP2937345B1
(fr)
|
2009-12-29 |
2018-03-21 |
Dana-Farber Cancer Institute, Inc. |
Inhibiteurs de la kinase raf de type ii
|
|
EP2528918B1
(fr)
|
2010-01-29 |
2014-09-10 |
Nerviano Medical Sciences S.r.l. |
Derives de 6,7-dihydroimidazo[1,5-a]pyrazin-8(5h)-one en tant que modulateurs de proteine kinase
|
|
KR101347303B1
(ko)
|
2010-01-29 |
2014-01-06 |
한미사이언스 주식회사 |
단백질 키나아제 저해활성을 갖는 티에노[3,2-d]피리미딘 유도체
|
|
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
|
|
KR102015402B1
(ko)
|
2010-05-20 |
2019-08-28 |
어레이 바이오파마 인크. |
Trk 키나제 저해제로서의 매크로시클릭 화합물
|
|
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
|
|
WO2012037155A2
(fr)
|
2010-09-13 |
2012-03-22 |
Gtx, Inc. |
Inhibiteurs des tyrosines kinases
|
|
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
|
|
RU2591191C2
(ru)
|
2011-01-26 |
2016-07-10 |
НЕРВИАНО МЕДИКАЛ САЙЕНСИЗ С.р.л. |
Трициклические пирроло производные, способ их получения и их применение в качестве ингибиторов киназы
|
|
US8916577B2
(en)
|
2011-01-26 |
2014-12-23 |
Nerviano Medical Sciences S.R.L. |
Tricyclic derivatives, process for their preparation and their use as kinase inhibitors
|
|
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
|
|
MA34948B1
(fr)
|
2011-02-07 |
2014-03-01 |
Plexxikon Inc |
Composes et procedes de modulation de kinase, et leurs indications
|
|
WO2012113774A1
(fr)
|
2011-02-24 |
2012-08-30 |
Nerviano Medical Sciences S.R.L. |
Dérivés de thiazolylphényl-benzènesulfonamido en tant qu'inhibiteurs de la kinase
|
|
AU2012220572A1
(en)
|
2011-02-25 |
2013-08-29 |
Irm Llc |
Compounds and compositions as trk inhibitors
|
|
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
|
|
EP3628665B1
(fr)
|
2011-04-01 |
2022-11-02 |
University of Utah Research Foundation |
Analogues substitués de n-phénylpyrimidine-2-amine en tant qu'inhibiteurs de la kinase axl
|
|
WO2012139930A1
(fr)
|
2011-04-11 |
2012-10-18 |
Nerviano Medical Sciences S.R.L. |
Dérivés pyrazolyl-pyrimidine en tant qu'inhibiteurs des kinases
|
|
BR112013026137B1
(pt)
|
2011-04-19 |
2020-12-01 |
Nerviano Medical Sciences S.R.L |
pirimidinil-pirróis substituídos ativos como inibidores da quinase
|
|
AR086042A1
(es)
*
|
2011-04-28 |
2013-11-13 |
Galapagos Nv |
Compuesto util para el tratamiento de enfermedades degenerativas e inflamatorias y composicion farmaceutica
|
|
CA2835478C
(fr)
|
2011-05-12 |
2019-02-05 |
Nerviano Medical Sciences S.R.L. |
Derives d'indazole substitues 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
|
|
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
|
|
EP2736514B1
(fr)
|
2011-07-28 |
2017-10-18 |
Nerviano Medical Sciences S.r.l. |
Pyrimidinyl-pyrroles substitués alcynyle agissant comme inhibiteurs de kinase
|
|
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
|
|
ES2704126T3
(es)
|
2011-08-23 |
2019-03-14 |
Found Medicine Inc |
Moléculas de fusión KIF5B-RET y usos de las mismas
|
|
MX370814B
(es)
|
2011-09-02 |
2020-01-08 |
Univ California |
Pirazolo[3,4-d]pirimidinas sustituidas y usos de las mismas.
|
|
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
|
|
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
|
|
WO2013042137A1
(fr)
|
2011-09-19 |
2013-03-28 |
Aurigene Discovery Technologies Limited |
Hétérocycles bicycliques convenant comme inhibiteurs de l'irak4
|
|
US9145418B2
(en)
|
2011-10-07 |
2015-09-29 |
Nerviano Medical Sciences S.R.L. |
Substituted 3,4-dihydropyrrolo[1,2-a]pyrazin-1(2H)-ones as protein kinase inhibitors
|
|
US9181258B2
(en)
|
2011-10-07 |
2015-11-10 |
Nerviano Medical Sciences S.R.L. |
Substituted 3,4-dihydropyrrolo[1,2-a]pyrazin-1(2H)-ones as protein kinase inhibitors
|
|
WO2013074518A1
(fr)
|
2011-11-14 |
2013-05-23 |
Tesaro, Inc. |
Modulation de certaines tyrosine kinases
|
|
KR20140100938A
(ko)
|
2011-11-30 |
2014-08-18 |
도쿠리츠교세이호진 고쿠리츠간켄큐센터 |
유도 악성 줄기세포
|
|
USRE47451E1
(en)
|
2011-12-30 |
2019-06-25 |
Hanmi Pharm. Co. Ltd. |
Thieno[3,2-D]pyrimidine derivatives having inhibitory activity for protein kinases
|
|
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
|
|
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
|
|
AU2013259267A1
(en)
|
2012-05-10 |
2014-11-06 |
Synta Pharmaceuticals Corp. |
Treating cancer with Hsp90 inhibitory compounds
|
|
KR102151963B1
(ko)
|
2012-05-23 |
2020-09-07 |
네르비아노 메디칼 사이언시스 에스.알.엘. |
N-[5-(3,5-디플루오로-벤질)-1h-인다졸-3-일]-4-(4-메틸-피페라진-1-일)-2-(테트라하이드로-피란-4-일아미노)-벤즈아미드의 제조 방법
|
|
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
|
|
US20150177246A1
(en)
|
2012-07-26 |
2015-06-25 |
Lsip, Llc |
Fusion gene of cep55 gene and ret gene
|
|
DK2880025T3
(en)
|
2012-08-02 |
2019-03-18 |
Nerviano Medical Sciences Srl |
SUBSTITUTED PYROLES ACTIVE AS KINase INHIBITORS
|
|
EP2892532B1
(fr)
|
2012-09-07 |
2019-02-13 |
Exelixis, Inc. |
Inhibiteurs de met, vegfr et ret pour l'utilisation dans le traitement de l'adénocarcinome pulmonaire
|
|
US10668075B2
(en)
|
2012-09-25 |
2020-06-02 |
Chugai Seiyaku Kabushiki Kaisha |
RET inhibitor
|
|
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
|
|
SG11201503560TA
(en)
|
2012-11-12 |
2015-06-29 |
Ignyta Inc |
Bendamustine derivatives and methods of using same
|
|
WO2014078378A1
(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
|
|
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
|
|
UA116455C2
(uk)
|
2012-11-13 |
2018-03-26 |
Еррей Біофарма Інк. |
Сполуки n-піролідинілсечовини, n'-піразолілсечовини, тіосечовини, гуанідину та ціаногуанідину як інгібітори кінази trka
|
|
US9790178B2
(en)
|
2012-11-13 |
2017-10-17 |
Array Biopharma Inc. |
Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
|
|
RU2664541C2
(ru)
|
2012-11-13 |
2018-08-20 |
Эррэй Биофарма Инк. |
Бициклические соединения мочевины, тиомочевины, гуанидина и цианогуанидина, пригодные для лечения боли
|
|
US9809578B2
(en)
|
2012-11-13 |
2017-11-07 |
Array Biopharma Inc. |
Pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trkA kinase inhibitors
|
|
US9981959B2
(en)
|
2012-11-13 |
2018-05-29 |
Array Biopharma Inc. |
Thiazolyl and oxazolyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
|
|
WO2014078331A1
(fr)
|
2012-11-13 |
2014-05-22 |
Array Biopharma Inc. |
Composés de n-(arylalkyle)-n'-pyrazolyle-urée, de thiourée, de guanidine et de cyanoguanidine en tant qu'inhibiteurs de la kinase trka
|
|
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
|
|
EP2925359A2
(fr)
|
2012-11-29 |
2015-10-07 |
Yeda Research and Development Co., Ltd. |
Méthodes de prévention d'une métastase tumorale, de traitement et de pronostic du cancer, et d'identification d'agents susceptibles de constituer des inhibiteurs de métastase
|
|
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
|
|
FR3000492B1
(fr)
|
2012-12-28 |
2015-09-11 |
Oribase Pharma |
Nouveaux derives azaindole en tant qu'inhibiteurs multikinases
|
|
ES2696700T3
(es)
|
2012-12-28 |
2019-01-17 |
Crystalgenomics Inc |
Derivado de 2,3-dihidro-isoindol-1-on como supresor de quinasa BTK y composición farmacéutica que incluye el mismo
|
|
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
|
|
BR122017003188A2
(pt)
|
2013-02-19 |
2019-09-10 |
Ono Pharmaceutical Co |
composto 1-{2-[4-(2-amino-5-cloro-3-piridinil)fenóxi]-5-pirimidinil}-3-[2-(metilsulfonil)-5-(trifluorometil)fenil]ureia, sal deste, composição farmacêutica compreendendo-os e uso destes para o tratamento de câncer
|
|
US20160151461A1
(en)
|
2013-03-14 |
2016-06-02 |
The Trustees Of The University Of Pennsylvania |
Cardio-Metabolic and Vascular Effects of GLP-1 Metabolites
|
|
MA38394B1
(fr)
|
2013-03-15 |
2018-04-30 |
Glaxosmithkline Ip Dev Ltd |
Dérivés pyridine utilisés comme inhibiteurs de la kinase réarrangée au cours de la transfection (ret)
|
|
UY35465A
(es)
|
2013-03-15 |
2014-10-31 |
Glaxosmithkline Ip Dev Ltd |
Nuevos compuestos como inhibidores de reorganizado durante la transfección (ret)
|
|
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
|
|
WO2014160521A1
(fr)
|
2013-03-15 |
2014-10-02 |
Blueprint Medicines Corporation |
Dérivés de pipérazine et leur utilisation comme modulateurs de kit
|
|
US9682083B2
(en)
|
2013-05-14 |
2017-06-20 |
Nerviano Medical Sciences S.R.L. |
Pyrrolo[2,3-D]pyrimidine derivatives, process for their preparation and their use as kinase inhibitors
|
|
AU2014274093B2
(en)
|
2013-05-30 |
2018-11-08 |
Plexxikon Inc. |
Compounds for kinase modulation, and indications therefor
|
|
WO2015017533A1
(fr)
|
2013-07-30 |
2015-02-05 |
Blueprint Medicines Corporation |
Fusions de ntrk2
|
|
EP3027654B1
(fr)
|
2013-07-30 |
2019-09-25 |
Blueprint Medicines Corporation |
Fusions de pik3c2g
|
|
US20150057335A1
(en)
|
2013-08-20 |
2015-02-26 |
National Cancer Center |
Novel fusion genes identified in lung cancer
|
|
CN105683182A
(zh)
|
2013-08-30 |
2016-06-15 |
埃姆比特生物科学公司 |
联芳基乙酰胺化合物及其使用方法
|
|
US9334263B2
(en)
|
2013-10-17 |
2016-05-10 |
Blueprint Medicines Corporation |
Compositions useful for treating disorders related to kit
|
|
LT3057969T
(lt)
|
2013-10-17 |
2018-07-10 |
Blueprint Medicines Corporation |
Kompozicijos, naudojamos gydyti sutrikimams, susijusiems su kit
|
|
DK3395814T3
(da)
|
2013-10-25 |
2022-07-04 |
Blueprint Medicines Corp |
Hæmmere af fibroblastvækstfaktorreceptoren
|
|
GB201321146D0
(en)
|
2013-11-29 |
2014-01-15 |
Cancer Rec Tech Ltd |
Quinazoline compounds
|
|
EP3076966A2
(fr)
|
2013-12-02 |
2016-10-12 |
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
|
|
AU2015209239C1
(en)
|
2014-01-24 |
2026-05-07 |
Turning Point Therapeutics, Inc. |
Diaryl macrocycles as modulators of protein kinases
|
|
AU2015218236B2
(en)
|
2014-02-14 |
2019-06-13 |
Exelixis, Inc. |
Crystalline solid forms of N-{4-[(6,7-dimethoxyquinolin-4-yl)oxy]phenyl}-N'-(4-fluorophenyl) cyclopropane-1, 1-dicarboxamide, processes for making, and methods of use
|
|
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
|
|
EP3132056B1
(fr)
|
2014-04-18 |
2021-11-24 |
Blueprint Medicines Corporation |
Fusions de pik3ca
|
|
EP3132054B1
(fr)
|
2014-04-18 |
2021-06-30 |
Blueprint Medicines Corporation |
Fusions de met
|
|
MY191956A
(en)
|
2014-05-15 |
2022-07-20 |
Array Biopharma Inc |
1-((3s,4r)-4-(3-fluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)-3-(4-methyl-3-(2-methylpyrimidin-5-yl)-1-phenyl-1h-pyrazol-5-yl)urea as a trka kinase inhibitor
|
|
US10378063B2
(en)
|
2014-06-10 |
2019-08-13 |
Blueprint Medicines Corporation |
RAF1 fusions
|
|
US10246750B2
(en)
|
2014-06-10 |
2019-04-02 |
Blueprint Medicines Corporation |
Method for detection of a TECR:PKN1 or an ANXA4:PKN1 gene fusion
|
|
US10370723B2
(en)
|
2014-07-17 |
2019-08-06 |
Blueprint Medicines Corporation |
TERT fusions
|
|
EP3169804B3
(fr)
|
2014-07-17 |
2019-09-18 |
Blueprint Medicines Corporation |
Fusions de fgr
|
|
WO2016011147A1
(fr)
|
2014-07-17 |
2016-01-21 |
Blueprint Medicines Corporation |
Fusions de prkc
|
|
CA2952083C
(fr)
|
2014-07-17 |
2023-01-24 |
Sunshine Lake Pharma Co., Ltd. |
Derives d'uree substitues et utilisations pharmaceutiques de ceux-ci
|
|
US9688680B2
(en)
|
2014-08-04 |
2017-06-27 |
Blueprint Medicines Corporation |
Compositions useful for treating disorders related to kit
|
|
CN106573913B
(zh)
|
2014-08-18 |
2019-11-19 |
小野药品工业株式会社 |
抑制Trk的化合物的酸加成盐
|
|
WO2016038519A1
(fr)
|
2014-09-08 |
2016-03-17 |
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
|
|
CR20170094A
(es)
|
2014-09-10 |
2017-05-08 |
Glaxosmithkline Ip Dev Ltd |
Nuevos compuestos como inhibidores de reorganizado durante la transfección (ret)
|
|
AU2015313841B2
(en)
|
2014-09-10 |
2018-03-08 |
Glaxosmithkline Intellectual Property Development Limited |
Pyridone derivatives as rearranged during transfection (RET) kinase inhibitors
|
|
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
|
|
KR102562866B1
(ko)
*
|
2014-11-14 |
2023-08-04 |
네르비아노 메디칼 사이언시스 에스.알.엘. |
단백질 키나아제 억제제로서의 6-아미노-7-바이사이클로-7-데아자-퓨린 유도체
|
|
JP6914834B2
(ja)
|
2014-11-16 |
2021-08-04 |
アレイ バイオファーマ インコーポレイテッド |
(S)−N−(5−((R)−2−(2,5−ジフルオロフェニル)−ピロリジン−1−イル)−ピラゾロ[1,5−a]ピリミジン−3−イル)−3−ヒドロキシピロリジン−1−カルボキサミド硫酸水素塩の結晶形
|
|
EP3221700B1
(fr)
|
2014-11-18 |
2022-06-22 |
Blueprint Medicines Corporation |
Fusions de prkacb
|
|
WO2016096709A1
(fr)
|
2014-12-16 |
2016-06-23 |
Eudendron S.R.L. |
Dérivés hétérocycliques modulant l'activité de certaines protéines kinases
|
|
WO2016127074A1
(fr)
|
2015-02-06 |
2016-08-11 |
Blueprint Medicines Corporation |
Utilisation de dérivés 2-(pyridine-3-yl)-pyrimidine en tant qu'inhibiteurs de ret
|
|
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
|
|
HUE053067T2
(hu)
*
|
2015-07-16 |
2021-06-28 |
Array Biopharma Inc |
Helyettesített pirazolo[1,5-A]piridin vegyületek, mint RET kináz inhibitorok
|
|
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
|
|
US10550124B2
(en)
|
2015-08-13 |
2020-02-04 |
San Diego State University Foundation |
Atropisomerism for increased kinase inhibitor selectivity
|
|
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
|
|
NZ742351A
(en)
|
2015-11-02 |
2023-03-31 |
Blueprint Medicines Corp |
Inhibitors of ret
|
|
WO2017097697A1
(fr)
|
2015-12-08 |
2017-06-15 |
Boehringer Ingelheim International Gmbh |
Procédé utilisant un gène de fusion ret comme biomarqueur pour sélectionner des patients atteints d'un cancer bronchique non à petites cellules (nsclc) et d'un cancer de la thyroïde pour un traitement anticancéreux
|
|
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
|
|
IL261107B2
(en)
|
2016-02-23 |
2023-11-01 |
Taiho Pharmaceutical Co Ltd |
A novel compressed pyrimidine compound or a salt thereof
|
|
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
|
|
UY37155A
(es)
|
2016-03-17 |
2017-10-31 |
Blueprint Medicines Corp |
Inhibidores de ret
|
|
US10045991B2
(en)
|
2016-04-04 |
2018-08-14 |
Loxo Oncology, Inc. |
Methods of treating pediatric cancers
|
|
EP3442980B1
(fr)
|
2016-04-15 |
2021-06-09 |
Cancer Research Technology Limited |
Composés hétérocycliques utilisés en tant qu'inhibiteurs de kinase ret
|
|
RS63609B1
(sr)
*
|
2016-04-15 |
2022-10-31 |
Cancer Research Tech Ltd |
Heterociklična jedinjenja kao inhibitori ret kinaze
|
|
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
|
|
TWI752098B
(zh)
*
|
2016-10-10 |
2022-01-11 |
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
|