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
|
US6677135B1
(en)
|
1996-05-08 |
2004-01-13 |
Biogen, Inc. |
Ret ligand (RetL) for stimulating neutral and renal growth
|
CN1163509C
(zh)
|
1996-05-08 |
2004-08-25 |
拜奥根有限公司 |
刺激神经和肾生长的RET配体(RetL)
|
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
|
NZ523105A
(en)
|
2000-06-22 |
2004-07-30 |
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
|
CA2493000A1
(fr)
|
2002-07-24 |
2004-01-29 |
University Of Cincinnati |
4-(4-methylpiperazin-1-ylmethyl)-n-[4 methyl-3-(4-pyridin-3yl)pyrimidin-2-ylamino)phenyl] benzamide utilise pour le traitement des maladies associees a une kinase ret mutee
|
JP4634367B2
(ja)
|
2003-02-20 |
2011-02-16 |
スミスクライン ビーチャム コーポレーション |
ピリミジン化合物
|
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
|
CA2543116A1
(fr)
|
2003-10-27 |
2005-05-19 |
Genelabs Technologies, Inc. |
Procedes de preparation de derives 7-(2'-.szlig.-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
|
KR20060117329A
(ko)
|
2003-11-21 |
2006-11-16 |
노파르티스 아게 |
단백질 키나제 저해제로서의 1h-이미다조퀴놀린 유도체
|
EP1689376A2
(fr)
|
2003-11-28 |
2006-08-16 |
Novartis AG |
Derives de diaryluree utilises en traitement de maladies dependant de proteines kinases
|
EP1696920B8
(fr)
|
2003-12-19 |
2015-05-06 |
Plexxikon Inc. |
Composes et methodes de developpement de modulateurs de ret
|
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
|
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
|
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
|
PE20051089A1
(es)
|
2004-01-22 |
2006-01-25 |
Novartis Ag |
Derivados de pirazolo [1,5-a] pirimidin-7-il-amina como inhibidores de 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
|
CN101257948A
(zh)
|
2005-02-18 |
2008-09-03 |
阿特努奥恩公司 |
嘧啶并二氮䓬衍生物及吲哚并蝶啶化合物
|
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
|
BRPI0610184A2
(pt)
|
2005-05-16 |
2012-09-25 |
Astrazeneca Ab |
composto, sal farmaceuticamente aceitável de um composto, processo para preparar um composto ou um sal farmaceuticamente aceitável do mesmo, uso de um composto ou um sal farmaceuticamente aceitável do mesmo, métodos para a inibição da atividade de trk, para o tratamento ou profilaxia de cáncer e para a produção de um efeito anti-proliferativo em um animal de sanque quente, e, composição farmacêutica
|
US20100047777A1
(en)
|
2005-05-26 |
2010-02-25 |
The Johns Hopkins University |
Methods for identifying mutations in coding and non-coding dna
|
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
|
CN101233129A
(zh)
|
2005-05-31 |
2008-07-30 |
普法尔家族联合企业(1996.7.9) |
取代的联芳杂环衍生物作为蛋白激酶抑制剂治疗癌症及其他疾病
|
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.
|
NZ565255A
(en)
*
|
2005-06-22 |
2010-04-30 |
Plexxikon Inc |
Pyrrolo[2,3-b] pyridine derivatives as protein kinase inhibitors
|
GB0515026D0
(en)
|
2005-07-21 |
2005-08-31 |
Novartis Ag |
Organic compounds
|
RS53195B2
(sr)
|
2005-08-25 |
2018-08-31 |
Creabilis Therapeutics Spa |
Polimerni konjugati k-252a i njihovi derivati
|
WO2007053776A1
(fr)
|
2005-11-03 |
2007-05-10 |
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
|
WO2007057399A2
(fr)
|
2005-11-15 |
2007-05-24 |
Boehringer Ingelheim International Gmbh |
Traitement du cancer
|
WO2007057397A1
(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
|
US7795273B2
(en)
|
2005-12-08 |
2010-09-14 |
Novartis Ag |
Pyrazolo[1,5-a]pyridine-3-carboxylic acids as EphB and VEGFR2 kinase inhibitors
|
JP5474354B2
(ja)
|
2005-12-30 |
2014-04-16 |
アステックス、セラピューティックス、リミテッド |
医薬化合物
|
WO2007087245A2
(fr)
|
2006-01-24 |
2007-08-02 |
Merck & Co., Inc. |
Inhibition de la tyrosine kinase ret
|
WO2007085188A1
(fr)
|
2006-01-27 |
2007-08-02 |
Shanghai Hengrui Pharmaceutical Co. Ltd. |
Composés de pyrrolo[3,2-c]pyridine-4-one 2-indolinone comme inhibiteurs de protéines kinases
|
CA2644356A1
(fr)
|
2006-03-16 |
2007-09-27 |
Novartis Ag |
Composes organiques
|
KR101549364B1
(ko)
|
2006-03-17 |
2015-09-01 |
암비트 바이오사이언시즈 코포레이션 |
질환 치료용 이미다졸로티아졸 화합물
|
NZ572202A
(en)
|
2006-03-27 |
2012-05-25 |
Nerviano Medical Sciences Srl |
Pyridyl- and pyrimidinyl-substituted pyrrole-, thiophene- and furane-derivatives as kinase inhibitors
|
CA2650611A1
(fr)
|
2006-05-15 |
2007-11-29 |
Irm Llc |
Compositions et procedes utilises en tant qu'inhibiteurs des kinases receptrices 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
|
US20110195072A1
(en)
|
2006-09-12 |
2011-08-11 |
Anne Boulay |
Non-neuroendocrine cancer therapy
|
AU2007294686B2
(en)
|
2006-09-15 |
2013-10-31 |
Equinox Sciences, Llc |
Kinase inhibitor compounds
|
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
|
WO2008058341A1
(fr)
|
2006-11-15 |
2008-05-22 |
Cytopia Research Pty Ltd |
Inhibiteurs de l'activité kinase
|
US7872018B2
(en)
|
2006-12-21 |
2011-01-18 |
Plexxikon, Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
WO2008079909A1
(fr)
|
2006-12-21 |
2008-07-03 |
Plexxikon, Inc. |
Composés et méthodes de modulation des kinases, et indications connexes
|
PE20121126A1
(es)
|
2006-12-21 |
2012-08-24 |
Plexxikon Inc |
Compuestos pirrolo [2,3-b] piridinas como moduladores de quinasa
|
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
|
US20100173954A1
(en)
|
2007-01-19 |
2010-07-08 |
Bayer Healthcare Llc |
Treatment of cancers having resistance to chemotherapeutic agents
|
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
|
BRPI0811516A2
(pt)
|
2007-05-04 |
2014-11-18 |
Irm Llc |
Compostos e composições como inibidores de c-kit e pdgfr cinase
|
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
|
EA201000092A1
(ru)
|
2007-07-09 |
2010-06-30 |
Астразенека Аб |
Тризамещенные пиримидиновые производные для лечения пролиферативных заболеваний
|
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
|
US20100190777A1
(en)
|
2007-07-17 |
2010-07-29 |
Plexxikon Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
BRPI0814441A2
(pt)
|
2007-07-19 |
2015-07-14 |
Schering Corp |
Compostos de amida heterocíclica como inibidores de proteína cinase
|
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
|
WO2009021137A2
(fr)
|
2007-08-07 |
2009-02-12 |
Purdue Research Foundation |
Inhibiteurs de kinase et leurs utilisations
|
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
|
KR20100089851A
(ko)
|
2007-10-23 |
2010-08-12 |
노파르티스 아게 |
호흡기 질환의 치료를 위한 trkb 항체의 용도
|
EP2215091B1
(fr)
|
2007-12-04 |
2016-03-30 |
Nerviano Medical Sciences S.r.l. |
Dérivés de dihydroptéridin-6-one substitués, procédé de préparation desdits dérivés et leur utilisation en tant qu'inhibiteurs de kinase
|
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
|
MX2010007841A
(es)
|
2008-01-17 |
2010-09-28 |
Irm Llc |
Anticuerpos anti-trkb mejorados.
|
JP2009203226A
(ja)
|
2008-01-31 |
2009-09-10 |
Eisai R & D Management Co Ltd |
ピリジン誘導体およびピリミジン誘導体を含有するレセプターチロシンキナーゼ阻害剤
|
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)
|
US8822500B2
(en)
|
2008-03-19 |
2014-09-02 |
Chembridge Corporation |
Tyrosine kinase inhibitors
|
JP5628145B2
(ja)
|
2008-03-19 |
2014-11-19 |
ケムブリッジ・コーポレーション |
新規チロシンキナーゼ阻害剤
|
ES2588193T3
(es)
|
2008-03-28 |
2016-10-31 |
Nerviano Medical Sciences S.R.L. |
Derivados de 3,4-dihidro-2H-pirazino[1,2-a]indol-1-ona activos como inhibidores de cinasa, proceso para su preparación y composiciones farmacéuticas que los comprenden
|
PE20091846A1
(es)
|
2008-05-19 |
2009-12-16 |
Plexxikon Inc |
DERIVADOS DE PIRROLO[2,3-d]-PIRIMIDINA COMO MODULADORES DE CINASAS
|
WO2009143018A2
(fr)
|
2008-05-19 |
2009-11-26 |
Plexxikon, Inc. |
Composés et procédés de modulation des kinases, et indications associées
|
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
|
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
|
CN102112478A
(zh)
|
2008-06-10 |
2011-06-29 |
普莱希科公司 |
用于激酶调节的5h-吡咯[2,3-b]吡嗪衍生物和其适应症
|
WO2009155527A2
(fr)
|
2008-06-19 |
2009-12-23 |
Progenics Pharmaceuticals, Inc. |
Inhibiteurs de phosphatidylinositol 3 kinase
|
CA2730190A1
(fr)
|
2008-07-14 |
2010-01-21 |
Queen's University At Kingston |
Compositions pharmaceutiques contenant des inhibiteurs de ret et procedes de traitement du cancer
|
CN102105151B
(zh)
|
2008-07-29 |
2013-12-18 |
内尔维阿诺医学科学有限公司 |
Cdk抑制剂在治疗神经胶质瘤中的应用
|
EP2352361B1
(fr)
|
2008-09-01 |
2014-09-24 |
Sharp Kabushiki Kaisha |
Panneau électroluminescent organique, affichage électroluminescent organique, éclairage électroluminescent organique et procédé de fabrication d un panneau, affichage et éclairage de ce genre
|
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
|
WO2010031816A1
(fr)
|
2008-09-19 |
2010-03-25 |
Nerviano Medical Sciences S.R.L. |
Dérivés de 3,4-dihydro-2h-pyrrolo[1,2-a]pyrazine-1-one
|
PL2350075T3
(pl)
|
2008-09-22 |
2014-07-31 |
Array Biopharma Inc |
Podstawione związki imidazo[1,2b]pirydazynowe jako inhibitory kinaz Trk
|
ES2435918T3
(es)
|
2008-09-26 |
2013-12-26 |
National Health Research Institutes |
Compuestos multicíclicos condensados como inhibidores de las proteína-cinasas
|
BRPI0919873B8
(pt)
|
2008-10-22 |
2021-05-25 |
Array Biopharma Inc |
compostos de pirazol[1,5-a]pirimidina substituídos como inibidores da trk quinase, seus processos de preparação e composições farmacêuticas
|
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
|
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
|
TWI484961B
(zh)
|
2009-05-08 |
2015-05-21 |
Astellas Pharma Inc |
Diamine heterocyclic methyl ester compounds
|
US8765747B2
(en)
|
2009-06-12 |
2014-07-01 |
Dana-Farber Cancer Institute, Inc. |
Fused 2-aminothiazole compounds
|
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
|
SG178454A1
(en)
|
2009-08-17 |
2012-03-29 |
Intellikine Inc |
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
|
MY173494A
(en)
|
2009-10-29 |
2020-01-29 |
Genosco |
Kinase inhibitors
|
KR101663637B1
(ko)
|
2009-11-13 |
2016-10-07 |
제노스코 |
키나아제 억제제
|
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
|
KR101483215B1
(ko)
|
2010-01-29 |
2015-01-16 |
한미약품 주식회사 |
단백질 키나아제 저해활성을 갖는 비시클릭 헤테로아릴 유도체
|
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
|
SG182361A1
(en)
|
2010-01-29 |
2012-08-30 |
Hanmi Science Co Ltd |
THIENO[3,2-d]PYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY ON PROTEIN KINASES
|
WO2011101408A1
(fr)
|
2010-02-18 |
2011-08-25 |
INSERM (Institut National de la Santé et de la Recherche Médicale) |
Procédé de prévention de la métastase cancéreuse
|
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
|
LT3205654T
(lt)
|
2010-05-20 |
2019-05-27 |
Array Biopharma, Inc. |
Makrocikliniai junginiai kaip trk kinazės slopikliai
|
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
|
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
|
JP5925808B2
(ja)
|
2011-01-26 |
2016-05-25 |
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 |
三環式誘導体、これらの調製方法およびこれらのキナーゼ阻害剤としての使用
|
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
|
PT2672967T
(pt)
|
2011-02-07 |
2018-12-07 |
Plexxikon Inc |
Compostos e métodos de modulação da quinase e suas indicações
|
CN103403002B
(zh)
|
2011-02-24 |
2016-06-22 |
内尔维阿诺医学科学有限公司 |
作为激酶抑制剂的噻唑基苯基-苯磺酰氨基衍生物
|
MA34969B1
(fr)
|
2011-02-25 |
2014-03-01 |
Irm Llc |
Composes et compositions en tant qu inibiteurs de trk
|
WO2012135631A1
(fr)
|
2011-03-30 |
2012-10-04 |
Arrien Pharmaeuticals Llc |
5-(pyrazin-2-yl)-1h-pyrazolo[3,4-b]pyridine substituée et dérivés de pyrazolo[3,4-b]pyridine en tant qu'inhibiteurs de protéine kinase
|
EP2693881B1
(fr)
|
2011-04-01 |
2019-09-04 |
University of Utah Research Foundation |
Analogues de n-phénylpyrimidine-2-amine substitués en tant qu'inhibiteurs de l'axl kinase
|
JP5976778B2
(ja)
|
2011-04-11 |
2016-08-24 |
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ピラゾリル−ピリミジン誘導体
|
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
|
SG194911A1
(en)
|
2011-05-12 |
2013-12-30 |
Nerviano Medical Sciences Srl |
Substituted indazole derivatives active as kinase inhibitors
|
AU2012256237B2
(en)
|
2011-05-13 |
2017-01-05 |
Array Biopharma Inc. |
Pyrrolidinyl urea and pyrrolidinyl thiourea compounds as TrkA kinase inhibitors
|
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
|
US8912200B2
(en)
|
2011-07-28 |
2014-12-16 |
Nerviano Medical Sciences S.R.L. |
Alkynyl substituted pyrimidinyl-pyrroles active as kinases inhibitors
|
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
|
JP6342805B2
(ja)
|
2011-09-02 |
2018-06-13 |
ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア |
置換ピラゾロ[3,4−d]ピリミジンおよびその用途
|
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
|
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
|
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
|
CA2854936A1
(fr)
|
2011-11-14 |
2013-05-23 |
Tesaro, Inc. |
Modulation de certaines tyrosine kinases
|
CA2853645A1
(fr)
|
2011-11-30 |
2013-06-06 |
National Cancer Center |
Cellules souches malignes induites
|
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
|
BR112014015720B1
(pt)
|
2011-12-30 |
2020-03-17 |
Hanmi Pharm. Co., Ltd. |
Derivados de tieno[3,2-d]pirimidina, composição farmacêutica e uso dos mesmos para a prevenção ou tratamento de uma doença causada por ativação anormal de uma proteína quinase
|
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
|
TW201350479A
(zh)
|
2012-04-26 |
2013-12-16 |
Ono Pharmaceutical Co |
Trk阻害化合物
|
US20150099721A1
(en)
|
2012-05-10 |
2015-04-09 |
Synta Pharmaceuticals Corp. |
Treating cancer with hsp90 inhibitory compounds
|
NZ703124A
(en)
|
2012-05-23 |
2016-07-29 |
Nerviano Medical Sciences Srl |
Process for the preparation of n-[5-(3,5-difluoro-benzyl)-1h-indazol-3-yl]-4-(4-methyl-piperazin-1-yl)-2-(tetrahydro-pyran-4-ylamino)-benzamide
|
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
|
SG11201500125QA
(en)
|
2012-07-11 |
2015-02-27 |
Blueprint Medicines Corp |
Inhibitors of the fibroblast growth factor receptor
|
EP2878672A4
(fr)
|
2012-07-26 |
2016-02-17 |
Nat Cancer Ct |
Gène de fusion formé par le gène cep55 et le gène ret
|
CN104507923B
(zh)
|
2012-08-02 |
2018-02-09 |
内尔维阿诺医学科学有限公司 |
作为激酶抑制剂的取代的吡咯类活性剂
|
CN114129566A
(zh)
|
2012-09-07 |
2022-03-04 |
埃克塞里艾克西斯公司 |
用于治疗肺腺癌的met、vegfr和ret的抑制剂
|
JP5759568B2
(ja)
|
2012-09-25 |
2015-08-05 |
中外製薬株式会社 |
Ret阻害剤
|
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
|
CA2890462A1
(fr)
|
2012-11-12 |
2014-05-15 |
Ignyta, Inc. |
Derives de bendamustine et leurs procedes d'utilisation
|
US9828360B2
(en)
|
2012-11-13 |
2017-11-28 |
Array Biopharma Inc. |
Pyrrolidinyl 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
|
US9546156B2
(en)
|
2012-11-13 |
2017-01-17 |
Array Biopharma Inc. |
N-bicyclic aryl,N'-pyrazolyl urea, thiourea, guanidine cyanoguanidine compounds as TrkA kinase inhibitors
|
HUE038512T2
(hu)
|
2012-11-13 |
2018-10-29 |
Array Biopharma Inc |
N-pirrolidinil-, N'-pirazolil-karbamid, tiokarbamid, guanidin és cianoguanidin vegyületek mint TrkA kináz inhibitorok
|
US9822118B2
(en)
|
2012-11-13 |
2017-11-21 |
Array Biopharma Inc. |
Bicyclic heteroaryl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
|
WO2014078417A1
(fr)
|
2012-11-13 |
2014-05-22 |
Array Biopharma Inc. |
Composés de pyrazolylurée, d'urée, de thiourée, de guanidine et de cyanoguianidine en tant qu'inhibiteurs de la trka kinase
|
US9790210B2
(en)
|
2012-11-13 |
2017-10-17 |
Array Biopharma Inc. |
N-(monocyclic aryl),N'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors
|
HUE031557T2
(en)
|
2012-11-13 |
2017-07-28 |
Array Biopharma Inc |
Bicyclic urea, thiourea, guanidine, and cyanoguadinine compounds used to treat pain
|
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
|
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
|
MX2015004626A
(es)
|
2012-11-29 |
2015-07-14 |
Yeda Res & Dev |
Metodos para prevenir metastasis de tumor, tratar y pronosticar cancer e identificar agentes que son inhibidores putativos de metastasis.
|
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
|
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
|
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
|
FR3000493A1
(fr)
|
2012-12-28 |
2014-07-04 |
Oribase Pharma |
Nouveaux 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
|
WO2014160524A1
(fr)
|
2013-03-14 |
2014-10-02 |
The Trustees Of The University Of Pennsylvania |
Effets cardiométaboliques et vasculaires de métabolites de glp-1
|
US9499522B2
(en)
|
2013-03-15 |
2016-11-22 |
Blueprint Medicines Corporation |
Compositions useful for treating disorders related to kit
|
US8937071B2
(en)
|
2013-03-15 |
2015-01-20 |
Glaxosmithkline Intellectual Property Development Limited |
Compounds as rearranged during transfection (RET) inhibitors
|
WO2014145485A2
(fr)
*
|
2013-03-15 |
2014-09-18 |
The Trustees Of Columbia University In The City Of New York |
Modulateurs de map kinase et utilisations de ceux-ci
|
JP2016516026A
(ja)
|
2013-03-15 |
2016-06-02 |
グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited |
Rearrangedduringtransfection(ret)キナーゼ阻害剤としてのピリジン誘導体
|
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
|
CN105228983A
(zh)
|
2013-05-30 |
2016-01-06 |
普莱希科公司 |
用于激酶调节的化合物及其适应症
|
US10407509B2
(en)
|
2013-07-30 |
2019-09-10 |
Blueprint Medicines Corporation |
NTRK2 fusions
|
WO2015017528A1
(fr)
|
2013-07-30 |
2015-02-05 |
Blueprint Medicines Corporation |
Fusions de pik3c2g
|
WO2015025866A1
(fr)
|
2013-08-20 |
2015-02-26 |
独立行政法人国立がん研究センター |
Nouveau gène de fusion détecté dans un cancer du poumon
|
CA2922230A1
(fr)
|
2013-08-30 |
2015-03-05 |
Ambit Biosciences Corporation |
Composes de biaryle acetamide et procedes d'utilisation de ceux-ci
|
US9334263B2
(en)
|
2013-10-17 |
2016-05-10 |
Blueprint Medicines Corporation |
Compositions useful for treating disorders related to kit
|
AU2014337314B2
(en)
|
2013-10-17 |
2018-12-13 |
Blueprint Medicines Corporation |
Compositions useful for treating disorders related to KIT
|
US9434700B2
(en)
|
2013-10-25 |
2016-09-06 |
Neil Bifulco, JR. |
Inhibitors of the fibroblast growth factor receptor
|
GB201321146D0
(en)
|
2013-11-29 |
2014-01-15 |
Cancer Rec Tech Ltd |
Quinazoline compounds
|
US9801880B2
(en)
|
2013-12-02 |
2017-10-31 |
Bergenbio As |
Use of kinase inhibitors
|
WO2015108992A1
(fr)
|
2014-01-15 |
2015-07-23 |
Blueprint Medicines Corporation |
Composés hétérobicycliques et leur utilisation en tant qu'inhibiteurs du récepteur fgfr4
|
HRP20221518T1
(hr)
|
2014-01-24 |
2023-02-17 |
Turning Point Therapeutics, Inc. |
Diaril makrociklični spojevi kao modulatori protein kinaza
|
CA3181899A1
(fr)
|
2014-02-14 |
2015-08-20 |
Exelixis, Inc. |
Formes solides cristallines du n-{4-[(6,7-dimethoxyquinolin-4-yl)oxy]phenyl}-n'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide, procedes de preparation, et methodes d'utilisation
|
US10231965B2
(en)
|
2014-02-20 |
2019-03-19 |
Ignyta, Inc. |
Molecules for administration to ROS1 mutant cancer cells
|
US20170044622A1
(en)
|
2014-04-18 |
2017-02-16 |
Blueprint Medicines Corporation |
Pik3ca fusions
|
EP3132054B1
(fr)
|
2014-04-18 |
2021-06-30 |
Blueprint Medicines Corporation |
Fusions de met
|
PL3154959T3
(pl)
|
2014-05-15 |
2019-12-31 |
Array Biopharma, Inc. |
1-((3S,4R)-4-(3-Fluorofenylo)-1-(2-metoksyetylo)pirolidyn-3-ylo)-3-(4-metylo-3- (2- metylopirymidyn-5-ylo)-1-fenylo-1H-pirazol-5-ilo)-mocznik jako inhibitor kinazy TrkA
|
WO2015191666A2
(fr)
|
2014-06-10 |
2015-12-17 |
Blueprint Medicines Corporation |
Fusions de raf1
|
US10246750B2
(en)
|
2014-06-10 |
2019-04-02 |
Blueprint Medicines Corporation |
Method for detection of a TECR:PKN1 or an ANXA4:PKN1 gene fusion
|
EP3169804B3
(fr)
|
2014-07-17 |
2019-09-18 |
Blueprint Medicines Corporation |
Fusions de fgr
|
EP3169808B1
(fr)
|
2014-07-17 |
2019-05-22 |
Blueprint Medicines Corporation |
Fusion trio:tert dans le cancer
|
JP6665154B2
(ja)
|
2014-07-17 |
2020-03-13 |
ノース・アンド・サウス・ブラザー・ファーマシー・インベストメント・カンパニー・リミテッド |
置換尿素誘導体及びその薬学的使用
|
EP3169809B1
(fr)
|
2014-07-17 |
2020-04-29 |
Blueprint Medicines Corporation |
Fusions de prkc
|
US9688680B2
(en)
|
2014-08-04 |
2017-06-27 |
Blueprint Medicines Corporation |
Compositions useful for treating disorders related to kit
|
HUE045237T2
(hu)
|
2014-08-18 |
2019-12-30 |
Ono Pharmaceutical Co |
TRK-inhibitáló vegyület savaddíciós sója
|
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
|
BR112017004897A2
(pt)
|
2014-09-10 |
2017-12-12 |
Glaxosmithkline Ip Dev Ltd |
compostos inovadores como inibidores rearranjados durante a transfecção (ret)
|
SG11201701694QA
(en)
|
2014-09-10 |
2017-04-27 |
Glaxosmithkline Ip Dev Ltd |
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
|
US10221181B2
(en)
|
2014-11-14 |
2019-03-05 |
Nerviano Medical Sciences S.R.L. |
6-amino-7-bicyclo-7-deaza-purine derivatives as protein kinase inhibitors
|
PL3699181T3
(pl)
|
2014-11-16 |
2023-05-22 |
Array Biopharma, Inc. |
Postać krystaliczna wodorosiarczanu (s)-n-(5-((r)-2-(2,5-difluorofenylo) - pirolidyn-1-ylo)-pirazolo[1,5-a]pirimidyn-3-ylo)-3-hydroksypirolidyno-1-karboksyamidu
|
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
|
AU2016226210A1
(en)
|
2015-03-03 |
2017-09-21 |
Caris Mpi, Inc. |
Molecular profiling for cancer
|
US10364247B2
(en)
|
2015-04-21 |
2019-07-30 |
Ruijin Hospital Affiliated To Shanghai Jiao Tong University School Of Medicine |
Preparation and use of novel protein kinase inhibitors
|
GB201512365D0
(en)
|
2015-07-15 |
2015-08-19 |
King S College London |
Novel therapy
|
CA2992586A1
(fr)
*
|
2015-07-16 |
2017-01-19 |
Array Biopharma, Inc. |
Composes substitues 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
|
EP3334430A4
(fr)
|
2015-08-13 |
2019-02-06 |
San Diego State University 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
|
EP4331585A3
(fr)
|
2015-11-02 |
2024-05-15 |
Blueprint Medicines Corporation |
Inhibiteurs 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
|
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
|
PT3269370T
(pt)
|
2016-02-23 |
2020-03-05 |
Taiho Pharmaceutical Co Ltd |
Novo composto de pirimidina condensada ou sal do mesmo
|
US10183928B2
(en)
|
2016-03-17 |
2019-01-22 |
Blueprint Medicines Corporation |
Inhibitors of RET
|
US10045991B2
(en)
|
2016-04-04 |
2018-08-14 |
Loxo Oncology, Inc. |
Methods of treating pediatric cancers
|
US10844067B2
(en)
*
|
2016-04-15 |
2020-11-24 |
Cancer Research Technology Limited |
Heterocyclic compounds as RET kinase inhibitors
|
KR102706837B1
(ko)
|
2016-04-15 |
2024-09-19 |
캔써 리서치 테크놀로지 리미티드 |
Ret 키나아제 억제제로서의 헤테로사이클릭 화합물
|
JOP20190077A1
(ar)
|
2016-10-10 |
2019-04-09 |
Array Biopharma Inc |
مركبات بيرازولو [1، 5-a]بيريدين بها استبدال كمثبطات كيناز 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
|