US4440929A
(en)
|
1981-07-16 |
1984-04-03 |
Usv Pharmaceutical Corporation |
Imidazoquinoxaline compounds
|
DK476885D0
(da)
|
1985-10-17 |
1985-10-17 |
Ferrosan As |
Heterocycliske forbindelser og fremgangsmaader til fremstilling heraf
|
US4859672A
(en)
|
1986-10-29 |
1989-08-22 |
Rorer Pharmaceutical Corporation |
Pyrido[2,3-d]pyrimidinone and imidazo[4,5-b]pyrimidinone
|
JPS63199347A
(ja)
|
1987-02-14 |
1988-08-17 |
Konica Corp |
鮮鋭性の向上した高感度ハロゲン化銀写真感光材料
|
IL90315A0
(en)
|
1988-06-01 |
1989-12-15 |
Ferrosan As |
Imidazoquinoxaline compounds,their preparation and pharmaceutical compositions containing them
|
DK626288D0
(da)
|
1988-11-10 |
1988-11-10 |
Ferrosan As |
Kemisk proces til fremstilling af imidazoquinoxaliner og mellemprodukter til brug i processen
|
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
|
DK588489D0
(da)
|
1989-11-22 |
1989-11-22 |
Ferrosan As |
Heterocykliske forbindelser, deres fremstilling og anvendelse
|
KR100207360B1
(ko)
|
1991-06-14 |
1999-07-15 |
돈 더블유. 슈미츠 |
이미다조[1,5,-a]퀸옥살린
|
AU4035893A
(en)
|
1991-12-17 |
1993-07-19 |
Upjohn Company, The |
3-substituted imidazo (1,5-a) and imidazo (1,5-a)-triazolo (1,5-c) quinoxalines and quinazolines with cns activity
|
EP0626966A1
(en)
|
1992-02-19 |
1994-12-07 |
PHARMACIA & UPJOHN COMPANY |
3-substituted imidazo(1,5-a)quinoxalines and quinazolines with cns activity
|
US6444656B1
(en)
|
1992-12-23 |
2002-09-03 |
Biochem Pharma, Inc. |
Antiviral phosphonate nucleotides
|
GB9226879D0
(en)
|
1992-12-23 |
1993-02-17 |
Iaf Biochem Int |
Anti-viral compounds
|
US5516774A
(en)
|
1993-07-29 |
1996-05-14 |
American Cyanamid Company |
Tricyclic diazepine vasopressin antagonists and oxytocin antagonists
|
US5521173A
(en)
|
1995-01-17 |
1996-05-28 |
American Home Products Corporation |
Tricyclic benzazepine vasopressin antagonists
|
ZA973884B
(en)
|
1996-05-23 |
1998-11-06 |
Du Pont Merck Pharma |
Tetrahydropteridines and pyridylpiperazines for treatment of neurological disorders
|
DE69824632T2
(de)
|
1997-11-12 |
2005-06-09 |
Mitsubishi Chemical Corp. |
Purinderivate und medikamente, welche dieselben als aktiven bestandteil enthalten
|
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
|
TW572758B
(en)
*
|
1997-12-22 |
2004-01-21 |
Sumitomo Pharma |
Type 2 helper T cell-selective immune response inhibitors comprising purine derivatives
|
CZ27399A3
(cs)
|
1999-01-26 |
2000-08-16 |
Ústav Experimentální Botaniky Av Čr |
Substituované dusíkaté heterocyklické deriváty, způsob jejich přípravy, tyto deriváty pro použití jako léčiva, farmaceutická kompozice a kombinovaný farmaceutický přípravek tyto deriváty obsahující a použití těchto derivátů pro výrobu léčiv
|
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
|
AU3540101A
(en)
|
2000-01-07 |
2001-07-16 |
Universitaire Instelling Antwerpen |
Purine derivatives, process for their preparation and use thereof
|
JP3675274B2
(ja)
|
2000-01-27 |
2005-07-27 |
ダイソー株式会社 |
9−(2−ヒドロキシアルキル)プリン誘導体および1−(2−ヒドロキシアルキル)ピリミジン誘導体の製造法
|
US20020040032A1
(en)
|
2000-07-07 |
2002-04-04 |
Glasky Michelle S. |
Methods for stimulation of synthesis of synaptophysin in the central nervous system
|
US20020040031A1
(en)
|
2000-07-07 |
2002-04-04 |
Glasky Michelle S. |
Methods for prevention of accumulation of amyloid beta peptide in the central nervous system
|
WO2002004449A2
(en)
|
2000-07-07 |
2002-01-17 |
Neotherapeutics, Inc. |
Methods for treatment of conditions affected by activity of multidrug transporters
|
ES2385931T3
(es)
|
2000-07-07 |
2012-08-03 |
Spectrum Pharmaceuticals, Inc. |
MÉTODOS PARA EL TRATAMIENTO DE NEUROPATíA PERIFÉRICA INDUCIDA POR UNA ENFERMEDAD Y AFECCIONES RELACIONADAS.
|
WO2002058736A2
(en)
|
2000-12-12 |
2002-08-01 |
Neotherapetics, Inc. |
Use of 9-substituted purine analogues and other molecules to stimulate neurogenesis
|
US6960595B2
(en)
|
2001-03-23 |
2005-11-01 |
Bristol-Myers Squibb Pharma Company |
5-6 to 5-7 Heterobicycles as factor Xa inhibitors
|
US20020156277A1
(en)
|
2001-04-20 |
2002-10-24 |
Fick David B. |
Synthesis and methods of use of purine analogues and derivatives
|
AU2003211993A1
(en)
|
2002-02-15 |
2003-09-04 |
Kyowa Hakko Kogyo Co., Ltd. |
(1,2,4)TRIAZOLO(1,5-c)PYRIMIDINE DERIVATIVES
|
WO2003072757A2
(en)
|
2002-02-28 |
2003-09-04 |
Biota, Inc. |
Nucleotide mimics and their prodrugs
|
US7247621B2
(en)
|
2002-04-30 |
2007-07-24 |
Valeant Research & Development |
Antiviral phosphonate compounds and methods therefor
|
ATE335744T1
(de)
|
2002-08-07 |
2006-09-15 |
Novartis Pharma Gmbh |
Organische verbindungen als mittel zur behandlung von aldosteronbedingten zuständen
|
US7371857B2
(en)
|
2002-08-08 |
2008-05-13 |
Valeant Research & Development |
Synthesis for hydroxyalkylated heterocyclic bases
|
US20040166137A1
(en)
|
2002-11-08 |
2004-08-26 |
Lackey John William |
Hetero-substituted benzimidazole compounds and antiviral uses thereof
|
JP2004217582A
(ja)
|
2003-01-16 |
2004-08-05 |
Abbott Japan Co Ltd |
9h−プリン誘導体
|
US20040180898A1
(en)
|
2003-03-03 |
2004-09-16 |
Bang-Chi Chen |
Processes for preparing imidazoquinoxalinones, heterocyclic-substituted imidazopyrazinones, imidazoquinoxalines and heterocyclic-substituted imidazopyrazines
|
RU2006102867A
(ru)
|
2003-07-02 |
2007-08-10 |
Ф.Хоффманн-Ля Рош Аг (Ch) |
Производные 5-замещенного хиназолинона
|
JP2006528184A
(ja)
|
2003-07-23 |
2006-12-14 |
ワイス |
5−ヒドロキシトリプタミン−6リガンドとしてのスルホニルジヒドロイミダゾピリジノン化合物
|
US20050043239A1
(en)
|
2003-08-14 |
2005-02-24 |
Jason Douangpanya |
Methods of inhibiting immune responses stimulated by an endogenous factor
|
US20050054614A1
(en)
|
2003-08-14 |
2005-03-10 |
Diacovo Thomas G. |
Methods of inhibiting leukocyte accumulation
|
WO2005067901A2
(en)
|
2004-01-08 |
2005-07-28 |
Michigan State University |
Methods for treating and preventing hypertension and hypertension-related disorders
|
AU2005214380A1
(en)
|
2004-02-18 |
2005-09-01 |
Astrazeneca Ab |
Fused hetrocyclic compounds and their use as metabotropic receptor antagonists for the treatment of gastrointestinal disorders
|
CA2566436C
(en)
|
2004-05-13 |
2011-05-10 |
Vanderbilt University |
Phosphoinositide 3-kinase delta selective inhibitors for inhibiting angiogenesis
|
WO2005117889A1
(en)
|
2004-05-25 |
2005-12-15 |
Icos Corporation |
Methods for treating and/or preventing aberrant proliferation of hematopoietic
|
CN101123968A
(zh)
|
2004-06-04 |
2008-02-13 |
艾科斯有限公司 |
肥大细胞病的治疗方法
|
CA2583536A1
(en)
|
2004-10-13 |
2006-04-27 |
Merck & Co., Inc. |
Cgrp receptor antagonists
|
SI1848718T1
(sl)
|
2005-02-04 |
2012-12-31 |
Millennium Pharmaceuticals, Inc. |
Inhibitorji E1 aktivacijskih enzimov
|
CA2598409A1
(en)
|
2005-02-17 |
2006-08-24 |
Icos Corporation |
Phosphoinositide 3-kinase inhibitors for inhibiting leukocyte accumulation
|
US7884109B2
(en)
|
2005-04-05 |
2011-02-08 |
Wyeth Llc |
Purine and imidazopyridine derivatives for immunosuppression
|
EP1874772A1
(en)
|
2005-04-05 |
2008-01-09 |
Pharmacopeia, Inc. |
Purine and imidazopyridine derivatives for immunosuppression
|
US20090023723A1
(en)
|
2005-09-21 |
2009-01-22 |
Pharmacopeia Drug Discovery, Inc. |
Purinone derivatives for treating neurodegenerative diseases
|
DE102005062987A1
(de)
|
2005-12-28 |
2007-07-05 |
Grünenthal GmbH |
Substituierte Propiolsäureamide und ihre Verwendung zur Herstellung von Arzneimitteln
|
US7989459B2
(en)
|
2006-02-17 |
2011-08-02 |
Pharmacopeia, Llc |
Purinones and 1H-imidazopyridinones as PKC-theta inhibitors
|
MX2008015008A
(es)
|
2006-05-26 |
2008-12-05 |
Novartis Ag |
INHIBIDORES DE SINTASA DE ALDOSTERONA Y/O DE 11ß-HIDROXILASA.
|
TW200817400A
(en)
|
2006-05-30 |
2008-04-16 |
Elbion Ag |
Pyrido [3,2-e] pyrazines, their use as inhibitors of phosphodiesterase 10, and processes for preparing them
|
WO2007149484A2
(en)
|
2006-06-20 |
2007-12-27 |
Dana-Farber Cancer Institute |
Inhibitors of usp1 deubiquitinating enzyme complex
|
EP2364702A3
(en)
*
|
2006-09-05 |
2012-01-25 |
Emory University |
Kinase inhibitors for preventing or treating pathogen infection and method of use thereof
|
US20100144738A1
(en)
|
2006-09-05 |
2010-06-10 |
William Bornmann |
Inhibitors of c-met and uses thereof
|
WO2008045529A1
(en)
|
2006-10-12 |
2008-04-17 |
Serenex, Inc. |
Purine and pyrimidine derivatives for treatment of cancer and inflammatory diseases
|
ES2383370T3
(es)
*
|
2006-10-19 |
2012-06-20 |
Signal Pharmaceuticals Llc |
Compuestos de heteroarilo, sus composiciones y uso de los mismos como inhibidores de proteína quinasa
|
US20080119496A1
(en)
|
2006-11-16 |
2008-05-22 |
Pharmacopeia Drug Discovery, Inc. |
7-Substituted Purine Derivatives for Immunosuppression
|
AU2006350748A1
(en)
|
2006-11-16 |
2008-05-22 |
Pharmacopeia, Llc |
7-substituted purine derivatives for immunosuppression
|
US7943617B2
(en)
|
2006-11-27 |
2011-05-17 |
Bristol-Myers Squibb Company |
Heterobicyclic compounds useful as kinase inhibitors
|
PE20081887A1
(es)
|
2007-03-20 |
2009-01-16 |
Dainippon Sumitomo Pharma Co |
Nuevo compuesto de adenina
|
WO2008118454A2
(en)
|
2007-03-23 |
2008-10-02 |
Amgen Inc. |
Derivatives of quinoline or benzopyrazine and their uses for the treatment of (inter alia) inflammatory diseases, autoimmune diseases or various kinds of cancer
|
WO2008117796A1
(ja)
|
2007-03-28 |
2008-10-02 |
Dainippon Sumitomo Pharma Co., Ltd. |
新規ムチリン誘導体
|
US20090182035A1
(en)
|
2007-04-11 |
2009-07-16 |
Alcon Research, Ltd. |
Use of a combination of olopatadine and cilomilast to treat non-infectious rhinitis and allergic conjunctivitis
|
TW200902025A
(en)
|
2007-04-11 |
2009-01-16 |
Alcon Res Ltd |
Use of an inhibitor of TNF α plus an antihistamine to treat allergic rhinitis and allergic conjunctivitis
|
GB0708258D0
(en)
|
2007-04-27 |
2007-06-06 |
Katholleke Universiteit Leuven |
New anti-viral nulceoside analogs
|
WO2008131501A2
(en)
|
2007-04-27 |
2008-11-06 |
Katholieke Universiteit Leuven |
New anti-viral nucleoside analogs
|
CA2686485A1
(en)
|
2007-05-23 |
2008-11-27 |
Pharmacopeia, Llc |
Purinones and 1h-imidazopyridinones as pkc-theta inhibitors
|
AU2008267444A1
(en)
|
2007-06-26 |
2008-12-31 |
Sanofi-Aventis |
A regioselective copper catalyzed synthesis of benzimidazoles and azabenzimidazoles
|
JP2009007273A
(ja)
|
2007-06-27 |
2009-01-15 |
Ajinomoto Co Inc |
ジアミノピリミジン化合物の製造方法
|
US20090118301A1
(en)
|
2007-11-02 |
2009-05-07 |
Arbor Vita Corporation |
Compositions and Methods for Treating Cancer
|
WO2009062059A2
(en)
|
2007-11-08 |
2009-05-14 |
Pharmacopeia, Inc. |
Isomeric purinones and 1h-imidazopyridinones as pkc-theta inhibitors
|
RU2010125220A
(ru)
|
2007-11-20 |
2011-12-27 |
Мерк Шарп Энд Домэ Корп. (Us) |
Ненуклеозидные ингибиторы обратной транскриптазы
|
US20090143392A1
(en)
|
2007-11-30 |
2009-06-04 |
Elbion Gmbh |
Methods of Treating Obesity and Metabolic Disorders
|
CA2706866A1
(en)
|
2007-11-30 |
2009-06-04 |
Biotie Therapies Gmbh |
Aryl and heteroaryl fused imidazo[1,5-a]pyrazines as inhibitors of phosphodiesterase 10
|
AU2008329072A1
(en)
|
2007-11-30 |
2009-06-04 |
Elbion Gmbh |
Aryl and heteroaryl fused imidazo (1,5-A) pyrazines as inhibitors of phosphodiesterase 10
|
EP2229394A1
(en)
|
2008-01-17 |
2010-09-22 |
Grünenthal GmbH |
Substituted sulfonamide derivatives
|
CA2712265A1
(en)
|
2008-01-17 |
2009-07-23 |
Gruenenthal Gmbh |
Substituted sulfonamide derivatives
|
EP2090576A1
(en)
|
2008-02-01 |
2009-08-19 |
Merz Pharma GmbH & Co.KGaA |
6-halo-pyrazolo[1,5-a]pyridines, a process for their preparation and their use as metabotropic glutamate receptor (mGluR) modulators
|
EP2085398A1
(en)
|
2008-02-01 |
2009-08-05 |
Merz Pharma GmbH & Co. KGaA |
Pyrazolopyrimidines, a process for their preparation and their use as medicine
|
JP2011515403A
(ja)
|
2008-03-21 |
2011-05-19 |
メルク・シャープ・エンド・ドーム・コーポレイション |
キノリジジノンm1受容体ポジティブアロステリックモジュレータ
|
CA2722308C
(en)
|
2008-04-15 |
2024-02-27 |
Rfs Pharma, Llc. |
Nucleoside derivatives for treatment of caliciviridae infections, including norovirus infections
|
WO2009137462A2
(en)
|
2008-05-05 |
2009-11-12 |
Envivo Pharmaceuticals, Inc. |
Methods for treating cognitive disorders using inhibitors of histone deacetylase
|
CN102131810B
(zh)
|
2008-06-25 |
2014-02-26 |
百时美施贵宝公司 |
作为抗hiv剂的二酮稠合的吡咯并哌啶类和吡咯并哌嗪类
|
JP5662319B2
(ja)
|
2008-09-09 |
2015-01-28 |
ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング |
アザ−ベンゾイミダゾロンキマーゼ阻害剤
|
CA2737527C
(en)
|
2008-09-16 |
2015-12-29 |
Proximagen Limited |
4,5,6,7-tetrahydroimidazo[4,5-c]pyridine compounds useful as inhibitors of ssao activity
|
CA2738429C
(en)
|
2008-09-26 |
2016-10-25 |
Intellikine, Inc. |
Heterocyclic kinase inhibitors
|
WO2010068520A2
(en)
|
2008-12-11 |
2010-06-17 |
Cara Therapeutics, Inc. |
Substituted imidazoheterocycle derivatives
|
CN101824036A
(zh)
|
2009-03-05 |
2010-09-08 |
上海恒瑞医药有限公司 |
四氢咪唑并[1,5-a]吡嗪衍生物的盐,其制备方法及其在医药上的应用
|
EP2493895B1
(en)
|
2009-10-29 |
2017-04-26 |
Vectura Limited |
N-containing heteroaryl derivatives as jak3 kinase inhibitors
|
JP2011136925A
(ja)
|
2009-12-28 |
2011-07-14 |
Dainippon Sumitomo Pharma Co Ltd |
含窒素二環性化合物
|
WO2011097333A1
(en)
|
2010-02-03 |
2011-08-11 |
Signal Pharmaceuticals, Llc |
Identification of lkb1 mutation as a predictive biomarker for sensitivity to tor kinase inhibitors
|
WO2011137320A2
(en)
|
2010-04-30 |
2011-11-03 |
Dana-Farber Cancer Institute, Inc. |
Small molecule inhibitors of usp1 deubiquitinating enzyme activity
|
WO2011156889A1
(en)
|
2010-06-14 |
2011-12-22 |
Trt Pharma Inc. |
Novel modulators of nrf2 and uses thereof
|
EP2397482A1
(en)
|
2010-06-15 |
2011-12-21 |
Almirall, S.A. |
Heteroaryl imidazolone derivatives as jak inhibitors
|
JP2012012332A
(ja)
|
2010-06-30 |
2012-01-19 |
Dainippon Sumitomo Pharma Co Ltd |
新規アザインドール誘導体
|
US20130165426A1
(en)
|
2010-07-06 |
2013-06-27 |
Université de Montréal |
Imidazopyridine, imidazopyrimidine and imidazopyrazine derivatives as melanocortin-4 receptor modulators
|
WO2012009258A2
(en)
|
2010-07-13 |
2012-01-19 |
Edward Roberts |
Peptidomimetic galanin receptor modulators
|
CN102372716A
(zh)
|
2010-08-09 |
2012-03-14 |
江苏恒瑞医药股份有限公司 |
酞嗪酮类衍生物、其制备方法及其在医药上的应用
|
DE102010040233A1
(de)
|
2010-09-03 |
2012-03-08 |
Bayer Schering Pharma Aktiengesellschaft |
Bicyclische Aza-Heterocyclen und ihre Verwendung
|
CN102485721B
(zh)
|
2010-12-03 |
2015-12-09 |
曹亚 |
取代的2,3-二氮杂萘酮化合物及其用途
|
TWI501967B
(zh)
|
2010-12-16 |
2015-10-01 |
Janssen R&D Ireland |
作為呼吸道融合病毒抗病毒劑之氮雜吲哚類
|
TWI527814B
(zh)
|
2010-12-16 |
2016-04-01 |
健生科學愛爾蘭無限公司 |
作為呼吸道融合病毒抗病毒劑之氮雜苯并咪唑類
|
TWI541241B
(zh)
|
2010-12-16 |
2016-07-11 |
健生科學愛爾蘭無限公司 |
作為呼吸道融合病毒抗病毒劑之咪唑并吡啶類
|
TWI515187B
(zh)
|
2010-12-16 |
2016-01-01 |
健生科學愛爾蘭無限公司 |
作為呼吸道融合病毒抗病毒劑之吲哚類
|
JP5990106B2
(ja)
|
2011-01-28 |
2016-09-07 |
佐藤製薬株式会社 |
縮環化合物
|
WO2012114252A1
(en)
|
2011-02-21 |
2012-08-30 |
Actelion Pharmaceuticals Ltd |
Novel indole and pyrrolopyridine amides
|
MX2013011096A
(es)
|
2011-03-26 |
2014-06-06 |
Envivo Pharmaceuticals Inc |
Metodos de tratamiento dirigido a degeneracion lobular frontotemporal.
|
WO2012136492A1
(en)
|
2011-04-04 |
2012-10-11 |
Siena Biotech S.P.A. |
Wnt pathway antagonists
|
WO2013025628A1
(en)
|
2011-08-15 |
2013-02-21 |
Ligand Pharmaceuticals Incorporated |
Janus kinase inhibitor compounds and methods
|
WO2013033899A1
(en)
|
2011-09-08 |
2013-03-14 |
Merck Sharp & Dohme Corp. |
Substituted benzofuran compounds and methods of use thereof for the treatment of viral diseases
|
EP2899183B1
(en)
|
2011-10-14 |
2018-09-19 |
Bristol-Myers Squibb Company |
Substituted Tetrahydroisoquinoline Compounds as Factor Xia Inhibitors
|
EP3659599B1
(en)
|
2011-10-19 |
2022-12-21 |
Signal Pharmaceuticals, LLC |
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 for use in the treatment of glioblastoma multiforme
|
US8501724B1
(en)
|
2012-01-31 |
2013-08-06 |
Pharmacyclics, Inc. |
Purinone compounds as kinase inhibitors
|
US9375443B2
(en)
|
2012-02-24 |
2016-06-28 |
Signal Pharmaceuticals, Llc |
Method for treating advanced non-small cell lung cancer (NSCLC) by administering a combination of a TOR kinase inhibitor and azacitidine or erlotinib
|
EP2822944A1
(en)
|
2012-03-05 |
2015-01-14 |
Amgen, Inc. |
Oxazolidinone compounds and derivatives thereof
|
US9338896B2
(en)
|
2012-07-25 |
2016-05-10 |
Enthone, Inc. |
Adhesion promotion in printed circuit boards
|
US9566310B2
(en)
|
2012-09-10 |
2017-02-14 |
Board Of Regents Of The Nevada System Of Higher Education On Behalf Of The University Of Nevada, Reno |
Methods of treating muscular dystrophy
|
WO2014043246A1
(en)
|
2012-09-11 |
2014-03-20 |
The Board Of Trustees Of The University Of Illinois |
Enoyl reductase inhibitors with antibacterial activity
|
AU2013202768B2
(en)
*
|
2012-10-18 |
2015-11-05 |
Signal Pharmaceuticals, Llc |
Treatment of cancer with TOR kinase inhibitors
|
AU2013370417A1
(en)
*
|
2012-12-28 |
2015-07-16 |
The United States Of America, As Represented By The Secretary, Department Of Health And Human Services |
Inhibitors of the USP1/UAF1 deubiquitinase complex and uses thereof
|
JP6024979B2
(ja)
|
2013-02-21 |
2016-11-16 |
学校法人金沢工業大学 |
難燃組成物、それを用いた難燃化処理方法および難燃材料
|
CN103923085B
(zh)
|
2013-02-25 |
2016-08-24 |
苏州云轩医药科技有限公司 |
具有刺猬通路拮抗剂活性的吡啶杂环化合物及其用途
|
WO2014134240A1
(en)
|
2013-02-28 |
2014-09-04 |
Signal Pharmaceuticals, Llc |
Treatment of cancer with tor kinase inhibitors
|
US9187454B2
(en)
|
2013-03-13 |
2015-11-17 |
Boston Biomedical, Inc. |
Inhibitors of kinases and cancer stem cells, and methods of preparation and use thereof
|
WO2014160017A1
(en)
|
2013-03-13 |
2014-10-02 |
Abbvie Inc. |
Pyridine cdk9 kinase inhibitors
|
US20160039825A1
(en)
|
2013-03-15 |
2016-02-11 |
Biogen Ma Inc. |
S1p and/or atx modulating agents
|
WO2014160592A2
(en)
|
2013-03-27 |
2014-10-02 |
Merck Sharp & Dohme Corp. |
FACTOR XIa INHIBITORS
|
ES2806135T3
(es)
|
2013-06-21 |
2021-02-16 |
Zenith Epigenetics Ltd |
Nuevos inhibidores de bromodominios bicíclicos
|
EP3160466A4
(en)
|
2014-06-25 |
2017-12-27 |
Epizyme, Inc. |
Prmt5 inhibitors and uses thereof
|
CN106467538B
(zh)
|
2015-08-14 |
2019-03-05 |
沈阳中化农药化工研发有限公司 |
一种取代的四氢异喹啉化合物与用途
|
MX2021001186A
(es)
|
2015-11-20 |
2022-10-11 |
Forma Therapeutics Inc |
Purinonas como inhibidores de proteasa especifica de ubiquitina 1.
|
CN107629071B
(zh)
|
2016-07-19 |
2019-12-27 |
上海勋和医药科技有限公司 |
取代2,4-(1h,3h)嘧啶二酮作为parp抑制剂及其应用
|
CN107629057B
(zh)
|
2016-07-19 |
2020-03-27 |
上海勋和医药科技有限公司 |
Bet蛋白抑制剂及其应用
|
WO2018119263A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds derivatives as pd-l1 internalization inducers
|
EP3897652A4
(en)
|
2018-12-20 |
2022-09-14 |
KSQ Therapeutics, Inc. |
SUBSTITUTED PYRAZOLOPYRIMIDINES AND SUBSTITUTED PURINES AND THEIR USE AS UBIQUITIN-SPECIFIC TREATMENT PROTEASE 1 INHIBITORS
|
CN113474346A
(zh)
|
2018-12-28 |
2021-10-01 |
福马治疗有限公司 |
用于抑制泛素特异性蛋白酶1的组合物
|