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
|
WO1998027108A2
(en)
|
1996-12-16 |
1998-06-25 |
Fujisawa Pharmaceutical Co., Ltd. |
New amide compounds and their use as nitric oxide synthase inhibitors
|
JPH10316853A
(ja)
|
1997-05-15 |
1998-12-02 |
Sumitomo Bakelite Co Ltd |
半導体多層配線用層間絶縁膜樹脂組成物及び該絶縁膜の製造方法
|
EP1019391A1
(en)
|
1997-10-02 |
2000-07-19 |
Merck & Co. Inc. |
Inhibitors of prenyl-protein transferase
|
AU2745899A
(en)
|
1998-03-05 |
1999-09-20 |
Nissan Chemical Industries Ltd. |
Anilide compounds and herbicide
|
JP2000128984A
(ja)
|
1998-10-28 |
2000-05-09 |
Sumitomo Bakelite Co Ltd |
ポリベンゾオキサゾール前駆体及び樹脂
|
JP2000128986A
(ja)
|
1998-10-28 |
2000-05-09 |
Sumitomo Bakelite Co Ltd |
ポリベンゾオキサゾール前駆体及びポリベンゾオキサゾール
|
JP2000128987A
(ja)
|
1998-10-28 |
2000-05-09 |
Sumitomo Bakelite Co Ltd |
ポリベンゾオキサゾール前駆体及びポリベンゾオキサゾール
|
US6297351B1
(en)
|
1998-12-17 |
2001-10-02 |
Sumitomo Bakelite Company Limited |
Polybenzoxazole resin and precursor thereof
|
WO2000035886A2
(en)
|
1998-12-18 |
2000-06-22 |
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
|
ID30204A
(id)
|
1999-12-27 |
2001-11-15 |
Japan Tobacco Inc |
Senyawa-senyawa cincin terfusi dan penggunaannya sebagai obat
|
US7041675B2
(en)
|
2000-02-01 |
2006-05-09 |
Abbott Gmbh & Co. Kg |
Heterocyclic compounds and their use as PARP inhibitors
|
US6521618B2
(en)
|
2000-03-28 |
2003-02-18 |
Wyeth |
3-cyanoquinolines, 3-cyano-1,6-naphthyridines, and 3-cyano-1,7-naphthyridines as protein kinase inhibitors
|
AU2001249679A1
(en)
|
2000-03-31 |
2001-10-15 |
Ortho-Mcneil Pharmaceutical, Inc. |
Phenyl-substituted imidazopyridines
|
WO2001081312A2
(en)
|
2000-04-24 |
2001-11-01 |
Merck Frosst Canada & Co. |
Method of treatment using phenyl and biaryl derivatives as prostaglandin e inhibitors and compounds useful therefore
|
ES2225624T3
(es)
|
2000-06-28 |
2005-03-16 |
Smithkline Beecham Plc |
Procedimiento de molienda por via humeda.
|
WO2002014321A1
(en)
|
2000-08-11 |
2002-02-21 |
The Regents Of The University Of California |
Use of stat-6 inhibitors as therapeutic agents
|
EP1343785A2
(de)
|
2000-12-13 |
2003-09-17 |
Basf Aktiengesellschaft |
Verwendung von substituierten imidazoazinen, neue imidazoazine, verfahren zu deren herstellung, sowie sie enthaltende mittel
|
JP2004518651A
(ja)
|
2000-12-15 |
2004-06-24 |
グラクソ グループ リミテッド |
治療用化合物
|
SE0100567D0
(sv)
|
2001-02-20 |
2001-02-20 |
Astrazeneca Ab |
Compounds
|
CA2438586A1
(en)
|
2001-03-14 |
2002-09-19 |
Eli Lilly And Company |
Retinoid x receptor modulators
|
EP1372643A1
(en)
|
2001-03-30 |
2004-01-02 |
Smithkline Beecham Corporation |
Pyrazolopyridines, process for their preparation and use as therapeutic compounds
|
EP1377575B1
(en)
|
2001-04-10 |
2006-07-05 |
SmithKline Beecham Corporation |
Antiviral pyrazolopyridine compounds
|
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
|
ATE296826T1
(de)
|
2001-04-27 |
2005-06-15 |
Smithkline Beecham Corp |
Pyrazolo(1,5)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
|
DE60220525T2
(de)
|
2001-09-07 |
2008-02-07 |
Smithkline Beecham Corp. |
Pyrazolo-pyridine für die behandlung von herpes-ansteckungen
|
TWI331526B
(en)
|
2001-09-21 |
2010-10-11 |
Bristol Myers Squibb Pharma Co |
Lactam-containing compounds and derivatives thereof as factor xa inhibitors
|
WO2003030901A1
(en)
|
2001-10-09 |
2003-04-17 |
Pharmacia & Upjohn Company |
Arylsulphonyl-substituted tetrahydro- and hexahydro-carbazoles as 5-ht-6 receptor ligands
|
US20030143199A1
(en)
|
2001-10-09 |
2003-07-31 |
Carson Dennis A. |
Use of STAT-6 inhibitors as therapeutic agents
|
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
|
WO2003087092A2
(en)
|
2002-04-11 |
2003-10-23 |
Vertex Pharmaceuticals Incorporated |
Inhibitors of serine proteases, particularly hepatitis c virus ns3 - ns4 protease
|
BR0309475A
(pt)
|
2002-04-23 |
2005-03-01 |
Shionogi & Co |
Derivados de pirazolo-[1,5-a]-pirimidina e inibidores de nad(p)h oxidase que contêm os mesmos
|
US20060004010A1
(en)
|
2002-07-10 |
2006-01-05 |
Hiromu Habashita |
Ccr4 antagonist and medical use thereof
|
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
|
EP1547996A4
(en)
|
2002-08-30 |
2006-08-02 |
Bf Res Inst Inc |
DIAGNOSTIC PROBES AND REMEDIES FOR DISEASES HAVING PRION PROTEIN ACCUMULATION AND METHOD OF MARKING
|
EP1546148A1
(en)
|
2002-10-03 |
2005-06-29 |
SmithKline Beecham Corporation |
Therapeutic compounds based on pyrazolopyridine derivatives
|
EP1551842A1
(en)
|
2002-10-15 |
2005-07-13 |
Smithkline Beecham Corporation |
Pyradazine compounds as gsk-3 inhibitors
|
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
|
SI1620429T1
(sl)
|
2003-04-11 |
2009-08-31 |
Glenmark Pharmaceuticals Sa |
Nove heterociklične spojine, uporabne za zdravljenje vnetnih in alergijskih motenj: postopek za njihovo pripravo in farmacevtski sestavki, ki jih vsebujejo
|
WO2005000833A1
(en)
|
2003-05-19 |
2005-01-06 |
Irm, Llc |
Immunosuppressant compounds and 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
|
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
|
EP1644370A4
(en)
|
2003-07-11 |
2008-06-04 |
Bristol Myers Squibb Co |
TETRAHYDROCHINOLINE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS
|
WO2005004863A1
(en)
|
2003-07-11 |
2005-01-20 |
Merck Patent Gmbh |
Benzimidazole carboxamides as raf kinase inhibitors
|
JPWO2005012221A1
(ja)
|
2003-08-04 |
2006-09-14 |
小野薬品工業株式会社 |
ジフェニルエーテル化合物、その製造方法および用途
|
WO2005014543A1
(ja)
|
2003-08-06 |
2005-02-17 |
Japan Tobacco Inc. |
縮合環化合物及びそのhcvポリメラーゼ阻害剤としての利用
|
US7504401B2
(en)
|
2003-08-29 |
2009-03-17 |
Locus Pharmaceuticals, Inc. |
Anti-cancer agents and uses thereof
|
JP4895811B2
(ja)
|
2003-09-11 |
2012-03-14 |
ケミア,インコーポレイテッド |
サイトカイン阻害剤
|
JP4758349B2
(ja)
|
2003-10-08 |
2011-08-24 |
アイアールエム・リミテッド・ライアビリティ・カンパニー |
タンパク質キナーゼ阻害剤としての化合物および組成物
|
US20070099938A1
(en)
|
2003-10-24 |
2007-05-03 |
Ono Pharmaceutical Co., Ltd. |
Antistress drug and medical use thereof
|
US20050288295A1
(en)
|
2003-11-11 |
2005-12-29 |
Currie Kevin S |
Certain imidazo[1,2-a]pyrazin-8-ylamines, method of making, and method of use thereof
|
WO2005063710A1
(de)
|
2003-12-23 |
2005-07-14 |
Basf Aktiengesellschaft |
3-trifluormethylpicolinsäureanilide und ihre verwendung als fungizide
|
EP1715867A4
(en)
|
2004-02-12 |
2009-04-15 |
Merck & Co Inc |
BIPYRIDYL AMIDES AS MODULATORS OF GLUTAMATE METABOTROPIC REPEATER-5
|
EP1717238A4
(en)
|
2004-02-16 |
2008-03-05 |
Daiichi Seiyaku Co |
FUNGICIDES HETEROCYCLIC COMPOUNDS
|
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
|
JP2007527908A
(ja)
|
2004-03-08 |
2007-10-04 |
ザ ユニバーシティ オブ ノース カロライナ アット チャペル ヒル |
抗原虫薬としての新規ジカチオン性イミダゾ[1,2−a]ピリジン、及び5,6,7,8−テトラヒドロ−イミダゾ[1,2−a]ピリジン
|
WO2005086904A2
(en)
|
2004-03-08 |
2005-09-22 |
Amgen Inc. |
Therapeutic modulation of ppar (gamma) activity
|
AU2005230902A1
(en)
|
2004-03-31 |
2005-10-20 |
Janssen Pharmaceutica, N.V. |
Non-imidazole heterocyclic compounds as histamine H3-receptor ligands
|
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
|
EP1735059A2
(en)
|
2004-04-06 |
2006-12-27 |
The Procter and Gamble Company |
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
|
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
(en)
|
2004-05-03 |
2013-09-24 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Cytokine inhibitors
|
PE20060748A1
(es)
|
2004-09-21 |
2006-10-01 |
Smithkline Beecham Corp |
Derivados de indolcarboxamida como inhibidores de quinasa ikk2
|
CN101035528A
(zh)
|
2004-09-23 |
2007-09-12 |
惠氏公司 |
治疗丙型肝炎病毒感染的咔唑和环戊二烯并吲哚衍生物
|
WO2006044687A2
(en)
|
2004-10-15 |
2006-04-27 |
Takeda San Diego, Inc. |
Kinase inhibitors
|
MX2007005643A
(es)
|
2004-11-10 |
2008-03-13 |
Cgi Pharmaceuticals Inc |
Ciertas imidazo [1,2-a] pirazin-8-ilaminas, metodo para su elaboracion y metodo de uso de las mismas.
|
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
|
EP1863766B1
(en)
|
2005-03-10 |
2015-05-20 |
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
|
WO2006125101A2
(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
(en)
|
2005-09-19 |
2007-03-29 |
Pfizer Products Inc. |
Diaryl-imidazole compounds condensed with a heterocycle as c3a receptor antagonists
|
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
|
WO2007061764A2
(en)
|
2005-11-22 |
2007-05-31 |
Merck & Co., Inc. |
Tricyclic compounds useful as inhibitors of kinases
|
WO2007067711A2
(en)
|
2005-12-08 |
2007-06-14 |
Amphora Discovery Corporation |
Certain chemical entities, compositions, and methods for modulating trpv1
|
EP1961745A1
(en)
|
2005-12-12 |
2008-08-27 |
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
(en)
|
2006-02-27 |
2007-08-30 |
Glenmark Pharmaceuticals S.A. |
Bicyclic heteroaryl derivatives as cannabinoid receptor modulators
|
WO2007102531A1
(ja)
|
2006-03-08 |
2007-09-13 |
Takeda Pharmaceutical Company Limited |
併用薬
|
WO2007113226A1
(en)
|
2006-03-31 |
2007-10-11 |
Novartis Ag |
Organic compounds
|
EP2023919A4
(en)
|
2006-05-08 |
2010-12-22 |
Molecular Neuroimaging Llc |
COMPOUNDS AND AMYLOID PROBES FOR THERAPY AND IMAGING USES
|
EP2035005A4
(en)
|
2006-06-09 |
2011-07-06 |
Kemia Inc |
THERAPY BASED ON CYTOKINE INHIBITORS
|
US20080280891A1
(en)
|
2006-06-27 |
2008-11-13 |
Locus Pharmaceuticals, Inc. |
Anti-cancer agents and uses thereof
|
EP2044061A2
(en)
|
2006-07-20 |
2009-04-08 |
Mehmet Kahraman |
Benzothiophene inhibitors of rho kinase
|
DE102006035018B4
(de)
|
2006-07-28 |
2009-07-23 |
Novaled Ag |
Oxazol-Triplett-Emitter für OLED-Anwendungen
|
WO2008021745A2
(en)
|
2006-08-16 |
2008-02-21 |
Itherx Pharmaceuticals, Inc. |
Hepatitis c virus entry inhibitors
|
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
|
US8263648B2
(en)
|
2006-09-11 |
2012-09-11 |
Mylan Laboratories Ltd. |
Diebenzofuran derivatives as inhibitors of PDE-4 and PDE-10
|
US7838523B2
(en)
|
2006-09-11 |
2010-11-23 |
Cgi Pharmaceuticals, Inc. |
Certain substituted amides, method of making, and method of use thereof
|
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
|
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.
|
AR063706A1
(es)
|
2006-09-11 |
2009-02-11 |
Cgi Pharmaceuticals Inc |
Determinadas amidas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmaceuticas que las comprenden.
|
FR2906250B1
(fr)
|
2006-09-22 |
2008-10-31 |
Sanofi Aventis Sa |
Derives de 2-aryl-6phenyl-imidazo(1,2-a) pyridines, leur preparation et leur application en therapeutique
|
EP2074107A2
(en)
|
2006-10-27 |
2009-07-01 |
Wyeth a Corporation of the State of Delaware |
Tricyclic compounds as matrix metalloproteinase inhibitors
|
GB0623209D0
(en)
|
2006-11-21 |
2007-01-03 |
F2G Ltd |
Antifungal agents
|
WO2008064317A1
(en)
|
2006-11-22 |
2008-05-29 |
University Of Medicine And Dentistry Of New Jersey |
Lipophilic opioid receptor active compounds
|
WO2008064318A2
(en)
|
2006-11-22 |
2008-05-29 |
University Of Medicine And Dentistry Of New Jersey |
Peripheral opioid receptor active compounds
|
US8513270B2
(en)
|
2006-12-22 |
2013-08-20 |
Incyte Corporation |
Substituted heterocycles as Janus kinase inhibitors
|
EP1964841A1
(en)
|
2007-02-28 |
2008-09-03 |
sanofi-aventis |
Imidazo[1,2-a]azine and their use as pharmaceuticals
|
EP1964840A1
(en)
|
2007-02-28 |
2008-09-03 |
sanofi-aventis |
Imidazo[1,2-a]pyridines and their use as pharmaceuticals
|
WO2008104077A1
(en)
|
2007-02-28 |
2008-09-04 |
Methylgene Inc. |
Small molecule inhibitors of protein arginine methyltransferases (prmts)
|
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
|
BRPI0809106A2
(pt)
|
2007-03-22 |
2014-08-26 |
Astrazeneca Ab |
Derivados de quinolina para o tratamento de doenças inflamatórias
|
US8653067B2
(en)
|
2007-04-24 |
2014-02-18 |
Shionogi & Co., Ltd. |
Pharmaceutical composition for treating Alzheimer's disease
|
WO2008134553A1
(en)
|
2007-04-26 |
2008-11-06 |
Xenon Pharmaceuticals Inc. |
Methods of using bicyclic compounds in treating sodium channel-mediated diseases
|
WO2008141239A1
(en)
|
2007-05-10 |
2008-11-20 |
Acadia Pharmaceuticals Inc. |
Imidazol [1,2-a] pyridines and related compounds with activity at cannabinoid cb2 receptors
|
WO2009027733A1
(en)
|
2007-08-24 |
2009-03-05 |
Astrazeneca Ab |
(2-pyridin-3-ylimidazo[1,2-b]pyridazin-6-yl) urea derivatives as antibacterial agents
|
EP2188252B1
(en)
|
2007-09-20 |
2011-04-13 |
Amgen Inc. |
1-(4-(4-benzylbenzamido)-benzyl)azetidine-3-carboxylic acid derivatives and related compounds as s1p receptor modulators for the treatment of immune disorders
|
CL2008002793A1
(es)
|
2007-09-20 |
2009-09-04 |
Cgi Pharmaceuticals Inc |
Compuestos derivados de amidas sustituidas, inhibidores de la actividad de btk; composicion farmaceutica que los comprende; utiles en el tratamiento del cancer, trastornos oseos, enfermedades autoinmunes, entre otras
|
DE102007048716A1
(de)
|
2007-10-11 |
2009-04-23 |
Merck Patent Gmbh |
Imidazo[1,2-a]pyrimidinderivate
|
TW200932219A
(en)
|
2007-10-24 |
2009-08-01 |
Astellas Pharma Inc |
Oxadiazolidinedione compound
|
US7868001B2
(en)
|
2007-11-02 |
2011-01-11 |
Hutchison Medipharma Enterprises Limited |
Cytokine inhibitors
|
WO2009062059A2
(en)
|
2007-11-08 |
2009-05-14 |
Pharmacopeia, Inc. |
Isomeric purinones and 1h-imidazopyridinones as pkc-theta inhibitors
|
US8431569B2
(en)
|
2007-12-13 |
2013-04-30 |
Merck Sharp & Dohme Corp. |
Inhibitors of 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
|
CA2707612A1
(en)
|
2007-12-19 |
2009-06-25 |
Syngenta Participations Ag |
Insecticidal compounds
|
WO2009086303A2
(en)
|
2007-12-21 |
2009-07-09 |
University Of Rochester |
Method for altering the lifespan of eukaryotic organisms
|
AU2008340182A1
(en)
|
2007-12-21 |
2009-07-02 |
The University Of Sydney |
Translocator protein ligands
|
RU2476431C2
(ru)
|
2008-01-18 |
2013-02-27 |
Эйсай Ар Энд Ди Менеджмент Ко., Лтд. |
Конденсированное производное аминодигидротиазина
|
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
|
EP2257552A1
(en)
|
2008-02-26 |
2010-12-08 |
Novartis AG |
Heterocyclic compounds as inhibitors of cxcr2
|
EP2095818A1
(en)
|
2008-02-29 |
2009-09-02 |
AEterna Zentaris GmbH |
Use of LHRH antagonists at non-castrating doses
|
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
|
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
|
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
|
EP2271646A1
(en)
|
2008-03-31 |
2011-01-12 |
Takeda Pharmaceutical Company Limited |
Apoptosis signal-regulating kinase 1 inhibitors
|
WO2009143156A2
(en)
|
2008-05-19 |
2009-11-26 |
Sepracor Inc. |
IMIDAZO[1,2-a]PYRIDINE COMPOUNDS
|
CA2726262A1
(en)
|
2008-05-29 |
2009-12-03 |
Sirtris Pharmaceuticals, Inc. |
Imidazopyridine and related analogs as sirtuin modulators
|
WO2010011837A1
(en)
|
2008-07-24 |
2010-01-28 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds useful as kinase modulators
|
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
|
EP2365970B1
(en)
|
2008-11-12 |
2018-03-21 |
Gilead Connecticut, Inc. |
Pyridazinones and their use as btk inhibitors
|
ES2403633T3
(es)
|
2008-12-04 |
2013-05-20 |
Proximagen Limited |
Compuestos de imidazopiridina
|
ES2539620T3
(es)
|
2008-12-19 |
2015-07-02 |
Cephalon, Inc. |
Pirrolotriazina como inhibidor de ALK y de JAK2
|
BRPI0922565A2
(pt)
|
2008-12-19 |
2015-12-15 |
Bristol Myers Squibb Co |
compostos de carbazol carboxamida úteis como inibidores de cinase
|
ES2490867T3
(es)
|
2008-12-19 |
2014-09-04 |
Bristol-Myers Squibb Company |
Inhibidores de carbazol y carbolina quinasas
|
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
|
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
|
JP2010202530A
(ja)
|
2009-02-27 |
2010-09-16 |
Tokyo Institute Of Technology |
含ヘテロ芳香族化合物および光学材料
|
KR20100101055A
(ko)
|
2009-03-07 |
2010-09-16 |
주식회사 메디젠텍 |
세포핵에서 세포질로의 gsk3의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 gsk3 이동 관련 질환의 치료 또는 예방용 약학적 조성물
|
AU2010233917B2
(en)
|
2009-04-02 |
2015-07-02 |
Merck Serono S.A. |
Dihydroorotate dehydrogenase inhibitors
|
WO2010119264A1
(en)
|
2009-04-16 |
2010-10-21 |
Centro Nacional De Investigaciones Oncólogicas (Cnio) |
Imidazopyrazines for use as kinase inhibitors
|
US8338441B2
(en)
|
2009-05-15 |
2012-12-25 |
Gilead Sciences, Inc. |
Inhibitors of human immunodeficiency virus replication
|
US8993604B2
(en)
|
2009-06-30 |
2015-03-31 |
Siga Technologies, Inc. |
Treatment and prevention of dengue virus infections
|
CA2763194A1
(en)
|
2009-06-30 |
2011-01-06 |
Siga Technologies, Inc. |
Treatment and prevention of dengue virus infections
|
TWI491606B
(zh)
|
2009-07-13 |
2015-07-11 |
Gilead Sciences Inc |
調節細胞凋亡信號之激酶的抑制劑
|
JP2011057661A
(ja)
|
2009-08-14 |
2011-03-24 |
Bayer Cropscience Ag |
殺虫性カルボキサミド類
|
UA108363C2
(uk)
|
2009-10-08 |
2015-04-27 |
|
Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування
|
US9095596B2
(en)
|
2009-10-15 |
2015-08-04 |
Southern Research Institute |
Treatment of neurodegenerative diseases, causation of memory enhancement, and assay for screening compounds for such
|
AU2010306646B2
(en)
|
2009-10-16 |
2016-09-01 |
Melinta Therapeutics, Inc. |
Antimicrobial compounds and methods of making and using the same
|
WO2011050245A1
(en)
|
2009-10-23 |
2011-04-28 |
Yangbo Feng |
Bicyclic heteroaryls as kinase inhibitors
|
EP2518072A4
(en)
|
2009-12-24 |
2014-06-04 |
Ajinomoto Kk |
IMIDAZOPYRIDAZINE COMPOUNDS
|
US20130022629A1
(en)
|
2010-01-04 |
2013-01-24 |
Sharpe Arlene H |
Modulators of Immunoinhibitory Receptor PD-1, and Methods of Use Thereof
|
US20130085133A1
(en)
|
2010-02-08 |
2013-04-04 |
Sourthern Research Institute Office of Commercialization and Intellectual Prop. |
Anti-viral treatment and assay to screenfor anti-viral agent
|
TW201136919A
(en)
|
2010-03-02 |
2011-11-01 |
Merck Sharp & Amp Dohme Corp |
Inhibitors of hepatitis C virus NS5B polymerase
|
WO2011109254A1
(en)
|
2010-03-04 |
2011-09-09 |
Merck Sharp & Dohme Corp. |
Inhibitors of catechol o-methyl transferase and their use in the treatment of psychotic disorders
|
US8865734B2
(en)
|
2010-03-18 |
2014-10-21 |
Institut Pasteur Korea |
Anti-infective compounds
|
US8410117B2
(en)
|
2010-03-26 |
2013-04-02 |
Hoffmann-La Roche Inc. |
Imidazopyrimidine derivatives
|
WO2011159857A1
(en)
|
2010-06-16 |
2011-12-22 |
Bristol-Myers Squibb Company |
Carboline carboxamide compounds useful as kinase inhibitors
|
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
(en)
|
2010-06-29 |
2012-01-04 |
Basf Se |
Pyrazole fused bicyclic compounds
|
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
(en)
|
2010-07-29 |
2012-02-02 |
President And Fellows Of Harvard College |
Ros1 kinase inhibitors for the treatment of glioblastoma and other p53-deficient cancers
|
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
|
CN103889428A
(zh)
|
2010-10-04 |
2014-06-25 |
肝炎与病毒研究所 |
乙型肝炎病毒抗原分泌的新型抑制剂
|
WO2012052745A1
(en)
|
2010-10-21 |
2012-04-26 |
Centro Nacional De Investigaciones Oncológicas (Cnio) |
Combinations of pi3k inhibitors with a second anti -tumor agent
|
EP2444084A1
(en)
|
2010-10-21 |
2012-04-25 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Use of PI3K inibitors for the treatment of obesity
|
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
|
AR084308A1
(es)
|
2010-12-17 |
2013-05-08 |
Syngenta Participations Ag |
Compuestos insecticidas derivados de triazol
|
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
|
MX347391B
(es)
|
2011-01-04 |
2017-04-25 |
Novartis Ag |
Compuestos de indol o análogos de los mismos útiles para el tratamiento de degeneración macular relacionada con la edad (amd).
|
WO2012100342A1
(en)
|
2011-01-27 |
2012-08-02 |
Université de Montréal |
Pyrazolopyridine and pyrazolopyrimidine derivatives as melanocortin-4 receptor modulators
|
WO2012125886A1
(en)
|
2011-03-17 |
2012-09-20 |
Bristol-Myers Squibb Company |
Pyrrolopyridazine jak3 inhibitors and their use for the treatment of inflammatory and autoimmune diseases
|
US9464065B2
(en)
|
2011-03-24 |
2016-10-11 |
The Scripps Research Institute |
Compounds and methods for inducing chondrogenesis
|
US9499502B2
(en)
|
2011-04-13 |
2016-11-22 |
Merck Sharp & Dohme Corp. |
5-substituted iminothiazines and their mono- and dioxides as BACE inhibitors, compositions, and their use
|
CN102796103A
(zh)
|
2011-05-23 |
2012-11-28 |
南京英派药业有限公司 |
6-(芳基甲酰)咪唑并[1,2-a]嘧啶和6-(芳基甲酰)[1,2,4]三唑并[4,3-a]嘧啶作为Hedgehog抑制剂及其应用
|
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
(en)
|
2011-06-24 |
2012-12-27 |
Pharminox Limited |
Fused pentacyclic anti - proliferative compounds
|
BR112014000314A2
(pt)
|
2011-07-08 |
2017-01-10 |
Novartis Ag |
derivados de pirrolo pirimidina
|
WO2013033901A1
(en)
|
2011-09-08 |
2013-03-14 |
Merck Sharp & Dohme Corp. |
Heterocyclic-substituted benzofuran derivatives and methods of use thereof for the treatment of viral diseases
|
WO2013040528A1
(en)
|
2011-09-16 |
2013-03-21 |
Microbiotix, Inc. |
Antimicrobial compounds
|
US9351973B2
(en)
|
2011-09-22 |
2016-05-31 |
Merck Sharp & Dohme Corp. |
Pyrazolopyridyl compounds as aldosterone synthase inhibitors
|
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
|
CA2852939A1
(en)
|
2011-10-20 |
2013-04-25 |
Glaxosmithkline Llc |
Substituted bicyclic aza-heterocycles and analogues as sirtuin modulators
|
EA201490807A1
(ru)
|
2011-10-21 |
2014-07-30 |
Торрент Фармасьютикалз Лимитед |
Новые замещенные имидазопиримидины как модуляторы рецептора gpbar1
|
WO2013120040A1
(en)
|
2012-02-10 |
2013-08-15 |
Children's Medical Center Corporation |
Targeted pathway inhibition to improve muscle structure, function and activity in muscular dystrophy
|
US9034882B2
(en)
|
2012-03-05 |
2015-05-19 |
Bristol-Myers Squibb Company |
Inhibitors of human immunodeficiency virus replication
|
WO2013133367A1
(ja)
|
2012-03-09 |
2013-09-12 |
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
(en)
|
2012-04-20 |
2013-10-24 |
Advinus Therapeutics Limited |
Bicyclic compounds, compositions and medicinal applications thereof
|
UY34750A
(es)
|
2012-04-20 |
2013-11-29 |
Gilead Sciences Inc |
?compuestos para el tratamiento del hiv, composiciones,métodos de preparación, intermediarios y métodos terapéuticos?.
|
WO2013163404A1
(en)
|
2012-04-27 |
2013-10-31 |
The Uab Research Foundation |
TREATING VIRAL INFECTIONS HAVING VIRAL RNAs TRANSLATED BY A NON-IRES MEDIATED MECHANISM
|
CN104379567A
(zh)
|
2012-06-18 |
2015-02-25 |
住友化学株式会社 |
稠合杂环化合物
|
US9630976B2
(en)
|
2012-07-03 |
2017-04-25 |
Ono Pharmaceutical Co., Ltd. |
Compound having agonistic activity on somatostatin receptor, and use thereof for medical purposes
|
GB201212513D0
(en)
|
2012-07-13 |
2012-08-29 |
Ucb Pharma Sa |
Therapeutic agents
|
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
|
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
|
WO2014039595A1
(en)
|
2012-09-06 |
2014-03-13 |
Bristol-Myers Squibb Company |
Imidazopyridazine jak3 inhibitors and their use for the treatment of inflammatory and autoimmune diseases
|
PL2900657T3
(pl)
|
2012-09-26 |
2020-07-27 |
F.Hoffmann-La Roche Ag |
Cykliczne związki eterowe pirazol-4-ilo-heterocyklilo-karboksyamidu i sposoby stosowania
|
WO2014061693A1
(ja)
|
2012-10-17 |
2014-04-24 |
塩野義製薬株式会社 |
新規非芳香族炭素環又は非芳香族複素環誘導体
|
EP2922548A4
(en)
|
2012-11-21 |
2016-06-01 |
Stategics Inc |
SUBSTITUTED TRIAZOLO-PYRIMIDINE COMPOUNDS FOR MODULATING CELL PROPOLATION, DIFFERENTIATION AND OVER LIVING
|
JP6037804B2
(ja)
|
2012-12-03 |
2016-12-07 |
富士フイルム株式会社 |
ガス分離膜
|
WO2014113388A1
(en)
|
2013-01-15 |
2014-07-24 |
Incyte Corporation |
Thiazolecarboxamides and pyridinecarboxamide compounds useful as pim kinase inhibitors
|
WO2014114532A1
(en)
|
2013-01-22 |
2014-07-31 |
F. Hoffmann-La Roche Ag |
Fluoro-[1,3]oxazines as bace1 inhibitors
|
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
(en)
|
2013-01-31 |
2014-08-07 |
Thomas Jefferson University |
Pd-l1 and pd-l2-based fusion proteins and uses thereof
|
BR112015020302B1
(pt)
|
2013-02-27 |
2023-04-18 |
Mochida Pharmaceutical Co., Ltd |
Derivado de pirazol, composição farmacêutica e composto intermediário
|
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
|
SG11201507395PA
(en)
|
2013-03-14 |
2015-10-29 |
Curadev Pharma Private Ltd |
Inhibitors of the kynurenine pathway
|
US9527842B2
(en)
|
2013-03-14 |
2016-12-27 |
VIIV Healthcare UK (No.5) Limited |
Inhibitors of human immunodeficiency virus replication
|
ES2705247T3
(es)
|
2013-03-14 |
2019-03-22 |
Univ Columbia |
4-fenilpiperidinas, su preparación y uso
|
RU2690489C2
(ru)
|
2013-03-14 |
2019-06-04 |
Селтакссис, Инк. |
Ингибиторы лейкотриен а4-гидролазы
|
WO2014181287A1
(en)
|
2013-05-09 |
2014-11-13 |
Piramal Enterprises Limited |
Heterocyclyl compounds and uses thereof
|
HUE040645T2
(hu)
|
2013-06-26 |
2019-03-28 |
Abbvie Inc |
BTK-inhibitor primer karboxamidok
|
ES2807599T3
(es)
|
2013-07-02 |
2021-02-23 |
Syngenta Participations Ag |
Heterociclos bi- o tricíclicos activos como plaguicidas con sustituyentes que contienen azufre
|
MY184572A
(en)
|
2013-07-17 |
2021-04-05 |
Otsuka Pharma Co Ltd |
Cyanotriazole compounds
|
AU2014292888B2
(en)
|
2013-07-25 |
2018-03-22 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of transcription factors and uses thereof
|
EP2835375A1
(en)
|
2013-08-09 |
2015-02-11 |
Fundació Institut Català d'Investigació Química |
Bis-salphen compounds and carbonaceous material composites comprising them
|
KR101715090B1
(ko)
|
2013-08-28 |
2017-03-13 |
한국화학연구원 |
신규한 화합물 또는 이의 약학적으로 허용가능한 염, 및 이를 유효성분으로 함유하는 인플루엔자 바이러스 감염으로 인한 질환의 예방 또는 치료용 약학적 조성물
|
SG11201601225RA
(en)
|
2013-09-04 |
2016-03-30 |
Bristol Myers Squibb Co |
Compounds useful as immunomodulators
|
KR102362277B1
(ko)
|
2013-09-06 |
2022-02-11 |
오리진 디스커버리 테크놀로지스 리미티드 |
면역조절제로서 1,2,4-옥사디아졸 유도체
|
PT3041828T
(pt)
|
2013-09-06 |
2018-10-09 |
Aurigene Discovery Tech Ltd |
Derivados 1,3,4-0xadiazoles como imonomoduladores
|
WO2015036927A1
(en)
|
2013-09-10 |
2015-03-19 |
Aurigene Discovery Technologies Limited |
Immunomodulating peptidomimetic derivatives
|
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
|
WO2015095337A2
(en)
|
2013-12-18 |
2015-06-25 |
The Rockefeller University |
PYRAZOLO[1,5-a]PYRIMIDINECARBOXAMIDE DERIVATIVES FOR TREATING COGNITIVE IMPAIRMENT
|
CA2935646A1
(en)
|
2014-01-03 |
2015-07-09 |
Bayer Animal Health Gmbh |
Novel pyrazolyl-heteroarylamides as pesticides
|
AU2015213735A1
(en)
|
2014-02-10 |
2016-08-04 |
Merck Sharp & Dohme Corp. |
Antibodies that bind to human Tau and assay for quantifying human Tau using the antibodies
|
MX2016011035A
(es)
|
2014-02-25 |
2017-03-09 |
Achillion Pharmaceuticals Inc |
Compuestos arilo, heteroarilo y heterociclicos para el tratamiento de trastornos mediados por complemento.
|
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
|
CR20160514A
(es)
|
2014-04-04 |
2017-07-26 |
Iomet Pharma Ltd |
Derivados de indol para uso en medicina
|
US9850225B2
(en)
|
2014-04-14 |
2017-12-26 |
Bristol-Myers Squibb Company |
Compounds useful as immunomodulators
|
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
|
JP2017530959A
(ja)
|
2014-09-17 |
2017-10-19 |
エピザイム,インコーポレイティド |
Carm1阻害剤およびその使用
|
NZ729603A
(en)
|
2014-10-06 |
2022-02-25 |
Merck Patent Gmbh |
Heteroaryl compounds as btk inhibitors and uses thereof
|
US10017520B2
(en)
|
2014-12-10 |
2018-07-10 |
Massachusetts Institute Of Technology |
Myc modulators and uses thereof
|
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
(en)
|
2015-04-02 |
2016-10-06 |
Bayer Cropscience Aktiengesellschaft |
Novel triazole compounds for controlling phytopathogenic harmful fungi
|
WO2017035405A1
(en)
|
2015-08-26 |
2017-03-02 |
Achillion Pharmaceuticals, Inc. |
Amino compounds for treatment of immune and inflammatory disorders
|
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
|
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
|
EA201891203A1
(ru)
*
|
2015-11-19 |
2018-12-28 |
Инсайт Корпорейшн |
Гетероциклические соединения в качестве иммуномодуляторов
|
US20170174671A1
(en)
|
2015-12-17 |
2017-06-22 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
BR112018012756A2
(pt)
|
2015-12-22 |
2018-12-04 |
Incyte Corp |
compostos heterocíclicos como imunomoduladores
|
WO2017107052A1
(en)
|
2015-12-22 |
2017-06-29 |
Merck Sharp & Dohme Corp. |
Soluble guanylate cyclase stimulators
|
WO2017109041A1
(en)
|
2015-12-22 |
2017-06-29 |
Synthon B.V. |
Pharmaceutical composition comprising amorphous lenalidomide and an antioxidant
|
CA3006911A1
(en)
|
2015-12-22 |
2017-06-29 |
Syngenta Participations Ag |
Pesticidally active pyrazole derivatives
|
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
|
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
|
TW201808950A
(zh)
|
2016-05-06 |
2018-03-16 |
英塞特公司 |
作為免疫調節劑之雜環化合物
|
US20170342060A1
(en)
|
2016-05-26 |
2017-11-30 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
AU2017280958A1
(en)
|
2016-06-20 |
2018-12-20 |
Ambrx, Inc. |
Pegylated porcine interferon and methods of use thereof
|
RS63673B1
(sr)
*
|
2016-06-20 |
2022-11-30 |
Incyte Corp |
Heterociklična jedinjenja kao imunomodulatori
|
JP7042812B2
(ja)
|
2016-06-20 |
2022-03-28 |
ノバルティス アーゲー |
トリアゾロピリミジン化合物の結晶形態
|
ES2870920T3
(es)
|
2016-06-21 |
2021-10-28 |
X4 Pharmaceuticals Inc |
Inhibidores de CXCR4 y usos de los mismos
|
ES2930092T3
(es)
|
2016-07-14 |
2022-12-07 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
JP2019530732A
(ja)
|
2016-08-03 |
2019-10-24 |
アライジング・インターナショナル・インコーポレイテッドArising International, Inc. |
免疫モジュレータとして有用な対称または半対称化合物
|
MA46045A
(fr)
|
2016-08-29 |
2021-04-28 |
Incyte Corp |
Composés hétérocycliques utilisés comme immunomodulateurs
|
EP3506908A1
(en)
|
2016-08-30 |
2019-07-10 |
Tetraphase Pharmaceuticals, Inc. |
Tetracycline compounds and methods of treatment
|
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
|
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
|
TWI798192B
(zh)
|
2016-12-22 |
2023-04-11 |
美商英塞特公司 |
免疫調節劑化合物及使用方法
|
ES2918974T3
(es)
|
2016-12-22 |
2022-07-21 |
Incyte Corp |
Compuestos heteroaromaticos biciclicos como inmunomoduladores
|
US20180179201A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
US20180177784A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
MY197635A
(en)
*
|
2016-12-22 |
2023-06-29 |
Incyte Corp |
Benzooxazole derivatives as immunomodulators
|
US20180179179A1
(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
|
AU2018306619B2
(en)
|
2017-07-28 |
2022-06-02 |
Chemocentryx, Inc. |
Immunomodulator compounds
|
WO2019032547A1
(en)
|
2017-08-08 |
2019-02-14 |
Chemocentryx, Inc. |
MACROCYCLIC IMMUNOMODULATORS
|
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
|
RS64055B1
(sr)
|
2018-03-30 |
2023-04-28 |
Incyte Corp |
Heterociklična jedinjenja kao imunomodulatori
|
CN111936475B
(zh)
|
2018-04-03 |
2024-05-10 |
贝达药业股份有限公司 |
免疫调节剂及其组合物和制备方法
|
TWI712412B
(zh)
|
2018-04-19 |
2020-12-11 |
美商基利科學股份有限公司 |
Pd‐1/pd‐l1抑制劑
|
WO2019217821A1
(en)
|
2018-05-11 |
2019-11-14 |
Incyte Corporation |
Tetrahydro-imidazo[4,5-c]pyridine derivatives as pd-l1 immunomodulators
|
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
|
TW202115059A
(zh)
|
2019-08-09 |
2021-04-16 |
美商英塞特公司 |
Pd—1/pd—l1抑制劑之鹽
|
PE20221038A1
(es)
|
2019-09-30 |
2022-06-17 |
Incyte Corp |
Compuestos de pirido[3,2-d] pirimidina como inmunomoduladores
|
WO2023049831A1
(en)
*
|
2021-09-24 |
2023-03-30 |
Incyte Corporation |
Treatment of human papillomavirus-associated cancers by pd-l1 inhibitors
|