US2985589A
(en)
|
1957-05-22 |
1961-05-23 |
Universal Oil Prod Co |
Continuous sorption process employing fixed bed of sorbent and moving inlets and outlets
|
US3832460A
(en)
|
1971-03-19 |
1974-08-27 |
C Kosti |
Anesthetic-vasoconstrictor-antihistamine composition for the treatment of hypertrophied oral tissue
|
US4140755A
(en)
|
1976-02-13 |
1979-02-20 |
Hoffmann-La Roche Inc. |
Sustained release tablet formulations
|
DE3036390A1
(de)
|
1980-09-26 |
1982-05-13 |
Troponwerke GmbH & Co KG, 5000 Köln |
Neue pyrrolo-pyrimidine, verfahren zu ihrer herstellung und ihre verwendung bei der herstellung von biologischen wirkstoffen
|
DE3220113A1
(de)
|
1982-05-28 |
1983-12-01 |
Basf Ag, 6700 Ludwigshafen |
Difluormethoxiphenylthiophosphorsaeureester
|
US4402832A
(en)
|
1982-08-12 |
1983-09-06 |
Uop Inc. |
High efficiency continuous separation process
|
US4548990A
(en)
|
1983-08-15 |
1985-10-22 |
Ciba-Geigy Corporation |
Crosslinked, porous polymers for controlled drug delivery
|
US4498991A
(en)
|
1984-06-18 |
1985-02-12 |
Uop Inc. |
Serial flow continuous separation process
|
NL8403224A
(nl)
|
1984-10-24 |
1986-05-16 |
Oce Andeno Bv |
Dioxafosforinanen, de bereiding ervan en de toepassing voor het splitsen van optisch actieve verbindingen.
|
CA1306260C
(en)
|
1985-10-18 |
1992-08-11 |
Shionogi & Co., Ltd. |
Condensed imidazopyridine derivatives
|
US4921947A
(en)
|
1986-03-31 |
1990-05-01 |
Eli Lilly And Company |
Process for preparing macrolide derivatives
|
JPH0710876Y2
(ja)
|
1989-08-31 |
1995-03-15 |
石垣機工株式会社 |
スクリュープレスにおける脱水筒の洗浄装置
|
DK0495982T3
(da)
|
1989-10-11 |
1996-07-01 |
Teijin Ltd |
Bicyklisk pyrimidinderivat, fremgangsmåde til fremstilling deraf og farmaceutisk præparat omfattende dette som en aktiv bestanddel
|
IT1258781B
(it)
|
1992-01-16 |
1996-02-29 |
Zambon Spa |
Composizione farmaceutica oftalmica contenente n-acetilcisteina e polivinilalcol
|
US5521184A
(en)
|
1992-04-03 |
1996-05-28 |
Ciba-Geigy Corporation |
Pyrimidine derivatives and processes for the preparation thereof
|
FR2695126B1
(fr)
|
1992-08-27 |
1994-11-10 |
Sanofi Elf |
Dérivés d'acide thiényl ou pyrrolyl carboxyliques, leur préparation et médicaments les contenant.
|
AU671491B2
(en)
|
1992-12-18 |
1996-08-29 |
F. Hoffmann-La Roche Ag |
N-oxycarbonyl substituted 5'-deoxy-5-fluorcytidines
|
JPH0710876A
(ja)
|
1993-06-24 |
1995-01-13 |
Teijin Ltd |
4位に環状アミノ基を有するピロロ[2,3―d]ピリミジン
|
EP0727217A3
(en)
|
1995-02-10 |
1997-01-15 |
Suntory Ltd |
Pharmaceutical and cosmetic compositions containing God-type ellagitannin as an active ingredient
|
US5856326A
(en)
|
1995-03-29 |
1999-01-05 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
IL117580A0
(en)
|
1995-03-29 |
1996-07-23 |
Merck & Co Inc |
Inhibitors of farnesyl-protein transferase and pharmaceutical compositions containing them
|
US6066638A
(en)
|
1995-07-05 |
2000-05-23 |
E. I. Du Pont De Nemours And Company |
Fungicidal pyrimidinones
|
MX9800215A
(es)
|
1995-07-06 |
1998-03-31 |
Novartis Ag |
Pirrolopirimidas y procesos para su preparacion.
|
US5630943A
(en)
|
1995-11-30 |
1997-05-20 |
Merck Patent Gesellschaft Mit Beschrankter Haftung |
Discontinuous countercurrent chromatographic process and apparatus
|
GB9604361D0
(en)
|
1996-02-29 |
1996-05-01 |
Pharmacia Spa |
4-Substituted pyrrolopyrimidine compounds as tyrosine kinase inhibitors
|
CA2250232A1
(en)
|
1996-04-03 |
1997-10-09 |
Allen I. Oliff |
A method of treating cancer
|
JP2000513711A
(ja)
|
1996-04-18 |
2000-10-17 |
メルク エンド カンパニー インコーポレーテッド |
癌の治療法
|
US5795909A
(en)
|
1996-05-22 |
1998-08-18 |
Neuromedica, Inc. |
DHA-pharmaceutical agent conjugates of taxanes
|
EP0934270A1
(en)
|
1996-05-30 |
1999-08-11 |
Merck & Co., Inc. |
A method of treating cancer
|
US6624138B1
(en)
|
2001-09-27 |
2003-09-23 |
Gp Medical |
Drug-loaded biological material chemically treated with genipin
|
CA2286239A1
(en)
|
1997-04-07 |
1998-10-15 |
Merck & Co., Inc. |
A method of treating cancer
|
US6063284A
(en)
|
1997-05-15 |
2000-05-16 |
Em Industries, Inc. |
Single column closed-loop recycling with periodic intra-profile injection
|
US6060038A
(en)
|
1997-05-15 |
2000-05-09 |
Merck & Co., Inc. |
Radiolabeled farnesyl-protein transferase inhibitors
|
US5919779A
(en)
|
1997-08-11 |
1999-07-06 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
5,6-Heteroaryl-dipyrido(2,3-B:3', 2'-F) azepines and their use in the prevention or treatment of HIV infection
|
US6075056A
(en)
|
1997-10-03 |
2000-06-13 |
Penederm, Inc. |
Antifungal/steroid topical compositions
|
US6025366A
(en)
|
1998-04-02 |
2000-02-15 |
Merck & Co., Inc. |
Antagonists of gonadotropin releasing hormone
|
HUP0102366A2
(hu)
|
1998-06-04 |
2001-11-28 |
Abbott Laboratories |
Sejttapadást gátló, gyulladáscsökkentő hatású vegyületek
|
US6232320B1
(en)
|
1998-06-04 |
2001-05-15 |
Abbott Laboratories |
Cell adhesion-inhibiting antiinflammatory compounds
|
PA8474101A1
(es)
|
1998-06-19 |
2000-09-29 |
Pfizer Prod Inc |
Compuestos de pirrolo [2,3-d] pirimidina
|
BR9911365A
(pt)
|
1998-06-19 |
2001-03-13 |
Pfizer Prod Inc |
Compostos pirrolo[2,3-d]pirimidina
|
AU5620299A
(en)
|
1998-08-11 |
2000-03-06 |
Novartis Ag |
Isoquinoline derivatives with angiogenesis inhibiting activity
|
JP2000119271A
(ja)
|
1998-08-12 |
2000-04-25 |
Hokuriku Seiyaku Co Ltd |
1h―イミダゾピリジン誘導体
|
CA2343148C
(en)
|
1998-09-10 |
2005-11-15 |
Nycomed Danmark A/S |
Quick release pharmaceutical compositions of drug substances
|
FR2785196B1
(fr)
|
1998-10-29 |
2000-12-15 |
Inst Francais Du Petrole |
Procede et dispositif de separation avec des zones chromatographiques a longueur variable
|
US6413419B1
(en)
|
1998-10-29 |
2002-07-02 |
Institut Francais Du Petrole |
Process and device for separation with variable-length chromatographic
|
US6375839B1
(en)
|
1998-10-29 |
2002-04-23 |
Institut Francais Du Petrole |
Process and device for separation with variable-length chromatographic zones
|
US6133031A
(en)
|
1999-08-19 |
2000-10-17 |
Isis Pharmaceuticals Inc. |
Antisense inhibition of focal adhesion kinase expression
|
EP1165084A4
(en)
|
1999-03-03 |
2002-05-15 |
Merck & Co Inc |
PRENYL PROTEIN TRANSFERASES INHIBITORS
|
GB9905075D0
(en)
|
1999-03-06 |
1999-04-28 |
Zeneca Ltd |
Chemical compounds
|
US6217895B1
(en)
|
1999-03-22 |
2001-04-17 |
Control Delivery Systems |
Method for treating and/or preventing retinal diseases with sustained release corticosteroids
|
US6239113B1
(en)
|
1999-03-31 |
2001-05-29 |
Insite Vision, Incorporated |
Topical treatment or prevention of ocular infections
|
WO2000063168A1
(en)
|
1999-04-16 |
2000-10-26 |
Coelacanth Chemical Corporation |
Synthesis of azetidine derivatives
|
US6921763B2
(en)
|
1999-09-17 |
2005-07-26 |
Abbott Laboratories |
Pyrazolopyrimidines as therapeutic agents
|
DE60013464T2
(de)
|
1999-10-13 |
2005-09-15 |
Banyu Pharmaceutical Co., Ltd. |
Substituierte imidazolin-derivate
|
HU229671B1
(en)
|
1999-12-10 |
2014-04-28 |
Pfizer Prod Inc |
Pyrrolo[2,3-d]pirimidine compounds
|
AP1917A
(en)
|
1999-12-24 |
2008-11-12 |
Aventis Pharma Ltd |
Azaindoles
|
GB0004890D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
US7235551B2
(en)
|
2000-03-02 |
2007-06-26 |
Smithkline Beecham Corporation |
1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases
|
DK1142566T3
(da)
|
2000-04-07 |
2004-02-09 |
Medidom Lab |
Oftalmologiske formuleringer på basis af ciclosporin, hyaluronsyre og polysorbat
|
WO2001081345A1
(fr)
|
2000-04-20 |
2001-11-01 |
Mitsubishi Pharma Corporation |
Composes d'amides aromatiques
|
US6518277B1
(en)
|
2000-04-25 |
2003-02-11 |
Icos Corporation |
Inhibitors of human phosphatidylinositol 3-kinase delta
|
US20030022819A1
(en)
|
2000-06-16 |
2003-01-30 |
Ling Leona E. |
Angiogenesis-modulating compositions and uses
|
US7498304B2
(en)
|
2000-06-16 |
2009-03-03 |
Curis, Inc. |
Angiogenesis-modulating compositions and uses
|
US6335342B1
(en)
|
2000-06-19 |
2002-01-01 |
Pharmacia & Upjohn S.P.A. |
Azaindole derivatives, process for their preparation, and their use as antitumor agents
|
KR20030011106A
(ko)
|
2000-06-23 |
2003-02-06 |
미쯔비시 웰 파마 가부시키가이샤 |
항종양 작용 강화제
|
PL359563A1
(en)
|
2000-06-26 |
2004-08-23 |
Pfizer Products Inc. |
Pyrrolo[2,3-d]pyrimidine compounds as immunosuppressive agents
|
EP1294358B1
(en)
|
2000-06-28 |
2004-08-18 |
Smithkline Beecham Plc |
Wet milling process
|
AU2001278790A1
(en)
|
2000-08-22 |
2002-03-04 |
Hokuriku Seiyaku Co. Ltd |
1h-imidazopyridine derivatives
|
DE60135676D1
(de)
|
2000-12-05 |
2008-10-16 |
Vertex Pharma |
Inhibitoren von c-jun n-terminalen kinasen (jnk) und anderen proteinkinasen
|
GB0100622D0
(en)
|
2001-01-10 |
2001-02-21 |
Vernalis Res Ltd |
Chemical compounds V111
|
US20040077654A1
(en)
|
2001-01-15 |
2004-04-22 |
Bouillot Anne Marie Jeanne |
Aryl piperidine and piperazine derivatives as inducers of ldl-receptor expression
|
EP1363702A4
(en)
|
2001-01-30 |
2007-08-22 |
Cytopia Pty Ltd |
PROCESS FOR INHIBITING KINASES
|
JP4316893B2
(ja)
|
2001-05-16 |
2009-08-19 |
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 |
Srcおよび他のプロテインキナーゼのインヒビター
|
US7301023B2
(en)
|
2001-05-31 |
2007-11-27 |
Pfizer Inc. |
Chiral salt resolution
|
GB0115109D0
(en)
|
2001-06-21 |
2001-08-15 |
Aventis Pharma Ltd |
Chemical compounds
|
GB0115393D0
(en)
|
2001-06-23 |
2001-08-15 |
Aventis Pharma Ltd |
Chemical compounds
|
US6852727B2
(en)
|
2001-08-01 |
2005-02-08 |
Merck & Co., Inc. |
Benzimisazo[4,5-f]isoquinolinone derivatives
|
PL369530A1
(en)
|
2001-09-19 |
2005-05-02 |
Aventis Pharma S.A. |
Chemical compounds
|
US6429231B1
(en)
|
2001-09-24 |
2002-08-06 |
Bradley Pharmaceuticals, Inc. |
Compositions containing antimicrobials and urea for the treatment of dermatological disorders and methods for their use
|
IL161156A0
(en)
|
2001-10-30 |
2004-08-31 |
Novartis Ag |
Staurosporine derivatives as inhibitors of flt3 receptor tyrosine kinase activity
|
JP2003155285A
(ja)
|
2001-11-19 |
2003-05-27 |
Toray Ind Inc |
環状含窒素誘導体
|
US6949668B2
(en)
|
2001-11-30 |
2005-09-27 |
Teijin Limited |
Process for producing 5-(3-cyanophenyl)-3-formylbenzoic acid compound
|
GT200200234A
(es)
|
2001-12-06 |
2003-06-27 |
|
Compuestos cristalinos novedosos
|
US6995144B2
(en)
|
2002-03-14 |
2006-02-07 |
Eisai Co., Ltd. |
Nitrogen containing heterocyclic compounds and medicines containing the same
|
TW200403058A
(en)
|
2002-04-19 |
2004-03-01 |
Bristol Myers Squibb Co |
Heterocyclo inhibitors of potassium channel function
|
WO2003091246A1
(en)
|
2002-04-26 |
2003-11-06 |
Vertex Pharmaceuticals Incorporated |
Pyrrole derivatives as inhibitors of erk2 and uses thereof
|
JP2005530745A
(ja)
|
2002-05-02 |
2005-10-13 |
メルク エンド カムパニー インコーポレーテッド |
チロシンキナーゼ阻害剤
|
BR0309844A
(pt)
|
2002-05-07 |
2005-02-15 |
Control Delivery Sys Inc |
Processos para formação de um dispositivo para a distribuição de droga
|
DE60317198T2
(de)
|
2002-05-23 |
2008-12-04 |
Cytopia Research Pty. Ltd., Richmond |
Proteinkinaseinhibitoren
|
PE20040522A1
(es)
|
2002-05-29 |
2004-09-28 |
Novartis Ag |
Derivados de diarilurea dependientes de la cinasa de proteina
|
CA2490340A1
(en)
|
2002-06-26 |
2004-01-08 |
Idemitsu Kosan Co., Ltd. |
Hydrogenated copolymer, production process for the same and hot melt adhesive composition using the same
|
GB0215676D0
(en)
|
2002-07-05 |
2002-08-14 |
Novartis Ag |
Organic compounds
|
GB0215844D0
(en)
|
2002-07-09 |
2002-08-14 |
Novartis Ag |
Organic compounds
|
WO2004007472A1
(ja)
|
2002-07-10 |
2004-01-22 |
Ono Pharmaceutical Co., Ltd. |
Ccr4アンタゴニストおよびその医薬用途
|
MXPA05003063A
(es)
|
2002-09-20 |
2005-05-27 |
Alcon Inc |
Uso de inhibidores de la sintesis de citosina para el tratamiento de trastornos de ojos secos.
|
US20040204404A1
(en)
|
2002-09-30 |
2004-10-14 |
Robert Zelle |
Human N-type calcium channel blockers
|
ATE371656T1
(de)
|
2002-11-04 |
2007-09-15 |
Vertex Pharma |
Heteroaryl-pyrimidinderivate als jak-inhibitoren
|
TWI335913B
(en)
|
2002-11-15 |
2011-01-11 |
Vertex Pharma |
Diaminotriazoles useful as inhibitors of protein kinases
|
US20040099204A1
(en)
|
2002-11-25 |
2004-05-27 |
Nestor John J. |
Sheet, page, line, position marker
|
PL378246A1
(pl)
|
2002-11-26 |
2006-03-20 |
Pfizer Products Inc. |
Sposób leczenia odrzucania przeszczepu
|
UA80767C2
(en)
|
2002-12-20 |
2007-10-25 |
Pfizer Prod Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
TWI335819B
(en)
|
2002-12-24 |
2011-01-11 |
Alcon Inc |
Use of oculosurface selective glucocorticoid in the treatment of dry eye
|
TW200418806A
(en)
|
2003-01-13 |
2004-10-01 |
Fujisawa Pharmaceutical Co |
HDAC inhibitor
|
US7167750B2
(en)
|
2003-02-03 |
2007-01-23 |
Enteromedics, Inc. |
Obesity treatment with electrically induced vagal down regulation
|
EP1611125A1
(en)
|
2003-02-07 |
2006-01-04 |
Vertex Pharmaceuticals Incorporated |
Heteroaryl substituted pyrolls useful as inhibitors of protein kinases
|
GB0305929D0
(en)
|
2003-03-14 |
2003-04-23 |
Novartis Ag |
Organic compounds
|
WO2004092154A1
(en)
|
2003-04-03 |
2004-10-28 |
Vertex Pharmaceuticals Incorporated |
Compositions useful as inhibitors of protein kinases
|
SE0301372D0
(sv)
|
2003-05-09 |
2003-05-09 |
Astrazeneca Ab |
Novel compounds
|
SE0301373D0
(sv)
|
2003-05-09 |
2003-05-09 |
Astrazeneca Ab |
Novel compounds
|
FR2857454B1
(fr)
|
2003-07-08 |
2006-08-11 |
Aventis Pasteur |
Dosage des acides techoiques des bacteries gram+
|
US20050043346A1
(en)
|
2003-08-08 |
2005-02-24 |
Pharmacia Italia S.P.A. |
Pyridylpyrrole derivatives active as kinase inhibitors
|
WO2005020921A2
(en)
|
2003-08-29 |
2005-03-10 |
Exelixis, Inc. |
C-kit modulators and methods of use
|
EP1678147B1
(en)
|
2003-09-15 |
2012-08-08 |
Lead Discovery Center GmbH |
Pharmaceutically active 4,6-disubstituted aminopyrimidine derivatives as modulators of protein kinases
|
PE20050952A1
(es)
|
2003-09-24 |
2005-12-19 |
Novartis Ag |
Derivados de isoquinolina como inhibidores de b-raf
|
DK1679074T3
(da)
|
2003-10-24 |
2011-03-21 |
Santen Pharmaceutical Co Ltd |
Terapeutisk middel til keratoconjunktive forstyrrelser
|
MY141220A
(en)
|
2003-11-17 |
2010-03-31 |
Astrazeneca Ab |
Pyrazole derivatives as inhibitors of receptor tyrosine kinases
|
EP1689407A1
(en)
|
2003-11-25 |
2006-08-16 |
Pfizer Products Inc. |
Method of treatment of atherosclerosis
|
CA2549485A1
(en)
|
2003-12-17 |
2005-07-07 |
Pfizer Products Inc. |
Pyrrolo [2,3-d] pyrimidine compounds for treating transplant rejection
|
PL1696920T3
(pl)
|
2003-12-19 |
2015-03-31 |
Plexxikon Inc |
Związki i sposoby opracowywania modulatorów Ret
|
ATE406356T1
(de)
|
2003-12-19 |
2008-09-15 |
Schering Corp |
Thiadiazole als cxc- und cc- chemokinrezeptorliganden
|
JP4928949B2
(ja)
|
2003-12-23 |
2012-05-09 |
アステックス、セラピューティックス、リミテッド |
タンパク質キナーゼモジュレーターとしてのピラゾール誘導体
|
US20050165029A1
(en)
|
2004-01-13 |
2005-07-28 |
Ambit Biosciences Corporation |
Pyrrolopyrimidine derivatives and analogs and their use in the treatment and prevention of diseases
|
US20050277629A1
(en)
|
2004-03-18 |
2005-12-15 |
The Brigham And Women's Hospital, Inc. |
Methods for the treatment of synucleinopathies (Lansbury)
|
KR101216372B1
(ko)
|
2004-03-30 |
2013-01-04 |
버텍스 파마슈티칼스 인코포레이티드 |
Jak 및 기타 단백질 키나제의 억제제로서 유용한 아자인돌
|
EP1750727A2
(en)
|
2004-04-23 |
2007-02-14 |
Exelixis, Inc. |
Kinase modulators and methods of use
|
US20060106020A1
(en)
|
2004-04-28 |
2006-05-18 |
Rodgers James D |
Tetracyclic inhibitors of Janus kinases
|
US7558717B2
(en)
|
2004-04-28 |
2009-07-07 |
Vertex Pharmaceuticals Incorporated |
Crystal structure of human JAK3 kinase domain complex and binding pockets thereof
|
CA2563569A1
(en)
|
2004-05-03 |
2005-11-10 |
Novartis Ag |
Combinations comprising a s1p receptor agonist and a jak3 kinase inhibitor
|
CA2566158A1
(en)
|
2004-05-14 |
2005-11-24 |
Abbott Laboratories |
Kinase inhibitors as therapeutic agents
|
PE20060426A1
(es)
|
2004-06-02 |
2006-06-28 |
Schering Corp |
DERIVADOS DE ACIDO TARTARICO COMO INHIBIDORES DE MMPs, ADAMs, TACE Y TNF-alfa
|
US7745437B2
(en)
|
2004-06-10 |
2010-06-29 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
EP1760071A4
(en)
|
2004-06-23 |
2008-03-05 |
Ono Pharmaceutical Co |
COMPOUND WITH S1P RECEPTOR BINDING ABILITY AND USE THEREOF
|
EP1765819B1
(en)
|
2004-06-30 |
2014-03-12 |
Vertex Pharmaceuticals Inc. |
Azaindoles useful as inhibitors of protein kinases
|
US7138423B2
(en)
|
2004-07-20 |
2006-11-21 |
Bristol-Myers Squibb Company |
Arylpyrrolidine derivatives as NK-1 /SSRI antagonists
|
FR2873691B1
(fr)
|
2004-07-29 |
2006-10-06 |
Sanofi Synthelabo |
Derives d'amino-piperidine, leur preparation et leur application en therapeutique
|
WO2006013114A1
(en)
|
2004-08-06 |
2006-02-09 |
Develogen Aktiengesellschaft |
Use of a timp-2 secreted protein product for preventing and treating pancreatic diseases and/or obesity and/or metabolic syndrome
|
CN101006186A
(zh)
|
2004-08-23 |
2007-07-25 |
财团法人牧岩生命工学研究所 |
用于检测sars冠状病毒的引物和探针,包括该引物和/或探针的试剂盒及其检测方法
|
US20070054916A1
(en)
|
2004-10-01 |
2007-03-08 |
Amgen Inc. |
Aryl nitrogen-containing bicyclic compounds and methods of use
|
JP2008515939A
(ja)
|
2004-10-13 |
2008-05-15 |
エフ.ホフマン−ラ ロシュ アーゲー |
Cdk2及び血管形成の阻害剤として、及び乳癌、結腸癌及び前立腺癌の治療に有用な2置換ピラゾロベンゾジアゼピン
|
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
|
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
|
CA2586375A1
(en)
|
2004-11-04 |
2006-05-18 |
Juan-Miguel Jimenez |
Pyrazolo[1,5-a]pyrimidines useful as inhibitors of protein kinases
|
MX2007006204A
(es)
|
2004-11-24 |
2007-06-20 |
Novartis Ag |
Combinaciones que comprenden inhibidores de jak y cuando menos uno de entre inhibidores de bcr-abl, flt-3, fak o raf cinasa.
|
US7517870B2
(en)
|
2004-12-03 |
2009-04-14 |
Fondazione Telethon |
Use of compounds that interfere with the hedgehog signaling pathway for the manufacture of a medicament for preventing, inhibiting, and/or reversing ocular diseases related with ocular neovascularization
|
US20060128803A1
(en)
|
2004-12-14 |
2006-06-15 |
Alcon, Inc. |
Method of treating dry eye disorders using 13(S)-HODE and its analogs
|
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.
|
WO2006067445A2
(en)
|
2004-12-22 |
2006-06-29 |
Astrazeneca Ab |
Csf-1r kinase inhibitors
|
WO2006077499A1
(en)
|
2005-01-20 |
2006-07-27 |
Pfizer Limited |
Chemical compounds
|
AU2006221065A1
(en)
|
2005-02-03 |
2006-09-14 |
Vertex Pharmaceuticals Incorporated |
Pyrrolopyrimidines useful as inhibitors of protein kinase
|
US7683171B2
(en)
|
2005-02-04 |
2010-03-23 |
Bristol-Myers Squibb Company |
1H-imidazo[4,5-d]thieno[3,2-b]pyridine based tricyclic compounds and pharmaceutical compositions comprising same
|
WO2006101783A2
(en)
|
2005-03-15 |
2006-09-28 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
JP2008534689A
(ja)
|
2005-04-05 |
2008-08-28 |
ファーマコペイア, インコーポレイテッド |
免疫抑制のためのプリン及びイミダゾピリジン誘導体
|
GB0510139D0
(en)
|
2005-05-18 |
2005-06-22 |
Addex Pharmaceuticals Sa |
Novel compounds B1
|
ATE540948T1
(de)
|
2005-05-20 |
2012-01-15 |
Vertex Pharma |
Pyrrolopyridine als proteinkinasehemmer
|
GB0510390D0
(en)
|
2005-05-20 |
2005-06-29 |
Novartis Ag |
Organic compounds
|
JP5225079B2
(ja)
|
2005-06-08 |
2013-07-03 |
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 |
Jak経路の阻害のための組成物および方法
|
WO2006136823A1
(en)
|
2005-06-21 |
2006-12-28 |
Astex Therapeutics Limited |
Heterocyclic containing amines as kinase b inhibitors
|
AU2006261993B2
(en)
|
2005-06-22 |
2011-11-17 |
Plexxikon, Inc. |
Pyrrolo (2, 3-B) pyridine derivatives as protein kinase inhibitors
|
EP2251341A1
(en)
|
2005-07-14 |
2010-11-17 |
Astellas Pharma Inc. |
Heterocyclic Janus kinase 3 inhibitors
|
FR2889662B1
(fr)
|
2005-08-11 |
2011-01-14 |
Galderma Res & Dev |
Emulsion de type huile-dans-eau pour application topique en dermatologie
|
US20070049591A1
(en)
|
2005-08-25 |
2007-03-01 |
Kalypsys, Inc. |
Inhibitors of MAPK/Erk Kinase
|
CA2621261C
(en)
|
2005-09-22 |
2014-05-20 |
Incyte Corporation |
Azepine inhibitors of janus kinases
|
EP1931674B1
(en)
|
2005-09-30 |
2012-12-12 |
Vertex Pharmaceuticals Incorporated |
Deazapurines useful as inhibitors of janus kinases
|
WO2007044894A2
(en)
|
2005-10-11 |
2007-04-19 |
Chembridge Research Laboratories, Inc. |
Cell-free protein expression systems and methods of use thereof
|
DK1937664T3
(da)
|
2005-10-14 |
2011-07-18 |
Sumitomo Chemical Co |
Hydrazidforbindelse og pesticid anvendelse af den samme
|
EP2388259A1
(en)
|
2005-10-28 |
2011-11-23 |
AstraZeneca AB |
4- (3-aminopyrazole) pyrimidine derivatives for use as tyrosine kinase inhibitors in the treatment of cancer
|
PT1951684T
(pt)
|
2005-11-01 |
2016-10-13 |
Targegen Inc |
Inibidores de cinases de tipo biaril-meta-pirimidina
|
WO2007062459A1
(en)
|
2005-11-29 |
2007-06-07 |
Cytopia Research Pty Ltd |
Selective kinase inhibitors based on pyridine scaffold
|
TWI553008B
(zh)
|
2005-12-13 |
2016-10-11 |
英塞特控股公司 |
作為傑納斯激酶(JANUS KINASE)抑制劑之經雜芳基取代之吡咯并[2,3-b]吡啶及吡咯并[2,3-b]嘧啶
|
US20130137681A1
(en)
|
2005-12-13 |
2013-05-30 |
Incyte Corporation |
HETEROARYL SUBSTITUTED PYRROLO[2,3-b]PYRIDINES AND PYRROLO[2,3-b]PYRIMIDINES AS JANUS KINASE INHIBITORS
|
WO2007076423A2
(en)
|
2005-12-22 |
2007-07-05 |
Smithkline Beecham Corporation |
INHIBITORS OF Akt ACTIVITY
|
SI1962830T1
(sl)
|
2005-12-23 |
2013-07-31 |
Glaxosmithkline Llc |
Azaindolni inhibitorji kinaz Aurora
|
WO2007084557A2
(en)
|
2006-01-17 |
2007-07-26 |
Vertex Pharmaceuticals Incorporated |
Azaindoles useful as inhibitors of janus kinases
|
CA2635899A1
(en)
|
2006-01-19 |
2007-07-26 |
Osi Pharmaceuticals, Inc. |
Fused heterobicyclic kinase inhibitors
|
EP1981887A2
(en)
|
2006-02-01 |
2008-10-22 |
SmithKline Beecham Corporation |
Pyrrolo[2,3,b]pyridine derivatives useful as raf kinase inhibitors
|
US7745477B2
(en)
|
2006-02-07 |
2010-06-29 |
Hoffman-La Roche Inc. |
Heteroaryl and benzyl amide compounds
|
MX2008011414A
(es)
|
2006-03-10 |
2008-09-22 |
Ono Pharmaceutical Co |
Derivado heterociclico nitrogenado y agente farmaceutico que comprende el derivado como ingrediente activo.
|
MX2008012738A
(es)
|
2006-04-03 |
2009-02-06 |
Astellas Pharma Inc |
Heterocompuesto.
|
MX2008012860A
(es)
|
2006-04-05 |
2009-01-07 |
Vertex Pharma |
Desazapurinas de utilidad como inhibidores de janus cinasas.
|
WO2007116313A2
(en)
|
2006-04-12 |
2007-10-18 |
Pfizer Limited |
Pyrrolidine derivatives as modulators of chemokine ccr5 receptors
|
WO2007129195A2
(en)
|
2006-05-04 |
2007-11-15 |
Pfizer Products Inc. |
4-pyrimidine-5-amino-pyrazole compounds
|
WO2007135461A2
(en)
|
2006-05-18 |
2007-11-29 |
Bayer Healthcare Ag |
Pharmaceutical compositions comprising implitapide and methods of using same
|
US7691811B2
(en)
|
2006-05-25 |
2010-04-06 |
Bodor Nicholas S |
Transporter-enhanced corticosteroid activity and methods and compositions for treating dry eye
|
JO3235B1
(ar)
|
2006-05-26 |
2018-03-08 |
Astex Therapeutics Ltd |
مركبات بيررولوبيريميدين و استعمالاتها
|
AU2007275221A1
(en)
|
2006-07-20 |
2008-01-24 |
Allen J. Borchardt |
Benzothiophene inhibitors of RHO kinase
|
WO2008013622A2
(en)
|
2006-07-27 |
2008-01-31 |
E. I. Du Pont De Nemours And Company |
Fungicidal azocyclic amides
|
US8492378B2
(en)
|
2006-08-03 |
2013-07-23 |
Takeda Pharmaceutical Company Limited |
GSK-3β inhibitor
|
US8318723B2
(en)
|
2006-08-16 |
2012-11-27 |
Boehringer Ingelheim International Gmbh |
Pyrazine compounds, their use and methods of preparation
|
BRPI0716598A2
(pt)
|
2006-09-08 |
2013-12-10 |
Novartis Ag |
Derivados de (hetero) arilsulfonamida de n-biarila úteis no tratamento de doenças medidas por interações de linfócitos
|
WO2008035376A2
(en)
|
2006-09-19 |
2008-03-27 |
Council Of Scientific & Industrial Research |
A novel bio-erodible insert for ophthalmic applications and a process for the preparation thereof
|
AR063141A1
(es)
|
2006-10-04 |
2008-12-30 |
Pharmacopeia Inc |
Derivados de 2- ( benzimidazolil ) purina 8- sustituida para inmunosupresion
|
AR063142A1
(es)
|
2006-10-04 |
2008-12-30 |
Pharmacopeia Inc |
Derivados de 2-(bencimidazolil) purina y purinonas 6-sustituidas utiles como inmunosupresores,y composiciones farmaceuticas que los contienen.
|
US20120225057A1
(en)
|
2006-10-11 |
2012-09-06 |
Deciphera Pharmaceuticals, Llc |
Methods and compositions for the treatment of myeloproliferative diseases and other proliferative diseases
|
CA2667487C
(en)
|
2006-11-06 |
2017-04-04 |
Supergen, Inc. |
Imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine derivatives and their use as protein kinase inhibitors
|
US20080119496A1
(en)
|
2006-11-16 |
2008-05-22 |
Pharmacopeia Drug Discovery, Inc. |
7-Substituted Purine Derivatives for Immunosuppression
|
DK2497470T3
(en)
|
2006-11-22 |
2015-12-07 |
Incyte Holdings Corp |
Imidazotriaziner and imidazopyrimidines as kinase inhibitors
|
WO2008067119A2
(en)
|
2006-11-27 |
2008-06-05 |
Smithkline Beecham Corporation |
Novel compounds
|
WO2008076356A1
(en)
|
2006-12-15 |
2008-06-26 |
Abbott Laboratories |
Novel oxadiazole compounds
|
CA2672903C
(en)
|
2006-12-20 |
2012-10-23 |
Amgen Inc. |
Heterocyclic compounds and their use in treating inflammation, angiogenesis and cancer
|
CA2672438A1
(en)
|
2006-12-20 |
2008-07-03 |
Amgen Inc. |
Substituted heterocycles and methods of use
|
SG176525A1
(en)
|
2006-12-22 |
2011-12-29 |
Sigma Tau Ind Farmaceuti |
Gel useful for the delivery of ophthalmic drugs
|
ES2415863T3
(es)
|
2006-12-22 |
2013-07-29 |
Incyte Corporation |
Heterociclos sustituidos como inhibidores de Janus Quinasas
|
WO2008082840A1
(en)
|
2006-12-29 |
2008-07-10 |
Abbott Laboratories |
Pim kinase inhibitors as cancer chemotherapeutics
|
WO2008082839A2
(en)
|
2006-12-29 |
2008-07-10 |
Abbott Laboratories |
Pim kinase inhibitors as cancer chemotherapeutics
|
KR20080062876A
(ko)
|
2006-12-29 |
2008-07-03 |
주식회사 대웅제약 |
신규한 항진균성 트리아졸 유도체
|
BRPI0808523A2
(pt)
|
2007-03-01 |
2014-08-19 |
Novartis Vaccines & Diagnostic |
Inibidores de pim cinase e métodos de seu uso
|
JP5374492B2
(ja)
|
2007-04-03 |
2013-12-25 |
アレイ バイオファーマ、インコーポレイテッド |
受容体チロシンキナーゼ阻害薬としてのイミダゾ[1,2−a]ピリジン化合物
|
GB0709031D0
(en)
|
2007-05-10 |
2007-06-20 |
Sareum Ltd |
Pharmaceutical compounds
|
EP2155689B1
(en)
|
2007-05-31 |
2015-07-08 |
Boehringer Ingelheim International GmbH |
Ccr2 receptor antagonists and uses thereof
|
GB0710528D0
(en)
|
2007-06-01 |
2007-07-11 |
Glaxo Group Ltd |
Novel compounds
|
ES2903444T3
(es)
|
2007-06-13 |
2022-04-01 |
Incyte Holdings Corp |
Uso de sales del inhibidor de quinasas Janus (R)-3-(4-(7H-pirrolo[2,3-d]pirimidin-4-il)-1H-pirazol-1-il)-3-ciclopentilpropanonitrilo
|
CL2008001709A1
(es)
|
2007-06-13 |
2008-11-03 |
Incyte Corp |
Compuestos derivados de pirrolo [2,3-b]pirimidina, moduladores de quinasas jak; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como cancer, psoriasis, artritis reumatoide, entre otras.
|
CN101743009A
(zh)
|
2007-07-11 |
2010-06-16 |
辉瑞大药厂 |
治疗干眼病的药物组合物和方法
|
KR20100038119A
(ko)
|
2007-08-01 |
2010-04-12 |
화이자 인코포레이티드 |
피라졸 화합물 및 raf 억제제로서 이의 용도
|
WO2009049028A1
(en)
|
2007-10-09 |
2009-04-16 |
Targegen Inc. |
Pyrrolopyrimidine compounds and their use as janus kinase modulators
|
EP2217235A4
(en)
|
2007-11-15 |
2011-01-12 |
Musc Found For Res Dev |
PROTEIN INHIBITORS PIM KINASES, COMPOSITIONS AND METHODS FOR TREATING CANCER
|
CN101910152B
(zh)
*
|
2007-11-16 |
2014-08-06 |
因塞特公司 |
作为janus激酶抑制剂的4-吡唑基-n-芳基嘧啶-2-胺和4-吡唑基-n-杂芳基嘧啶-2-胺
|
GB0723815D0
(en)
|
2007-12-05 |
2008-01-16 |
Glaxo Group Ltd |
Compounds
|
LT3133080T
(lt)
|
2008-01-18 |
2018-11-12 |
Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic |
Naujieji citostatiniai 7-deazapurino nukleozidai
|
AU2009212462B2
(en)
|
2008-02-04 |
2012-09-13 |
Mercury Therapeutics, Inc. |
AMPK modulators
|
UY31679A1
(es)
|
2008-03-03 |
2009-09-30 |
|
Inhibidores de cinasa pim y metodos para su uso
|
EA017218B1
(ru)
*
|
2008-03-11 |
2012-10-30 |
Инсайт Корпорейшн |
Производные азетидина и циклобутана как ингибиторы jak-киназ
|
AU2009227013B2
(en)
|
2008-03-21 |
2013-01-10 |
Novartis Ag |
Novel heterocyclic compounds and uses therof
|
US8344144B2
(en)
|
2008-06-18 |
2013-01-01 |
Merck Sharp & Dohme Corp. |
Inhibitors of Janus kinases
|
ES2761664T3
(es)
|
2008-06-26 |
2020-05-20 |
Anterios Inc |
Entrega dérmica
|
TWI461423B
(zh)
|
2008-07-02 |
2014-11-21 |
Astrazeneca Ab |
用於治療Pim激酶相關病狀及疾病之噻唑啶二酮化合物
|
FR2933409B1
(fr)
|
2008-07-03 |
2010-08-27 |
Centre Nat Rech Scient |
NOUVEAUX PYRROLO °2,3-a! CARBAZOLES ET LEUR UTILISATION COMME INHIBITEURS DES KINASES PIM
|
TWI496779B
(zh)
|
2008-08-19 |
2015-08-21 |
Array Biopharma Inc |
作為pim激酶抑制劑之三唑吡啶化合物
|
WO2010022081A1
(en)
|
2008-08-19 |
2010-02-25 |
Array Biopharma Inc. |
Triazolopyridine compounds as pim kinase inhibitors
|
CN102131812B
(zh)
|
2008-08-20 |
2014-04-09 |
硕腾有限责任公司 |
吡咯并[2,3-d]嘧啶化合物
|
EP2342190A1
(en)
|
2008-09-02 |
2011-07-13 |
Novartis AG |
Bicyclic kinase inhibitors
|
WO2010026122A1
(en)
|
2008-09-02 |
2010-03-11 |
Novartis Ag |
Heterocyclic pim-kinase inhibitors
|
GEP20135849B
(en)
|
2008-09-02 |
2013-06-10 |
Novartis Ag |
Picolinamide derivatives as kinase inhibitors
|
CL2009001884A1
(es)
|
2008-10-02 |
2010-05-14 |
Incyte Holdings Corp |
Uso de 3-ciclopentil-3-[4-(7h-pirrolo[2,3-d]pirimidin-4-il)-1h-pirazol-1-il)propanonitrilo, inhibidor de janus quinasa, y uso de una composición que lo comprende para el tratamiento del ojo seco.
|
JOP20190230A1
(ar)
|
2009-01-15 |
2017-06-16 |
Incyte Corp |
طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به
|
EP2210890A1
(en)
|
2009-01-19 |
2010-07-28 |
Almirall, S.A. |
Oxadiazole derivatives as S1P1 receptor agonists
|
US8263601B2
(en)
|
2009-02-27 |
2012-09-11 |
Concert Pharmaceuticals, Inc. |
Deuterium substituted xanthine derivatives
|
CN102458581B
(zh)
|
2009-05-22 |
2016-03-30 |
因塞特控股公司 |
作为JANUS激酶抑制剂的吡唑-4-基-吡咯并[2,3-d]嘧啶和吡咯-3-基-吡咯并[2,3-d]嘧啶的N-(杂)芳基-吡咯烷衍生物
|
ME03556B
(me)
|
2009-05-22 |
2020-07-20 |
Incyte Holdings Corp |
3-[4-(7h-pirolo[2,3-d]pirimidin-4-il)-1 h-pirazol-1-il]oktan- ili нертan - niтril kао јак inhibiтori
|
UA110324C2
(en)
|
2009-07-02 |
2015-12-25 |
Genentech Inc |
Jak inhibitory compounds based on pyrazolo pyrimidine
|
TW201105674A
(en)
|
2009-07-08 |
2011-02-16 |
Leo Pharma As |
Novel JAK receptor and protein tyrosine kinase inhibitors and pharmaceutical use thereof
|
WO2011025685A1
(en)
|
2009-08-24 |
2011-03-03 |
Merck Sharp & Dohme Corp. |
Jak inhibition blocks rna interference associated toxicities
|
TW201111385A
(en)
|
2009-08-27 |
2011-04-01 |
Biocryst Pharm Inc |
Heterocyclic compounds as janus kinase inhibitors
|
AR078012A1
(es)
|
2009-09-01 |
2011-10-05 |
Incyte Corp |
Derivados heterociclicos de las pirazol-4-il- pirrolo (2,3-d) pirimidinas como inhibidores de la quinasa janus
|
SG10201405568UA
(en)
|
2009-09-08 |
2014-11-27 |
Hoffmann La Roche |
4-substituted pyridin-3-yl-carboxamide compounds and methods of use
|
EP2305660A1
(en)
|
2009-09-25 |
2011-04-06 |
Almirall, S.A. |
New thiadiazole derivatives
|
PL2486041T3
(pl)
|
2009-10-09 |
2014-01-31 |
Incyte Holdings Corp |
Pochodne hydroksylowe, keto i glukuronidowe 3-(4-(7H-pirolo[2,3-d]pirymidyn-4-ylo)-1H-pirazol-1-ilo)-3-cyklopentylopropanonitrylu
|
EP2491039A1
(en)
|
2009-10-20 |
2012-08-29 |
Cellzome Limited |
Heterocyclyl pyrazolopyrimidine analogues as jak inhibitors
|
EP2332917B1
(en)
|
2009-11-11 |
2012-08-01 |
Sygnis Bioscience GmbH & Co. KG |
Compounds for PIM kinase inhibition and for treating malignancy
|
KR20120118088A
(ko)
|
2009-11-24 |
2012-10-25 |
앨더바이오 홀딩스 엘엘씨 |
Ⅰl-6에 대한 항체 및 이들의 용도
|
WO2011069141A2
(en)
|
2009-12-04 |
2011-06-09 |
Board Of Regents, The University Of Texas System |
Interferon therapies in combination with blockade of stat3 activation
|
AR079984A1
(es)
|
2010-01-12 |
2012-03-07 |
Hoffmann La Roche |
Compuestos heterociclicos triciclicos, composiciones y su uso en el tratamiento de enfermedades mediadas por la inhibicion de jak1
|
SA111320200B1
(ar)
|
2010-02-17 |
2014-02-16 |
ديبيوفارم اس ايه |
مركبات ثنائية الحلقة واستخداماتها كمثبطات c-src/jak مزدوجة
|
MX2012009541A
(es)
|
2010-02-18 |
2012-10-01 |
Incyte Corp |
Derivados de ciclobutano y metilciclobutano como inhibidores de janus cinasa.
|
RS60680B1
(sr)
|
2010-03-10 |
2020-09-30 |
Incyte Holdings Corp |
Piperidin-4-il azetidin derivati kao inhibitori jak1
|
CA2796388A1
(en)
*
|
2010-04-14 |
2011-10-20 |
Array Biopharma Inc. |
5, 7-substituted-imidazo [1, 2-c] pyrimidines as inhibitors of jak kinases
|
EP2390252A1
(en)
|
2010-05-19 |
2011-11-30 |
Almirall, S.A. |
New pyrazole derivatives
|
PL2574168T3
(pl)
|
2010-05-21 |
2016-10-31 |
|
Preparaty inhibitora kinazy janusowej do stosowania miejscowego
|
US8637529B2
(en)
|
2010-06-11 |
2014-01-28 |
AbbYie Inc. |
Pyrazolo[3,4-d]pyrimidine compounds
|
US9351943B2
(en)
|
2010-07-01 |
2016-05-31 |
Matthew T. McLeay |
Anti-fibroblastic fluorochemical emulsion therapies
|
JP5833392B2
(ja)
*
|
2010-09-17 |
2015-12-16 |
公益財団法人相模中央化学研究所 |
(トリフルオロビニル)ベンゼン類およびその製造方法
|
WO2012045020A1
(en)
|
2010-09-30 |
2012-04-05 |
Portola Pharmaceuticals, Inc. |
Combinations of 4-(cyclopropylamino)-2-(4-(4-(ethylsulfonyl)piperazin-1-yl)phenylamino)pyrimidine-5-carboxamide and fludarabine
|
AR083933A1
(es)
|
2010-11-19 |
2013-04-10 |
Incyte Corp |
Derivados de pirrolopiridina y pirrolopirimidina sustituidos con ciclobutilo como inhibidores de jak
|
EP2640725B1
(en)
|
2010-11-19 |
2015-01-07 |
Incyte Corporation |
Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors
|
CN103370068A
(zh)
|
2010-12-03 |
2013-10-23 |
Ym生物科学澳大利亚私人有限公司 |
Jak-2 介导的病症的治疗
|
MX357939B
(es)
|
2011-02-18 |
2018-07-31 |
Novartis Pharma Ag |
Terapia de combinacion de inhibidor de objetivo de rapamicina en mamifero/janus cinasa (mtor/jak).
|
CA2839767A1
(en)
|
2011-06-20 |
2012-12-27 |
Incyte Corporation |
Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors
|
WO2013007768A1
(en)
|
2011-07-13 |
2013-01-17 |
F. Hoffmann-La Roche Ag |
Tricyclic heterocyclic compounds, compositions and methods of use thereof as jak inhibitors
|
WO2013007765A1
(en)
|
2011-07-13 |
2013-01-17 |
F. Hoffmann-La Roche Ag |
Fused tricyclic compounds for use as inhibitors of janus kinases
|
US9358229B2
(en)
|
2011-08-10 |
2016-06-07 |
Novartis Pharma Ag |
JAK PI3K/mTOR combination therapy
|
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
|
UA111854C2
(uk)
*
|
2011-09-07 |
2016-06-24 |
Інсайт Холдінгс Корпорейшн |
Способи і проміжні сполуки для отримання інгібіторів jak
|
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
|
US10155987B2
(en)
|
2012-06-12 |
2018-12-18 |
Dana-Farber Cancer Institute, Inc. |
Methods of predicting resistance to JAK inhibitor therapy
|
EP2890691B1
(en)
|
2012-08-31 |
2018-04-25 |
Principia Biopharma Inc. |
Benzimidazole derivatives as itk inhibitors
|
TWI646099B
(zh)
|
2012-11-01 |
2019-01-01 |
英塞特控股公司 |
作爲jak抑制劑之三環稠合噻吩衍生物
|
LT2919766T
(lt)
|
2012-11-15 |
2021-09-27 |
Incyte Holdings Corporation |
Ruksolitinibo pailginto atpalaidavimo vaisto formos
|
SI2964650T1
(sl)
|
2013-03-06 |
2019-05-31 |
Incyte Holdings Corporation |
Postopki in vmesne spojine za izdelavo inhibitorja JAK
|
EA039660B1
(ru)
|
2013-05-17 |
2022-02-24 |
Инсайт Корпорейшн |
Твердая форма производного бипиразола
|
HUE049345T2
(hu)
|
2013-08-07 |
2020-09-28 |
Incyte Corp |
Nyújtott hatóanyag-leadású dózisformák JAK1 inhibitorhoz
|
TW201529074A
(zh)
|
2013-08-20 |
2015-08-01 |
Incyte Corp |
在c-反應蛋白含量較高之實體腫瘤患者中的存活益處
|
SG11201607083VA
(en)
|
2014-02-28 |
2016-09-29 |
Incyte Corp |
Jak1 inhibitors for the treatment of myelodysplastic syndromes
|
KR102717075B1
(ko)
|
2014-04-08 |
2024-10-15 |
인사이트 홀딩스 코포레이션 |
Jak 및 pi3k 억제제 조합에 의한 b-세포 악성종양의 치료
|
MA39987A
(fr)
|
2014-04-30 |
2017-03-08 |
Incyte Corp |
Procédés de préparation d'un inhibiteur de jak1 et nouvelles formes associées
|
US9498467B2
(en)
|
2014-05-30 |
2016-11-22 |
Incyte Corporation |
Treatment of chronic neutrophilic leukemia (CNL) and atypical chronic myeloid leukemia (aCML) by inhibitors of JAK1
|