|
US3272781A
(en)
|
1963-08-07 |
1966-09-13 |
American Potash & Chem Corp |
Boroureas of phosphinoborine polymers
|
|
FR1425700A
(fr)
|
1965-02-22 |
1966-01-24 |
Basf Ag |
Composés formant des complexes métalliques et procédé pour les préparer et les utiliser
|
|
US4208328A
(en)
|
1978-04-27 |
1980-06-17 |
General Electric Company |
Alkyl 3,5-dihydroxy-4-(2-benzothiazolyl)benzoates
|
|
US4789711A
(en)
|
1986-12-02 |
1988-12-06 |
Ciba-Geigy Corporation |
Multifunctional epoxide resins
|
|
JPH0611031Y2
(ja)
|
1988-02-27 |
1994-03-23 |
タマパック株式会社 |
ゴルフ用パッティンググリーン
|
|
DE3828535A1
(de)
|
1988-08-23 |
1990-03-08 |
Basf Ag |
Benzimidazol-2-carbonsaeureanilide, ihre verwendung als lichtschutzmittel fuer organisches material und mit diesen aniliden stabilisiertes organisches material
|
|
US5077164A
(en)
|
1989-06-21 |
1991-12-31 |
Minolta Camera Kabushiki Kaisha |
Photosensitive member containing an azo dye
|
|
DE69421982T2
(de)
|
1993-09-20 |
2000-03-30 |
Fuji Photo Film Co., Ltd. |
Positiv arbeitende Photoresistzusammensetzung
|
|
JP3461397B2
(ja)
|
1995-01-11 |
2003-10-27 |
富士写真フイルム株式会社 |
ポジ型フオトレジスト組成物
|
|
WO1998027108A2
(fr)
|
1996-12-16 |
1998-06-25 |
Fujisawa Pharmaceutical Co., Ltd. |
Nouveaux composes amide
|
|
JPH10316853A
(ja)
|
1997-05-15 |
1998-12-02 |
Sumitomo Bakelite Co Ltd |
半導体多層配線用層間絶縁膜樹脂組成物及び該絶縁膜の製造方法
|
|
EP1019391A1
(fr)
|
1997-10-02 |
2000-07-19 |
Merck & Co. Inc. |
Inhibiteurs de la prenyl-proteine transferase
|
|
AU2745899A
(en)
|
1998-03-05 |
1999-09-20 |
Nissan Chemical Industries Ltd. |
Anilide compounds and herbicide
|
|
JP2000128984A
(ja)
|
1998-10-28 |
2000-05-09 |
Sumitomo Bakelite Co Ltd |
ポリベンゾオキサゾール前駆体及び樹脂
|
|
JP2000128986A
(ja)
|
1998-10-28 |
2000-05-09 |
Sumitomo Bakelite Co Ltd |
ポリベンゾオキサゾール前駆体及びポリベンゾオキサゾール
|
|
JP2000128987A
(ja)
|
1998-10-28 |
2000-05-09 |
Sumitomo Bakelite Co Ltd |
ポリベンゾオキサゾール前駆体及びポリベンゾオキサゾール
|
|
US6297351B1
(en)
|
1998-12-17 |
2001-10-02 |
Sumitomo Bakelite Company Limited |
Polybenzoxazole resin and precursor thereof
|
|
UA70976C2
(uk)
|
1998-12-18 |
2004-11-15 |
Аксіз Фармасьютікелз, Інк. |
(гетеро)арилбіциклічні гетероарильні похідні, їх одержання та використання як інгібіторів протеаз
|
|
JP2000212281A
(ja)
|
1999-01-27 |
2000-08-02 |
Sumitomo Bakelite Co Ltd |
ポリベンゾオキサゾ―ル前駆体及びポリベンゾオキサゾ―ル樹脂
|
|
WO2001007409A1
(fr)
|
1999-07-23 |
2001-02-01 |
Astrazeneca Uk Limited |
Derives de carbazole et leur utilisation en tant que ligands du recepteur de neuropeptide y5
|
|
JP2001114893A
(ja)
|
1999-10-15 |
2001-04-24 |
Sumitomo Bakelite Co Ltd |
ポリベンゾオキサゾール樹脂およびその前駆体
|
|
US6372907B1
(en)
|
1999-11-03 |
2002-04-16 |
Apptera Corporation |
Water-soluble rhodamine dye peptide conjugates
|
|
JP2001163975A
(ja)
|
1999-12-03 |
2001-06-19 |
Sumitomo Bakelite Co Ltd |
ポリベンゾオキサゾール樹脂及びその前駆体
|
|
SK13752001A3
(sk)
|
1999-12-27 |
2002-07-02 |
Japan Tobacco, Inc. |
Zlúčeniny s fúzovanými kruhmi a ich použitie ako liečiv
|
|
AU2001240542A1
(en)
|
2000-02-01 |
2001-08-14 |
Basf Aktiengesellschaft |
Heterocyclic compounds and their use as parp inhibitors
|
|
US6521618B2
(en)
|
2000-03-28 |
2003-02-18 |
Wyeth |
3-cyanoquinolines, 3-cyano-1,6-naphthyridines, and 3-cyano-1,7-naphthyridines as protein kinase inhibitors
|
|
AU2001249679A1
(en)
|
2000-03-31 |
2001-10-15 |
Ortho-Mcneil Pharmaceutical, Inc. |
Phenyl-substituted imidazopyridines
|
|
WO2001081312A2
(fr)
|
2000-04-24 |
2001-11-01 |
Merck Frosst Canada & Co. |
Methode de traitement se basant sur l'utilisation de derives de phenyle et de biaryle comme inhibiteurs de prostaglandine e
|
|
KR100786927B1
(ko)
|
2000-06-28 |
2007-12-17 |
스미스클라인비이참피이엘시이 |
습식 분쇄방법
|
|
WO2002014321A1
(fr)
|
2000-08-11 |
2002-02-21 |
The Regents Of The University Of California |
Utilisation d'inhibiteurs de stat-6 comme agents therapeutiques
|
|
EP1343785A2
(fr)
|
2000-12-13 |
2003-09-17 |
Basf Aktiengesellschaft |
Utilisation d'imidazoazines substituees, nouvelles imidazoazines, procede permettant de les produire et agents les contenant
|
|
WO2002048147A2
(fr)
|
2000-12-15 |
2002-06-20 |
Glaxo Group Limited |
Composes therapeutiques
|
|
SE0100567D0
(sv)
|
2001-02-20 |
2001-02-20 |
Astrazeneca Ab |
Compounds
|
|
JP2004532194A
(ja)
|
2001-03-14 |
2004-10-21 |
エリ リリー アンド カンパニー |
レチノイドxレセプターモジュレータ
|
|
US7034030B2
(en)
|
2001-03-30 |
2006-04-25 |
Smithkline Beecham Corporation |
Pyralopyridines, process for their preparation and use as therapeutic compounds
|
|
EP1377575B1
(fr)
|
2001-04-10 |
2006-07-05 |
SmithKline Beecham Corporation |
Composes de pyrazolopyridine antiviraux
|
|
JP2002316966A
(ja)
|
2001-04-19 |
2002-10-31 |
Ueno Seiyaku Oyo Kenkyusho:Kk |
ビナフトール誘導体およびその製法
|
|
WO2002088124A2
(fr)
|
2001-04-27 |
2002-11-07 |
Smithkline Beecham Corporation |
Composes therapeutiques
|
|
AR035543A1
(es)
|
2001-06-26 |
2004-06-16 |
Japan Tobacco Inc |
Agente terapeutico para la hepatitis c que comprende un compuesto de anillo condensado, compuesto de anillo condensado, composicion farmaceutica que lo comprende, compuestos de benzimidazol, tiazol y bifenilo utiles como intermediarios para producir dichos compuestos, uso del compuesto de anillo con
|
|
JP2005507878A
(ja)
|
2001-09-07 |
2005-03-24 |
スミスクライン ビーチャム コーポレーション |
ヘルペス感染症を治療するためのピラゾロ−ピリジン類
|
|
TWI320039B
(en)
|
2001-09-21 |
2010-02-01 |
|
Lactam-containing compounds and derivatives thereof as factor xa inhibitors
|
|
CA2461369A1
(fr)
|
2001-10-09 |
2003-04-17 |
Pharmacia & Upjohn Company |
Carbazoles arylsulfonyl tetrahydro et hexahydro substitues utiles comme ligands du recepteur 5-ht-6
|
|
WO2003031587A2
(fr)
|
2001-10-09 |
2003-04-17 |
The Regents Of The University Of California |
Utilisation d'inhibiteurs de stat-6 comme agents therapeutiques
|
|
CA2466279A1
(fr)
|
2001-11-13 |
2003-05-22 |
Dana-Farber Cancer Institute, Inc. |
Agents modulant l'activite de cellules immunes et procedes d'utilisation associes
|
|
JP4024579B2
(ja)
|
2002-01-22 |
2007-12-19 |
住友ベークライト株式会社 |
プラスチック光導波路用材料及び光導波路
|
|
NZ575692A
(en)
|
2002-04-11 |
2009-10-30 |
Vertex Pharma |
Inhibitors of Serine Proteases, Particularly Hepatitis C Virus NS3-NS4 Protease
|
|
BR0309475A
(pt)
|
2002-04-23 |
2005-03-01 |
Shionogi & Co |
Derivados de pirazolo-[1,5-a]-pirimidina e inibidores de nad(p)h oxidase que contêm os mesmos
|
|
US20060004010A1
(en)
|
2002-07-10 |
2006-01-05 |
Hiromu Habashita |
Ccr4 antagonist and medical use thereof
|
|
WO2004006906A2
(fr)
|
2002-07-15 |
2004-01-22 |
Combinatorx, Incorporated |
Methodes de traitement de neoplasmes
|
|
JP2004059761A
(ja)
|
2002-07-30 |
2004-02-26 |
Sumitomo Bakelite Co Ltd |
ポリベンゾオキサゾール樹脂、その前駆体及びこれらを用いた光導波路材料並びに光導波路
|
|
JP2004091369A
(ja)
|
2002-08-30 |
2004-03-25 |
Sumitomo Pharmaceut Co Ltd |
新規ビフェニル化合物
|
|
JPWO2004035522A1
(ja)
|
2002-08-30 |
2006-02-16 |
株式会社 ビーエフ研究所 |
プリオン蛋白蓄積性疾患の診断プローブおよび治療薬ならびにプリオン蛋白の染色剤
|
|
US7153863B2
(en)
|
2002-10-03 |
2006-12-26 |
Smithkline Beecham Corporation |
Therapeutic compounds based on pyrazolopyridline derivatives
|
|
US7582630B2
(en)
|
2002-10-15 |
2009-09-01 |
Smithkline Beecham Corporation |
Pyradazine compounds as GSK-3 inhibitors
|
|
ES2367430T3
(es)
|
2002-12-23 |
2011-11-03 |
Wyeth Llc |
Anticuerpos contra pd-1 y sus usos.
|
|
KR100624406B1
(ko)
|
2002-12-30 |
2006-09-18 |
삼성에스디아이 주식회사 |
비페닐 유도체 및 이를 채용한 유기 전계 발광 소자
|
|
US7320989B2
(en)
|
2003-02-28 |
2008-01-22 |
Encysive Pharmaceuticals, Inc. |
Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-II receptor antagonists
|
|
US7078419B2
(en)
|
2003-03-10 |
2006-07-18 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Cytokine inhibitors
|
|
AR043633A1
(es)
|
2003-03-20 |
2005-08-03 |
Schering Corp |
Ligandos de receptores de canabinoides
|
|
JP4595288B2
(ja)
|
2003-03-25 |
2010-12-08 |
住友ベークライト株式会社 |
ポリベンゾオキサゾール樹脂、その前駆体及びこれらを用いた光導波路材料並びに光導波路
|
|
WO2004089940A1
(fr)
|
2003-04-11 |
2004-10-21 |
Glenmark Pharmaceuticals S.A. |
Nouveaux composes heterocycliques pour le traitement des affections inflammatoires et allergiques, leur procede de preparation et compositions pharmaceutiques les contenant
|
|
JP2005002330A
(ja)
|
2003-05-19 |
2005-01-06 |
Sumitomo Electric Ind Ltd |
光学樹脂材料、光学素子、光モジュール、フッ素化ポリマー前駆体及びフッ素化ポリマー
|
|
ES2467160T3
(es)
|
2003-05-19 |
2014-06-12 |
Irm Llc |
Compuestos y composiciones inmunosupresores
|
|
US20060183746A1
(en)
|
2003-06-04 |
2006-08-17 |
Currie Kevin S |
Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds
|
|
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
|
|
US20070010573A1
(en)
|
2003-06-23 |
2007-01-11 |
Xianqi Kong |
Methods and compositions for treating amyloid-related diseases
|
|
US7393848B2
(en)
|
2003-06-30 |
2008-07-01 |
Cgi Pharmaceuticals, Inc. |
Certain heterocyclic substituted imidazo[1,2-A]pyrazin-8-ylamines and methods of inhibition of Bruton's tyrosine kinase by such compounds
|
|
WO2005007628A1
(fr)
|
2003-07-11 |
2005-01-27 |
Bristol-Myers Squibb Company |
Derives de tetrahydroquinoleine constituant des modulateurs des recepteurs des cannabinoides
|
|
WO2005004863A1
(fr)
|
2003-07-11 |
2005-01-20 |
Merck Patent Gmbh |
Benzimidazole carboxamides utilises en tant qu'inhibiteurs de la kinase raf
|
|
EP1661879A4
(fr)
|
2003-08-04 |
2006-11-29 |
Ono Pharmaceutical Co |
Compose d'ether de diphenyle, sa methode de preparation et d'utilisation
|
|
WO2005014543A1
(fr)
|
2003-08-06 |
2005-02-17 |
Japan Tobacco Inc. |
Compose a cycle condense utilise comme inhibiteur de la polymerase du vhc
|
|
US7504401B2
(en)
|
2003-08-29 |
2009-03-17 |
Locus Pharmaceuticals, Inc. |
Anti-cancer agents and uses thereof
|
|
JP4895811B2
(ja)
|
2003-09-11 |
2012-03-14 |
ケミア,インコーポレイテッド |
サイトカイン阻害剤
|
|
EP1673343A4
(fr)
|
2003-10-08 |
2008-09-10 |
Irm Llc |
Composes et compositions convenant comme inhibiteurs de proteine-kinases
|
|
EP1679309A4
(fr)
|
2003-10-24 |
2007-03-28 |
Ono Pharmaceutical Co |
Medicament antistress et usage medical correspondant
|
|
WO2005047290A2
(fr)
|
2003-11-11 |
2005-05-26 |
Cellular Genomics Inc. |
Certaines imidazo[1,2-a]pyrazin-8-ylamines, procede de fabrication et methode d'utilisation
|
|
WO2005063710A1
(fr)
|
2003-12-23 |
2005-07-14 |
Basf Aktiengesellschaft |
Anilides d'acide 3-trifluoromethylpicolinique et leur utilisation comme fongicides
|
|
EP1715867A4
(fr)
|
2004-02-12 |
2009-04-15 |
Merck & Co Inc |
Amides bipyridyles en tant que modulateurs du r cepteur-5 metabotropique du glutamate
|
|
JPWO2005077948A1
(ja)
|
2004-02-16 |
2008-01-10 |
第一製薬株式会社 |
抗真菌作用複素環化合物
|
|
GB0403864D0
(en)
|
2004-02-20 |
2004-03-24 |
Ucl Ventures |
Modulator
|
|
JP2005248082A
(ja)
|
2004-03-05 |
2005-09-15 |
Sumitomo Electric Ind Ltd |
ポリベンゾオキサゾール樹脂前駆体の製造方法およびポリベンゾオキサゾール樹脂の製造方法
|
|
US7432278B2
(en)
|
2004-03-08 |
2008-10-07 |
The University Of North Carolina At Chapel Hill |
Dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridines as antiprotozoal agents
|
|
AU2005221140A1
(en)
|
2004-03-08 |
2005-09-22 |
Amgen Inc. |
Therapeutic modulation of PPAR (gamma) activity
|
|
EP1761496A2
(fr)
|
2004-03-31 |
2007-03-14 |
Janssen Pharmaceutica N.V. |
Heterocycles ne comprenant pas d`imidazole utilisables comme ligands des recepteurs histamine h3
|
|
JP2005290301A
(ja)
|
2004-04-02 |
2005-10-20 |
Sumitomo Electric Ind Ltd |
ポリベンゾオキサゾール樹脂前駆体の製造方法およびポリベンゾオキサゾール樹脂の製造方法
|
|
WO2005099656A2
(fr)
|
2004-04-06 |
2005-10-27 |
The Procter & Gamble Company |
Composes de teinture de la keratine, compositions de teinture de la keratine contenant ces composes et leurs utilisations
|
|
NZ550114A
(en)
|
2004-04-20 |
2011-02-25 |
Transtech Pharma Inc |
Substituted thiazole and pyrimidine derivatives as melanocortin receptor modulators
|
|
DE102004021716A1
(de)
|
2004-04-30 |
2005-12-01 |
Grünenthal GmbH |
Substituierte Imidazo[1,2-a]pyridin-Verbindungen und Arzneimittel enthaltend substituierte Imidazo[1,2-a]pyridin-Verbindungen
|
|
CA2560387C
(fr)
|
2004-05-03 |
2013-09-24 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Inhibiteurs de cytokines
|
|
PE20060748A1
(es)
|
2004-09-21 |
2006-10-01 |
Smithkline Beecham Corp |
Derivados de indolcarboxamida como inhibidores de quinasa ikk2
|
|
JP2008514611A
(ja)
|
2004-09-23 |
2008-05-08 |
ワイス |
C型肝炎ウイルスによる感染を処置するためのカルバゾールおよびシクロペンタインドールの誘導体
|
|
US7713973B2
(en)
|
2004-10-15 |
2010-05-11 |
Takeda Pharmaceutical Company Limited |
Kinase inhibitors
|
|
AU2005304473A1
(en)
|
2004-11-10 |
2006-05-18 |
Cgi Pharmaceuticals, Inc. |
Imidazo[1 , 2-a] pyrazin-8-ylamines useful as modulators of kinase activity
|
|
DE102004054665A1
(de)
|
2004-11-12 |
2006-05-18 |
Bayer Cropscience Gmbh |
Substituierte bi- und tricyclische Pyrazol-Derivate Verfahren zur Herstellung und Verwendung als Herbizide und Pflanzenwachstumsregulatoren
|
|
AU2006218403A1
(en)
|
2005-03-03 |
2006-09-08 |
Sirtris Pharmaceuticals, Inc. |
Fused heterocyclic compounds and their use as sirtuin modulators
|
|
JP2008533032A
(ja)
|
2005-03-10 |
2008-08-21 |
シージーアイ ファーマシューティカルズ,インコーポレイティド |
或る種の置換アミド、その製造方法及び使用方法
|
|
JP2006290883A
(ja)
|
2005-03-17 |
2006-10-26 |
Nippon Nohyaku Co Ltd |
置換ヘテロ環カルボン酸アニリド誘導体、その中間体及び農園芸用薬剤並びにその使用方法
|
|
US7906522B2
(en)
|
2005-04-28 |
2011-03-15 |
Kyowa Hakko Kirin Co., Ltd |
2-aminoquinazoline derivatives
|
|
AU2006244885B2
(en)
|
2005-05-09 |
2011-03-31 |
E. R. Squibb & Sons, L.L.C. |
Human monoclonal antibodies to programmed death 1(PD-1) and methods for treating cancer using anti-PD-1 antibodies alone or in combination with other immunotherapeutics
|
|
BRPI0610863A2
(pt)
|
2005-05-20 |
2010-08-03 |
Array Biopharma Inc |
compostos inibidores de raf e métodos para sua utilização
|
|
AU2006265108C1
(en)
|
2005-07-01 |
2013-01-17 |
E. R. Squibb & Sons, L.L.C. |
Human monoclonal antibodies to programmed death ligand 1 (PD-L1)
|
|
US20080220968A1
(en)
|
2005-07-05 |
2008-09-11 |
Ge Healthcare Bio-Sciences Ab |
[1, 2, 4] Triazolo [1, 5-A] Pyrimidine Derivatives as Chromatographic Adsorbent for the Selective Adsorption of Igg
|
|
WO2007034282A2
(fr)
|
2005-09-19 |
2007-03-29 |
Pfizer Products Inc. |
Composes de biphenylimidazole utilises comme antagonistes du recepteur du c3a
|
|
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
|
|
EP2597087B1
(fr)
|
2005-10-25 |
2016-03-30 |
Shionogi&Co., Ltd. |
Dérivés dihydrooxazine et tétrahydropyrimidine comme inhibiteurs de BACE 1
|
|
US8518964B2
(en)
|
2005-11-22 |
2013-08-27 |
Merck Sharp & Dohme Corp. |
Tricyclic compounds useful as inhibitors of kinases
|
|
WO2007067711A2
(fr)
|
2005-12-08 |
2007-06-14 |
Amphora Discovery Corporation |
Certains types d'entites chimiques, compositions et methode de modulation de trpv1
|
|
JPWO2007069565A1
(ja)
|
2005-12-12 |
2009-05-21 |
小野薬品工業株式会社 |
二環式複素環化合物
|
|
US20090281075A1
(en)
|
2006-02-17 |
2009-11-12 |
Pharmacopeia, Inc. |
Isomeric purinones and 1h-imidazopyridinones as pkc-theta inhibitors
|
|
WO2007096764A2
(fr)
|
2006-02-27 |
2007-08-30 |
Glenmark Pharmaceuticals S.A. |
Dérivés d'hétéroaryles bicycliques en tant que modulateurs des récepteurs cannabinoïdes
|
|
JPWO2007102531A1
(ja)
|
2006-03-08 |
2009-07-23 |
武田薬品工業株式会社 |
併用薬
|
|
AU2007233709A1
(en)
|
2006-03-31 |
2007-10-11 |
Novartis Ag |
Organic compounds
|
|
EP2023919A4
(fr)
|
2006-05-08 |
2010-12-22 |
Molecular Neuroimaging Llc |
Composés et sondes amyloïdes de ceux-ci pour des utilisations thérapeutiques et en imagerie
|
|
WO2007146712A2
(fr)
|
2006-06-09 |
2007-12-21 |
Kemia, Inc. |
Thérapie à base d'inhibiteurs de cytokine
|
|
US20080280891A1
(en)
|
2006-06-27 |
2008-11-13 |
Locus Pharmaceuticals, Inc. |
Anti-cancer agents and uses thereof
|
|
EP2044061A2
(fr)
|
2006-07-20 |
2009-04-08 |
Mehmet Kahraman |
Inhibiteurs de la rho kinase à base de benzothiophène
|
|
DE102006035018B4
(de)
|
2006-07-28 |
2009-07-23 |
Novaled Ag |
Oxazol-Triplett-Emitter für OLED-Anwendungen
|
|
WO2008021745A2
(fr)
|
2006-08-16 |
2008-02-21 |
Itherx Pharmaceuticals, Inc. |
Inhibiteurs de la pénétration du virus de l'hépatite c
|
|
TWI389895B
(zh)
|
2006-08-21 |
2013-03-21 |
Infinity Discovery Inc |
抑制bcl蛋白質與結合夥伴間之交互作用的化合物及方法
|
|
WO2008027812A2
(fr)
|
2006-08-28 |
2008-03-06 |
Forest Laboratories Holdings Limited |
Dérivés d'imidazopyridine et d'imidazopyrimidine
|
|
US20100160292A1
(en)
|
2006-09-11 |
2010-06-24 |
Cgi Pharmaceuticals, Inc |
Kinase Inhibitors, and Methods of Using and Identifying Kinase Inhibitors
|
|
US7838523B2
(en)
|
2006-09-11 |
2010-11-23 |
Cgi Pharmaceuticals, Inc. |
Certain substituted amides, method of making, and method of use thereof
|
|
CN101573348A
(zh)
|
2006-09-11 |
2009-11-04 |
矩阵实验室有限公司 |
作为pde-4和pde-10的抑制剂的二苯并呋喃衍生物
|
|
PE20081370A1
(es)
|
2006-09-11 |
2008-11-28 |
Cgi Pharmaceuticals Inc |
Determinadas amidas sustituidas, metodo de elaboracion y metodo de uso de las mismas
|
|
AR063706A1
(es)
|
2006-09-11 |
2009-02-11 |
Cgi Pharmaceuticals Inc |
Determinadas amidas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmaceuticas que las comprenden.
|
|
FR2906250B1
(fr)
|
2006-09-22 |
2008-10-31 |
Sanofi Aventis Sa |
Derives de 2-aryl-6phenyl-imidazo(1,2-a) pyridines, leur preparation et leur application en therapeutique
|
|
EP2074107A2
(fr)
|
2006-10-27 |
2009-07-01 |
Wyeth a Corporation of the State of Delaware |
Composes tricycliques servant d'inhibiteurs des metalloproteases matricielles
|
|
HRP20130626T1
(en)
|
2006-11-08 |
2013-08-31 |
Bristol-Myers Squibb Company |
Pyridinone compounds
|
|
GB0623209D0
(en)
|
2006-11-21 |
2007-01-03 |
F2G Ltd |
Antifungal agents
|
|
WO2008064317A1
(fr)
|
2006-11-22 |
2008-05-29 |
University Of Medicine And Dentistry Of New Jersey |
Composés actifs de récepteurs opioïdes lipophiles
|
|
WO2008064318A2
(fr)
|
2006-11-22 |
2008-05-29 |
University Of Medicine And Dentistry Of New Jersey |
Composés actifs de récepteurs opioïdes périphériques
|
|
JP2010513253A
(ja)
|
2006-12-14 |
2010-04-30 |
ベーリンガー インゲルハイム インテルナショナール ゲーエムベーハー |
炎症の治療に有用なベンゾオキサゾール類
|
|
ES2415863T3
(es)
|
2006-12-22 |
2013-07-29 |
Incyte Corporation |
Heterociclos sustituidos como inhibidores de Janus Quinasas
|
|
EP1964841A1
(fr)
|
2007-02-28 |
2008-09-03 |
sanofi-aventis |
Imidazo[1,2-a]azine et son utilisation en tant que produit pharmaceutique
|
|
EP2137158A4
(fr)
|
2007-02-28 |
2012-04-18 |
Methylgene Inc |
Inhibiteurs à petite molécule de protéines arginine méthyltransférases (prmt)
|
|
EP1964840A1
(fr)
|
2007-02-28 |
2008-09-03 |
sanofi-aventis |
Imidazo[1,2-a]pyridines et leur utilisation en tant que produits pharmaceutiques
|
|
JP2008218327A
(ja)
|
2007-03-07 |
2008-09-18 |
Hitachi Ltd |
電解質、電解質膜、それを用いた膜電極接合体、燃料電池電源及び燃料電池電源システム
|
|
JP2010120852A
(ja)
|
2007-03-09 |
2010-06-03 |
Daiichi Sankyo Co Ltd |
新規なジアミド誘導体
|
|
CN101679350B
(zh)
|
2007-03-22 |
2014-03-12 |
阿斯利康(瑞典)有限公司 |
用于治疗炎性疾病的喹啉衍生物
|
|
AU2008245082B8
(en)
|
2007-04-24 |
2012-09-13 |
Shionogi & Co., Ltd. |
Aminodihydrothiazine derivatives substituted with a cyclic group
|
|
JP5383483B2
(ja)
|
2007-04-24 |
2014-01-08 |
塩野義製薬株式会社 |
アルツハイマー症治療用医薬組成物
|
|
WO2008134553A1
(fr)
|
2007-04-26 |
2008-11-06 |
Xenon Pharmaceuticals Inc. |
Procédés de traitement de maladies associées aux canaux sodiques au moyen de composés bicycliques
|
|
WO2008141249A1
(fr)
|
2007-05-10 |
2008-11-20 |
Acadia Pharmaceuticals Inc. |
Imidazol (1,2-a)pyridines et composés associés à activité au niveau des récepteurs cannabinoïdes cb2
|
|
CA2691357C
(fr)
|
2007-06-18 |
2014-09-23 |
N.V. Organon |
Anticorps diriges contre le recepteur humain de mort programmee pd-1
|
|
WO2009027733A1
(fr)
|
2007-08-24 |
2009-03-05 |
Astrazeneca Ab |
Dérivés de (2-pyridin-3-ylimidazo[1,2-b]pyridazin-6-yl)urée en tant qu'agents antibactériens
|
|
US8080542B2
(en)
|
2007-09-20 |
2011-12-20 |
Amgen, Inc. |
S1P receptor modulating compounds and use thereof
|
|
CL2008002793A1
(es)
|
2007-09-20 |
2009-09-04 |
Cgi Pharmaceuticals Inc |
Compuestos derivados de amidas sustituidas, inhibidores de la actividad de btk; composicion farmaceutica que los comprende; utiles en el tratamiento del cancer, trastornos oseos, enfermedades autoinmunes, entre otras
|
|
DE102007048716A1
(de)
|
2007-10-11 |
2009-04-23 |
Merck Patent Gmbh |
Imidazo[1,2-a]pyrimidinderivate
|
|
TW200932219A
(en)
|
2007-10-24 |
2009-08-01 |
Astellas Pharma Inc |
Oxadiazolidinedione compound
|
|
JP2011500778A
(ja)
|
2007-10-25 |
2011-01-06 |
アストラゼネカ・アクチエボラーグ |
ピリジン及びピラジン誘導体−083
|
|
US7868001B2
(en)
|
2007-11-02 |
2011-01-11 |
Hutchison Medipharma Enterprises Limited |
Cytokine inhibitors
|
|
WO2009062059A2
(fr)
|
2007-11-08 |
2009-05-14 |
Pharmacopeia, Inc. |
Purinones et 1h-imidazopyridinones isomères comme inhibiteurs de pkc-thêta
|
|
JP5489296B2
(ja)
|
2007-12-13 |
2014-05-14 |
メルク・シャープ・アンド・ドーム・コーポレーション |
Janusキナーゼの阻害剤
|
|
RU2364597C1
(ru)
|
2007-12-14 |
2009-08-20 |
Андрей Александрович Иващенко |
ГЕТЕРОЦИКЛИЧЕСКИЕ ИНГИБИТОРЫ Hh-СИГНАЛЬНОГО КАСКАДА, ЛЕКАРСТВЕННЫЕ КОМПОЗИЦИИ НА ИХ ОСНОВЕ И СПОСОБ ЛЕЧЕНИЯ ЗАБОЛЕВАНИЙ, СВЯЗАННЫХ С АББЕРАНТНОЙ АКТИВНОСТЬЮ Hh СИГНАЛЬНОЙ СИСТЕМЫ
|
|
EP2230913B1
(fr)
|
2007-12-19 |
2017-10-18 |
Syngenta Participations AG |
Composés insecticides
|
|
AU2008345225A1
(en)
|
2007-12-21 |
2009-07-09 |
University Of Rochester |
Method for altering the lifespan of eukaryotic organisms
|
|
EP2231659A4
(fr)
|
2007-12-21 |
2011-10-26 |
Univ Sydney |
Ligands de la protéine de translocation
|
|
HUE026064T2
(en)
|
2008-01-18 |
2016-05-30 |
Eisai R&D Man Co Ltd |
Condensed aminodihydrothiazine derivatives
|
|
WO2009096202A1
(fr)
|
2008-01-31 |
2009-08-06 |
Konica Minolta Holdings, Inc. |
Composé aromatique polycyclique halogéné et son procédé de production
|
|
MX2010009416A
(es)
|
2008-02-26 |
2010-09-24 |
Novartis Ag |
Compuestos heterociclicos como inhibidores de cxcr2.
|
|
EP2095818A1
(fr)
|
2008-02-29 |
2009-09-02 |
AEterna Zentaris GmbH |
Utilisation d'antagonistes LHRH dans des doses n'impliquant pas de castration
|
|
EP2262837A4
(fr)
|
2008-03-12 |
2011-04-06 |
Merck Sharp & Dohme |
Protéines de liaison avec pd-1
|
|
FR2928921B1
(fr)
|
2008-03-21 |
2010-04-23 |
Sanofi Aventis |
Derives polysubstitues de 2-aryl-6-phenyl-imidazo°1,2-a!pyridines, leur preparation et leur application en therapeutique
|
|
FR2928922B1
(fr)
|
2008-03-21 |
2010-04-23 |
Sanofi Aventis |
Derives de 2-aryl-6-phenyl-imidazo°1,2-a!pyridines polysubstitues, leur preparation et leur application en therapeutique
|
|
FR2928924B1
(fr)
|
2008-03-21 |
2010-04-23 |
Sanofi Aventis |
Derives polysubstitues de 6-heteroaryle-imidazo°1,2-a! pyridines, leur preparation et leur application en therapeutique
|
|
EP2271646A1
(fr)
|
2008-03-31 |
2011-01-12 |
Takeda Pharmaceutical Company Limited |
Inhibiteurs de kinase 1 de régulation de signal d'apoptose
|
|
KR101034351B1
(ko)
|
2008-05-14 |
2011-05-16 |
한국화학연구원 |
신규 벤즈옥사졸로 치환된 피리딘 유도체 또는 이의약학적으로 허용가능한 염, 이의 제조방법 및 이를유효성분으로 함유하는 이상세포 성장 질환의 예방 및치료용 약학적 조성물
|
|
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.
|
|
EP2280946B1
(fr)
|
2008-06-05 |
2016-02-10 |
Glaxo Group Limited |
Dérivés de 4-carboxamide indazole utiles en tant qu'inhibiteurs de p13 kinases
|
|
US8476430B2
(en)
|
2008-07-24 |
2013-07-02 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds useful as kinase modulators
|
|
US9540322B2
(en)
|
2008-08-18 |
2017-01-10 |
Yale University |
MIF modulators
|
|
US9643922B2
(en)
|
2008-08-18 |
2017-05-09 |
Yale University |
MIF modulators
|
|
JP2011231017A
(ja)
|
2008-09-09 |
2011-11-17 |
Nissan Chem Ind Ltd |
光学活性エポキシ化合物及び光学活性スルホキシド化合物の製造方法、並びに該方法に用いる配位子、錯体及び該錯体の製造方法
|
|
PL2342226T3
(pl)
|
2008-09-26 |
2017-01-31 |
Dana-Farber Cancer Institute, Inc. |
Ludzkie przeciwciała anty-PD-1, PD-L1 i PD-L2 oraz ich zastosowania
|
|
US8598174B2
(en)
|
2008-11-12 |
2013-12-03 |
Genetech, Inc. |
Pyridazinones, method of making, and method of use thereof
|
|
WO2010064020A1
(fr)
|
2008-12-04 |
2010-06-10 |
Proximagen Ltd. |
Composés imidazopyridines
|
|
PT2376535T
(pt)
|
2008-12-09 |
2017-06-23 |
Hoffmann La Roche |
Anticorpos anti-pd-l1 e a sua utilização para a melhoria do funcionamento das células t
|
|
ES2490867T3
(es)
|
2008-12-19 |
2014-09-04 |
Bristol-Myers Squibb Company |
Inhibidores de carbazol y carbolina quinasas
|
|
AR074830A1
(es)
|
2008-12-19 |
2011-02-16 |
Cephalon Inc |
Pirrolotriazinas como inhibidores de alk y jak2
|
|
SG171815A1
(en)
|
2008-12-19 |
2011-07-28 |
Bristol Myers Squibb Co |
Carbazole carboxamide compounds useful as kinase inhibitors
|
|
JP5624275B2
(ja)
|
2008-12-22 |
2014-11-12 |
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
|
|
RU2505540C2
(ru)
|
2008-12-23 |
2014-01-27 |
Эббви Инк. |
Антивирусные соединения
|
|
WO2010074284A1
(fr)
|
2008-12-26 |
2010-07-01 |
味の素株式会社 |
Composé de pyrazolopyrimidine
|
|
EP3192811A1
(fr)
|
2009-02-09 |
2017-07-19 |
Université d'Aix-Marseille |
Anticorps pd-1 et pd-l1 et leurs utilisations
|
|
JP2010202530A
(ja)
|
2009-02-27 |
2010-09-16 |
Tokyo Institute Of Technology |
含ヘテロ芳香族化合物および光学材料
|
|
KR20100101055A
(ko)
|
2009-03-07 |
2010-09-16 |
주식회사 메디젠텍 |
세포핵에서 세포질로의 gsk3의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 gsk3 이동 관련 질환의 치료 또는 예방용 약학적 조성물
|
|
CN104030987B
(zh)
|
2009-04-02 |
2017-04-12 |
默克雪兰诺有限公司 |
二氢乳清酸脱氢酶抑制剂
|
|
KR20120034613A
(ko)
|
2009-04-16 |
2012-04-12 |
센트로 내셔널 드 인베스티가시오네스 온콜로지카스 (씨엔아이오) |
키나아제 억제제로서 사용을 위한 이미다조피라진
|
|
US8338441B2
(en)
|
2009-05-15 |
2012-12-25 |
Gilead Sciences, Inc. |
Inhibitors of human immunodeficiency virus replication
|
|
EP2448410A4
(fr)
|
2009-06-30 |
2013-12-18 |
Siga Technologies Inc |
Traitement et prévention d'infections par le virus de la dengue
|
|
US8993604B2
(en)
|
2009-06-30 |
2015-03-31 |
Siga Technologies, Inc. |
Treatment and prevention of dengue virus infections
|
|
TWI491606B
(zh)
|
2009-07-13 |
2015-07-11 |
Gilead Sciences Inc |
調節細胞凋亡信號之激酶的抑制劑
|
|
JP2011057661A
(ja)
|
2009-08-14 |
2011-03-24 |
Bayer Cropscience Ag |
殺虫性カルボキサミド類
|
|
UA108363C2
(uk)
|
2009-10-08 |
2015-04-27 |
|
Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування
|
|
US9095596B2
(en)
|
2009-10-15 |
2015-08-04 |
Southern Research Institute |
Treatment of neurodegenerative diseases, causation of memory enhancement, and assay for screening compounds for such
|
|
DK2488525T3
(en)
|
2009-10-16 |
2018-08-06 |
Melinta Therapeutics Inc |
ANTIMICROBIAL COMPOUNDS AND PROCEDURES FOR PREPARING AND USING THEREOF
|
|
WO2011050245A1
(fr)
|
2009-10-23 |
2011-04-28 |
Yangbo Feng |
Hétéroaryles bicycliques formant inhibiteurs de la kinase
|
|
EP2504028A4
(fr)
|
2009-11-24 |
2014-04-09 |
Amplimmune Inc |
Inhibition simultanée de pd-l1/pd-l2
|
|
JPWO2011078221A1
(ja)
|
2009-12-24 |
2013-05-09 |
味の素株式会社 |
イミダゾピリダジン化合物
|
|
US20130022629A1
(en)
|
2010-01-04 |
2013-01-24 |
Sharpe Arlene H |
Modulators of Immunoinhibitory Receptor PD-1, and Methods of Use Thereof
|
|
WO2011097607A1
(fr)
|
2010-02-08 |
2011-08-11 |
Southern Research Institute |
Traitement antiviral et dosage pour cribler des antiviraux
|
|
TW201136919A
(en)
|
2010-03-02 |
2011-11-01 |
Merck Sharp & Amp Dohme Corp |
Inhibitors of hepatitis C virus NS5B polymerase
|
|
WO2011109254A1
(fr)
|
2010-03-04 |
2011-09-09 |
Merck Sharp & Dohme Corp. |
Inhibiteurs de catéchol o-méthyl transférase et utilisation associée dans le traitement de troubles psychotiques
|
|
KR101732212B1
(ko)
|
2010-03-18 |
2017-05-02 |
재단법인 한국파스퇴르연구소 |
항감염성 화합물
|
|
US8410117B2
(en)
|
2010-03-26 |
2013-04-02 |
Hoffmann-La Roche Inc. |
Imidazopyrimidine derivatives
|
|
US8685969B2
(en)
|
2010-06-16 |
2014-04-01 |
Bristol-Myers Squibb Company |
Carboline carboxamide compounds useful as kinase inhibitors
|
|
US9163087B2
(en)
|
2010-06-18 |
2015-10-20 |
The Brigham And Women's Hospital, Inc. |
Bi-specific antibodies against TIM-3 and PD-1 for immunotherapy in chronic immune conditions
|
|
US8907053B2
(en)
|
2010-06-25 |
2014-12-09 |
Aurigene Discovery Technologies Limited |
Immunosuppression modulating compounds
|
|
CN102295642B
(zh)
|
2010-06-25 |
2016-04-06 |
中国人民解放军军事医学科学院毒物药物研究所 |
2-芳基咪唑并[1,2-a]吡啶-3-乙酰胺衍生物、其制备方法及用途
|
|
EP2402345A1
(fr)
|
2010-06-29 |
2012-01-04 |
Basf Se |
Composés pyrazoliques bicycliques condenses
|
|
CN101891895B
(zh)
|
2010-07-28 |
2011-11-30 |
南京航空航天大学 |
基于桥联双水杨醛结构的苯并噻唑类金属配位聚合物及其制法及应用
|
|
WO2012016133A2
(fr)
|
2010-07-29 |
2012-02-02 |
President And Fellows Of Harvard College |
Inhibiteurs de la ros1 kinase pour le traitement de glioblastome et d'autres cancers déficients en p53
|
|
US8633200B2
(en)
|
2010-09-08 |
2014-01-21 |
Bristol-Myers Squibb Company |
Inhibitors of human immunodeficiency virus replication
|
|
CN101993415B
(zh)
|
2010-09-15 |
2013-08-14 |
北京韩美药品有限公司 |
作为Hedgehog通路抑制剂的化合物以及包含该化合物的药物组合物及其应用
|
|
US8921381B2
(en)
|
2010-10-04 |
2014-12-30 |
Baruch S. Blumberg Institute |
Inhibitors of secretion of hepatitis B virus antigens
|
|
WO2012052745A1
(fr)
|
2010-10-21 |
2012-04-26 |
Centro Nacional De Investigaciones Oncológicas (Cnio) |
Combinaisons d'inhibiteurs de pi3k avec un second agent antitumoral
|
|
EP2444084A1
(fr)
|
2010-10-21 |
2012-04-25 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Utilisation d'inhibiteurs de PI3K pour le traitement de l'obésité
|
|
US20140243324A1
(en)
|
2010-11-18 |
2014-08-28 |
Ligand Pharmaceuticals Incorporated |
Use of hematopoietic growth factor mimetics
|
|
UY33808A
(es)
|
2010-12-17 |
2012-07-31 |
Syngenta Participations Ag |
Compuestos insecticidas
|
|
TWI617559B
(zh)
|
2010-12-22 |
2018-03-11 |
江蘇恆瑞醫藥股份有限公司 |
2-芳基咪唑并[1,2-b]嗒.2-苯基咪唑并[1,2-a]吡啶,和2-苯基咪唑并[1,2-a]吡衍生物
|
|
PE20140471A1
(es)
|
2011-01-04 |
2014-04-13 |
Novartis Ag |
Moduladores de la via del complemento y usos de los mismos
|
|
CA2825098C
(fr)
|
2011-01-27 |
2020-03-10 |
Universite De Montreal |
Pyrazolopyridine et derives de pyrazolopyrimidine en tant que modulateurs du recepteur de la melanocortine-4
|
|
US8921368B2
(en)
|
2011-03-17 |
2014-12-30 |
Bristol-Myers Squibb Company |
Pyrrolopyridazine JAK3 inhibitors and their use for the treatment of inflammatory and autoimmune diseases
|
|
US9464065B2
(en)
|
2011-03-24 |
2016-10-11 |
The Scripps Research Institute |
Compounds and methods for inducing chondrogenesis
|
|
US9499502B2
(en)
|
2011-04-13 |
2016-11-22 |
Merck Sharp & Dohme Corp. |
5-substituted iminothiazines and their mono- and dioxides as BACE inhibitors, compositions, and their use
|
|
CN102796103A
(zh)
|
2011-05-23 |
2012-11-28 |
南京英派药业有限公司 |
6-(芳基甲酰)咪唑并[1,2-a]嘧啶和6-(芳基甲酰)[1,2,4]三唑并[4,3-a]嘧啶作为Hedgehog抑制剂及其应用
|
|
DK2713722T3
(en)
|
2011-05-31 |
2017-07-03 |
Celgene Int Ii Sarl |
Newly known GLP-1 receptor stabilizers and modulators
|
|
GB201109763D0
(en)
|
2011-06-10 |
2011-07-27 |
Ucl Business Plc |
Compounds
|
|
WO2012175991A1
(fr)
|
2011-06-24 |
2012-12-27 |
Pharminox Limited |
Composés pentacycliques fusionnés anti-prolifératifs
|
|
CN103732596B
(zh)
|
2011-07-08 |
2016-06-01 |
诺华股份有限公司 |
吡咯并嘧啶衍生物
|
|
EP2548877A1
(fr)
|
2011-07-19 |
2013-01-23 |
MSD Oss B.V. |
Dérivés de 4-(pyridine condensée à 5 chaînons)benzamide comme inhibiteurs de BTK
|
|
WO2013033901A1
(fr)
|
2011-09-08 |
2013-03-14 |
Merck Sharp & Dohme Corp. |
Dérivés benzofuranes substitués par un hétérocycle et leurs procédés d'utilisation pour le traitement de maladies virales
|
|
WO2013040528A1
(fr)
|
2011-09-16 |
2013-03-21 |
Microbiotix, Inc. |
Composés antimicrobiens
|
|
WO2013043521A1
(fr)
|
2011-09-22 |
2013-03-28 |
Merck Sharp & Dohme Corp. |
Composés pyrazolopyridyle à utiliser en tant qu'inhibiteurs de l'aldostérone synthase
|
|
JP6040677B2
(ja)
|
2011-09-29 |
2016-12-07 |
東洋インキScホールディングス株式会社 |
太陽電池封止材用樹脂組成物
|
|
KR20140084146A
(ko)
|
2011-10-13 |
2014-07-04 |
노파르티스 아게 |
신규 옥사진 유도체 및 질환의 치료에서의 그의 용도
|
|
CA2852939A1
(fr)
|
2011-10-20 |
2013-04-25 |
Glaxosmithkline Llc |
Aza-heterocycles bicycliques substitues et analogues en tant que modulateurs des sirtuines
|
|
JP2014530850A
(ja)
|
2011-10-21 |
2014-11-20 |
トレント・ファーマシューティカルズ・リミテッドTorrent Pharmaceuticals Limited |
Gpbar1受容体調節剤としての新規置換イミダゾピリミジン
|
|
WO2013120040A1
(fr)
|
2012-02-10 |
2013-08-15 |
Children's Medical Center Corporation |
Inhibition d'une voie ciblée pour améliorer la structure, le fonctionnement et l'activité musculaires dans la dystrophie musculaire
|
|
US9034882B2
(en)
|
2012-03-05 |
2015-05-19 |
Bristol-Myers Squibb Company |
Inhibitors of human immunodeficiency virus replication
|
|
IN2014MN01897A
(fr)
|
2012-03-09 |
2015-07-10 |
Carna Biosciences Inc |
|
|
RU2711077C9
(ru)
|
2012-03-15 |
2020-08-11 |
Селджен Кар Ллс |
Соли ингибитора киназы рецептора эпидермального фактора роста
|
|
SG11201401189WA
(en)
|
2012-04-20 |
2014-09-26 |
Gilead Sciences Inc |
Benzothiazol- 6 -yl acetic acid derivatives and their use for treating an hiv infection
|
|
WO2013157021A1
(fr)
|
2012-04-20 |
2013-10-24 |
Advinus Therapeutics Limited |
Composés bicycliques, compositions et applications médicinales de ceux-ci
|
|
WO2013163404A1
(fr)
|
2012-04-27 |
2013-10-31 |
The Uab Research Foundation |
Traitement d'infections virales avec arn viraux traduits par un mécanisme non médié par l'ires
|
|
WO2013191113A1
(fr)
|
2012-06-18 |
2013-12-27 |
住友化学株式会社 |
Composé hétérocyclique fusionné
|
|
WO2014007228A1
(fr)
|
2012-07-03 |
2014-01-09 |
小野薬品工業株式会社 |
Composé ayant une activité agoniste sur un récepteur de la somatostatine, et leur utilisation à des fins médicales
|
|
JP6259823B2
(ja)
|
2012-07-13 |
2018-01-10 |
ユーシービー バイオファルマ エスピーアールエル |
Tnf活性の調節物質としてのイミダゾピリジン誘導体
|
|
GB201212513D0
(en)
|
2012-07-13 |
2012-08-29 |
Ucb Pharma Sa |
Therapeutic agents
|
|
JP2015178457A
(ja)
|
2012-07-25 |
2015-10-08 |
杏林製薬株式会社 |
ピラゾロピリジン誘導体、またはその薬理学的に許容される塩
|
|
EP2892899B1
(fr)
|
2012-09-06 |
2018-03-21 |
Bristol-Myers Squibb Company |
Inhibiteurs de jak3 de type imidazopyridazine et leur utilisation pour le traitement de maladies inflammatoires et auto-immunes
|
|
BR112015006019B1
(pt)
|
2012-09-26 |
2021-01-05 |
F. Hoffmann-La Roche Ag |
composto e uso de um composto
|
|
WO2014061693A1
(fr)
|
2012-10-17 |
2014-04-24 |
塩野義製薬株式会社 |
Nouveau dérivé carbocyclique non aromatique ou hétérocyclique non aromatique
|
|
US9163027B2
(en)
|
2012-11-21 |
2015-10-20 |
Stategics, Inc. |
Substituted triazolo-pyrimidine compounds for modulating cell proliferation differentiation and survival
|
|
JP6037804B2
(ja)
|
2012-12-03 |
2016-12-07 |
富士フイルム株式会社 |
ガス分離膜
|
|
AU2014207691B2
(en)
|
2013-01-15 |
2018-08-30 |
Incyte Holdings Corporation |
Thiazolecarboxamides and pyridinecarboxamide compounds useful as Pim kinase inhibitors
|
|
CN104968660A
(zh)
|
2013-01-22 |
2015-10-07 |
霍夫曼-拉罗奇有限公司 |
作为bace1抑制剂的氟-[1,3]噁嗪类化合物
|
|
CN103933036B
(zh)
|
2013-01-23 |
2017-10-13 |
中国人民解放军军事医学科学院毒物药物研究所 |
2‑芳基咪唑并[1,2‑α]吡啶‑3‑乙酰胺衍生物在制备防治PTSD的药物中的用途
|
|
WO2014121085A1
(fr)
|
2013-01-31 |
2014-08-07 |
Thomas Jefferson University |
Protéines de fusion à base de pd-l1 et pd-l2 et leurs utilisations
|
|
AU2014221799B2
(en)
|
2013-02-27 |
2017-09-28 |
Mochida Pharmaceutical Co., Ltd. |
Novel pyrazole derivative
|
|
KR20150124985A
(ko)
|
2013-03-08 |
2015-11-06 |
암젠 인크 |
베타-세크레타제 억제제로서 퍼플루오르화된 사이클로프로필 융합된 1,3-옥사진-2-아민 화합물 및 그의 사용 방법
|
|
JP2016516399A
(ja)
|
2013-03-13 |
2016-06-09 |
オーストラリアン ニュークリア サイエンス アンド テクノロジー オーガニゼーション |
非機能性tspo遺伝子を有するトランスジェニック非ヒト生物
|
|
CN104045552B
(zh)
|
2013-03-13 |
2019-06-11 |
江苏先声药业有限公司 |
作为神经保护剂的药用化合物
|
|
ES2705247T3
(es)
|
2013-03-14 |
2019-03-22 |
Univ Columbia |
4-fenilpiperidinas, su preparación y uso
|
|
US9527842B2
(en)
|
2013-03-14 |
2016-12-27 |
VIIV Healthcare UK (No.5) Limited |
Inhibitors of human immunodeficiency virus replication
|
|
CA2906086A1
(fr)
|
2013-03-14 |
2014-09-25 |
Celtaxsys, Inc. |
Inhibiteurs de la leucotriene a4 hydrolase
|
|
PE20151719A1
(es)
|
2013-03-14 |
2015-11-19 |
Curadev Pharma Private Ltd |
Inhibidores de la ruta de quinurenina
|
|
US9308236B2
(en)
|
2013-03-15 |
2016-04-12 |
Bristol-Myers Squibb Company |
Macrocyclic inhibitors of the PD-1/PD-L1 and CD80(B7-1)/PD-L1 protein/protein interactions
|
|
BR112015021983B1
(pt)
|
2013-03-15 |
2022-03-03 |
Plexxikon, Inc |
Compostos heterocíclicos, composições farmacêuticas que os compreendem e usos dos mesmos
|
|
WO2014181287A1
(fr)
|
2013-05-09 |
2014-11-13 |
Piramal Enterprises Limited |
Composés hétérocyclyliques et leurs utilisations
|
|
UY35630A
(es)
|
2013-06-26 |
2015-01-30 |
Abbvie Inc |
Carboxamidas primarias como inhibidores de btk
|
|
HUE049733T2
(hu)
|
2013-07-02 |
2020-10-28 |
Syngenta Participations Ag |
Növényvédõszerként aktív biciklusos vagy triciklusos heterociklusok kéntartalmú szubsztituensekkel
|
|
SG10201800325PA
(en)
|
2013-07-17 |
2018-02-27 |
Otsuka Pharma Co Ltd |
Cyanotriazole compounds
|
|
KR20160034379A
(ko)
|
2013-07-25 |
2016-03-29 |
다나-파버 캔서 인스티튜트 인크. |
전사 인자의 억제제 및 그의 용도
|
|
EP2835375A1
(fr)
|
2013-08-09 |
2015-02-11 |
Fundació Institut Català d'Investigació Química |
Composés salphen bis et composites de matériau carboné les comprenant
|
|
KR101715090B1
(ko)
|
2013-08-28 |
2017-03-13 |
한국화학연구원 |
신규한 화합물 또는 이의 약학적으로 허용가능한 염, 및 이를 유효성분으로 함유하는 인플루엔자 바이러스 감염으로 인한 질환의 예방 또는 치료용 약학적 조성물
|
|
SG11201601225RA
(en)
|
2013-09-04 |
2016-03-30 |
Bristol Myers Squibb Co |
Compounds useful as immunomodulators
|
|
HUE039014T2
(hu)
|
2013-09-06 |
2018-12-28 |
Aurigene Discovery Tech Ltd |
1,3,4-Oxadiazol és 1,3,4-tiadiazol származékok, mint immunomodulátorok
|
|
DK3041827T3
(en)
|
2013-09-06 |
2018-07-16 |
Aurigene Discovery Tech Ltd |
1,2,4-OXADIAZOLD DERIVATIVES AS IMMUNE MODULATORS
|
|
WO2015036927A1
(fr)
|
2013-09-10 |
2015-03-19 |
Aurigene Discovery Technologies Limited |
Dérivés peptidomimétiques d'immunomodulation
|
|
JP6336870B2
(ja)
|
2013-09-30 |
2018-06-06 |
日本ポリプロ株式会社 |
ビフェノール化合物及びそれを用いるオレフィン重合用触媒並びにオレフィン重合体の製造方法
|
|
FR3012140B1
(fr)
|
2013-10-18 |
2016-08-26 |
Arkema France |
Unite et procede pour la purification de methacrylate de methyle brut
|
|
GB201321733D0
(en)
|
2013-12-09 |
2014-01-22 |
Ucb Pharma Sa |
Therapeutic agents
|
|
GB201321746D0
(en)
|
2013-12-09 |
2014-01-22 |
Ucb Pharma Sa |
Therapeutic agents
|
|
GB201321743D0
(en)
|
2013-12-09 |
2014-01-22 |
Ucb Pharma Sa |
Therapeutic agents
|
|
GB201321736D0
(en)
|
2013-12-09 |
2014-01-22 |
Ucb Pharma Sa |
Therapeutic agents
|
|
WO2015095337A2
(fr)
|
2013-12-18 |
2015-06-25 |
The Rockefeller University |
Dérivés pyrazolo [1,5-a]pyrimidine carboxamide pour le traitement de troubles cognitifs
|
|
TW201540705A
(zh)
|
2014-01-03 |
2015-11-01 |
拜耳作物科學股份有限公司 |
做為殺蟲劑之新穎吡唑基雜芳基醯胺類
|
|
US20160356794A1
(en)
|
2014-02-10 |
2016-12-08 |
Merck Sharp & Dohme Corp. |
Antibodies that bind to human tau and assay for quantifying human tau using the antibodies
|
|
US9695205B2
(en)
|
2014-02-25 |
2017-07-04 |
Achillion Pharmaceuticals, Inc. |
Amide compounds for treatment of complement mediated disorders
|
|
US9394365B1
(en)
|
2014-03-12 |
2016-07-19 |
Yeda Research And Development Co., Ltd |
Reducing systemic regulatory T cell levels or activity for treatment of alzheimer's disease
|
|
JP6490464B2
(ja)
|
2014-03-26 |
2019-03-27 |
三井化学株式会社 |
遷移金属化合物、オレフィン重合用触媒およびオレフィン系重合体の製造方法
|
|
DK3125883T3
(da)
|
2014-04-04 |
2020-10-19 |
Iomet Pharma Ltd |
Indolderivater til anvendelse i medicin
|
|
US9850225B2
(en)
|
2014-04-14 |
2017-12-26 |
Bristol-Myers Squibb Company |
Compounds useful as immunomodulators
|
|
WO2015175678A1
(fr)
|
2014-05-14 |
2015-11-19 |
President And Fellows Of Harvard College |
Matériaux pour diodes électroluminescentes organiques
|
|
CN106065009B
(zh)
|
2014-06-28 |
2019-03-01 |
广东东阳光药业有限公司 |
作为丙型肝炎抑制剂的化合物及其在药物中的应用
|
|
CN104211726B
(zh)
|
2014-08-11 |
2017-06-16 |
中南民族大学 |
非茂类三齿双核钛配合物、制备方法及用途
|
|
EP3193608A4
(fr)
|
2014-09-17 |
2018-05-02 |
Epizyme, Inc. |
Inhibiteurs de carm1 et leurs utilisations
|
|
JP6777638B2
(ja)
|
2014-09-19 |
2020-10-28 |
マッカイ メディカル ファンデーション ザ プレスビュテロス チャーチ イン タイワン マッカイ メモリアル ホスピタル |
ベンゾ複素環化合物および薬剤
|
|
BR112017006305B1
(pt)
|
2014-10-06 |
2024-02-20 |
Merck Patent Gmbh |
Compostos heteroarila, seus usos, e composição farmacêutica
|
|
WO2016094688A1
(fr)
|
2014-12-10 |
2016-06-16 |
Massachusetts Institute Of Technology |
Dérivés fusionnés de 1,3-azole utiles pour le traitement de maladies prolifératives
|
|
JP6853619B2
(ja)
|
2015-01-16 |
2021-03-31 |
大塚製薬株式会社 |
シアノトリアゾール化合物の医薬用途
|
|
DE112016000383A5
(de)
|
2015-01-20 |
2017-10-05 |
Cynora Gmbh |
Organische Moleküle, insbesondere zur Verwendung in optoelektronischen Bauelementen
|
|
WO2016118404A1
(fr)
|
2015-01-20 |
2016-07-28 |
Merck Sharp & Dohme Corp. |
Dioxydes d'iminothiadiazine portant un substituant lié à une amine, utilisés en tant qu'inhibiteurs de bace, compositions les contenant et leur utilisation
|
|
WO2016156282A1
(fr)
|
2015-04-02 |
2016-10-06 |
Bayer Cropscience Aktiengesellschaft |
Nouveaux composés de triazole pour contrôler des champignons nocifs phytopathogènes
|
|
WO2017035405A1
(fr)
|
2015-08-26 |
2017-03-02 |
Achillion Pharmaceuticals, Inc. |
Composés amino pour le traitement de troubles immunitaires et inflammatoires
|
|
US10745382B2
(en)
|
2015-10-15 |
2020-08-18 |
Bristol-Myers Squibb Company |
Compounds useful as immunomodulators
|
|
WO2017070089A1
(fr)
|
2015-10-19 |
2017-04-27 |
Incyte Corporation |
Composés hétérocycliques utilisés comme immunomodulateurs
|
|
US10633370B2
(en)
|
2015-10-21 |
2020-04-28 |
University of Pittsburgh—of the Commonwealth System of Higher Education |
Phenyl indole allosteric inhibitors of p97 ATPase
|
|
US9603950B1
(en)
|
2015-10-25 |
2017-03-28 |
Institute Of Nuclear Energy Research |
Compounds of imaging agent with HDAC inhibitor for treatment of Alzheimer syndrome and method of synthesis thereof
|
|
KR101717601B1
(ko)
|
2015-11-10 |
2017-03-20 |
한국화학연구원 |
신규한 화합물 또는 이의 약학적으로 허용가능한 염, 및 이를 유효성분으로 함유하는 인플루엔자 바이러스 감염으로 인한 질환의 예방 또는 치료용 약학적 조성물
|
|
ES2928856T3
(es)
|
2015-11-19 |
2022-11-23 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
|
WO2017106634A1
(fr)
|
2015-12-17 |
2017-06-22 |
Incyte Corporation |
Dérivés de n-phényl-pyridine-2-carboxamide et leur utilisation comme modulateurs d'interactions protéine/protéine pd-1/pd-l1
|
|
HRP20210698T1
(hr)
|
2015-12-22 |
2021-09-17 |
Immatics Biotechnologies Gmbh |
Peptidi i kombinacija peptida za uporabu u imunoterapiji protiv karcinoma dojke i drugih karcinoma
|
|
WO2017107052A1
(fr)
|
2015-12-22 |
2017-06-29 |
Merck Sharp & Dohme Corp. |
Activateurs solubles de guanylate cyclase
|
|
MX2018007527A
(es)
|
2015-12-22 |
2018-09-07 |
Syngenta Participations Ag |
Derivados de pirazol activos como pesticidas.
|
|
TWI850624B
(zh)
|
2015-12-22 |
2024-08-01 |
美商英塞特公司 |
作為免疫調節劑之雜環化合物
|
|
AU2016378482A1
(en)
|
2015-12-22 |
2018-07-12 |
Synthon B.V. |
Pharmaceutical composition comprising amorphous lenalidomide and an antioxidant
|
|
KR101653560B1
(ko)
|
2016-02-02 |
2016-09-12 |
한국화학연구원 |
신규한 화합물 또는 이의 약학적으로 허용가능한 염, 및 이를 유효성분으로 함유하는 인플루엔자 바이러스 감염으로 인한 질환의 예방 또는 치료용 약학적 조성물
|
|
EP3445339B1
(fr)
|
2016-04-22 |
2023-08-23 |
Incyte Corporation |
Formulations d'un inhibiteur de lsd1
|
|
ES2906460T3
(es)
|
2016-05-06 |
2022-04-18 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
|
TW201808902A
(zh)
|
2016-05-26 |
2018-03-16 |
美商英塞特公司 |
作為免疫調節劑之雜環化合物
|
|
RU2754856C2
(ru)
|
2016-06-20 |
2021-09-08 |
Новартис Аг |
Кристаллические формы соединения триазолопиримидина
|
|
PT3472167T
(pt)
|
2016-06-20 |
2022-11-11 |
Incyte Corp |
Compostos heterocíclicos como imunomoduladores
|
|
PL3471755T3
(pl)
|
2016-06-20 |
2020-10-19 |
Elanco Us Inc. |
Pegylowany interferon świni i sposoby jego stosowania
|
|
JP7054529B2
(ja)
|
2016-06-21 |
2022-04-14 |
エックス4 ファーマシューティカルズ, インコーポレイテッド |
Cxcr4阻害剤およびその使用
|
|
US20180016260A1
(en)
|
2016-07-14 |
2018-01-18 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
|
AU2017305399A1
(en)
|
2016-08-03 |
2019-01-31 |
Arising International, Inc. |
Symmetric or semi-symmetric compounds useful as immunomodulators
|
|
MA46045A
(fr)
|
2016-08-29 |
2021-04-28 |
Incyte Corp |
Composés hétérocycliques utilisés comme immunomodulateurs
|
|
CN110167560B
(zh)
|
2016-08-30 |
2023-08-18 |
四相制药公司 |
四环素化合物和治疗方法
|
|
MY203083A
(en)
|
2016-12-21 |
2024-06-07 |
Acerta Pharma Bv |
Imidazopyrazine inhibitors of bruton's tyrosine kinase
|
|
TWI795381B
(zh)
|
2016-12-21 |
2023-03-11 |
比利時商健生藥品公司 |
作為malt1抑制劑之吡唑衍生物
|
|
EP3558973B1
(fr)
|
2016-12-22 |
2021-09-15 |
Incyte Corporation |
Dérivés pyridine utilisés en tant qu'immunomodulateurs
|
|
TW201835049A
(zh)
|
2016-12-22 |
2018-10-01 |
美商英塞特公司 |
作為免疫調節劑之雜環化合物
|
|
US20180179201A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
|
US20180177784A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
|
SG10201911240PA
(en)
|
2016-12-22 |
2020-02-27 |
Calithera Biosciences Inc |
Compositions and methods for inhibiting arginase activity
|
|
RS63710B1
(sr)
|
2016-12-22 |
2022-11-30 |
Incyte Corp |
Derivati tetrahidro imidazo[4,5-c] piridina kao induktori internalizacije pd-l1
|
|
JP7101678B2
(ja)
|
2016-12-22 |
2022-07-15 |
インサイト・コーポレイション |
免疫調節剤としての複素環式化合物
|
|
JOP20180040A1
(ar)
|
2017-04-20 |
2019-01-30 |
Gilead Sciences Inc |
مثبطات pd-1/pd-l1
|
|
AU2018306619B2
(en)
|
2017-07-28 |
2022-06-02 |
Chemocentryx, Inc. |
Immunomodulator compounds
|
|
EP3664793B1
(fr)
|
2017-08-08 |
2022-06-29 |
ChemoCentryx, Inc. |
Immunomodulateurs macrocycliques
|
|
US11787766B2
(en)
|
2017-08-18 |
2023-10-17 |
Shanghai Ennovabio Pharmaceuticals Co., Ltd. |
Compound having PD-L1 inhibitory activity, preparation method therefor and use thereof
|
|
TWI796596B
(zh)
|
2018-02-13 |
2023-03-21 |
美商基利科學股份有限公司 |
Pd‐1/pd‐l1抑制劑
|
|
RS66699B1
(sr)
|
2018-03-30 |
2025-05-30 |
Incyte Corp |
Heterociklična jedinjenja kao imunomodulatori
|
|
CN111936475B
(zh)
|
2018-04-03 |
2024-05-10 |
贝达药业股份有限公司 |
免疫调节剂及其组合物和制备方法
|
|
KR102591947B1
(ko)
|
2018-04-19 |
2023-10-25 |
길리애드 사이언시즈, 인코포레이티드 |
Pd-1/pd-l1 억제제
|
|
TW202425987A
(zh)
|
2018-05-11 |
2024-07-01 |
美商英塞特公司 |
作為免疫調節劑之雜環化合物
|
|
WO2020036491A1
(fr)
|
2018-08-15 |
2020-02-20 |
Moonshine Solutions As |
Procédé et dispositif d'alimentation d'un liquide à un revêtement
|
|
JP7158577B2
(ja)
|
2018-10-24 |
2022-10-21 |
ギリアード サイエンシーズ, インコーポレイテッド |
Pd-1/pd-l1阻害剤
|
|
KR20210089195A
(ko)
|
2018-11-02 |
2021-07-15 |
상하이 맥시노벨 파마수티컬스 씨오., 엘티디. |
비페닐계 화합물, 이의 중간체, 제조 방법, 약학 조성물 및 용도
|
|
US11596692B1
(en)
|
2018-11-21 |
2023-03-07 |
Incyte Corporation |
PD-L1/STING conjugates and methods of use
|
|
CN120463702A
(zh)
|
2019-01-31 |
2025-08-12 |
贝达药业股份有限公司 |
免疫调节剂,组合物及其方法
|
|
GB201911210D0
(en)
|
2019-08-06 |
2019-09-18 |
Amlo Biosciences Ltd |
Clinical management of oropharyngeal squamous cell carcinoma
|
|
TW202115059A
(zh)
|
2019-08-09 |
2021-04-16 |
美商英塞特公司 |
Pd—1/pd—l1抑制劑之鹽
|
|
CA3155090A1
(fr)
|
2019-09-20 |
2021-03-25 |
Transgene |
Combinaison d'un poxvirus codant pour des polypeptides hpv et il-2 avec un anticorps anti-pd-l1
|
|
JP7559059B2
(ja)
|
2019-09-30 |
2024-10-01 |
インサイト・コーポレイション |
免疫調節剤としてのピリド[3,2-d]ピリミジン化合物
|
|
PH12022551136A1
(en)
|
2019-11-11 |
2023-10-09 |
Incyte Corp |
Salts and crystalline forms of a pd-1/pd-l1 inhibitor
|
|
EP4146216A4
(fr)
|
2020-05-04 |
2024-05-29 |
Beyondspring Pharmaceuticals Inc. |
Trithérapie pour améliorer la destruction de cellules cancéreuses dans des cancers à faible immunogénicité
|
|
TW202233615A
(zh)
|
2020-11-06 |
2022-09-01 |
美商英塞特公司 |
Pd—1/pd—l1抑制劑之結晶形式
|
|
TW202233616A
(zh)
|
2020-11-06 |
2022-09-01 |
美商英塞特公司 |
用於製備pd-1/pd-l1抑制劑以及其鹽及結晶形式之方法
|
|
US11780836B2
(en)
|
2020-11-06 |
2023-10-10 |
Incyte Corporation |
Process of preparing a PD-1/PD-L1 inhibitor
|
|
TW202241420A
(zh)
|
2020-12-18 |
2022-11-01 |
美商英塞特公司 |
Pd-l1抑制劑之口服調配物
|
|
US20230149409A1
(en)
|
2021-09-24 |
2023-05-18 |
Incyte Corporation |
Treatment of human papillomavirus-associated cancers by pd-l1 inhibitors
|