|
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
|
|
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
|
|
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
|
|
JPH0395163A
(ja)
|
1989-09-08 |
1991-04-19 |
Daicel Chem Ind Ltd |
2.2.4.4.6―ペンタメチル―2.3.4.5―テトラヒドロピリミジンの製造法
|
|
US5859205A
(en)
|
1989-12-21 |
1999-01-12 |
Celltech Limited |
Humanised antibodies
|
|
ATE255131T1
(de)
|
1991-06-14 |
2003-12-15 |
Genentech Inc |
Humanisierter heregulin antikörper
|
|
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
|
|
ATE219517T1
(de)
|
1995-08-18 |
2002-07-15 |
Morphosys Ag |
Protein-/(poly)peptidbibliotheken
|
|
US20020077461A1
(en)
|
1996-04-24 |
2002-06-20 |
Soren Bjorn |
Pharmaceutical formulation
|
|
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
|
|
WO2001019828A2
(en)
*
|
1999-09-17 |
2001-03-22 |
Basf Aktiengesellschaft |
Kinase inhibitors as therapeutic agents
|
|
US6770666B2
(en)
|
1999-12-27 |
2004-08-03 |
Japan Tobacco Inc. |
Fused-ring compounds and use thereof as drugs
|
|
EP1162196A4
(en)
|
1999-12-27 |
2003-04-16 |
Japan Tobacco Inc |
COMPOUNDS WITH JOINED CYCLES AND THEIR USE AS MEDICAMENTS
|
|
KR100786927B1
(ko)
|
2000-06-28 |
2007-12-17 |
스미스클라인비이참피이엘시이 |
습식 분쇄방법
|
|
CN1309421C
(zh)
|
2001-04-06 |
2007-04-11 |
惠氏公司 |
诸如雷帕霉素和吉西他滨或氟尿嘧啶的抗肿瘤联合
|
|
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
|
|
GB0221697D0
(en)
|
2002-09-18 |
2002-10-30 |
Unilever Plc |
Novel compouds and their uses
|
|
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
|
|
RU2005118421A
(ru)
|
2002-11-15 |
2006-01-20 |
Айденикс (Кайман) Лимитед (Ky) |
2'-разветвленные нуклеозиды и мутация flaviviridae
|
|
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
|
|
US20050008625A1
(en)
|
2003-02-13 |
2005-01-13 |
Kalobios, Inc. |
Antibody affinity engineering by serial epitope-guided complementarity replacement
|
|
CA2517034A1
(en)
|
2003-03-13 |
2004-09-30 |
Synta Pharmaceuticals Corp. |
Fused pyrrole compounds
|
|
KR20050122210A
(ko)
|
2003-03-17 |
2005-12-28 |
다케다 샌디에고, 인코포레이티드 |
히스톤 탈아세틸화 효소 억제제
|
|
EP1610768B1
(en)
|
2003-03-26 |
2008-07-02 |
Egalet A/S |
Matrix compositions for controlled delivery of drug substances
|
|
DE602004029252D1
(de)
|
2003-06-13 |
2010-11-04 |
Biogen Idec Inc |
Aglycosyl-anti-cd154 (cd40-ligand) antikörper und deren verwendungen
|
|
FR2857966A1
(fr)
|
2003-07-24 |
2005-01-28 |
Aventis Pharma Sa |
Produits aryl-heteroaromatiques, compositions les contenant et utilisation
|
|
CN1871259A
(zh)
|
2003-08-22 |
2006-11-29 |
比奥根艾迪克Ma公司 |
具有改变的效应物功能的经改进的抗体和制备它的方法
|
|
US20050203063A1
(en)
|
2003-09-12 |
2005-09-15 |
Raymond Deshaies |
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
|
|
HRP20090495T1
(hr)
|
2004-04-02 |
2009-10-31 |
Osi Pharmaceuticals |
Heterobiciklički inhibitori protein kinaze supstituirani 6,6-bicikličkim prstenom
|
|
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
|
|
AR053090A1
(es)
*
|
2004-07-20 |
2007-04-25 |
Osi Pharm Inc |
Imidazotriazinas como inhibidores de proteina quinasas y su uso para la preparacion de medicamentos
|
|
US20070043057A1
(en)
|
2005-02-09 |
2007-02-22 |
Threshold Pharmaceuticals, Inc. |
Lonidamine analogs
|
|
US20070015771A1
(en)
|
2004-07-29 |
2007-01-18 |
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
|
|
KR20070085433A
(ko)
|
2004-11-24 |
2007-08-27 |
노파르티스 아게 |
Jak 저해제들과 bcr-abl, flt-3, fak 또는raf 키나제 저해제들 중 하나 이상의 조합물
|
|
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
|
|
ES2436877T3
(es)
*
|
2005-11-17 |
2014-01-07 |
OSI Pharmaceuticals, LLC |
Intermedios para la preparación de inhibidores de mTOR bicíclicos condensados
|
|
US7514435B2
(en)
|
2005-11-18 |
2009-04-07 |
Bristol-Myers Squibb Company |
Pyrrolotriazine kinase inhibitors
|
|
PE20070855A1
(es)
*
|
2005-12-02 |
2007-10-14 |
Bayer Pharmaceuticals Corp |
Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
|
|
KR101461680B1
(ko)
|
2005-12-02 |
2014-11-19 |
바이엘 헬스케어 엘엘씨 |
과다-증식성 장애 및 맥관형성과 관련된 질환의 치료에유용한 치환된 4-아미노-피롤로트리아진 유도체
|
|
US8338594B2
(en)
|
2005-12-02 |
2012-12-25 |
Bayer Healthcare Llc |
Pyrrolotriazine derivatives useful for treating cancer through inhibition of aurora kinase
|
|
CN103214484B
(zh)
|
2005-12-13 |
2016-07-06 |
因塞特控股公司 |
作为两面神激酶抑制剂的杂芳基取代的吡咯并[2,3-b]吡啶和吡咯并[2,3-b]嘧啶
|
|
JP5400388B2
(ja)
|
2005-12-15 |
2014-01-29 |
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 |
キナーゼインヒビターおよびその利用
|
|
TW200801008A
(en)
|
2005-12-29 |
2008-01-01 |
Abbott Lab |
Protein kinase inhibitors
|
|
TW200808805A
(en)
|
2006-04-12 |
2008-02-16 |
Vertex Pharma |
Tetrahydropteridines useful as inhibitors of protein kinases
|
|
DK2010528T3
(en)
|
2006-04-19 |
2018-01-15 |
Novartis Ag |
6-O-Substituted Benzoxazole and Benzothiazole Compounds and Methods for Inhibiting CSF-1R Signaling
|
|
WO2007125315A2
(en)
|
2006-04-25 |
2007-11-08 |
Astex Therapeutics Limited |
Pharmaceutical compounds
|
|
ATE528002T1
(de)
|
2006-05-19 |
2011-10-15 |
Bayer Pharma AG |
Pyridoncarboxamidderivate zur behandlung hyperproliferativer und angiogenese-vermittelter leiden
|
|
EP2032560B1
(en)
|
2006-06-29 |
2013-05-01 |
Merck Sharp & Dohme Corp. |
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
|
|
ES2560435T3
(es)
*
|
2006-11-22 |
2016-02-19 |
Incyte Holdings Corporation |
Imidazotriazinas e imidazopirimidinas como inhibidores de la quinasa
|
|
WO2008073282A2
(en)
|
2006-12-07 |
2008-06-19 |
Schering Corporation |
Ph sensitive matrix formulation
|
|
CN101646671A
(zh)
|
2006-12-14 |
2010-02-10 |
弗特克斯药品有限公司 |
用作蛋白激酶抑制剂的化合物
|
|
AU2007342005A1
(en)
|
2006-12-29 |
2008-07-10 |
Rigel Pharmaceuticals, Inc. |
N3-heteroaryl substituted triazoles and N5-heteroaryl substituted triazoles useful as Axl inhibitors
|
|
PT2078010E
(pt)
|
2006-12-29 |
2014-05-07 |
Rigel Pharmaceuticals Inc |
Triazoles substituídos com heteroarilos policíclicos úteis como inibidores de axl
|
|
EP2114954B1
(en)
|
2006-12-29 |
2013-02-13 |
Rigel Pharmaceuticals, Inc. |
Bicyclic aryl and bicyclic heteroaryl substituted triazoles useful as axl inhibitors
|
|
SI2114980T1
(sl)
|
2007-01-12 |
2012-11-30 |
Biocryst Pharm Inc |
Protivirusni nukleozidni analogi
|
|
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
|
|
CA2680680A1
(en)
|
2007-03-29 |
2009-02-19 |
Panacea Biotec Limited |
Modified dosage forms of tacrolimus
|
|
US8124759B2
(en)
|
2007-05-09 |
2012-02-28 |
Abbott Laboratories |
Inhibitors of protein kinases
|
|
AU2008251555B2
(en)
|
2007-05-10 |
2012-08-30 |
Biocryst Pharmaceuticals, Inc. |
Tetrahydrofuro [3 4-D] dioxolane compounds for use in the treatment of viral infections and cancer
|
|
KR20120029480A
(ko)
|
2007-06-12 |
2012-03-26 |
콘서트 파마슈티컬즈, 인크. |
아자펩티드 유도체
|
|
US20090263397A1
(en)
|
2007-07-06 |
2009-10-22 |
Buck Elizabeth A |
Combination anti-cancer therapy
|
|
JP2010532756A
(ja)
|
2007-07-06 |
2010-10-14 |
オーエスアイ・ファーマスーティカルズ・インコーポレーテッド |
mTORC1及びmTORC2の両方の阻害剤を含む組み合わせ抗癌療法
|
|
CA2695753A1
(en)
|
2007-08-15 |
2009-02-19 |
Vertex Pharmaceuticals Incorporated |
Compounds useful as protein kinases inhibitors
|
|
MX2010003269A
(es)
|
2007-09-25 |
2010-08-02 |
Bayer Healthcare Llc |
Derivados de pirrolotriazina utiles para tratar cancer a traves de la inhibicion de la aurora quinasa.
|
|
GB0719803D0
(en)
|
2007-10-10 |
2007-11-21 |
Cancer Rec Tech Ltd |
Therapeutic compounds and their use
|
|
JP2011500778A
(ja)
|
2007-10-25 |
2011-01-06 |
アストラゼネカ・アクチエボラーグ |
ピリジン及びピラジン誘導体−083
|
|
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
|
|
MX2010006457A
(es)
|
2007-12-19 |
2010-07-05 |
Amgen Inc |
Compuestos fusionados de piridina, pirimidina y triazina como inhibidores de ciclo celular.
|
|
AR070127A1
(es)
|
2008-01-11 |
2010-03-17 |
Novartis Ag |
Pirrolo - pirimidinas y pirrolo -piridinas
|
|
JP2011515410A
(ja)
|
2008-03-19 |
2011-05-19 |
オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド |
塩の形のmTOR阻害剤
|
|
JP5746015B2
(ja)
|
2008-04-16 |
2015-07-08 |
マックス プランク ゲゼルシャフト ツゥアー フェデルゥン デル ヴィッセンシャフテン エー フォー |
Axlキナーゼ阻害剤としてのキノリン誘導体
|
|
HRP20130048T1
(hr)
|
2008-04-23 |
2013-02-28 |
Gilead Sciences, Inc. |
Karba-nukleozidni analozi za antivirusnu terapiju
|
|
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
|
|
MX346186B
(es)
|
2008-06-23 |
2017-03-10 |
Vertex Pharma |
Inhibidores de proteina cinasas.
|
|
EP2313102A2
(en)
|
2008-07-03 |
2011-04-27 |
Biota Scientific Management |
Bycyclic nucleosides and nucleotides as therapeutic agents
|
|
JP5592884B2
(ja)
|
2008-07-09 |
2014-09-17 |
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 |
Axl阻害剤として有用な多環式ヘテロアリール置換トリアゾール
|
|
US8431594B2
(en)
|
2008-07-09 |
2013-04-30 |
Rigel Pharmaceuticals, Inc. |
Bridged bicyclic 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
|
|
EP2158913A1
(en)
|
2008-08-25 |
2010-03-03 |
Ratiopharm GmbH |
Pharmaceutical composition comprising N-[3-chhloro-4-[(3-fluorophenyl)methoxy]phenyl]6-(5[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furyl]-4-quinazolinamine
|
|
US20100075973A1
(en)
|
2008-08-28 |
2010-03-25 |
Takeda Pharmaceutical Company Limited |
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
|
|
US8476282B2
(en)
|
2008-11-03 |
2013-07-02 |
Intellikine Llc |
Benzoxazole kinase inhibitors and methods of use
|
|
EP2376491B1
(en)
|
2008-12-19 |
2015-03-04 |
Cephalon, Inc. |
Pyrrolotriazines as alk and jak2 inhibitors
|
|
US20100204265A1
(en)
|
2009-02-09 |
2010-08-12 |
Genelabs Technologies, Inc. |
Certain Nitrogen Containing Bicyclic Chemical Entities for Treating Viral Infections
|
|
JP2012517426A
(ja)
|
2009-02-09 |
2012-08-02 |
アステックス ファーマシューティカルズ インコーポレイテッド |
ピロロピリミジニルaxlキナーゼ阻害剤
|
|
WO2010099139A2
(en)
|
2009-02-25 |
2010-09-02 |
Osi Pharmaceuticals, Inc. |
Combination anti-cancer therapy
|
|
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
|
|
WO2010126960A1
(en)
|
2009-04-29 |
2010-11-04 |
Locus Pharmaceuticals, Inc. |
Pyrrolotriazine compounds
|
|
MY156727A
(en)
|
2009-05-22 |
2016-03-15 |
Incyte Corp |
N-(hetero)aryl-pyrrolidine derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines and pyrrol-3-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors
|
|
EP2845856A1
(en)
*
|
2009-06-29 |
2015-03-11 |
Incyte Corporation |
Pyrimidinones as PI3K inhibitors
|
|
WO2011014726A1
(en)
|
2009-07-31 |
2011-02-03 |
Osi Pharmaceuticals, Inc. |
Mtor inhibitor and angiogenesis inhibitor combination therapy
|
|
TW201113285A
(en)
|
2009-09-01 |
2011-04-16 |
Incyte Corp |
Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors
|
|
AU2010295373B2
(en)
|
2009-09-21 |
2016-09-29 |
Gilead Sciences, Inc. |
2' -fluoro substituted carba-nucleoside analogs for antiviral treatment
|
|
US8455451B2
(en)
|
2009-09-21 |
2013-06-04 |
Gilead Sciences, Inc. |
2'-fluoro substituted carba-nucleoside analogs for antiviral treatment
|
|
WO2011035250A1
(en)
|
2009-09-21 |
2011-03-24 |
Gilead Sciences, Inc. |
Processes and intermediates for the preparation of 1'-substituted carba-nucleoside analogs
|
|
NZ599342A
(en)
|
2009-09-25 |
2014-04-30 |
Vertex Pharma |
Methods for preparing pyrimidine derivatives useful as protein kinase inhibitors
|
|
AU2010303567B2
(en)
|
2009-10-06 |
2016-06-09 |
Millennium Pharmaceuticals, Inc |
Heterocyclic compounds useful as PDK1 inhibitors
|
|
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
|
|
WO2011075630A1
(en)
|
2009-12-18 |
2011-06-23 |
Incyte Corporation |
Substituted fused aryl and heteroaryl derivatives as pi3k inhibitors
|
|
WO2011089400A1
(en)
|
2010-01-22 |
2011-07-28 |
Centro Nacional De Investigaciones Oncológicas (Cnio) |
Inhibitors of pi3 kinase
|
|
EP3354652B1
(en)
|
2010-03-10 |
2020-05-06 |
Incyte Holdings Corporation |
Piperidin-4-yl azetidine derivatives as jak1 inhibitors
|
|
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
|
|
EP2566866A1
(en)
|
2010-05-05 |
2013-03-13 |
Vertex Pharmaceuticals Incorporated |
4 substituted pyrazolopyrimidines useful as pkc-theta inhibitors
|
|
WO2011141713A1
(en)
|
2010-05-13 |
2011-11-17 |
Centro Nacional De Investigaciones Oncologicas (Cnio) |
New bicyclic compounds as pi3-k and mtor inhibitors
|
|
WO2011146313A1
(en)
|
2010-05-19 |
2011-11-24 |
The University Of North Carolina At Chapel Hill |
Pyrazolopyrimidine compounds for the treatment of cancer
|
|
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
|
|
EA025311B1
(ru)
|
2010-07-19 |
2016-12-30 |
Гайлид Сайэнсиз, Инк. |
Способы получения диастереомерно чистых фосфорамидатных пролекарств
|
|
ES2524356T3
(es)
|
2010-07-22 |
2014-12-05 |
Gilead Sciences, Inc. |
Métodos y compuestos para tratar infecciones provocadas por virus Paramyxoviridae
|
|
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 |
吉李德科學股份有限公司 |
用於抗病毒治療之2’-氟取代之碳-核苷類似物
|
|
EP2623505B1
(en)
|
2010-09-29 |
2015-07-29 |
Kissei Pharmaceutical Co., Ltd. |
(aza)indolizine derivatives as xanthine oxidase inhibitors
|
|
JP2013539759A
(ja)
|
2010-10-08 |
2013-10-28 |
エラン ファーマシューティカルズ,インコーポレイテッド |
ポロ様キナーゼの阻害剤
|
|
US9181234B2
(en)
|
2010-10-08 |
2015-11-10 |
Biota Europe Ltd. |
Antibacterial compounds
|
|
ITRM20100537A1
(it)
|
2010-10-12 |
2012-04-12 |
Consiglio Nazionale Ricerche |
Aptamero inibitore del recettore tirosina chinasi axl per uso in terapia
|
|
CA2818542A1
(en)
|
2010-11-19 |
2012-05-24 |
Incyte Corporation |
Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors
|
|
WO2012068440A1
(en)
|
2010-11-19 |
2012-05-24 |
Incyte Corporation |
Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors
|
|
TW201249844A
(en)
|
2010-12-20 |
2012-12-16 |
Incyte Corp |
N-(1-(substituted-phenyl)ethyl)-9H-purin-6-amines as PI3K inhibitors
|
|
EP2678016B1
(en)
|
2011-02-23 |
2016-08-10 |
Intellikine, LLC |
Heterocyclic compounds and uses thereof
|
|
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
|
|
RU2568258C2
(ru)
|
2011-02-28 |
2015-11-20 |
Саншайн Лейк Фарма Ко., Лтд |
Замещенные соединения хинолина и способы их использования
|
|
DK2937349T3
(en)
|
2011-03-23 |
2017-02-20 |
Amgen Inc |
CONDENSED TRICYCLIC DUAL INHIBITORS OF CDK 4/6 AND FLT3
|
|
EP3628665B1
(en)
|
2011-04-01 |
2022-11-02 |
University of Utah Research Foundation |
Substituted n-phenylpyrimidin-2-amine analogs as inhibitors of the axl kinase
|
|
ES2618489T3
(es)
|
2011-05-04 |
2017-06-21 |
Intellikine, Llc |
Composiciones farmacéuticas combinadas y usos de las mismas
|
|
WO2012154608A1
(en)
|
2011-05-06 |
2012-11-15 |
Intellikine, Llc |
Reactive mtor and pi3 kinase inhibitors and uses thereof
|
|
EA025496B1
(ru)
|
2011-05-17 |
2016-12-30 |
Принсипиа Биофарма Инк. |
Ингибиторы тирозинкиназы
|
|
HUE048834T2
(hu)
|
2011-05-17 |
2020-08-28 |
Univ California |
Kináz inhibitorok
|
|
WO2012158795A1
(en)
|
2011-05-17 |
2012-11-22 |
Principia Biopharma Inc. |
Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors
|
|
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
|
|
MY165963A
(en)
|
2011-06-20 |
2018-05-18 |
Incyte Holdings Corp |
Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors
|
|
JP5955953B2
(ja)
|
2011-07-01 |
2016-07-20 |
バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH |
Alk1阻害剤としてのヒドロキシメチルアリール−置換ピロロトリアジン
|
|
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
|
|
UA121539C2
(uk)
|
2011-09-02 |
2020-06-25 |
Інсайт Холдинґс Корпорейшн |
Гетероцикліламіни як інгібітори рі3к
|
|
CN103826630B
(zh)
|
2011-09-18 |
2016-12-07 |
杭州民生药物研究院有限公司 |
药物组合物
|
|
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
|
|
US9273056B2
(en)
|
2011-10-03 |
2016-03-01 |
The University Of North Carolina At Chapel Hill |
Pyrrolopyrimidine compounds for the treatment of cancer
|
|
CN106924741A
(zh)
|
2011-11-08 |
2017-07-07 |
因特利凯有限责任公司 |
使用多种药剂的治疗方案
|
|
UY34451A
(es)
|
2011-11-14 |
2013-05-31 |
Cephalon Inc |
Derivados de uracilo como inhibidores de la quinasa axl y c-met
|
|
US20130209543A1
(en)
|
2011-11-23 |
2013-08-15 |
Intellikine Llc |
Enhanced treatment regimens using mtor inhibitors
|
|
WO2013082210A1
(en)
|
2011-11-29 |
2013-06-06 |
Perosphere Inc. |
Anticoagulant reversal agents
|
|
WO2013085802A1
(en)
|
2011-12-06 |
2013-06-13 |
Merck Sharp & Dohme Corp. |
Pyrrolopyrimidines as janus kinase inhibitors
|
|
UY34484A
(es)
|
2011-12-15 |
2013-07-31 |
Bayer Ip Gmbh |
Benzotienilo-pirrolotriazinas disustituidas y sus usos
|
|
JP6047582B2
(ja)
|
2011-12-15 |
2016-12-21 |
バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH |
置換ベンゾチエニル−ピロロトリアジンおよび癌の処置におけるその使用
|
|
MY165215A
(en)
|
2012-01-31 |
2018-03-09 |
Daiichi Sankyo Co Ltd |
Pyridone derivatives
|
|
CN104080789B
(zh)
|
2012-01-31 |
2016-05-11 |
南京奥昭生物科技有限公司 |
作为布鲁顿酪氨酸激酶抑制剂的环状分子
|
|
CA2865021C
(en)
|
2012-02-23 |
2020-06-30 |
Bayer Intellectual Property Gmbh |
Substituted benzothienyl-pyrrolotriazines and uses thereof
|
|
US20150057243A1
(en)
|
2012-04-02 |
2015-02-26 |
Northern 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
|
|
DK2861599T3
(da)
|
2012-06-18 |
2020-03-02 |
Principia Biopharma Inc |
Reversible kovalente pyrrolo- eller pyrazolopyrimidiner, der er nyttige til behandling af cancer og autoimmunsygdomme
|
|
KR20150021120A
(ko)
|
2012-06-19 |
2015-02-27 |
선오비온 파마슈티컬스 인코포레이티드 |
헤테로아릴 화합물 및 이의 이용 방법
|
|
US9260436B2
(en)
|
2012-06-22 |
2016-02-16 |
Sumitomo Chemical Company, Limited |
Fused heterocyclic compound
|
|
WO2014022569A1
(en)
|
2012-08-03 |
2014-02-06 |
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
|
|
CN104981247A
(zh)
|
2012-09-06 |
2015-10-14 |
普莱希科公司 |
用于激酶调节的化合物和方法及其适应症
|
|
WO2014042433A2
(en)
|
2012-09-14 |
2014-03-20 |
Kainos Medicine, Inc. |
Compounds and compositions for modulating adenosine a3 receptor activity
|
|
MX2015003874A
(es)
*
|
2012-09-26 |
2015-12-16 |
Univ California |
Modulacion de ire1.
|
|
EP2909211A4
(en)
|
2012-10-17 |
2016-06-22 |
Univ North Carolina |
PYRAZOLOPYRIMIDINE COMPOUNDS FOR CANCER TREATMENT
|
|
WO2014059901A1
(en)
|
2012-10-17 |
2014-04-24 |
Merck Sharp & Dohme Corp. |
2'-cyano substituted nucleoside derivatives and methods of use thereof for treatment of viral diseases
|
|
EP2909210A4
(en)
|
2012-10-17 |
2016-04-06 |
Merck Sharp & Dohme |
2'-DISUBSTITUTED NUCLEOSIDE DERIVATIVES AND METHOD FOR THE USE THEREOF FOR THE TREATMENT OF VIRUS DISEASES
|
|
JP6359546B2
(ja)
|
2012-11-01 |
2018-07-18 |
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阻害薬としての三環式縮合チオフェン誘導体
|
|
WO2014078778A2
(en)
|
2012-11-16 |
2014-05-22 |
Biocryst Pharmaceuticals, Inc. |
Antiviral azasugar-containing nucleosides
|
|
WO2014079545A1
(en)
|
2012-11-20 |
2014-05-30 |
Ktb Tumorforschungsgesellschaft Mbh |
Thioether derivatives as protein kinase inhibitors
|
|
US20140199728A1
(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
|
|
WO2014113620A2
(en)
|
2013-01-18 |
2014-07-24 |
Bristol-Myers Squibb Company |
Phthalazinones and isoquinolinones as rock inhibitors
|
|
WO2014113942A1
(en)
|
2013-01-23 |
2014-07-31 |
Merck Sharp & Dohme Corp. |
Btk inhibitors
|
|
US20140357636A1
(en)
|
2013-02-21 |
2014-12-04 |
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
|
|
WO2014164729A1
(en)
|
2013-03-12 |
2014-10-09 |
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
|
|
CA2922058A1
(en)
|
2013-10-18 |
2015-04-23 |
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
|
|
ES2685661T3
(es)
|
2013-11-08 |
2018-10-10 |
Ono Pharmaceutical Co., Ltd. |
Derivado de pirrolopirimidina
|
|
WO2015081783A1
(zh)
|
2013-12-06 |
2015-06-11 |
江苏奥赛康药业股份有限公司 |
吡咯并[2,1-f][1,2,4]三嗪类衍生物及其制备方法和用途
|
|
CN105916859A
(zh)
*
|
2014-02-03 |
2016-08-31 |
卡迪拉保健有限公司 |
杂环化合物
|
|
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
|
|
GB201420285D0
(en)
|
2014-11-14 |
2014-12-31 |
Bergenbio As |
Process
|
|
ES2746839T3
(es)
|
2014-12-18 |
2020-03-09 |
Pfizer |
Derivados de pirimidina y triazina y su uso como inhibidores de AXL
|
|
US9840503B2
(en)
|
2015-05-11 |
2017-12-12 |
Incyte Corporation |
Heterocyclic compounds and uses thereof
|
|
AU2016298227B9
(en)
|
2015-07-30 |
2019-10-31 |
Macrogenics, Inc. |
PD-1-binding molecules and methods of use thereof
|
|
WO2017027717A1
(en)
*
|
2015-08-12 |
2017-02-16 |
Incyte Corporation |
Bicyclic fused pyrimidine compounds as tam inhibitors
|
|
US10053465B2
(en)
|
2015-08-26 |
2018-08-21 |
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
|
|
ES2956011T3
(es)
|
2015-10-13 |
2023-12-11 |
Nihon Nohyaku Co Ltd |
Compuesto heterocíclico condensado que contiene un grupo oxima o sales del mismo e insecticida agrícola y hortícola que contiene dicho compuesto y método para el uso del mismo
|
|
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
|
|
CN114456176B
(zh)
*
|
2016-03-28 |
2024-08-30 |
因赛特公司 |
作为tam抑制剂的吡咯并三嗪化合物
|
|
US10166221B2
(en)
|
2016-04-22 |
2019-01-01 |
Incyte Corporation |
Formulations of an LSD1 inhibitor
|
|
AR108875A1
(es)
|
2016-06-24 |
2018-10-03 |
Incyte Corp |
COMPUESTOS HETEROCÍCLICOS COMO INHIBIDORES DE PI3K-g
|
|
ES2935658T3
(es)
|
2016-07-15 |
2023-03-09 |
Ionis Pharmaceuticals Inc |
Compuestos y métodos para la modulación de 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
|
|
JOP20190257A1
(ar)
|
2017-04-28 |
2019-10-28 |
Novartis Ag |
مركبات أريل غير متجانسة ثنائية الحلقة مندمجة 6-6 واستخدامها كمثبطات lats
|
|
KR102739325B1
(ko)
|
2017-09-27 |
2024-12-09 |
인사이트 코포레이션 |
Tam 억제제로서 유용한 피롤로트리아진 유도체의 염
|
|
US11241438B2
(en)
|
2018-06-29 |
2022-02-08 |
Incyte Corporation |
Formulations of an AXL/MER inhibitor
|
|
PH12022552347A1
(en)
|
2020-03-06 |
2024-01-29 |
Incyte Corp |
Combination therapy comprising axl/mer and pd-1/pd-l1 inhibitors
|