US4242513A
(en)
|
1979-03-05 |
1980-12-30 |
Appleton Papers Inc. |
Lactone compounds containing a heterocyclic radical
|
WO1986007059A2
(en)
|
1985-05-25 |
1986-12-04 |
Yoshitomi Pharmaceutical Industries, Ltd. |
Oxodiazine compounds
|
AU6355190A
(en)
|
1989-06-13 |
1991-01-17 |
Smithkline Beecham Corporation |
Inhibition of interleukin-1 and tumor necrosis factor production by monocytes and/or macrophages
|
KR920702606A
(ko)
|
1989-06-13 |
1992-10-06 |
스튜어트 알. 슈터 |
모노킨(Monokine)의 활성저해
|
AU622330B2
(en)
|
1989-06-23 |
1992-04-02 |
Takeda Chemical Industries Ltd. |
Condensed heterocyclic compounds having a nitrogen atom in the bridgehead for use as fungicides
|
KR910011852A
(ko)
|
1989-12-04 |
1991-08-07 |
폴 디. 매튜카이티스 |
신경독 장해 치료용 이미다조[1,2-a]피리디닐알킬 화합물
|
WO1991019497A1
(en)
|
1990-06-12 |
1991-12-26 |
Smithkline Beecham Corporation |
Inhibition of 5-lipoxygenase and cyclooxygenase pathway mediated diseases
|
US5137876A
(en)
|
1990-10-12 |
1992-08-11 |
Merck & Co., Inc. |
Nucleoside antiviral and anti-inflammatory compounds and compositions and methods for using same
|
EP0563286A4
(en)
|
1990-12-13 |
1995-01-11 |
Smithkline Beecham Corp |
Novel csaids
|
WO1992010190A1
(en)
|
1990-12-13 |
1992-06-25 |
Smithkline Beecham Corporation |
Novel csaids
|
US5486525A
(en)
|
1993-12-16 |
1996-01-23 |
Abbott Laboratories |
Platelet activating factor antagonists: imidazopyridine indoles
|
US5869486A
(en)
|
1995-02-24 |
1999-02-09 |
Ono Pharmaceutical Co., Ltd. |
Fused pyrimidines and pyriazines as pharmaceutical compounds
|
WO1996034866A1
(en)
|
1995-05-01 |
1996-11-07 |
Fujisawa Pharmaceutical Co., Ltd. |
Imidazo 1,2-a pyridine and imidazo 1,2-a pyridezine derivatives and their use as bone resorption inhibitors
|
US6992188B1
(en)
|
1995-12-08 |
2006-01-31 |
Pfizer, Inc. |
Substituted heterocyclic derivatives
|
US20010007867A1
(en)
|
1999-12-13 |
2001-07-12 |
Yuhpyng L. Chen |
Substituted 6,5-hetero-bicyclic derivatives
|
CZ68199A3
(cs)
*
|
1996-08-28 |
1999-11-17 |
Pfizer Inc. |
6,5-Heterobicyklické deriváty, farmaceutická kompozice na jejich bázi a způsob léčení chorob
|
EP0970082A2
(en)
|
1997-02-18 |
2000-01-12 |
Neurocrine Biosciences, Inc. |
Biazacyclic crf antagonists
|
AU6691798A
(en)
|
1997-03-07 |
1998-09-22 |
Metabasis Therapeutics, Inc. |
Novel indole and azaindole inhibitors of fructose-1,6-bisphosphatase
|
EP1012151B1
(en)
|
1997-09-02 |
2002-08-07 |
Bristol-Myers Squibb Pharma Company |
Heterocyclyl-substituted ring-fused pyridines and pyrimidines as corticotropin releasing hormone (crh) antagonists, useful for treating cns and stress-related disorders
|
US6248755B1
(en)
|
1999-04-06 |
2001-06-19 |
Merck & Co., Inc. |
Pyrrolidine modulators of chemokine receptor activity
|
JP4032566B2
(ja)
|
1999-06-21 |
2008-01-16 |
東レ株式会社 |
発光素子
|
JP2001057292A
(ja)
|
1999-08-20 |
2001-02-27 |
Toray Ind Inc |
発光素子
|
GB9919778D0
(en)
|
1999-08-21 |
1999-10-27 |
Zeneca Ltd |
Chemical compounds
|
IL139197A0
(en)
|
1999-10-29 |
2001-11-25 |
Pfizer Prod Inc |
Use of corticotropin releasing factor antagonists and related compositions
|
CA2398956A1
(en)
|
2000-02-14 |
2001-08-16 |
Japan Tobacco Inc. |
A pharmaceutical composition for prophylaxis or therapy of a postoperative stress
|
EP1149583A3
(en)
|
2000-04-13 |
2001-11-14 |
Pfizer Products Inc. |
Combinations of corticotropin releasing factor antagonists and growth hormone secretagogues
|
US6403588B1
(en)
|
2000-04-27 |
2002-06-11 |
Yamanouchi Pharmaceutical Co., Ltd. |
Imidazopyridine derivatives
|
HUP0301801A2
(hu)
|
2000-07-14 |
2003-09-29 |
Bristol-Myers Squibb Pharma Company |
Imidazo[1,2-a]pirazin-származékok és az ezeket tartalmazó gyógyszerkészítmények
|
AU2001295992A1
(en)
|
2000-10-24 |
2002-05-06 |
Sankyo Company Limited |
Imidazopyridine derivatives
|
US20040058938A1
(en)
|
2000-12-13 |
2004-03-25 |
Oliver Cullmann |
Use of substituted imidazoazines, novel imidazoazines, methods for the production thereof, and agents containing these compounds
|
WO2002057287A2
(en)
|
2001-01-22 |
2002-07-25 |
Merck & Co., Inc. |
Nucleoside derivatives as inhibitors of rna-dependent rna viral polymerase
|
TWI312347B
(en)
|
2001-02-08 |
2009-07-21 |
Eisai R&D Man Co Ltd |
Bicyclic nitrogen-containing condensed ring compounds
|
GB0103926D0
(en)
|
2001-02-17 |
2001-04-04 |
Astrazeneca Ab |
Chemical compounds
|
SE0100568D0
(sv)
|
2001-02-20 |
2001-02-20 |
Astrazeneca Ab |
Compounds
|
ES2316546T3
(es)
|
2001-02-20 |
2009-04-16 |
Astrazeneca Ab |
2-arilamino-pirimidinas para el tratamiento de trastornos asociados a gsk3.
|
MXPA03007779A
(es)
|
2001-03-14 |
2004-11-12 |
Lilly Co Eli |
Moduladores de los receptores de retinoides x.
|
DE60227794D1
(de)
|
2001-04-26 |
2008-09-04 |
Eisai R&D Man Co Ltd |
Stickstoffhaltige verbindung mit kondensiertem ring und pyrazolylgruppe als substituent und medizinische zusammensetzung davon
|
WO2002096363A2
(en)
|
2001-05-30 |
2002-12-05 |
Alteon, Inc. |
Method for treating fibrotic diseases or other indications
|
WO2002096318A2
(en)
|
2001-05-30 |
2002-12-05 |
Alteon, Inc. |
Method for treating glaucoma v
|
HUP0400266A2
(hu)
|
2001-06-21 |
2004-08-30 |
Smithkline Beecham Corp. |
Imidazo[1,2-a]piridin-származékok, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk herpeszvírus-fertőzések megelőzésére vagy kezelésére
|
CA2450555A1
(en)
|
2001-06-25 |
2003-01-03 |
Merck & Co., Inc. |
(pyrimidyl)(phenyl)substituted fused heteroaryl p38 inhibiting and pkg kinase inhibiting compounds
|
IL159811A0
(en)
|
2001-07-13 |
2004-06-20 |
Neurogen Corp |
Heteroaryl substituted fused bicyclic heteroaryl compounds as gabaa receptor ligands
|
JP2005508955A
(ja)
|
2001-10-05 |
2005-04-07 |
スミスクライン ビーチャム コーポレーション |
ヘルペスウイルス感染の治療で使用されるためのイミダゾ−ピリジン誘導体
|
AU2003207646C1
(en)
|
2002-01-22 |
2008-09-18 |
Vanderbilt University |
Treating stress response with chemokine receptor CCR5 modulators
|
ES2276048T3
(es)
|
2002-03-05 |
2007-06-16 |
Eli Lilly And Company |
Derivados de purina como inhibidores de cinasa.
|
JP2003313126A
(ja)
|
2002-04-23 |
2003-11-06 |
Sankyo Co Ltd |
イミダゾピリジン誘導体を有効成分とする医薬
|
JP2004002826A
(ja)
|
2002-04-24 |
2004-01-08 |
Sankyo Co Ltd |
高分子イミダゾピリジン誘導体
|
CA2484631A1
(en)
|
2002-05-13 |
2003-11-27 |
Merck & Co., Inc. |
Phenyl substituted imidazopyridines and phenyl substituted benzimidazoles
|
US20040014957A1
(en)
|
2002-05-24 |
2004-01-22 |
Anne Eldrup |
Oligonucleotides having modified nucleoside units
|
JP2005539000A
(ja)
|
2002-07-31 |
2005-12-22 |
スミスクライン・ビーチャム・コーポレイション |
Alk5阻害剤としての2−フェニルピリジン−4−イル誘導体
|
GB0217783D0
(en)
|
2002-07-31 |
2002-09-11 |
Glaxo Group Ltd |
Compounds
|
EP1554272B1
(en)
|
2002-08-09 |
2006-10-25 |
Eli Lilly And Company |
Benzimidazoles and benzothiazoles as inhibitors of map kinase
|
AU2003255845A1
(en)
|
2002-08-22 |
2004-03-11 |
Piramed Limited |
Phosphadidylinositol 3,5-biphosphate inhibitors as anti-viral agents
|
UA80296C2
(en)
|
2002-09-06 |
2007-09-10 |
Biogen Inc |
Imidazolopyridines and methods of making and using the same
|
AU2003270489A1
(en)
|
2002-09-09 |
2004-03-29 |
Cellular Genomics, Inc. |
6-ARYL-IMIDAZO(1,2-a)PYRAZIN-8-YLAMINES, METHOD OF MAKING, AND METHOD OF USE THEREOF
|
EP1539749A4
(en)
|
2002-09-13 |
2007-06-13 |
Merck & Co Inc |
BY CONDENSED HETEROBICYCLOGRUPPEN SUBSTITUTED PHENYL COMPOUNDS AS METOBOTROPE GLUTAMATE-5 MODULATORS
|
ES2293068T3
(es)
|
2002-09-19 |
2008-03-16 |
Schering Corporation |
Imidazopiridinas como inhibidores de quinasas dependientes de ciclina.
|
US7576085B2
(en)
|
2002-09-23 |
2009-08-18 |
Schering Corporation |
Imidazopyrazines as cyclin dependent kinase inhibitors
|
CN1694706A
(zh)
|
2002-09-23 |
2005-11-09 |
先灵公司 |
用作依赖细胞周期蛋白的激酶抑制剂的新的咪唑并吡嗪
|
EP1543008B1
(en)
|
2002-09-23 |
2007-11-07 |
Schering Corporation |
Imidazopyrazines as cyclin dependent kinase inhibitors
|
AU2003271185A1
(en)
|
2002-10-15 |
2004-05-04 |
Takeda Pharmaceutical Company Limited |
Imidazopyridine derivative, process for producing the same, and use
|
ATE426600T1
(de)
*
|
2002-10-22 |
2009-04-15 |
Eisai R&D Man Co Ltd |
7-phenylpyrazolopyridinverbindungen
|
EP1576138B1
(en)
|
2002-11-15 |
2017-02-01 |
Idenix Pharmaceuticals LLC. |
2'-methyl nucleosides in combination with interferon and flaviviridae mutation
|
US20070004736A1
(en)
|
2002-11-22 |
2007-01-04 |
Keiji Kubo |
Imidazole derivative, process for producing the same, and use
|
WO2004063159A1
(ja)
|
2003-01-10 |
2004-07-29 |
Idemitsu Kosan Co., Ltd. |
含窒素複素環誘導体及びそれを用いた有機エレクトロルミネッセンス素子
|
WO2004072081A1
(en)
|
2003-02-10 |
2004-08-26 |
Cellular Genomics, Inc. |
Certain 8-heteroaryl-6-phenyl-imidazo[1,2-a]pyrazines as modulators of kinase activity
|
US7186832B2
(en)
|
2003-02-20 |
2007-03-06 |
Sugen Inc. |
Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
|
US7329668B2
(en)
|
2003-02-25 |
2008-02-12 |
Bristol-Myers Squibb Company |
Pyrazolopurine-based tricyclic compounds and pharmaceutical compositions comprising same
|
PA8595001A1
(es)
|
2003-03-04 |
2004-09-28 |
Pfizer Prod Inc |
Nuevos compuestos heteroaromaticos condensados que son inhibidores del factor de crecimiento transforante (tgf)
|
US7041671B2
(en)
|
2003-04-02 |
2006-05-09 |
Pfizer Inc |
Pyrrolo[1,2-b]pyridazine compounds and their uses
|
US20060100235A1
(en)
|
2003-04-11 |
2006-05-11 |
Novo Nordisk A/S |
Pharmaceutical use of substituted 1,2,4-triazoles
|
WO2004089416A2
(en)
|
2003-04-11 |
2004-10-21 |
Novo Nordisk A/S |
Combination of an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and an antihypertensive agent
|
US20060094699A1
(en)
|
2003-04-11 |
2006-05-04 |
Kampen Gita Camilla T |
Combination therapy using an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and a glucocorticoid receptor agonist to minimize the side effects associated with glucocorticoid receptor agonist therapy
|
WO2004103991A1
(fr)
|
2003-05-20 |
2004-12-02 |
'chemical Diversity Research Institute', Ltd. |
Piperidines 2-substituees, bibliotheque focalisee et composition pharmaceutique
|
WO2005020885A2
(en)
|
2003-05-21 |
2005-03-10 |
Isis Pharmaceuticals, Inc. |
Compositions and methods for the treatment of severe acute respiratory syndrome (sars)
|
EP1630152A4
(en)
|
2003-05-30 |
2009-09-23 |
Takeda Pharmaceutical |
CONNECTION WITH CONDENSED RING
|
WO2005014599A1
(en)
|
2003-06-04 |
2005-02-17 |
Cellular Genomics, Inc. |
Imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of bruton’s tyrosine kinase by such compounds
|
WO2005005429A1
(en)
|
2003-06-30 |
2005-01-20 |
Cellular Genomics, Inc. |
Certain heterocyclic substituted imidazo[1,2-a]pyrazin-8-ylamines and methods of inhibition of bruton’s tyrosine kinase by such compounds
|
EP2287166A3
(en)
|
2003-07-14 |
2011-06-22 |
Arena Pharmaceuticals, Inc. |
Fused-aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto
|
US7259164B2
(en)
|
2003-08-11 |
2007-08-21 |
Cgi Pharmaceuticals, Inc. |
Certain substituted imidazo[1,2-a]pyrazines, as modulators of kinase activity
|
KR100553752B1
(ko)
|
2003-10-13 |
2006-02-20 |
삼성에스디아이 주식회사 |
이미다졸 고리 함유 화합물 및 이를 이용한 유기 전계발광 소자
|
JP2007509960A
(ja)
|
2003-10-28 |
2007-04-19 |
セプラコア インコーポレーテッド |
イミダゾ[1,2−a]ピリジン抗不安薬
|
US20050288295A1
(en)
|
2003-11-11 |
2005-12-29 |
Currie Kevin S |
Certain imidazo[1,2-a]pyrazin-8-ylamines, method of making, and method of use thereof
|
US20090023737A1
(en)
|
2004-02-12 |
2009-01-22 |
Neurogen Corporation |
Imidazo-Pyridazines, Triazolo-Pyridazines and Related Benzodiazepine Receptor Ligands
|
US7306631B2
(en)
|
2004-03-30 |
2007-12-11 |
The Procter & Gamble Company |
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
|
JP2005343889A
(ja)
|
2004-05-06 |
2005-12-15 |
Taisho Pharmaceut Co Ltd |
イミダゾピリジン誘導体
|
DE602005013085D1
(de)
|
2004-06-09 |
2009-04-16 |
Oncalis Ag |
Proteinkinaseinhibitoren
|
GB0413605D0
(en)
|
2004-06-17 |
2004-07-21 |
Addex Pharmaceuticals Sa |
Novel compounds
|
US7718801B2
(en)
|
2004-08-31 |
2010-05-18 |
Banyu Pharmaceutical Co., Ltd. |
Substituted imidazole derivative
|
AU2005295734A1
(en)
|
2004-10-15 |
2006-04-27 |
Biogen Idec Ma Inc. |
Methods of treating vascular injuries
|
RU2007119637A
(ru)
|
2004-10-28 |
2008-12-10 |
Айрм Ллк (Bm) |
Соединения и композиции в качестве модуляторов hedgehog-пути
|
CN101098870B
(zh)
|
2004-11-08 |
2010-11-03 |
万有制药株式会社 |
新型稠环咪唑衍生物
|
MX2007005643A
(es)
|
2004-11-10 |
2008-03-13 |
Cgi Pharmaceuticals Inc |
Ciertas imidazo [1,2-a] pirazin-8-ilaminas, metodo para su elaboracion y metodo de uso de las mismas.
|
EP1838312A4
(en)
|
2004-12-17 |
2010-01-20 |
Smithkline Beecham Corp |
CHEMICAL COMPOUNDS
|
WO2006070943A1
(ja)
|
2004-12-28 |
2006-07-06 |
Takeda Pharmaceutical Company Limited |
縮合イミダゾール化合物およびその用途
|
AU2006218403A1
(en)
|
2005-03-03 |
2006-09-08 |
Sirtris Pharmaceuticals, Inc. |
Fused heterocyclic compounds and their use as sirtuin modulators
|
ATE424402T1
(de)
|
2005-03-21 |
2009-03-15 |
Lilly Co Eli |
Imidazopyridinverbindungen
|
US7666880B2
(en)
|
2005-03-21 |
2010-02-23 |
S*Bio Pte Ltd. |
Imidazo[1,2-A]pyridine derivatives: preparation and pharmaceutical applications
|
US20080255358A1
(en)
|
2005-03-24 |
2008-10-16 |
Mark James Bamford |
Derivatives of Imidazo [1,2-A] Pyridine Useful as Medicaments For Treating Gastrointestinal Diseases
|
US7557103B2
(en)
|
2005-04-05 |
2009-07-07 |
Eli Lilly And Company |
Imidazopyridazine compounds
|
US7572807B2
(en)
|
2005-06-09 |
2009-08-11 |
Bristol-Myers Squibb Company |
Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors
|
GB0513423D0
(en)
|
2005-06-30 |
2005-08-03 |
Glaxo Group Ltd |
Novel compounds
|
CA2611607A1
(en)
|
2005-07-11 |
2007-01-18 |
Novartis Ag |
Indolylmaleimide derivatives
|
US20100216798A1
(en)
|
2005-07-29 |
2010-08-26 |
Astellas Pharma Inc |
Fused heterocycles as lck inhibitors
|
US20070185063A1
(en)
|
2005-08-23 |
2007-08-09 |
Idenix Pharmaceuticals, Inc. |
Seven-membered ring nucleosides
|
WO2007025090A2
(en)
|
2005-08-25 |
2007-03-01 |
Kalypsys, Inc. |
Heterobicyclic and - tricyclic inhibitors of mapk/erk kinase
|
TW200800213A
(en)
|
2005-09-02 |
2008-01-01 |
Abbott Lab |
Novel imidazo based heterocycles
|
US7723336B2
(en)
|
2005-09-22 |
2010-05-25 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds useful as kinase modulators
|
US20070078136A1
(en)
|
2005-09-22 |
2007-04-05 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds useful as kinase modulators
|
ATE463495T1
(de)
|
2005-09-27 |
2010-04-15 |
Hoffmann La Roche |
Oxadiazolylpyrazolopyrimidine als mglur2- antagonisten
|
UY29826A1
(es)
|
2005-09-30 |
2007-04-30 |
Astrazeneca Ab |
Derivados de pirimidina, sales farmaceuticamente aceptables, esteres de los mismos hidrolisables in vivo, procesos de preparacion y aplicaciones
|
JO2769B1
(en)
|
2005-10-26 |
2014-03-15 |
جانسين فارماسوتيكا ان. في |
Rapid decomposition of physiologically antagonistic agents of the 2-dopamine receptor
|
EP1945644A2
(en)
|
2005-11-10 |
2008-07-23 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
US20070105864A1
(en)
|
2005-11-10 |
2007-05-10 |
Schering Corporation |
Methods for inhibiting protein kinases
|
EP1959962A2
(en)
|
2005-12-16 |
2008-08-27 |
Cytokinetics, Inc. |
Certain chemical entities, compositions, and methods
|
JP5498703B2
(ja)
|
2006-01-23 |
2014-05-21 |
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 |
プロテインキナーゼのインヒビターとして有用なチオフェン−カルボキサミド
|
JP2009524689A
(ja)
|
2006-01-25 |
2009-07-02 |
スミスクライン ビーチャム コーポレーション |
化合物
|
EP1993539A4
(en)
|
2006-03-02 |
2010-05-19 |
Glaxosmithkline Llc |
THIAZOLONE AS A PI3 KINASE INHIBITOR
|
TW200808802A
(en)
|
2006-06-06 |
2008-02-16 |
Schering Corp |
Imidazopyrazines as protein kinase inhibitors
|
US20090175852A1
(en)
|
2006-06-06 |
2009-07-09 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
ITVA20060041A1
(it)
|
2006-07-05 |
2008-01-06 |
Dialectica Srl |
Uso di composti derivati amminotiazolici, di loro composizioni farmaceutiche, nel trattamento di malattie caratterizzate dalla anormale repressione della trascrizione genica, particolarmente il morbo di huntington
|
BRPI0713187A2
(pt)
|
2006-07-20 |
2012-10-16 |
Mehmet Kahraman |
método de inibir rho-quinase, método de tratamento de doença mediada por rho-quinase, composto e composição farmacêutica
|
JP2009544723A
(ja)
|
2006-07-24 |
2009-12-17 |
スミスクライン・ビーチャム・コーポレイション |
Pi3キナーゼ阻害剤としてのチオゾリジンジオン誘導体
|
US7563797B2
(en)
|
2006-08-28 |
2009-07-21 |
Forest Laboratories Holding Limited |
Substituted imidazo(1,2-A)pyrimidines and imidazo(1,2-A) pyridines as cannabinoid receptor ligands
|
US20100144743A1
(en)
|
2006-09-05 |
2010-06-10 |
Board Of Regents, The University Of Texas System |
Compositions and methods for inhibition of tyrosine kinases
|
US8268809B2
(en)
|
2006-09-05 |
2012-09-18 |
Emory University |
Kinase inhibitors for preventing or treating pathogen infection and method of use thereof
|
US20110021513A1
(en)
|
2006-09-07 |
2011-01-27 |
Biogen Idec Ma Inc. |
Modulators of interleukin-1 receptor-associated kinase
|
JP2010505855A
(ja)
|
2006-10-06 |
2010-02-25 |
アボット・ラボラトリーズ |
新規なイミダゾチアゾール類およびイミダゾオキサゾール類
|
WO2008053285A1
(en)
|
2006-10-30 |
2008-05-08 |
Draximage Limited |
Methods for preparing 2-methoxyisobutylisonitrile and tetrakis(2-methoxyisobutylisonitrile)copper(i) tetrafluoroborate
|
WO2008057402A2
(en)
|
2006-11-02 |
2008-05-15 |
Cytovia, Inc. |
N-aryl-isoxazolopyrimidin-4-amines and related compounds as activators of caspases and inducers of apoptosis and the use thereof
|
MX2009005011A
(es)
|
2006-11-08 |
2009-05-20 |
Schering Corp |
Imidazopirazinas como inhibidores de proteina quinasa.
|
AU2007321922A1
(en)
|
2006-11-20 |
2008-05-29 |
Alantos Pharmaceuticals Holding, Inc. |
Heterobicyclic matrix metalloprotease inhibitors
|
US7622584B2
(en)
|
2006-11-24 |
2009-11-24 |
Samsung Mobile Display Co., Ltd. |
Imidazopyridine-based compound and organic light emitting diode including organic layer comprising the imidazopyridine-based compound
|
RU2469034C2
(ru)
|
2006-12-04 |
2012-12-10 |
Астразенека Аб |
Химические соединения
|
US7977336B2
(en)
|
2006-12-28 |
2011-07-12 |
Banyu Pharmaceutical Co. Ltd |
Aminopyrimidine derivatives as PLK1 inhibitors
|
JP5271917B2
(ja)
|
2007-01-12 |
2013-08-21 |
メルク・シャープ・アンド・ドーム・コーポレーション |
スピロクロマノン誘導体
|
US20080242862A1
(en)
|
2007-03-27 |
2008-10-02 |
Calderwood David J |
Novel imidazo based heterocycles
|
WO2008121687A2
(en)
|
2007-03-28 |
2008-10-09 |
Array Biopharma Inc. |
Imidazo[1,2-a]pyridine compounds as receptor tyrosine kinase inhibitors
|
PT2137184E
(pt)
|
2007-04-03 |
2013-08-01 |
Array Biopharma Inc |
Compostos imidazo[1,2-a]piridina como inibidores do receptor de tirosina quinase
|
BRPI0809567A2
(pt)
|
2007-04-10 |
2014-09-23 |
Lundbeck & Co As H |
Composto, composição farmacêutica, método para modular a atividade de um receptor de p2x7, para tratar uma condição responsiva à modulação do receptor de p2x7 em um paciente, para inibir a morte de células do gânglio retinal em um paciente, e para determinar a presença ou ausência do receptor de p2x7 em uma amostra, preparação farmacêutica acondiciaonada, e, uso de um composto
|
WO2008133192A1
(ja)
|
2007-04-19 |
2008-11-06 |
Takeda Pharmaceutical Company Limited |
縮合イミダゾール化合物およびその用途
|
WO2008134553A1
(en)
|
2007-04-26 |
2008-11-06 |
Xenon Pharmaceuticals Inc. |
Methods of using bicyclic compounds in treating sodium channel-mediated diseases
|
AU2008250328A1
(en)
|
2007-05-09 |
2008-11-20 |
Novartis Ag |
Substituted imidazopyridazines as PI3K lipid kinase inhibitors
|
DK2155758T3
(da)
|
2007-05-10 |
2012-11-05 |
Biocryst Pharm Inc |
Tetrahydrofuro[3,4-d]dioxolanforbindelser til anvendelse i behandlingen af virusinfektioner og cancer
|
CN101932580B
(zh)
|
2007-06-01 |
2013-05-22 |
葛兰素史密丝克莱恩有限责任公司 |
咪唑并吡啶激酶抑制剂
|
AR066958A1
(es)
|
2007-06-14 |
2009-09-23 |
Schering Corp |
Imidazopirazinas como inhibidores de proteina quinasa
|
KR101030007B1
(ko)
|
2007-06-15 |
2011-04-20 |
삼성모바일디스플레이주식회사 |
헤테로방향환 함유 화합물, 이의 제조 방법 및 이를 이용한유기 발광 소자
|
WO2009002534A1
(en)
|
2007-06-26 |
2008-12-31 |
Gilead Colorado, Inc. |
Imidazopyridinyl thiazolyl histone deacetylase inhibitors
|
FR2918061B1
(fr)
|
2007-06-28 |
2010-10-22 |
Sanofi Aventis |
Derives de 6-cycloamino-3-(pyridin-4-yl)imidazo°1,2-b!- pyridazine,leur preparation et leur application en therapeutique.
|
US8188083B2
(en)
|
2007-06-28 |
2012-05-29 |
Abbott Laboratories |
Triazolopyridazines
|
FR2918986B1
(fr)
|
2007-07-19 |
2009-09-04 |
Sanofi Aventis Sa |
Derives de 6-cycloamino-3-(pyridazin-4-yl)imidazo[1,2-b]- pyridazine, leur preparation et leur application en therapeutique
|
TW200904799A
(en)
|
2007-07-27 |
2009-02-01 |
Actelion Pharmaceuticals Ltd |
Trans-3-aza-bicyclo[3.1.0]hexane derivatives
|
BRPI0814874A2
(pt)
|
2007-07-31 |
2019-09-24 |
Schering Corp |
combinação de agente antimitótico e inibidor da aurora quinase como tratamento anticâncer.
|
AU2008287421A1
(en)
|
2007-08-10 |
2009-02-19 |
Glaxosmithkline Llc |
Nitrogen containing bicyclic chemical entities for treating viral infections
|
KR20100049589A
(ko)
|
2007-08-14 |
2010-05-12 |
바이엘 쉐링 파마 악티엔게젤샤프트 |
암 치료를 위한 융합된 이미다졸
|
WO2009023253A2
(en)
|
2007-08-15 |
2009-02-19 |
Arena Pharmaceuticals Inc. |
IMIDAZO[L,2-α]PYRIDINE DERIVATIVES AS MODULATORS OF THE 5-HT2A SEROTONIN RECEPTOR USEFUL FOR THE TREATMENT OF DISORDERS RELATED THERETO
|
GB0716292D0
(en)
|
2007-08-21 |
2007-09-26 |
Biofocus Dpi Ltd |
Imidazopyrazine compounds
|
US20110046127A1
(en)
|
2007-11-08 |
2011-02-24 |
Paolo Pevarello |
Imidazopyridazines for Use as Protein Kinase Inhibitors
|
EP2217069A4
(en)
|
2007-11-09 |
2012-03-14 |
Salk Inst For Biological Studi |
INHIBITORS OF NON-NUCLEOSIDE INHIBITORS OF THE REVERSE TRANSCRIPTASE
|
WO2009077334A1
(en)
|
2007-12-14 |
2009-06-25 |
F. Hoffmann-La Roche Ag |
Novel imidazo[1,2-a]pyridine and imidazo[1,2-b]pyridazine derivatives
|
EP2231660A1
(en)
|
2007-12-21 |
2010-09-29 |
Wyeth LLC |
Imidazo [1,2-a] pyridine compounds
|
CA2710458A1
(en)
|
2007-12-21 |
2009-07-09 |
Wyeth Llc |
Imidazo [1,2-b] pyridazine compounds as modulators of liver x receptors
|
WO2009081857A1
(ja)
|
2007-12-21 |
2009-07-02 |
Idemitsu Kosan Co., Ltd. |
有機エレクトロルミネッセンス素子
|
FR2926556B1
(fr)
|
2008-01-22 |
2010-02-19 |
Sanofi Aventis |
Derives de carboxamides n-azabicycliques, leur preparation et leur application en therapeutique
|
CA2710929A1
(en)
|
2008-01-28 |
2009-08-06 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
US8329697B2
(en)
|
2008-02-26 |
2012-12-11 |
Merck Sharp & Dohme Corp. |
Imidizo[1,2-A]pyrazines useful as AHCY hydrolase inhibitors
|
MX2010010151A
(es)
|
2008-03-20 |
2010-10-25 |
Amgen Inc |
Moduladores de cinasa aurora y metodo de uso.
|
DE102008017853A1
(de)
|
2008-04-09 |
2009-10-15 |
Merck Patent Gmbh |
Thienopyrimidine
|
TW201000107A
(en)
|
2008-04-09 |
2010-01-01 |
Infinity Pharmaceuticals Inc |
Inhibitors of fatty acid amide hydrolase
|
WO2009132135A1
(en)
|
2008-04-23 |
2009-10-29 |
Gilead Sciences, Inc. |
1' -substituted carba-nucleoside analogs for antiviral treatment
|
US8507488B2
(en)
*
|
2008-05-13 |
2013-08-13 |
Irm Llc |
Fused nitrogen containing heterocycles and compositions thereof as kinase inhibitors
|
WO2010036407A2
(en)
|
2008-05-15 |
2010-04-01 |
Biocryst Pharmaceuticals, Inc. |
Antiviral nucleoside analogs
|
JP5774982B2
(ja)
|
2008-05-19 |
2015-09-09 |
サノビオン ファーマシューティカルズ インクSunovion Pharmaceuticals Inc. |
イミダゾ[1,2−a]ピリジン化合物
|
MX2010012961A
(es)
|
2008-05-29 |
2011-03-03 |
Sirtris Pharmaceuticals Inc Star |
Imidazopiridina y analogos relacionados como moduladores de sirtuina.
|
AR072008A1
(es)
|
2008-06-13 |
2010-07-28 |
Merck & Co Inc |
Compuestos heterobiciclicos como agentes de inhibicion de quinasa p38
|
EP2297131A2
(en)
*
|
2008-06-25 |
2011-03-23 |
Envivo Pharmaceuticals, Inc. |
Di-substituted phenyl compounds as phosphodiesterase 10 inhibitors
|
EP2306836B1
(en)
|
2008-07-01 |
2016-09-07 |
PTC Therapeutics, Inc. |
Bmi-1 protein expression modulators
|
US8124764B2
(en)
|
2008-07-14 |
2012-02-28 |
Gilead Sciences, Inc. |
Fused heterocyclyc inhibitor compounds
|
WO2010011837A1
(en)
|
2008-07-24 |
2010-01-28 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds useful as kinase modulators
|
JP5576370B2
(ja)
|
2008-08-06 |
2014-08-20 |
ファイザー・インク |
Chk−1阻害剤としての6置換2−ヘテロシクリルアミノピラジン化合物
|
FR2934994B1
(fr)
|
2008-08-12 |
2010-09-17 |
Sanofi Aventis |
Derives de 2-alkyl-6cycloamino-3-(pyridin-4-yl)imidaz°1,2-b! pyridazine, leur preparation et leur application en therapeutique
|
US8198449B2
(en)
|
2008-09-11 |
2012-06-12 |
Bristol-Myers Squibb Company |
Compounds for the treatment of hepatitis C
|
US20120021519A1
(en)
|
2008-09-19 |
2012-01-26 |
Presidents And Fellows Of Harvard College |
Efficient induction of pluripotent stem cells using small molecule compounds
|
WO2010048149A2
(en)
|
2008-10-20 |
2010-04-29 |
Kalypsys, Inc. |
Heterocyclic modulators of gpr119 for treatment of disease
|
JP5416944B2
(ja)
|
2008-10-23 |
2014-02-12 |
ユー・ディー・シー アイルランド リミテッド |
有機電界発光素子
|
WO2010059838A2
(en)
|
2008-11-20 |
2010-05-27 |
Decode Genetics Ehf |
Pde4 inhibitors selective for the long form of pde4 for treating inflammation and avoiding side effects
|
WO2010059836A1
(en)
|
2008-11-20 |
2010-05-27 |
Decode Genetics Ehf |
Substituted aza-bridged bicyclics for cardiovascular and cns disease
|
GB0822981D0
(en)
|
2008-12-17 |
2009-01-21 |
Summit Corp Plc |
Compounds for treatment of duchenne muscular dystrophy
|
JP5210187B2
(ja)
|
2009-01-22 |
2013-06-12 |
ユー・ディー・シー アイルランド リミテッド |
有機電界発光素子
|
EP2210891A1
(en)
|
2009-01-26 |
2010-07-28 |
Domain Therapeutics |
New adenosine receptor ligands and uses thereof
|
WO2010088518A2
(en)
|
2009-01-31 |
2010-08-05 |
Kalypsys, Inc. |
Heterocyclic modulators of gpr119 for treatment of disease
|
US8367222B2
(en)
|
2009-02-27 |
2013-02-05 |
Idemitsu Kosan Co., Ltd. |
Organic electroluminescent device
|
WO2010108074A2
(en)
|
2009-03-20 |
2010-09-23 |
Amgen Inc. |
Inhibitors of pi3 kinase
|
US8604466B2
(en)
|
2009-03-24 |
2013-12-10 |
Idemitsu Kosan Co., Ltd. |
Organic electroluminescent element
|
EP2419429B1
(en)
|
2009-04-16 |
2014-03-26 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Imidazopyrazines as inhibitors of protein kinases
|
TW201107329A
(en)
|
2009-07-30 |
2011-03-01 |
Oncotherapy Science Inc |
Fused imidazole derivative having ttk inhibitory action
|
WO2011021520A1
(ja)
|
2009-08-19 |
2011-02-24 |
出光興産株式会社 |
芳香族アミン誘導体及びそれを用いた有機エレクトロルミネッセンス素子
|
MX2012004990A
(es)
*
|
2009-10-30 |
2012-06-12 |
Janssen Pharmaceutica Nv |
Deribados de imidazo [1,2-b] pirimideazina y su uso como inhibidores de la enzima fosfodiesterasa 10.
|
CN102596907B
(zh)
|
2009-11-16 |
2014-12-17 |
出光兴产株式会社 |
芳香族胺衍生物和使用其的有机电致发光元件
|
EP2526102B1
(en)
|
2010-01-22 |
2017-03-08 |
Fundación Centro Nacional de Investigaciones Oncológicas Carlos III |
Inhibitors of PI3 kinase
|
AR080754A1
(es)
*
|
2010-03-09 |
2012-05-09 |
Janssen Pharmaceutica Nv |
Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10
|
WO2012146644A1
(en)
|
2011-04-28 |
2012-11-01 |
Janssen Pharmaceutica Nv |
Salt of an inhibitor of phosphodiesterase 10 enzyme
|