US4242513A
(en)
|
1979-03-05 |
1980-12-30 |
Appleton Papers Inc. |
Lactone compounds containing a heterocyclic radical
|
DE3666434D1
(de)
|
1985-05-25 |
1989-11-23 |
Yoshitomi Pharmaceutical |
Oxodiazine compounds
|
WO1991000092A1
(en)
|
1989-06-13 |
1991-01-10 |
Smithkline Beecham Corporation |
Inhibition of interleukin-1 and tumor necrosis factor production by monocytes and/or macrophages
|
JPH04506215A
(ja)
|
1989-06-13 |
1992-10-29 |
スミスクライン・ビーチャム・コーポレイション |
モノカイン活性干渉
|
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
|
KR930700104A
(ko)
|
1990-06-12 |
1993-03-13 |
원본미기재 |
5-리프옥시게나제 및 사이클로옥시게나제 경로 개재된 질병의 억제
|
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
|
JPH11505524A
(ja)
|
1995-05-01 |
1999-05-21 |
藤沢薬品工業株式会社 |
イミダゾ1,2−aピリジンおよびイミダゾ1,2−aピリデジン誘導体、および骨吸収阻害剤としてのその用途
|
US6992188B1
(en)
|
1995-12-08 |
2006-01-31 |
Pfizer, Inc. |
Substituted heterocyclic derivatives
|
CN1080260C
(zh)
*
|
1996-06-25 |
2002-03-06 |
美国辉瑞有限公司 |
取代的吲哚衍生物以及它们作为iv型磷酸二酯酶(pde)和肿瘤坏死因子(tnf)抑制剂的用途
|
US20010007867A1
(en)
|
1999-12-13 |
2001-07-12 |
Yuhpyng L. Chen |
Substituted 6,5-hetero-bicyclic derivatives
|
JP2001511813A
(ja)
|
1997-02-18 |
2001-08-14 |
ニューロクライン バイオサイエンシーズ,インコーポレイテッド |
Crfレセプターアンタゴニストおよびそれらに関連する方法
|
AU6691798A
(en)
|
1997-03-07 |
1998-09-22 |
Metabasis Therapeutics, Inc. |
Novel indole and azaindole inhibitors of fructose-1,6-bisphosphatase
|
WO1999011643A1
(en)
|
1997-09-02 |
1999-03-11 |
Du Pont Pharmaceuticals 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
|
KR20030016222A
(ko)
|
2000-02-14 |
2003-02-26 |
니뽄 다바코 산교 가부시키가이샤 |
수술후 스트레스 예방ㆍ치료제
|
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
|
WO2002006286A2
(en)
|
2000-07-14 |
2002-01-24 |
Bristol-Myers Squibb Pharma Company |
IMIDAZO[1,2-a]PYRAZINES FOR THE TREATMENT OF NEUROLOGICAL DISORDERS
|
AU2001295992A1
(en)
|
2000-10-24 |
2002-05-06 |
Sankyo Company Limited |
Imidazopyridine derivatives
|
AU2002224927A1
(en)
|
2000-12-13 |
2002-06-24 |
Basf Aktiengesellschaft |
Use of substituted imidazoazines, novel imidazoazines, methods for the production thereof, and agents containing these compounds
|
MY134070A
(en)
|
2001-01-22 |
2007-11-30 |
Isis Pharmaceuticals 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
|
IL156784A0
(en)
|
2001-02-20 |
2004-02-08 |
Astrazeneca Ab |
2-arylamino-pyrimidines for the treatment of gsk3-related disorders
|
SE0100568D0
(sv)
|
2001-02-20 |
2001-02-20 |
Astrazeneca Ab |
Compounds
|
CA2438586A1
(en)
|
2001-03-14 |
2002-09-19 |
Eli Lilly And Company |
Retinoid x receptor modulators
|
EP1382603B1
(en)
|
2001-04-26 |
2008-07-23 |
Eisai R&D Management Co., Ltd. |
Nitrogenous fused-ring compound having pyrazolyl group as substituent and medicinal composition thereof
|
CA2448317A1
(en)
|
2001-05-30 |
2002-12-05 |
Alteon Inc. |
Method for treating glaucoma v
|
EP1406611A2
(en)
|
2001-05-30 |
2004-04-14 |
Alteon, Inc. |
Method for treating fibrotic diseases or other indications
|
PL366827A1
(en)
|
2001-06-21 |
2005-02-07 |
Smithkline Beecham Corporation |
Imidazo[1,2-a]pyridine derivatives for the prophylaxis and treatment of herpes viral infections
|
US7196095B2
(en)
|
2001-06-25 |
2007-03-27 |
Merck & Co., Inc. |
(Pyrimidinyl) (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
|
WO2003031446A1
(en)
|
2001-10-05 |
2003-04-17 |
Smithkline Beecham Corporation |
Imidazo-pyridine derivatives for use in the treatment of herpes viral infection
|
WO2003061659A1
(en)
|
2002-01-22 |
2003-07-31 |
Merck & Co., Inc. |
Treating stress response with chemokine receptor ccr5 modulators
|
KR100974770B1
(ko)
|
2002-03-05 |
2010-08-06 |
일라이 릴리 앤드 캄파니 |
키나제 억제제로서의 퓨린 유도체
|
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
|
AU2003229004A1
(en)
|
2002-05-13 |
2003-12-02 |
Merck & Co., Inc. |
Phenyl substituted imidazopyridines and phenyl substituted benzimidazoles
|
AU2003237249A1
(en)
|
2002-05-24 |
2003-12-12 |
Isis Pharmaceuticals, Inc. |
Oligonucleotides having modified nucleoside units
|
GB0217783D0
(en)
|
2002-07-31 |
2002-09-11 |
Glaxo Group Ltd |
Compounds
|
AR040726A1
(es)
|
2002-07-31 |
2005-04-20 |
Smithkline Beecham Corp |
Compuesto de 2- fenilpiridin-4-il-heterociclico, composicion farmaceutica que lo comprende y su uso para la fabricacion de un medicamento
|
US7320995B2
(en)
|
2002-08-09 |
2008-01-22 |
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
|
WO2004022562A1
(en)
|
2002-09-09 |
2004-03-18 |
Cellular Genomics, Inc. |
6-ARYL-IMIDAZO[1,2-a]PYRAZIN-8-YLAMINES, METHOD OF MAKING, AND METHOD OF USE THEREOF
|
JP2006503038A
(ja)
|
2002-09-13 |
2006-01-26 |
メルク エンド カムパニー インコーポレーテッド |
融合ヘテロビシクロ置換フェニル代謝型グルタミン酸−5修飾因子
|
MXPA05003058A
(es)
|
2002-09-19 |
2005-05-27 |
Schering Corp |
Nuevas imidazopiridinas como inhibidores de cinasa dependientes de ciclina.
|
CN1694886A
(zh)
|
2002-09-23 |
2005-11-09 |
先灵公司 |
作为周期素依赖性激酶抑制剂的咪唑并吡嗪
|
AU2003275031B2
(en)
|
2002-09-23 |
2006-08-17 |
Schering Corporation |
Novel imidazopyrazines as cyclin dependent kinase inhibitors
|
US7576085B2
(en)
|
2002-09-23 |
2009-08-18 |
Schering Corporation |
Imidazopyrazines as cyclin dependent kinase inhibitors
|
WO2004035579A1
(ja)
|
2002-10-15 |
2004-04-29 |
Takeda Pharmaceutical Company Limited |
イミダゾピリジン誘導体、その製造法および用途
|
BR0316363A
(pt)
|
2002-11-15 |
2005-10-04 |
Idenix Cayman Ltd |
Nucleosìdeos 2'-ramificado e mutação de flaviviridae
|
WO2004048363A1
(ja)
|
2002-11-22 |
2004-06-10 |
Takeda Pharmaceutical Company Limited |
イミダゾール誘導体、その製造法および用途
|
EP1582516B1
(en)
|
2003-01-10 |
2013-07-17 |
Idemitsu Kosan Co., Ltd. |
Nitrogenous heterocyclic derivative and organic electroluminescent element employing the same
|
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
|
WO2004075846A2
(en)
|
2003-02-25 |
2004-09-10 |
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)
|
CA2527691C
(en)
|
2003-05-30 |
2013-01-22 |
Takeda Pharmaceutical Company Limited |
Condensed ring compound
|
US7405295B2
(en)
|
2003-06-04 |
2008-07-29 |
Cgi Pharmaceuticals, Inc. |
Certain 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
|
EP2287165A3
(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
|
WO2005047290A2
(en)
|
2003-11-11 |
2005-05-26 |
Cellular Genomics Inc. |
Imidazo[1,2-a] pyrazin-8-ylamines as kinase inhibitors
|
WO2005080355A1
(en)
|
2004-02-12 |
2005-09-01 |
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
|
WO2005120513A1
(en)
|
2004-06-09 |
2005-12-22 |
Oncalis Ag |
Protein kinase inhibitors
|
GB0413605D0
(en)
|
2004-06-17 |
2004-07-21 |
Addex Pharmaceuticals Sa |
Novel compounds
|
MXPA06014699A
(es)
*
|
2004-07-05 |
2007-03-26 |
Astellas Pharma Inc |
Derivados de pirazolo-piridina.
|
JP4972804B2
(ja)
|
2004-08-31 |
2012-07-11 |
Msd株式会社 |
新規置換イミダゾール誘導体
|
EP1804801A2
(en)
|
2004-10-15 |
2007-07-11 |
Biogen Idec MA, Inc. |
Methods of treating vascular injuries
|
CA2583812A1
(en)
|
2004-10-28 |
2006-05-11 |
Irm Llc |
Compounds and compositions as hedgehog pathway modulators
|
CA2586259A1
(en)
|
2004-11-08 |
2006-05-11 |
Banyu Pharmaceutical Co., Ltd. |
Novel fused imidazole derivative
|
WO2006053121A2
(en)
|
2004-11-10 |
2006-05-18 |
Cgi Pharmaceuticals, Inc. |
Imidazo[1 , 2-a] pyrazin-8-ylamines useful as modulators of kinase activity
|
AU2005323311A1
(en)
*
|
2004-11-23 |
2006-07-13 |
Venkateswara Rao Batchu |
Novel bicyclic heterocyclic compounds, process for their preparation and compositions containing them
|
JP2008524255A
(ja)
|
2004-12-17 |
2008-07-10 |
スミスクライン ビーチャム コーポレーション |
化学物質
|
US20080167314A1
(en)
|
2004-12-28 |
2008-07-10 |
Osamu Uchikawa |
Condensed Imidazole Compound And Use Thereof
|
CA2599987A1
(en)
|
2005-03-03 |
2006-09-08 |
Sirtris Pharmaceuticals, Inc. |
Fused heterocyclic compounds and their use as sirtuin modulators
|
US7666880B2
(en)
|
2005-03-21 |
2010-02-23 |
S*Bio Pte Ltd. |
Imidazo[1,2-A]pyridine derivatives: preparation and pharmaceutical applications
|
BRPI0608857A2
(pt)
*
|
2005-03-21 |
2012-08-28 |
Lilly Co Eli |
composto, e, composição farmacêutica
|
WO2006100119A1
(en)
|
2005-03-24 |
2006-09-28 |
Glaxo Group Limited |
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
|
KR20080023732A
(ko)
|
2005-07-11 |
2008-03-14 |
노파르티스 아게 |
인돌릴말레이미드 유도체
|
WO2007013673A1
(en)
|
2005-07-29 |
2007-02-01 |
Astellas Pharma Inc. |
Fused heterocycles as lck inhibitors
|
WO2007025043A2
(en)
|
2005-08-23 |
2007-03-01 |
Idenix Pharmaceuticals, Inc. |
Seven-membered ring nucleosides
|
US20070049591A1
(en)
|
2005-08-25 |
2007-03-01 |
Kalypsys, Inc. |
Inhibitors of MAPK/Erk Kinase
|
TW200800213A
(en)
|
2005-09-02 |
2008-01-01 |
Abbott Lab |
Novel imidazo based heterocycles
|
US20070078136A1
(en)
*
|
2005-09-22 |
2007-04-05 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds useful as kinase modulators
|
US7723336B2
(en)
|
2005-09-22 |
2010-05-25 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds useful as kinase modulators
|
CN101273040B
(zh)
|
2005-09-27 |
2011-11-09 |
弗·哈夫曼-拉罗切有限公司 |
作为mglur2拮抗剂的*二唑基吡唑并嘧啶类化合物
|
KR20080049130A
(ko)
|
2005-09-30 |
2008-06-03 |
아스트라제네카 아베 |
세포 증식 억제 활성을 갖는 이미다조 [1,2-a] 피리딘
|
JO2769B1
(en)
|
2005-10-26 |
2014-03-15 |
جانسين فارماسوتيكا ان. في |
Rapid decomposition of physiologically antagonistic agents of the 2-dopamine receptor
|
JP2009515882A
(ja)
|
2005-11-10 |
2009-04-16 |
シェーリング コーポレイション |
プロテインキナーゼを阻害するための方法
|
KR20080074963A
(ko)
|
2005-11-10 |
2008-08-13 |
쉐링 코포레이션 |
단백질 키나제 억제제로서의 이미다조피라진
|
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
|
US20100227880A1
(en)
|
2006-01-25 |
2010-09-09 |
Kristjan Gudmundsson |
Chemical compounds
|
US20090203732A1
(en)
|
2006-03-02 |
2009-08-13 |
Dashyant Dhanak |
Thiazolones for Use as P13 Kinase Inhibitors
|
US20090176829A1
(en)
*
|
2006-05-02 |
2009-07-09 |
Pfizer Inc |
Bicyclic heteroaryl compounds as pde10 inhibitors
|
US20090175852A1
(en)
|
2006-06-06 |
2009-07-09 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
AR061229A1
(es)
|
2006-06-06 |
2008-08-13 |
Schering Corp |
Imidazopirazinas como inhibidores de la proteina quinasa
|
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
|
WO2008014219A2
(en)
|
2006-07-24 |
2008-01-31 |
Smithkline Beecham Corporation |
Thiozolidinedione derivatives as p13 kinase inhibitors
|
WO2008027812A2
(en)
|
2006-08-28 |
2008-03-06 |
Forest Laboratories Holdings Limited |
Imidazopyridine and imidazopyrimidine derivatives
|
US20100144743A1
(en)
|
2006-09-05 |
2010-06-10 |
Board Of Regents, The University Of Texas System |
Compositions and methods for inhibition of tyrosine kinases
|
CA2662677C
(en)
|
2006-09-05 |
2016-05-31 |
Emory University |
Kinase inhibitors for preventing or treating pathogen infection and method of use thereof
|
JP2010502716A
(ja)
|
2006-09-07 |
2010-01-28 |
バイオジェン・アイデック・エムエイ・インコーポレイテッド |
インターロイキン1受容体関連キナーゼの調節物質
|
MX2009003650A
(es)
|
2006-10-06 |
2009-04-22 |
Abbott Lab |
Nuevos imidazotiazoles e imidazoxazoles.
|
CA2612656A1
(en)
|
2006-10-30 |
2008-04-30 |
Draxis Specialty Pharmaceuticals Inc. |
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
|
EP2079746A2
(en)
|
2006-11-08 |
2009-07-22 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
CA2670042A1
(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
|
EP2102199B1
(en)
|
2006-12-04 |
2011-04-27 |
AstraZeneca AB |
Antibacterial polycyclic urea compounds
|
US7977336B2
(en)
|
2006-12-28 |
2011-07-12 |
Banyu Pharmaceutical Co. Ltd |
Aminopyrimidine derivatives as PLK1 inhibitors
|
WO2008088692A2
(en)
|
2007-01-12 |
2008-07-24 |
Merck & Co., Inc. |
Spirochromanon derivatives
|
US20080242862A1
(en)
|
2007-03-27 |
2008-10-02 |
Calderwood David J |
Novel imidazo based heterocycles
|
US20100144751A1
(en)
|
2007-03-28 |
2010-06-10 |
Array Biopharma Inc. |
IMIDAZO[1,2-a]PYRIDINE COMPOUNDS AS RECEPTOR TYROSINE KINASE INHIBITORS
|
MY157724A
(en)
|
2007-04-03 |
2016-07-15 |
Array Biopharma Inc |
IMIDAZO[1,2-a]PYRIDINE COMPOUNDS AS RECEPTOR TYROSINE KINASE INHIBITORS
|
MX2009010523A
(es)
|
2007-04-10 |
2009-12-15 |
Lundbeck & Co As H |
Análogos de amidas heteroarílicas como antagonistas de p2x7.
|
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
|
JP2011513195A
(ja)
|
2007-05-10 |
2011-04-28 |
バイオクライスト ファーマシューティカルズ, インコーポレイテッド |
ウイルス感染およびがんの処置に使用するためのテトラヒドロフロ[3,4−d]ジオキソラン化合物
|
EP2162454B1
(en)
|
2007-06-01 |
2013-01-02 |
GlaxoSmithKline LLC |
Imidazopyridine kinase inhibitors
|
CN101772500A
(zh)
|
2007-06-14 |
2010-07-07 |
先灵公司 |
作为蛋白质激酶抑制剂的咪唑并吡嗪
|
KR101030007B1
(ko)
|
2007-06-15 |
2011-04-20 |
삼성모바일디스플레이주식회사 |
헤테로방향환 함유 화합물, 이의 제조 방법 및 이를 이용한유기 발광 소자
|
EP2170882A1
(en)
|
2007-06-26 |
2010-04-07 |
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.
|
EP2170337A4
(en)
|
2007-06-28 |
2013-12-18 |
Abbvie Inc |
NEW TRIAZOLOPYRIDAZINE
|
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
|
ATE493386T1
(de)
|
2007-07-27 |
2011-01-15 |
Actelion Pharmaceuticals Ltd |
Trans-3-aza-bicyclo-ä3.1.0ü-hexan-derivate
|
JP2010535201A
(ja)
|
2007-07-31 |
2010-11-18 |
シェーリング コーポレイション |
抗癌治療としての抗有糸***薬およびオーロラキナーゼ阻害薬
|
CN101842098A
(zh)
|
2007-08-10 |
2010-09-22 |
基因实验室技术有限公司 |
用于治疗病毒感染的含氮的二环化学实体
|
DE602008005894D1
(de)
|
2007-08-14 |
2011-05-12 |
Bayer Schering Pharma Ag |
Kondensierte imidazole zur krebsbehandlung
|
EP2190844B3
(en)
|
2007-08-15 |
2013-07-17 |
Arena Pharmaceuticals, Inc. |
Imidazo[1,2-a]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
|
CA2704645A1
(en)
|
2007-11-09 |
2009-05-14 |
The Salk Institute For Biological Studies |
Non-nucleoside reverse transcriptase inhibitors
|
CA2708361C
(en)
|
2007-12-14 |
2016-06-07 |
F. Hoffmann-La Roche Ag |
Novel imidazo[1,2-a]pyridine and imidazo[1,2-b]pyridazine derivatives
|
CN101904028A
(zh)
|
2007-12-21 |
2010-12-01 |
出光兴产株式会社 |
有机电致发光元件
|
US20110112135A1
(en)
|
2007-12-21 |
2011-05-12 |
Singhaus Jr Robert Ray |
Imidazo [1,2-A] Pyridine Compounds
|
JP2011507902A
(ja)
|
2007-12-21 |
2011-03-10 |
ワイス・エルエルシー |
肝臓X受容体のモジュレーターとしてのイミダゾ[1,2−b]ピリダジン化合物
|
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
|
WO2009108546A1
(en)
|
2008-02-26 |
2009-09-03 |
Merck & Co., Inc. |
Ahcy hydrolase inhibitors for treatment of hyper homocysteinemia
|
AU2009226024B2
(en)
|
2008-03-20 |
2012-07-12 |
Amgen Inc. |
Aurora kinase modulators and method of use
|
WO2009126691A1
(en)
|
2008-04-09 |
2009-10-15 |
Infinity Pharmaceuticals, Inc |
Inhibitors of fatty acid amide hydrolase
|
DE102008017853A1
(de)
|
2008-04-09 |
2009-10-15 |
Merck Patent Gmbh |
Thienopyrimidine
|
DK2280973T3
(da)
|
2008-04-23 |
2013-03-04 |
Gilead Sciences Inc |
Carbanukleosidanaloge til antiviral behandling
|
WO2010036407A2
(en)
|
2008-05-15 |
2010-04-01 |
Biocryst Pharmaceuticals, Inc. |
Antiviral nucleoside analogs
|
CA2724842A1
(en)
|
2008-05-19 |
2009-11-26 |
Sunovion Pharmaceuticals Inc. |
Imidazo[1,2-a]pyridine compounds
|
AR072008A1
(es)
|
2008-06-13 |
2010-07-28 |
Merck & Co Inc |
Compuestos heterobiciclicos como agentes de inhibicion de quinasa p38
|
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
|
CN102164604A
(zh)
|
2008-07-24 |
2011-08-24 |
百时美施贵宝公司 |
用作激酶调节剂的稠合杂环化合物
|
ES2378513T3
(es)
|
2008-08-06 |
2012-04-13 |
Pfizer Inc. |
Compuestos 2-heterociclilamino piracinas sustituidas en posición 6 como inhibidores de CHK-1
|
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
|
WO2010033906A2
(en)
|
2008-09-19 |
2010-03-25 |
President 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
|
WO2010059836A1
(en)
|
2008-11-20 |
2010-05-27 |
Decode Genetics Ehf |
Substituted aza-bridged bicyclics for cardiovascular and cns disease
|
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
|
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
|
MX2011009796A
(es)
|
2009-03-20 |
2011-12-14 |
Amgen Inc |
Inhibidores de la cinasa pi3.
|
WO2010110277A1
(ja)
|
2009-03-24 |
2010-09-30 |
出光興産株式会社 |
有機エレクトロルミネッセンス素子
|
KR101792837B1
(ko)
|
2009-04-16 |
2017-11-02 |
푼다시온 센트로 나시오날 드 인베스티가시오네스 온콜로기카스 카를로스Ⅲ |
키나아제 억제제로서 사용을 위한 이미다조피라진
|
TW201107329A
(en)
|
2009-07-30 |
2011-03-01 |
Oncotherapy Science Inc |
Fused imidazole derivative having ttk inhibitory action
|
EP2468725B1
(en)
|
2009-08-19 |
2019-07-17 |
Idemitsu Kosan Co., Ltd. |
Aromatic amine derivatives and organic electroluminescent elements using same
|
CN102596961B
(zh)
*
|
2009-10-30 |
2015-12-02 |
詹森药业有限公司 |
咪唑并[1,2-b]哒嗪衍生物及其作为PDE10抑制剂的用途
|
WO2011059099A1
(ja)
|
2009-11-16 |
2011-05-19 |
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
|
US9073927B2
(en)
|
2010-01-22 |
2015-07-07 |
Fundacion Centro Nacional De Investigaciones Oncologicas 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
|