EP0010061B1
(en)
|
1978-09-25 |
1983-07-13 |
Stuart John Mc Farlane |
Pharmaceutical preparations containing a mollusc extract
|
JP2602037B2
(ja)
|
1987-10-31 |
1997-04-23 |
持田製薬株式会社 |
1−アシル−2,3−ジヒドロ−4(1h)−キノリノン−4−オキシム誘導体、その製法およびそれらを主成分とする利尿、降圧、抗浮腫および腹水除去用医薬組成物
|
GB8814277D0
(en)
|
1988-06-16 |
1988-07-20 |
Glaxo Group Ltd |
Chemical compounds
|
JPH02264757A
(ja)
|
1989-04-06 |
1990-10-29 |
Nippon Steel Chem Co Ltd |
ニトロインドール類の製造方法
|
US5210092A
(en)
|
1990-09-25 |
1993-05-11 |
Fujisawa Pharmaceutical Co., Ltd. |
Angiotensin ii antagonizing heterocyclic derivatives
|
US5215994A
(en)
|
1990-09-25 |
1993-06-01 |
Fujisawa Pharmaceutical Co., Ltd. |
Angiotenin II antagonizing heterocyclic derivatives
|
US5354759A
(en)
|
1991-09-12 |
1994-10-11 |
Fujisawa Pharmaceutical Co., Ltd. |
Angiotenin II antagonizing heterocyclic compounds
|
WO1993006082A1
(en)
|
1991-09-13 |
1993-04-01 |
Merck & Co., Inc. |
Process for the preparation of 4-substituted-1,4-dihydropyridines
|
DE4136489A1
(de)
|
1991-11-06 |
1993-05-13 |
Bayer Ag |
Neue diethylentriamin-derivate und deren verwendung zu diagnostischen und therapeutischen zwecken
|
TW212798B
(xx)
|
1991-11-25 |
1993-09-11 |
Takeda Pharm Industry Co Ltd |
|
EP0545478A1
(en)
|
1991-12-03 |
1993-06-09 |
MERCK SHARP & DOHME LTD. |
Heterocyclic compounds as tachykinin antagonists
|
AU658729B2
(en)
|
1992-03-27 |
1995-04-27 |
Kyoto Pharmaceutical Industries, Ltd. |
3-(1H-imidazol-1-ylmethyl)-1H-indole derivatives
|
JP3229654B2
(ja)
|
1992-06-05 |
2001-11-19 |
ティーディーケイ株式会社 |
有機el素子用化合物および有機el素子
|
CA2116863A1
(en)
|
1992-07-03 |
1994-01-20 |
Sumio Yokota |
Condensed heterocyclic derivatives and herbicides
|
GB2271991A
(en)
|
1992-11-02 |
1994-05-04 |
Merck Sharp & Dohme |
N-(2-oxo-1H-1,4-benzodiazepin-3-yl)-ureas
|
EP0639573A1
(de)
|
1993-08-03 |
1995-02-22 |
Hoechst Aktiengesellschaft |
Benzokondensierte 5-Ringheterocyclen, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament, ihre Verwendung als Diagnostikum, sowie sie enthaltendes Medikament
|
US5354763A
(en)
|
1993-11-17 |
1994-10-11 |
American Home Products Corporation |
Substituted N-heteroaryl and N-aryl-1,2-diaminocyclobutene-3,4-diones
|
CN1067386C
(zh)
|
1994-02-10 |
2001-06-20 |
辉瑞大药厂 |
作为苯并二氮杂䓬受体位的兴奋剂和拮抗药的5-杂芳基吲哚衍生物
|
RU2152385C1
(ru)
|
1994-07-27 |
2000-07-10 |
Санкио Компани Лимитед |
Гетероциклические соединения, применимые в качестве аллостерических эффекторов при мускариновых рецепторах
|
FR2723739B1
(fr)
|
1994-08-19 |
1997-02-14 |
Sanofi Sa |
Derives de glycinamide, procedes pour leur preparation et medicaments les contenant.
|
JPH08225535A
(ja)
|
1994-11-15 |
1996-09-03 |
Dai Ichi Seiyaku Co Ltd |
インダゾール誘導体
|
EP0717143A1
(de)
|
1994-12-16 |
1996-06-19 |
Lignozym GmbH |
Mehrkomponentensystem zum Verändern, Abbau oder Bleichen von Lignin, ligninhaltigen Materialien oder ähnlichen Stoffen sowie Verfahren zu seiner Anwendung
|
ES2175079T3
(es)
|
1995-04-10 |
2002-11-16 |
Fujisawa Pharmaceutical Co |
Derivados de indol utiles como inhibidores de cgmp-pde.
|
WO1997010214A1
(fr)
|
1995-09-14 |
1997-03-20 |
Shionogi & Co., Ltd. |
Nouveaux derives d'acide phenylacetique et compositions medicinales les contenant
|
US6069162A
(en)
|
1996-05-27 |
2000-05-30 |
Fujisawa Pharmaceutical Co., Ltd. |
Indolyl and benzofuranyl carboxamides as inhibitors of nitric oxide production
|
US5629325A
(en)
|
1996-06-06 |
1997-05-13 |
Abbott Laboratories |
3-pyridyloxymethyl heterocyclic ether compounds useful in controlling chemical synaptic transmission
|
US5861398A
(en)
|
1996-08-26 |
1999-01-19 |
Alanex Corporation |
Benzoperimidine-carboxylic acids and derivatives thereof
|
WO1998043969A1
(en)
|
1997-03-31 |
1998-10-08 |
Dupont Pharmaceuticals Company |
Indazoles of cyclic ureas useful as hiv protease inhibitors
|
SE9704544D0
(sv)
|
1997-12-05 |
1997-12-05 |
Astra Pharma Prod |
Novel compounds
|
SE9704545D0
(sv)
|
1997-12-05 |
1997-12-05 |
Astra Pharma Prod |
Novel compounds
|
JP2002515891A
(ja)
|
1997-12-19 |
2002-05-28 |
スミスクライン・ビーチャム・コーポレイション |
新規なピペリジン含有化合物
|
EP1047692B1
(en)
|
1998-01-14 |
2004-07-21 |
The Uab Research Foundation |
Methods of synthesizing and screening inhibitors of bacterial nad synthetase enzyme, compounds thereof and methods of treating bacterial and microbial infections with these inhibitors
|
CA2260499A1
(en)
|
1998-01-29 |
1999-07-29 |
Sumitomo Pharmaceuticals Company Limited |
Pharmaceutical compositions for the treatment of ischemic brain damage
|
WO1999059973A1
(en)
|
1998-05-15 |
1999-11-25 |
Guilford Pharmaceuticals Inc. |
Carboxamide compounds, compositions, and methods for inhibiting parp activity
|
AU4981199A
(en)
|
1998-07-08 |
2000-02-01 |
Gregory N. Beatch |
Compositions and methods for modulating sexual activity
|
RU2237663C2
(ru)
|
1998-07-15 |
2004-10-10 |
Тейдзин Лимитед |
Производное тиобензимидазола и содержащие его фармацевтические композиции
|
DE19842354A1
(de)
|
1998-09-16 |
2000-03-23 |
Bayer Ag |
Isothiazolcarbonsäureamide
|
FR2783520B1
(fr)
|
1998-09-21 |
2000-11-10 |
Oreal |
Nouveaux 4-hydroxyindoles cationiques, leur utilisation pour la teinture d'oxydation des fibres keratiniques, compositions tinctoriales et procede de teinture
|
AU1738900A
(en)
|
1998-11-19 |
2000-06-05 |
Nortran Pharmaceuticals Inc. |
Serotonin ligands as pro-erectile compounds
|
AR021509A1
(es)
|
1998-12-08 |
2002-07-24 |
Lundbeck & Co As H |
Derivados de benzofurano, su preparacion y uso
|
CZ27399A3
(cs)
|
1999-01-26 |
2000-08-16 |
Ústav Experimentální Botaniky Av Čr |
Substituované dusíkaté heterocyklické deriváty, způsob jejich přípravy, tyto deriváty pro použití jako léčiva, farmaceutická kompozice a kombinovaný farmaceutický přípravek tyto deriváty obsahující a použití těchto derivátů pro výrobu léčiv
|
WO2001032621A1
(fr)
|
1999-10-29 |
2001-05-10 |
Wakunaga Pharmaceutical Co., Ltd. |
Nouveaux derives d'indole, et medicaments contenant lesdits derives comme principe actif
|
CN1105722C
(zh)
|
1999-11-12 |
2003-04-16 |
中国科学院上海药物研究所 |
含氮杂环基的青蒿素衍生物及其制备方法
|
EP1289958A2
(en)
|
2000-05-22 |
2003-03-12 |
Leo Pharma A/S |
BENZOPHENONES AS INHIBITORS OF IL-1$g(b) AND TNF-$g(a)
|
US6995268B2
(en)
|
2000-06-20 |
2006-02-07 |
Wayne State University |
N- and O-substituted 4-[2-(diphenylmethoxy)-ethyl]-1- (phenyl) methyl) piperidine analogs and methods of treating CNS disorders therewith
|
JP2002017387A
(ja)
|
2000-07-06 |
2002-01-22 |
Mitsubishi Rayon Co Ltd |
インドール誘導体の製造法
|
JP2002017386A
(ja)
|
2000-07-06 |
2002-01-22 |
Mitsubishi Rayon Co Ltd |
インドール−3−カルボン酸誘導体の製造法
|
WO2002018363A2
(en)
|
2000-08-29 |
2002-03-07 |
Abbott Laboratories |
3-phenyl-propanoic acid derivatives as protein tyrosine phosphatase inhibitors
|
DE10046934A1
(de)
|
2000-09-21 |
2002-04-18 |
Consortium Elektrochem Ind |
Verfahren zur fermentativen Herstellung von nicht-proteinogenen L-Aminosäuren
|
JP2004512335A
(ja)
|
2000-10-25 |
2004-04-22 |
アストラゼネカ アクチボラグ |
キナゾリン誘導体
|
BR0115077A
(pt)
|
2000-11-01 |
2003-12-23 |
Merck Patent Ges Mit Beschroen |
Métodos e composições para o tratamento de doenças dos olhos
|
AU2002239277A1
(en)
|
2000-11-20 |
2002-05-27 |
Cor Therapeutics, Inc. |
Adenine based inhibitors of adenylyl cyclase, pharmaceutical compositions and method of use thereof
|
US6387992B1
(en)
|
2000-11-27 |
2002-05-14 |
Ciba Specialty Chemicals Corporation |
Substituted 5-heteroaryl-2-(2-hydroxyphenyl)-2h-benzotriazole UV absorbers, a process for preparation thereof and compositions stabilized therewith
|
GB0031315D0
(en)
|
2000-12-21 |
2001-02-07 |
Glaxo Group Ltd |
Indole derivatives
|
US20040087620A1
(en)
|
2001-01-18 |
2004-05-06 |
Tatsuo Tsuri |
Terphenyl compounds bearing substituted amino groups
|
US20040087604A1
(en)
|
2001-01-22 |
2004-05-06 |
Tatsuo Tsuri |
Hetero-tricyclic compounds having substituted amino groups
|
MXPA03006950A
(es)
|
2001-02-02 |
2003-11-18 |
Schering Corp |
Ciclobuteno-1,2-dionas 3,4-disustituidas como antagonistas de receptor de quimiocina cxc.
|
WO2002072549A1
(en)
|
2001-03-12 |
2002-09-19 |
Millennium Pharmaceuticals, Inc. |
Functionalized heterocycles as modulators of chemokine receptor function and methods of use therefor
|
GB0106586D0
(en)
|
2001-03-16 |
2001-05-09 |
Smithkline Beecham Plc |
Novel compounds
|
CA2444031C
(en)
|
2001-04-16 |
2012-02-21 |
Schering Corporation |
3,4-di-substituted cyclobutene-1,2-diones as cxc-chemokine receptor ligands
|
US7199147B2
(en)
|
2001-06-12 |
2007-04-03 |
Dainippon Sumitomo Pharma Co., Ltd. |
Rho kinase inhibitors
|
DE60221391T2
(de)
*
|
2001-06-20 |
2008-04-17 |
Wyeth |
Substituierte indolsäurederivate als inhibitoren von plasminogen-aktivator-inhibitor-1 (pai-1)
|
EP1844771A3
(en)
|
2001-06-20 |
2007-11-07 |
Wyeth |
Substituted indole acid derivatives as inhibitors of plasminogen activator inhibitor-1 (PAI-1)
|
WO2003004027A1
(en)
|
2001-07-05 |
2003-01-16 |
Synaptic Pharmaceutical Corporation |
Substituted anilinic piperidines as mch selective antagonists
|
BR0211604A
(pt)
|
2001-08-01 |
2004-08-24 |
Merck Patent Gmbh |
Inibidores de integrina para o tratamento de doenças do olho
|
CA2459224C
(en)
|
2001-09-03 |
2012-05-08 |
Takeda Chemical Industries, Ltd. |
1,3-benzothiazinone derivatives and the use thereof
|
CN1599734A
(zh)
|
2001-10-12 |
2005-03-23 |
先灵公司 |
作为cxc趋化因子受体拮抗剂的3,4-二取代的马来酰亚胺化合物
|
EP1441725A1
(en)
|
2001-10-26 |
2004-08-04 |
Aventis Pharmaceuticals Inc. |
Benzimidazoles and analogues and their use as protein kinases inhibitors
|
FR2831536A1
(fr)
|
2001-10-26 |
2003-05-02 |
Aventis Pharma Sa |
Nouveaux derives de benzimidazoles, leur procede de preparation, leur application a titre de medicament, compositions pharmaceutiques et nouvelle utilisation notamment comme inhibiteurs de kdr
|
WO2003035005A2
(en)
|
2001-10-26 |
2003-05-01 |
University Of Connecticut |
Heteroindanes: a new class of potent cannabimimetic ligands
|
US20030187026A1
(en)
|
2001-12-13 |
2003-10-02 |
Qun Li |
Kinase inhibitors
|
US6933316B2
(en)
|
2001-12-13 |
2005-08-23 |
National Health Research Institutes |
Indole compounds
|
SE0104331D0
(sv)
|
2001-12-19 |
2001-12-19 |
Astrazeneca Ab |
Novel compounds
|
JP2003192716A
(ja)
|
2001-12-27 |
2003-07-09 |
Mitsui Chemicals Inc |
オレフィン重合用触媒および該触媒を用いたオレフィンの重合方法
|
ATE420847T1
(de)
|
2002-02-21 |
2009-01-15 |
Asahi Kasei Pharma Corp |
Substituiertes phenylalkansäurederivat und dessen verwendung
|
JP2005532280A
(ja)
*
|
2002-04-03 |
2005-10-27 |
アストラゼネカ アクチボラグ |
化合物
|
JP2005530804A
(ja)
|
2002-05-14 |
2005-10-13 |
ベイラー カレッジ オブ メディスン |
Her2発現の小分子阻害剤
|
WO2003099206A2
(en)
|
2002-05-21 |
2003-12-04 |
Bristol-Myers Squibb Company |
Indole compounds useful as impdh inhibitors
|
AU2003281205A1
(en)
|
2002-07-09 |
2004-01-23 |
Fujisawa Pharmaceutical Co., Ltd. |
Remedy for urinary frequency and urinary incontinence
|
US6972336B2
(en)
|
2002-07-18 |
2005-12-06 |
Novartis Ag |
N-alkylation of indole derivatives
|
AU2003255767A1
(en)
|
2002-08-10 |
2004-02-25 |
Astex Technology Limited |
3-(carbonyl) 1h-indazole compounds as cyclin dependent kinases (cdk) inhibitors
|
FR2845382A1
(fr)
|
2002-10-02 |
2004-04-09 |
Sanofi Synthelabo |
Derives d'indazolecarboxamides, leur preparation et leur utilisation en therapeutique
|
FR2846656B1
(fr)
|
2002-11-05 |
2004-12-24 |
Servier Lab |
Nouveaux derives d'imidazopyridine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
|
AU2003295776B2
(en)
|
2002-11-21 |
2011-05-12 |
Novartis Vaccines And Diagnostics, Inc. |
2,4,6-trisubstituted pyrimidines as phosphotidylinositol (PI) 3-kinase inhibitors and their use in the treatment of cancer
|
IS7839A
(is)
|
2002-11-22 |
2004-05-23 |
Merck Frosst Canada Ltd. |
4-oxó-1-(3-setið fenýl-1,4-díhýdró-1,8-naftýridín-3-karboxamíð fosfódíesterasa-4 hindrar
|
PT1581492E
(pt)
|
2002-11-28 |
2008-09-19 |
Suven Life Sciences Ltd |
Indoles n-arilsulfonil-3-substituídos possuindo afinidade de receptor de serotonina, processo para a sua preparação e composição farmacêutica contendo os mesmos
|
WO2004063155A1
(en)
|
2003-01-06 |
2004-07-29 |
Eli Lilly And Company |
Fused heterocyclic derivatives as ppar modulators
|
WO2004092131A1
(en)
|
2003-01-06 |
2004-10-28 |
Eli Lilly And Company |
Indole derivatives as ppar modulators
|
CL2004000234A1
(es)
|
2003-02-12 |
2005-04-15 |
Biogen Idec Inc |
Compuestos derivados 3-(piridin-2-il)-4-heteroaril-pirazol sustituidos, antagonistas de aik5 y/o aik4; composicion farmaceutica y uso del compuesto en el tratamiento de desordenes fibroticos como esclerodermia, lupus nefritico, cicatrizacion de herid
|
ITMI20030287A1
(it)
|
2003-02-18 |
2004-08-19 |
Acraf |
Indazolammidi dotate di attivita' analgesica metodo, per
|
BRPI0407662B8
(pt)
|
2003-02-21 |
2021-05-25 |
Chiesi Farm Spa |
derivados do ácido 1-fenilalcanocarboxílico para o tratamento de doenças neurodegenerativas
|
JP2004284997A
(ja)
|
2003-03-24 |
2004-10-14 |
Taoka Chem Co Ltd |
高純度インドールカルボン酸類の製造方法
|
JP2004284998A
(ja)
|
2003-03-24 |
2004-10-14 |
Taoka Chem Co Ltd |
1−アルキルインドール類の製造方法
|
EP1615697A2
(en)
|
2003-04-11 |
2006-01-18 |
Novo Nordisk A/S |
New pyrazolo[1,5-a] pyrimidine derivatives and pharmaceutical use thereof
|
JP2006522750A
(ja)
|
2003-04-11 |
2006-10-05 |
ノボ ノルディスク アクティーゼルスカブ |
代謝性症候群ならびに関連の疾患および障害を治療するために、11β−ヒドロキシステロイドデヒドロゲナーゼ1型阻害剤および抗高血圧剤を使用する併用療法
|
WO2004089380A2
(en)
|
2003-04-11 |
2004-10-21 |
Novo Nordisk A/S |
Pharmaceutical use of fused 1,2,4-triazoles
|
JP2006522745A
(ja)
|
2003-04-11 |
2006-10-05 |
ノボ ノルディスク アクティーゼルスカブ |
置換1,2,4−トリアゾールの薬学的使用
|
EP1615667A2
(en)
|
2003-04-11 |
2006-01-18 |
Novo Nordisk A/S |
Combinations of an 11-beta-hydroxysteroid dehydrogenase type 1 inhibitor and a glucocorticoid receptor agonist
|
JP4629657B2
(ja)
|
2003-04-11 |
2011-02-09 |
ハイ・ポイント・ファーマスーティカルズ、エルエルシー |
11β−ヒドロキシステロイドデヒドロゲナーゼ1型化活性化合物
|
MXPA05011539A
(es)
|
2003-04-30 |
2006-01-23 |
Inst For Pharm Discovery Inc |
Acidos carboxilicos sustituidos con heterociclo como inhibidores de la proteina tirosina-fosfatasa-1b.
|
US7119205B2
(en)
|
2003-05-16 |
2006-10-10 |
Abbott Laboratories |
Thienopyridones as AMPK activators for the treatment of diabetes and obesity
|
US7429596B2
(en)
|
2003-06-20 |
2008-09-30 |
The Regents Of The University Of California |
1H-pyrrolo [2,3-D] pyrimidine derivatives and methods of use thereof
|
US20070197603A1
(en)
|
2003-07-04 |
2007-08-23 |
Alessandra Consonni |
Substituted indole ligands for the orl-1 receptor
|
WO2005014554A1
(en)
|
2003-08-08 |
2005-02-17 |
Astex Therapeutics Limited |
1h-indazole-3-carboxamide compounds as mapkap kinase modulators
|
US7470807B2
(en)
|
2003-08-14 |
2008-12-30 |
Asahi Kasei Pharma Corporation |
Substituted arylalkanoic acid derivatives and use thereof
|
EP2468729B1
(en)
|
2003-10-15 |
2013-12-25 |
Ube Industries, Ltd. |
Novel indazole derivative
|
JP4458819B2
(ja)
|
2003-11-13 |
2010-04-28 |
株式会社リコー |
アゾ置換インドール化合物及びこれを用いた光記録媒体
|
JP2005145859A
(ja)
|
2003-11-13 |
2005-06-09 |
Nippon Steel Chem Co Ltd |
脱水素化方法及び芳香族複素環化合物の製造方法
|
KR20060120694A
(ko)
|
2003-12-22 |
2006-11-27 |
메모리 파마슈티칼스 코포레이션 |
인돌, 1h-인다졸, 1,2-벤즈이속사졸 및1,2-벤즈이소티아졸, 및 이들의 제법 및 용도
|
CA2560741C
(en)
|
2004-03-25 |
2013-08-06 |
Memory Pharmaceuticals Corporation |
Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, and preparation and uses thereof
|
WO2005097203A2
(en)
|
2004-04-01 |
2005-10-20 |
Cardiome Pharma Corp. |
Serum protein conjugates of ion channel modulating compounds and uses thereof
|
JP4510500B2
(ja)
|
2004-04-15 |
2010-07-21 |
株式会社リコー |
アゾ置換インドール化合物及びアゾ金属キレート化合物、並びに光記録媒体
|
JP2007538011A
(ja)
|
2004-05-07 |
2007-12-27 |
メモリー・ファーマシューティカルズ・コーポレイション |
1h−インダゾール、ベンゾチアゾール、1,2−ベンゾイソキサゾール、1,2−ベンゾイソチアゾール、およびクロモン、ならびにそれらの調製および使用
|
EP1758899A1
(en)
|
2004-06-03 |
2007-03-07 |
Brandeis University |
Asymmetric michael and aldol addition using bifunctional cinchona-alkaloid-based catalysts
|
CA2570365A1
(en)
|
2004-06-18 |
2005-12-29 |
Biolipox Ab |
Indoles useful in the treatment of inflammation
|
CN101006053A
(zh)
|
2004-06-18 |
2007-07-25 |
比奥里波克斯公司 |
用于治疗炎症的吲哚
|
WO2006012504A2
(en)
|
2004-07-23 |
2006-02-02 |
Daiamed, Inc. |
Compounds and methods for treatment of thrombosis
|
EP1781639B1
(en)
|
2004-07-28 |
2012-01-25 |
Janssen Pharmaceutica NV |
Substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase
|
US20070015771A1
(en)
|
2004-07-29 |
2007-01-18 |
Threshold Pharmaceuticals, Inc. |
Lonidamine analogs
|
JP2006045119A
(ja)
|
2004-08-04 |
2006-02-16 |
Toray Ind Inc |
ピラジン誘導体及びそれを有効成分とする腎炎治療薬
|
US20060035893A1
(en)
|
2004-08-07 |
2006-02-16 |
Boehringer Ingelheim International Gmbh |
Pharmaceutical compositions for treatment of respiratory and gastrointestinal disorders
|
NZ588431A
(en)
|
2004-09-17 |
2012-02-24 |
Whitehead Biomedical Inst |
Using Benzimidazole or Indole compounds with a 1,2-diazole group to Inhibit Alpha-Synuclein Toxicity
|
US20070299114A1
(en)
|
2004-10-05 |
2007-12-27 |
Shionogi & Co., Ltd. |
Biaryl Derivatives
|
JP2008516962A
(ja)
|
2004-10-15 |
2008-05-22 |
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 |
血管傷害を治療する方法
|
JP2006131519A
(ja)
|
2004-11-04 |
2006-05-25 |
Idemitsu Kosan Co Ltd |
縮合環含有化合物及びそれを用いた有機エレクトロルミネッセンス素子
|
DE102004054666A1
(de)
|
2004-11-12 |
2006-05-18 |
Bayer Cropscience Gmbh |
Substituierte Pyrazol-3-carboxamide, Verfahren zur Herstellung und Verwendung als Herbizide und Pflanzenwachstumsregulatoren
|
JPWO2006051937A1
(ja)
|
2004-11-15 |
2008-05-29 |
塩野義製薬株式会社 |
ヘテロ5員環誘導体
|
PL1828179T3
(pl)
|
2004-12-22 |
2010-08-31 |
Memory Pharm Corp |
Ligandy dla receptorów nikotynowych alfa-7 przeciwko chorobom związanym z OUN
|
KR20060079121A
(ko)
|
2004-12-31 |
2006-07-05 |
에스케이케미칼주식회사 |
당뇨 및 비만 치료예방에 유효한 퀴나졸린 유도체
|
FR2882054B1
(fr)
|
2005-02-17 |
2007-04-13 |
Sanofi Aventis Sa |
Derives de 1,5-diarylpyrrole, leur preparation et leur application en therapeutique
|
WO2006109933A1
(en)
|
2005-03-30 |
2006-10-19 |
Daewoong Pharmaceutical Co., Ltd. |
Antifungal triazole derivatives
|
WO2006110516A1
(en)
|
2005-04-11 |
2006-10-19 |
Abbott Laboratories |
Acylhydrazide p2x7 antagonists and uses thereof
|
CA2605594A1
(en)
|
2005-04-22 |
2006-11-02 |
Daiichi Sankyo Company, Limited |
Heterocyclic compound
|
HUE031979T2
(en)
|
2005-05-17 |
2017-08-28 |
Sarcode Bioscience Inc |
Preparations and methods for treating eye disorders
|
WO2006130437A2
(en)
|
2005-05-27 |
2006-12-07 |
Brandeis University |
Asymmetric carbon-carbon-bond-forming reactions catalyzed by bifunctional cinchona alkaloids
|
WO2006130453A1
(en)
|
2005-05-27 |
2006-12-07 |
Brandeis University |
Asymmetric aldol additions using bifunctional cinchona-alkaloid-based catalysts
|
JP4981794B2
(ja)
|
2005-06-03 |
2012-07-25 |
アボット・ラボラトリーズ |
シクロブチルアミン誘導体
|
US20090291988A1
(en)
|
2005-06-14 |
2009-11-26 |
Renata Oballa |
Reversible Inhibitors of Monoamine Oxidase A and B
|
US20080221088A1
(en)
|
2005-06-23 |
2008-09-11 |
Vijay Kumar Potluri |
3,4-Substituted Thiazoles as Ampk Activators
|
CA2611296A1
(en)
|
2005-06-27 |
2007-01-04 |
Sanofi-Aventis |
Pyrazolopyridine derivatives as inhibitors of beta-adrenergic receptor kinase 1
|
CN101273022A
(zh)
|
2005-07-04 |
2008-09-24 |
雷迪博士实验室有限公司 |
作为ampk激活剂的噻唑衍生物
|
JP2007015952A
(ja)
|
2005-07-06 |
2007-01-25 |
Shionogi & Co Ltd |
ナフタレン誘導体
|
EP1931632A4
(en)
|
2005-08-18 |
2011-05-11 |
Microbia Inc |
USEFUL INDOOR CONNECTIONS
|
EP1754483A1
(en)
|
2005-08-18 |
2007-02-21 |
Merck Sante |
Use of thienopyridone derivatives as AMPK activators and pharmaceutical compositions containing them
|
US8106066B2
(en)
|
2005-09-23 |
2012-01-31 |
Memory Pharmaceuticals Corporation |
Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, pyrazolopyridines, isothiazolopyridines, and preparation and uses thereof
|
JP2009514893A
(ja)
|
2005-11-03 |
2009-04-09 |
イリプサ, インコーポレイテッド |
多価インドール化合物およびホスホリパーゼa2インヒビターとしてのその使用
|
CA2627349A1
(en)
|
2005-11-03 |
2007-05-18 |
Ilypsa, Inc. |
Azaindole compounds and use thereof as phospholipase-a2 inhibitors
|
AU2006311765A1
(en)
|
2005-11-03 |
2007-05-18 |
Ilypsa, Inc. |
Phospholipase inhibitors, including multi-valent phospholipase inhibitors, and use thereof, including as lumen-localized phospholipase inhibitors
|
JP2009514980A
(ja)
|
2005-11-09 |
2009-04-09 |
メモリー・ファーマシューティカルズ・コーポレイション |
1h−インダゾール類、ベンゾチアゾール類、1,2−ベンゾイソオキサゾール類、1,2−ベンゾイソチアゾール類、および/クロモン類と、それらの製造と用途
|
WO2007058504A1
(en)
|
2005-11-21 |
2007-05-24 |
Lg Life Sciences, Ltd. |
Novel compounds as agonist for ppar gamma and ppar alpha, method for preparation of the same, and pharmaceutical composition containing the same
|
CN1978445B
(zh)
|
2005-12-02 |
2010-09-01 |
中国科学院上海药物研究所 |
一种可用作人源腺苷单核苷酸激活蛋白激酶激活剂的化合物及其制备方法和应用
|
WO2007070818A1
(en)
|
2005-12-14 |
2007-06-21 |
Bristol-Myers Squibb Company |
Six-membered heterocycles useful as serine protease inhibitors
|
WO2007070826A1
(en)
|
2005-12-14 |
2007-06-21 |
Bristol-Myers Squibb Company |
Arylpropionamide, arylacrylamide, arylpropynamide, or arylmethylurea analogs as factor xia inhibitors
|
WO2007079173A2
(en)
|
2005-12-30 |
2007-07-12 |
Emergent Biosolutions Inc. |
Novel 2-heteroaryloxy-phenol derivatives as antibacterial agents
|
AU2007212126B2
(en)
|
2006-02-03 |
2012-07-19 |
Eli Lilly And Company |
Compounds and methods for modulating FX-receptors
|
GB0603041D0
(en)
|
2006-02-15 |
2006-03-29 |
Angeletti P Ist Richerche Bio |
Therapeutic compounds
|
JPWO2007114213A1
(ja)
|
2006-03-30 |
2009-08-13 |
旭化成ファーマ株式会社 |
置換二環式環状誘導体及びその用途
|
EP2001480A4
(en)
|
2006-03-31 |
2011-06-15 |
Abbott Lab |
Indazole CONNECTIONS
|
CA2647256A1
(en)
|
2006-04-18 |
2007-10-25 |
Abbott Laboratories |
Antagonists of the vanilloid receptor subtype 1 (vr1) and uses thereof
|
PL2018380T3
(pl)
|
2006-05-19 |
2012-05-31 |
Abbvie Bahamas Ltd |
Skondensowane azabicykliczne pochodne alkanowe podstawione bicykloheterocyklem o aktywności wobec OUN
|
CA2651378C
(en)
|
2006-05-24 |
2012-08-28 |
Eli Lilly And Company |
Fxr agonists
|
TW200815398A
(en)
|
2006-06-08 |
2008-04-01 |
Ube Industries |
A novel indazole derivative having spirocyclic structure in the side chain
|
NZ573371A
(en)
|
2006-07-03 |
2011-01-28 |
Biovitrum Ab Publ |
Indoles as 5-ht6 modulators
|
FR2903695B1
(fr)
|
2006-07-13 |
2008-10-24 |
Merck Sante Soc Par Actions Si |
Utilisation de derives d'imidazole activateurs de l'ampk, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
|
KR100826108B1
(ko)
|
2006-08-04 |
2008-04-29 |
한국화학연구원 |
퓨란-2-카복실산 유도체 및 그의 제조 방법
|
EA018724B1
(ru)
|
2006-08-07 |
2013-10-30 |
Айронвуд Фармасьютикалз, Инк. |
Соединения индола
|
JP2008063278A
(ja)
|
2006-09-07 |
2008-03-21 |
Fujifilm Finechemicals Co Ltd |
1−ピリジン−4−イル−インドール類の製造方法
|
JP2008106037A
(ja)
|
2006-09-29 |
2008-05-08 |
Osaka Prefecture Univ |
インドール化合物の製造方法およびインドール化合物
|
WO2008054748A2
(en)
|
2006-10-31 |
2008-05-08 |
Arena Pharmaceuticals, Inc. |
Indazole derivatives as modulators of the 5-ht2a serotonin receptor useful for the treatment of disorders related thereto
|
CA2671543A1
(en)
|
2006-12-05 |
2008-06-12 |
Chung-Ming Sun |
Indazole compounds
|
WO2008072850A1
(en)
|
2006-12-11 |
2008-06-19 |
Amorepacific Corporation |
Triazine derivatives having inhibitory activity against acetyl-coa carboxylase
|
AU2007331676A1
(en)
|
2006-12-14 |
2008-06-19 |
Bayer Schering Pharma Aktiengesellschaft |
Dihydropyridine derivatives useful as protein kinase inhibitors
|
CA2672205A1
(en)
|
2006-12-18 |
2008-06-26 |
Ambrx, Inc. |
Compositions containing, methods involving, and uses of non-natural amino acids and polypeptides
|
CA2672639A1
(en)
|
2006-12-22 |
2008-07-03 |
Novartis Ag |
Indol-4-yl-pyrimidinyl-2-yl-amine derivatives and use thereof as cyclin dependant kinase inhibitors
|
EP2079694B1
(en)
|
2006-12-28 |
2017-03-01 |
Rigel Pharmaceuticals, Inc. |
N-substituted-heterocycloalkyloxybenzamide compounds and methods of use
|
PE20081559A1
(es)
|
2007-01-12 |
2008-11-20 |
Merck & Co Inc |
DERIVADOS DE ESPIROCROMANONA SUSTITUIDOS COMO INHIBIDORES DE ACETIL CoA CARBOXILASA
|
EP2120952A4
(en)
|
2007-01-15 |
2011-09-21 |
Us Of America As Represented By The Secretary Of The Army On Behalf Of The U S Army Res Inst Of Infe |
ANTIVIRAL COMPOUNDS AND METHOD FOR THEIR USE
|
DE102007002717A1
(de)
|
2007-01-18 |
2008-07-24 |
Merck Patent Gmbh |
Heterocyclische Indazolderivate
|
JP2008179567A
(ja)
|
2007-01-25 |
2008-08-07 |
Toray Ind Inc |
ピラジン誘導体を有効成分とする抗がん剤
|
AR065093A1
(es)
|
2007-02-05 |
2009-05-13 |
Merck Frosst Canada Ltd |
Compuestos farmacéuticos inhibidores de la biosintesis de leucotrienos
|
US20090047246A1
(en)
|
2007-02-12 |
2009-02-19 |
Intermune, Inc. |
Novel inhibitors of hepatitis c virus replication
|
JP5107589B2
(ja)
|
2007-02-13 |
2012-12-26 |
旭化成株式会社 |
インドール誘導体
|
JP2008208074A
(ja)
|
2007-02-27 |
2008-09-11 |
Toray Ind Inc |
ピラジン誘導体を有効成分とする抗がん剤
|
JP2008222576A
(ja)
|
2007-03-09 |
2008-09-25 |
Japan Enviro Chemicals Ltd |
インドール化合物の製造方法
|
WO2008110863A1
(en)
|
2007-03-15 |
2008-09-18 |
Glenmark Pharmaceuticals S.A. |
Indazole derivatives and their use as vanilloid receptor ligands
|
WO2008118822A1
(en)
|
2007-03-23 |
2008-10-02 |
Rigel Pharmaceuticals, Inc. |
Compositions and methods for inhibition of the jak pathway
|
EP2142547A1
(en)
|
2007-03-28 |
2010-01-13 |
NeuroSearch A/S |
Purinyl derivatives and their use as potassium channel modulators
|
WO2008136642A1
(en)
|
2007-05-07 |
2008-11-13 |
Mazence Inc. |
Naphthoquinone-based pharmaceutical composition for treatment or prevention of diseases involving obesity, diabetes, metabolic syndrome, neuro-degenerative diseases and mitochondria dysfunction diseases
|
WO2008150899A1
(en)
|
2007-05-29 |
2008-12-11 |
Emory University |
Combination therapies for treatment of cancer and inflammatory diseases
|
FR2917735B1
(fr)
|
2007-06-21 |
2009-09-04 |
Sanofi Aventis Sa |
Nouveaux indazoles substitutes, leur preparation et leur utilisation en therapeutique
|
TW200906823A
(en)
|
2007-07-16 |
2009-02-16 |
Lilly Co Eli |
Compounds and methods for modulating FXR
|
AR067770A1
(es)
|
2007-08-03 |
2009-10-21 |
Betagenon Ab |
Derivados de tiazol y ditiazol para el tratamiento de diabetes
|
KR20090016804A
(ko)
|
2007-08-13 |
2009-02-18 |
주식회사 티지 바이오텍 |
신규 벤질에스테르계 화합물 및 이를 유효성분으로함유하는 비만, 당뇨 및 고지혈증의 예방 및 치료용 조성물
|
WO2009026107A1
(en)
|
2007-08-17 |
2009-02-26 |
Portola Pharmaceuticals, Inc. |
Protein kinase inhibitors
|
EP2197842B1
(en)
|
2007-08-29 |
2012-05-23 |
Schering Corporation |
2, 3-substituted indole derivatives for treating viral infections
|
PE20090630A1
(es)
|
2007-08-29 |
2009-05-16 |
Schering Corp |
Derivados de indol 2-carboxi sustituidos y metodos para su utilizacion
|
US8415358B2
(en)
|
2007-09-17 |
2013-04-09 |
Neurosearch A/S |
Pyrazine derivatives and their use as potassium channel modulators
|
US8404713B2
(en)
|
2007-10-26 |
2013-03-26 |
Janssen Pharmaceutica Nv |
Quinolinone derivatives as PARP inhibitors
|
US20090124680A1
(en)
|
2007-10-31 |
2009-05-14 |
Mazence Inc. |
Use of prodrug composition containing naphthoquinone-based compound for manufacture of medicament for treatment or prevention of diseases involving metabolic syndrome
|
CA2705947C
(en)
|
2007-11-16 |
2016-08-09 |
Rigel Pharmaceuticals, Inc. |
Carboxamide, sulfonamide and amine compounds for metabolic disorders
|
MX2010005355A
(es)
|
2007-11-16 |
2010-06-02 |
Schering Corp |
Derivados de indol sustituidos con 3-aminosulfonilo y metodos de uso de los mismos.
|
US20100311965A1
(en)
|
2007-12-28 |
2010-12-09 |
Carna Biosciences Inc. |
2-aminoquinazoline derivative
|
EP2258950A1
(en)
|
2008-01-31 |
2010-12-08 |
National University Corporation Yokohama National University |
Fluid machine
|
BRPI0905952A2
(pt)
|
2008-02-04 |
2015-06-30 |
Mercury Therapeutics |
Composto e sais do mesmo e compição farmacêutica
|
WO2009115874A2
(en)
|
2008-03-17 |
2009-09-24 |
Matrix Laboratories Ltd. |
Novel heterocyclic compounds, pharmaceutical compositions containing them and processes for their preparation
|
EP2257545B1
(en)
|
2008-03-20 |
2011-08-31 |
F. Hoffmann-La Roche AG |
Pyrrolidinyl derivatives and uses thereof
|
WO2009120783A1
(en)
|
2008-03-25 |
2009-10-01 |
The Johns Hopkins University |
High affinity inhibitors of hepatitis c virus ns3/4a protease
|
CA2716932C
(en)
|
2008-03-27 |
2017-07-04 |
Eddy Jean Edgard Freyne |
Aza-bicyclohexyl substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase
|
NZ589136A
(en)
|
2008-04-11 |
2012-06-29 |
Merck Patent Gmbh |
Thienopyridone derivatives as amp-activated protein kinase (ampk) activators
|
NZ588652A
(en)
|
2008-04-23 |
2012-09-28 |
Rigel Pharmaceuticals Inc |
Carboxamide compounds for the treatment of metabolic disorders
|
KR20160038065A
(ko)
|
2008-05-05 |
2016-04-06 |
메르크 파텐트 게엠베하 |
Amp-활성화된 단백질 키나아제 (ampk) 활성화제로서의 티에노피리돈 유도체
|
GB0808282D0
(en)
|
2008-05-07 |
2008-06-11 |
Medical Res Council |
Compounds for use in stabilizing p53 mutants
|
DK2285786T3
(da)
|
2008-06-16 |
2013-11-04 |
Merck Patent Gmbh |
Quinoxalindion-derivater
|
JP2011524880A
(ja)
|
2008-06-20 |
2011-09-08 |
グラクソ グループ リミテッド |
化合物
|
DE102008031480A1
(de)
|
2008-07-03 |
2010-01-07 |
Merck Patent Gmbh |
Salze enthaltend ein Pyrimidincarbonsäure-Derivat
|
WO2010009190A1
(en)
|
2008-07-16 |
2010-01-21 |
King Pharmaceuticals Research And Development, Inc. |
Methods of treating atherosclerosis
|
WO2010010186A1
(en)
|
2008-07-25 |
2010-01-28 |
Galapagos Nv |
Novel compounds useful for the treatment of degenerative and inflammatory diseases
|
WO2010036910A1
(en)
|
2008-09-26 |
2010-04-01 |
Yoshikazu Ohta |
Heart protection by administering an amp-activated protein kinase activator
|
KR20110061640A
(ko)
|
2008-09-26 |
2011-06-09 |
에프. 호프만-라 로슈 아게 |
Hcv 치료용 피린 또는 피라진 유도체
|
US8410284B2
(en)
|
2008-10-22 |
2013-04-02 |
Merck Sharp & Dohme Corp |
Cyclic benzimidazole derivatives useful as anti-diabetic agents
|
CA2741300A1
(en)
|
2008-10-29 |
2010-05-06 |
Merck Sharp & Dohme Corp. |
Novel cyclic benzimidazole derivatives useful anti-diabetic agents
|
CN102271509A
(zh)
|
2008-10-31 |
2011-12-07 |
默沙东公司 |
用于抗糖尿病药的新型环苯并咪唑衍生物
|
WO2010056041A2
(ko)
|
2008-11-13 |
2010-05-20 |
주식회사 머젠스 |
허혈 또는 허혈 재관류에 의해 유발되는 심장질환의 치료 및 예방을 위한 약제 조성물
|
CA2741511C
(en)
|
2008-11-21 |
2017-01-24 |
Raqualia Pharma Inc. |
Novel pyrazole-3-carboxamide derivative having 5-ht2b receptor antagonist activity
|
KR101061599B1
(ko)
*
|
2008-12-05 |
2011-09-02 |
한국과학기술연구원 |
비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물
|
WO2010068287A2
(en)
|
2008-12-11 |
2010-06-17 |
Angion Biomedica Corp. |
Small molecule modulators of hepatocyte growth factor (scatter factor) activity
|
AU2009327133B2
(en)
|
2008-12-18 |
2016-04-14 |
Merck Serono S.A. |
Oxadiazole fused heterocyclic derivatives useful for the treatment of multiple sclerosis
|
US20120122889A1
(en)
|
2008-12-23 |
2012-05-17 |
President And Fellows Of Harvard College |
Small molecule inhibitors of necroptosis
|
WO2010073011A2
(en)
|
2008-12-23 |
2010-07-01 |
Betagenon Ab |
Compounds useful as medicaments
|
UA106600C2
(uk)
|
2009-01-28 |
2014-09-25 |
Райджел Фармасьютікалз, Інк. |
Карбоксамідні сполуки і способи їхнього застосування
|
WO2010086613A1
(en)
|
2009-01-30 |
2010-08-05 |
Betagenon Ab |
Compounds useful as inhibitors as ampk
|
US20100210682A1
(en)
|
2009-02-19 |
2010-08-19 |
Abbott Laboratories |
Repeated Dosing of TRPV1 Antagonists
|
SG172951A1
(en)
|
2009-03-24 |
2011-08-29 |
Sumitomo Chemical Co |
Method for manufacturing a boronic acid ester compound
|
AU2010231058A1
(en)
|
2009-03-31 |
2011-11-10 |
Renascience Co., Ltd. |
Plasminogen activator inhibitor-1 inhibitor
|
US8927576B2
(en)
|
2009-04-06 |
2015-01-06 |
PTC Therpeutics, Inc. |
HCV inhibitor and therapeutic agent combinations
|
WO2011004162A2
(en)
|
2009-07-08 |
2011-01-13 |
Betagenon Ab |
Compounds useful as medicaments
|
CN102574787B
(zh)
|
2009-07-30 |
2014-12-31 |
新加坡国立大学 |
具有潜在的抗癌活性的小分子异戊二烯基半胱氨酸羧基甲基转移酶抑制剂
|
GB0915892D0
(en)
|
2009-09-10 |
2009-10-14 |
Smithkline Beecham Corp |
Compounds
|
WO2011032320A1
(en)
|
2009-09-21 |
2011-03-24 |
F. Hoffmann-La Roche Ag |
Novel alkene oxindole derivatives
|
WO2011069298A1
(en)
|
2009-12-11 |
2011-06-16 |
F. Hoffmann-La Roche Ag |
Novel cyclopropane indolinone derivatives
|
JP2013047189A
(ja)
|
2009-12-25 |
2013-03-07 |
Kyorin Pharmaceutical Co Ltd |
新規パラバン酸誘導体及びそれらを有効成分とする医薬
|
EP2519527B1
(en)
|
2009-12-29 |
2013-12-18 |
Poxel |
Thieno[2,3-b]pyridinedione activators of ampk and therapeutic uses thereof
|
EP2538784B1
(en)
|
2010-02-25 |
2015-09-09 |
Merck Sharp & Dohme Corp. |
Benzimidazole derivatives useful anti-diabetic agents
|
US8796254B2
(en)
|
2010-03-31 |
2014-08-05 |
Rigel Pharmaceuticals, Inc. |
Methods for using carboxamide, sulfonamide and amine compounds
|
US8344137B2
(en)
|
2010-04-14 |
2013-01-01 |
Hoffman-La Roche Inc. |
3,3-dimethyl tetrahydroquinoline derivatives
|
EP2566868A1
(en)
|
2010-05-05 |
2013-03-13 |
GlaxoSmithKline LLC |
Pyrrolo [3, 2 -d]pyrimidin-3 -yl derivatives used as activators of ampk
|
US8592594B2
(en)
|
2010-07-02 |
2013-11-26 |
Hoffmann-La Roche Inc. |
Tetrahydro-quinoline derivatives
|
SG186850A1
(en)
|
2010-07-29 |
2013-02-28 |
Rigel Pharmaceuticals Inc |
Ampk-activating heterocyclic compounds and methods for using the same
|
KR101190141B1
(ko)
|
2010-08-24 |
2012-10-12 |
서울대학교산학협력단 |
Ampk를 활성화시키는 화합물을 함유하는 약학조성물
|
JP2013230986A
(ja)
|
2010-08-25 |
2013-11-14 |
Kyorin Pharmaceutical Co Ltd |
新規ヒダントイン誘導体及びそれらを有効成分とする医薬
|
WO2012027548A1
(en)
|
2010-08-25 |
2012-03-01 |
The Feinstein Institute For Medical Research |
Compounds and methods for prevention and treatment of alzheimer's and other diseases
|
CA2811025C
(en)
|
2010-09-10 |
2018-07-17 |
Shionogi & Co., Ltd. |
Hetero ring-fused imidazole derivative having ampk activating effect
|
WO2012040499A2
(en)
|
2010-09-22 |
2012-03-29 |
Surface Logix, Inc. |
Metabolic inhibitors
|
US8546427B2
(en)
|
2010-10-20 |
2013-10-01 |
Hoffmann-La Roche Inc. |
Tetrahydroquinoline derivatives
|
US8809369B2
(en)
|
2011-01-26 |
2014-08-19 |
Hoffmann-La Roche Inc. |
Tetrahydroquinoline derivatives
|
JP5728099B2
(ja)
|
2011-02-25 |
2015-06-03 |
メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. |
抗糖尿病剤として有用な新規環状アザベンゾイミダゾール誘導体
|
WO2012119979A1
(en)
|
2011-03-07 |
2012-09-13 |
Glaxosmithkline Llc |
1H-PYROLLO[3,2-d]PYRIMIDINEDIONE DERIVATIVES
|
CA2830706A1
(en)
|
2011-03-07 |
2012-09-13 |
Glaxosmithkline Llc |
Quinolinone derivatives
|
EP2742040B1
(en)
|
2011-08-12 |
2016-04-06 |
F.Hoffmann-La Roche Ag |
Indazole compounds, compositions and methods of use
|
WO2013124158A1
(en)
|
2012-02-21 |
2013-08-29 |
Aziende Chimiche Riunite Angelini Francesco A.C.R.A.F. S.P.A. |
1h-indazole-3-carboxamide compounds as glycogen synthase kinase 3 beta inhibitors
|
US8889730B2
(en)
*
|
2012-04-10 |
2014-11-18 |
Pfizer Inc. |
Indole and indazole compounds that activate AMPK
|