US3507866A
(en)
|
1967-08-08 |
1970-04-21 |
Merck & Co Inc |
1h - imidazo(4,5-b)pyrazin - 2 - one and processes for their preparation
|
US3567725A
(en)
|
1968-11-20 |
1971-03-02 |
Merck & Co Inc |
Process for preparation of 1h-imidazo-(4,5-b)pyrazin-2-ones
|
US4317909A
(en)
|
1980-03-24 |
1982-03-02 |
Sterling Drug Inc. |
Preparation of 1,3-dihydro-5-(pyridinyl)-2H-imidazo[4,5-b]pyridin-2-ones
|
US4294836A
(en)
|
1980-03-24 |
1981-10-13 |
Sterling Drug Inc. |
1,3-Dihydro-6-(pyridinyl)-2H-imidazo[4,5-b]pyridin-2-ones and -imidazo[4,5-b]-pyridine-2-thiones and their cardiotonic use
|
US4294837A
(en)
|
1980-03-28 |
1981-10-13 |
Sterling Drug Inc. |
1,3-Dihydro-6-(pyridinyl)-2H-imidazo[4,5-b]pyridin-2-ones and -imidazo[4,5-b]pyridine-2-thiones and their cardiotonic use
|
US4309537A
(en)
|
1980-03-28 |
1982-01-05 |
Sterling Drug Inc. |
Production of imidazo[4,5-b]pyridin-2-ones or thiones
|
GB8709448D0
(en)
|
1987-04-21 |
1987-05-28 |
Pfizer Ltd |
Heterobicyclic quinoline derivatives
|
JPS63275582A
(ja)
|
1987-05-02 |
1988-11-14 |
Naade Kenkyusho:Kk |
2−アミノイミダゾ〔4,5−b〕ピリジン誘導体の製造方法
|
DD262026A1
(de)
|
1987-07-10 |
1988-11-16 |
Akad Wissenschaften Ddr |
Verfahren zur herstellung von 4-substituierten 6-(pyrid-4-yl)-2,4-dihydro-1h-imidazo[4,5-b]pyrid-2-onen
|
FR2643903A1
(fr)
|
1989-03-03 |
1990-09-07 |
Union Pharma Scient Appl |
Nouveaux derives de benzimidazole, leurs procedes de preparation, intermediaires de synthese, compositions pharmaceutiques les contenant, utiles notamment pour le traitement des maladies cardiovasculaires, et des ulceres duodenaux
|
US4963561A
(en)
|
1990-02-28 |
1990-10-16 |
Sterling Drug Inc. |
Imidazopyridines, their preparation and use
|
TW274550B
(es)
|
1992-09-26 |
1996-04-21 |
Hoechst Ag |
|
DE19601627A1
(de)
|
1996-01-18 |
1997-07-24 |
Bayer Ag |
Heteroatomhaltige Cyclopentanopyridyl-Oxazolidinone
|
US6031105A
(en)
|
1996-04-09 |
2000-02-29 |
Pfizer Inc |
Substituted pyridines
|
HUP0004024A3
(en)
|
1997-09-26 |
2001-10-29 |
Zentaris Gmbh |
Azabenzimidazole-based compounds, process for their preparation and pharmaceutical composition thereof
|
EP1036844A4
(en)
|
1997-11-27 |
2002-12-04 |
Chugai Pharmaceutical Co Ltd |
Test methods, test reagent and remedies for diseases caused by changes in the LKB1 gene
|
ZA9810490B
(en)
|
1997-12-03 |
1999-05-20 |
Dainippon Pharmaceutical Co |
2-Aryl-8-oxodihydropurine derivative process for the preparation thereof pharmaceutical composition containing the same and intermediate therefor
|
AU4951300A
(en)
|
1999-05-31 |
2000-12-18 |
Chugai Research Institute For Molecular Medicine, Inc. |
Lkb1 gene knockout animals
|
JP2003146987A
(ja)
|
1999-05-31 |
2003-05-21 |
Dainippon Pharmaceut Co Ltd |
2−アリールプリン−9−アセトアミド誘導体
|
JP3814125B2
(ja)
|
1999-06-02 |
2006-08-23 |
大日本住友製薬株式会社 |
2−アリール−8−オキソジヒドロプリン誘導体からなる医薬
|
JP2002100363A
(ja)
|
2000-09-25 |
2002-04-05 |
Mitsubishi Chemicals Corp |
リチウム二次電池用正極材料、リチウム二次電池用正極及びリチウム二次電池
|
JP2002167387A
(ja)
|
2000-11-29 |
2002-06-11 |
Dainippon Pharmaceut Co Ltd |
2−(7,8−ジヒドロ−8−オキソ−9h−プリン−9−イル)酢酸誘導体
|
EP1347982B1
(en)
|
2000-12-12 |
2005-11-16 |
Neurogen Corporation |
Spiro isobenzofuran-1,4'-piperidin]-3-ones and 3h-spiroisobenzofuran-1,4'-piperidines
|
WO2002076954A1
(en)
|
2001-03-23 |
2002-10-03 |
Smithkline Beecham Corporation |
Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
|
EA007062B1
(ru)
|
2001-09-04 |
2006-06-30 |
Бёрингер Ингельхайм Фарма Гмбх Унд Ко. Кг |
Новые дигидроптеридиноны, способы их получения и их применение в качестве лекарственных средств
|
EP1438048A1
(en)
|
2001-10-18 |
2004-07-21 |
Boehringer Ingelheim Pharmaceuticals Inc. |
1,4-disubstituted benzo-fused urea compounds as cytokine inhibitors
|
AU2003208415B2
(en)
|
2002-02-14 |
2009-05-28 |
Immunomedics, Inc. |
Anti-CD20 antibodies and fusion proteins thereof and methods of use
|
PE20030968A1
(es)
|
2002-02-28 |
2004-01-12 |
Novartis Ag |
Derivados de 5-feniltiazol como inhibidores de cinasas
|
US7247621B2
(en)
|
2002-04-30 |
2007-07-24 |
Valeant Research & Development |
Antiviral phosphonate compounds and methods therefor
|
MXPA04010983A
(es)
|
2002-05-06 |
2005-02-14 |
Genelabs Tech Inc |
Derivados de nucleosidos para tratar infecciones por el virus de la hepatitis c.
|
WO2004042002A2
(en)
|
2002-08-05 |
2004-05-21 |
University Of Massachusetts |
Compounds for modulating rna interference
|
EP1556053A4
(en)
|
2002-10-31 |
2006-04-19 |
Amgen Inc |
ANTI-INFLAMMATORY AGENTS
|
AU2003295776B2
(en)
|
2002-11-21 |
2011-05-12 |
Novartis Vaccines And Diagnostics, Inc. |
2,4,6-trisubstituted pyrimidines as phosphotidylinositol (PI) 3-kinase inhibitors and their use in the treatment of cancer
|
DE602004021558D1
(de)
|
2003-01-17 |
2009-07-30 |
Warner Lambert Co |
2-aminopyridin-substituierteheterocyclen als inhibitoren der zellulären proliferation
|
RS52386B
(en)
|
2003-02-26 |
2013-02-28 |
Boehringer Ingelheim Pharma Gmbh & Co.Kg. |
DIHYDROPTERIDINONE, PROCEDURE FOR THEIR PREPARATION AND THEIR APPLICATION AS A MEDICINE
|
US8084582B2
(en)
|
2003-03-03 |
2011-12-27 |
Xencor, Inc. |
Optimized anti-CD20 monoclonal antibodies having Fc variants
|
GB0305152D0
(en)
|
2003-03-06 |
2003-04-09 |
Novartis Ag |
Organic compounds
|
GB2400101A
(en)
|
2003-03-28 |
2004-10-06 |
Biofocus Discovery Ltd |
Compounds capable of binding to the active site of protein kinases
|
TW200519106A
(en)
|
2003-05-02 |
2005-06-16 |
Novartis Ag |
Organic compounds
|
AR044388A1
(es)
|
2003-05-20 |
2005-09-07 |
Applied Molecular Evolution |
Moleculas de union a cd20
|
CA2734055A1
(en)
|
2003-05-30 |
2005-01-13 |
Pharmasset, Inc. |
Modified fluorinated nucleoside analogues
|
US7476665B2
(en)
|
2003-06-26 |
2009-01-13 |
Merck & Co., Inc. |
Benzodiazepine CGRP receptor antagonists
|
ATE392433T1
(de)
|
2003-07-17 |
2008-05-15 |
Univ Dundee |
Verfahren zur anwendung eines an lkb1/strad/mo25- komplexes
|
US8147832B2
(en)
|
2003-08-14 |
2012-04-03 |
Merck Patent Gmbh |
CD20-binding polypeptide compositions and methods
|
GB0320197D0
(en)
|
2003-08-28 |
2003-10-01 |
Novartis Ag |
Organic compounds
|
US20080194019A1
(en)
|
2003-09-09 |
2008-08-14 |
Beth Israel Deaconess Medical Center, Inc. |
Tumor Suppressor Lkb1 Kinase Directly Activates Amp-Activated Kinase
|
CA2569406A1
(en)
|
2004-06-04 |
2005-12-22 |
Icos Corporation |
Methods for treating mast cell disorders
|
DE102004029784A1
(de)
|
2004-06-21 |
2006-01-05 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Neue 2-Benzylaminodihydropteridinone, Verfahren zur deren Herstellung und deren Verwendung als Arzneimittel
|
WO2006001266A1
(ja)
|
2004-06-23 |
2006-01-05 |
Banyu Pharmaceutical Co., Ltd. |
2-アリールプリン誘導体の製造方法
|
US20060058311A1
(en)
|
2004-08-14 |
2006-03-16 |
Boehringer Ingelheim International Gmbh |
Combinations for the treatment of diseases involving cell proliferation
|
GB0420719D0
(en)
|
2004-09-17 |
2004-10-20 |
Addex Pharmaceuticals Sa |
Novel allosteric modulators
|
AU2005289644A1
(en)
|
2004-09-24 |
2006-04-06 |
Janssen Pharmaceutica, N.V. |
Imidazo{4,5-b}pyrazinone inhibitors of protein kinases
|
GB0423653D0
(en)
|
2004-10-25 |
2004-11-24 |
Piramed Ltd |
Pharmaceutical compounds
|
KR20070085286A
(ko)
|
2004-10-29 |
2007-08-27 |
티보텍 파마슈티칼즈 리미티드 |
Hiv를 저해하는 바이사이클릭 피리미딘 유도체
|
WO2006050076A1
(en)
|
2004-10-29 |
2006-05-11 |
Janssen Pharmaceutica, N.V. |
Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders
|
SE0403006D0
(sv)
|
2004-12-09 |
2004-12-09 |
Biovitrum Ab |
New compounds
|
WO2006065703A1
(en)
|
2004-12-13 |
2006-06-22 |
Sunesis Pharmaceuticals, Inc. |
Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as raf kinase inhibitors
|
DK1853588T3
(da)
|
2005-02-16 |
2008-09-15 |
Astrazeneca Ab |
Kemiske forbindelser
|
WO2006091737A1
(en)
|
2005-02-24 |
2006-08-31 |
Kemia, Inc. |
Modulators of gsk-3 activity
|
EP1871377A1
(en)
|
2005-02-25 |
2008-01-02 |
Kudos Pharmaceuticals Ltd |
2,4-diamino-pyridopyrimidine derivatives and their use as mtor inhibitors
|
EP1877388A2
(en)
|
2005-02-25 |
2008-01-16 |
Kudos Pharmaceuticals Ltd |
Hydrazinomethyl, hydrazonomethyl and 5-membered heterocylic compounds which act as mtor inhibitors and their use as anti cancer agents
|
AU2006231784B2
(en)
|
2005-03-31 |
2010-10-14 |
Biomedics Inc. |
Anti-CD-20 monoclonal antibody
|
WO2006108103A1
(en)
|
2005-04-05 |
2006-10-12 |
Pharmacopeia, Inc. |
Purine and imidazopyridine derivatives for immunosuppression
|
CA2610234A1
(en)
|
2005-06-02 |
2006-12-07 |
Astrazeneca Ab |
Antibodies directed to cd20 and uses thereof
|
PL1940839T3
(pl)
|
2005-10-07 |
2013-12-31 |
Exelixis Inc |
Pirydopirymidynonowe inhibitory PI3Kalfa
|
AU2006302179C1
(en)
|
2005-10-07 |
2013-06-20 |
Exelixis, Inc. |
N- (3-amino-quinoxalin-2-yl) -sulfonamide derivatives and their use as phosphatidylinositol 3-kinase inhibitors
|
EP1931670B1
(en)
|
2005-10-07 |
2012-09-12 |
Exelixis, Inc. |
Pyridopyrimidinone inhibitors of pi3k
|
WO2007047754A2
(en)
|
2005-10-18 |
2007-04-26 |
George Mason Intellectual Properties, Inc. |
Mtor pathway theranostic
|
WO2007061737A2
(en)
|
2005-11-17 |
2007-05-31 |
Osi Pharmaceuticals, Inc. |
FUSED BICYCLIC mTOR INHIBITORS
|
WO2007060404A1
(en)
|
2005-11-22 |
2007-05-31 |
Kudos Pharmaceuticals Limited |
PYRIDO-,PYRAZO- AND PYRIMIDO-PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
GB0525080D0
(en)
|
2005-12-09 |
2006-01-18 |
Astrazeneca Ab |
Pyrimidine derivatives
|
GB0525083D0
(en)
|
2005-12-09 |
2006-01-18 |
Astrazeneca Ab |
Pyrimidine derivatives
|
WO2007080382A1
(en)
|
2006-01-11 |
2007-07-19 |
Astrazeneca Ab |
Morpholino pyrimidine derivatives and their use in therapy
|
US20090281075A1
(en)
|
2006-02-17 |
2009-11-12 |
Pharmacopeia, Inc. |
Isomeric purinones and 1h-imidazopyridinones as pkc-theta inhibitors
|
EP2043655A2
(en)
|
2006-04-25 |
2009-04-08 |
Astex Therapeutics Limited |
Purine and deazapurine derivatives as pharmaceutical compounds
|
CL2007001165A1
(es)
|
2006-04-26 |
2008-01-25 |
Hoffmann La Roche |
2-(1h-indazol-4-il)-6-(4-metanosulfonil-piperazin-1-ilmetil)-4-morfolin-4-il-tieno[3,2-d]pirimidina; procedimiento de preparacion; composicion farmaceutica; proceso de preparacion de dicha composicion; kit farmaceutico; y uso para tratar enfermedades tales como cancer, desordenes inmunes y enfermedades cardiovasculares.
|
CN101484452A
(zh)
|
2006-05-03 |
2009-07-15 |
阿斯利康(瑞典)有限公司 |
噻唑衍生物及其作为抗肿瘤药物的用途
|
EP2016068A1
(en)
|
2006-05-03 |
2009-01-21 |
AstraZeneca AB |
Pyrazole derivatives and their use as pi3k inhibitors
|
CN101448827A
(zh)
|
2006-05-22 |
2009-06-03 |
阿斯利康(瑞典)有限公司 |
吲哚衍生物
|
DK2069352T5
(en)
|
2006-08-02 |
2017-04-03 |
Cytokinetics Inc |
SPECIFIC CHEMICAL UNITS, COMPOSITIONS AND PROCEDURES
|
ES2648388T3
(es)
|
2006-08-23 |
2018-01-02 |
Kudos Pharmaceuticals Limited |
Derivados de 2-metilmorfolin pirido-, pirazo- y pirimido-pirimidina como inhibidores de mTOR
|
US20100144738A1
(en)
|
2006-09-05 |
2010-06-10 |
William Bornmann |
Inhibitors of c-met and uses thereof
|
CA2662677C
(en)
|
2006-09-05 |
2016-05-31 |
Emory University |
Kinase inhibitors for preventing or treating pathogen infection and method of use thereof
|
US20100022534A1
(en)
|
2006-09-14 |
2010-01-28 |
Astrazeneca |
2-benzimidazolyl-6-morpholino-4- (azetidine, pyrrolidine, piperidine or azepine) pyrimidine derivatives as pi3k and mtor inhibitors for the treatment of proliferative disorders
|
WO2008032036A1
(en)
|
2006-09-14 |
2008-03-20 |
Astrazeneca Ab |
6-benzimidaz0lyl-2-m0rph0lin0-4- (azetidine, pyrrolidine, piperidine or azepine) pyrimidine derivatives as pi3k and mtor inhibitors for the treatment of proliferative disorders
|
US20090270390A1
(en)
|
2006-09-14 |
2009-10-29 |
Astrazeneca |
Pyrimidine derivatives
|
WO2008032027A1
(en)
|
2006-09-14 |
2008-03-20 |
Astrazeneca Ab |
Pyrimidine derivatives
|
EP2064203A1
(en)
|
2006-09-14 |
2009-06-03 |
AstraZeneca AB |
2-benzimidaz0lyl-6-m0rph0lin0-4-piperidin-4-ylpyrimidine derivatives as pi3k and mtor inhibitors for the treatment of proliferative disorders
|
WO2008032089A1
(en)
|
2006-09-14 |
2008-03-20 |
Astrazeneca Ab |
4-benzimidaz0lyl-2-m0rph0lin0-6-piperidin-4-ylpyrimidine derivatives as pi3k and mtor inhibitors for the treatment of proliferative disorders
|
WO2008032060A1
(en)
|
2006-09-14 |
2008-03-20 |
Astrazeneca Ab |
4-benzimidaz0lyl-6-m0rph0lin0-2-piperazinylpyrimidine derivatives as p13k and mtor inhibitors for the treatment of proliferative disorders
|
WO2008032033A1
(en)
|
2006-09-14 |
2008-03-20 |
Astrazeneca Ab |
4-benzimidazolyl-2-morpholino-6-piperazinylpyrimidine derivatives as pi3k and mtor inhibitors for the treatment of proliferative disorders
|
WO2008032091A1
(en)
|
2006-09-14 |
2008-03-20 |
Astrazeneca Ab |
4-benzimidaz0lyl-6-m0rph0lin0-2-piperidin-4-ylpyrimidine derivatives as pi3k and mtor inhibitors for the treatment of proliferative disorders
|
WO2008032077A1
(en)
|
2006-09-14 |
2008-03-20 |
Astrazeneca Ab |
Pyrimidine derivatives
|
DK2428513T3
(en)
|
2006-09-26 |
2017-08-21 |
Celgene Corp |
5-substituted quinazolinone derivatives as anti-cancer agents
|
US7902187B2
(en)
|
2006-10-04 |
2011-03-08 |
Wyeth Llc |
6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression
|
WO2008043031A1
(en)
|
2006-10-04 |
2008-04-10 |
Pharmacopeia, Inc. |
6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression
|
CN101679432B
(zh)
|
2006-10-19 |
2015-04-22 |
西格诺药品有限公司 |
杂芳基化合物、其组合物及其作为蛋白激酶抑制剂的用途
|
NZ576278A
(en)
*
|
2006-10-19 |
2011-12-22 |
Signal Pharm Llc |
Heteroaryl compounds, compositions thereof, and their use as protein kinase inhibitors
|
CN106045993A
(zh)
|
2006-11-20 |
2016-10-26 |
诺华股份有限公司 |
化合物的盐和晶型
|
US20080234262A1
(en)
|
2007-03-21 |
2008-09-25 |
Wyeth |
Pyrazolopyrimidine analogs and their use as mtor kinase and pi3 kinase inhibitors
|
UA99284C2
(ru)
|
2007-05-11 |
2012-08-10 |
Елі Ліллі Енд Компані |
ИНГИБИТОРЫ р70 S6-КИНАЗЫ
|
KR20100042280A
(ko)
|
2007-07-09 |
2010-04-23 |
아스트라제네카 아베 |
Mtor 키나제 및/또는 pi3k와 연관된 질환에 사용되는 모르폴리노 피리미딘 유도체
|
AR067478A1
(es)
|
2007-07-09 |
2009-10-14 |
Astrazeneca Ab |
Compuestos derivados de morfolina pirimidina
|
WO2009007751A2
(en)
|
2007-07-09 |
2009-01-15 |
Astrazeneca Ab |
Trisubstituted pyrimidine derivatives for the treatment of proliferative diseases
|
JP5588865B2
(ja)
|
2007-07-31 |
2014-09-10 |
リジェネロン・ファーマシューティカルズ・インコーポレイテッド |
ヒトcd20に対するヒト抗体及びその使用方法
|
EP2197918B1
(en)
|
2007-09-05 |
2013-12-18 |
F. Hoffmann-La Roche AG |
Combination therapy with type i and type ii anti-cd20 antibodies
|
RU2476432C2
(ru)
|
2007-09-26 |
2013-02-27 |
Селджин Корпорейшн |
6-, 7- или 8-замещенные производные хиназолинона и композиции, включающие их, и способы их использования
|
JP2011500702A
(ja)
|
2007-10-16 |
2011-01-06 |
ワイス・エルエルシー |
チエノピリミジンおよびピラゾロピリミジン化合物ならびにmTORキナーゼおよびPI3キナーゼ阻害剤としてのその使用
|
CA2709784A1
(en)
|
2007-12-21 |
2009-07-09 |
University Of Rochester |
Method for altering the lifespan of eukaryotic organisms
|
EP2252296A1
(en)
|
2008-01-15 |
2010-11-24 |
Wyeth LLC |
3h-[1,2,3]triazolo[4,5-d]pyrimidine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses
|
WO2009102986A1
(en)
|
2008-02-15 |
2009-08-20 |
Catholic Healthcare West (D/B/A St. Joseph's Hospital And Medical Center) |
Treatment of adenocarcinoma expressing lkb1 with mtor inhibitor in combination with cox1 inhibitor
|
EP3549934A1
(en)
|
2008-06-27 |
2019-10-09 |
Celgene CAR LLC |
Heteroaryl compounds and uses thereof
|
US20110224223A1
(en)
|
2008-07-08 |
2011-09-15 |
The Regents Of The University Of California, A California Corporation |
MTOR Modulators and Uses Thereof
|
US8110578B2
(en)
*
|
2008-10-27 |
2012-02-07 |
Signal Pharmaceuticals, Llc |
Pyrazino[2,3-b]pyrazine mTOR kinase inhibitors for oncology indications and diseases associated with the mTOR/PI3K/Akt pathway
|
AU2009313878B2
(en)
*
|
2008-11-13 |
2016-01-07 |
Gilead Calistoga Llc |
Therapies for hematologic malignancies
|
WO2010068483A2
(en)
|
2008-11-25 |
2010-06-17 |
University Of Rochester |
Mlk inhibitors and methods of use
|
CN102448472A
(zh)
|
2009-05-25 |
2012-05-09 |
国立大学法人东京工业大学 |
包含与中枢神经细胞的增殖和分化相关的核因子的药物组合物
|
US8476270B2
(en)
|
2009-09-14 |
2013-07-02 |
Gilead Sciences, Inc. |
Dihydropyrido[4,3-b]pyrazine-3-ones as modulators of toll-like receptors
|
CA2778615C
(en)
*
|
2009-10-26 |
2019-04-23 |
Signal Pharmaceuticals, Llc |
Methods of synthesis and purification of heteroaryl compounds
|
PH12012501122A1
(en)
|
2009-12-23 |
2012-10-29 |
Elan Pharm Inc |
Pteridinones as inhibitors of polo-like kinase
|
EP2992878A1
(en)
|
2010-02-03 |
2016-03-09 |
Signal Pharmaceuticals, LLC |
Identification of lkb1 mutation as a predictive biomarker for sensitivity to tor kinase inhibitors
|
JP2013522236A
(ja)
|
2010-03-12 |
2013-06-13 |
セルジーン コーポレイション |
レナリドミドを使用する非ホジキンリンパ腫の治療方法、並びに予測因子としての遺伝子及びタンパク質バイオマーカー
|
US20110318336A1
(en)
|
2010-03-29 |
2011-12-29 |
George Mason Intellectual Properties, Inc. |
Identification and Treatment of Aggressive Lung Cancer Tumors
|
US20120028972A1
(en)
*
|
2010-07-30 |
2012-02-02 |
Lilly Wong |
Biomarker assays for detecting or measuring inhibition of tor kinase activity
|
SG192947A1
(en)
*
|
2011-03-11 |
2013-09-30 |
Celgene Corp |
Use of 3-(5-amino-2-methyl-4-oxoquinazolin-3(4h)-yl)piperidine-2-6-dione in treatment of immune-related and inflammatory diseases
|
JP2014524240A
(ja)
|
2011-08-03 |
2014-09-22 |
シグナル ファーマシューティカルズ,エルエルシー |
Lkb1の状態についての予測バイオマーカーとしての、遺伝子発現プロファイルの同定
|
IN2014CN02887A
(es)
*
|
2011-10-19 |
2015-07-03 |
Signal Pharm Llc |
|
BR112014013332B1
(pt)
*
|
2011-12-02 |
2022-09-06 |
Signal Pharmaceuticals, Llc |
Composições farmacêuticas de 7-(6-(2-hidroxi-propan-2-il)piridin-3-il)-1-((trans)-4- metoxicicloexil)-3,4-diidropirazino [2,3-b]pirazin-2(1h)-ona, uma forma sólida dessa e métodos de seu uso
|
KR102064626B1
(ko)
|
2012-02-24 |
2020-01-09 |
시그날 파마소티칼 엘엘씨 |
Tor 키나제 억제자 복합 치료법을 사용한 비소세포 폐암의 치료 방법
|
CN104271139A
(zh)
|
2012-03-15 |
2015-01-07 |
西格诺药品有限公司 |
用tor激酶抑制剂治疗癌症
|
US20130245029A1
(en)
|
2012-03-15 |
2013-09-19 |
Signal Pharmaceuticals, Llc |
Treatment of cancer with tor kinase inhibitors
|
UA114315C2
(uk)
|
2012-03-15 |
2017-05-25 |
Сігнал Фармасьютікалз, Елелсі |
Лікування раку інгібіторами тоr-кінази
|
NZ628420A
(en)
|
2012-03-15 |
2016-04-29 |
Signal Pharm Llc |
Treatment of cancer with tor kinase inhibitors
|
AU2013203714B2
(en)
|
2012-10-18 |
2015-12-03 |
Signal Pharmaceuticals, Llc |
Inhibition of phosphorylation of PRAS40, GSK3-beta or P70S6K1 as a marker for TOR kinase inhibitory activity
|
WO2014172426A1
(en)
|
2013-04-17 |
2014-10-23 |
Signal Pharmaceuticals, Llc |
Treatment of cancer with dihydropyrazino-pyrazines
|
MX2015014455A
(es)
*
|
2013-04-17 |
2016-07-21 |
Signal Pharm Llc |
Terapia de combinacion que comprende un inhibidor de tor cinasa y n-(3-(5-fluoro-2-(4-(2-metoxietoxi)fenilamino)pirimidin-4-ilamino )fenil)acrilamida para tratar cancer.
|
MX364101B
(es)
|
2013-04-17 |
2019-04-12 |
Signal Pharm Llc |
Terapia de combinación que comprende un compuesto de dihidropirazino-pirazina y un antagonista de receptor de andrógenos para tratar cáncer de próstata.
|
WO2014172429A1
(en)
*
|
2013-04-17 |
2014-10-23 |
Signal Pharmaceuticals, Llc |
Combination therapy comprising a tor kinase inhibitor and an imid compound for treating cancer
|
EP2986297A1
(en)
|
2013-04-17 |
2016-02-24 |
Signal Pharmaceuticals, LLC |
Treatment of cancer with dihydropyrazino-pyrazines
|
US9782427B2
(en)
|
2013-04-17 |
2017-10-10 |
Signal Pharmaceuticals, Llc |
Methods for treating cancer using TOR kinase inhibitor combination therapy
|
US9359364B2
(en)
|
2013-04-17 |
2016-06-07 |
Signal Pharmaceuticals, Llc |
Pharmaceutical formulations, processes, solid forms and methods of use relating to 1-ethyl-7-(2-methyl-6-(1H-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b] pyrazin-2(1H)-one
|
UA119538C2
(uk)
|
2013-04-17 |
2019-07-10 |
Сігнал Фармасьютікалз, Елелсі |
Лікування злоякісної пухлини дигідропіразинопіразинами
|