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
|
US5702688A
(en)
*
|
1986-12-23 |
1997-12-30 |
Tristrata Technology, Inc. |
Amphoteric compositions and polymeric forms of alpha hydroxyacids, and their therapeutic use
|
ES2087916T3
(es)
|
1989-10-11 |
1996-08-01 |
Teijin Ltd |
Derivado de pirimidina biciclico, metodo para producir el mismo, y preparacion farmaceutica que contiene el mismo como ingrediente activo.
|
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
|
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
|
IL117580A0
(en)
|
1995-03-29 |
1996-07-23 |
Merck & Co Inc |
Inhibitors of farnesyl-protein transferase and pharmaceutical compositions containing them
|
US5856326A
(en)
|
1995-03-29 |
1999-01-05 |
Merck & Co., Inc. |
Inhibitors of farnesyl-protein transferase
|
WO1997002262A1
(en)
|
1995-07-05 |
1997-01-23 |
E.I. Du Pont De Nemours And Company |
Fungicidal pyrimidinones
|
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
|
WO1997036587A1
(en)
|
1996-04-03 |
1997-10-09 |
Merck & Co., Inc. |
A method of treating cancer
|
WO1997038664A2
(en)
|
1996-04-18 |
1997-10-23 |
Merck & Co., Inc. |
A method of treating cancer
|
US5795909A
(en)
|
1996-05-22 |
1998-08-18 |
Neuromedica, Inc. |
DHA-pharmaceutical agent conjugates of taxanes
|
WO1997045412A1
(en)
|
1996-05-30 |
1997-12-04 |
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
|
AU724216B2
(en)
|
1997-04-07 |
2000-09-14 |
Merck & Co., Inc. |
A method of treating cancer
|
US6060038A
(en)
|
1997-05-15 |
2000-05-09 |
Merck & Co., Inc. |
Radiolabeled farnesyl-protein transferase inhibitors
|
US6063284A
(en)
|
1997-05-15 |
2000-05-16 |
Em Industries, Inc. |
Single column closed-loop recycling with periodic intra-profile injection
|
WO1999007379A1
(en)
|
1997-08-11 |
1999-02-18 |
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
|
US6232320B1
(en)
|
1998-06-04 |
2001-05-15 |
Abbott Laboratories |
Cell adhesion-inhibiting antiinflammatory compounds
|
HUP0102366A2
(hu)
|
1998-06-04 |
2001-11-28 |
Abbott Laboratories |
Sejttapadást gátló, gyulladáscsökkentő hatású vegyületek
|
PA8474101A1
(es)
|
1998-06-19 |
2000-09-29 |
Pfizer Prod Inc |
Compuestos de pirrolo [2,3-d] pirimidina
|
BR9912938B1
(pt)
|
1998-08-11 |
2011-06-28 |
|
derivados de isoquinolina, composição que os compreende, processo para preparação e uso dos mesmos.
|
JP2000119271A
(ja)
|
1998-08-12 |
2000-04-25 |
Hokuriku Seiyaku Co Ltd |
1h―イミダゾピリジン誘導体
|
EP1109534B1
(en)
|
1998-09-10 |
2003-02-12 |
Nycomed Danmark A/S |
Quick release pharmaceutical compositions of drug substances
|
US6375839B1
(en)
|
1998-10-29 |
2002-04-23 |
Institut Francais Du Petrole |
Process and device for separation with variable-length chromatographic zones
|
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
|
US6333384B1
(en)
|
1998-11-02 |
2001-12-25 |
Gil Technologies |
Vinyl-terminated polybutadiene and butadiene-styrene copolymers containing urethane and/or ester residues, and the electrical laminates obtained therefrom
|
US6133031A
(en)
|
1999-08-19 |
2000-10-17 |
Isis Pharmaceuticals Inc. |
Antisense inhibition of focal adhesion kinase expression
|
AU3248600A
(en)
|
1999-03-03 |
2000-09-21 |
Merck & Co., Inc. |
Inhibitors of prenyl-protein transferases
|
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
|
US6699880B1
(en)
|
1999-10-13 |
2004-03-02 |
Banyu Pharmaceutical Co., Ltd. |
Substituted imidazolidinone derivatives
|
DZ3248A1
(fr)
|
1999-12-10 |
2001-06-14 |
Pfizer Prod Inc |
Composés à base de pyrrolo[2,3-d]pyrimidine
|
IL150388A0
(en)
|
1999-12-24 |
2002-12-01 |
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
|
DE60100866T2
(de)
|
2000-04-07 |
2004-07-29 |
Laboratoire Medidom S.A. |
Cyklosporin, Hyaluronsäure und Polysorbate enthaltenes Augenarzneimittel
|
WO2001081345A1
(fr)
|
2000-04-20 |
2001-11-01 |
Mitsubishi Pharma Corporation |
Composes d'amides aromatiques
|
KR100785363B1
(ko)
|
2000-04-25 |
2007-12-18 |
이코스 코포레이션 |
인간 포스파티딜-이노시톨 3-키나제 델타의 억제제
|
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
|
WO2001097849A1
(fr)
|
2000-06-23 |
2001-12-27 |
Mitsubishi Pharma Corporation |
Potentialisateurs d'effet antitumoral
|
YU83302A
(sh)
|
2000-06-26 |
2005-09-19 |
Pfizer Products Inc. |
Jedinjenja pirolo (2,3-d) pirimidina kao imunosupresivni agensi
|
MXPA03000051A
(es)
|
2000-06-28 |
2003-08-19 |
Smithkline Beecham Plc |
Procedimiento de molido en humedo.
|
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
|
CA2436487A1
(en)
|
2001-01-30 |
2002-08-08 |
Cytopia Pty Ltd. |
Methods of inhibiting kinases
|
EP1404669A2
(en)
|
2001-05-16 |
2004-04-07 |
Vertex Pharmaceuticals Incorporated |
Heterocyclic substituted pyrazoles as inhibitors of src and other protein kinases
|
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
|
EP1414443B1
(en)
|
2001-08-01 |
2006-11-15 |
Merck & Co., Inc. |
BENZIMIDAZO 4,5-f|ISOQUINOLINONE DERIVATIVES
|
IL160915A0
(en)
|
2001-09-19 |
2004-08-31 |
Aventis Pharma Sa |
Indolizines inhibiting kinase proteins
|
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
|
KR100926194B1
(ko)
|
2001-10-30 |
2009-11-09 |
노파르티스 아게 |
Flt3 수용체 티로신 키나아제 활성의 억제제로서의스타우로스포린 유도체
|
JP2003155285A
(ja)
|
2001-11-19 |
2003-05-27 |
Toray Ind Inc |
環状含窒素誘導体
|
KR20040058340A
(ko)
|
2001-11-30 |
2004-07-03 |
데이진 가부시키가이샤 |
5-(3-시아노페닐)-3-포르밀벤조산 화합물의 제조 방법
|
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
|
US7122550B2
(en)
|
2002-05-23 |
2006-10-17 |
Cytopia Pty Ltd |
Protein kinase inhibitors
|
TW200406374A
(en)
|
2002-05-29 |
2004-05-01 |
Novartis Ag |
Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases
|
EP1535934A4
(en)
|
2002-06-26 |
2005-11-02 |
Idemitsu Kosan Co |
HYDROGENATED COPOLYMER, METHOD FOR THE PRODUCTION THEREOF AND THIS CONTAINING HOTMELT ADHESIVE COMPOSITION
|
GB0215676D0
(en)
|
2002-07-05 |
2002-08-14 |
Novartis Ag |
Organic compounds
|
GB0215844D0
(en)
|
2002-07-09 |
2002-08-14 |
Novartis Ag |
Organic compounds
|
JPWO2004007472A1
(ja)
|
2002-07-10 |
2005-11-17 |
小野薬品工業株式会社 |
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
|
AR042052A1
(es)
|
2002-11-15 |
2005-06-08 |
Vertex Pharma |
Diaminotriazoles utiles como inhibidores de proteinquinasas
|
US20040099204A1
(en)
|
2002-11-25 |
2004-05-27 |
Nestor John J. |
Sheet, page, line, position marker
|
NZ539901A
(en)
|
2002-11-26 |
2007-09-28 |
Pfizer Prod Inc |
Method of treatment of transplant rejection
|
UA80767C2
(en)
|
2002-12-20 |
2007-10-25 |
Pfizer Prod Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
UY28126A1
(es)
|
2002-12-24 |
2004-06-30 |
Alcon Inc |
Uso de glucocorticoides selectivos para la superficie ocular en el tratamiento de la sequedad ocular
|
US7135493B2
(en)
|
2003-01-13 |
2006-11-14 |
Astellas Pharma Inc. |
HDAC inhibitor
|
US7444183B2
(en)
|
2003-02-03 |
2008-10-28 |
Enteromedics, Inc. |
Intraluminal electrode apparatus and method
|
AU2004212421B2
(en)
|
2003-02-07 |
2009-08-20 |
Vertex Pharmaceuticals Incorporated |
Heteroaryl substituted pyrolls useful as inhibitors of protein kinases
|
GB0305929D0
(en)
|
2003-03-14 |
2003-04-23 |
Novartis Ag |
Organic compounds
|
EP1615906A1
(en)
|
2003-04-03 |
2006-01-18 |
Vertex Pharmaceuticals Incorporated |
Compositions useful as inhibitors of protein kinases
|
SE0301373D0
(sv)
|
2003-05-09 |
2003-05-09 |
Astrazeneca Ab |
Novel compounds
|
SE0301372D0
(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
|
US8362017B2
(en)
|
2003-08-29 |
2013-01-29 |
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
|
AR045944A1
(es)
|
2003-09-24 |
2005-11-16 |
Novartis Ag |
Derivados de isoquinolina 1.4-disustituidas
|
DE602004030470D1
(de)
|
2003-10-24 |
2011-01-20 |
Santen Pharmaceutical Co Ltd |
Therapeutisches mittel für keratokonjunktive erkrankungen
|
MY141220A
(en)
|
2003-11-17 |
2010-03-31 |
Astrazeneca Ab |
Pyrazole derivatives as inhibitors of receptor tyrosine kinases
|
JP2007512316A
(ja)
|
2003-11-25 |
2007-05-17 |
ファイザー・プロダクツ・インク |
アテローム性動脈硬化症の治療方法
|
EP1734967A2
(en)
|
2003-12-17 |
2006-12-27 |
Pfizer Products Incorporated |
Pyrrolo [2,3-d] pyrimidine compounds for treating transplant rejection
|
TW200528450A
(en)
|
2003-12-19 |
2005-09-01 |
Schering Corp |
Thiadiazoles as cxc-and cc-chemokine receptor ligands
|
WO2005062795A2
(en)
|
2003-12-19 |
2005-07-14 |
Plexxikon, Inc. |
Compounds and methods for development of ret modulators
|
EP1706385B1
(en)
|
2003-12-23 |
2010-10-06 |
Astex Therapeutics Limited |
Pyrazole derivatives as protein kinase modulators
|
WO2005069865A2
(en)
|
2004-01-13 |
2005-08-04 |
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)
|
TWI471133B
(zh)
|
2004-03-30 |
2015-02-01 |
Vertex Pharma |
適合作為jak及其它蛋白質激酶抑制劑之氮雜吲哚
|
WO2005117909A2
(en)
|
2004-04-23 |
2005-12-15 |
Exelixis, Inc. |
Kinase modulators and methods of use
|
US20060106020A1
(en)
|
2004-04-28 |
2006-05-18 |
Rodgers James D |
Tetracyclic inhibitors of Janus kinases
|
WO2005105988A2
(en)
|
2004-04-28 |
2005-11-10 |
Vertex Pharmaceuticals Incorporated |
Crystal structure of human jak3 kinase domain complex and binding pockets thereof
|
WO2005105146A1
(en)
|
2004-05-03 |
2005-11-10 |
Novartis Ag |
Combinations comprising a s1p receptor agonist and a jak3 kinase inhibitor
|
US20060074102A1
(en)
|
2004-05-14 |
2006-04-06 |
Kevin Cusack |
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
|
MXPA06014247A
(es)
|
2004-06-10 |
2007-03-12 |
Irm Llc |
Compuestos y composiciones como inhibidores de la proteina quinasa.
|
WO2006001463A1
(ja)
|
2004-06-23 |
2006-01-05 |
Ono Pharmaceutical Co., Ltd. |
S1p受容体結合能を有する化合物およびその用途
|
CA2572058A1
(en)
|
2004-06-30 |
2006-01-12 |
Vertex Pharmaceuticals Incorporated |
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
|
WO2006022459A1
(en)
|
2004-08-23 |
2006-03-02 |
Mogam Biotechnology Institute |
Primer and probe for detection of sars coronavirus, kit comprising the primer and/or the probe, and detection method thereof
|
US20070054916A1
(en)
|
2004-10-01 |
2007-03-08 |
Amgen Inc. |
Aryl nitrogen-containing bicyclic compounds and methods of use
|
PT1802625E
(pt)
|
2004-10-13 |
2008-08-06 |
Hoffmann La Roche |
Pirazolobenzodiazepinas di-substituídas, úteis como inibidores de cdc2 e de angiogénese e para o tratamento de cancro da mama, do cólon, do pulmão e da próstata
|
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
|
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
|
NZ555236A
(en)
|
2004-11-04 |
2010-10-29 |
Vertex Pharma |
Pyrazolo[1,5-a]pyrimidines useful as inhibitors of protein kinases
|
RU2007123675A
(ru)
|
2004-11-24 |
2008-12-27 |
Новартис АГ (CH) |
Комбинации ингибиторов jak
|
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
|
AR053992A1
(es)
|
2004-12-22 |
2007-05-30 |
Astrazeneca Ab |
Compuestos quimicos con actividad anticancerosa, un procedimiento para su preparacion, su uso en la preparacion de medicamentos y composicion farmaceutica.
|
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.
|
EP1844037A1
(en)
|
2005-01-20 |
2007-10-17 |
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
|
MX2007011316A
(es)
|
2005-03-15 |
2007-11-12 |
Irm Llc |
Compuestos y composiciones como inhibidores de cinasa de proteina.
|
CA2604161A1
(en)
|
2005-04-05 |
2006-10-12 |
Pharmacopeia, Inc. |
Purine and imidazopyridine derivatives for immunosuppression
|
GB0510139D0
(en)
|
2005-05-18 |
2005-06-22 |
Addex Pharmaceuticals Sa |
Novel compounds B1
|
GB0510390D0
(en)
|
2005-05-20 |
2005-06-29 |
Novartis Ag |
Organic compounds
|
RU2435769C2
(ru)
|
2005-05-20 |
2011-12-10 |
Вертекс Фармасьютикалз Инкорпорейтед |
Пирролопиридины, полезные в качестве ингибиторов протеинкиназы
|
NZ563454A
(en)
|
2005-06-08 |
2011-03-31 |
Rigel Pharmaceuticals Inc |
2,4-diaminopyrimidine derivatives for inhibition of the JAK pathway
|
WO2006136823A1
(en)
|
2005-06-21 |
2006-12-28 |
Astex Therapeutics Limited |
Heterocyclic containing amines as kinase b inhibitors
|
ATE518860T1
(de)
|
2005-06-22 |
2011-08-15 |
Plexxikon Inc |
Pyrroloä2,3-büpyridinderivate als proteinkinaseinhibitoren
|
CN102127078A
(zh)
|
2005-07-14 |
2011-07-20 |
安斯泰来制药株式会社 |
Janus激酶3的杂环类抑制剂
|
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
|
US20070149506A1
(en)
|
2005-09-22 |
2007-06-28 |
Arvanitis Argyrios G |
Azepine inhibitors of Janus kinases
|
JP2009513571A
(ja)
|
2005-09-30 |
2009-04-02 |
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 |
ヤヌスキナーゼ阻害剤として有用なデアザプリン
|
US20070128633A1
(en)
|
2005-10-11 |
2007-06-07 |
Chembridge Research Laboratories, Inc. |
Cell-free protein expression systems and methods of use thereof
|
KR101315574B1
(ko)
|
2005-10-14 |
2013-10-08 |
스미또모 가가꾸 가부시끼가이샤 |
히드라지드 화합물 및 이의 살충 용도
|
WO2007049041A1
(en)
|
2005-10-28 |
2007-05-03 |
Astrazeneca Ab |
4- (3-aminopyrazole) pyrimidine derivatives for use as tyrosine kinase inhibitors in the treatment of cancer
|
BR122021011788B1
(pt)
|
2005-11-01 |
2022-01-25 |
Impact Biomedicines, Inc |
Inibidores de biaril meta pirimidina de cinases, composição farmacêutica e processo para preparar uma composição farmacêutica
|
WO2007062459A1
(en)
|
2005-11-29 |
2007-06-07 |
Cytopia Research Pty Ltd |
Selective kinase inhibitors based on pyridine scaffold
|
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
|
ES2373688T3
(es)
|
2005-12-13 |
2012-02-07 |
Incyte Corporation |
Pirrolo[2,3-b]piridinas y pirrolo[2,3-b]pirimidinas sustituidas con heteroarilo como inhibidores de quinasas janus.
|
WO2007076423A2
(en)
|
2005-12-22 |
2007-07-05 |
Smithkline Beecham Corporation |
INHIBITORS OF Akt ACTIVITY
|
EP1962830B1
(en)
|
2005-12-23 |
2013-03-27 |
GlaxoSmithKline LLC |
Azaindole inhibitors of aurora kinases
|
CN102532133A
(zh)
|
2006-01-17 |
2012-07-04 |
沃泰克斯药物股份有限公司 |
适用作詹纳斯激酶抑制剂的吖吲哚类
|
EP1979353A2
(en)
|
2006-01-19 |
2008-10-15 |
OSI Pharmaceuticals, Inc. |
Fused heterobicyclic kinase inhibitors
|
JP2009525350A
(ja)
|
2006-02-01 |
2009-07-09 |
スミスクライン ビーチャム コーポレーション |
Rafキナーゼ阻害薬として有用なピロロ[2,3,b]ピリジン誘導体
|
US7745477B2
(en)
|
2006-02-07 |
2010-06-29 |
Hoffman-La Roche Inc. |
Heteroaryl and benzyl amide compounds
|
CN101443322A
(zh)
|
2006-03-10 |
2009-05-27 |
小野药品工业株式会社 |
含氮杂环衍生物及含有该衍生物作为活性成分的药物
|
FR2898498B1
(fr)
*
|
2006-03-15 |
2008-11-28 |
Galderma Sa |
Nouvelles compositions topiques sous forme d'emulsion h/e comprenant un glycol pro-penetrant
|
MX356221B
(es)
|
2006-04-03 |
2018-05-18 |
Astellas Pharma Inc |
Heterocompuesto.
|
KR20090018895A
(ko)
|
2006-04-05 |
2009-02-24 |
버텍스 파마슈티칼스 인코포레이티드 |
야누스 키나제의 억제제로서 유용한 데아자푸린
|
JP2009533416A
(ja)
|
2006-04-12 |
2009-09-17 |
ファイザー・リミテッド |
ケモカインccr5受容体の調節剤としてのピロリジン誘導体
|
WO2007129195A2
(en)
|
2006-05-04 |
2007-11-15 |
Pfizer Products Inc. |
4-pyrimidine-5-amino-pyrazole compounds
|
EP2040704A2
(en)
|
2006-05-18 |
2009-04-01 |
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
|
TWI398252B
(zh)
|
2006-05-26 |
2013-06-11 |
Novartis Ag |
吡咯并嘧啶化合物及其用途
|
CN101790527A
(zh)
|
2006-07-20 |
2010-07-28 |
凯利普西斯公司 |
Rho激酶的苯并噻吩抑制剂
|
US8715700B2
(en)
*
|
2006-07-21 |
2014-05-06 |
Dow Pharmaceutical Sciences, Inc. |
Alpha hydroxy acid sustained release formulation
|
WO2008013622A2
(en)
|
2006-07-27 |
2008-01-31 |
E. I. Du Pont De Nemours And Company |
Fungicidal azocyclic amides
|
WO2008016123A1
(fr)
|
2006-08-03 |
2008-02-07 |
Takeda Pharmaceutical Company Limited |
INHIBITEUR DE LA GSK-3β
|
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
|
CL2007002866A1
(es)
|
2006-10-04 |
2008-07-04 |
Pharmacopeia Inc |
Compuestos derivados de 6-sustituidos-2-(bencimidazolil) purina y purinona; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto en el tratamiento de enfermedades autoinmunes, enfermedad inflamatoria, enfermedad mediada por m
|
US7915268B2
(en)
|
2006-10-04 |
2011-03-29 |
Wyeth Llc |
8-substituted 2-(benzimidazolyl)purine derivatives for immunosuppression
|
US20120225057A1
(en)
|
2006-10-11 |
2012-09-06 |
Deciphera Pharmaceuticals, Llc |
Methods and compositions for the treatment of myeloproliferative diseases and other proliferative diseases
|
KR101546493B1
(ko)
|
2006-11-06 |
2015-08-21 |
톨레로 파마수티컬스, 인크. |
이미다조[1,2-b]피리다진 및 피라졸로[1,5-a]피리미딘 유도체 및 단백질 키나제 억제제로서의 이의 용도
|
US20080119496A1
(en)
|
2006-11-16 |
2008-05-22 |
Pharmacopeia Drug Discovery, Inc. |
7-Substituted Purine Derivatives for Immunosuppression
|
RS57741B1
(sr)
|
2006-11-22 |
2018-12-31 |
Incyte Holdings Corp |
Imidazotriazini i imidazopirimidini kao inhibitori kinaze
|
WO2008067119A2
(en)
|
2006-11-27 |
2008-06-05 |
Smithkline Beecham Corporation |
Novel compounds
|
KR20090095648A
(ko)
|
2006-12-15 |
2009-09-09 |
아보트 러보러터리즈 |
신규한 옥사디아졸 화합물
|
MX2009006543A
(es)
|
2006-12-20 |
2009-06-26 |
Amgen Inc |
Compuestos heterociclicos y su uso en el tratamiento de la inflamacion, angiogenesis y cancer.
|
CA2672438A1
(en)
|
2006-12-20 |
2008-07-03 |
Amgen Inc. |
Substituted heterocycles and methods of use
|
EP2094236A1
(en)
|
2006-12-22 |
2009-09-02 |
SIGMA-TAU Industrie Farmaceutiche Riunite S.p.A. |
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
|
WO2008124323A1
(en)
|
2007-04-03 |
2008-10-16 |
Array Biopharma Inc. |
Imidazo[1,2-a]pyridine compounds as receptor tyrosine kinase inhibitors
|
GB0709031D0
(en)
|
2007-05-10 |
2007-06-20 |
Sareum Ltd |
Pharmaceutical compounds
|
CA2687931C
(en)
|
2007-05-31 |
2016-05-24 |
Boehringer Ingelheim International Gmbh |
Ccr2 receptor antagonists and uses thereof
|
GB0710528D0
(en)
|
2007-06-01 |
2007-07-11 |
Glaxo Group Ltd |
Novel compounds
|
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.
|
EP2173752B2
(en)
|
2007-06-13 |
2022-07-13 |
Incyte Holdings Corporation |
Salts of the janus kinase inhibitor (r)-3-(4-(7h-pyrrolo(2,3-d)pyrimidin-4-yl)-1h-pyrazol-1-yl)-3-cyclopentylpropanenitrile
|
ES2523303T3
(es)
|
2007-07-11 |
2014-11-24 |
Pfizer Inc. |
Composiciones farmacéuticas y procedimientos de tratamiento de trastornos del ojo seco
|
WO2009016460A2
(en)
|
2007-08-01 |
2009-02-05 |
Pfizer Inc. |
Pyrazole compounds and their use as raf inhibitors
|
WO2009049028A1
(en)
|
2007-10-09 |
2009-04-16 |
Targegen Inc. |
Pyrrolopyrimidine compounds and their use as janus kinase modulators
|
CA2743756A1
(en)
|
2007-11-15 |
2009-05-22 |
Musc Foundation For Research Development |
Inhibitors of pim protein kinases, compositions, and methods for treating cancer
|
NZ585139A
(en)
|
2007-11-16 |
2012-05-25 |
Incyte Corp |
4-pyrazolyl-n-arylpyrimidin-2-amines and 4-pyrazolyl-n-heteroarylpyrimidin-2-amines as jak inhibitors
|
GB0723815D0
(en)
|
2007-12-05 |
2008-01-16 |
Glaxo Group Ltd |
Compounds
|
EP3133080B1
(en)
|
2008-01-18 |
2018-08-01 |
Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic |
Novel cytostatic 7-deazapurine nucleosides
|
EP2240016A4
(en)
|
2008-02-04 |
2011-11-16 |
Mercury Therapeutics Inc |
AMPK MODULATORS
|
PE20091577A1
(es)
|
2008-03-03 |
2009-11-05 |
Novartis Ag |
Inhibidores de cinasa pim y metodos para su uso
|
AU2009223640B2
(en)
|
2008-03-11 |
2013-07-04 |
Incyte Holdings Corporation |
Azetidine and cyclobutane derivatives as jak inhibitors
|
KR20130040258A
(ko)
|
2008-03-21 |
2013-04-23 |
노파르티스 아게 |
신규한 헤테로시클릭 화합물 및 그의 용도
|
BRPI0914630A2
(pt)
*
|
2008-06-26 |
2019-09-24 |
Anterios Inc |
liberação dérmica
|
UY31952A
(es)
|
2008-07-02 |
2010-01-29 |
Astrazeneca Ab |
5-metilideno-1,3-tiazolidina-2,4-dionas sustituidas como inhibidores de quinasa pim
|
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
|
US8557809B2
(en)
|
2008-08-19 |
2013-10-15 |
Array Biopharma Inc. |
Triazolopyridine compounds as PIM kinase inhibitors
|
BRPI0917459B1
(pt)
|
2008-08-20 |
2017-09-12 |
Zoetis Services Llc |
N-methyl-1- [trans-4- [methyl (7h-pyrrol [2,3-d] pyridol [2,3-d] pyrimidine compounds, use of these in therapy and crystalline a form of n-methyl- pyrimidin-4-yl) amino] cyclohexyl} methanosulphonamide
|
EP2342190A1
(en)
|
2008-09-02 |
2011-07-13 |
Novartis AG |
Bicyclic kinase inhibitors
|
EA020136B1
(ru)
|
2008-09-02 |
2014-08-29 |
Новартис Аг |
Производные пиколинамида в качестве ингибиторов киназы
|
EP2344473B1
(en)
|
2008-09-02 |
2014-04-16 |
Novartis AG |
Heterocyclic pim-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.
|
EP2350054A4
(en)
|
2008-10-17 |
2012-03-28 |
Merck Canada Inc |
AZETIDINE DERIVATIVES AS INHIBITORS OF THE STEAROYL COENZYME A DELTA 9 DESATURASE
|
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
|
PL2432472T3
(pl)
|
2009-05-22 |
2020-03-31 |
Incyte Holdings Corporation |
3-[4-(7H-Pirolo[2,3-d]pirymidyn-4-ylo)-1H-pirazol-1-ilo]oktano- lub heptano-nitryle jako inhibitory JAK
|
UA110324C2
(en)
|
2009-07-02 |
2015-12-25 |
Genentech Inc |
Jak inhibitory compounds based on pyrazolo pyrimidine
|
CN101958119B
(zh)
|
2009-07-16 |
2012-02-29 |
中兴通讯股份有限公司 |
一种改进的离散余弦变换域音频丢帧补偿器和补偿方法
|
WO2011066371A2
(en)
|
2009-11-24 |
2011-06-03 |
Alder Biopharmaceuticals, Inc. |
Antibodies to il-6 and 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
|
WO2011028685A1
(en)
|
2009-09-01 |
2011-03-10 |
Incyte Corporation |
Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors
|
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
|
KR101921850B1
(ko)
|
2009-10-09 |
2018-11-23 |
인사이트 홀딩스 코포레이션 |
3-(4-(7H-피롤로〔2,3-d〕피리미딘-4-일)-1H-피라졸-1-일)-3-사이클로펜틸프로판니트릴의 하이드록실, 케토 및 글루쿠로나이드 유도체
|
WO2011048082A1
(en)
|
2009-10-20 |
2011-04-28 |
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
|
EP2506852A4
(en)
|
2009-12-04 |
2013-06-19 |
Univ Texas |
INTERFERONTHERAPIES IN COMBINATION WITH BLOCKING OF STAT3 ACTIVATION
|
RU2012132278A
(ru)
|
2010-01-12 |
2014-02-20 |
Ф. Хоффманн-Ля Рош Аг |
Трициклические гетероциклические соединения, содержащие их композиции и способы их применения
|
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.
|
TWI592413B
(zh)
|
2010-03-10 |
2017-07-21 |
英塞特公司 |
作為jak1抑制劑之哌啶-4-基三亞甲亞胺衍生物
|
SG184870A1
(en)
|
2010-04-14 |
2012-11-29 |
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
|
ME02445B
(me)
|
2010-05-21 |
2016-09-20 |
Incyte Holdings Corp |
Topikalna formulacija za inhibiciju jak-a
|
US8637529B2
(en)
|
2010-06-11 |
2014-01-28 |
AbbYie Inc. |
Pyrazolo[3,4-d]pyrimidine compounds
|
WO2012003457A1
(en)
|
2010-07-01 |
2012-01-05 |
Mtm Research Llc |
Anti-fibroblastic fluorochemical emulsion therapies
|
EP2621489A1
(en)
|
2010-09-30 |
2013-08-07 |
Portola Pharmaceuticals, Inc. |
Combinations of 4-(cyclopropylamino)-2-(4-(4-(ethylsulfonyl)piperazin-1-yl)phenylamino)pyrimidine-5-carboxamide and fludarabine
|
CA2818545C
(en)
|
2010-11-19 |
2019-04-16 |
Incyte Corporation |
Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors
|
CA2818542A1
(en)
|
2010-11-19 |
2012-05-24 |
Incyte Corporation |
Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors
|
CA2819560A1
(en)
|
2010-12-03 |
2012-06-07 |
Ym Biosciences Australia Pty Ltd |
Treatment of jak2-mediated conditions
|
WO2012112847A1
(en)
|
2011-02-18 |
2012-08-23 |
Novartis Pharma Ag |
mTOR/JAK INHIBITOR COMBINATION THERAPY
|
MY165963A
(en)
|
2011-06-20 |
2018-05-18 |
Incyte Holdings Corp |
Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors
|
HK1198579A1
(en)
|
2011-08-10 |
2015-04-30 |
Novartis Pharma Ag |
Jak p13k/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
|
US9193733B2
(en)
|
2012-05-18 |
2015-11-24 |
Incyte Holdings Corporation |
Piperidinylcyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as JAK inhibitors
|
US10155987B2
(en)
|
2012-06-12 |
2018-12-18 |
Dana-Farber Cancer Institute, Inc. |
Methods of predicting resistance to JAK inhibitor therapy
|
US9573958B2
(en)
|
2012-08-31 |
2017-02-21 |
Principia Biopharma, Inc. |
Benzimidazole derivatives as ITK inhibitors
|
MX2015005428A
(es)
|
2012-11-01 |
2015-07-21 |
Incyte Corp |
Derivados triciclicos fusionados de tiofeno como inhibidores de la cinasa janus (jak).
|
PL2919766T3
(pl)
|
2012-11-15 |
2021-10-04 |
Incyte Holdings Corporation |
Postacie dawkowania ruksolitynibu o przedłużonym uwalnianiu
|
HRP20211922T1
(hr)
|
2013-03-06 |
2022-03-04 |
Incyte Holdings Corporation |
Postupci i intermedijeri za pripravu jak inhibitora
|
AR096330A1
(es)
|
2013-05-17 |
2015-12-23 |
Incyte Corp |
Derivados del bipirazol como inhibidores jak
|
ES2792549T3
(es)
|
2013-08-07 |
2020-11-11 |
Incyte Corp |
Formas de dosificación de liberación sostenida para un inhibidor de JAK1
|
AR097388A1
(es)
|
2013-08-20 |
2016-03-09 |
Incyte Corp |
Beneficio de supervivencia en pacientes con tumores sólidos con niveles elevados de proteína c reactiva
|
CN106456773A
(zh)
|
2014-02-28 |
2017-02-22 |
因赛特公司 |
用于治疗骨髓增生异常综合征的jak1抑制剂
|
PL3129021T3
(pl)
|
2014-04-08 |
2021-05-31 |
Incyte Corporation |
Leczenie nowotworów złośliwych z komórek b za pomocą skojarzenia inhibitora jak i pi3k
|
WO2015168246A1
(en)
|
2014-04-30 |
2015-11-05 |
Incyte Corporation |
Processes of preparing a jak1 inhibitor and new forms thereto
|
ES2946179T3
(es)
|
2014-05-28 |
2023-07-13 |
Onco Tracker Inc |
Efectos antineoplásicos de inhibidores de JAK2 en combinación con derivados de talidomida y glucocorticoides
|
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
|