US4399216A
(en)
|
1980-02-25 |
1983-08-16 |
The Trustees Of Columbia University |
Processes for inserting DNA into eucaryotic cells and for producing proteinaceous materials
|
US4634665A
(en)
|
1980-02-25 |
1987-01-06 |
The Trustees Of Columbia University In The City Of New York |
Processes for inserting DNA into eucaryotic cells and for producing proteinaceous materials
|
US5179017A
(en)
|
1980-02-25 |
1993-01-12 |
The Trustees Of Columbia University In The City Of New York |
Processes for inserting DNA into eucaryotic cells and for producing proteinaceous materials
|
US5156840A
(en)
|
1982-03-09 |
1992-10-20 |
Cytogen Corporation |
Amine-containing porphyrin derivatives
|
US5057313A
(en)
|
1986-02-25 |
1991-10-15 |
The Center For Molecular Medicine And Immunology |
Diagnostic and therapeutic antibody conjugates
|
US4908056A
(en)
|
1986-04-25 |
1990-03-13 |
E. I. Du Pont De Nemours And Company |
Heterocyclic acyl sulfonamides
|
EP0307434B2
(en)
|
1987-03-18 |
1998-07-29 |
Scotgen Biopharmaceuticals, Inc. |
Altered antibodies
|
EP0352575A3
(de)
|
1988-07-28 |
1991-08-21 |
Bayer Ag |
Substituierte anellierte Pyrrole
|
IL162181A
(en)
|
1988-12-28 |
2006-04-10 |
Pdl Biopharma Inc |
A method of producing humanized immunoglubulin, and polynucleotides encoding the same
|
US5530101A
(en)
|
1988-12-28 |
1996-06-25 |
Protein Design Labs, Inc. |
Humanized immunoglobulins
|
DE3920358A1
(de)
|
1989-06-22 |
1991-01-17 |
Behringwerke Ag |
Bispezifische und oligospezifische, mono- und oligovalente antikoerperkonstrukte, ihre herstellung und verwendung
|
US5859205A
(en)
|
1989-12-21 |
1999-01-12 |
Celltech Limited |
Humanised antibodies
|
LU91067I2
(fr)
|
1991-06-14 |
2004-04-02 |
Genentech Inc |
Trastuzumab et ses variantes et dérivés immuno chimiques y compris les immotoxines
|
DE69233528T2
(de)
|
1991-11-25 |
2006-03-16 |
Enzon, Inc. |
Verfahren zur Herstellung von multivalenten antigenbindenden Proteinen
|
US5714350A
(en)
|
1992-03-09 |
1998-02-03 |
Protein Design Labs, Inc. |
Increasing antibody affinity by altering glycosylation in the immunoglobulin variable region
|
US5827690A
(en)
|
1993-12-20 |
1998-10-27 |
Genzyme Transgenics Corporatiion |
Transgenic production of antibodies in milk
|
IT1269176B
(it)
|
1994-01-11 |
1997-03-21 |
Isagro Srl |
Eterobicicli ad attivita' fungicida
|
US5731168A
(en)
|
1995-03-01 |
1998-03-24 |
Genentech, Inc. |
Method for making heteromultimeric polypeptides
|
US5869046A
(en)
|
1995-04-14 |
1999-02-09 |
Genentech, Inc. |
Altered polypeptides with increased half-life
|
CA2229043C
(en)
|
1995-08-18 |
2016-06-07 |
Morphosys Gesellschaft Fur Proteinoptimierung Mbh |
Protein/(poly)peptide libraries
|
EP1047761A1
(en)
|
1997-10-14 |
2000-11-02 |
The Procter & Gamble Company |
Hard surface cleaning compositions comprising mid-chain branched surfactants
|
US6982265B1
(en)
|
1999-05-21 |
2006-01-03 |
Bristol Myers Squibb Company |
Pyrrolotriazine inhibitors of kinases
|
ES2299434T3
(es)
|
1999-09-17 |
2008-06-01 |
ABBOTT GMBH & CO. KG |
Inhibidores de kinasa utilizados como agentes terapeuticos.
|
US6770666B2
(en)
|
1999-12-27 |
2004-08-03 |
Japan Tobacco Inc. |
Fused-ring compounds and use thereof as drugs
|
RU2223761C2
(ru)
|
1999-12-27 |
2004-02-20 |
Джапан Тобакко Инк. |
Соединения с конденсированным кольцом и их использование в качестве лекарственных средств
|
KR100786927B1
(ko)
|
2000-06-28 |
2007-12-17 |
스미스클라인비이참피이엘시이 |
습식 분쇄방법
|
CA2442849A1
(en)
|
2001-04-06 |
2002-10-17 |
Wyeth |
Antineoplastic combinations such as rapamycin together with gemcitabine or fluorouracil
|
AR035543A1
(es)
|
2001-06-26 |
2004-06-16 |
Japan Tobacco Inc |
Agente terapeutico para la hepatitis c que comprende un compuesto de anillo condensado, compuesto de anillo condensado, composicion farmaceutica que lo comprende, compuestos de benzimidazol, tiazol y bifenilo utiles como intermediarios para producir dichos compuestos, uso del compuesto de anillo con
|
AU2003272175A1
(en)
|
2002-10-21 |
2004-05-04 |
Aprea Ab |
Reactivation of wild type p53 in human tumour cells by a low molecular weight compound
|
EP1576138B1
(en)
|
2002-11-15 |
2017-02-01 |
Idenix Pharmaceuticals LLC. |
2'-methyl nucleosides in combination with interferon and flaviviridae mutation
|
EP2368578A1
(en)
|
2003-01-09 |
2011-09-28 |
Macrogenics, Inc. |
Identification and engineering of antibodies with variant Fc regions and methods of using same
|
US20050079574A1
(en)
|
2003-01-16 |
2005-04-14 |
Genentech, Inc. |
Synthetic antibody phage libraries
|
WO2004072266A2
(en)
|
2003-02-13 |
2004-08-26 |
Kalobios Inc. |
Antibody affinity engineering by serial epitope-guided complementarity replacement
|
TW200505915A
(en)
|
2003-03-13 |
2005-02-16 |
Synta Pharmaceuticals Corp |
Fused pyrrole compounds
|
KR20050122210A
(ko)
|
2003-03-17 |
2005-12-28 |
다케다 샌디에고, 인코포레이티드 |
히스톤 탈아세틸화 효소 억제제
|
DK1639014T3
(da)
|
2003-06-13 |
2011-01-17 |
Biogen Idec Inc |
Aglycosyl-anti-CD154 (CD40-ligand)-antistoffer og anvendelser deraf
|
FR2857966A1
(fr)
|
2003-07-24 |
2005-01-28 |
Aventis Pharma Sa |
Produits aryl-heteroaromatiques, compositions les contenant et utilisation
|
AU2004266159A1
(en)
|
2003-08-22 |
2005-03-03 |
Biogen Idec Ma Inc. |
Improved antibodies having altered effector function and methods for making the same
|
WO2005025515A2
(en)
|
2003-09-12 |
2005-03-24 |
California Institute Of Technology |
Proteasome pathway inhibitors and related methods
|
US7306631B2
(en)
|
2004-03-30 |
2007-12-11 |
The Procter & Gamble Company |
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
|
UY28931A1
(es)
|
2004-06-03 |
2005-12-30 |
Bayer Pharmaceuticals Corp |
Derivados de pirrolotriazina utiles para tratar trastornos hiper-proliferativos y enfermedades asociadas con angiogenesis
|
TW200613306A
(en)
*
|
2004-07-20 |
2006-05-01 |
Osi Pharm Inc |
Imidazotriazines as protein kinase inhibitors
|
US20070015771A1
(en)
|
2004-07-29 |
2007-01-18 |
Threshold Pharmaceuticals, Inc. |
Lonidamine analogs
|
US20070043057A1
(en)
|
2005-02-09 |
2007-02-22 |
Threshold Pharmaceuticals, Inc. |
Lonidamine analogs
|
UY29177A1
(es)
|
2004-10-25 |
2006-05-31 |
Astex Therapeutics Ltd |
Derivados sustituidos de purina, purinona y deazapurina, composiciones que los contienen métodos para su preparación y sus usos
|
WO2006056399A2
(en)
|
2004-11-24 |
2006-06-01 |
Novartis Ag |
Combinations of jak inhibitors and at least one of bcr-abl, flt-3, fak or raf kinase inhibitors
|
WO2006124874A2
(en)
|
2005-05-12 |
2006-11-23 |
Kalypsys, Inc. |
Inhibitors of b-raf kinase
|
JP5116687B2
(ja)
|
2005-11-02 |
2013-01-09 |
バイエル・ファルマ・アクチェンゲゼルシャフト |
がんおよび他の過剰増殖性疾患の処置のためのピロロ[2,1−f][1,2,4]トリアジン−4−イルアミンIGF−1Rキナーゼ阻害剤
|
CN101316845A
(zh)
|
2005-11-17 |
2008-12-03 |
Osi医药有限公司 |
稠合双环mTOR抑制剂
|
US7514435B2
(en)
|
2005-11-18 |
2009-04-07 |
Bristol-Myers Squibb Company |
Pyrrolotriazine kinase inhibitors
|
MX2008007103A
(es)
|
2005-12-02 |
2008-09-12 |
Bayer Healthcare Llc |
Derivados 4-amino-pirrolotriazina sustituidos, útiles para tratar trastornos hiperproliferativos y enfermedades asociadas con angiogenesis.
|
PE20070855A1
(es)
*
|
2005-12-02 |
2007-10-14 |
Bayer Pharmaceuticals Corp |
Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
|
EP1957078B1
(en)
|
2005-12-02 |
2013-08-28 |
Bayer HealthCare, LLC |
Pyrrolotriazine derivatives useful for treating cancer through inhibition of aurora kinase
|
KR101391900B1
(ko)
|
2005-12-13 |
2014-05-02 |
인사이트 코포레이션 |
야누스 키나아제 억제제로서의 헤테로아릴 치환된 피롤로[2,3-b]피리딘 및 피롤로[2,3-b]피리미딘
|
CA2633035C
(en)
|
2005-12-15 |
2016-05-10 |
Rigel Pharmaceuticals, Inc. |
Kinase inhibitors and their uses
|
ES2545907T3
(es)
|
2005-12-29 |
2015-09-16 |
Abbvie Inc. |
Inhibidores de proteína quinasa
|
US7763629B2
(en)
|
2006-04-12 |
2010-07-27 |
Vertex Pharmaceuticals Incorporated |
Tetrahydropteridines useful as inhibitors of protein kinases
|
HUE035654T2
(en)
|
2006-04-19 |
2018-05-28 |
Novartis Ag |
6-o-substituted benzoxazole and benzothiazole compounds and methods for inhibiting CSF-1R signaling
|
US20090253718A1
(en)
|
2006-04-25 |
2009-10-08 |
Astex Therapeutics Limited |
Pharmaceutical Compounds
|
WO2008005262A1
(en)
|
2006-06-29 |
2008-01-10 |
Schering Corporation |
Substituted bicyclic and tricyclic thrombin receptor antagonists
|
WO2008012635A2
(en)
|
2006-07-26 |
2008-01-31 |
Pfizer Products Inc. |
Amine derivatives useful as anticancer agents
|
WO2008045978A1
(en)
|
2006-10-10 |
2008-04-17 |
Rigel Pharmaceuticals, Inc. |
Pinane-substituted pyrimidinediamine derivatives useful as axl inhibitors
|
MY188335A
(en)
*
|
2006-11-22 |
2021-11-30 |
Incyte Holdings Corp |
Imidazotriazines and imidazopyrimidines as kinase inhibitors
|
EP2428204A3
(en)
|
2006-12-07 |
2012-07-04 |
Schering Corporation |
pH sensitive matrix formulation
|
EP2102210B1
(en)
|
2006-12-14 |
2011-02-09 |
Vertex Pharmceuticals Incorporated |
Compounds useful as protein kinase inhibitors
|
US9650391B2
(en)
|
2006-12-29 |
2017-05-16 |
Rigel Pharmaceuticals Inc. |
N3-heteroaryl substituted triazoles and N5-heteroaryl substituted triazoles useful as Axl inhibitors
|
EP2078010B1
(en)
|
2006-12-29 |
2014-01-29 |
Rigel Pharmaceuticals, Inc. |
Polycyclic heteroaryl substituted triazoles useful as axl inhibitors
|
ES2406930T3
(es)
|
2006-12-29 |
2013-06-10 |
Rigel Pharmaceuticals, Inc. |
Triazoles sustituidos con arilo bicíclico y heteroarilo bicíclico útiles como inhibidores de AXL
|
CN101611046A
(zh)
|
2007-01-12 |
2009-12-23 |
拜奥克里斯特制药公司 |
抗病毒的核苷类似物
|
WO2008098139A2
(en)
|
2007-02-07 |
2008-08-14 |
The Regents Of The University Of Colorado |
Axl tyrosine kinase inhibitors and methods of making and using the same
|
US8124759B2
(en)
|
2007-05-09 |
2012-02-28 |
Abbott Laboratories |
Inhibitors of protein kinases
|
US8242085B2
(en)
|
2007-05-10 |
2012-08-14 |
Biocryst Pharmaceuticals, Inc. |
Tetrahydrofuro [3,4-D] dioxolane compounds for use in the treatment of viral infections and cancer
|
US20090274698A1
(en)
|
2007-07-06 |
2009-11-05 |
Shripad Bhagwat |
Combination anti-cancer therapy
|
WO2009009016A1
(en)
|
2007-07-06 |
2009-01-15 |
Osi Pharmaceuticals, Inc. |
Combination anti-cancer therapy
|
CA2695753A1
(en)
|
2007-08-15 |
2009-02-19 |
Vertex Pharmaceuticals Incorporated |
Compounds useful as protein kinases inhibitors
|
WO2009042543A1
(en)
|
2007-09-25 |
2009-04-02 |
Bayer Healthcare Llc |
Pyrrolotriazine derivatives useful for treating cancer through inhibition of aurora kinase
|
GB0719803D0
(en)
|
2007-10-10 |
2007-11-21 |
Cancer Rec Tech Ltd |
Therapeutic compounds and their use
|
WO2009053737A2
(en)
|
2007-10-25 |
2009-04-30 |
Astrazeneca Ab |
Pyridine and pyrazine derivatives useful in the treatment of cell proliferative disorders
|
CA2704052C
(en)
|
2007-10-26 |
2015-04-21 |
Rigel Pharmaceuticals, Inc. |
Polycyclic aryl substituted triazoles and polycyclic heteroaryl substituted triazoles useful as axl inhibitors
|
DE102007051762A1
(de)
|
2007-10-30 |
2009-05-07 |
Bayer Healthcare Ag |
Substituierte Pyrrolotriazine und ihre Verwendung
|
BRPI0821209A2
(pt)
|
2007-12-19 |
2019-09-24 |
Amgen Inc |
composto, composição farmacêutica, métodos de tratar câncer, para reduzir o tamanho de tumor, para tratar distúrbios, e para reduzir metástase em um tumor.
|
AR070127A1
(es)
|
2008-01-11 |
2010-03-17 |
Novartis Ag |
Pirrolo - pirimidinas y pirrolo -piridinas
|
US8557814B2
(en)
|
2008-03-19 |
2013-10-15 |
OSI Pharmaceuticals, LLC |
mTOR inhibitor salt forms
|
RU2010146474A
(ru)
|
2008-04-16 |
2012-05-27 |
Макс-Планк-Гезелльшафт Цур Фердерунг Дер Виссеншафтен Е.Ф. (De) |
Производные хинолина в качестве ингибиторов axl киназ
|
PL2937350T3
(pl)
|
2008-04-23 |
2018-06-29 |
Gilead Sciences, Inc. |
1'-podstawione analogi karba-nukleozydów do leczenia przeciwwirusowego
|
TWI539953B
(zh)
|
2008-04-28 |
2016-07-01 |
瑞波若斯治療學公司 |
用於治療乳癌之組成物和方法
|
KR20110018376A
(ko)
|
2008-06-23 |
2011-02-23 |
스미또모 가가꾸 가부시키가이샤 |
조성물 및 상기 조성물을 이용하여 이루어지는 발광 소자
|
AU2009271658B2
(en)
|
2008-06-23 |
2014-04-10 |
Vertex Pharmaceuticals Incorporated |
Protein kinase inhibitors
|
EP2313102A2
(en)
|
2008-07-03 |
2011-04-27 |
Biota Scientific Management |
Bycyclic nucleosides and nucleotides as therapeutic agents
|
DK2328888T3
(da)
|
2008-07-09 |
2013-02-11 |
Rigel Pharmaceuticals Inc |
Broforbundne, bicykliske heteroarylsubstituerede triazoler, der er anvendelige som axl-inhitorer
|
US8349838B2
(en)
|
2008-07-09 |
2013-01-08 |
Rigel Pharmaceuticals, Inc. |
Polycyclic heteroaryl substituted triazoles useful as Axl inhibitors
|
WO2010014755A1
(en)
|
2008-07-29 |
2010-02-04 |
The Regents Of The University Of Colorado |
Methods and compounds for enhancing anti-cancer therapy
|
WO2010025073A1
(en)
|
2008-08-28 |
2010-03-04 |
Takeda Pharmaceutical Company Limited |
Dihydroimidazo [ 1, 5-f] pteridines as polo-like kinase inhibitors
|
EP2350317A4
(en)
|
2008-10-20 |
2012-06-27 |
Univ Colorado Regents |
BIOLOGICAL MARKERS FOR PREDICTING THE ANTICIPATE RESPONSE TO INSULINARY GROWTH FACTOR 1 RECEPTOR KINASE INHIBITORS
|
US8476431B2
(en)
|
2008-11-03 |
2013-07-02 |
Itellikine LLC |
Benzoxazole kinase inhibitors and methods of use
|
TW201035100A
(en)
|
2008-12-19 |
2010-10-01 |
Cephalon Inc |
Pyrrolotriazines as ALK and JAK2 inhibitors
|
AU2010210986A1
(en)
|
2009-02-09 |
2011-08-25 |
Supergen, Inc. |
Pyrrolopyrimidinyl Axl kinase inhibitors
|
US20100204265A1
(en)
|
2009-02-09 |
2010-08-12 |
Genelabs Technologies, Inc. |
Certain Nitrogen Containing Bicyclic Chemical Entities for Treating Viral Infections
|
EP2400985A2
(en)
|
2009-02-25 |
2012-01-04 |
OSI Pharmaceuticals, LLC |
Combination of an either an anti-igf-1r antibody or an igf binding protein and a small molecule igf-1r kinase inhibitor
|
WO2010104306A2
(ko)
|
2009-03-07 |
2010-09-16 |
주식회사 메디젠텍 |
세포핵에서 세포질로의 gsk3의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 gsk3 이동에 의해 발생되는 질환의 치료 또는 예방용 약학적 조성물
|
US8765754B2
(en)
|
2009-04-29 |
2014-07-01 |
Locus Pharmaceuticals, Inc. |
Pyrrolotriazine compounds
|
ES2487542T3
(es)
|
2009-05-22 |
2014-08-21 |
Incyte Corporation |
Derivados de N-(hetero)aril-pirrolidina de pirazol-4-il-pirrolo[2,3-d]pirimidinas y pirrol-3-il-pirrolo[2,3-d]pirimidinas como inhibidores de cinasas Janus
|
BRPI1015135B1
(pt)
*
|
2009-06-29 |
2021-08-03 |
Incyte Holdings Corporation |
Pirimidinonas inibidoras de pi3k, composição compreendendo tais compostos, bem como usos dos mesmos
|
US20120128670A1
(en)
|
2009-07-31 |
2012-05-24 |
OSI Pharmaceuticals, LLC |
mTOR INHIBITOR AND ANGIOGENESIS INHIBITOR COMBINATION THERAPY
|
US9249145B2
(en)
|
2009-09-01 |
2016-02-02 |
Incyte Holdings Corporation |
Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors
|
US8455451B2
(en)
|
2009-09-21 |
2013-06-04 |
Gilead Sciences, Inc. |
2'-fluoro substituted carba-nucleoside analogs for antiviral treatment
|
PL2480559T3
(pl)
|
2009-09-21 |
2013-11-29 |
Gilead Sciences Inc |
Sposoby i związki pośrednie do wytwarzania analogów 11cyjanokarbanukleozydowych
|
ME02656B
(me)
|
2009-09-21 |
2017-06-20 |
Gilead Sciences Inc |
2' -fluoro supstituisani karba-nukleozidni analozi za antiviralno lečenje
|
JP2013512860A
(ja)
|
2009-09-25 |
2013-04-18 |
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 |
プロテインキナーゼ阻害剤として有用なピリミジン誘導体の調製方法
|
LT2485731T
(lt)
|
2009-10-06 |
2016-09-12 |
Millennium Pharmaceuticals, Inc. |
Heterocikliniai junginiai, tinkami naudoti kaip pdk1 inhibitoriai
|
EP2311809A1
(en)
|
2009-10-16 |
2011-04-20 |
Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. |
Quinolinyloxyphenylsulfonamides
|
US8604217B2
(en)
|
2009-11-12 |
2013-12-10 |
Selvita S.A. |
Compound, a process for its preparation, a pharmaceutical composition, use of a compound, a method for modulating or regulating serine/threonine kinases and a serine/threonine kinases modulating agent
|
TW201130842A
(en)
|
2009-12-18 |
2011-09-16 |
Incyte Corp |
Substituted fused aryl and heteroaryl derivatives as PI3K inhibitors
|
ES2627703T3
(es)
|
2010-01-22 |
2017-07-31 |
Fundación Centro Nacional De Investigaciones Oncológicas Carlos Iii |
Inhibidores de PI3·quinasa
|
SI3050882T1
(en)
|
2010-03-10 |
2018-06-29 |
Incyte Holdings Corporation |
Piperidin-4-yl azetidine derivatives, as inhibitors of JAK1
|
JP5752232B2
(ja)
*
|
2010-03-31 |
2015-07-22 |
ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company |
プロテインキナーゼ阻害剤としての置換ピロロトリアジン化合物
|
CA2761074A1
(en)
|
2010-05-05 |
2011-11-10 |
Vertex Pharmaceuticals Incorporated |
4 substituted pyrazolopyrimidines useful as pkc-theta inhibitors
|
US20130131057A1
(en)
|
2010-05-13 |
2013-05-23 |
Centro Nacional De Investigaciones Oncologicas (Cnio |
New bicyclic compounds as pi3-k and mtor inhibitors
|
TW201201815A
(en)
|
2010-05-28 |
2012-01-16 |
Gilead Sciences Inc |
1'-substituted-carba-nucleoside prodrugs for antiviral treatment
|
GB2480814A
(en)
|
2010-06-01 |
2011-12-07 |
Summit Corp Plc |
Compounds for the treatment of clostridium difficile-associated disease
|
WO2012012465A1
(en)
|
2010-07-19 |
2012-01-26 |
Clarke, Michael, O'neil Hanrahan |
Methods for the preparation of diasteromerically pure phosphoramidate prodrugs
|
CN103052631B
(zh)
|
2010-07-22 |
2015-11-25 |
吉里德科学公司 |
用于治疗副黏病毒科病毒感染的方法和化合物
|
EP2423208A1
(en)
|
2010-08-28 |
2012-02-29 |
Lead Discovery Center GmbH |
Pharmaceutically active compounds as Axl inhibitors
|
US20120077814A1
(en)
|
2010-09-10 |
2012-03-29 |
Zhong Wang |
Sulfonamide, sulfamate, and sulfamothioate derivatives
|
TW201305185A
(zh)
|
2010-09-13 |
2013-02-01 |
Gilead Sciences Inc |
用於抗病毒治療之2’-氟取代之碳-核苷類似物
|
JP5906191B2
(ja)
|
2010-09-29 |
2016-04-20 |
キッセイ薬品工業株式会社 |
(アザ)インドリジン誘導体及びその医薬用途
|
AU2011313820A1
(en)
|
2010-10-08 |
2013-04-11 |
Biota Europe Ltd |
Antibacterial compounds
|
BR112013008526A2
(pt)
|
2010-10-08 |
2016-07-12 |
Elan Pharm Inc |
inibidores de quinase do tipo polo
|
ITRM20100537A1
(it)
|
2010-10-12 |
2012-04-12 |
Consiglio Nazionale Ricerche |
Aptamero inibitore del recettore tirosina chinasi axl per uso in terapia
|
PE20140146A1
(es)
|
2010-11-19 |
2014-02-06 |
Incyte Corp |
Derivados de pirrolopiridina y pirrolopirimidina sustituidos con ciclobutilo como inhibidores de jak
|
JP5917544B2
(ja)
|
2010-11-19 |
2016-05-18 |
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阻害剤としての複素環置換ピロロピリジンおよびピロロピリミジン
|
JP5961187B2
(ja)
|
2010-12-20 |
2016-08-02 |
インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation |
Pi3k阻害剤としてのn−(1−(置換フェニル)エチル)−9h−プリン−6−アミン
|
CA2828483A1
(en)
|
2011-02-23 |
2012-11-01 |
Intellikine, Llc |
Combination of kinase inhibitors and uses thereof
|
EP2678016B1
(en)
|
2011-02-23 |
2016-08-10 |
Intellikine, LLC |
Heterocyclic compounds and uses thereof
|
JP5707518B2
(ja)
|
2011-02-28 |
2015-04-30 |
カリトル サイエンシズ, エルエルシー |
置換型キノリン化合物及び使用方法
|
EP2688887B1
(en)
|
2011-03-23 |
2015-05-13 |
Amgen Inc. |
Fused tricyclic dual inhibitors of cdk 4/6 and flt3
|
PL2693881T3
(pl)
|
2011-04-01 |
2020-03-31 |
University Of Utah Research Foundation |
Podstawione analogi N-fenylopirymidyno-2-aminy jako inhibitory kinazy AXL
|
US20140357651A1
(en)
|
2011-05-04 |
2014-12-04 |
Yi Liu |
Combination pharmaceutical compositions and uses thereof
|
WO2012154608A1
(en)
|
2011-05-06 |
2012-11-15 |
Intellikine, Llc |
Reactive mtor and pi3 kinase inhibitors and uses thereof
|
CA2836410C
(en)
|
2011-05-17 |
2019-08-20 |
Principia Biopharma Inc. |
Tyrosine kinase inhibitors
|
WO2012158795A1
(en)
|
2011-05-17 |
2012-11-22 |
Principia Biopharma Inc. |
Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors
|
KR102052670B1
(ko)
|
2011-05-17 |
2019-12-06 |
더 리젠츠 오브 더 유니버시티 오브 캘리포니아 |
키나아제 저해제
|
AR086913A1
(es)
|
2011-06-14 |
2014-01-29 |
Novartis Ag |
4-metil-3-[[4-(3-piridinil)-2-pirimidinil]-amino]-n-[5-(4-metil-1h-imidazol-1-il)-3-(trifluoro-metil)-fenil]-benzamida amorfa, forma de dosificacion que la contiene y metodo para prepararlas
|
ES2560611T3
(es)
|
2011-06-20 |
2016-02-22 |
Incyte Holdings Corporation |
Derivados de fenil de azetidinilo, carboxamida de piridilo o pirazinilo como inhibidores de JAK
|
CN103764657B
(zh)
*
|
2011-07-01 |
2016-05-25 |
拜耳知识产权有限责任公司 |
作为alk1抑制剂的羟甲基芳基取代的吡咯并三嗪
|
EP2548877A1
(en)
|
2011-07-19 |
2013-01-23 |
MSD Oss B.V. |
4-(5-Membered fused pyridinyl)benzamides as BTK-inhibitors
|
TW201313721A
(zh)
|
2011-08-18 |
2013-04-01 |
Incyte Corp |
作為jak抑制劑之環己基氮雜環丁烷衍生物
|
WO2013033569A1
(en)
|
2011-09-02 |
2013-03-07 |
Incyte Corporation |
Heterocyclylamines as pi3k inhibitors
|
AU2012308453B2
(en)
|
2011-09-18 |
2016-11-10 |
Euro-Celtique S.A. |
Pharmaceutical compositions
|
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
|
ES2650630T3
(es)
|
2011-10-03 |
2018-01-19 |
The University Of North Carolina At Chapel Hill |
Compuestos de pirrolopirimidina para el tratamiento del cáncer
|
CN104080786A
(zh)
|
2011-11-08 |
2014-10-01 |
因特利凯有限责任公司 |
使用多种药剂的治疗方案
|
ES2614824T3
(es)
|
2011-11-14 |
2017-06-02 |
Ignyta, Inc. |
Derivados de uracil como inhibidores de la quinasa axl y c-met
|
EP2793893A4
(en)
|
2011-11-23 |
2015-07-08 |
Intellikine Llc |
IMPROVED TREATMENT REGIMES USING MTOR INHIBITORS
|
WO2013085802A1
(en)
|
2011-12-06 |
2013-06-13 |
Merck Sharp & Dohme Corp. |
Pyrrolopyrimidines as janus kinase inhibitors
|
WO2013087647A1
(en)
|
2011-12-15 |
2013-06-20 |
Bayer Intellectual Property Gmbh |
Substituted benzothienyl - pyrrolotriazines and uses thereof in the treatment cancer
|
UY34484A
(es)
|
2011-12-15 |
2013-07-31 |
Bayer Ip Gmbh |
Benzotienilo-pirrolotriazinas disustituidas y sus usos
|
DK2810937T3
(en)
|
2012-01-31 |
2017-03-13 |
Daiichi Sankyo Co Ltd |
PYRIDONE DERIVATIVES
|
JP5985658B2
(ja)
|
2012-01-31 |
2016-09-06 |
ナンジン アルゲン ファルマ カンパニー リミテッドNanjing Allgen Pharma Co. Ltd. |
ブルトンチロシンキナーゼ阻害薬としての環状分子
|
CN104136439B
(zh)
|
2012-02-23 |
2017-01-18 |
拜耳知识产权有限责任公司 |
取代的苯并噻吩基‑吡咯并三嗪及其用途
|
WO2013151975A1
(en)
|
2012-04-02 |
2013-10-10 |
Northeastern University |
Compositions and methods for the inhibition of methyltransferases
|
CN103373996A
(zh)
|
2012-04-20 |
2013-10-30 |
山东亨利医药科技有限责任公司 |
作为crth2受体拮抗剂的二并环衍生物
|
WO2013162061A1
(ja)
|
2012-04-26 |
2013-10-31 |
第一三共株式会社 |
二環性ピリミジン化合物
|
TW201406761A
(zh)
|
2012-05-18 |
2014-02-16 |
Incyte Corp |
做爲jak抑制劑之哌啶基環丁基取代之吡咯并吡啶及吡咯并嘧啶衍生物
|
CN104487441B
(zh)
|
2012-06-18 |
2018-06-01 |
普林斯匹亚生物制药公司 |
有用于治疗癌症和自身免疫性疾病的可逆的共价吡咯并嘧啶或吡唑并嘧啶
|
IN2015DN00345A
(pt)
|
2012-06-19 |
2015-06-12 |
Sunovion Pharmaceuticals Inc |
|
EP2865671B1
(en)
|
2012-06-22 |
2017-11-01 |
Sumitomo Chemical Company, Ltd |
Fused heterocyclic compound
|
US9572811B2
(en)
|
2012-08-03 |
2017-02-21 |
Principia Biopharma Inc. |
Treatment of dry eye
|
WO2014035140A2
(en)
|
2012-08-30 |
2014-03-06 |
Kainos Medicine, Inc. |
Compounds and compositions for modulating histone methyltransferase activity
|
MX2015002887A
(es)
|
2012-09-06 |
2015-07-06 |
Plexxikon Inc |
Compuestos y metodos para la modulacion de cinasas, e indicaciones para ello.
|
WO2014042433A2
(en)
|
2012-09-14 |
2014-03-20 |
Kainos Medicine, Inc. |
Compounds and compositions for modulating adenosine a3 receptor activity
|
CA2886240A1
(en)
*
|
2012-09-26 |
2014-04-03 |
The Regents Of The University Of California |
Modulation of ire1
|
US9457039B2
(en)
|
2012-10-17 |
2016-10-04 |
Merck Sharp & Dohme Corp. |
2′-disubstituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases
|
WO2014062774A1
(en)
|
2012-10-17 |
2014-04-24 |
The University Of North Carolina At Chapel Hill |
Pyrazolopyrimidine compounds for the treatment of cancer
|
EP2909209B1
(en)
|
2012-10-17 |
2022-08-03 |
Merck Sharp & Dohme LLC |
2'-cyano substituted nucleoside derivatives and methods of use thereof for treatment of viral diseases
|
AR093308A1
(es)
|
2012-11-01 |
2015-05-27 |
Incyte Corp |
Derivados triciclicos fusionados de tiofeno como inhibidores de jak
|
WO2014078778A2
(en)
|
2012-11-16 |
2014-05-22 |
Biocryst Pharmaceuticals, Inc. |
Antiviral azasugar-containing nucleosides
|
JP6218848B2
(ja)
|
2012-11-20 |
2017-10-25 |
プロキナーゼ ゲゼルシャフト ミット ベシュレンクテル ハフツング |
プロテインキナーゼ阻害剤としてのチオエーテル誘導体
|
WO2014109858A1
(en)
|
2013-01-14 |
2014-07-17 |
Amgen Inc. |
Methods of using cell-cycle inhibitors to modulate one or more properties of a cell culture
|
MX2015008741A
(es)
|
2013-01-18 |
2015-11-06 |
Squibb Bristol Myers Co |
Ftalazinonas e isoquinolinonas como inhibidores de cinasa rho.
|
WO2014113942A1
(en)
|
2013-01-23 |
2014-07-31 |
Merck Sharp & Dohme Corp. |
Btk inhibitors
|
WO2014130856A2
(en)
|
2013-02-21 |
2014-08-28 |
Wayne Rothbaum |
Treatment of skeletal-related disorders
|
US9050345B2
(en)
|
2013-03-11 |
2015-06-09 |
Bristol-Myers Squibb Company |
Pyrrolotriazines as potassium ion channel inhibitors
|
US9012466B2
(en)
|
2013-03-12 |
2015-04-21 |
Arqule Inc. |
Substituted tricyclic pyrazolo-pyrimidine compounds
|
TWI649308B
(zh)
|
2013-07-24 |
2019-02-01 |
小野藥品工業股份有限公司 |
喹啉衍生物
|
EP3057970A1
(en)
|
2013-10-18 |
2016-08-24 |
Medivation Technologies, Inc. |
Heterocyclic compounds and methods of use
|
WO2015066371A1
(en)
|
2013-10-31 |
2015-05-07 |
Forum Pharmaceuticals, Inc. |
SPIRO-OXADIAZOLINE COMPOUNDS AS AGONISTS OF α-7-NICOTINIC ACETYLCHOLINE RECEPTORS
|
JP6493218B2
(ja)
|
2013-11-08 |
2019-04-03 |
小野薬品工業株式会社 |
ピロロピリミジン誘導体
|
BR112016016844A2
(pt)
*
|
2014-02-03 |
2017-08-08 |
Cadila Healthcare Ltd |
Compostos heterocíclicos
|
US9936723B2
(en)
|
2014-02-12 |
2018-04-10 |
Senomyx, Inc. |
Process for the synthesis of substituted 1-benzyl-3-(1-(isoxazol-4-ylmethyl)-1h-pyrazol-4-yl)imidazolidine-2,4-diones
|
JP6621477B2
(ja)
|
2014-12-18 |
2019-12-18 |
ファイザー・インク |
ピリミジンおよびトリアジン誘導体ならびにaxl阻害薬としてのそれらの使用
|
US9840503B2
(en)
|
2015-05-11 |
2017-12-12 |
Incyte Corporation |
Heterocyclic compounds and uses thereof
|
US9708333B2
(en)
|
2015-08-12 |
2017-07-18 |
Incyte Corporation |
Fused bicyclic 1,2,4-triazine compounds as TAM inhibitors
|
WO2017035366A1
(en)
|
2015-08-26 |
2017-03-02 |
Incyte Corporation |
Pyrrolopyrimidine derivatives as tam inhibitors
|
WO2017062797A1
(en)
|
2015-10-07 |
2017-04-13 |
The University Of North Carolina At Chapel Hill |
The methods for treatment of tumors
|
CN108137568A
(zh)
|
2015-10-13 |
2018-06-08 |
日本农药株式会社 |
具有肟基的稠杂环化合物或其盐类及含有该化合物的农业园艺用杀虫剂以及其使用方法
|
EP3373932B1
(en)
|
2015-11-14 |
2022-03-30 |
Sunshine Lake Pharma Co., Ltd. |
Crystalline form of a substituted quinoline compound and pharmaceutical compositions thereof
|
US9695150B2
(en)
|
2015-11-14 |
2017-07-04 |
Calitor Sciences, Llc |
Crystalline form of a substituted quinoline compound and pharmaceutical compositions thereof
|
CN114456176A
(zh)
|
2016-03-28 |
2022-05-10 |
因赛特公司 |
作为tam抑制剂的吡咯并三嗪化合物
|
EA201892395A1
(ru)
|
2016-04-22 |
2019-04-30 |
Инсайт Корпорейшн |
Лекарственные составы ингибитора lsd1
|
AR108875A1
(es)
|
2016-06-24 |
2018-10-03 |
Incyte Corp |
COMPUESTOS HETEROCÍCLICOS COMO INHIBIDORES DE PI3K-g
|
HRP20221378T1
(hr)
|
2016-07-15 |
2023-01-06 |
Ionis Pharmaceuticals, Inc. |
Spojevi i postupci za modulaciju smn2
|
JOP20170153A1
(ar)
|
2016-07-15 |
2019-01-30 |
Lilly Co Eli |
نظائر urocortin-2 جديدة معدلة بحمض دهني لعلاج داء السكري وأمراض الكلى المزمنة
|
PE20210002A1
(es)
|
2017-09-27 |
2021-01-05 |
Incyte Corp |
Sales de derivados de pirrolotriazina utiles como inhibidores tam
|
SG11202013163TA
(en)
|
2018-06-29 |
2021-01-28 |
Incyte Corp |
Formulations of an axl/mer inhibitor
|
KR20230017165A
(ko)
|
2020-03-06 |
2023-02-03 |
인사이트 코포레이션 |
Axl/mer 및 pd-1/pd-l1 억제제를 포함하는 병행 요법
|