|
CN1615873A
(zh)
|
1999-12-24 |
2005-05-18 |
阿文蒂斯药物有限公司 |
氮杂吲哚类化合物
|
|
GB0115109D0
(en)
|
2001-06-21 |
2001-08-15 |
Aventis Pharma Ltd |
Chemical compounds
|
|
EP2335700A1
(en)
*
|
2001-07-25 |
2011-06-22 |
Boehringer Ingelheim (Canada) Ltd. |
Hepatitis C virus polymerase inhibitors with a heterobicylic structure
|
|
TWI329105B
(en)
*
|
2002-02-01 |
2010-08-21 |
Rigel Pharmaceuticals Inc |
2,4-pyrimidinediamine compounds and their uses
|
|
GB0202679D0
(en)
*
|
2002-02-05 |
2002-03-20 |
Glaxo Group Ltd |
Novel compounds
|
|
TW200307542A
(en)
|
2002-05-30 |
2003-12-16 |
Astrazeneca Ab |
Novel compounds
|
|
CA2495216A1
(en)
|
2002-08-12 |
2004-02-19 |
Sugen, Inc. |
3-pyrrolyl-pyridopyrazoles and 3-pyrrolyl-indazoles as novel kinase inhibitors
|
|
SE0202463D0
(sv)
*
|
2002-08-14 |
2002-08-14 |
Astrazeneca Ab |
Novel compounds
|
|
US20050043212A1
(en)
*
|
2002-10-09 |
2005-02-24 |
Ford Kirschenbaum |
Differential inhibition of p38 map kinase isoforms
|
|
US20050288299A1
(en)
*
|
2002-10-09 |
2005-12-29 |
Mavunkel Babu J |
Azaindole derivatives as inhibitors of p38 kinase
|
|
CN1713910A
(zh)
*
|
2002-10-09 |
2005-12-28 |
西奥斯股份有限公司 |
作为p38激酶抑制剂的氮杂吲哚衍生物
|
|
US7098231B2
(en)
*
|
2003-01-22 |
2006-08-29 |
Boehringer Ingelheim International Gmbh |
Viral polymerase inhibitors
|
|
US7223785B2
(en)
|
2003-01-22 |
2007-05-29 |
Boehringer Ingelheim International Gmbh |
Viral polymerase inhibitors
|
|
GB0305142D0
(en)
*
|
2003-03-06 |
2003-04-09 |
Eisai London Res Lab Ltd |
Synthesis
|
|
SE0301372D0
(sv)
*
|
2003-05-09 |
2003-05-09 |
Astrazeneca Ab |
Novel compounds
|
|
AU2004275694B2
(en)
*
|
2003-06-30 |
2008-03-06 |
Bizbiotech Co., Ltd. |
Compounds, compositions and methods
|
|
US7202363B2
(en)
|
2003-07-24 |
2007-04-10 |
Abbott Laboratories |
Thienopyridine and furopyridine kinase inhibitors
|
|
ES2421139T3
(es)
|
2003-07-30 |
2013-08-29 |
Rigel Pharmaceuticals, Inc. |
Compuestos de 2,4-pirimidindiamina para su uso en el tratamiento o la prevención de enfermedades autoinmunitarias
|
|
WO2005056547A2
(en)
|
2003-12-04 |
2005-06-23 |
Vertex Pharmaceuticals Incorporated |
Quinoxalines useful as inhibitors of protein kinases
|
|
EP1694686A1
(en)
|
2003-12-19 |
2006-08-30 |
Takeda San Diego, Inc. |
Kinase inhibitors
|
|
KR20120091276A
(ko)
*
|
2004-02-20 |
2012-08-17 |
베링거 인겔하임 인터내셔날 게엠베하 |
바이러스 폴리머라제 억제제
|
|
PT1730146E
(pt)
*
|
2004-03-30 |
2011-07-11 |
Vertex Pharma |
Azaindoles úteis como inibidores de jak e outras proteínas quinases
|
|
FR2868422B1
(fr)
|
2004-03-31 |
2006-07-14 |
Aventis Pharma Sa |
Nouveaux derives pyrrolo(2,3-b) pyridine, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases
|
|
WO2005097129A2
(en)
*
|
2004-04-05 |
2005-10-20 |
Takeda Pharmaceutical Company Limited |
6-azaindole compound
|
|
WO2005105788A1
(en)
*
|
2004-04-23 |
2005-11-10 |
Takeda San Diego, Inc. |
Indole derivatives and use thereof as kinase inhibitors
|
|
KR20070053237A
(ko)
*
|
2004-07-27 |
2007-05-23 |
에스지엑스 파마슈티컬스, 인코포레이티드 |
피롤로-피리딘 키나제 조절제
|
|
CA2573538C
(en)
|
2004-07-30 |
2014-11-25 |
Methylgene Inc. |
Inhibitors of vegf receptor and hgf receptor signaling
|
|
BRPI0514094A
(pt)
*
|
2004-08-02 |
2008-05-27 |
Osi Pharm Inc |
composto, composição, e, método de tratamento de distúrbio hiperproliferativo
|
|
EP1778669A2
(en)
|
2004-08-18 |
2007-05-02 |
Takeda San Diego, Inc. |
Kinase inhibitors
|
|
JP2008510792A
(ja)
*
|
2004-08-26 |
2008-04-10 |
ファイザー・インク |
タンパク質チロシンキナーゼ阻害剤としてのアミノヘテロアリール化合物
|
|
FR2876103B1
(fr)
|
2004-10-01 |
2008-02-22 |
Aventis Pharma Sa |
Nouveaux derives bis-azaindoles, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases
|
|
ATE479687T1
(de)
|
2004-10-15 |
2010-09-15 |
Takeda Pharmaceutical |
Kinaseinhibitoren
|
|
MY179032A
(en)
*
|
2004-10-25 |
2020-10-26 |
Cancer Research Tech Ltd |
Ortho-condensed pyridine and pyrimidine derivatives (e.g.purines) as protein kinase inhibitors
|
|
EP1814882A1
(en)
*
|
2004-11-22 |
2007-08-08 |
Vertex Pharmaceuticals Incorporated |
Pyrrolopyrazines and pyrazolopyrazines useful as inhibitors of protein kinases
|
|
JP4954086B2
(ja)
*
|
2004-12-08 |
2012-06-13 |
グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー |
1h−ピロロ[2,3−b]ピリジン
|
|
AR054416A1
(es)
|
2004-12-22 |
2007-06-27 |
Incyte Corp |
Pirrolo [2,3-b]piridin-4-il-aminas y pirrolo [2,3-b]pirimidin-4-il-aminas como inhibidores de las quinasas janus. composiciones farmaceuticas.
|
|
US7786113B2
(en)
*
|
2004-12-23 |
2010-08-31 |
Hoffman-La Roche Inc. |
Heterocyclic carbamate derivatives, their manufacture and use as pharmaceutical agents
|
|
EP1874769B1
(de)
*
|
2005-04-25 |
2011-09-14 |
Merck Patent GmbH |
Neuartige aza-heterozyklen als kinase-inhibitoren
|
|
FR2884821B1
(fr)
*
|
2005-04-26 |
2007-07-06 |
Aventis Pharma Sa |
Pyrrolopyridines substitues, compositions les contenant, procede de fabrication et utilisation
|
|
AU2006343808B2
(en)
|
2005-05-20 |
2012-03-29 |
Mirati Therapeutics, Inc. |
Inhibitors of VEGF receptor and HGF receptor signaling
|
|
CA2608726C
(en)
|
2005-05-20 |
2013-07-09 |
Methylgene Inc. |
Inhibitors of vegf receptor and hgf receptor signaling
|
|
EP1881983B1
(en)
|
2005-05-20 |
2012-01-11 |
Vertex Pharmaceuticals, Inc. |
Pyrrolopyridines useful as inhibitors of protein kinase
|
|
JP2008543855A
(ja)
|
2005-06-13 |
2008-12-04 |
ライジェル ファーマシューティカルズ, インコーポレイテッド |
変形性骨疾患を処置するための方法および組成物
|
|
EP1734251B1
(en)
*
|
2005-06-17 |
2007-01-24 |
MAGNETI MARELLI POWERTRAIN S.p.A. |
Fuel injector
|
|
UA95244C2
(ru)
|
2005-06-22 |
2011-07-25 |
Плексикон, Инк. |
Соединения и способ модулирования активности киназ, и показания для их применения
|
|
KR101142363B1
(ko)
*
|
2005-06-27 |
2012-05-21 |
주식회사유한양행 |
피롤로피리딘 유도체를 포함하는 항암제 조성물
|
|
EP2251341A1
(en)
*
|
2005-07-14 |
2010-11-17 |
Astellas Pharma Inc. |
Heterocyclic Janus kinase 3 inhibitors
|
|
EP1915378A4
(en)
*
|
2005-08-12 |
2009-07-22 |
Boehringer Ingelheim Int |
VIRUS POLYMERASE INHIBITORS
|
|
US8119655B2
(en)
|
2005-10-07 |
2012-02-21 |
Takeda Pharmaceutical Company Limited |
Kinase inhibitors
|
|
US7576218B2
(en)
|
2005-10-11 |
2009-08-18 |
Chemocentryx, Inc. |
4-phenylpiperdine-pyrazole CCR1 antagonists
|
|
US7371862B2
(en)
|
2005-11-11 |
2008-05-13 |
Pfizer Italia S.R.L. |
Azaindolylidene derivatives as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them
|
|
JP2009515984A
(ja)
|
2005-11-15 |
2009-04-16 |
バーテックス ファーマシューティカルズ インコーポレイテッド |
キナーゼ阻害剤として有用なアザインダゾール
|
|
EP1963320A1
(en)
*
|
2005-12-07 |
2008-09-03 |
OSI Pharmaceuticals, Inc. |
Pyrrolopyridine kinase inhibiting compounds
|
|
DK3184526T3
(en)
|
2005-12-13 |
2019-01-14 |
Incyte Holdings Corp |
PYRROLO [2,3-D] PYRIMIDINE DERIVATIVES AS A JANUS-KINASE INHIBITOR
|
|
EP1968961A2
(en)
|
2005-12-21 |
2008-09-17 |
Decode Genetics EHF |
Biaryl nitrogen heterocycle inhibitors of lta4h for treating inflammation
|
|
NZ601687A
(en)
|
2006-01-17 |
2014-03-28 |
Vertex Pharma |
Azaindoles useful as inhibitors of janus kinases
|
|
CN101466676B
(zh)
*
|
2006-04-12 |
2012-07-18 |
默沙东公司 |
吡啶基酰胺类t-型钙通道拮抗剂
|
|
PL2026775T3
(pl)
*
|
2006-05-09 |
2015-12-31 |
Novaremed Ltd |
Zastosowanie inhibitorów kinazy tyrozynowej Syk w leczeniu komórkowych zaburzeń proliferacyjnych
|
|
US8604031B2
(en)
*
|
2006-05-18 |
2013-12-10 |
Mannkind Corporation |
Intracellular kinase inhibitors
|
|
GB0617161D0
(en)
*
|
2006-08-31 |
2006-10-11 |
Vernalis R&D Ltd |
Enzyme inhibitors
|
|
CL2007002617A1
(es)
|
2006-09-11 |
2008-05-16 |
Sanofi Aventis |
Compuestos derivados de pirrolo[2,3-b]pirazin-6-ilo; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar inflamacion de las articulaciones, artritis reumatoide, tumores, linfoma de las celulas del manto.
|
|
JP2010505961A
(ja)
*
|
2006-10-09 |
2010-02-25 |
タケダ サン ディエゴ インコーポレイテッド |
キナーゼ阻害剤
|
|
JP2010505962A
(ja)
|
2006-10-09 |
2010-02-25 |
武田薬品工業株式会社 |
キナーゼ阻害剤
|
|
WO2008063888A2
(en)
|
2006-11-22 |
2008-05-29 |
Plexxikon, Inc. |
Compounds modulating c-fms and/or c-kit activity and uses therefor
|
|
CA2673472A1
(en)
|
2006-12-21 |
2008-07-03 |
Vertex Pharmaceuticals Incorporated |
5-cyan0-4- (pyrrolo) [2, 3b] pyridine-3-yl) -pyrimidine derivatives useful as protein kinase inhibitors
|
|
PE20081581A1
(es)
*
|
2006-12-21 |
2008-11-12 |
Plexxikon Inc |
COMPUESTOS PIRROLO[2,3-b]PIRIDINAS COMO MODULADORES DE QUINASA
|
|
TW200833711A
(en)
*
|
2006-12-22 |
2008-08-16 |
Genentech Inc |
Antibodies to insulin-like growth factor receptor
|
|
BRPI0809542A8
(pt)
|
2007-03-29 |
2015-09-15 |
Asubio Pharma Co Ltd |
Compostos derivados de indol tendo atividade de inibição de cpla2, composição farmacêutica, e métodos de produção dos referidos compostos
|
|
DK2740731T3
(en)
|
2007-06-13 |
2016-04-11 |
Incyte Holdings Corp |
CRYSTALLINE SALTS OF JANUSKINASEINHIBITOREN (R) -3- (4- (7H-pyrrolo [2,3-d] pyrimidin-4-yl) -1H-pyrazol-1-yl) -3-CYCLOPENTYLPROPANNITRIL
|
|
SG183036A1
(en)
|
2007-07-17 |
2012-08-30 |
Plexxikon Inc |
Compounds and methods for kinase modulation, and indications therefor
|
|
GB2467670B
(en)
|
2007-10-04 |
2012-08-01 |
Intellikine Inc |
Chemical entities and therapeutic uses thereof
|
|
CA2701594C
(en)
|
2007-10-24 |
2014-02-18 |
Merck Sharp & Dohme Corp. |
Heterocycle phenyl amide t-type calcium channel antagonists
|
|
AU2008317352A1
(en)
*
|
2007-10-24 |
2009-04-30 |
Merck Sharp & Dohme Corp. |
Heterocycle amide T-type calcium channel antagonists
|
|
EP2247595B1
(en)
|
2008-02-25 |
2011-07-20 |
F. Hoffmann-La Roche AG |
Pyrrolopyrazine kinase inhibitors
|
|
ES2372908T3
(es)
|
2008-02-25 |
2012-01-27 |
F. Hoffmann-La Roche Ag |
Inhibidores de la pirrolopirazina quinasa.
|
|
KR20100114095A
(ko)
|
2008-02-25 |
2010-10-22 |
에프. 호프만-라 로슈 아게 |
피롤로피라진 키나아제 저해제
|
|
CN101952294B
(zh)
|
2008-02-25 |
2014-11-26 |
霍夫曼-拉罗奇有限公司 |
吡咯并吡嗪激酶抑制剂
|
|
PL2247592T3
(pl)
|
2008-02-25 |
2012-01-31 |
Hoffmann La Roche |
Pirolopirazynowe inhibitory kinazy
|
|
KR20100137495A
(ko)
|
2008-03-05 |
2010-12-30 |
메틸진 인코포레이티드 |
단백질 티로신 키나아제 활성의 억제제
|
|
US8993580B2
(en)
|
2008-03-14 |
2015-03-31 |
Intellikine Llc |
Benzothiazole kinase inhibitors and methods of use
|
|
US8637542B2
(en)
|
2008-03-14 |
2014-01-28 |
Intellikine, Inc. |
Kinase inhibitors and methods of use
|
|
US9273077B2
(en)
|
2008-05-21 |
2016-03-01 |
Ariad Pharmaceuticals, Inc. |
Phosphorus derivatives as kinase inhibitors
|
|
PL2300013T5
(pl)
|
2008-05-21 |
2025-04-28 |
Takeda Pharmaceutical Company Limited |
Pochodne fosforu jako inhibitor kinazy
|
|
EP2313411A1
(en)
*
|
2008-06-10 |
2011-04-27 |
Plexxikon, Inc. |
5h-pyrr0l0 [2,3-b]pyrazine derivatives for kinase modulation, and indications therefor
|
|
BRPI0915231A2
(pt)
*
|
2008-07-08 |
2018-06-12 |
Intellikine Inc |
compostos inibidores de quinase e métodos de uso
|
|
US8476282B2
(en)
|
2008-11-03 |
2013-07-02 |
Intellikine Llc |
Benzoxazole kinase inhibitors and methods of use
|
|
US8846664B2
(en)
|
2008-11-12 |
2014-09-30 |
Ariad Pharmaceuticals, Inc. |
Pyrazinopyrazines and derivatives as kinase inhibitors
|
|
CN102232076B
(zh)
*
|
2008-12-05 |
2014-12-31 |
霍夫曼-拉罗奇有限公司 |
吡咯并吡嗪基脲激酶抑制剂
|
|
UA103351C2
(uk)
|
2008-12-05 |
2013-10-10 |
Ебботт Леборетріз |
ПОХІДНІ ТІЄНО[3,2-c]ПІРИДИНУ ЯК ІНГІБІТОРИ КІНАЗ ДЛЯ ЗАСТОСУВАННЯ В ЛІКУВАННІ РАКУ
|
|
CA2744563A1
(en)
*
|
2008-12-12 |
2010-06-17 |
Ariad Pharmaceuticals, Inc. |
Azaindole derivatives as kinase inhibitors
|
|
MY201120A
(en)
|
2009-02-25 |
2024-02-06 |
Takeda Pharmaceuticals Co |
Intermediates for use in a process of producing pyrrole compounds
|
|
US20110112101A1
(en)
*
|
2009-03-05 |
2011-05-12 |
Sanofi-Aventis |
Treatment for ocular-related disorders
|
|
EA022924B1
(ru)
|
2009-04-03 |
2016-03-31 |
Ф.Хоффманн-Ля Рош Аг |
ТВЁРДАЯ ФОРМА {3-[5-(4-ХЛОРФЕНИЛ)-1Н-ПИРРОЛО[2,3-b]ПИРИДИН-3-КАРБОНИЛ]-2,4-ДИФТОРФЕНИЛ}АМИДА ПРОПАН-1-СУЛЬФОНОВОЙ КИСЛОТЫ И ЕЁ ПРИМЕНЕНИЕ
|
|
WO2010135411A2
(en)
*
|
2009-05-19 |
2010-11-25 |
The Regents Of The University Of Colorado |
Aurora-a copy number and sensitivity to inhibitors
|
|
WO2010146059A2
(en)
|
2009-06-16 |
2010-12-23 |
F. Hoffmann-La Roche Ag |
Biomarkers for igf-1r inhibitor therapy
|
|
PH12015501678B1
(en)
|
2009-06-17 |
2022-07-06 |
Vertex Pharma |
Inhibitors of influenza viruses replication
|
|
US8329724B2
(en)
|
2009-08-03 |
2012-12-11 |
Hoffmann-La Roche Inc. |
Process for the manufacture of pharmaceutically active compounds
|
|
FR2949467B1
(fr)
|
2009-09-03 |
2011-11-25 |
Sanofi Aventis |
Nouveaux derives de 5,6,7,8-tetrahydroindolizine inhibiteurs d'hsp90, compositions les contenant et utilisation
|
|
MA33975B1
(fr)
|
2009-11-06 |
2013-02-01 |
Plexxikon Inc |
Composés et méthodes de modulation des kinases et leurs indications d'emploi
|
|
EP2338890A1
(en)
|
2009-12-22 |
2011-06-29 |
Bayer CropScience AG |
4,7-Diazaindole derivatives and their use as fungicides
|
|
PL2516434T3
(pl)
|
2009-12-23 |
2015-11-30 |
Takeda Pharmaceuticals Co |
Skondensowane heteroaromatyczne pirolidynony jako inhibitory SYK
|
|
CA2787079A1
(en)
*
|
2010-01-27 |
2011-08-04 |
Vertex Pharmaceuticals Incorporated |
Pyrazolopyrazine kinase inhibitors
|
|
WO2011109932A1
(en)
*
|
2010-03-09 |
2011-09-15 |
F.Hoffmann-La Roche Ag |
Novel process for the manufacture of 5-halogenated-7-azaindoles
|
|
AU2011224484A1
(en)
|
2010-03-10 |
2012-09-27 |
Incyte Holdings Corporation |
Piperidin-4-yl azetidine derivatives as JAK1 inhibitors
|
|
US8481541B2
(en)
|
2010-03-22 |
2013-07-09 |
Hoffmann-La Roche Inc. |
Pyrrolopyrazine kinase inhibitors
|
|
US8518945B2
(en)
|
2010-03-22 |
2013-08-27 |
Hoffmann-La Roche Inc. |
Pyrrolopyrazine kinase inhibitors
|
|
CA2798970A1
(en)
|
2010-05-20 |
2011-11-24 |
F. Hoffmann-La Roche Ag |
Pyrrolopyrazine derivatives as syk and jak inhibitors
|
|
JP2013529204A
(ja)
*
|
2010-05-20 |
2013-07-18 |
エフ.ホフマン−ラ ロシュ アーゲー |
ピロロ[2,3−b]ピラジン−7−カルボキサミド誘導体とJAK及びSYK及び阻害剤としてのそれらの使用
|
|
MY161078A
(en)
|
2010-05-21 |
2017-04-14 |
Incyte Holdings Corp |
Topical formulation for a jak inhibitor
|
|
CA2800176C
(en)
*
|
2010-05-24 |
2018-08-28 |
University Of Rochester |
Bicyclic heteroaryl kinase inhibitors and methods of use
|
|
US9265739B2
(en)
|
2010-06-02 |
2016-02-23 |
The Trustees Of The University Of Pennsylvania |
Methods and use of compounds that bind to HER2/neu receptor complex
|
|
WO2011153049A1
(en)
|
2010-06-02 |
2011-12-08 |
The Trustees Of The University Of Pennsylvania |
Methods and use of compounds that bind to her2/neu receptor complex
|
|
EP2635556B1
(en)
*
|
2010-11-01 |
2017-06-21 |
Portola Pharmaceuticals, Inc. |
Benzamides and nicotinamides as syk modulators
|
|
EP2640723A1
(en)
|
2010-11-19 |
2013-09-25 |
Incyte Corporation |
Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors
|
|
AU2011343642A1
(en)
|
2010-12-16 |
2013-05-02 |
Vertex Pharmaceuticals Incorporated |
Inhibitors of influenza viruses replication
|
|
WO2012088266A2
(en)
|
2010-12-22 |
2012-06-28 |
Incyte Corporation |
Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3
|
|
JP5941069B2
(ja)
|
2011-02-07 |
2016-06-29 |
プレキシコン インコーポレーテッドPlexxikon Inc. |
キナーゼ調節のための化合物および方法、ならびにそれに対する適応症
|
|
TWI558702B
(zh)
|
2011-02-21 |
2016-11-21 |
普雷辛肯公司 |
醫藥活性物質的固態形式
|
|
JP6130305B2
(ja)
|
2011-02-23 |
2017-05-17 |
インテリカイン, エルエルシー |
キナーゼ阻害剤の組み合わせおよびそれらの使用
|
|
EP2704572B1
(en)
|
2011-05-04 |
2015-12-30 |
Ariad Pharmaceuticals, Inc. |
Compounds for inhibiting cell proliferation in egfr-driven cancers
|
|
EP2706852B1
(en)
|
2011-05-10 |
2018-08-22 |
Merck Sharp & Dohme Corp. |
Bipyridylaminopyridines as syk inhibitors
|
|
US9120785B2
(en)
|
2011-05-10 |
2015-09-01 |
Merck Sharp & Dohme Corp. |
Pyridyl aminopyridines as Syk inhibitors
|
|
WO2012154519A1
(en)
|
2011-05-10 |
2012-11-15 |
Merck Sharp & Dohme Corp. |
Aminopyrimidines as syk inhibitors
|
|
KR20140040819A
(ko)
|
2011-06-20 |
2014-04-03 |
인사이트 코포레이션 |
Jak 저해제로서의 아제티디닐 페닐, 피리딜 또는 피라지닐 카르복스아미드 유도체
|
|
US9056873B2
(en)
|
2011-06-22 |
2015-06-16 |
Takeda Pharmaceutical Company Limited |
Substituted 6-aza-isoindolin-1-one derivatives
|
|
CN103702998A
(zh)
|
2011-07-05 |
2014-04-02 |
沃泰克斯药物股份有限公司 |
生产氮杂吲哚类的方法和中间体
|
|
WO2013012909A1
(en)
|
2011-07-20 |
2013-01-24 |
Abbott Laboratories |
Kinase inhibitor with improved aqueous solubility
|
|
UA118010C2
(uk)
|
2011-08-01 |
2018-11-12 |
Вертекс Фармасьютікалз Інкорпорейтед |
Інгібітори реплікації вірусів грипу
|
|
DE102011111400A1
(de)
*
|
2011-08-23 |
2013-02-28 |
Merck Patent Gmbh |
Bicyclische heteroaromatische Verbindungen
|
|
EP3473099A1
(en)
|
2011-09-14 |
2019-04-24 |
Samumed, LLC |
Indazole-3-carboxamides and their use as wnt/b-catenin signaling pathway inhibitors
|
|
EP2763976B1
(en)
|
2011-10-05 |
2016-05-18 |
Merck Sharp & Dohme Corp. |
2-pyridyl carboxamide-containing spleen tyrosine kinase (syk) inhibitors
|
|
EP2763974B1
(en)
|
2011-10-05 |
2016-09-14 |
Merck Sharp & Dohme Corp. |
Phenyl carboxamide-containing spleen tyrosine kinase (syk) inhibitors
|
|
WO2013052393A1
(en)
|
2011-10-05 |
2013-04-11 |
Merck Sharp & Dohme Corp. |
3-PYRIDYL CARBOXAMIDE-CONTAINING SPLEEN TYROSINE KINASE (Syk) INHIBITORS
|
|
PH12017500997A1
(en)
|
2012-04-04 |
2018-02-19 |
Samumed Llc |
Indazole inhibitors of the wnt signal pathway and therapeutic uses thereof
|
|
JP6182593B2
(ja)
|
2012-04-20 |
2017-08-16 |
アドヴィーナス セラピューティクス リミテッド |
置換ヘテロ二環化合物、組成物及び医薬並びにそれらの用途
|
|
JP6469567B2
(ja)
|
2012-05-05 |
2019-02-13 |
アリアド・ファーマシューティカルズ・インコーポレイテッド |
Egfr発動性がんの細胞増殖阻害用化合物
|
|
US9150570B2
(en)
|
2012-05-31 |
2015-10-06 |
Plexxikon Inc. |
Synthesis of heterocyclic compounds
|
|
ES2984771T3
(es)
|
2012-06-13 |
2024-10-31 |
Incyte Holdings Corp |
Compuestos tricíclicos sustituidos como inhibidores de FGFR
|
|
US9487504B2
(en)
|
2012-06-20 |
2016-11-08 |
Merck Sharp & Dohme Corp. |
Imidazolyl analogs as syk inhibitors
|
|
WO2013192125A1
(en)
|
2012-06-20 |
2013-12-27 |
Merck Sharp & Dohme Corp. |
Pyrazolyl derivatives as syk inhibitors
|
|
EP2863915B1
(en)
|
2012-06-22 |
2017-12-06 |
Merck Sharp & Dohme Corp. |
SUBSTITUTED DIAZINE AND TRIAZINE SPLEEN TYROSINE KINASE (Syk) INHIBITORS
|
|
WO2013192098A1
(en)
|
2012-06-22 |
2013-12-27 |
Merck Sharp & Dohme Corp. |
SUBSTITUTED PYRIDINE SPLEEN TYROSINE KINASE (Syk) INHIBITORS
|
|
CN102718694B
(zh)
*
|
2012-06-27 |
2014-04-02 |
上海大学 |
3-氰基取代吲哚化合物及其合成方法
|
|
WO2014026125A1
(en)
|
2012-08-10 |
2014-02-13 |
Incyte Corporation |
Pyrazine derivatives as fgfr inhibitors
|
|
US9353066B2
(en)
|
2012-08-20 |
2016-05-31 |
Merck Sharp & Dohme Corp. |
Substituted phenyl-Spleen Tyrosine Kinase (Syk) inhibitors
|
|
PH12020551186B1
(en)
|
2012-11-15 |
2024-03-20 |
Incyte Holdings Corp |
Sustained-release dosage forms of ruxolitinib
|
|
EP2738172A1
(en)
*
|
2012-11-28 |
2014-06-04 |
Almirall, S.A. |
New bicyclic compounds as crac channel modulators
|
|
US9266892B2
(en)
|
2012-12-19 |
2016-02-23 |
Incyte Holdings Corporation |
Fused pyrazoles as FGFR inhibitors
|
|
US9908867B2
(en)
|
2013-01-08 |
2018-03-06 |
Samumed, Llc |
3-(benzoimidazol-2-yl)-indazole inhibitors of the Wnt signaling pathway and therapeutic uses thereof
|
|
US9468681B2
(en)
|
2013-03-01 |
2016-10-18 |
California Institute Of Technology |
Targeted nanoparticles
|
|
JP6397831B2
(ja)
|
2013-03-06 |
2018-09-26 |
インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation |
Jak阻害剤の製造方法及びその中間体
|
|
SG11201507486SA
(en)
|
2013-03-13 |
2015-10-29 |
Forma Therapeutics Inc |
Novel compounds and compositions for inhibition of fasn
|
|
TW201446763A
(zh)
*
|
2013-03-14 |
2014-12-16 |
Abbvie Inc |
吡咯并[2,3-b]吡啶cdk9激酶抑制劑
|
|
CN105246890A
(zh)
*
|
2013-03-14 |
2016-01-13 |
艾伯维公司 |
吡咯并[2,3-b]吡啶cdk9激酶抑制剂
|
|
US9611283B1
(en)
|
2013-04-10 |
2017-04-04 |
Ariad Pharmaceuticals, Inc. |
Methods for inhibiting cell proliferation in ALK-driven cancers
|
|
EA035095B1
(ru)
|
2013-04-19 |
2020-04-27 |
Инсайт Холдингс Корпорейшн |
Бициклические гетероциклы в качестве ингибиторов fgfr
|
|
KR20160045081A
(ko)
|
2013-08-07 |
2016-04-26 |
인사이트 코포레이션 |
Jak1 억제제용 지속 방출 복용 형태
|
|
JPWO2015029447A1
(ja)
*
|
2013-08-30 |
2017-03-02 |
興和株式会社 |
光学活性カルビノール化合物の製造方法
|
|
JP6615755B2
(ja)
|
2013-11-13 |
2019-12-04 |
バーテックス ファーマシューティカルズ インコーポレイテッド |
インフルエンザウイルスの複製の阻害剤
|
|
AU2014348752C1
(en)
|
2013-11-13 |
2019-11-21 |
Vertex Pharmaceuticals Incorporated |
Methods of preparing inhibitors of influenza viruses replication
|
|
WO2016040181A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof
|
|
WO2016040184A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof
|
|
WO2016040185A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
2-(1h-indazol-3-yl)-3h-imidazo[4,5-b]pyridine and therapeutic uses thereof
|
|
WO2016040190A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridine and therapeutic uses thereof
|
|
WO2016040193A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridine and therapeutic uses thereof
|
|
WO2016040180A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
3-(1h-benzo[d]imidazol-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof
|
|
US10851105B2
(en)
|
2014-10-22 |
2020-12-01 |
Incyte Corporation |
Bicyclic heterocycles as FGFR4 inhibitors
|
|
SG11201704685TA
(en)
*
|
2014-12-11 |
2017-07-28 |
Beta Pharma Inc |
Substituted 2-anilinopyrimidine derivatives as egfr modulators
|
|
EA038045B1
(ru)
|
2015-02-20 |
2021-06-28 |
Инсайт Корпорейшн |
Бициклические гетероциклы в качестве ингибиторов fgfr
|
|
MA41551A
(fr)
|
2015-02-20 |
2017-12-26 |
Incyte Corp |
Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
|
|
US9580423B2
(en)
|
2015-02-20 |
2017-02-28 |
Incyte Corporation |
Bicyclic heterocycles as FGFR4 inhibitors
|
|
WO2016183120A1
(en)
|
2015-05-13 |
2016-11-17 |
Vertex Pharmaceuticals Incorporated |
Inhibitors of influenza viruses replication
|
|
JP6704416B2
(ja)
|
2015-05-13 |
2020-06-03 |
バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated |
インフルエンザウイルスの複製の阻害剤を調製する方法
|
|
JP6914860B2
(ja)
|
2015-07-01 |
2021-08-04 |
カリフォルニア インスティチュート オブ テクノロジー |
カチオン性粘液酸ポリマー系デリバリーシステム
|
|
US10206909B2
(en)
|
2015-08-03 |
2019-02-19 |
Samumed, Llc |
3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
|
US10285982B2
(en)
|
2015-08-03 |
2019-05-14 |
Samumed, Llc |
3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof
|
|
US10206908B2
(en)
|
2015-08-03 |
2019-02-19 |
Samumed, Llc |
3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof
|
|
WO2017023986A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc |
3-(1h-indol-2-yl)-1h-indazoles and therapeutic uses thereof
|
|
WO2017024015A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
|
US10226453B2
(en)
|
2015-08-03 |
2019-03-12 |
Samumed, Llc |
3-(1H-indol-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
|
US10166218B2
(en)
|
2015-08-03 |
2019-01-01 |
Samumed, Llc |
3-(1H-indol-2-yl)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof
|
|
US10350199B2
(en)
|
2015-08-03 |
2019-07-16 |
Samumed, Llc |
3-(1h-pyrrolo[2,3-b]pyridin-2-yl)-1h-indazoles and therapeutic uses thereof
|
|
WO2017023987A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(1h-pyrrolo[3,2-c]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridines and therapeutic uses thereof
|
|
WO2017023989A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(1h-benzo[d]imidazol-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
|
US10231956B2
(en)
|
2015-08-03 |
2019-03-19 |
Samumed, Llc |
3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
|
WO2017023972A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
|
US10285983B2
(en)
|
2015-08-03 |
2019-05-14 |
Samumed, Llc |
3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[3,4-B] pyridines and therapeutic uses thereof
|
|
US10188634B2
(en)
|
2015-08-03 |
2019-01-29 |
Samumed, Llc |
3-(3H-imidazo[4,5-C]pyridin-2-yl)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
|
US10519169B2
(en)
|
2015-08-03 |
2019-12-31 |
Samumed, Llc |
3-(1H-pyrrolo[2,3-C]pyridin-2-yl)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
|
US10383861B2
(en)
|
2015-08-03 |
2019-08-20 |
Sammumed, LLC |
3-(1H-pyrrolo[2,3-C]pyridin-2-yl)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof
|
|
WO2017024010A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(1h-pyrrolo[3,2-c]pyridin-2-yl)-1h-indazoles and therapeutic uses thereof
|
|
EP3362449B1
(en)
*
|
2015-10-13 |
2021-06-16 |
Institut National de la Santé et de la Recherche Médicale (INSERM) |
Sibiriline derivatives for use for preventing and/or treating disorders associated with cellular necroptosis
|
|
WO2017079759A1
(en)
|
2015-11-06 |
2017-05-11 |
Samumed, Llc |
2-(1h-indazol-3-yl)-3h-imidazo[4,5-c]pyridines and their anti-inflammatory uses thereof
|
|
US9938273B2
(en)
*
|
2015-12-07 |
2018-04-10 |
Plexxikon Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
|
AR107030A1
(es)
|
2015-12-09 |
2018-03-14 |
Padlock Therapeutics Inc |
Inhibidores aza-bencimidazol de pad4
|
|
WO2017151409A1
(en)
|
2016-02-29 |
2017-09-08 |
University Of Florida Research Foundation, Incorporated |
Chemotherapeutic methods
|
|
EP3464266B1
(en)
|
2016-06-01 |
2021-10-20 |
Bayer Animal Health GmbH |
Substituted indazoles useful for treatment and prevention of allergic and/or inflammatory diseases in animals
|
|
SG10201912248RA
(en)
|
2016-06-01 |
2020-02-27 |
Samumed Llc |
Process for preparing n-(5-(3-(7-(3-fluorophenyl)-3h-imidazo[4,5-c]pyridin-2-yl)-1h-indazol-5-yl)pyridin-3-yl)-3-methylbutanamide
|
|
CN106008306A
(zh)
*
|
2016-06-28 |
2016-10-12 |
山东大学 |
取代吲哚类衍生物及其制备方法与应用
|
|
AU2017345699A1
(en)
|
2016-10-21 |
2019-05-16 |
Samumed, Llc |
Methods of using indazole-3-carboxamides and their use as Wnt/B-catenin signaling pathway inhibitors
|
|
WO2018085865A1
(en)
|
2016-11-07 |
2018-05-11 |
Samumed, Llc |
Single-dose, ready-to-use injectable formulations
|
|
AR111960A1
(es)
|
2017-05-26 |
2019-09-04 |
Incyte Corp |
Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
|
|
US10428067B2
(en)
|
2017-06-07 |
2019-10-01 |
Plexxikon Inc. |
Compounds and methods for kinase modulation
|
|
TW201904577A
(zh)
|
2017-06-16 |
2019-02-01 |
美商貝達醫藥公司 |
N-(2-(2-二甲胺基)乙氧基)-4-甲氧基-5-((4-(1-甲基-1h-吲哚-3-基)嘧啶-2-基)胺基)苯基)丙烯醯胺及其鹽之醫藥調配物
|
|
WO2019113487A1
(en)
|
2017-12-08 |
2019-06-13 |
Incyte Corporation |
Low dose combination therapy for treatment of myeloproliferative neoplasms
|
|
CN112105608B
(zh)
|
2018-01-30 |
2023-07-14 |
因赛特公司 |
制备(1-(3-氟-2-(三氟甲基)异烟碱基)哌啶-4-酮)的方法
|
|
SMT202400306T1
(it)
|
2018-03-30 |
2024-09-16 |
Incyte Corp |
Trattamento dell'idrosadenite suppurativa utilizzando inibitori di jak.
|
|
CN108358894B
(zh)
*
|
2018-04-26 |
2021-05-07 |
四川大学 |
一种抑制组蛋白乙酰转移酶的化合物及其制备方法与应用
|
|
US11174257B2
(en)
|
2018-05-04 |
2021-11-16 |
Incyte Corporation |
Salts of an FGFR inhibitor
|
|
RS66310B1
(sr)
|
2018-05-04 |
2025-01-31 |
Incyte Corp |
Čvrsti oblici inhibitora fgfr i procesi za njegovu pripremu
|
|
US20190381188A1
(en)
|
2018-06-13 |
2019-12-19 |
California Institute Of Technology |
Nanoparticles For Crossing The Blood Brain Barrier And Methods Of Treatment Using The Same
|
|
TWI767148B
(zh)
|
2018-10-10 |
2022-06-11 |
美商弗瑪治療公司 |
抑制脂肪酸合成酶(fasn)
|
|
CN113382633A
(zh)
|
2018-10-29 |
2021-09-10 |
福马治疗股份有限公司 |
(4-(2-氟-4-(1-甲基-1H-苯并[d]咪唑-5-基)苯甲酰基)哌嗪-1-基)(1-羟基环丙基)甲酮的固体形式
|
|
ES2974634T3
(es)
|
2018-12-21 |
2024-06-28 |
Celgene Corp |
Inhibidores de tienopiridinas de RIPK2
|
|
TW202043205A
(zh)
|
2018-12-31 |
2020-12-01 |
美商拜歐米富士恩有限公司 |
Menin-mll相互作用之抑制劑
|
|
MX2021007925A
(es)
|
2018-12-31 |
2021-10-26 |
Biomea Fusion Llc |
Inhibidores irreversibles de la interaccion menina-mll.
|
|
JP7532385B2
(ja)
*
|
2019-01-31 |
2024-08-13 |
杏林製薬株式会社 |
15-pgdh阻害薬
|
|
WO2020185532A1
(en)
|
2019-03-08 |
2020-09-17 |
Incyte Corporation |
Methods of treating cancer with an fgfr inhibitor
|
|
CN111171001B
(zh)
*
|
2019-05-16 |
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|
|
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|
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|
|
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|
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|
|
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|
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|
|
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(en)
|
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|
|
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(en)
|
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|
|
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|
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|
|
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|
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|
|
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(en)
*
|
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|
|
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(en)
|
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|
|
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(ja)
|
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|
|
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(zh)
|
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|
|
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|
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|
|
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(en)
|
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|
|
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|
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|
|
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(en)
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|
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|
|
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|
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