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
|
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
|
JP2001505585A
(ja)
|
1996-12-16 |
2001-04-24 |
藤沢薬品工業株式会社 |
新規アミド化合物およびそれらの一酸化窒素シンターゼ阻害剤としての用途
|
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
|
WO1999018096A1
(fr)
|
1997-10-02 |
1999-04-15 |
Merck & Co., Inc. |
Inhibiteurs de la prenyl-proteine transferase
|
WO1999044992A1
(fr)
|
1998-03-05 |
1999-09-10 |
Nissan Chemical Industries, Ltd. |
Composes d'anilide et herbicide
|
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
|
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
|
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
|
US6867200B1
(en)
|
1998-12-18 |
2005-03-15 |
Axys Pharmaceuticals, Inc. |
(Hetero)aryl-bicyclic heteroaryl derivatives, their preparation and their use as protease inhibitors
|
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
|
AU6000900A
(en)
|
1999-07-23 |
2001-02-13 |
Astrazeneca Uk Limited |
Carbazole derivatives and their use as neuropeptide y5 receptor ligands
|
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
|
CN1623984A
(zh)
|
1999-12-27 |
2005-06-08 |
日本烟草产业株式会社 |
稠环化合物及其药物用途
|
WO2001057038A1
(fr)
|
2000-02-01 |
2001-08-09 |
Basf Aktiengesellschaft |
Composes heterocycliques et leur utilisation comme inhibiteurs de parp
|
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
|
WO2001074815A2
(fr)
|
2000-03-31 |
2001-10-11 |
Ortho Mcneil Pharmaceutical, Inc. |
Imidazopyridines phenyle-substituees
|
AU2001254555A1
(en)
|
2000-04-24 |
2001-11-07 |
Merck Frosst Canada & Co |
Method of treatment using phenyl and biaryl derivatives as prostaglandin E inhibitors and compounds useful therefore
|
CA2413330A1
(fr)
|
2000-06-28 |
2002-01-03 |
Smithkline Beecham P.L.C. |
Procede de broyage par voie humide
|
WO2002014321A1
(fr)
|
2000-08-11 |
2002-02-21 |
The Regents Of The University Of California |
Utilisation d'inhibiteurs de stat-6 comme agents therapeutiques
|
WO2002048146A2
(fr)
|
2000-12-13 |
2002-06-20 |
Basf Aktiengesellschaft |
Utilisation d'imidazoazines substituees, nouvelles imidazoazines, procede permettant de les produire et agents les contenant
|
DE60112609T2
(de)
|
2000-12-15 |
2006-01-19 |
Glaxo Group Ltd., Greenford |
Pyrazolopyridine
|
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
|
WO2002083672A1
(fr)
|
2001-04-10 |
2002-10-24 |
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
|
DE60204452T2
(de)
|
2001-04-27 |
2005-12-15 |
Smithkline Beecham Corp. |
Pyrazolo[1,5a]Pyridinderivate
|
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
|
AU2002334969A1
(en)
|
2001-10-09 |
2003-04-22 |
Sylvie Barchechath |
Use of stat-6 inhibitors as therapeutic agents
|
BR0213208A
(pt)
|
2001-10-09 |
2004-08-31 |
Upjohn Co |
Compostos de tetraidro- e hexaidro-carbazóis de arilsulfonila substituìda, suas composições e usos
|
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
|
PL373399A1
(en)
|
2002-04-11 |
2005-08-22 |
Vertex Pharmaceuticals Incorporated |
Inhibitors of serine proteases, particularly hcv ns3-ns4a 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
|
WO2004007472A1
(fr)
|
2002-07-10 |
2004-01-22 |
Ono Pharmaceutical Co., Ltd. |
Antagoniste du ccr4 et utilisation medicinale correspondante
|
AU2003249244A1
(en)
|
2002-07-15 |
2004-02-02 |
Combinatorx, Incorporated |
Methods for the treatment of neoplasms
|
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
|
EP1547996A4
(fr)
|
2002-08-30 |
2006-08-02 |
Bf Res Inst Inc |
Sondes de diagnostic et remedes contre des maladies presentant une accumulation de la proteine du prion et methode de marquage
|
WO2004033454A1
(fr)
|
2002-10-03 |
2004-04-22 |
Smithkline Beecham Corporation |
Composes therapeutiques a base de derives de pyrazolopyridine
|
WO2004035588A1
(fr)
|
2002-10-15 |
2004-04-29 |
Smithkline Beecham Corporation |
Composes de pyradazine utiles comme inhibiteurs de gsk-3
|
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
|
TW200505902A
(en)
|
2003-03-20 |
2005-02-16 |
Schering Corp |
Cannabinoid receptor ligands
|
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
|
PT1620429E
(pt)
|
2003-04-11 |
2009-04-28 |
Glenmark Pharmaceuticals Sa |
Novos compostos heterocíclicos úteis para o tratamento de perturbações inflamatórias e alérgicas: processo para a sua preparação e composições farmacêuticas que os contêm
|
CA2524048C
(fr)
|
2003-05-19 |
2013-06-25 |
Irm Llc |
Composes immunosuppresseurs et compositions
|
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
|
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
|
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
|
WO2005005429A1
(fr)
|
2003-06-30 |
2005-01-20 |
Cellular Genomics, Inc. |
Certaines imidazo[1,2-a]pyrazin-8-ylamines substituees heterocycliques et methodes d'inhibition de la tyrosine kinase de bruton utilisant ces composes
|
WO2005007111A2
(fr)
|
2003-07-11 |
2005-01-27 |
Bristol-Myers Squibb Company |
Derives de tetrahydroquinoleine constituant des modulateurs des recepteurs des cannabinoides
|
JP5001650B2
(ja)
|
2003-07-11 |
2012-08-15 |
メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング |
ベンズイミダゾールカルボキサミド
|
US20100267778A1
(en)
|
2003-08-04 |
2010-10-21 |
Shinya Kusuda |
Diphenyl ether compound, process for producing the same, and use
|
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
|
AU2004270733B2
(en)
|
2003-09-11 |
2011-05-19 |
Itherx Pharma, Inc. |
Cytokine inhibitors
|
EP1673343A4
(fr)
|
2003-10-08 |
2008-09-10 |
Irm Llc |
Composes et compositions convenant comme inhibiteurs de proteine-kinases
|
JPWO2005040135A1
(ja)
|
2003-10-24 |
2007-03-08 |
小野薬品工業株式会社 |
抗ストレス薬およびその医薬用途
|
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
|
AU2005215379A1
(en)
|
2004-02-12 |
2005-09-01 |
Merck & Co., Inc. |
Bipyridyl amides as modulators of metabotropic glutamate receptor-5
|
WO2005077948A1
(fr)
|
2004-02-16 |
2005-08-25 |
Daiichi Pharmaceutical Co., Ltd. |
Composes heterocycliques fongicides
|
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
|
US20050250820A1
(en)
|
2004-03-08 |
2005-11-10 |
Amgen Inc. |
Therapeutic modulation of PPARgamma activity
|
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
|
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
|
JP4879165B2
(ja)
|
2004-04-20 |
2012-02-22 |
トランス テック ファーマ,インコーポレイテッド |
メラノコルチン受容体の調節因子としての置換チアゾール及びピリミジン誘導体
|
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
|
WO2005108387A2
(fr)
|
2004-05-03 |
2005-11-17 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Inhibiteurs de cytokines
|
TW200626142A
(en)
|
2004-09-21 |
2006-08-01 |
Glaxo Group Ltd |
Chemical compounds
|
US7250441B2
(en)
|
2004-09-23 |
2007-07-31 |
Wyeth |
Carbazole and cyclopentaindole derivatives to treat infection with Hepatitis C virus
|
US7713973B2
(en)
|
2004-10-15 |
2010-05-11 |
Takeda Pharmaceutical Company Limited |
Kinase inhibitors
|
BRPI0517619A
(pt)
|
2004-11-10 |
2008-10-14 |
Cgi Pharmaceuticals Inc |
entidades quìmicas de imidazo[1,2-a] pirazin-8-ilaminas, suas composições farmacêuticas, uso dos referidos compostos na preparação de medicamento, processo de preparação de medicamento e métodos de utilização dos referidos compostos
|
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
|
MX2007011041A
(es)
|
2005-03-10 |
2008-02-22 |
Cgi Pharmaceuticals Inc |
Ciertas amidas sustituidas, metodo de elaboracion y metodo de uso de las mismas.
|
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
|
AU2006247118A1
(en)
|
2005-05-20 |
2006-11-23 |
Array Biopharma Inc. |
Raf inhibitor compounds and methods of use thereof
|
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
|
CN103936690B
(zh)
|
2005-10-25 |
2016-06-08 |
盐野义制药株式会社 |
氨基二氢噻嗪衍生物
|
JP5249772B2
(ja)
|
2005-11-22 |
2013-07-31 |
メルク・シャープ・アンド・ドーム・コーポレーション |
キナーゼの阻害剤として有用な三環式化合物
|
WO2007067711A2
(fr)
|
2005-12-08 |
2007-06-14 |
Amphora Discovery Corporation |
Certains types d'entites chimiques, compositions et methode de modulation de trpv1
|
US20090281120A1
(en)
|
2005-12-12 |
2009-11-12 |
Ono Pharmaceutical Co., Ltd |
Bicyclic heterocyclic compound
|
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
|
MX2008012617A
(es)
|
2006-03-31 |
2008-10-10 |
Novartis Ag |
Compuestos organicos.
|
US7700616B2
(en)
|
2006-05-08 |
2010-04-20 |
Molecular Neuroimaging, Llc. |
Compounds and amyloid probes thereof for therapeutic and imaging uses
|
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
|
WO2008011557A2
(fr)
|
2006-07-20 |
2008-01-24 |
Borchardt Allen J |
Inhibiteurs hétéroaryliques de la kinase rho
|
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
|
US7563797B2
(en)
|
2006-08-28 |
2009-07-21 |
Forest Laboratories Holding Limited |
Substituted imidazo(1,2-A)pyrimidines and imidazo(1,2-A) pyridines as cannabinoid receptor ligands
|
PE20080839A1
(es)
|
2006-09-11 |
2008-08-23 |
Cgi Pharmaceuticals Inc |
Determinadas amidas sustituidas, metodo de elaboracion y metodo de uso de las mismas
|
PE20081370A1
(es)
|
2006-09-11 |
2008-11-28 |
Cgi Pharmaceuticals Inc |
Determinadas amidas sustituidas, metodo de elaboracion y metodo de uso de las mismas
|
JP2010502751A
(ja)
|
2006-09-11 |
2010-01-28 |
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 |
キナーゼ阻害物質、およびキナーゼ阻害物質の使用および同定方法
|
US7838523B2
(en)
|
2006-09-11 |
2010-11-23 |
Cgi Pharmaceuticals, Inc. |
Certain substituted amides, method of making, and method of use thereof
|
SG174810A1
(en)
|
2006-09-11 |
2011-10-28 |
Matrix Lab Ltd |
Dibenzofuran derivatives as inhibitors of pde-4 and pde-10
|
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
|
CA2667644A1
(fr)
|
2006-10-27 |
2008-05-15 |
Wyeth |
Composes tricycliques servant d'inhibiteurs des metalloproteases matricielles
|
EP2089364B1
(fr)
|
2006-11-08 |
2013-06-12 |
Bristol-Myers Squibb Company |
Composés de pyridinone
|
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
|
CA2673038C
(fr)
|
2006-12-22 |
2015-12-15 |
Incyte Corporation |
Composes heteroaryls tricycliques substitues comme inhibiteurs de kinase janus
|
EP1964840A1
(fr)
|
2007-02-28 |
2008-09-03 |
sanofi-aventis |
Imidazo[1,2-a]pyridines et leur utilisation en tant que produits pharmaceutiques
|
US8338437B2
(en)
|
2007-02-28 |
2012-12-25 |
Methylgene Inc. |
Amines as small molecule inhibitors
|
EP1964841A1
(fr)
|
2007-02-28 |
2008-09-03 |
sanofi-aventis |
Imidazo[1,2-a]azine et son utilisation en tant que produit pharmaceutique
|
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
|
JP2010522227A
(ja)
|
2007-03-22 |
2010-07-01 |
アストラゼネカ・アクチエボラーグ |
炎症性疾患の処置のためのキノリン誘導体
|
EP2151435A4
(fr)
|
2007-04-24 |
2011-09-14 |
Shionogi & Co |
Composition pharmaceutique pour le traitement de la maladie d'alzheimer
|
KR20100017255A
(ko)
|
2007-04-24 |
2010-02-16 |
시오노기 앤드 컴파니, 리미티드 |
환식기로 치환된 아미노다이하이드로싸이아진 유도체
|
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
|
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
|
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
|
AU2008302746B2
(en)
|
2007-09-20 |
2014-07-03 |
Amgen Inc. |
1-(4-(benzylbenzamid0) -benzyl) azetidine-3-carboxylic acid derivatives and related compounds as SlP receptor modulators for the treatment of immune disorders
|
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
|
CN101910158A
(zh)
|
2007-10-25 |
2010-12-08 |
阿斯利康(瑞典)有限公司 |
可用于治疗细胞增殖性病症的吡啶衍生物和吡嗪衍生物
|
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
|
EP2231143B1
(fr)
|
2007-12-13 |
2013-07-03 |
Merck Sharp & Dohme Corp. |
5H-pyrido[4,3-b]indoles comme iNHIBITEURS DE JANUS KINASES
|
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
|
GEP20125588B
(en)
|
2007-12-19 |
2012-07-25 |
Syngenta Participations Ag |
Insecticidal compounds
|
EP2219646A4
(fr)
|
2007-12-21 |
2010-12-22 |
Univ Rochester |
Procédé permettant de modifier la durée de vie d'organismes eucaryotes
|
EP2231659A4
(fr)
|
2007-12-21 |
2011-10-26 |
Univ Sydney |
Ligands de la protéine de translocation
|
PL2233474T3
(pl)
|
2008-01-18 |
2015-12-31 |
Eisai R&D Man Co Ltd |
Skondensowana pochodna aminodihydrotiazyny
|
WO2009096202A1
(fr)
|
2008-01-31 |
2009-08-06 |
Konica Minolta Holdings, Inc. |
Composé aromatique polycyclique halogéné et son procédé de production
|
AU2009218515A1
(en)
|
2008-02-26 |
2009-09-03 |
Novartis Ag |
Heterocyclic compounds as inhibitors of CXCR2
|
EP2095818A1
(fr)
|
2008-02-29 |
2009-09-02 |
AEterna Zentaris GmbH |
Utilisation d'antagonistes LHRH dans des doses n'impliquant pas de castration
|
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
|
JP5432982B2
(ja)
|
2008-03-31 |
2014-03-05 |
武田薬品工業株式会社 |
アポトーシスシグナル調節キナーゼ1阻害剤
|
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
|
CA2724842A1
(fr)
|
2008-05-19 |
2009-11-26 |
Sunovion Pharmaceuticals Inc. |
Composes imidazo[1,2-a]pyridines
|
JP2011521960A
(ja)
|
2008-05-29 |
2011-07-28 |
サートリス ファーマシューティカルズ, インコーポレイテッド |
サーチュイン調節薬としてのイミダゾピリジンおよび関連する類似体
|
ES2566339T3
(es)
|
2008-06-05 |
2016-04-12 |
Glaxo Group Limited |
Derivados de 4-carboxamida indazol útiles como inhibidores de PI3-quinasas
|
JP2011529073A
(ja)
|
2008-07-24 |
2011-12-01 |
ブリストル−マイヤーズ スクイブ カンパニー |
キナーゼ調節因子として有用な縮合ヘテロ環化合物
|
US9643922B2
(en)
|
2008-08-18 |
2017-05-09 |
Yale University |
MIF modulators
|
US9540322B2
(en)
|
2008-08-18 |
2017-01-10 |
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
|
WO2010056875A1
(fr)
|
2008-11-12 |
2010-05-20 |
Cgi Pharmaceuticals, Inc. |
Pyridazinones et leur utilisation comme inhibiteurs de la btk
|
WO2010064020A1
(fr)
|
2008-12-04 |
2010-06-10 |
Proximagen Ltd. |
Composés imidazopyridines
|
JP5557849B2
(ja)
|
2008-12-19 |
2014-07-23 |
ブリストル−マイヤーズ スクイブ カンパニー |
カルバゾールおよびカルボリンキナーゼ阻害剤
|
TW201035100A
(en)
|
2008-12-19 |
2010-10-01 |
Cephalon Inc |
Pyrrolotriazines as ALK and JAK2 inhibitors
|
CA2747670A1
(fr)
|
2008-12-19 |
2010-07-15 |
Bristol-Myers Squibb Company |
Composes carbazole carboxamide utiles comme inhibiteurs de kinases
|
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
|
JP2012513409A
(ja)
|
2008-12-23 |
2012-06-14 |
アボット・ラボラトリーズ |
抗ウイルス化合物
|
WO2010074284A1
(fr)
|
2008-12-26 |
2010-07-01 |
味の素株式会社 |
Composé de pyrazolopyrimidine
|
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
|
WO2010104307A2
(fr)
|
2009-03-07 |
2010-09-16 |
주식회사 메디젠텍 |
Compositions pharmaceutiques pour traiter ou prévenir des maladies causées par la translocation de gsk3 du noyau cellulaire au cytoplasme, contenant des composés inhibant la translocation de gsk3 du noyau cellulaire au cytoplasme
|
CN102574786A
(zh)
|
2009-04-02 |
2012-07-11 |
默克雪兰诺有限公司 |
二氢乳清酸脱氢酶抑制剂
|
DK2419429T3
(da)
|
2009-04-16 |
2014-06-23 |
Ct Nac De Investigaciones Oncológicas Cnio |
Imidazopyraziner som inhibitorer af proteinkinaser
|
US8338441B2
(en)
|
2009-05-15 |
2012-12-25 |
Gilead Sciences, Inc. |
Inhibitors of human immunodeficiency virus replication
|
JP2012532102A
(ja)
|
2009-06-30 |
2012-12-13 |
シガ・テクノロジーズ・インコーポレーテッド |
デングウイルス感染の治療法および予防法
|
US8993604B2
(en)
|
2009-06-30 |
2015-03-31 |
Siga Technologies, Inc. |
Treatment and prevention of dengue virus infections
|
TWI598347B
(zh)
|
2009-07-13 |
2017-09-11 |
基利科學股份有限公司 |
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
|
CA2777734A1
(fr)
|
2009-10-16 |
2011-04-21 |
Rib-X Pharmaceuticals, Inc. |
Composes anti-microbiens et procedes permettant de fabriquer et d'utiliser ces composes
|
WO2011050245A1
(fr)
|
2009-10-23 |
2011-04-28 |
Yangbo Feng |
Hétéroaryles bicycliques formant inhibiteurs de la kinase
|
WO2011078221A1
(fr)
|
2009-12-24 |
2011-06-30 |
味の素株式会社 |
Composés d'imidazopyridazine
|
WO2011082400A2
(fr)
|
2010-01-04 |
2011-07-07 |
President And Fellows Of Harvard College |
Modulateurs du récepteur immunosuppresseur pd-1 et procédés d'utilisation de ceux-ci
|
WO2011097607A1
(fr)
|
2010-02-08 |
2011-08-11 |
Southern Research Institute |
Traitement antiviral et dosage pour cribler des antiviraux
|
AR080433A1
(es)
|
2010-03-02 |
2012-04-11 |
Merck Sharp & Dohme |
Derivados de benzofurancarboxamidas utiles para tratar o prevenir infecciones por vhc y composiciones farmaceuticas que los contienen.
|
US9024032B2
(en)
|
2010-03-04 |
2015-05-05 |
Merck Sharp & Dohme Corp. |
Inhibitors of catechol O-methyl transferase and their use in the treatment of psychotic disorders
|
RU2576662C2
(ru)
|
2010-03-18 |
2016-03-10 |
Энститю Пастер Корея |
Противоинфекционные соединения
|
US8410117B2
(en)
|
2010-03-26 |
2013-04-02 |
Hoffmann-La Roche Inc. |
Imidazopyrimidine derivatives
|
WO2011159857A1
(fr)
|
2010-06-16 |
2011-12-22 |
Bristol-Myers Squibb Company |
Composés de carboline-carboxamide utiles en tant qu'inhibiteurs de kinases
|
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
|
WO2012047856A2
(fr)
|
2010-10-04 |
2012-04-12 |
Institute For Hepatitis And Virus Research |
Nouveaux inhibiteurs de la sécrétion d'antigènes du virus de l'hépatite b
|
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
|
WO2012052745A1
(fr)
|
2010-10-21 |
2012-04-26 |
Centro Nacional De Investigaciones Oncológicas (Cnio) |
Combinaisons d'inhibiteurs de pi3k avec un second agent antitumoral
|
WO2012068406A2
(fr)
|
2010-11-18 |
2012-05-24 |
Ligand Pharmaceuticals Incorporated |
Utilisation de mimétiques d'un facteur de croissance hématopoïétique
|
WO2012080376A1
(fr)
|
2010-12-17 |
2012-06-21 |
Syngenta Participations Ag |
Composés insecticides
|
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
|
KR20140027090A
(ko)
|
2011-01-04 |
2014-03-06 |
노파르티스 아게 |
연령-관련 황반 변성 (amd)의 치료에 유용한 인돌 화합물 또는 그의 유사체
|
US9018395B2
(en)
|
2011-01-27 |
2015-04-28 |
Université de Montréal |
Pyrazolopyridine and pyrazolopyrimidine derivatives as melanocortin-4 receptor modulators
|
EP2685981B1
(fr)
|
2011-03-17 |
2016-08-24 |
Bristol-Myers Squibb Company |
Inhibiteurs de jak3 de type pyrrolopyridazine et leur utilisation pour traiter les maladies inflammatoires et auto-immunes
|
WO2012129562A2
(fr)
|
2011-03-24 |
2012-09-27 |
The Scripps Research Institute |
Composés et procédés pour l'induction de la chondrogenèse
|
WO2012139425A1
(fr)
|
2011-04-13 |
2012-10-18 |
Schering Corporation |
Iminothiazines 5-substituées et leur monoxydes et dioxydes comme inhibiteurs de bace, leurs compositions et leur utilisation
|
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
|
EP2713722B1
(fr)
|
2011-05-31 |
2017-03-15 |
Receptos, LLC |
Nouveaux stabilisants et modulateurs du récepteur de glp-1
|
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
|
CA2841111A1
(fr)
|
2011-07-08 |
2013-01-17 |
Novartis Ag |
Nouveaux derives de pyrrolopyrimidine
|
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
|
WO2013054291A1
(fr)
|
2011-10-13 |
2013-04-18 |
Novartis Ag |
Nouveaux dérivés d'oxazine et leur utilisation dans le traitement de maladie
|
CN103998451A
(zh)
|
2011-10-20 |
2014-08-20 |
葛兰素史密斯克莱有限责任公司 |
用作沉默调节蛋白调节剂的取代的双环氮杂杂环化合物和类似物
|
EP2768832A1
(fr)
|
2011-10-21 |
2014-08-27 |
Torrent Pharmaceuticals Limited |
Nouveaux imidazopiridines substitues comme modulateurs recepteurs gpbar1
|
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
|
JPWO2013133367A1
(ja)
|
2012-03-09 |
2015-07-30 |
カルナバイオサイエンス株式会社 |
新規トリアジン誘導体
|
WO2013157021A1
(fr)
|
2012-04-20 |
2013-10-24 |
Advinus Therapeutics Limited |
Composés bicycliques, compositions et applications médicinales de ceux-ci
|
PE20141558A1
(es)
|
2012-04-20 |
2014-11-06 |
Gilead Sciences Inc |
Derivados de acido benzotiazol-6-il acetico y su uso para tratar una infeccion por vih
|
US20150105433A1
(en)
|
2012-04-27 |
2015-04-16 |
The Uab Research Foundation |
TREATING VIRAL INFECTIONS HAVING VIRAL RNAs TRANSLATED BY A NON-IRES MEDIATED MECHANISM
|
EP2862853B1
(fr)
|
2012-06-18 |
2020-01-22 |
Sumitomo Chemical Co., Ltd |
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
|
EP2900657B1
(fr)
|
2012-09-26 |
2020-03-11 |
F.Hoffmann-La Roche Ag |
Composés de pyrazol-4-yl-hétérocyclyl-carboxamide substitués par ethers cycliques et leurs méthodes d'utilisation
|
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
|
EP2922548A4
(fr)
|
2012-11-21 |
2016-06-01 |
Stategics Inc |
Composés triazolo-pyrimidines substitués pour la modulation de la prolifération, la différentiation et la survie cellulaires
|
JP6037804B2
(ja)
|
2012-12-03 |
2016-12-07 |
富士フイルム株式会社 |
ガス分離膜
|
EA035929B1
(ru)
|
2013-01-15 |
2020-09-02 |
Инсайт Холдингс Корпорейшн |
ТИАЗОЛКАРБОКСАМИДЫ И ПИРИДИНКАРБОКСАМИДЫ, ИСПОЛЬЗУЕМЫЕ В КАЧЕСТВЕ ИНГИБИТОРОВ Pim-КИНАЗЫ
|
CA2896185A1
(fr)
|
2013-01-22 |
2014-07-31 |
F. Hoffmann-La Roche Ag |
Fluoro-[1,3]oxazines servant d'inhibiteurs de la bace1
|
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
|
US9657082B2
(en)
|
2013-01-31 |
2017-05-23 |
Thomas Jefferson University |
PD-L1 and PD-L2-based fusion proteins and uses thereof
|
KR102169426B1
(ko)
|
2013-02-27 |
2020-10-23 |
모찌다 세이야쿠 가부시끼가이샤 |
신규 피라졸 유도체
|
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
|
AU2014231768A1
(en)
|
2013-03-13 |
2015-09-24 |
Australian Nuclear Science And Technology Organisation |
Transgenic non-human organisms with non-functional TSPO genes
|
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
|
DK2968304T3
(en)
|
2013-03-14 |
2019-01-28 |
Univ Columbia |
4-PHENYLPIPERIDINES, THEIR PREPARATION AND USE.
|
CN105189503B
(zh)
|
2013-03-14 |
2017-03-22 |
百时美施贵宝公司 |
人免疫缺陷病毒复制的抑制剂
|
EP2968265A4
(fr)
|
2013-03-14 |
2016-12-28 |
Celtaxsys Inc |
Inhibiteurs de la leucotriène a4 hydrolase
|
MA38461B1
(fr)
|
2013-03-14 |
2021-10-29 |
Curadev Pharma Private Ltd |
Inhibiteurs de la voie de la kynurénine
|
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
|
WO2014181287A1
(fr)
|
2013-05-09 |
2014-11-13 |
Piramal Enterprises Limited |
Composés hétérocyclyliques et leurs utilisations
|
ME03307B
(fr)
|
2013-06-26 |
2019-10-20 |
Abbvie Inc |
Carboxamides primaires servant d'inhibiteurs de la btk
|
WO2015000715A1
(fr)
|
2013-07-02 |
2015-01-08 |
Syngenta Participations Ag |
Hétérocycles bi- ou tricycliques à action pesticide avec substituants soufrés
|
SG11201600108PA
(en)
|
2013-07-17 |
2016-02-26 |
Otsuka Pharma Co Ltd |
Cyanotriazole compounds
|
RU2016105108A
(ru)
|
2013-07-25 |
2017-08-30 |
Дана-Фарбер Кэнсер Инститьют, Инк. |
Ингибиторы факторов транскрипции и их применение
|
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
|
ES2642074T3
(es)
*
|
2013-09-04 |
2017-11-15 |
Bristol-Myers Squibb Company |
Compuestos útiles como inmunomoduladores
|
ES2788848T3
(es)
|
2013-09-06 |
2020-10-23 |
Aurigene Discovery Tech Ltd |
Derivados de 1,2,4-oxadiazol como inmunomoduladores
|
PT3041828T
(pt)
|
2013-09-06 |
2018-10-09 |
Aurigene Discovery Tech Ltd |
Derivados 1,3,4-0xadiazoles como imonomoduladores
|
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
|
GB201321736D0
(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
|
WO2015095337A2
(fr)
|
2013-12-18 |
2015-06-25 |
The Rockefeller University |
Dérivés pyrazolo [1,5-a]pyrimidine carboxamide pour le traitement de troubles cognitifs
|
ES2683693T3
(es)
|
2014-01-03 |
2018-09-27 |
Bayer Animal Health Gmbh |
Nuevas pirazolil-heteroarilamidas como agentes plaguicidas
|
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
|
US9732103B2
(en)
|
2014-02-25 |
2017-08-15 |
Achillion Pharmaceuticals, Inc. |
Carbamate, ester, and ketone 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
|
EP3125883B1
(fr)
|
2014-04-04 |
2020-08-12 |
Iomet Pharma Ltd. |
Dérivés indolés destinés à être utilisés dans le domaine de la médecine
|
US9850225B2
(en)
|
2014-04-14 |
2017-12-26 |
Bristol-Myers Squibb Company |
Compounds useful as immunomodulators
|
WO2015197028A1
(fr)
|
2014-06-28 |
2015-12-30 |
Sunshine Lake Pharma Co., Ltd. |
Composés en tant qu'inhibiteurs du virus de l'hépatite c (vhc) et leurs utilisations en médecine
|
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
|
WO2016041511A1
(fr)
|
2014-09-19 |
2016-03-24 |
Yen-Ta Lu |
Composés benzo-hétérocycliques et leurs applications
|
SG11201701573QA
(en)
|
2014-10-06 |
2017-03-30 |
Merck Patent Gmbh |
Heteroaryl compounds as btk inhibitors and uses thereof
|
AU2015360416A1
(en)
|
2014-12-10 |
2017-06-08 |
Massachusetts Institute Of Technology |
Fused 1,3-azole derivatives useful for the treatment of proliferative diseases
|
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
|
US10071998B2
(en)
|
2015-01-20 |
2018-09-11 |
Merck Sharp & Dohme Corp. |
Iminothiadiazine dioxides bearing an amine-linked substituent as BACE inhibitors, compositions, and their use
|
DE112016000383A5
(de)
|
2015-01-20 |
2017-10-05 |
Cynora Gmbh |
Organische Moleküle, insbesondere zur Verwendung in optoelektronischen Bauelementen
|
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
|
MA52119A
(fr)
|
2015-10-19 |
2018-08-29 |
Ncyte Corp |
Composés hétérocycliques utilisés comme immunomodulateurs
|
WO2017070320A1
(fr)
|
2015-10-21 |
2017-04-27 |
University Of Pittsburgh - Of The Commonwealth System Of Higher Education |
Inhibiteurs allostériques de phényl indole de l'atpase p97
|
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
|
SG11201804152RA
(en)
|
2015-11-19 |
2018-06-28 |
Incyte Corp |
Heterocyclic compounds as immunomodulators
|
TW201726623A
(zh)
|
2015-12-17 |
2017-08-01 |
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
|
JP6943857B2
(ja)
|
2015-12-22 |
2021-10-06 |
シンジェンタ パーティシペーションズ アーゲー |
有害生物防除活性ピラゾール誘導体
|
SG10202111399YA
(en)
|
2015-12-22 |
2021-11-29 |
Immatics Biotechnologies Gmbh |
Peptides and combination of peptides for use in immunotherapy against breast cancer and other cancers
|
WO2017107052A1
(fr)
|
2015-12-22 |
2017-06-29 |
Merck Sharp & Dohme Corp. |
Activateurs solubles de guanylate cyclase
|
EP4292650A3
(fr)
|
2015-12-22 |
2024-02-28 |
Incyte Corporation |
Composés hétérocycliques en tant qu'immunomodulateurs
|
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
|
AR109452A1
(es)
|
2016-04-22 |
2018-12-12 |
Incyte Corp |
Formulación farmacéutica de un inhibidor de lsd1 y método de tratamiento
|
AR108396A1
(es)
|
2016-05-06 |
2018-08-15 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
WO2017205464A1
(fr)
|
2016-05-26 |
2017-11-30 |
Incyte Corporation |
Composés hétérocycliques utilisés comme immunomodulateurs
|
MX2018016331A
(es)
|
2016-06-20 |
2019-05-20 |
Novartis Ag |
Formas cristalinas de compuesto de triazolopirimidina.
|
CN109641034B
(zh)
|
2016-06-20 |
2023-08-15 |
伊兰科美国公司 |
聚乙二醇化的猪干扰素及其使用方法
|
KR102685249B1
(ko)
|
2016-06-20 |
2024-07-17 |
인사이트 코포레이션 |
면역조절제로서의 복소환식 화합물
|
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
|
MA45669A
(fr)
|
2016-07-14 |
2019-05-22 |
Incyte Corp |
Composés hétérocycliques utilisés comme immunomodulateurs
|
CA3030773A1
(fr)
|
2016-08-03 |
2018-02-08 |
Arising International, Inc. |
Composes symetriques ou semi-symetriques utiles comme immunomodulateurs
|
US20180057486A1
(en)
|
2016-08-29 |
2018-03-01 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
SG11201901390TA
(en)
|
2016-08-30 |
2019-03-28 |
Tetraphase Pharmaceuticals Inc |
Tetracycline compounds and methods of treatment
|
JP7022131B2
(ja)
|
2016-12-21 |
2022-02-17 |
アセルタ ファーマ ビー.ブイ. |
ブルトン型チロシンキナーゼのイミダゾピラジン阻害剤
|
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
|
WO2018119221A1
(fr)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Dérivés pyridine utilisés en tant qu'immunomodulateurs
|
AU2017382405B2
(en)
|
2016-12-22 |
2021-12-16 |
Calithera Biosciences, Inc. |
Compositions and methods for inhibiting arginase activity
|
PL3558990T3
(pl)
|
2016-12-22 |
2022-12-19 |
Incyte Corporation |
Pochodne tetrahydroimidazo[4,5-c]pirydyny jako induktory internalizacji pd-l1
|
WO2018119286A1
(fr)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Composés hétéroaromatiques bicycliques utilisés en tant qu'immunomodulateurs
|
US20180179201A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
US10308644B2
(en)
|
2016-12-22 |
2019-06-04 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
US20180177784A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
JOP20180040A1
(ar)
|
2017-04-20 |
2019-01-30 |
Gilead Sciences Inc |
مثبطات pd-1/pd-l1
|
CA3070794A1
(fr)
|
2017-07-28 |
2019-01-31 |
Chemocentryx, Inc. |
Composes immunomodulateurs
|
EP3664793B1
(fr)
|
2017-08-08 |
2022-06-29 |
ChemoCentryx, Inc. |
Immunomodulateurs macrocycliques
|
EP3669872A4
(fr)
|
2017-08-18 |
2021-05-05 |
Shanghai Ennovabio Pharmaceuticals Co., Ltd. |
Composé ayant une activité inhibitrice de pd-l1, sa méthode de préparation et son utilisation
|
WO2019191707A1
(fr)
|
2018-03-30 |
2019-10-03 |
Incyte Corporation |
Composés hétérocycliques utilisés comme immunomodulateurs
|
JP2021520342A
(ja)
|
2018-04-03 |
2021-08-19 |
ベータ ファーマシューティカルズ カンパニー リミテッド |
免疫調節物質、組成物及びそれらの方法
|
JP7242702B2
(ja)
|
2018-04-19 |
2023-03-20 |
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
|
DK3790877T3
(da)
|
2018-05-11 |
2023-04-24 |
Incyte Corp |
Tetrahydro-imidazo[4,5-c]pyridinderivater som pd-l1-immunmodulatorer
|
KR102635333B1
(ko)
|
2018-10-24 |
2024-02-15 |
길리애드 사이언시즈, 인코포레이티드 |
Pd-1/pd-l1 억제제
|
JP2022513592A
(ja)
|
2018-11-02 |
2022-02-09 |
シャンハイ マキシノベル ファーマシューティカルズ カンパニー リミテッド |
ビフェニル系化合物、その中間体、製造方法、医薬組成物及び使用
|
CN113365995A
(zh)
|
2019-01-31 |
2021-09-07 |
贝达药业股份有限公司 |
免疫调节剂,组合物及其方法
|
US11753406B2
(en)
|
2019-08-09 |
2023-09-12 |
Incyte Corporation |
Salts of a PD-1/PD-L1 inhibitor
|
KR20220075382A
(ko)
|
2019-09-30 |
2022-06-08 |
인사이트 코포레이션 |
면역조절제로서의 피리도[3,2-d]피리미딘 화합물
|
BR112022009031A2
(pt)
|
2019-11-11 |
2022-10-11 |
Incyte Corp |
Sais e formas cristalinas de um inibidor de pd-1/pd-l1
|
WO2022099018A1
(fr)
|
2020-11-06 |
2022-05-12 |
Incyte Corporation |
Procédé de préparation d'un inhibiteur de pd-1/pd-l1
|
AU2021373044A1
(en)
|
2020-11-06 |
2023-06-08 |
Incyte Corporation |
Process for making a pd-1/pd-l1 inhibitor and salts and crystalline forms thereof
|
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
|
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
|