|
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
|
|
AU9781098A
(en)
|
1997-10-02 |
1999-04-27 |
Merck & Co., Inc. |
Inhibitors of prenyl-protein transferase
|
|
WO1999044992A1
(fr)
|
1998-03-05 |
1999-09-10 |
Nissan Chemical Industries, Ltd. |
Composes d'anilide et 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
|
|
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
|
|
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
|
|
US6297351B1
(en)
|
1998-12-17 |
2001-10-02 |
Sumitomo Bakelite Company Limited |
Polybenzoxazole resin and precursor thereof
|
|
EA200100675A1
(ru)
|
1998-12-18 |
2001-12-24 |
Аксис Фармасьютикалз, Инк. |
Ингибиторы протеазы
|
|
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
|
|
WO2001047883A1
(fr)
|
1999-12-27 |
2001-07-05 |
Japan Tobacco Inc. |
Composes a cycles accoles et leur utilisation comme medicaments
|
|
DE50112961D1
(de)
|
2000-02-01 |
2007-10-18 |
Abbott Gmbh & Co Kg |
Heterozyklische verbindungen und deren anwendung als parp-inhibitoren
|
|
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
|
|
EP1268478B1
(fr)
|
2000-03-31 |
2007-05-02 |
Ortho-McNeil Pharmaceutical, Inc. |
Imidazopyridines phenyle-substituees
|
|
EP1278734A2
(fr)
|
2000-04-24 |
2003-01-29 |
Merck Frosst Canada & Co. |
Methode de traitement se basant sur l'utilisation de derives de phenyle et de biaryle comme inhibiteurs de prostaglandine e
|
|
NZ522783A
(en)
|
2000-06-28 |
2004-07-30 |
Smithkline Beecham P |
Wet milling process for pharmaceuticals with agitator or chamber having nylon with internal lubricant
|
|
AU2001294515A1
(en)
|
2000-08-11 |
2002-02-25 |
The Regents Of The University Of California |
Use of stat-6 inhibitors as therapeutic agents
|
|
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
|
|
MXPA03007779A
(es)
|
2001-03-14 |
2004-11-12 |
Lilly Co Eli |
Moduladores de los receptores de retinoides x.
|
|
EP1372643A1
(fr)
|
2001-03-30 |
2004-01-02 |
Smithkline Beecham Corporation |
Pyralopyridines, leur procede de preparation et leur utilisation en tant que composes therapeutiques
|
|
DE60212949T2
(de)
|
2001-04-10 |
2007-01-04 |
Smithkline Beecham Corp. |
Antivirale pyrazolopyridin verbindungen
|
|
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
|
|
EP1385847B1
(fr)
|
2001-04-27 |
2005-06-01 |
SmithKline Beecham Corporation |
Derives de pyrazolo (1,5-a) pyridine
|
|
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
|
|
ES2286272T3
(es)
|
2001-09-07 |
2007-12-01 |
Smithkline Beecham Corporation |
Pirizolo-piridinas para el tratamiento de infecciones por herpes.
|
|
TWI331526B
(en)
|
2001-09-21 |
2010-10-11 |
Bristol Myers Squibb Pharma Co |
Lactam-containing compounds and derivatives thereof as factor xa inhibitors
|
|
US20030143199A1
(en)
|
2001-10-09 |
2003-07-31 |
Carson Dennis A. |
Use of STAT-6 inhibitors as therapeutic agents
|
|
US6727274B2
(en)
|
2001-10-09 |
2004-04-27 |
Pharmacia & Upjohn Company |
Arylsulphonyl substituted-tetrahydro- and hexahydro-carbazoles
|
|
WO2003042402A2
(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
|
|
KR20040099425A
(ko)
|
2002-04-11 |
2004-11-26 |
버텍스 파마슈티칼스 인코포레이티드 |
세린 프로테아제, 특히 c형 간염 바이러스 ns3-ns4프로테아제의 억제제
|
|
US7662826B2
(en)
|
2002-04-23 |
2010-02-16 |
Shionogi & Co., Ltd. |
Pyrazolo [1,5-a] pyrimidine derivative and nad (p) h oxidase inhibitor containing the same
|
|
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
|
|
JP2006504755A
(ja)
|
2002-10-15 |
2006-02-09 |
スミスクライン ビーチャム コーポレーション |
Gsk−3阻害薬としてのピリダジン化合物
|
|
JP4511943B2
(ja)
|
2002-12-23 |
2010-07-28 |
ワイス エルエルシー |
Pd−1に対する抗体およびその使用
|
|
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
|
|
CL2004001120A1
(es)
|
2003-05-19 |
2005-04-15 |
Irm Llc |
Compuestos derivados de amina sustituidas con heterociclos, inmunosupresores; composicion farmaceutica; y uso para tratar enfermedades mediadas por interacciones de linfocito, tales como enfermedades autoinmunes, inflamatorias, infecciosas, cancer.
|
|
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
|
|
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
|
|
US7276608B2
(en)
|
2003-07-11 |
2007-10-02 |
Bristol-Myers Squibb Company |
Tetrahydroquinoline derivatives as cannabinoid receptor modulators
|
|
CA2531856C
(fr)
|
2003-07-11 |
2013-07-30 |
Merck Patent Gesellschaft Mit Beschraenkter Haftung |
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
|
|
BRPI0414313A
(pt)
|
2003-09-11 |
2006-11-07 |
Kemia Inc |
inibidores de citocinas
|
|
BRPI0415210A
(pt)
|
2003-10-08 |
2006-12-05 |
Irm Llc |
compostos e composições como inibidores de proteìna cinase
|
|
US20070099938A1
(en)
|
2003-10-24 |
2007-05-03 |
Ono Pharmaceutical Co., Ltd. |
Antistress drug and medical use thereof
|
|
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
|
|
EP1717238A4
(fr)
|
2004-02-16 |
2008-03-05 |
Daiichi Seiyaku Co |
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
|
|
JP2007527918A
(ja)
|
2004-03-08 |
2007-10-04 |
アムジェン インコーポレイテッド |
Pparガンマ活性の治療的調節
|
|
AU2005220882A1
(en)
|
2004-03-08 |
2005-09-22 |
Georgia State University Research Foundation, Inc |
Novel dicationic imidazo(1,2-a)pyridines and 5,6,7,8-tetrahydro-imidazo(1,2a)pyridines as antiprotozoal agents
|
|
JP2007531753A
(ja)
|
2004-03-31 |
2007-11-08 |
ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ |
非イミダゾール系複素環式化合物
|
|
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
|
|
CN1937994A
(zh)
|
2004-04-06 |
2007-03-28 |
宝洁公司 |
角蛋白染色化合物、包含它们的角蛋白染色组合物以及它们的应用
|
|
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
|
|
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
|
|
EP1793819A2
(fr)
|
2004-09-23 |
2007-06-13 |
Wyeth a Corporation of the State of Delaware |
Derives de carbazole et de cyclopentaindole destines a traiter une infection par le virus de l'hepatite c
|
|
ATE479687T1
(de)
|
2004-10-15 |
2010-09-15 |
Takeda Pharmaceutical |
Kinaseinhibitoren
|
|
WO2006053121A2
(fr)
|
2004-11-10 |
2006-05-18 |
Cgi Pharmaceuticals, Inc. |
Certaines imidazo[1,2-a] pyrazin-8-ylamines et les procédés de fabrication et d'utilisation correspondants
|
|
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
|
|
US7998974B2
(en)
|
2005-03-03 |
2011-08-16 |
Sirtris Pharmaceuticals, Inc. |
Fused heterocyclic compounds and their use as sirtuin modulators
|
|
AU2006223409B2
(en)
|
2005-03-10 |
2011-07-21 |
Gilead Connecticut, Inc. |
Certain substituted amides, method of making, and method of use thereof
|
|
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
|
|
WO2006118256A1
(fr)
|
2005-04-28 |
2006-11-09 |
Kyowa Hakko Kogyo Co., Ltd. |
Dérivés de 2-aminoquinazoline
|
|
EP2439273B1
(fr)
|
2005-05-09 |
2019-02-27 |
Ono Pharmaceutical Co., Ltd. |
Anticorps monoclonaux humains pour mort programmée 1 (PD-1) et procédés de traitement du cancer à l'aide d'anticorps anti-PD-1 seuls ou combinés à d'autres formulations immunothérapeutiques
|
|
EP1902056A2
(fr)
|
2005-05-20 |
2008-03-26 |
Array Biopharma, Inc. |
Composes inhibiteurs raf et procedes d'utilisation de ceux-ci
|
|
HRP20151102T1
(xx)
|
2005-07-01 |
2015-11-20 |
E. R. Squibb & Sons, L.L.C. |
Humana monoklonska antitijela za ligand programirane smrti 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
|
|
ES2537898T3
(es)
|
2005-10-25 |
2015-06-15 |
Shionogi & Co., Ltd. |
Derivados de aminotiazolidina y aminotetrahidrotiazepina como inhibidores 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
|
|
WO2007069565A1
(fr)
|
2005-12-12 |
2007-06-21 |
Ono Pharmaceutical Co., Ltd. |
Compose heterocyclique bicyclique
|
|
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
|
|
JP2009531390A
(ja)
|
2006-03-31 |
2009-09-03 |
ノバルティス アクチエンゲゼルシャフト |
有機化合物
|
|
WO2008118122A2
(fr)
|
2006-05-08 |
2008-10-02 |
Molecular Neuroimaging, Llc |
Composés et sondes amyloïdes de ceux-ci pour des utilisations thérapeutiques et en imagerie
|
|
AU2007257959A1
(en)
|
2006-06-09 |
2007-12-21 |
Kemia, Inc. |
Therapy using cytokine inhibitors
|
|
US20080280891A1
(en)
|
2006-06-27 |
2008-11-13 |
Locus Pharmaceuticals, Inc. |
Anti-cancer agents and uses thereof
|
|
BRPI0713187A2
(pt)
|
2006-07-20 |
2012-10-16 |
Mehmet Kahraman |
método de inibir rho-quinase, método de tratamento de doença mediada por rho-quinase, composto e composição farmacêutica
|
|
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
|
|
WO2008032171A1
(fr)
|
2006-09-11 |
2008-03-20 |
Matrix Laboratories Ltd. |
Nouveaux composés hétérocycliques utiles pour traiter les maladies allergiques et inflammatoires, compositions pharmaceutiques les contenant et procédés servant à les préparer
|
|
US7838523B2
(en)
|
2006-09-11 |
2010-11-23 |
Cgi Pharmaceuticals, Inc. |
Certain substituted amides, method of making, and method of use thereof
|
|
WO2008033858A2
(fr)
|
2006-09-11 |
2008-03-20 |
Cgi Pharmaceuticals, Inc. |
Inhibiteurs de kinase et procédés d'utilisation et d'identification des inhibiteurs de kinase
|
|
PE20080839A1
(es)
|
2006-09-11 |
2008-08-23 |
Cgi Pharmaceuticals Inc |
Determinadas amidas sustituidas, metodo de elaboracion y metodo de uso de las mismas
|
|
AR063707A1
(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 farmacéuticas 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
|
|
WO2008057254A2
(fr)
|
2006-10-27 |
2008-05-15 |
Wyeth |
Composés tricycliques servant d'inhibiteurs des métalloprotéases matricielles
|
|
TWI409259B
(zh)
|
2006-11-08 |
2013-09-21 |
必治妥美雅史谷比公司 |
吡啶酮化合物
|
|
GB0623209D0
(en)
|
2006-11-21 |
2007-01-03 |
F2G Ltd |
Antifungal agents
|
|
WO2008064318A2
(fr)
|
2006-11-22 |
2008-05-29 |
University Of Medicine And Dentistry Of New Jersey |
Composés actifs de récepteurs opioïdes périphériques
|
|
WO2008064317A1
(fr)
|
2006-11-22 |
2008-05-29 |
University Of Medicine And Dentistry Of New Jersey |
Composés actifs de récepteurs opioïdes lipophiles
|
|
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
|
|
US8513270B2
(en)
|
2006-12-22 |
2013-08-20 |
Incyte Corporation |
Substituted heterocycles as Janus kinase inhibitors
|
|
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
|
|
EP2139879B1
(fr)
|
2007-03-22 |
2012-07-11 |
AstraZeneca AB |
Dérivés de quinoléine destinés au traitement de maladies inflammatoires
|
|
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
|
|
JP2010526836A
(ja)
|
2007-05-10 |
2010-08-05 |
ジーイー・ヘルスケア・リミテッド |
カンナビノイドCB2レセプターに対して活性を有するイミダゾール(1,2−a)ピリジン及び関連化合物
|
|
PT2170959E
(pt)
|
2007-06-18 |
2014-01-07 |
Merck Sharp & Dohme |
Anticorpos para o receptor humano de morte programada 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
|
|
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
|
|
ES2360929T3
(es)
|
2007-09-20 |
2011-06-10 |
Amgen Inc. |
Derivados del ácido 1-(4-(4-bencilbenzamido)-bencil)azetidin-3-carboxílico y compuestos relacionados como moduladores del receptor s1p para el tratamiento de trastornos inmunitarios.
|
|
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
|
|
WO2009053737A2
(fr)
|
2007-10-25 |
2009-04-30 |
Astrazeneca Ab |
Dérivés de pyridine et de pyrazine - 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
|
|
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
|
|
WO2009077197A1
(fr)
|
2007-12-19 |
2009-06-25 |
Syngenta Participations Ag |
Composés insecticides
|
|
JP2011506487A
(ja)
|
2007-12-21 |
2011-03-03 |
ザ・ユニバーシティ・オブ・シドニー |
トランスロケータータンパク質リガンド
|
|
US8642660B2
(en)
|
2007-12-21 |
2014-02-04 |
The University Of Rochester |
Method for altering the lifespan of eukaryotic organisms
|
|
SI2233474T1
(sl)
|
2008-01-18 |
2015-11-30 |
Eisai R&D Management Co., Ltd. |
Kondenziran derivat aminodihidrotiazina
|
|
JP5381718B2
(ja)
|
2008-01-31 |
2014-01-08 |
コニカミノルタ株式会社 |
ハロ多環芳香族化合物及びその製造方法
|
|
CA2714500A1
(fr)
|
2008-02-26 |
2009-09-03 |
Novartis Ag |
Composes heterocycliques comme inhibiteurs 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
|
|
US8168757B2
(en)
|
2008-03-12 |
2012-05-01 |
Merck Sharp & Dohme Corp. |
PD-1 binding proteins
|
|
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
|
|
US8461163B2
(en)
|
2008-03-31 |
2013-06-11 |
Takeda Pharmaceutical Company Limited |
Substituted N-(pyrazolo[1,5-a]pyrimidin-5-yl)amides as inhibitors of apoptosis signal-regulating kinase 1
|
|
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
|
|
EP2300470A2
(fr)
|
2008-05-19 |
2011-03-30 |
Sepracor Inc. |
Composés imidazo[1,2-a]pyridines
|
|
WO2009146358A1
(fr)
|
2008-05-29 |
2009-12-03 |
Sirtris Pharmaceuticals, Inc. |
Imidazopyridine et analogues liés en tant que modulateurs de la sirtuine
|
|
US8163743B2
(en)
|
2008-06-05 |
2012-04-24 |
GlaxoGroupLimited |
4-carboxamide indazole derivatives useful as inhibitors of PI3-kinases
|
|
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
|
|
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
|
|
JP6087503B2
(ja)
|
2008-09-26 |
2017-03-08 |
ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド |
ヒト抗pd−1、pd−l1、及びpd−l2抗体とその用途
|
|
US8598174B2
(en)
|
2008-11-12 |
2013-12-03 |
Genetech, Inc. |
Pyridazinones, method of making, and method of use thereof
|
|
US20120010188A1
(en)
|
2008-12-04 |
2012-01-12 |
Promimagen Ltd. |
Imidazopyridine Compounds
|
|
SMT202500126T1
(it)
|
2008-12-09 |
2025-05-12 |
Hoffmann La Roche |
Anticorpi anti-pd-l1 e loro uso per potenziare la funzione dei linfociti t
|
|
WO2010080474A1
(fr)
|
2008-12-19 |
2010-07-15 |
Bristol-Myers Squibb Company |
Carbazole et inhibiteurs de la carboline kinase
|
|
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
|
|
CA2740193A1
(fr)
|
2008-12-23 |
2010-07-01 |
Abbott Laboratories |
Composes antiviraux
|
|
JP5578490B2
(ja)
|
2008-12-26 |
2014-08-27 |
味の素株式会社 |
ピラゾロピリミジン化合物
|
|
ES2629337T3
(es)
|
2009-02-09 |
2017-08-08 |
Inserm - Institut National De La Santé Et De La Recherche Médicale |
Anticuerpos contra PD-1 y anticuerpos contra PD-L1 y usos de los mismos
|
|
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
|
|
WO2010104306A2
(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
|
|
WO2010115736A2
(fr)
|
2009-04-02 |
2010-10-14 |
Merck Serono S.A. |
Inhibiteurs de la dihydroorotate déshydrogénase
|
|
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
|
|
CN102469788A
(zh)
|
2009-06-30 |
2012-05-23 |
西佳技术公司 |
登革病毒感染的治疗和预防
|
|
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
|
|
WO2011047129A1
(fr)
|
2009-10-15 |
2011-04-21 |
Southern Research Institute |
Traitement de maladies neurodégénératives, cause d'amélioration de la mémoire et analyse pour évaluer des composés associés
|
|
WO2011047319A2
(fr)
|
2009-10-16 |
2011-04-21 |
Rib-X Pharmaceuticals, Inc. |
Composés anti-microbiens et procédés permettant de fabriquer et d'utiliser ces composés
|
|
WO2011050245A1
(fr)
|
2009-10-23 |
2011-04-28 |
Yangbo Feng |
Hétéroaryles bicycliques formant inhibiteurs de la kinase
|
|
JP2013512251A
(ja)
|
2009-11-24 |
2013-04-11 |
アンプリミューン、インコーポレーテッド |
Pd−l1/pd−l2の同時阻害
|
|
EP2518072A4
(fr)
|
2009-12-24 |
2014-06-04 |
Ajinomoto Kk |
Composés d'imidazopyridazine
|
|
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
|
|
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.
|
|
ES2862931T3
(es)
|
2010-03-04 |
2021-10-08 |
Merck Sharp & Dohme |
Inhibidores de la catecol O-metil transferasa y su uso en el tratamiento de trastornos psicóticos
|
|
CN102869661B
(zh)
|
2010-03-18 |
2015-08-05 |
韩国巴斯德研究所 |
抗感染化合物
|
|
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
|
|
JP2013532153A
(ja)
|
2010-06-18 |
2013-08-15 |
ザ ブリガム アンド ウィメンズ ホスピタル インコーポレイテッド |
慢性免疫病に対する免疫治療のためのtim−3およびpd−1に対する二重特異性抗体
|
|
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
|
|
EP2624837A4
(fr)
|
2010-10-04 |
2014-03-26 |
Inst Hepatitis & Virus Res |
Nouveaux inhibiteurs de la sécrétion d'antigènes du virus de l'hépatite b
|
|
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
|
|
CN103282034A
(zh)
|
2010-11-18 |
2013-09-04 |
利亘制药公司 |
造血生长因子模拟物的用途
|
|
CN103261188A
(zh)
|
2010-12-17 |
2013-08-21 |
先正达参股股份有限公司 |
杀虫化合物
|
|
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
|
|
CN103402996B
(zh)
|
2011-01-04 |
2015-02-11 |
诺瓦提斯公司 |
可用于治疗年龄相关性黄斑变性(amd)的吲哚化合物或其类似物
|
|
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
|
|
US9464065B2
(en)
|
2011-03-24 |
2016-10-11 |
The Scripps Research Institute |
Compounds and methods for inducing chondrogenesis
|
|
AU2012243329B2
(en)
|
2011-04-13 |
2015-09-17 |
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
|
|
JP6007417B2
(ja)
|
2011-05-31 |
2016-10-12 |
レセプトス エルエルシー |
新規glp−1受容体安定剤および調節剤
|
|
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
|
|
BR112014000314A2
(pt)
|
2011-07-08 |
2017-01-10 |
Novartis Ag |
derivados de pirrolo pirimidina
|
|
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
|
|
AU2012322329A1
(en)
|
2011-10-13 |
2014-05-01 |
Novartis Ag |
Novel oxazine derivatives and their use in the treatment of disease
|
|
KR20140077965A
(ko)
|
2011-10-20 |
2014-06-24 |
글락소스미스클라인 엘엘씨 |
시르투인 조절제로서의 치환된 비시클릭 아자-헤테로사이클 및 유사체
|
|
SG11201401359SA
(en)
|
2011-10-21 |
2014-05-29 |
Torrent Pharmaceuticals Ltd |
Novel substituted imidazopyrimidines as gpbar1 receptor modulators
|
|
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
|
|
WO2013133367A1
(fr)
|
2012-03-09 |
2013-09-12 |
カルナバイオサイエンス株式会社 |
Nouveau dérivé de triazine
|
|
JP6317320B2
(ja)
|
2012-03-15 |
2018-04-25 |
セルジーン シーエーアール エルエルシー |
上皮成長因子受容体キナーゼ阻害剤の塩
|
|
MD20140063A2
(ro)
|
2012-04-20 |
2014-12-31 |
Gilead Sciences, Inc. |
Derivaţi de acid benzotiazol-6-il acetic şi utilizarea acestora pentru tratarea unei infecţii HIV
|
|
WO2013157021A1
(fr)
|
2012-04-20 |
2013-10-24 |
Advinus Therapeutics Limited |
Composés bicycliques, compositions et applications médicinales de ceux-ci
|
|
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
|
|
WO2013191113A1
(fr)
|
2012-06-18 |
2013-12-27 |
住友化学株式会社 |
Composé hétérocyclique fusionné
|
|
JP6299591B2
(ja)
|
2012-07-03 |
2018-03-28 |
小野薬品工業株式会社 |
ソマトスタチン受容体作動活性を有する化合物およびその医薬用途
|
|
ES2689429T3
(es)
|
2012-07-13 |
2018-11-14 |
Ucb Biopharma Sprl |
Derivados de imidazopiridina como moduladores de actividad de TNF
|
|
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
|
|
US9428511B2
(en)
|
2012-09-06 |
2016-08-30 |
Bristol-Myers Squibb Company |
Imidazopyridazine JAK3 inhibitors and their use for the treatment of inflammatory and autoimmune diseases
|
|
KR102281288B1
(ko)
|
2012-09-26 |
2021-07-26 |
에프. 호프만-라 로슈 아게 |
환형 에터 피라졸-4-일-헤테로사이클릴-카복사마이드 화합물 및 이의 사용 방법
|
|
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
|
|
TW201932456A
(zh)
|
2013-01-15 |
2019-08-16 |
美商英塞特控股公司 |
適用作pim激酶抑制劑之噻唑甲醯胺及吡啶甲醯胺化合物
|
|
WO2014114532A1
(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
|
|
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
|
|
CN103143948A
(zh)
|
2013-03-07 |
2013-06-12 |
江苏汤臣汽车零部件有限公司 |
一种轻量化平衡轴支座的车架连接钻孔工装
|
|
AP2015008716A0
(en)
|
2013-03-08 |
2015-09-30 |
Amgen Inc |
Perfluorinated cyclopropyl fused 1,3-oxazin-2-amine compounds as beta-secretase inhibitors and methods of use
|
|
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
|
|
CN105283552A
(zh)
|
2013-03-13 |
2016-01-27 |
澳大利亚核科学和技术组织 |
具有非功能性tspo基因的转基因非人类生物体
|
|
ES2705247T3
(es)
|
2013-03-14 |
2019-03-22 |
Univ Columbia |
4-fenilpiperidinas, su preparación y uso
|
|
AU2014265957A1
(en)
|
2013-03-14 |
2015-09-10 |
Curadev Pharma Private Ltd. |
Inhibitors of the kynurenine pathway
|
|
EP2968265A4
(fr)
|
2013-03-14 |
2016-12-28 |
Celtaxsys Inc |
Inhibiteurs de la leucotriène a4 hydrolase
|
|
ES2623904T3
(es)
|
2013-03-14 |
2017-07-12 |
VIIV Healthcare UK (No.5) Limited |
Inhibidores de la replicación del virus de la inmunodeficiencia humana
|
|
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
|
|
PT2970265T
(pt)
|
2013-03-15 |
2018-10-23 |
Plexxikon Inc |
Compostos heterocíclicos e suas utilizações
|
|
WO2014181287A1
(fr)
|
2013-05-09 |
2014-11-13 |
Piramal Enterprises Limited |
Composés hétérocyclyliques et leurs utilisations
|
|
MX355943B
(es)
|
2013-06-26 |
2018-05-07 |
Abbvie Inc |
Carboxamidas primarias como inhibidores de btk.
|
|
JP6677637B2
(ja)
|
2013-07-02 |
2020-04-08 |
シンジェンタ パーティシペーションズ アーゲー |
有害生物防除的に活性な、硫黄含有置換基を有する二環式または三環式複素環
|
|
KR102377635B1
(ko)
|
2013-07-17 |
2022-03-24 |
오츠카 세이야쿠 가부시키가이샤 |
시아노트리아졸 화합물
|
|
BR112016001457A2
(pt)
|
2013-07-25 |
2017-08-29 |
Dana Farber Cancer Inst Inc |
Inibidores de fatores de transcrição e usos dos mesmos
|
|
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
|
|
KR102276644B1
(ko)
|
2013-09-04 |
2021-07-13 |
브리스톨-마이어스 스큅 컴퍼니 |
면역조절제로서 유용한 화합물
|
|
CU24345B1
(es)
|
2013-09-06 |
2018-05-08 |
Aurigene Discovery Tech Ltd |
Derivados de 1,3,4-oxadiazol y 1,3,4-tiadiazol como inmunomoduladores
|
|
HRP20181052T1
(hr)
|
2013-09-06 |
2018-09-07 |
Aurigene Discovery Technologies Limited |
Derivati 1,2,4-oksadiazola kao imunomodulatori
|
|
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
|
|
KR20160104065A
(ko)
|
2014-01-03 |
2016-09-02 |
바이엘 애니멀 헬스 게엠베하 |
농약으로서의 신규 피라졸릴헤테로아릴아미드
|
|
EP3105251A4
(fr)
|
2014-02-10 |
2017-11-15 |
Merck Sharp & Dohme Corp. |
Anticorps qui se lient à la protéine tau humaine et dosage pour quantifier la protéine tau humaine au moyen des anticorps
|
|
EP3110423A4
(fr)
|
2014-02-25 |
2017-09-20 |
Achillion Pharmaceuticals, Inc. |
Composés d'éther pour le traitement de troubles dans lequel intervient le complément
|
|
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
|
|
BR112016022785B8
(pt)
|
2014-04-04 |
2020-09-15 |
Iomet Pharma Ltd |
composto inibidor de triptofano-2,3-dioxigenase (tdo) e/ou indoleamina-2,3-dioxigenase (ido), composição farmacêutica, e, uso de composto inibidor de triptofano-2,3-dioxigenase (tdo) e/ou indoleamina-2,3dioxigenase (ido) ou de um sal farmaceuticamente aceitável do mesmo para fabricação de um medicamento
|
|
US9850225B2
(en)
|
2014-04-14 |
2017-12-26 |
Bristol-Myers Squibb Company |
Compounds useful as immunomodulators
|
|
CN106661001A
(zh)
|
2014-05-14 |
2017-05-10 |
哈佛学院院长等 |
有机发光二极管材料
|
|
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
|
|
WO2016041511A1
(fr)
|
2014-09-19 |
2016-03-24 |
Yen-Ta Lu |
Composés benzo-hétérocycliques et leurs applications
|
|
BR112017006305B1
(pt)
|
2014-10-06 |
2024-02-20 |
Merck Patent Gmbh |
Compostos heteroarila, seus usos, e composição farmacêutica
|
|
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
|
|
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
|
|
TW201718581A
(zh)
|
2015-10-19 |
2017-06-01 |
英塞特公司 |
作為免疫調節劑之雜環化合物
|
|
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
|
|
SG10202004618TA
(en)
|
2015-11-19 |
2020-06-29 |
Incyte Corp |
Heterocyclic compounds as immunomodulators
|
|
US20170174671A1
(en)
|
2015-12-17 |
2017-06-22 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
|
EP3393457A1
(fr)
|
2015-12-22 |
2018-10-31 |
Synthon B.V. |
Composition pharmaceutique comprenant du lénalidomide amorphe et un antioxydant
|
|
SI3394033T1
(sl)
|
2015-12-22 |
2021-03-31 |
Incyte Corporation |
Heterociklične spojine kot imunomodulatorji
|
|
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
|
|
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
|
|
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
|
|
BR112018071585B1
(pt)
|
2016-04-22 |
2024-01-02 |
Incyte Corporation |
Formulações de um inibidor de lsd1, seus usos e método de preparação das mesmas
|
|
AR108396A1
(es)
|
2016-05-06 |
2018-08-15 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
|
MA45116A
(fr)
|
2016-05-26 |
2021-06-02 |
Incyte Corp |
Composés hétérocycliques comme immunomodulateurs
|
|
KR102409470B1
(ko)
|
2016-06-20 |
2022-06-16 |
엘랑코 유에스 인코포레이티드 |
Peg화된 돼지 인터페론 및 그의 사용 방법
|
|
IL263429B
(en)
|
2016-06-20 |
2022-08-01 |
Novartis Ag |
Crystalline forms of triazolopyrimidine compound
|
|
ES2927984T3
(es)
|
2016-06-20 |
2022-11-14 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
|
WO2017223239A1
(fr)
|
2016-06-21 |
2017-12-28 |
X4 Pharmaceuticals, Inc. |
Inhibiteurs de cxcr4 et leurs utilisations
|
|
ES2930092T3
(es)
|
2016-07-14 |
2022-12-07 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
|
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
|
|
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
|
|
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
|
|
ES2929193T3
(es)
|
2016-12-22 |
2022-11-25 |
Incyte Corp |
Derivados de tetrahidro imidazo[4,5-c]piridina como inductores de la internalización de PD-L1
|
|
WO2018119221A1
(fr)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Dérivés pyridine utilisés en tant qu'immunomodulateurs
|
|
MX391981B
(es)
|
2016-12-22 |
2025-03-21 |
Incyte Corp |
Derivados de benzooxazol como inmunomoduladores.
|
|
US20180177784A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
|
WO2018119236A1
(fr)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Dérivés de triazolo[1,5-a]pyridine en tant qu'immunomodulateurs
|
|
EP3558963B1
(fr)
|
2016-12-22 |
2022-03-23 |
Incyte Corporation |
Composés hétéroaromatiques bicycliques utilisés en tant qu'immunomodulateurs
|
|
HUE054272T2
(hu)
|
2016-12-22 |
2021-09-28 |
Calithera Biosciences Inc |
Összetételek és módszerek az argináz-tevékenység gátlásához
|
|
JOP20180040A1
(ar)
|
2017-04-20 |
2019-01-30 |
Gilead Sciences Inc |
مثبطات pd-1/pd-l1
|
|
WO2019023575A1
(fr)
|
2017-07-28 |
2019-01-31 |
Chemocentryx, Inc. |
Composés immunomodulateurs
|
|
JP7198269B2
(ja)
|
2017-08-08 |
2022-12-28 |
ケモセントリックス,インコーポレイティド |
大員環免疫調節剤
|
|
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
|
|
KR102708681B1
(ko)
|
2018-02-13 |
2024-09-26 |
길리애드 사이언시즈, 인코포레이티드 |
Pd-1/pd-l1 억제제
|
|
SMT202300065T1
(it)
|
2018-03-30 |
2023-05-12 |
Incyte Corp |
Composti eterociclici come immunomodulatori
|
|
US20210040118A1
(en)
|
2018-04-03 |
2021-02-11 |
Betta Pharmaceuticals Co., Ltd |
Immunomodulators, compositions and methods thereof
|
|
EP3781556B1
(fr)
|
2018-04-19 |
2025-06-18 |
Gilead Sciences, Inc. |
Inhibiteurs pd-1/pd-l1
|
|
PL3790877T3
(pl)
|
2018-05-11 |
2023-06-12 |
Incyte Corporation |
Pochodne tetrahydroimidazo[4,5-c]pirydyny jako immunomodulatory pd-l1
|
|
WO2020036491A1
(fr)
|
2018-08-15 |
2020-02-20 |
Moonshine Solutions As |
Procédé et dispositif d'alimentation d'un liquide à un revêtement
|
|
CA3117199C
(fr)
|
2018-10-24 |
2024-03-19 |
Gilead Sciences, Inc. |
Inhibiteurs de pd-1/pd-l1
|
|
AU2019373702A1
(en)
|
2018-11-02 |
2021-06-24 |
Shanghai Maxinovel Pharmaceuticals Co., Ltd. |
Diphenyl-like compound, intermediate thereof, preparation method therefor, pharmaceutical composition thereof and uses thereof
|
|
US11596692B1
(en)
|
2018-11-21 |
2023-03-07 |
Incyte Corporation |
PD-L1/STING conjugates and methods of use
|
|
JP7579789B2
(ja)
|
2019-01-31 |
2024-11-08 |
ベッタ ファーマシューティカルズ カンパニー リミテッド |
免疫調節剤、組成物およびその使用方法
|
|
GB201911210D0
(en)
|
2019-08-06 |
2019-09-18 |
Amlo Biosciences Ltd |
Clinical management of oropharyngeal squamous cell carcinoma
|
|
WO2021030162A1
(fr)
|
2019-08-09 |
2021-02-18 |
Incyte Corporation |
Sels d'un inhibiteur de pd-1/pd-l1
|
|
MX2022002883A
(es)
|
2019-09-20 |
2022-03-25 |
Transgene |
Combinacion de un poxvirus que codifica para polipeptidos de virus de papiloma humano (vph) e interleucina 2 (il-2) con un anticuerpo anti ligando 1 de muerte programada (pd-l1).
|
|
IL291471B2
(en)
|
2019-09-30 |
2025-04-01 |
Incyte Corp |
Pyrimido[3,2–D]pyrimidine compounds as immunomodulators
|
|
CN114829366A
(zh)
|
2019-11-11 |
2022-07-29 |
因赛特公司 |
Pd-1/pd-l1抑制剂的盐及结晶形式
|
|
AU2021266969A1
(en)
|
2020-05-04 |
2022-12-08 |
Beyondspring Pharmaceuticals, Inc. |
Triple combination therapy for enhancing cancer cell killing in cancers with low immunogenicity
|
|
US11866434B2
(en)
|
2020-11-06 |
2024-01-09 |
Incyte Corporation |
Process for making a PD-1/PD-L1 inhibitor and salts and crystalline forms thereof
|
|
WO2022099018A1
(fr)
|
2020-11-06 |
2022-05-12 |
Incyte Corporation |
Procédé de préparation d'un inhibiteur de pd-1/pd-l1
|
|
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
|
|
WO2022133176A1
(fr)
|
2020-12-18 |
2022-06-23 |
Incyte Corporation |
Formulation orale pour un inhibiteur de pd-l1
|
|
US20230149409A1
(en)
*
|
2021-09-24 |
2023-05-18 |
Incyte Corporation |
Treatment of human papillomavirus-associated cancers by pd-l1 inhibitors
|