|
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
|
|
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
|
|
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
|
|
DE3883899T3
(de)
|
1987-03-18 |
1999-04-22 |
Sb2, Inc., Danville, Calif. |
Geänderte antikörper.
|
|
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
|
|
DE122004000008I1
(de)
|
1991-06-14 |
2005-06-09 |
Genentech Inc |
Humanisierter Heregulin Antikörper.
|
|
WO1993011161A1
(en)
|
1991-11-25 |
1993-06-10 |
Enzon, Inc. |
Multivalent antigen-binding proteins
|
|
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
|
|
WO1997008320A1
(en)
|
1995-08-18 |
1997-03-06 |
Morphosys Gesellschaft Für Proteinoptimierung Mbh |
Protein/(poly)peptide libraries
|
|
US20020077461A1
(en)
|
1996-04-24 |
2002-06-20 |
Soren Bjorn |
Pharmaceutical formulation
|
|
JP2001520268A
(ja)
|
1997-10-14 |
2001-10-30 |
ザ、プロクター、エンド、ギャンブル、カンパニー |
中鎖分枝鎖界面活性剤を包含する硬質表面クリーニング組成物
|
|
US6982265B1
(en)
|
1999-05-21 |
2006-01-03 |
Bristol Myers Squibb Company |
Pyrrolotriazine inhibitors of kinases
|
|
DE60037455T2
(de)
|
1999-09-17 |
2008-11-27 |
Abbott Gmbh & Co. Kg |
Kinaseinhibitoren als arzneimittel
|
|
US6770666B2
(en)
|
1999-12-27 |
2004-08-03 |
Japan Tobacco Inc. |
Fused-ring compounds and use thereof as drugs
|
|
WO2001047883A1
(fr)
|
1999-12-27 |
2001-07-05 |
Japan Tobacco Inc. |
Composes a cycles accoles et leur utilisation comme medicaments
|
|
NZ522783A
(en)
|
2000-06-28 |
2004-07-30 |
Smithkline Beecham P |
Wet milling process for pharmaceuticals with agitator or chamber having nylon with internal lubricant
|
|
ATE406892T1
(de)
|
2001-04-06 |
2008-09-15 |
Wyeth Corp |
Antineoplastische kombinationspräparate enthaltend cci-779 (rapamycin derivat) zusammen mit gemcitabin oder fluoro-uracil
|
|
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
|
|
WO2004035580A1
(en)
|
2002-10-21 |
2004-04-29 |
Aprea Ab |
Reactivation of wild type p53 in human tumour cells by a low molecular weight compound
|
|
US7824851B2
(en)
|
2002-11-15 |
2010-11-02 |
Idenix Pharmaceuticals, Inc. |
2′-branched nucleosides 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
|
|
CA2510003A1
(en)
|
2003-01-16 |
2004-08-05 |
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
|
|
TW200505915A
(en)
|
2003-03-13 |
2005-02-16 |
Synta Pharmaceuticals Corp |
Fused pyrrole compounds
|
|
EP1608628A2
(en)
|
2003-03-17 |
2005-12-28 |
Takeda San Diego, Inc. |
Histone deacetylase inhibitors
|
|
JP4989217B2
(ja)
|
2003-03-26 |
2012-08-01 |
エガレット エイ/エス |
薬剤物質の送達制御用マトリックス組成物
|
|
CA2528551A1
(en)
|
2003-06-13 |
2005-01-13 |
Biogen Idec Ma Inc. |
Aglycosyl anti-cd154 (cd40 ligand) antibodies and uses thereof
|
|
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
|
|
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
|
|
CN102924458B
(zh)
|
2004-04-02 |
2014-11-05 |
Osi制药有限责任公司 |
6,6-双环取代的杂双环蛋白激酶抑制剂
|
|
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
|
|
WO2007056170A2
(en)
|
2005-11-02 |
2007-05-18 |
Bayer Healthcare Ag |
Pyrrolo[2,1-f] [1,2,4] triazin-4-ylamines igf-1r kinase inhibitors for the treatment of cancer and other hyperproliferative diseases
|
|
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
|
|
JP5193876B2
(ja)
|
2005-12-02 |
2013-05-08 |
バイエル・ヘルスケア・エルエルシー |
オーロラキナーゼの阻害により癌を処置するために有用なピロロトリアジン誘導体
|
|
PE20070855A1
(es)
*
|
2005-12-02 |
2007-10-14 |
Bayer Pharmaceuticals Corp |
Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
|
|
CA2631741C
(en)
|
2005-12-02 |
2014-01-28 |
Bayer Healthcare Llc |
Substituted 4-amino-pyrrolotriazine derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis
|
|
EP3838903B1
(en)
|
2005-12-13 |
2023-11-22 |
Incyte Holdings Corporation |
Pyrrolo[2,3-d]pyrimidine derivative as janus kinase inhibitor
|
|
WO2007070872A1
(en)
|
2005-12-15 |
2007-06-21 |
Rigel Pharmaceuticals, Inc. |
Kinase inhibitors and their uses
|
|
CN101389630A
(zh)
|
2005-12-29 |
2009-03-18 |
艾博特公司 |
蛋白激酶抑制剂
|
|
NZ571969A
(en)
|
2006-04-12 |
2011-10-28 |
Vertex Pharma |
4, 5-dihydro- [1, 2, 4] triazolo [4, 3-f] pteridines as protein kinase plk1 inhibitors for the treatment of proliferative disorders
|
|
AU2007237904B2
(en)
|
2006-04-19 |
2011-03-03 |
Novartis Ag |
6-O-substituted benzoxazole and benzothiazole compounds and methods of 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
|
|
AU2007269830A1
(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
|
|
EP3443958A1
(en)
*
|
2006-11-22 |
2019-02-20 |
Incyte Holdings Corporation |
Imidazotriazines and imidazopyrimidines as kinase inhibitors
|
|
JP2010512317A
(ja)
|
2006-12-07 |
2010-04-22 |
シェーリング コーポレイション |
pH感受性マトリクス処方物
|
|
EP2102210B1
(en)
|
2006-12-14 |
2011-02-09 |
Vertex Pharmceuticals Incorporated |
Compounds useful as protein kinase inhibitors
|
|
SI2078010T1
(sl)
|
2006-12-29 |
2014-06-30 |
Rigel Pharmaceuticals, Inc., |
Policiklični heteroaril substituirani triazoli uporabni kot inhibitorji AXL
|
|
CA2710043C
(en)
|
2006-12-29 |
2016-02-09 |
Rigel Pharmaceuticals, Inc. |
Bicyclic aryl and bicyclic heteroaryl substituted triazoles useful as axl inhibitors
|
|
ES2607065T3
(es)
|
2006-12-29 |
2017-03-29 |
Rigel Pharmaceuticals, Inc. |
Triazoles N3-heteroaril sustituidos y triazoles N5-heteroaril sustituidos útiles como inhibidores de axl
|
|
EP2535345A1
(en)
|
2007-01-12 |
2012-12-19 |
BioCryst Pharmaceuticals, Inc. |
Anticancer nucleoside analogs
|
|
US8168415B2
(en)
|
2007-02-07 |
2012-05-01 |
The Regents Of The University Of Colorado |
Axl fusion proteins as Axl tyrosine kinase inhibitors
|
|
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
|
|
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
|
|
JP2010529196A
(ja)
|
2007-06-12 |
2010-08-26 |
コンサート ファーマシューティカルズ インコーポレイテッド |
アザペプチド誘導体
|
|
EP2178563A2
(en)
|
2007-07-06 |
2010-04-28 |
OSI Pharmaceuticals, Inc. |
Combination anti-cancer therapy comprising an inhibitor of both mtorc1 and mtorc2
|
|
WO2009009016A1
(en)
|
2007-07-06 |
2009-01-15 |
Osi Pharmaceuticals, Inc. |
Combination anti-cancer therapy
|
|
CN101952291A
(zh)
|
2007-08-15 |
2011-01-19 |
弗特克斯药品有限公司 |
用作人蛋白激酶plk1至plk4的抑制剂以治疗增殖疾病的4-(9-(3,3-二氟环戊基)-5,7,7-三甲基-6-氧代-6,7,8,9-四氢-5h-嘧啶并[4,5-b][1,4]二氮杂䓬-2-基氨基)-3-甲氧基苯甲酰胺衍生物
|
|
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
|
|
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
|
|
AU2008343932B2
(en)
|
2007-12-19 |
2013-08-15 |
Amgen Inc. |
Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors
|
|
AR070127A1
(es)
|
2008-01-11 |
2010-03-17 |
Novartis Ag |
Pirrolo - pirimidinas y pirrolo -piridinas
|
|
CN101977912A
(zh)
|
2008-03-19 |
2011-02-16 |
Osi医药有限公司 |
mTOR抑制剂的盐形式
|
|
KR101325237B1
(ko)
|
2008-04-16 |
2013-11-04 |
막스-플랑크-게젤샤프트 츄어 푀르더룽 데어 비쎈샤프텐 에.파우. |
Axl 키나아제 억제제인 퀴놀린 유도체
|
|
EA020659B1
(ru)
|
2008-04-23 |
2014-12-30 |
Джилид Сайэнс, Инк. |
1'-замещённые карбануклеозидные аналоги для противовирусной терапии
|
|
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
|
|
WO2010002877A2
(en)
|
2008-07-03 |
2010-01-07 |
Biota Scientific Management |
Bycyclic nucleosides and nucleotides as therapeutic agents
|
|
HRP20130045T1
(hr)
|
2008-07-09 |
2013-02-28 |
Rigel Pharmaceuticals, Inc. |
Premošteni bicikliäśki heteroaril supstituirani triazoli koji su korisni kao axl inhibitori
|
|
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
|
|
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
|
|
JP2012506238A
(ja)
|
2008-10-20 |
2012-03-15 |
ザ リージェンツ オブ ザ ユニバーシティ オブ コロラド,ア ボディー コーポレイト |
インスリン様増殖因子−1受容体キナーゼ阻害剤に対する抗がん反応を予測する生物学的マーカー
|
|
US8476431B2
(en)
|
2008-11-03 |
2013-07-02 |
Itellikine LLC |
Benzoxazole kinase inhibitors and methods of use
|
|
AR074830A1
(es)
|
2008-12-19 |
2011-02-16 |
Cephalon Inc |
Pirrolotriazinas como inhibidores de alk y jak2
|
|
US20100204265A1
(en)
|
2009-02-09 |
2010-08-12 |
Genelabs Technologies, Inc. |
Certain Nitrogen Containing Bicyclic Chemical Entities for Treating Viral Infections
|
|
CA2748943A1
(en)
|
2009-02-09 |
2010-08-12 |
Supergen, Inc. |
Pyrrolopyrimidinyl axl kinase inhibitors
|
|
US20120189641A1
(en)
|
2009-02-25 |
2012-07-26 |
OSI Pharmaceuticals, LLC |
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
|
|
EP2424368B1
(en)
|
2009-04-29 |
2014-12-31 |
Locus Pharmaceuticals, Inc. |
Pyrrolotriazine compounds
|
|
US8716303B2
(en)
|
2009-05-22 |
2014-05-06 |
Incyte Corporation |
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
|
|
CN104945420A
(zh)
*
|
2009-06-29 |
2015-09-30 |
因塞特公司 |
作为pi3k抑制剂的嘧啶酮类
|
|
US20120128670A1
(en)
|
2009-07-31 |
2012-05-24 |
OSI Pharmaceuticals, LLC |
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
|
|
US8455451B2
(en)
|
2009-09-21 |
2013-06-04 |
Gilead Sciences, Inc. |
2'-fluoro substituted carba-nucleoside analogs for antiviral treatment
|
|
CN102596979B
(zh)
|
2009-09-21 |
2014-12-10 |
吉里德科学公司 |
用于制备1’-取代碳核苷类似物的方法和中间体
|
|
CA2773772C
(en)
|
2009-09-21 |
2018-06-26 |
Gilead Sciences, Inc. |
2'-fluoro substituted carba-nucleoside analogs for antiviral treatment
|
|
SG179207A1
(en)
|
2009-09-25 |
2012-04-27 |
Vertex Pharma |
Methods for preparing pyrimidine derivatives useful as protein kinase inhibitors
|
|
RU2615130C2
(ru)
|
2009-10-06 |
2017-04-04 |
Милленниум Фармасьютикалз, Инк |
Гетероциклические соединения, используемые в качестве ингибиторов pdk1
|
|
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
|
|
AR079529A1
(es)
|
2009-12-18 |
2012-02-01 |
Incyte Corp |
Derivados arilo y heteroarilo sustituidos y fundidos como inhibidores de la pi3k
|
|
US9073927B2
(en)
|
2010-01-22 |
2015-07-07 |
Fundacion Centro Nacional De Investigaciones Oncologicas Carlos Iii |
Inhibitors of PI3 kinase
|
|
ME02386B
(me)
|
2010-03-10 |
2016-09-20 |
Incyte Holdings Corp |
Derivati piperidin-4-il azetidina kao inhibitori jak1
|
|
US8791257B2
(en)
|
2010-03-31 |
2014-07-29 |
Bristol-Myers Squibb Company |
Substituted pyrrolotriazines as protein kinase inhibitors
|
|
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
|
|
ES2524398T3
(es)
|
2010-07-19 |
2014-12-09 |
Gilead Sciences, Inc. |
Métodos para la preparación de profármacos de fosforoamidato diastereoméricamente puros
|
|
EA025252B1
(ru)
|
2010-07-22 |
2016-12-30 |
Гайлид Сайэнсиз, Инк. |
Способы и соединения для лечения вирусных инфекций 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 |
Gilead Sciences Inc |
用於抗病毒治療之2’-氟取代之碳-核苷類似物
|
|
WO2012043638A1
(ja)
|
2010-09-29 |
2012-04-05 |
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
|
|
US9181234B2
(en)
|
2010-10-08 |
2015-11-10 |
Biota Europe Ltd. |
Antibacterial compounds
|
|
EP2661268A2
(en)
|
2010-10-08 |
2013-11-13 |
Elan Pharmaceuticals Inc. |
Inhibitors of polo-like kinase
|
|
ITRM20100537A1
(it)
|
2010-10-12 |
2012-04-12 |
Consiglio Nazionale Ricerche |
Aptamero inibitore del recettore tirosina chinasi axl per uso in terapia
|
|
TW201249845A
(en)
|
2010-11-19 |
2012-12-16 |
Incyte Corp |
Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as JAK inhibitors
|
|
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
|
|
CA2822070C
(en)
|
2010-12-20 |
2019-09-17 |
Incyte Corporation |
N-(1-(substituted-phenyl)ethyl)-9h-purin-6-amines as pi3k inhibitors
|
|
WO2012116237A2
(en)
|
2011-02-23 |
2012-08-30 |
Intellikine, Llc |
Heterocyclic compounds and uses thereof
|
|
EP2678018A4
(en)
|
2011-02-23 |
2015-09-30 |
Intellikine Llc |
COMBINATION OF CHINESE HEMMER AND USES THEREOF
|
|
BR112013014708B1
(pt)
|
2011-02-28 |
2021-10-19 |
Sunshine Lake Pharma Co., Ltd. |
Composto, composição farmacêutica, e, uso de um composto ou composição farmacêutica
|
|
WO2012129344A1
(en)
|
2011-03-23 |
2012-09-27 |
Amgen Inc. |
Fused tricyclic dual inhibitors of cdk 4/6 and flt3
|
|
EP2693881B1
(en)
|
2011-04-01 |
2019-09-04 |
University of Utah Research Foundation |
Substituted n-phenylpyrimidin-2-amine analogs as inhibitors of the axl kinase
|
|
WO2012151562A1
(en)
|
2011-05-04 |
2012-11-08 |
Intellikine, Llc |
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
|
|
KR102027598B1
(ko)
|
2011-05-17 |
2019-10-01 |
프린시피아 바이오파마, 인코퍼레이티드 |
타이로신 키나아제 저해제
|
|
US9580427B2
(en)
|
2011-05-17 |
2017-02-28 |
The Regents Of The University Of California |
Kinase inhibitors
|
|
US9376438B2
(en)
|
2011-05-17 |
2016-06-28 |
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
|
|
KR20140040819A
(ko)
|
2011-06-20 |
2014-04-03 |
인사이트 코포레이션 |
Jak 저해제로서의 아제티디닐 페닐, 피리딜 또는 피라지닐 카르복스아미드 유도체
|
|
SG195100A1
(en)
|
2011-07-01 |
2013-12-30 |
Bayer Ip Gmbh |
Hydroxymethylaryl-substituted pyrrolotriazines as alk1 inhibitors
|
|
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
|
|
AR087760A1
(es)
|
2011-09-02 |
2014-04-16 |
Incyte Corp |
Heterociclilaminas como inhibidores de pi3k
|
|
PT2758052T
(pt)
|
2011-09-18 |
2018-03-29 |
Euro Celtique Sa |
Composição farmacêutica que compreende um inibidor de hdac e um ciclopolissacárido
|
|
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
|
|
KR102063098B1
(ko)
|
2011-10-03 |
2020-01-08 |
더 유니버시티 오브 노쓰 캐롤라이나 엣 채플 힐 |
암 치료를 위한 피롤로피리미딘 화합물
|
|
CA2854926A1
(en)
|
2011-11-08 |
2013-05-16 |
Intellikine, Llc |
Treatment regimens using multiple pharmaceutical agents
|
|
CN103958497B
(zh)
|
2011-11-14 |
2017-09-01 |
亚尼塔公司 |
作为AXL和c‑MET激酶抑制剂的尿嘧啶衍生物
|
|
WO2013078440A2
(en)
|
2011-11-23 |
2013-05-30 |
Intellikine, Llc |
Enhanced treatment regimens using mtor inhibitors
|
|
EP2785700B1
(en)
|
2011-11-29 |
2016-03-09 |
Perosphere, Inc. |
Anticoagulant reversal agents
|
|
US8993756B2
(en)
|
2011-12-06 |
2015-03-31 |
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
|
|
WO2013113097A1
(en)
|
2012-01-31 |
2013-08-08 |
Beta Pharma Canada Inc. |
Cyclic molecules as bruton's tyrosine kinase inhibitors
|
|
RS55728B1
(sr)
|
2012-01-31 |
2017-07-31 |
Daiichi Sankyo Co Ltd |
Derivat piridona
|
|
WO2013124316A1
(en)
|
2012-02-23 |
2013-08-29 |
Bayer Intellectual Property Gmbh |
Substituted benzothienyl-pyrrolotriazines and uses thereof
|
|
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
|
|
WO2013191965A1
(en)
|
2012-06-18 |
2013-12-27 |
Principia Biopharma Inc. |
Reversible covalent pyrrolo- or pyrazolopyrimidines useful for the treatment cancer and autoimmune diseases
|
|
SG11201408178TA
(en)
|
2012-06-19 |
2015-01-29 |
Sunovion Pharmaceuticals Inc |
Heteroaryl compounds and methods of use thereof
|
|
EP2865671B1
(en)
|
2012-06-22 |
2017-11-01 |
Sumitomo Chemical Company, Ltd |
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
|
|
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
|
|
WO2014052669A1
(en)
*
|
2012-09-26 |
2014-04-03 |
The Regents Of The University Of California |
Modulation of ire1
|
|
US9242988B2
(en)
|
2012-10-17 |
2016-01-26 |
Merck Sharp & Dohme Corp. |
2′-cyano substituted 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
|
|
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
|
|
SG11201503141TA
(en)
|
2012-11-01 |
2015-06-29 |
Incyte Corp |
Tricyclic fused thiophene derivatives as jak inhibitors
|
|
CA2890905A1
(en)
|
2012-11-16 |
2014-05-22 |
Biocryst Pharmaceuticals, Inc. |
Antiviral azasugar-containing nucleosides
|
|
US9925193B2
(en)
|
2012-11-20 |
2018-03-27 |
Proqinase Gmbh |
Thioether derivatives as protein kinase inhibitors
|
|
US20150353542A1
(en)
|
2013-01-14 |
2015-12-10 |
Amgen Inc. |
Methods of using cell-cycle inhibitors to modulate one or more properties of a cell culture
|
|
BR112015017008A2
(pt)
|
2013-01-18 |
2017-07-11 |
Bristol Myers Squibb Co |
ftalazinonas e isoquinolinonas como inibidores de rock
|
|
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
|
|
WO2015058084A1
(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
|
|
EP3067356B1
(en)
|
2013-11-08 |
2018-07-04 |
ONO Pharmaceutical Co., Ltd. |
Pyrrolo pyrimidine derivative
|
|
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
|
|
CA2934989C
(en)
*
|
2014-02-03 |
2017-08-08 |
Cadila Healthcare Limited |
Novel heterocyclic compounds
|
|
HK1232076A1
(zh)
|
2014-02-12 |
2018-01-05 |
Senomyx, Inc. |
用於取代的1-苄基-3-(1-(异恶唑-4-基甲基)-1h-吡唑-4-基)咪唑烷-2,4-二酮的合成的改进方法
|
|
GB201420285D0
(en)
|
2014-11-14 |
2014-12-31 |
Bergenbio As |
Process
|
|
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
|
|
WO2016183071A1
(en)
|
2015-05-11 |
2016-11-17 |
Incyte Corporation |
Hetero-tricyclic compounds and their use for the treatment of cancer
|
|
CR20200423A
(es)
|
2015-07-30 |
2021-01-20 |
Macrogenics Inc |
Moléculas de unión a pd-1 y métodos de uso de las mismas (divisional 2018-0062)
|
|
WO2017027717A1
(en)
|
2015-08-12 |
2017-02-16 |
Incyte Corporation |
Bicyclic fused pyrimidine compounds as tam inhibitors
|
|
WO2017035366A1
(en)
|
2015-08-26 |
2017-03-02 |
Incyte Corporation |
Pyrrolopyrimidine derivatives as tam inhibitors
|
|
US20180296561A1
(en)
|
2015-10-07 |
2018-10-18 |
The University Of North Carolina At Chapel Hill |
The Methods For Treatment Of Tumors
|
|
MX2018004516A
(es)
|
2015-10-13 |
2018-08-01 |
Nihon Nohyaku Co Ltd |
Compuesto heterociclico condensado con contenido de grupo oxima o su sal, insecticida agricola y horticola que comprende el compuesto y metodo para usar el insecticida.
|
|
EP3373934B1
(en)
|
2015-11-14 |
2020-05-20 |
Sunshine Lake Pharma Co., Ltd. |
Crystalline form of a substituted quinoline compound and pharmaceutical compositions thereof
|
|
ES2911678T3
(es)
|
2015-11-14 |
2022-05-20 |
Sunshine Lake Pharma Co Ltd |
Forma cristalina de un compuesto de quinolina sustituida y composiciones farmacéuticas de la misma
|
|
HUE064656T2
(hu)
|
2016-03-28 |
2024-04-28 |
Incyte Corp |
Pirrolotriazin vegyületek mint TAM inhibitorok
|
|
BR112018071585B1
(pt)
|
2016-04-22 |
2024-01-02 |
Incyte Corporation |
Formulações de um inibidor de lsd1, seus usos e método de preparação das mesmas
|
|
WO2017223414A1
(en)
|
2016-06-24 |
2017-12-28 |
Incyte Corporation |
HETEROCYCLIC COMPOUNDS AS PI3K-γ INHIBITORS
|
|
JOP20170153A1
(ar)
|
2016-07-15 |
2019-01-30 |
Lilly Co Eli |
نظائر urocortin-2 جديدة معدلة بحمض دهني لعلاج داء السكري وأمراض الكلى المزمنة
|
|
EP4206213A1
(en)
|
2016-07-15 |
2023-07-05 |
Ionis Pharmaceuticals, Inc. |
Compounds and methods for modulation of smn2
|
|
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
|
|
ES3031110T3
(en)
|
2018-06-29 |
2025-07-04 |
Incyte Corp |
Formulations of an axl/mer inhibitor
|
|
AU2021230385A1
(en)
|
2020-03-06 |
2022-09-22 |
Incyte Corporation |
Combination therapy comprising AXL/MER and PD-1/PD-L1 inhibitors
|