US2234705A
(en)
|
1940-04-12 |
1941-03-11 |
Eastman Kodak Co |
Cellulose organic derivative composition containing esters of monoalkoxy benzoic acids
|
US2413258A
(en)
|
1942-07-07 |
1946-12-24 |
United Gas Improvement Co |
Polystyrene-type resins plasticized with high boiling fatty acid alkyl esters
|
GB1141949A
(en)
|
1966-02-23 |
1969-02-05 |
Sterling Drug Inc |
7-azaindole derivatives
|
BR6794063D0
(pt)
|
1966-10-21 |
1973-09-18 |
Minnesota Mining & Mfg |
Processo para preparar perfluoral-quilsulfonamidas n-substituidas e composicoes herbicidas e fitoreguladoras nelas baseadas
|
IL46853A0
(en)
|
1974-03-20 |
1975-05-22 |
Bayer Ag |
Novel alkoxycarbonylphenylureas,their preparation and their use as herbicides
|
DE2413258A1
(de)
|
1974-03-20 |
1975-10-02 |
Bayer Ag |
Alkoxycarbonylphenylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide
|
GB1573212A
(en)
|
1976-04-15 |
1980-08-20 |
Technicon Instr |
Immunoassay for gentamicin
|
US4301159A
(en)
|
1980-06-20 |
1981-11-17 |
Shionogi & Co., Ltd. |
N-(Diethylaminoethyl)-2-alkoxy-benzamide derivatives
|
AU547405B2
(en)
|
1981-07-08 |
1985-10-17 |
Sanofi |
Amidobenzamides
|
US4664504A
(en)
|
1983-01-20 |
1987-05-12 |
Tokyo Shibaura Denki Kabushiki Kaisha |
Image forming apparatus
|
US4568649A
(en)
|
1983-02-22 |
1986-02-04 |
Immunex Corporation |
Immediate ligand detection assay
|
US4626513A
(en)
|
1983-11-10 |
1986-12-02 |
Massachusetts General Hospital |
Method and apparatus for ligand detection
|
AU567140B2
(en)
|
1984-01-06 |
1987-11-12 |
Shionogi & Co., Ltd. |
Sulphonamido-benzamide derivatives
|
ATE56096T1
(de)
|
1984-03-15 |
1990-09-15 |
Immunex Corp |
Test zur sofortigen feststellung von liganden, testsatz und seine herstellung.
|
IT1196133B
(it)
|
1984-06-06 |
1988-11-10 |
Ausonia Farma Srl |
Derivati furanici con attivita' antiulcera
|
US4714693A
(en)
|
1986-04-03 |
1987-12-22 |
Uop Inc. |
Method of making a catalyst composition comprising uniform size metal components on carrier
|
DE3642315A1
(de)
|
1986-12-11 |
1988-06-23 |
Boehringer Mannheim Gmbh |
Neue pyrrolobenzimidazole, verfahren zu ihrer herstellung sowie arzneimittel
|
US5688655A
(en)
|
1988-02-10 |
1997-11-18 |
Ict Pharmaceuticals, Inc. |
Method of screening for protein inhibitors and activators
|
US5700637A
(en)
|
1988-05-03 |
1997-12-23 |
Isis Innovation Limited |
Apparatus and method for analyzing polynucleotide sequences and method of generating oligonucleotide arrays
|
US6054270A
(en)
|
1988-05-03 |
2000-04-25 |
Oxford Gene Technology Limited |
Analying polynucleotide sequences
|
US5658775A
(en)
|
1988-05-17 |
1997-08-19 |
Sloan-Kettering Institute For Cancer Research |
Double copy retroviral vector
|
JP2528706B2
(ja)
|
1988-05-30 |
1996-08-28 |
ゼリア新薬工業株式会社 |
ジヒドロピリジン化合物の製剤組成物
|
WO1990002806A1
(en)
|
1988-09-01 |
1990-03-22 |
Whitehead Institute For Biomedical Research |
Recombinant retroviruses with amphotropic and ecotropic host ranges
|
US5703055A
(en)
|
1989-03-21 |
1997-12-30 |
Wisconsin Alumni Research Foundation |
Generation of antibodies through lipid mediated DNA delivery
|
US5744101A
(en)
|
1989-06-07 |
1998-04-28 |
Affymax Technologies N.V. |
Photolabile nucleoside protecting groups
|
US5143854A
(en)
|
1989-06-07 |
1992-09-01 |
Affymax Technologies N.V. |
Large scale photolithographic solid phase synthesis of polypeptides and receptor binding screening thereof
|
US5527681A
(en)
|
1989-06-07 |
1996-06-18 |
Affymax Technologies N.V. |
Immobilized molecular synthesis of systematically substituted compounds
|
US5800992A
(en)
|
1989-06-07 |
1998-09-01 |
Fodor; Stephen P.A. |
Method of detecting nucleic acids
|
US5360822A
(en)
|
1990-02-07 |
1994-11-01 |
Nippon Shinyaku Co. Ltd. |
Sulfonanilide derivatives and medicine
|
WO1991018088A1
(en)
|
1990-05-23 |
1991-11-28 |
The United States Of America, Represented By The Secretary, United States Department Of Commerce |
Adeno-associated virus (aav)-based eucaryotic vectors
|
DE4022414A1
(de)
|
1990-07-13 |
1992-01-16 |
Bayer Ag |
Substituierte pyrrolo-pyridine
|
US5124335A
(en)
|
1991-01-30 |
1992-06-23 |
Merck & Co., Inc. |
Substituted pyrollo-fused 6 membered heterocycles as angiotensin ii antagonists
|
KR0182801B1
(ko)
|
1991-04-16 |
1999-05-01 |
아만 히데아키 |
고체 분산체의 제조방법
|
WO1993002556A1
(en)
|
1991-07-26 |
1993-02-18 |
University Of Rochester |
Cancer therapy utilizing malignant cells
|
US5632957A
(en)
|
1993-11-01 |
1997-05-27 |
Nanogen |
Molecular biological diagnostic systems including electrodes
|
FR2687402B1
(fr)
|
1992-02-14 |
1995-06-30 |
Lipha |
Nouveaux azaindoles, procedes de preparation et medicaments les contenant.
|
JPH05236997A
(ja)
|
1992-02-28 |
1993-09-17 |
Hitachi Ltd |
ポリヌクレオチド捕捉用チップ
|
AU686115B2
(en)
|
1992-11-02 |
1998-02-05 |
Fujisawa Pharmaceutical Co., Ltd. |
Imidazo (I,2-a) pyridine derivatives as bradykinin antagonists, pharmaceuticals and processes for their preparation
|
US5576319A
(en)
|
1993-03-01 |
1996-11-19 |
Merck, Sharp & Dohme Ltd. |
Pyrrolo-pyridine derivatives
|
HUT71799A
(en)
|
1993-03-01 |
1996-02-28 |
Merck Sharp & Dohme |
Pyrrolo-pyridine derivatives, pharmaceutical compositions containing the same, process for producing them
|
DE69420394T2
(de)
|
1993-03-01 |
2000-04-13 |
Merck Sharp & Dohme |
Pyrrolopyridinderivate als dopaminrezeptor liganden
|
US5840485A
(en)
|
1993-05-27 |
1998-11-24 |
Selectide Corporation |
Topologically segregated, encoded solid phase libraries
|
JP3394777B2
(ja)
|
1993-05-27 |
2003-04-07 |
セレクタイド コーポレーション |
位相学的に分離された、コードされた固相ライブラリー
|
US5631236A
(en)
|
1993-08-26 |
1997-05-20 |
Baylor College Of Medicine |
Gene therapy for solid tumors, using a DNA sequence encoding HSV-Tk or VZV-Tk
|
US5426039A
(en)
|
1993-09-08 |
1995-06-20 |
Bio-Rad Laboratories, Inc. |
Direct molecular cloning of primer extended DNA containing an alkane diol
|
JP3545461B2
(ja)
|
1993-09-10 |
2004-07-21 |
エーザイ株式会社 |
二環式ヘテロ環含有スルホンアミド誘導体
|
US6045996A
(en)
|
1993-10-26 |
2000-04-04 |
Affymetrix, Inc. |
Hybridization assays on oligonucleotide arrays
|
US6468742B2
(en)
|
1993-11-01 |
2002-10-22 |
Nanogen, Inc. |
Methods for determination of single nucleic acid polymorphisms using bioelectronic microchip
|
US5965452A
(en)
|
1996-07-09 |
1999-10-12 |
Nanogen, Inc. |
Multiplexed active biologic array
|
US5486525A
(en)
|
1993-12-16 |
1996-01-23 |
Abbott Laboratories |
Platelet activating factor antagonists: imidazopyridine indoles
|
EP1195372A1
(en)
|
1994-04-18 |
2002-04-10 |
Mitsubishi Pharma Corporation |
N-heterocyclic substituted benzamide derivatives with antihypertensive activity
|
GB9408577D0
(en)
|
1994-04-29 |
1994-06-22 |
Fujisawa Pharmaceutical Co |
New compound
|
US5807522A
(en)
|
1994-06-17 |
1998-09-15 |
The Board Of Trustees Of The Leland Stanford Junior University |
Methods for fabricating microarrays of biological samples
|
US5763198A
(en)
|
1994-07-22 |
1998-06-09 |
Sugen, Inc. |
Screening assays for compounds
|
GB9416189D0
(en)
|
1994-08-10 |
1994-09-28 |
Merck Sharp & Dohme |
Therapeutic agents
|
GB9416162D0
(en)
|
1994-08-10 |
1994-09-28 |
Merck Sharp & Dohme |
Therapeutic agents
|
US5556752A
(en)
|
1994-10-24 |
1996-09-17 |
Affymetrix, Inc. |
Surface-bound, unimolecular, double-stranded DNA
|
US5830645A
(en)
|
1994-12-09 |
1998-11-03 |
The Regents Of The University Of California |
Comparative fluorescence hybridization to nucleic acid arrays
|
GB2298199A
(en)
|
1995-02-21 |
1996-08-28 |
Merck Sharp & Dohme |
Synthesis of azaindoles
|
GB9503400D0
(en)
|
1995-02-21 |
1995-04-12 |
Merck Sharp & Dohme |
Therpeutic agents
|
US5959098A
(en)
|
1996-04-17 |
1999-09-28 |
Affymetrix, Inc. |
Substrate preparation process
|
US6117681A
(en)
|
1995-03-29 |
2000-09-12 |
Bavarian Nordic Research Inst. A/S |
Pseudotyped retroviral particles
|
GB2299581A
(en)
|
1995-04-07 |
1996-10-09 |
Merck Sharp & Dohme |
3-(Tetrahydropyridin-1-yl-methyl)pyrrolo[2,3-b]pyridine derivatives as ligands for dopamine receptor subtypes
|
GB9507291D0
(en)
|
1995-04-07 |
1995-05-31 |
Merck Sharp & Dohme |
Therapeutic agents
|
US6110456A
(en)
|
1995-06-07 |
2000-08-29 |
Yale University |
Oral delivery or adeno-associated viral vectors
|
US5856174A
(en)
|
1995-06-29 |
1999-01-05 |
Affymetrix, Inc. |
Integrated nucleic acid diagnostic device
|
US5866411A
(en)
|
1995-09-08 |
1999-02-02 |
Pedersen; Finn Skou |
Retroviral vector, a replication system for said vector and avian or mammalian cells transfected with said vector
|
US5747276A
(en)
|
1995-09-15 |
1998-05-05 |
The Scripps Research Institute |
Screening methods for the identification of novel antibiotics
|
WO1997016533A1
(en)
|
1995-10-31 |
1997-05-09 |
The Regents Of The University Of California |
Mammalian artificial chromosomes and methods of using same
|
US6022963A
(en)
|
1995-12-15 |
2000-02-08 |
Affymetrix, Inc. |
Synthesis of oligonucleotide arrays using photocleavable protecting groups
|
US6013440A
(en)
|
1996-03-11 |
2000-01-11 |
Affymetrix, Inc. |
Nucleic acid affinity columns
|
US6025155A
(en)
|
1996-04-10 |
2000-02-15 |
Chromos Molecular Systems, Inc. |
Artificial chromosomes, uses thereof and methods for preparing artificial chromosomes
|
US5804585A
(en)
|
1996-04-15 |
1998-09-08 |
Texas Biotechnology Corporation |
Thieno-pyridine sulfonamides derivatives thereof and related compounds that modulate the activity of endothelin
|
EP0956865B2
(en)
|
1996-08-12 |
2010-08-18 |
Mitsubishi Tanabe Pharma Corporation |
MEDICINES COMPRISING Rho KINASE INHIBITOR
|
US6294330B1
(en)
|
1997-01-31 |
2001-09-25 |
Odyssey Pharmaceuticals Inc. |
Protein fragment complementation assays for the detection of biological or drug interactions
|
WO1998039471A1
(en)
|
1997-03-07 |
1998-09-11 |
Tropix, Inc. |
Protease inhibtor assay
|
US5977131A
(en)
|
1997-04-09 |
1999-11-02 |
Pfizer Inc. |
Azaindole-ethylamine derivatives as nicotinic acetylcholine receptor binding agents
|
US6096718A
(en)
|
1997-06-05 |
2000-08-01 |
Gene Targeting Corp. |
Tissue specific adenovirus vectors for breast cancer treatment
|
SG72827A1
(en)
|
1997-06-23 |
2000-05-23 |
Hoffmann La Roche |
Phenyl-and aminophenyl-alkylsulfonamide and urea derivatives
|
RU2199532C2
(ru)
|
1997-06-27 |
2003-02-27 |
Фудзисава Фармасьютикал Ко., Лтд. |
Сульфонамидное соединение
|
US6235769B1
(en)
|
1997-07-03 |
2001-05-22 |
Sugen, Inc. |
Methods of preventing and treating neurological disorders with compounds that modulate the function of the C-RET receptor protein tyrosine kinase
|
US6826296B2
(en)
|
1997-07-25 |
2004-11-30 |
Affymetrix, Inc. |
Method and system for providing a probe array chip design database
|
ES2287971T3
(es)
|
1997-08-11 |
2007-12-16 |
Pfizer Products Inc. |
Dispersiones farmaceuticas solidas con biodisponibilidad incrementada.
|
US6161776A
(en)
|
1997-08-12 |
2000-12-19 |
Nibco Inc. |
Multi-layered, porous mat turf irrigation apparatus and method
|
ATE319986T1
(de)
|
1997-09-11 |
2006-03-15 |
Bioventures Inc |
Verfahren zur herstellung von arrays hoher dichte
|
US6178384B1
(en)
|
1997-09-29 |
2001-01-23 |
The Trustees Of Columbia University In The City Of New York |
Method and apparatus for selecting a molecule based on conformational free energy
|
US6465178B2
(en)
|
1997-09-30 |
2002-10-15 |
Surmodics, Inc. |
Target molecule attachment to surfaces
|
US6048695A
(en)
|
1998-05-04 |
2000-04-11 |
Baylor College Of Medicine |
Chemically modified nucleic acids and methods for coupling nucleic acids to solid support
|
EP1085846A2
(en)
|
1998-06-08 |
2001-03-28 |
Advanced Medicine, Inc. |
Multibinding inhibitors of microsomal triglyceride transferase protein
|
US6113913A
(en)
|
1998-06-26 |
2000-09-05 |
Genvec, Inc. |
Recombinant adenovirus
|
CA2307285C
(en)
|
1998-08-17 |
2009-03-31 |
Senju Pharmaceutical Co., Ltd. |
Agent for prophylaxis and treatment of glaucoma
|
US6350786B1
(en)
|
1998-09-22 |
2002-02-26 |
Hoffmann-La Roche Inc. |
Stable complexes of poorly soluble compounds in ionic polymers
|
US6277628B1
(en)
|
1998-10-02 |
2001-08-21 |
Incyte Genomics, Inc. |
Linear microarrays
|
US6277489B1
(en)
|
1998-12-04 |
2001-08-21 |
The Regents Of The University Of California |
Support for high performance affinity chromatography and other uses
|
CN1198803C
(zh)
|
1999-03-05 |
2005-04-27 |
第一三得利制药株式会社 |
具有激活烟碱性乙酰胆碱α4β2受体作用的杂环化合物
|
US6653309B1
(en)
|
1999-04-26 |
2003-11-25 |
Vertex Pharmaceuticals Incorporated |
Inhibitors of IMPDH enzyme technical field of the invention
|
US6221653B1
(en)
|
1999-04-27 |
2001-04-24 |
Agilent Technologies, Inc. |
Method of performing array-based hybridization assays using thermal inkjet deposition of sample fluids
|
FR2793793B1
(fr)
|
1999-05-19 |
2004-02-27 |
Adir |
Nouveaux derives dimeriques substitues, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
|
US6653151B2
(en)
|
1999-07-30 |
2003-11-25 |
Large Scale Proteomics Corporation |
Dry deposition of materials for microarrays using matrix displacement
|
US20010008765A1
(en)
|
1999-12-06 |
2001-07-19 |
Fuji Photo Film Co., Ltd. |
DNA chip and reactive solid carrier
|
US20020010203A1
(en)
|
1999-12-22 |
2002-01-24 |
Ken Lipson |
Methods of modulating c-kit tyrosine protein kinase function with indolinone compounds
|
ES2246922T3
(es)
|
1999-12-28 |
2006-03-01 |
Eisai Co., Ltd. |
Compuestos heterociclicos que tienen grupos de sulfonamida.
|
JP2001278886A
(ja)
|
2000-03-28 |
2001-10-10 |
Dai Ichi Seiyaku Co Ltd |
ベンゾオキサジン誘導体及びこれを含有する医薬
|
GB0017256D0
(en)
*
|
2000-07-13 |
2000-08-30 |
Merck Sharp & Dohme |
Therapeutic agents
|
KR20030080013A
(ko)
|
2001-02-21 |
2003-10-10 |
에자이 가부시키가이샤 |
인테그린 발현 억제를 통한 혈관 신생 억제제의 효과를검정하는 방법
|
WO2002067893A2
(en)
|
2001-02-27 |
2002-09-06 |
Astrazeneca Ab |
Pharmaceutical formulation comprising bicalutamide
|
WO2002083175A1
(fr)
|
2001-04-11 |
2002-10-24 |
Senju Pharmaceutical Co., Ltd. |
Agents ameliorant la fonction visuelle
|
GB0114417D0
(en)
|
2001-06-13 |
2001-08-08 |
Boc Group Plc |
Lubricating systems for regenerative vacuum pumps
|
EP1267111A1
(en)
|
2001-06-15 |
2002-12-18 |
Dsm N.V. |
Pressurized fluid conduit
|
GB0115109D0
(en)
|
2001-06-21 |
2001-08-15 |
Aventis Pharma Ltd |
Chemical compounds
|
US6858860B2
(en)
|
2001-07-24 |
2005-02-22 |
Seiko Epson Corporation |
Apparatus and method for measuring natural period of liquid
|
EP1452525A4
(en)
|
2001-10-30 |
2005-01-26 |
Nippon Shinyaku Co Ltd |
AMIDE DERIVATIVES AND CORRESPONDING MEDICAMENTS
|
US7361665B2
(en)
|
2002-07-09 |
2008-04-22 |
Vertex Pharmaceuticals Incorporated |
Inhibitors of c-Jun N-terminal kinases (JNK) and other protein kinases
|
TW200403243A
(en)
|
2002-07-18 |
2004-03-01 |
Wyeth Corp |
1-Heterocyclylalkyl-3-sulfonylazaindole or-azaindazole derivatives as 5-hydroxytryptamine-6 ligands
|
TWI329112B
(en)
|
2002-07-19 |
2010-08-21 |
Bristol Myers Squibb Co |
Novel inhibitors of kinases
|
EP1388341A1
(en)
|
2002-08-07 |
2004-02-11 |
Aventis Pharma Deutschland GmbH |
Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals
|
US6878887B2
(en)
|
2002-08-07 |
2005-04-12 |
Matsushita Electric Industrial Co., Ltd. |
Anti-malfunction mechanism for variable output device
|
SE0202463D0
(sv)
|
2002-08-14 |
2002-08-14 |
Astrazeneca Ab |
Novel compounds
|
ES2666694T3
(es)
|
2002-09-06 |
2018-05-07 |
Cerulean Pharma Inc. |
Polímeros a base de ciclodextrina para el suministro de los agentes terapéuticos enlazados covalentemente a ellos
|
WO2004024895A2
(en)
|
2002-09-16 |
2004-03-25 |
Plexxikon, Inc. |
Crystal structure of pim-1 kinase
|
US7183241B2
(en)
|
2002-10-15 |
2007-02-27 |
Exxonmobil Research And Engineering Company |
Long life lubricating oil composition with very low phosphorus content
|
SE0203654D0
(sv)
|
2002-12-09 |
2002-12-09 |
Astrazeneca Ab |
New compounds
|
ATE405269T1
(de)
|
2002-12-13 |
2008-09-15 |
Smithkline Beecham Corp |
Cyclohexylverbindungen als ccr5-antagonisten
|
UA80171C2
(en)
|
2002-12-19 |
2007-08-27 |
Pfizer Prod Inc |
Pyrrolopyrimidine derivatives
|
US7696225B2
(en)
|
2003-01-06 |
2010-04-13 |
Osi Pharmaceuticals, Inc. |
(2-carboxamido)(3-Amino) thiophene compounds
|
SE0300119D0
(sv)
|
2003-01-17 |
2003-01-17 |
Astrazeneca Ab |
Novel compounds
|
SE0300120D0
(sv)
|
2003-01-17 |
2003-01-17 |
Astrazeneca Ab |
Novel compounds
|
US20050085463A1
(en)
|
2003-01-23 |
2005-04-21 |
Weiner David M. |
Use of N-desmethylclozapine to treat human neuropsychiatric disease
|
JP4783278B2
(ja)
|
2003-02-03 |
2011-09-28 |
ノバルティス アーゲー |
医薬製剤
|
TW200418830A
(en)
|
2003-02-14 |
2004-10-01 |
Wyeth Corp |
Heterocyclyl-3-sulfonylazaindole or-azaindazole derivatives as 5-hydroxytryptamine-6 ligands
|
JP2007524374A
(ja)
|
2003-02-28 |
2007-08-30 |
プレキシコン,インコーポレーテッド |
Pyk2結晶構造および使用
|
EP1599475A2
(en)
|
2003-03-06 |
2005-11-30 |
Eisai Co., Ltd. |
Jnk inhibitors
|
WO2004101565A2
(en)
|
2003-05-16 |
2004-11-25 |
Eisai Co., Ltd. |
Jnk inhibitors
|
TWI339206B
(en)
|
2003-09-04 |
2011-03-21 |
Vertex Pharma |
Compositions useful as inhibitors of protein kinases
|
WO2005044181A2
(en)
|
2003-09-09 |
2005-05-19 |
Temple University-Of The Commonwealth System Of Higher Education |
Protection of tissues and cells from cytotoxic effects of ionizing radiation by abl inhibitors
|
US20050164300A1
(en)
|
2003-09-15 |
2005-07-28 |
Plexxikon, Inc. |
Molecular scaffolds for kinase ligand development
|
US20060281803A1
(en)
|
2003-09-23 |
2006-12-14 |
Lindsley Craig W |
Pyrazole modulators of metabotropic glutamate receptors
|
CN1863774B
(zh)
|
2003-10-08 |
2010-12-15 |
Irm责任有限公司 |
用作蛋白激酶抑制剂的化合物和组合物
|
DE10357510A1
(de)
|
2003-12-09 |
2005-07-07 |
Bayer Healthcare Ag |
Heteroarylsubstituierte Benzole
|
JP5138938B2
(ja)
|
2003-12-19 |
2013-02-06 |
プレキシコン インコーポレーテッド |
Ret調節剤の開発のための化合物および方法
|
US20070066641A1
(en)
|
2003-12-19 |
2007-03-22 |
Prabha Ibrahim |
Compounds and methods for development of RET modulators
|
GB0330042D0
(en)
|
2003-12-24 |
2004-01-28 |
Pharmacia Italia Spa |
Pyrrolo [2,3-b] pyridine derivatives active as kinase inhibitors process for their preparation and pharmaceutical compositions them
|
WO2005066347A1
(en)
|
2003-12-24 |
2005-07-21 |
Danisco A/S |
Proteins
|
GB0330043D0
(en)
|
2003-12-24 |
2004-01-28 |
Pharmacia Italia Spa |
Pyrrolo [2,3-b] pyridine derivatives active as kinase inhibitors process for their preparation and pharmaceutical compositions comprising them
|
GB0403635D0
(en)
|
2004-02-18 |
2004-03-24 |
Devgen Nv |
Pyridinocarboxamides with improved activity as kinase inhibitors
|
GB0405055D0
(en)
|
2004-03-05 |
2004-04-07 |
Eisai London Res Lab Ltd |
JNK inhibitors
|
CA2555914A1
(en)
|
2004-03-08 |
2005-09-22 |
Amgen Inc. |
Therapeutic modulation of ppar (gamma) activity
|
KR20050091462A
(ko)
|
2004-03-12 |
2005-09-15 |
한국과학기술연구원 |
푸로피리미딘 화합물 및 이를 포함하는 ddr2 티로신키나아제 활성 저해제
|
CN101676285A
(zh)
|
2004-03-30 |
2010-03-24 |
沃泰克斯药物股份有限公司 |
用作jak和其它蛋白激酶抑制剂的氮杂吲哚
|
TW200604168A
(en)
|
2004-04-02 |
2006-02-01 |
Vertex Pharma |
Azaindoles useful as inhibitors of rock and other protein kinases
|
EP1773305A2
(en)
|
2004-05-25 |
2007-04-18 |
Yale University Corporation |
Method for treating skeletal disorders resulting from fgfr malfunction
|
WO2005115374A1
(en)
|
2004-05-29 |
2005-12-08 |
7Tm Pharma A/S |
Crth2 receptor ligands for therapeutic use
|
CA2570817A1
(en)
|
2004-06-17 |
2006-01-26 |
Plexxikon, Inc. |
Azaindoles modulating c-kit activity and uses therefor
|
US7498342B2
(en)
|
2004-06-17 |
2009-03-03 |
Plexxikon, Inc. |
Compounds modulating c-kit activity
|
AU2005260689B2
(en)
|
2004-06-30 |
2012-05-10 |
Vertex Pharmaceuticals Incorporated |
Azaindoles useful as inhibitors of protein kinases
|
US7140816B2
(en)
|
2004-07-20 |
2006-11-28 |
H&S Tool, Inc. |
Multi-functional tube milling head
|
US7709645B2
(en)
|
2004-07-27 |
2010-05-04 |
Sgx Pharmaceuticals, Inc. |
Pyrrolo-pyridine kinase modulators
|
CN101027302B
(zh)
*
|
2004-07-27 |
2011-05-11 |
Sgx药物公司 |
吡咯并吡啶激酶调节剂
|
EP1778687A2
(en)
|
2004-07-27 |
2007-05-02 |
SGX Pharmaceuticals, Inc. |
Fused ring heterocycle kinase modulators
|
US7361764B2
(en)
|
2004-07-27 |
2008-04-22 |
Sgx Pharmaceuticals, Inc. |
Pyrrolo-pyridine kinase modulators
|
US7626021B2
(en)
|
2004-07-27 |
2009-12-01 |
Sgx Pharmaceuticals, Inc. |
Fused ring heterocycle kinase modulators
|
NZ553267A
(en)
|
2004-07-27 |
2010-09-30 |
Sgx Pharmaceuticals Inc |
Pyrrolo-pyridine kinase modulators
|
US20060024361A1
(en)
|
2004-07-28 |
2006-02-02 |
Isa Odidi |
Disintegrant assisted controlled release technology
|
EP1789393A2
(en)
|
2004-07-30 |
2007-05-30 |
GPC Biotech AG |
Pyridinylamines
|
WO2006063167A1
(en)
|
2004-12-08 |
2006-06-15 |
Smithkline Beecham Corporation |
1h-pyrrolo[2,3-b]pyridines
|
CN101087787A
(zh)
*
|
2004-12-23 |
2007-12-12 |
霍夫曼-拉罗奇有限公司 |
苯甲酰胺衍生物,它们的制备及作为药剂的应用
|
WO2006082373A1
(en)
*
|
2005-02-01 |
2006-08-10 |
Astrazeneca Ab |
Pyrimidine compounds having ties (tek) inhibitory activity
|
US20060183758A1
(en)
*
|
2005-02-17 |
2006-08-17 |
Cb Research And Development, Inc. |
Method for synthesis of AZA-annelated pyrroles, thiophenes, and furans
|
CA2605738C
(en)
|
2005-04-25 |
2013-10-01 |
Merck Patent Gesellschaft Mit Beschraenkter Haftung |
Novel azaheterocyclic compounds as kinase inhibitors
|
FR2884821B1
(fr)
|
2005-04-26 |
2007-07-06 |
Aventis Pharma Sa |
Pyrrolopyridines substitues, compositions les contenant, procede de fabrication et utilisation
|
EP1885723A2
(en)
|
2005-05-17 |
2008-02-13 |
Plexxikon, Inc. |
Pyrrolo[2,3-b]pyridine derivatives as protein kinase inhibitors
|
US8921376B2
(en)
|
2005-05-20 |
2014-12-30 |
Vertex Pharmaceuticals Incorporated |
Pyrrolopyridines useful as inhibitors of protein kinase
|
KR20090130887A
(ko)
|
2005-06-21 |
2009-12-24 |
미쓰이 가가쿠 가부시키가이샤 |
아미드 유도체 및 이 화합물을 함유하는 살충제
|
RS52010B
(en)
|
2005-06-22 |
2012-04-30 |
Plexxikon Inc. |
DERIVATI PIROLO [2, 3-B] PIRIDINA KAO INHIBITORI PROTEIN KINAZE
|
DE102005034406A1
(de)
|
2005-07-22 |
2007-02-01 |
Ratiopharm Gmbh |
Neue Salze von Rosiglitazon
|
GB0516156D0
(en)
|
2005-08-05 |
2005-09-14 |
Eisai London Res Lab Ltd |
JNK inhibitors
|
US7754717B2
(en)
|
2005-08-15 |
2010-07-13 |
Amgen Inc. |
Bis-aryl amide compounds and methods of use
|
JP2009530415A
(ja)
|
2006-03-20 |
2009-08-27 |
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 |
医薬組成物
|
PT2848610T
(pt)
|
2006-11-15 |
2017-11-14 |
Ym Biosciences Australia Pty |
Inibidores da atividade de quinases
|
WO2008063888A2
(en)
|
2006-11-22 |
2008-05-29 |
Plexxikon, Inc. |
Compounds modulating c-fms and/or c-kit activity and uses therefor
|
GB0624084D0
(en)
|
2006-12-01 |
2007-01-10 |
Selamine Ltd |
Ramipril amino acid salts
|
WO2008079909A1
(en)
|
2006-12-21 |
2008-07-03 |
Plexxikon, Inc. |
Pyrrolo [2,3-b] pyridines as kinase modulators
|
PE20121126A1
(es)
|
2006-12-21 |
2012-08-24 |
Plexxikon Inc |
Compuestos pirrolo [2,3-b] piridinas como moduladores de quinasa
|
EP2155166A2
(en)
|
2007-05-11 |
2010-02-24 |
F. Hoffmann-Roche AG |
Pharmaceutical compositions for poorly soluble drugs
|
TW200908968A
(en)
|
2007-05-29 |
2009-03-01 |
Sgx Pharmaceuticals Inc |
Substituted pyrrolopyridines and pyrazolopyridines as kinase modulators
|
CA2695004C
(en)
|
2007-07-17 |
2016-01-19 |
Plexxikon, Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
CA2691752C
(en)
|
2007-07-23 |
2016-01-26 |
Evangelos Karavas |
Pharmaceutical composition containing dihydropyridine calcium channel antagonist and method for the preparation thereof
|
AU2008281543A1
(en)
|
2007-08-01 |
2009-02-05 |
Pfizer Inc. |
Pyrazole compounds and their use as Raf inhibitors
|
CA2716949A1
(en)
|
2008-02-29 |
2009-09-11 |
Array Biopharma Inc. |
N- (6-aminopyridin-3-yl) -3- (sulfonamido) benzamide derivatives as b-raf inhibitors for the treatment of cancer
|
CA2716947A1
(en)
|
2008-02-29 |
2009-09-11 |
Array Biopharma Inc. |
Imidazo [4,5-b] pyridine derivatives used as raf inhibitors
|
JP2011513330A
(ja)
|
2008-02-29 |
2011-04-28 |
アレイ バイオファーマ、インコーポレイテッド |
Raf阻害化合物およびその使用方法
|
AR072657A1
(es)
|
2008-02-29 |
2010-09-15 |
Genentech Inc |
Compuestos inhibidores de raf y metodos para su uso
|
UA103319C2
(en)
|
2008-05-06 |
2013-10-10 |
Глаксосмитклайн Ллк |
Thiazole- and oxazole-benzene sulfonamide compounds
|
NZ594398A
(en)
|
2009-04-03 |
2014-03-28 |
Plexxikon Inc |
Propane-1-sulfonic acid (3-[5-(4-chloro-phenyl)-1h-pyrrol [2, 3-b] pyridine-3-carbonyl]-2,4-difluoro-phenyl} -amide compositions and uses thereof
|
TW201041888A
(en)
|
2009-05-06 |
2010-12-01 |
Plexxikon Inc |
Compounds and methods for kinase modulation, and indications therefor
|
US8329724B2
(en)
|
2009-08-03 |
2012-12-11 |
Hoffmann-La Roche Inc. |
Process for the manufacture of pharmaceutically active compounds
|
US8779150B2
(en)
|
2010-07-21 |
2014-07-15 |
Hoffmann-La Roche Inc. |
Processes for the manufacture of propane-1-sulfonic acid {3-[5-(4-chloro-phenyl)-1 H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide
|