DE280853C
(hu)
|
|
|
|
|
US850370A
(en)
|
1906-06-05 |
1907-04-16 |
William L Hynes |
Water-automobile.
|
DE2156720A1
(de)
|
1971-11-16 |
1973-05-24 |
Bayer Ag |
Pyrimido eckige klammer auf 4,5-d eckige klammer zu pyrimidine
|
US3984021A
(en)
|
1972-09-11 |
1976-10-05 |
Uhlig Gerhardt E |
Safety closure container
|
US3894021A
(en)
|
1974-01-28 |
1975-07-08 |
Squibb & Sons Inc |
Derivatives of 1,7-dihydro-2H-pyrazolo{8 4{40 ,3{40 :5,6{9 pyrido{8 4,3-D{9 pyrimidine-2,4-(3H)-diones
|
JPS5120580B2
(hu)
|
1974-06-19 |
1976-06-25 |
|
|
US4347348A
(en)
|
1978-06-05 |
1982-08-31 |
Chernikhov Alexei Y |
Heat-resistant heterocyclic polymers and methods for producing same
|
FR2428654A1
(fr)
|
1978-06-13 |
1980-01-11 |
Chernikhov Alexei |
Polymeres heterocycliques thermostables et leurs procedes de preparation
|
CH635828A5
(de)
|
1978-08-30 |
1983-04-29 |
Ciba Geigy Ag |
N-substituierte imide und bisimide.
|
CH641470A5
(de)
|
1978-08-30 |
1984-02-29 |
Ciba Geigy Ag |
Imidgruppen enthaltende silane.
|
US4339267A
(en)
|
1980-01-18 |
1982-07-13 |
E. I. Du Pont De Nemours And Company |
Herbicidal sulfonamides
|
US4405519A
(en)
|
1980-10-22 |
1983-09-20 |
Plastics Engineering Company |
Di-Acetylene-terminated polyimide derivatives
|
US4402878A
(en)
|
1980-10-22 |
1983-09-06 |
Plastics Engineering Company |
Addition products of di-acetylene-terminated polyimide derivatives with a polyimide having terminal non-conjugated acetylene groups
|
US4405786A
(en)
|
1980-10-22 |
1983-09-20 |
Plastics Engineering Company |
Addition products of di-acetylene-terminated polyimide derivatives and an dienophile having ethylene groups
|
US4405520A
(en)
|
1980-10-22 |
1983-09-20 |
Plastics Engineering Company |
Addition products of di-acetylene-terminated polymide derivatives and dienophiles having terminal maleimide grops
|
US4460773A
(en)
|
1982-02-05 |
1984-07-17 |
Lion Corporation |
1-Phenyl-1H-pyrazolo [3,4-b]pyrazine derivatives and process for preparing same
|
DE3432983A1
(de)
|
1983-09-07 |
1985-04-18 |
Lion Corp., Tokio/Tokyo |
1,5-disubstituierte 1h-pyrazolo(3,4-b)-pyrazin-derivate und antitumormittel, die diese enthalten
|
JPS62273979A
(ja)
|
1986-05-21 |
1987-11-28 |
Lion Corp |
1,5−置換−1H−ピラゾロ〔3,4−b〕ピラジン誘導体及び該化合物を含有する抗腫瘍剤
|
JPS6310630A
(ja)
|
1986-06-23 |
1988-01-18 |
Teijin Ltd |
芳香族ポリアミドイミドエ−テルの製造法
|
JPS6317882A
(ja)
|
1986-07-09 |
1988-01-25 |
Lion Corp |
5−置換−1H−ピラゾロ〔3,4−b〕ピラジン誘導体及び該化合物を含有する抗腫瘍剤
|
US4859672A
(en)
|
1986-10-29 |
1989-08-22 |
Rorer Pharmaceutical Corporation |
Pyrido[2,3-d]pyrimidinone and imidazo[4,5-b]pyrimidinone
|
US4874803A
(en)
|
1987-09-21 |
1989-10-17 |
Pennwalt Corporation |
Dianhydride coupled polymer stabilizers
|
DE3814549A1
(de)
|
1987-10-30 |
1989-05-18 |
Bayer Ag |
N-substituierte derivate von 1-desoxynojirimycin und 1-desoxymannonojirimycin, verfahren zu deren herstellung und deren verwendung in arzneimitteln
|
JPH029895A
(ja)
|
1988-06-28 |
1990-01-12 |
Lion Corp |
ヌクレオシド類似化合物及び抗腫瘍剤
|
DD280853A1
(de)
|
1989-03-21 |
1990-07-18 |
Akad Nauk Sssr |
Bindemittel fuer elektroden, vorzugsweise fuer polymerelektroden
|
US5159054A
(en)
|
1989-05-16 |
1992-10-27 |
The United States Of America As Represented By The Secretary Of The Navy |
Synthesis of phthalonitrile resins containing ether and imide linkages
|
JP2845957B2
(ja)
|
1989-07-17 |
1999-01-13 |
三井化学株式会社 |
イミド環を有する新規ジフェノール類およびその製造方法
|
US5726302A
(en)
|
1989-09-15 |
1998-03-10 |
Gensia Inc. |
Water soluble adenosine kinase inhibitors
|
DE3937633A1
(de)
|
1989-11-11 |
1991-05-16 |
Bayer Ag |
Heterocyclische verbindungen und deren verwendung als pigmente und farbstoffe
|
US5329046A
(en)
|
1989-12-28 |
1994-07-12 |
Hoechst Aktiengesellschaft |
Biscationic acid amide and imide derivatives and processes for their preparation
|
CA2072560A1
(en)
|
1989-12-28 |
1991-06-29 |
Hans-Tobias Macholdt |
Biscationic acid amide and acid imide derivatives as charge controllers
|
JP2883670B2
(ja)
|
1990-03-23 |
1999-04-19 |
三井化学株式会社 |
イミド環を有する新規ビスフェノール類およびその製造方法
|
GB9113137D0
(en)
|
1990-07-13 |
1991-08-07 |
Ici Plc |
Thioxo heterocycles
|
NZ240089A
(en)
|
1990-10-03 |
1993-04-28 |
Commw Scient Ind Res Org |
Diaminobisimide compounds and compositions comprising such compounds for curing epoxy resins
|
JPH04158084A
(ja)
|
1990-10-22 |
1992-06-01 |
Fuji Photo Film Co Ltd |
記録材料
|
JPH04179576A
(ja)
|
1990-11-14 |
1992-06-26 |
Fuji Photo Film Co Ltd |
記録材料
|
JPH04328121A
(ja)
|
1991-04-26 |
1992-11-17 |
Sumitomo Bakelite Co Ltd |
半導体封止用エポキシ樹脂組成物
|
KR100207360B1
(ko)
|
1991-06-14 |
1999-07-15 |
돈 더블유. 슈미츠 |
이미다조[1,5,-a]퀸옥살린
|
DE4119767A1
(de)
|
1991-06-15 |
1992-12-17 |
Dresden Arzneimittel |
Verfahren zur herstellung von (pyrimid-2-yl-thio- bzw. seleno)-essigsaeurederivaten
|
US5521184A
(en)
|
1992-04-03 |
1996-05-28 |
Ciba-Geigy Corporation |
Pyrimidine derivatives and processes for the preparation thereof
|
JP3279635B2
(ja)
|
1992-05-18 |
2002-04-30 |
鐘淵化学工業株式会社 |
ヒドロシリル基含有イミド化合物
|
JP3232123B2
(ja)
|
1992-05-20 |
2001-11-26 |
鐘淵化学工業株式会社 |
硬化性組成物
|
WO1993024488A1
(en)
|
1992-05-28 |
1993-12-09 |
Commonwealth Scientific And Industrial Research Organisation |
Bismaleimide compounds
|
JPH08504196A
(ja)
|
1992-12-07 |
1996-05-07 |
コモンウェルス・サイエンティフィック・アンド・インダストリアル・リサーチ・オーガニゼイション |
ビスナドイミド
|
EP0678106A4
(en)
|
1993-01-11 |
1995-12-27 |
Univ Pennsylvania |
POLYCYCLIC AROMATIC COMPOUNDS WITH NON-LINEAR OPTICAL PROPERTIES.
|
WO1994025438A1
(en)
|
1993-04-28 |
1994-11-10 |
The Du Pont Merck Pharmaceutical Company |
Novel trisubstituted aromatic amines useful for the treatment of cognitive deficits
|
US5536725A
(en)
|
1993-08-25 |
1996-07-16 |
Fmc Corporation |
Insecticidal substituted-2,4-diamino-5,6,7,8-tetrahydroquinazolines
|
CA2276946A1
(en)
|
1993-11-30 |
1995-06-08 |
G.D. Searle & Co. |
Substituted pyrazolyl benzenesulfonamides and pharmaceutical compositions containing the same
|
EP0746320B1
(en)
|
1994-02-02 |
2001-01-31 |
Eli Lilly And Company |
Hiv protease inhibitors and intermediates
|
US5480887A
(en)
|
1994-02-02 |
1996-01-02 |
Eli Lilly And Company |
Protease inhibitors
|
MX9702245A
(es)
|
1994-11-14 |
1997-06-28 |
Warner Lambert Co |
Seis-aril-pirido(2,3-d)pirimidinas y naftiridinas para inhibir la proliferacion celular mediada por la proteina cinasa tirosina.
|
US7067664B1
(en)
|
1995-06-06 |
2006-06-27 |
Pfizer Inc. |
Corticotropin releasing factor antagonists
|
US5783577A
(en)
|
1995-09-15 |
1998-07-21 |
Trega Biosciences, Inc. |
Synthesis of quinazolinone libraries and derivatives thereof
|
JPH09188812A
(ja)
|
1996-01-11 |
1997-07-22 |
Mitsui Toatsu Chem Inc |
結晶化促進剤
|
AU2980797A
(en)
|
1996-06-11 |
1998-01-07 |
Yoshitomi Pharmaceutical Industries, Ltd. |
Fused heterocyclic compounds and medicinal uses thereof
|
TR199900228T2
(xx)
|
1996-08-06 |
1999-03-22 |
Pfizer Inc. |
�kameli/katk�l� pirido-veya pirimido-i�eren 6,6-veya 6,7-bisiklik t�revler.
|
WO1998006703A1
(en)
|
1996-08-14 |
1998-02-19 |
Warner-Lambert Company |
2-phenyl benzimidazole derivatives as mcp-1 antagonists
|
JP3669783B2
(ja)
|
1996-08-21 |
2005-07-13 |
三井化学株式会社 |
有機電界発光素子
|
US5994364A
(en)
|
1996-09-13 |
1999-11-30 |
Schering Corporation |
Tricyclic antitumor farnesyl protein transferase inhibitors
|
AU6908398A
(en)
|
1996-10-28 |
1998-05-22 |
Versicor Inc |
Fused 2,4-pyrimidinedione combinatorial libraries and biologically active fused 2,4-pyramidinediones
|
JP2001507349A
(ja)
|
1996-12-23 |
2001-06-05 |
セルテック セラピューティックス リミテッド |
縮合多環式2−アミノピリミジン誘導体、それらの製造およびたんぱく質チロシンキナーゼ抑制因子としてのそれらの使用
|
AU749750B2
(en)
|
1997-02-05 |
2002-07-04 |
Warner-Lambert Company |
Pyrido {2,3-d} pyrimidines and 4-aminopyrimidines as inhibitors of cellular proliferation
|
JP2001521523A
(ja)
|
1997-04-11 |
2001-11-06 |
アボツト・ラボラトリーズ |
化学的シナプス伝達の制御において有用なフロピリジン、チエノピリジン、ピロロピリジンおよび関連するピリミジン、ピリダジンおよびトリアジン化合物
|
AU751188C
(en)
|
1997-05-28 |
2005-06-30 |
Aventis Pharmaceuticals Inc. |
Quinoline and quinoxaline compounds which inhibit platelet-derived growth factor and/or p56lck tyrosine kinases
|
GB9716231D0
(en)
|
1997-07-31 |
1997-10-08 |
Amersham Int Ltd |
Base analogues
|
JP2001512742A
(ja)
|
1997-08-11 |
2001-08-28 |
シーオーアール セラピューティクス インコーポレイテッド |
選択的Xa因子阻害剤
|
WO1999009030A1
(en)
|
1997-08-20 |
1999-02-25 |
Warner-Lambert Company |
Naphthyridinones for inhibiting protein tyrosine kinase and cell cycle kinase mediated cellular proliferation
|
US6465484B1
(en)
|
1997-09-26 |
2002-10-15 |
Merck & Co., Inc. |
Angiogenesis inhibitors
|
JPH11171865A
(ja)
|
1997-12-04 |
1999-06-29 |
Yoshitomi Pharmaceut Ind Ltd |
縮合ヘテロ環化合物
|
KR20010041109A
(ko)
|
1998-02-20 |
2001-05-15 |
다케다 야쿠힌 고교 가부시키가이샤 |
아미노구아니딘 히드라존 유도체, 이의 제조방법 및 이의약제
|
EP1077946A1
(en)
|
1998-05-15 |
2001-02-28 |
Guilford Pharmaceuticals Inc. |
Fused tricyclic compounds which inhibit parp activity
|
US20040044012A1
(en)
|
1998-05-26 |
2004-03-04 |
Dobrusin Ellen Myra |
Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation
|
EP1080092B1
(en)
|
1998-05-26 |
2008-07-23 |
Warner-Lambert Company LLC |
Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation
|
WO1999064400A1
(en)
|
1998-06-12 |
1999-12-16 |
Vertex Pharmaceuticals Incorporated |
INHIBITORS OF p38
|
JP4516690B2
(ja)
|
1998-08-11 |
2010-08-04 |
ノバルティス アーゲー |
血管形成阻害活性を有するイソキノリン誘導体
|
JP2000123973A
(ja)
|
1998-10-09 |
2000-04-28 |
Canon Inc |
有機発光素子
|
AU769989B2
(en)
|
1998-10-23 |
2004-02-12 |
F. Hoffmann-La Roche Ag |
Bicyclic nitrogen heterocycles
|
GB9823103D0
(en)
|
1998-10-23 |
1998-12-16 |
Pfizer Ltd |
Pharmaceutically active compounds
|
US6133031A
(en)
|
1999-08-19 |
2000-10-17 |
Isis Pharmaceuticals Inc. |
Antisense inhibition of focal adhesion kinase expression
|
GB9905075D0
(en)
|
1999-03-06 |
1999-04-28 |
Zeneca Ltd |
Chemical compounds
|
DE19912638A1
(de)
|
1999-03-20 |
2000-09-21 |
Bayer Ag |
Naphthylcarbonsäureamid-substituierte Sulfonamide
|
DE19920790A1
(de)
|
1999-05-06 |
2000-11-09 |
Bayer Ag |
Bis-Sulfonamide mit anti-HCMV-Wirkung
|
PE20010306A1
(es)
|
1999-07-02 |
2001-03-29 |
Agouron Pharma |
Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa
|
JP4041624B2
(ja)
|
1999-07-21 |
2008-01-30 |
三井化学株式会社 |
有機電界発光素子
|
PL207590B1
(pl)
|
1999-09-24 |
2011-01-31 |
Janssen Pharmaceutica Nv |
Cząstka stanowiąca dyspersję stałą oraz postać dawkowania, sposób ich otrzymywania i zastosowanie
|
DE19946289A1
(de)
|
1999-09-28 |
2001-03-29 |
Basf Ag |
Benzodiazepin-Derivate, deren Herstellung und Anwendung
|
ATE349447T1
(de)
|
1999-10-21 |
2007-01-15 |
Hoffmann La Roche |
Alkylamino-substituierte bicyclische heterocyclen als p38 protein kinase inhibitoren
|
RU2265606C2
(ru)
|
1999-10-21 |
2005-12-10 |
Ф.Хоффманн-Ля Рош Аг |
ГЕТЕРОАЛКИЛАМИНОЗАМЕЩЕННЫЕ БИЦИКЛИЧЕСКИЕ АЗОТСОДЕРЖАЩИЕ ГЕТЕРОЦИКЛЫ В КАЧЕСТВЕ ИНГИБИТОРОВ ПРОТЕИНКИНАЗЫ р38
|
TWI271406B
(en)
|
1999-12-13 |
2007-01-21 |
Eisai Co Ltd |
Tricyclic condensed heterocyclic compounds, preparation method of the same and pharmaceuticals comprising the same
|
EP1242382B1
(en)
|
1999-12-29 |
2007-02-07 |
Wyeth |
Tricyclic protein kinase inhibitors
|
OA12316A
(en)
|
2000-01-24 |
2006-05-15 |
Warner Lambert Co |
3-Aminoquinazolin-2,4-dione antibacterial agents.
|
CN1433417A
(zh)
|
2000-01-27 |
2003-07-30 |
沃尼尔·朗伯公司 |
用于治疗神经变性疾病的吡啶并嘧啶酮衍生物
|
ATE372337T1
(de)
|
2000-02-01 |
2007-09-15 |
Abbott Gmbh & Co Kg |
Heterozyklische verbindungen und deren anwendung als parp-inhibitoren
|
WO2001057037A1
(en)
|
2000-02-04 |
2001-08-09 |
Cor Therapeutics, Inc. |
Platelet adp receptor inhibitors
|
ES2241781T3
(es)
|
2000-02-09 |
2005-11-01 |
Novartis Ag |
Derivados de piridina inhibidores de la angiogenesis y/o del receptor tirosina quinasa de vegf.
|
GB0004890D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
US7498335B2
(en)
|
2000-03-06 |
2009-03-03 |
Astrazeneca Ab |
Method of producing an antiangiogenic or vascular permeability reducing effect
|
DE10012549A1
(de)
|
2000-03-15 |
2001-09-20 |
Bayer Ag |
Arzneimittel gegen virale Erkrankungen
|
JP2001265031A
(ja)
|
2000-03-15 |
2001-09-28 |
Fuji Xerox Co Ltd |
電子写真感光体、プロセスカートリッジ、及び、電子写真装置
|
KR100901221B1
(ko)
|
2000-04-28 |
2009-06-08 |
아카디아 파마슈티칼스 인코포레이티드 |
무스카린성 작용제
|
CA2408156A1
(en)
|
2000-05-05 |
2001-11-15 |
Millennium Pharmaceuticals, Inc. |
Heterobicyclic sulfonamides and their use as platelet adp receptor inhibitors
|
AU2001268712A1
(en)
|
2000-06-23 |
2002-01-08 |
Bristol-Myers Squibb Company |
1 - (heteroaryl-phenyl) - condensed pyrazol derivatives as factor Xa inhibitors
|
PL202623B1
(pl)
|
2000-06-28 |
2009-07-31 |
Smithkline Beecham Plc |
Sposób wytwarzania drobno zmielonego preparatu substancji leczniczej, drobno zmielona substancja lecznicza wytworzona tym sposobem i zawierająca ją kompozycja farmaceutyczna
|
US20050009876A1
(en)
|
2000-07-31 |
2005-01-13 |
Bhagwat Shripad S. |
Indazole compounds, compositions thereof and methods of treatment therewith
|
AU2001285401A1
(en)
|
2000-08-07 |
2002-02-18 |
Neurogen Corporation |
Heterocyclic compounds as ligands of the GABAa receptor
|
ATE320427T1
(de)
|
2000-08-14 |
2006-04-15 |
Ortho Mcneil Pharm Inc |
Substituierte pyrazole
|
MXPA03001963A
(es)
|
2000-09-06 |
2004-03-18 |
Johnson & Johnson |
Un metodo para tratar alergias usando pirazoles sustituidos.
|
GB0025782D0
(en)
|
2000-10-20 |
2000-12-06 |
Pfizer Ltd |
Use of inhibitors
|
EP1217000A1
(en)
|
2000-12-23 |
2002-06-26 |
Aventis Pharma Deutschland GmbH |
Inhibitors of factor Xa and factor VIIa
|
GB0100621D0
(en)
|
2001-01-10 |
2001-02-21 |
Vernalis Res Ltd |
Chemical compounds VI
|
GB0103926D0
(en)
|
2001-02-17 |
2001-04-04 |
Astrazeneca Ab |
Chemical compounds
|
AP1699A
(en)
|
2001-03-21 |
2006-12-26 |
Warner Lambert Co |
New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors
|
US6998408B2
(en)
|
2001-03-23 |
2006-02-14 |
Bristol-Myers Squibb Pharma Company |
6-5, 6-6, or 6-7 Heterobicycles as factor Xa inhibitors
|
JP2002296731A
(ja)
|
2001-03-30 |
2002-10-09 |
Fuji Photo Film Co Ltd |
熱現像カラー画像記録材料
|
ATE449763T1
(de)
|
2001-04-16 |
2009-12-15 |
Eisai R&D Man Co Ltd |
1h-indazolverbindungen die jnk hemmen
|
JP4310109B2
(ja)
|
2001-04-26 |
2009-08-05 |
エーザイ・アール・アンド・ディー・マネジメント株式会社 |
ピラゾリル基を置換基として有する含窒素縮合環化合物およびその医薬組成物
|
US7279474B2
(en)
|
2001-04-30 |
2007-10-09 |
Glaxo Group Limited |
Substituted pyrrolo[2,3-d]pyrimidines as antagonists of the corticotropin releasing factor (CRF)
|
WO2002094825A1
(fr)
|
2001-05-22 |
2002-11-28 |
Banyu Pharmaceutical Co., Ltd. |
Nouveau derive de spiropiperidine
|
US20030114448A1
(en)
|
2001-05-31 |
2003-06-19 |
Millennium Pharmaceuticals, Inc. |
Inhibitors of factor Xa
|
MXPA03009894A
(es)
|
2001-06-19 |
2004-02-17 |
Warner Lambert Co |
Agentes antibacterianos.
|
GB0115109D0
(en)
|
2001-06-21 |
2001-08-15 |
Aventis Pharma Ltd |
Chemical compounds
|
US20030114467A1
(en)
|
2001-06-21 |
2003-06-19 |
Shakespeare William C. |
Novel pyrazolo- and pyrrolo-pyrimidines and uses thereof
|
WO2003000690A1
(en)
|
2001-06-25 |
2003-01-03 |
Aventis Pharmaceuticals Inc. |
Synthesis of heterocyclic compounds employing microwave technology
|
US20040235867A1
(en)
|
2001-07-24 |
2004-11-25 |
Bilodeau Mark T. |
Tyrosine kinase inhibitors
|
US7205417B2
(en)
|
2001-08-07 |
2007-04-17 |
Banyu Pharmaceutical Co., Ltd. |
Spiro compounds
|
DE60230890D1
(de)
|
2001-09-19 |
2009-03-05 |
Aventis Pharma Sa |
Indolizine als kinaseproteinhemmer
|
DE60213842T2
(de)
|
2001-10-30 |
2007-09-06 |
Novartis Ag |
Staurosporin-derivate als hemmer der flt3-rezeptor-tyrosinkinase-wirkung
|
US7514445B2
(en)
|
2001-11-01 |
2009-04-07 |
Janssen Pharmaceutica N.V. |
Heteroaryl amines as glycogen synthase kinase 3β inhibitors (GSK3 inhibitors)
|
CN1582284A
(zh)
|
2001-11-07 |
2005-02-16 |
霍夫曼-拉罗奇有限公司 |
氨基嘧啶类和吡啶类化合物
|
JP4488740B2
(ja)
|
2001-11-13 |
2010-06-23 |
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 |
免疫細胞活性化を調節する作用剤およびその使用方法
|
GB0129476D0
(en)
|
2001-12-10 |
2002-01-30 |
Syngenta Participations Ag |
Organic compounds
|
SI1470124T1
(sl)
|
2002-01-22 |
2006-04-30 |
Warner Lambert Co |
2-(piridin-2-ilamino)-pirido(2,3-d)pirimidin-7-oni
|
BRPI0308208B8
(pt)
|
2002-03-05 |
2021-05-25 |
Axys Pharm Inc |
compostos inibidores de catepsina cisteína protease e composições farmacêuticas compreendendo os mesmos
|
US6815519B2
(en)
|
2002-03-22 |
2004-11-09 |
Chung-Shan Institute Of Science & Technology |
Acidic fluorine-containing poly (siloxane amideimide) silica hybrids
|
RU2310657C2
(ru)
|
2002-04-03 |
2007-11-20 |
Ф.Хоффманн-Ля Рош Аг |
Имидазоконденсированные соединения и фармацевтическая композиция, содержащая их
|
CN100396670C
(zh)
|
2002-05-15 |
2008-06-25 |
詹森药业有限公司 |
作为pdfg受体抑制剂的n-取代的3-氨基苯并环戊二烯并吡唑及药用组合物和用途
|
JP4499342B2
(ja)
|
2002-05-16 |
2010-07-07 |
株式会社カネカ |
SiH基を含有する含窒素有機系化合物の製造方法
|
PT1551834E
(pt)
|
2002-05-23 |
2010-09-30 |
Novartis Vaccines & Diagnostic |
Compostos de quinazolinona substituídos
|
TW200406374A
(en)
|
2002-05-29 |
2004-05-01 |
Novartis Ag |
Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases
|
US7119111B2
(en)
|
2002-05-29 |
2006-10-10 |
Amgen, Inc. |
2-oxo-1,3,4-trihydroquinazolinyl derivatives and methods of use
|
US7105526B2
(en)
|
2002-06-28 |
2006-09-12 |
Banyu Pharmaceuticals Co., Ltd. |
Benzimidazole derivatives
|
GB0215676D0
(en)
|
2002-07-05 |
2002-08-14 |
Novartis Ag |
Organic compounds
|
PA8577501A1
(es)
|
2002-07-25 |
2004-02-07 |
Warner Lambert Co |
Inhibidores de quinasas
|
DE60330466D1
(de)
|
2002-07-29 |
2010-01-21 |
Rigel Pharmaceuticals Inc |
VERFAHREN ZUR BEHANDLUNG ODER PRuVENTION VON AUTOIMMUNKRANKHEITEN MIT 2,4-PYRIMIDINDIAMIN-VERBINDUNGEN
|
CN100432073C
(zh)
|
2002-08-06 |
2008-11-12 |
霍夫曼-拉罗奇有限公司 |
作为p-38map激酶抑制剂的6-烷氧基-吡啶并-嘧啶
|
EP1388541A1
(en)
|
2002-08-09 |
2004-02-11 |
Centre National De La Recherche Scientifique (Cnrs) |
Pyrrolopyrazines as kinase inhibitors
|
US7084270B2
(en)
|
2002-08-14 |
2006-08-01 |
Hoffman-La Roche Inc. |
Pyrimido compounds having antiproliferative activity
|
GB0220187D0
(en)
|
2002-08-30 |
2002-10-09 |
Novartis Ag |
Organic compounds
|
GB0223349D0
(en)
|
2002-10-08 |
2002-11-13 |
Merck Sharp & Dohme |
Therapeutic agents
|
TW200413381A
(en)
|
2002-11-04 |
2004-08-01 |
Hoffmann La Roche |
Novel amino-substituted dihydropyrimido [4,5-d]pyrimidinone derivatives, their manufacture and use as pharmaceutical agents
|
US7129351B2
(en)
|
2002-11-04 |
2006-10-31 |
Hoffmann-La Roche Inc. |
Pyrimido compounds having antiproliferative activity
|
WO2004043367A2
(en)
|
2002-11-06 |
2004-05-27 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds and use thereof
|
AR042052A1
(es)
|
2002-11-15 |
2005-06-08 |
Vertex Pharma |
Diaminotriazoles utiles como inhibidores de proteinquinasas
|
MXPA05005028A
(es)
|
2002-11-18 |
2005-08-03 |
Hoffmann La Roche |
Diazinopirimidinas.
|
MXPA05005547A
(es)
|
2002-11-28 |
2005-07-26 |
Schering Ag |
Pirimidinas inhibidoras de chk, pdk y akt, su produccion y uso como agentes farmaceuticos.
|
AU2003298034B2
(en)
|
2002-12-06 |
2011-04-21 |
Purdue Research Foundation |
Pyridines for treating injured mammalian nerve tissue
|
JP4666256B2
(ja)
|
2002-12-10 |
2011-04-06 |
小野薬品工業株式会社 |
含窒素複素環化合物およびその医薬用途
|
UA80171C2
(en)
|
2002-12-19 |
2007-08-27 |
Pfizer Prod Inc |
Pyrrolopyrimidine derivatives
|
UA80767C2
(en)
|
2002-12-20 |
2007-10-25 |
Pfizer Prod Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
US7098332B2
(en)
|
2002-12-20 |
2006-08-29 |
Hoffmann-La Roche Inc. |
5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones
|
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
|
JP2004203749A
(ja)
|
2002-12-24 |
2004-07-22 |
Kanegafuchi Chem Ind Co Ltd |
SiH基を含有する含窒素有機系化合物の製造方法
|
MXPA05007503A
(es)
|
2003-01-17 |
2005-09-21 |
Warner Lambert Co |
Heterociclicos 2-aminopiridina sustituidos como inhibidores de proliferacion celular.
|
GB0305929D0
(en)
|
2003-03-14 |
2003-04-23 |
Novartis Ag |
Organic compounds
|
US7135469B2
(en)
|
2003-03-18 |
2006-11-14 |
Bristol Myers Squibb, Co. |
Linear chain substituted monocyclic and bicyclic derivatives as factor Xa inhibitors
|
KR20050122220A
(ko)
|
2003-03-25 |
2005-12-28 |
다케다 샌디에고, 인코포레이티드 |
디펩티딜 펩티다제 억제제
|
GB0308208D0
(en)
|
2003-04-09 |
2003-05-14 |
Glaxo Group Ltd |
Chemical compounds
|
CN100497339C
(zh)
|
2003-04-10 |
2009-06-10 |
霍夫曼-拉罗奇有限公司 |
嘧啶并化合物
|
WO2004099209A1
(en)
|
2003-05-05 |
2004-11-18 |
F. Hoffmann-La-Roche Ag |
Fused pyrimidine derivatives with crf activity
|
JP2004346145A
(ja)
|
2003-05-21 |
2004-12-09 |
Teijin Ltd |
イミド組成物およびそれからなる樹脂組成物、及びその製造方法
|
WO2004112793A1
(en)
|
2003-05-23 |
2004-12-29 |
Chiron Corporation |
Guanidino-substituted quinazolinone compounds as mc4-r agonists
|
NZ543636A
(en)
|
2003-06-06 |
2009-07-31 |
Arexis Ab |
Use of fused heterocyclic compounds as SCCE inhibitors for the treatment of skin conditions or cancer
|
IL156495A0
(en)
|
2003-06-17 |
2004-01-04 |
Prochon Biotech Ltd |
Use of fgfr3 antagonists for treating t cell mediated diseases
|
JP4631703B2
(ja)
|
2003-06-18 |
2011-02-16 |
宇部興産株式会社 |
ピリミジン−4−オン化合物の製造方法
|
JP2005015395A
(ja)
|
2003-06-26 |
2005-01-20 |
Japan Science & Technology Agency |
新規ピリミドピリミジンヌクレオシドとその構造類縁体
|
NZ544472A
(en)
|
2003-07-03 |
2009-04-30 |
Myriad Genetics Inc |
Compounds and therapeutical use thereof
|
AR045037A1
(es)
|
2003-07-10 |
2005-10-12 |
Aventis Pharma Sa |
Tetrahidro-1h-pirazolo [3,4-c] piridinas sustituidas, composiciones que las contienen y su utilizacion.
|
AU2004260689B8
(en)
|
2003-07-29 |
2008-05-15 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
US7390820B2
(en)
|
2003-08-25 |
2008-06-24 |
Amgen Inc. |
Substituted quinolinone derivatives and methods of use
|
EP1675858A2
(en)
|
2003-09-03 |
2006-07-05 |
Neurogen Corporation |
5-aryl-pyrazolo [4,3-d] pyrimidines, pyridines, and pyrazines and related compounds
|
KR20060070572A
(ko)
|
2003-09-18 |
2006-06-23 |
콘포마 세러퓨틱스 코포레이션 |
Hsp90-저해제로서의 신규 헤테로시클릭 화합물
|
ATE433974T1
(de)
|
2003-09-19 |
2009-07-15 |
Gilead Sciences Inc |
Azachinolinolphosphonatverbindungen als integraseinhibitoren
|
AR045944A1
(es)
|
2003-09-24 |
2005-11-16 |
Novartis Ag |
Derivados de isoquinolina 1.4-disustituidas
|
EP1670761B1
(en)
|
2003-10-01 |
2009-01-28 |
Xention Limited |
Tetrahydro-naphthalene and urea derivatives
|
AU2004279427B2
(en)
*
|
2003-10-08 |
2008-07-03 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
US20090099165A1
(en)
|
2003-10-14 |
2009-04-16 |
Arizona Board Of Regents On Behalf Of The University Of Arizona |
Protein Kinase Inhibitors
|
CN1897950A
(zh)
|
2003-10-14 |
2007-01-17 |
惠氏公司 |
稠合芳基和杂芳基衍生物及其使用方法
|
CA2546192C
(en)
|
2003-11-17 |
2010-04-06 |
Pfizer Products Inc. |
Pyrrolopyrimidine compounds useful in treatment of cancer
|
WO2005056524A2
(en)
|
2003-12-09 |
2005-06-23 |
Euro-Celtique S.A. |
Therapeutic agents useful for treating pain
|
US20080188527A1
(en)
|
2003-12-23 |
2008-08-07 |
Cashman John R |
Synthetic Compounds and Derivatives as Modulators of Smoking or Nicotine Ingestion and Lung Cancer
|
KR100703068B1
(ko)
|
2003-12-30 |
2007-04-05 |
에스케이케미칼주식회사 |
피리딘 유도체와 이의 제조방법, 및 이를 포함하는약제조성물
|
US20050222171A1
(en)
|
2004-01-22 |
2005-10-06 |
Guido Bold |
Organic compounds
|
ATE444068T1
(de)
|
2004-01-23 |
2009-10-15 |
Janssen Pharmaceutica Nv |
Chinolinderivate und ihre verwendung als mycobakterielle inhibitoren
|
AU2005206562A1
(en)
|
2004-01-23 |
2005-08-04 |
Amgen Inc. |
Vanilloid receptor ligands and their use in treatments
|
US20060019952A1
(en)
|
2004-01-29 |
2006-01-26 |
Elixir Pharmaceuticals, Inc. |
Anti-viral therapeutics
|
GB0402137D0
(en)
|
2004-01-30 |
2004-03-03 |
Smithkline Beecham Corp |
Novel compounds
|
AU2005214352B2
(en)
|
2004-02-14 |
2009-11-12 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
CA2555724A1
(en)
|
2004-02-18 |
2005-09-09 |
Warner-Lambert Company Llc |
2-(pyridin-3-ylamino)-pyrido[2,3-d]pyrimidin-7-ones
|
RU2006134021A
(ru)
|
2004-02-27 |
2008-04-10 |
Ф.Хоффманн-Ля Рош Аг (Ch) |
Производные гетероарил-конденсированного пиразола
|
KR100843526B1
(ko)
|
2004-02-27 |
2008-07-03 |
에프. 호프만-라 로슈 아게 |
피라졸의 접합 유도체
|
WO2005087765A1
(en)
|
2004-03-04 |
2005-09-22 |
Arena Pharmaceuticals, Inc. |
Ligands of follicle stimulating hormone receptor and methods of use thereof
|
WO2005085210A1
(ja)
|
2004-03-10 |
2005-09-15 |
Ono Pharmaceutical Co., Ltd. |
ニトリル化合物およびその化合物を有効成分として含有する医薬組成物
|
EP1736476A4
(en)
|
2004-03-29 |
2010-04-07 |
Mitsui Chemicals Inc |
NEW CONNECTION AND ORGANIC ELECTRONIC DEVICE USING SUCH A CONNECTION
|
WO2005105097A2
(en)
*
|
2004-04-28 |
2005-11-10 |
Gpc Biotech Ag |
Pyridopyrimidines for treating inflammatory and other diseases
|
JP2005320288A
(ja)
|
2004-05-10 |
2005-11-17 |
Mitsui Chemicals Inc |
テトラカルボン酸誘導体、および該化合物を用いた電子写真感光体、電子写真装置
|
US20050256309A1
(en)
|
2004-05-12 |
2005-11-17 |
Altenbach Robert J |
Tri-and bi-cyclic heteroaryl histamine-3 receptor ligands
|
WO2005116035A1
(en)
|
2004-05-27 |
2005-12-08 |
Pfizer Products Inc. |
Pyrrolopyrimidine derivatives useful in cancer treatment
|
PE20060426A1
(es)
|
2004-06-02 |
2006-06-28 |
Schering Corp |
DERIVADOS DE ACIDO TARTARICO COMO INHIBIDORES DE MMPs, ADAMs, TACE Y TNF-alfa
|
EP1761539A1
(en)
|
2004-06-02 |
2007-03-14 |
Takeda Pharmaceutical Company Limited |
Indole derivative and use for treatment of cancer
|
EP1758892B1
(en)
|
2004-06-10 |
2012-10-17 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
SI2298768T1
(en)
|
2004-06-11 |
2013-01-31 |
Japan Tobacco Inc |
5-amino-2,4,7-trioxo-3,4,7,8-tetrahydro-2H-pyridoS2,3-dCpyrimidine derivatives and related compounds for the treatment of cancer
|
GB0512324D0
(en)
|
2005-06-16 |
2005-07-27 |
Novartis Ag |
Organic compounds
|
JP2006028027A
(ja)
|
2004-07-12 |
2006-02-02 |
Mitsui Chemicals Inc |
テトラカルボン酸誘導体、および該化合物を用いた電子写真感光体、電子写真装置
|
ATE425166T1
(de)
|
2004-08-31 |
2009-03-15 |
Hoffmann La Roche |
Amidderivate von 3-phenyldihydropyrimidoä4,5- düpyrimidinonen, deren herstellung und verwendung als pharmazeutische mittel
|
AU2005279337A1
(en)
|
2004-08-31 |
2006-03-09 |
F. Hoffmann-La Roche Ag |
Amide derivatives of 7-amino-3-phenyl-dihydropyrimido [4,5-d]pyrimidinones, their manufacture and use as pharmaceutical agents
|
WO2006024834A1
(en)
|
2004-08-31 |
2006-03-09 |
Astrazeneca Ab |
Quinazolinone derivatives and their use as b-raf inhibitors
|
DE102004042667A1
(de)
|
2004-09-01 |
2006-03-30 |
Ewald Dörken Ag |
Mehrschichtige Gebäudewand
|
KR101165653B1
(ko)
|
2004-09-10 |
2012-07-17 |
우베 고산 가부시키가이샤 |
변성 폴리이미드 수지 및 경화가능 수지 조성물
|
AU2005336092B2
(en)
|
2004-09-14 |
2010-05-27 |
Cynthia C. Bamdad |
Methods for diagnosis and treatment of cancer
|
GB0420719D0
(en)
|
2004-09-17 |
2004-10-20 |
Addex Pharmaceuticals Sa |
Novel allosteric modulators
|
WO2006038112A1
(en)
|
2004-10-01 |
2006-04-13 |
Warner-Lambert Company Llc |
Use of kinase inhibitors to promote neochondrogenesis
|
FR2876582B1
(fr)
|
2004-10-15 |
2007-01-05 |
Centre Nat Rech Scient Cnrse |
Utilisation de derives de pyrrolo-pyrazines pour la fabrication de medicaments pour le traitement de la mucoviscidose et de maladies liees a un defaut d'adressage des proteines dans les cellules
|
US20060135553A1
(en)
|
2004-10-28 |
2006-06-22 |
Campbell David A |
Imidazole derivatives
|
US7855205B2
(en)
|
2004-10-29 |
2010-12-21 |
Janssen Pharmaceutica Nv |
Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders
|
JP2008519036A
(ja)
|
2004-11-08 |
2008-06-05 |
バクスター・インターナショナル・インコーポレイテッド |
チューブリン阻害化合物のナノ粒子組成物
|
CA2587153A1
(en)
|
2004-11-18 |
2006-05-26 |
Incyte Corporation |
Inhibitors of 11-.beta. hydroxyl steroid dehydrogenase type 1 and methods of using the same
|
RU2394825C2
(ru)
|
2004-11-22 |
2010-07-20 |
Вертекс Фармасьютикалз Инкорпорейтед |
Пирролопиразины, пригодные в качестве ингибиторов киназы аврора а
|
KR20070085433A
(ko)
|
2004-11-24 |
2007-08-27 |
노파르티스 아게 |
Jak 저해제들과 bcr-abl, flt-3, fak 또는raf 키나제 저해제들 중 하나 이상의 조합물
|
MY140748A
(en)
|
2004-12-06 |
2010-01-15 |
Astrazeneca Ab |
Novel pyrrolo [3,2-d] pyrimidin-4-one derivatives and their use in therapy
|
JP5111113B2
(ja)
|
2004-12-13 |
2012-12-26 |
サネシス ファーマシューティカルズ, インコーポレイテッド |
Rafキナーゼ阻害剤として有用なピリドピリミジノン、ジヒドロピリミドピリミジノンおよびプテリジノン
|
US20100152206A1
(en)
|
2005-01-07 |
2010-06-17 |
Ralph Mazitschek |
Bicyclic Dihydropyrimidines and Uses Thereof
|
DE102005008310A1
(de)
|
2005-02-17 |
2006-08-24 |
Schering Ag |
Verwendung von CDKII Inhibitoren zur Fertilitätskontrolle
|
US20090111837A1
(en)
|
2005-03-01 |
2009-04-30 |
Peter Cox |
Use of pde7 inhibitors for the treatment of neuropathic pain
|
US7297700B2
(en)
|
2005-03-24 |
2007-11-20 |
Renovis, Inc. |
Bicycloheteroaryl compounds as P2X7 modulators and uses thereof
|
WO2006105448A2
(en)
|
2005-03-30 |
2006-10-05 |
Minerva Biotechnologies Corporation |
Proliferation of muc1 expressing cells
|
JP2006284843A
(ja)
|
2005-03-31 |
2006-10-19 |
Mitsui Chemicals Inc |
テトラカルボン酸誘導体を用いた電子写真感光体、電子写真装置
|
US20060223993A1
(en)
|
2005-04-01 |
2006-10-05 |
Connor Daniel M |
Colorant compounds, intermediates, and compositions
|
JP2006316054A
(ja)
|
2005-04-15 |
2006-11-24 |
Tanabe Seiyaku Co Ltd |
高コンダクタンス型カルシウム感受性kチャネル開口薬
|
KR100781704B1
(ko)
|
2005-04-20 |
2007-12-03 |
에스케이케미칼주식회사 |
피리딘 유도체와 이의 제조방법, 및 이를 포함하는약제조성물
|
EP1885369B1
(en)
|
2005-05-04 |
2015-09-23 |
Evotec AG |
Fused heterocyclic compounds, and compositions and uses thereof
|
RU2406760C3
(ru)
|
2005-05-09 |
2017-11-28 |
Оно Фармасьютикал Ко., Лтд. |
Моноклональные антитела человека к белку программируемой смерти 1 (pd-1) и способы лечения рака с использованием анти-pd-1-антител самостоятельно или в комбинации с другими иммунотерапевтическими средствами
|
WO2006124731A2
(en)
*
|
2005-05-12 |
2006-11-23 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
JP5016593B2
(ja)
|
2005-05-13 |
2012-09-05 |
アイアールエム・リミテッド・ライアビリティ・カンパニー |
プロテイン・キナーゼ阻害剤としての化合物および組成物
|
WO2006135821A2
(en)
|
2005-06-09 |
2006-12-21 |
Achille Carlisle Tisdelle |
Vehicular head and neck safety system and method
|
GB0512844D0
(en)
|
2005-06-23 |
2005-08-03 |
Novartis Ag |
Organic compounds
|
KR101607288B1
(ko)
|
2005-07-01 |
2016-04-05 |
이. 알. 스퀴부 앤드 선즈, 엘.엘.씨. |
예정 사멸 리간드 1 (피디-엘1)에 대한 인간 모노클로날 항체
|
US7932257B2
(en)
|
2005-07-22 |
2011-04-26 |
Sunesis Pharmaceuticals, Inc. |
Substituted pyrazolo[4,3-d]pyrimidines as aurora kinase inhibitors
|
US20100216798A1
(en)
|
2005-07-29 |
2010-08-26 |
Astellas Pharma Inc |
Fused heterocycles as lck inhibitors
|
ES2270715B1
(es)
|
2005-07-29 |
2008-04-01 |
Laboratorios Almirall S.A. |
Nuevos derivados de pirazina.
|
ATE482958T1
(de)
|
2005-08-09 |
2010-10-15 |
Irm Llc |
Verbindungen und zusammensetzungen als proteinkinaseinhibitoren
|
BRPI0614578A2
(pt)
|
2005-08-16 |
2011-04-05 |
Irm Llc |
composto, composição farmacêutica como inibidores de proteìna cinases, bem como seu método e uso
|
CN101242832B
(zh)
|
2005-08-25 |
2011-08-10 |
霍夫曼-拉罗奇有限公司 |
用作p38 MAP激酶抑制剂的稠合吡唑
|
US7678917B2
(en)
|
2005-09-01 |
2010-03-16 |
Hoffman-La Roche Inc. |
Factor Xa inhibitors
|
AU2006287771A1
(en)
|
2005-09-06 |
2007-03-15 |
Smithkline Beecham Corporation |
Regioselective process for preparing benzimidazole thiophenes
|
KR20080046728A
(ko)
|
2005-09-15 |
2008-05-27 |
아스카 세이야쿠 가부시키가이샤 |
복소환 화합물, 그의 제조 방법 및 용도
|
US20070116984A1
(en)
|
2005-09-21 |
2007-05-24 |
Doosan Corporation |
Spiro-compound for electroluminescent display device and electroluminescent display device comprising the same
|
CN101309925A
(zh)
|
2005-09-23 |
2008-11-19 |
先灵公司 |
作为治疗药物的稠合四环类代谢型谷氨酸受体1拮抗剂
|
DE102005048072A1
(de)
|
2005-09-24 |
2007-04-05 |
Bayer Cropscience Ag |
Thiazole als Fungizide
|
WO2007044729A2
(en)
|
2005-10-07 |
2007-04-19 |
Exelixis, Inc. |
N- (3-amino-quinoxalin-2-yl) -sulfonamide derivatives and their use as phosphatidylinositol 3-kinase inhibitors
|
CN102746298A
(zh)
|
2005-10-07 |
2012-10-24 |
埃克塞里艾克西斯公司 |
PI3Kα的吡啶并嘧啶酮抑制剂
|
WO2007061554A2
(en)
|
2005-10-21 |
2007-05-31 |
Purdue Research Foundation |
Dosage of 4-aminopyridine derivatives for treatment of central nervous system injuries
|
EP1943231A1
(en)
|
2005-10-26 |
2008-07-16 |
Boehringer Ingelheim International Gmbh |
(hetero)aryl compounds with mch antagonistic activity and medicaments comprising these compounds
|
MX362412B
(es)
|
2005-11-01 |
2019-01-15 |
Targegen Inc |
Inhibidores de biaril meta-pirimidina de cinasas.
|
US8067457B2
(en)
|
2005-11-01 |
2011-11-29 |
Millennium Pharmaceuticals, Inc. |
Compounds useful as antagonists of CCR2
|
US8604042B2
(en)
|
2005-11-01 |
2013-12-10 |
Targegen, Inc. |
Bi-aryl meta-pyrimidine inhibitors of kinases
|
WO2007056075A2
(en)
|
2005-11-02 |
2007-05-18 |
Targegen, Inc. |
Six membered heteroaromatic inhibitors targeting resistant kinase mutations
|
ES2401099T3
(es)
|
2005-11-02 |
2013-04-16 |
Bayer Intellectual Property Gmbh |
Pirrolo[2,1-F] [1,2,4]-triazin-4-ilaminas como inhibidores de la quinasa IGF-1R para el tratamiento del cáncer y de otras enfermedades hiperproliferativas
|
NZ568292A
(en)
|
2005-11-10 |
2011-08-26 |
Msd Kk |
Spiro[cyclohexane-1,1'-(3'H)-4'-azaisobenzofuran]-4-carboxamide derivatives
|
EP2314590A1
(en)
|
2005-11-10 |
2011-04-27 |
ChemoCentryx, Inc. |
Substituted quinolones and methods of use
|
WO2007058626A1
(en)
|
2005-11-16 |
2007-05-24 |
S*Bio Pte Ltd |
Indazole compounds
|
AR057986A1
(es)
|
2005-11-21 |
2008-01-09 |
Japan Tobacco Inc |
Compuesto heterociclico y su uso farmaceutico
|
CN101466710B
(zh)
|
2005-12-02 |
2013-05-29 |
拜尔健康护理有限责任公司 |
用于治疗与血管生成有关的过度增殖性病症和疾病的取代的4-氨基-吡咯并三嗪衍生物
|
PE20070855A1
(es)
|
2005-12-02 |
2007-10-14 |
Bayer Pharmaceuticals Corp |
Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
|
JP2009519908A
(ja)
|
2005-12-08 |
2009-05-21 |
ミレニアム・ファーマシューティカルズ・インコーポレイテッド |
キナーゼ阻害活性を有する二環式化合物
|
WO2007066189A2
(en)
|
2005-12-09 |
2007-06-14 |
Pfizer Products Inc. |
Salts, prodrugs and formulations of 1-[5-(4-amino-7-isopropyl-7h-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-2-methoxy-phenyl]-3-(2,4-dichloro-phenyl)-urea
|
EP1968950A4
(en)
|
2005-12-19 |
2010-04-28 |
Genentech Inc |
PYRIMIDINKINASEINHIBITOREN
|
AU2006326989B2
(en)
|
2005-12-21 |
2011-11-24 |
Novartis Ag |
Pyrimidinyl aryl urea derivatives being FGF inhibitors
|
US7998959B2
(en)
|
2006-01-12 |
2011-08-16 |
Incyte Corporation |
Modulators of 11-β hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same
|
PE20071025A1
(es)
|
2006-01-31 |
2007-10-17 |
Mitsubishi Tanabe Pharma Corp |
Compuesto amina trisustituido
|
WO2007092879A2
(en)
|
2006-02-08 |
2007-08-16 |
Janssen Pharmaceutica, N.V. |
Substituted thiatriazaacenaphthylene-6-carbonitrile kinase inhibitors
|
JP2009528989A
(ja)
|
2006-02-17 |
2009-08-13 |
ファイザー・リミテッド |
Tlr7変調剤としての3−デアザプリン誘導体
|
WO2007109334A2
(en)
|
2006-03-21 |
2007-09-27 |
Epix Delaware, Inc. |
Sip receptor modulating compounds and use thereof
|
CA2680789C
(en)
|
2006-03-28 |
2016-02-16 |
Atir Holding S.A. |
Heterocyclic compounds and uses thereof in the treatment of sexual disorders
|
WO2007112347A1
(en)
|
2006-03-28 |
2007-10-04 |
Takeda Pharmaceutical Company Limited |
Dipeptidyl peptidase inhibitors
|
EP2007373A4
(en)
|
2006-03-29 |
2012-12-19 |
Foldrx Pharmaceuticals Inc |
INHIBITION OF ALPHA SYNUCLEINE TOXICITY
|
CA2648324A1
(en)
|
2006-04-06 |
2007-10-18 |
Wisconsin Alumni Research Foundation |
2-methylene-1.alpha.,25-dihydroxy-19,21-dinorvitamin d3 analogs and uses thereof
|
US20090286813A1
(en)
|
2006-04-13 |
2009-11-19 |
Astrazeneca Ab |
Thioxanthine Derivatives and Their Use as Inhibitors of MPO
|
GB0608386D0
(en)
|
2006-04-27 |
2006-06-07 |
Senexis Ltd |
Compounds
|
US7998978B2
(en)
|
2006-05-01 |
2011-08-16 |
Pfizer Inc. |
Substituted 2-amino-fused heterocyclic compounds
|
JP5241704B2
(ja)
|
2006-05-11 |
2013-07-17 |
アイアールエム・リミテッド・ライアビリティ・カンパニー |
プロテインキナーゼ阻害剤としての化合物および組成物
|
RU2008149245A
(ru)
|
2006-05-15 |
2010-06-20 |
Айрм Ллк (Bm) |
Композиции и способы ингибирования рецепторных киназ fgf
|
US7910108B2
(en)
|
2006-06-05 |
2011-03-22 |
Incyte Corporation |
Sheddase inhibitors combined with CD30-binding immunotherapeutics for the treatment of CD30 positive diseases
|
DE102006027156A1
(de)
|
2006-06-08 |
2007-12-13 |
Bayer Schering Pharma Ag |
Sulfimide als Proteinkinaseinhibitoren
|
AU2007262670B2
(en)
|
2006-06-22 |
2012-12-20 |
Prana Biotechnology Limited |
Method of treatment of glioma brain tumour
|
US20090281115A1
(en)
|
2006-06-30 |
2009-11-12 |
Board of Regents, The University of Texas System, a Texas University |
Inhibitors of c-kit and uses thereof
|
TW200817391A
(en)
|
2006-06-30 |
2008-04-16 |
Astrazeneca Ab |
Novel compounds
|
CA2654670A1
(en)
|
2006-07-06 |
2008-01-10 |
Boehringer Ingelheim International Gmbh |
New compounds
|
US8030487B2
(en)
|
2006-07-07 |
2011-10-04 |
Targegen, Inc. |
2-amino—5-substituted pyrimidine inhibitors
|
TW200811134A
(en)
|
2006-07-12 |
2008-03-01 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
WO2008012635A2
(en)
|
2006-07-26 |
2008-01-31 |
Pfizer Products Inc. |
Amine derivatives useful as anticancer agents
|
WO2008021851A2
(en)
|
2006-08-09 |
2008-02-21 |
Smithkline Beecham Corporation |
Novel compounds as antagonists or inverse agonists for opioid receptors
|
EP2056829B9
(en)
|
2006-08-16 |
2012-09-26 |
Exelixis, Inc. |
Using pi3k and mek modulators in treatments of cancer
|
DE102006041382A1
(de)
|
2006-08-29 |
2008-03-20 |
Bayer Schering Pharma Ag |
Carbamoyl-Sulfoximide als Proteinkinaseinhibitoren
|
PL2061765T3
(pl)
|
2006-09-01 |
2015-04-30 |
Senhwa Biosciences Inc |
Modulatory białkowych kinaz serynowo-treoninowych i PARP
|
CA2662677C
(en)
|
2006-09-05 |
2016-05-31 |
Emory University |
Kinase inhibitors for preventing or treating pathogen infection and method of use thereof
|
EP2270200A3
(en)
|
2006-09-11 |
2011-07-13 |
CGI Pharmaceuticals, Inc. |
Kinase inhibitors, and methods of using and identifying kinase inhibitors
|
US7897762B2
(en)
|
2006-09-14 |
2011-03-01 |
Deciphera Pharmaceuticals, Llc |
Kinase inhibitors useful for the treatment of proliferative diseases
|
JP5372759B2
(ja)
|
2006-09-21 |
2013-12-18 |
ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング |
グルコピラノシル−置換ジフルオロベンジル−ベンゼン誘導体、該化合物を含有する医薬品及びその使用と調製方法
|
TW200836724A
(en)
|
2006-09-22 |
2008-09-16 |
Glaxo Group Ltd |
Novel compounds
|
CA2664375A1
(en)
|
2006-09-28 |
2008-04-03 |
Novartis Ag |
Pyrazolo [1, 5-a] pyrimidine derivatives and their therapeutic use
|
CA2663366C
(en)
|
2006-10-02 |
2012-02-07 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
WO2008052934A1
(en)
|
2006-10-30 |
2008-05-08 |
Glaxo Group Limited |
Novel substituted pyrimidines as cysteine protease inhibitors
|
US7858645B2
(en)
|
2006-11-01 |
2010-12-28 |
Hoffmann-La Roche Inc. |
Indazole derivatives
|
WO2008060907A2
(en)
|
2006-11-10 |
2008-05-22 |
Bristol-Myers Squibb Company |
Pyrrolo-pyridine kinase inhibitors
|
WO2008063583A1
(en)
|
2006-11-17 |
2008-05-29 |
Polyera Corporation |
Acene-based organic semiconductor materials and methods of preparing and using the same
|
EP2086974B1
(en)
|
2006-11-17 |
2013-07-24 |
Polyera Corporation |
Diimide-based semiconductor materials and methods of preparing and using the same
|
KR20080045536A
(ko)
|
2006-11-20 |
2008-05-23 |
에스케이케미칼주식회사 |
피리딘 화합물을 포함하는 간염 치료 및 예방 또는 간 보호효능을 갖는 약제 조성물
|
EP3443958A1
(en)
|
2006-11-22 |
2019-02-20 |
Incyte Holdings Corporation |
Imidazotriazines and imidazopyrimidines as kinase inhibitors
|
MX2009006466A
(es)
|
2006-12-13 |
2009-06-26 |
Schering Corp |
Metodos de tratamiento de cancer con inhibidores del receptor del factor 1 de crecimiento similar a la insulina.
|
WO2008071455A1
(en)
|
2006-12-15 |
2008-06-19 |
Bayer Schering Pharma Aktiengesellschaft |
Bicyclic acyltryptophanols
|
WO2008074068A1
(en)
|
2006-12-20 |
2008-06-26 |
Prana Biotechnology Limited |
Substituted quinoline derivatives as antiamyloidogeneic agents
|
US7737149B2
(en)
|
2006-12-21 |
2010-06-15 |
Astrazeneca Ab |
N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]-4-(3,5-dimethylpiperazin-1-yl)benzamide and salts thereof
|
CN101679409B
(zh)
|
2006-12-22 |
2014-11-26 |
Astex治疗学有限公司 |
双环杂环衍生化合物、其医药组合物和其用途
|
WO2008078091A1
(en)
|
2006-12-22 |
2008-07-03 |
Astex Therapeutics Limited |
Bicyclic heterocyclic compounds as fgfr inhibitors
|
CN101568529A
(zh)
|
2006-12-22 |
2009-10-28 |
诺瓦提斯公司 |
作为cdk抑制剂、用于治疗癌症、炎症和病毒感染的杂芳基-杂芳基化合物
|
FR2911140B1
(fr)
|
2007-01-05 |
2009-02-20 |
Sanofi Aventis Sa |
Nouveaux derives de 2-anilino 4-heteroaryle pyrimides, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
|
KR20090117730A
(ko)
|
2007-01-08 |
2009-11-12 |
폴리에라 코퍼레이션 |
아렌-비스(디카르복스이미드)-기재 반도체 물질, 및 이를 제조하기 위한 관련된 중간체의 제조 방법
|
CN101007778A
(zh)
|
2007-01-10 |
2007-08-01 |
复旦大学 |
一种链延长型芴基双马来酰亚胺及其制备方法
|
MX2009007333A
(es)
|
2007-01-12 |
2009-08-31 |
Biocryst Pharm Inc |
Analogos de nucleosidos antivirales.
|
WO2008084861A1
(ja)
|
2007-01-12 |
2008-07-17 |
Astellas Pharma Inc. |
縮合ピリジン化合物
|
FR2911604B1
(fr)
|
2007-01-19 |
2009-04-17 |
Sanofi Aventis Sa |
Derives de n-(heteroaryl-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique
|
JP5358962B2
(ja)
|
2007-02-06 |
2013-12-04 |
住友化学株式会社 |
組成物及び該組成物を用いてなる発光素子
|
JP2008198769A
(ja)
|
2007-02-13 |
2008-08-28 |
Nippon Steel Chem Co Ltd |
有機エレクトロルミネッセント素子
|
CA2678492A1
(en)
|
2007-03-06 |
2008-09-12 |
Novartis Ag |
Bicyclic organic compounds suitable for the treatment of inflammatory or allergic conditions
|
US20080221128A1
(en)
|
2007-03-07 |
2008-09-11 |
Christian Gege |
Metalloprotease inhibitors containing a squaramide moiety
|
RU2498983C2
(ru)
|
2007-03-12 |
2013-11-20 |
Юм Биосайнсес Аустралия Пти Лтд |
Соединения фениламинопиримидина и их применения
|
US20080234262A1
(en)
|
2007-03-21 |
2008-09-25 |
Wyeth |
Pyrazolopyrimidine analogs and their use as mtor kinase and pi3 kinase inhibitors
|
EP2132207A2
(en)
|
2007-03-23 |
2009-12-16 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
EP2896624B1
(en)
|
2007-03-28 |
2016-07-13 |
Atir Holding S.A. |
Heterotricyclic compounds as serotonergic and/or dopaminergic agents and uses thereof
|
KR20080091948A
(ko)
|
2007-04-10 |
2008-10-15 |
에스케이케미칼주식회사 |
락탐형 피리딘 화합물을 포함하는 허혈성 질환의 예방 및치료용 약학조성물
|
US20100112211A1
(en)
|
2007-04-12 |
2010-05-06 |
Advanced Technology Materials, Inc. |
Zirconium, hafnium, titanium, and silicon precursors for ald/cvd
|
CN101754961A
(zh)
|
2007-04-20 |
2010-06-23 |
先灵公司 |
嘧啶酮衍生物及其使用方法
|
EP1985612A1
(en)
|
2007-04-26 |
2008-10-29 |
Bayer Schering Pharma Aktiengesellschaft |
Arymethylen substituted N-Acyl-gamma-aminoalcohols
|
JP2010526823A
(ja)
|
2007-05-10 |
2010-08-05 |
グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー |
Pi3キナーゼ阻害物質としてのキノキサリン誘導体
|
EP1990342A1
(en)
|
2007-05-10 |
2008-11-12 |
AEterna Zentaris GmbH |
Pyridopyrazine Derivatives, Process of Manufacturing and Uses thereof
|
WO2008144253A1
(en)
|
2007-05-14 |
2008-11-27 |
Irm Llc |
Protein kinase inhibitors and methods for using thereof
|
GB2449293A
(en)
|
2007-05-17 |
2008-11-19 |
Evotec |
Compounds having Hsp90 inhibitory activity
|
JP5622568B2
(ja)
|
2007-06-03 |
2014-11-12 |
バンダービルト ユニバーシティ |
ベンズアミドmGluR5の正のアロステリック調節因子ならびにその作製および使用方法
|
JP2010529120A
(ja)
|
2007-06-07 |
2010-08-26 |
メルク・シャープ・エンド・ドーム・コーポレイション |
三環式アニリド複素環cgrp受容体アンタゴニスト
|
US8633186B2
(en)
|
2007-06-08 |
2014-01-21 |
Senomyx Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
US7928111B2
(en)
|
2007-06-08 |
2011-04-19 |
Senomyx, Inc. |
Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
|
SI2168966T1
(sl)
|
2007-06-15 |
2017-03-31 |
Msd K.K. |
Derivat biciklo anilina
|
CN104945508B
(zh)
|
2007-06-18 |
2019-02-22 |
默沙东有限责任公司 |
针对人程序性死亡受体pd-1的抗体
|
EP2018859A1
(en)
|
2007-07-26 |
2009-01-28 |
Bayer Schering Pharma Aktiengesellschaft |
Arylmethylene substituted N-acyl-beta-amino alcohols
|
CA2694261A1
(en)
|
2007-07-26 |
2009-01-29 |
Novartis Ag |
Organic compounds
|
EP2020404A1
(en)
|
2007-08-01 |
2009-02-04 |
Bayer Schering Pharma Aktiengesellschaft |
Cyanomethyl substituted N-Acyl Tryptamines
|
JP2010535804A
(ja)
|
2007-08-09 |
2010-11-25 |
グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー |
Pi3キナーゼ阻害薬としてのキノキサリン誘導体
|
WO2009019518A1
(en)
|
2007-08-09 |
2009-02-12 |
Astrazeneca Ab |
Pyrimidine compounds having a fgfr inhibitory effect
|
US7960400B2
(en)
|
2007-08-27 |
2011-06-14 |
Duquesne University Of The Holy Ghost |
Tricyclic compounds having cytostatic and/or cytotoxic activity and methods of use thereof
|
WO2009029625A1
(en)
|
2007-08-27 |
2009-03-05 |
Kalypsys, Inc. |
4- [heterocyclyl-methyl] -8-fluoro-quinolin-2-ones useful as nitric oxide synthase inhibitors
|
EP2200436B1
(en)
|
2007-09-04 |
2015-01-21 |
The Scripps Research Institute |
Substituted pyrimidinyl-amines as protein kinase inhibitors
|
WO2009030871A1
(en)
|
2007-09-07 |
2009-03-12 |
Vernalis R & D Ltd |
Pyrrolopyrimidine derivatives having hsp90 inhibitory activity
|
TW200920357A
(en)
|
2007-09-10 |
2009-05-16 |
Curis Inc |
HSP90 inhibitors containing a zinc binding moiety
|
JP5792955B2
(ja)
|
2007-10-01 |
2015-10-14 |
アイシス ファーマシューティカルズ, インコーポレーテッド |
線維芽細胞増殖因子受容体4発現のアンチセンスモジュレーション
|
AU2008308092B2
(en)
|
2007-10-05 |
2013-07-11 |
Msd K.K. |
Benzoxazinone derivative
|
WO2009047255A1
(en)
|
2007-10-09 |
2009-04-16 |
Ucb Pharma, S.A. |
Heterobicyclic compounds as histamine h4-receptor antagonists
|
WO2009049018A1
(en)
|
2007-10-10 |
2009-04-16 |
Syndax Pharmaceuticals, Inc. |
Novel compounds and methods of using them
|
US8513233B2
(en)
|
2007-10-11 |
2013-08-20 |
Shanghai Institute Of Materia Medica, Cas |
Pyrimidinyl-propionic acid derivatives and their use as PPAR agonists
|
GB0720038D0
(en)
|
2007-10-12 |
2007-11-21 |
Astex Therapeutics Ltd |
New compounds
|
GB0720041D0
(en)
|
2007-10-12 |
2007-11-21 |
Astex Therapeutics Ltd |
New Compounds
|
JP5273052B2
(ja)
|
2007-10-13 |
2013-08-28 |
コニカミノルタ株式会社 |
有機エレクトロルミネッセンス素子、表示装置及び照明装置
|
CA2702838A1
(en)
|
2007-10-16 |
2009-04-23 |
Wyeth Llc |
Thienopyrimidine and pyrazolopyrimidine compounds and their use as mtor kinase and pi3 kinase inhibitors
|
ES2393430T3
(es)
|
2007-10-17 |
2012-12-21 |
Novartis Ag |
Derivados de imidazo[1,2-A]-piridina útiles como inhibidores de ALK
|
RU2007139634A
(ru)
|
2007-10-25 |
2009-04-27 |
Сергей Олегович Бачурин (RU) |
Новые тиазол-, триазол- или оксадиазол-содержащие тетрациклические соединения
|
KR20100089090A
(ko)
|
2007-10-25 |
2010-08-11 |
아스트라제네카 아베 |
세포 증식 장애의 치료에 유용한 피리딘 및 피라진 유도체
|
WO2009056886A1
(en)
|
2007-11-01 |
2009-05-07 |
Astrazeneca Ab |
Pyrimidine derivatives and their use as modulators of fgfr activity
|
MX2010005671A
(es)
|
2007-11-28 |
2010-06-25 |
Dana Farber Cancer Inst Inc |
Inhibidores de miristato de moleculas pequeñas contra bcr-abl y metodos de uso.
|
JP2011505407A
(ja)
|
2007-12-03 |
2011-02-24 |
ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング |
過剰な又は異常な細胞増殖を特徴とする疾患を治療するためのジアミノピリジン
|
EP2231656A1
(en)
|
2007-12-19 |
2010-09-29 |
Amgen Inc. |
Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors
|
US20100331333A1
(en)
|
2007-12-21 |
2010-12-30 |
Wyeth Llc |
Imidazo [1,2-B] Pyridazine Compounds
|
JP2011507910A
(ja)
|
2007-12-21 |
2011-03-10 |
ユニバーシティー オブ ロチェスター |
真核生物の寿命を変更するための方法
|
WO2009086509A2
(en)
|
2007-12-27 |
2009-07-09 |
Purdue Research Foundation |
Reagents for biomolecular labeling, detection and quantification employing raman spectroscopy
|
FR2926297B1
(fr)
|
2008-01-10 |
2013-03-08 |
Centre Nat Rech Scient |
Molecules chimiques inhibitrices du mecanisme d'epissage pour traiter des maladies resultant d'anomalies d'epissage.
|
US20100292188A1
(en)
|
2008-01-24 |
2010-11-18 |
Ucb Pharma S.A. |
Compounds Comprising A Cyclobutoxy Group
|
EP2248814A4
(en)
|
2008-01-24 |
2011-01-12 |
Alla Chem Llc |
SUBSTITUTED CYCLOALKAN [E AND D] PYRAZOLO [1,5-A] PYRIMIDINES / ANTAGONISTS OF SEROTONIN 5-HT6 RECEPTORS AND PROCESS FOR THEIR PREPARATION AND THEIR USE
|
KR20100119776A
(ko)
|
2008-01-24 |
2010-11-10 |
알라 캠, 엘엘씨 |
2-알킬아미노-3-아릴설포닐-사이클로알카노[e 또는 d]피라졸로[1,5-A]피리미딘/세로토닌 5-HT6 수용체의 길항제, 이의 제조방법 및 이의 용도
|
WO2009094528A1
(en)
|
2008-01-25 |
2009-07-30 |
High Point Pharmaceuticals, Llc |
TRICYCLIC COMPOUNDS AS MODULATORS OF TNF-α SYNTHESIS AND AS PDE4 INHIBITORS
|
CN101981037B
(zh)
|
2008-01-30 |
2013-09-04 |
吉宁特有限公司 |
吡唑并嘧啶pi3k抑制剂化合物及使用方法
|
JP2011511005A
(ja)
|
2008-02-04 |
2011-04-07 |
オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド |
2−アミノピリジン系キナーゼ阻害薬
|
JP2011513233A
(ja)
|
2008-02-22 |
2011-04-28 |
アイアールエム・リミテッド・ライアビリティ・カンパニー |
Gpr119活性モジュレーターとしての化合物および組成物
|
BRPI0907577A2
(pt)
|
2008-02-22 |
2015-07-21 |
Hoffmann La Roche |
Moduladores para amiloide beta
|
JP5451646B2
(ja)
|
2008-02-27 |
2014-03-26 |
ヴァイティー ファーマシューティカルズ,インコーポレイテッド |
11β−ヒドロキシステロイドデヒドロゲナーゼ1型の阻害剤
|
WO2009108827A1
(en)
|
2008-02-29 |
2009-09-03 |
Wyeth |
Fused tricyclic pyrazolo[1, 5-a]pyrimidines, methods for preparation and uses thereof
|
ITTV20080039A1
(it)
|
2008-03-06 |
2009-09-07 |
Alpinestars Research Srl |
Collare di protezione in particolare per guidatori di motoveicoli
|
EP2262837A4
(en)
|
2008-03-12 |
2011-04-06 |
Merck Sharp & Dohme |
PD-1 BINDING PROTEINS
|
GB0804701D0
(en)
|
2008-03-13 |
2008-04-16 |
Amura Therapeutics Ltd |
Compounds
|
WO2009114874A2
(en)
|
2008-03-14 |
2009-09-17 |
Intellikine, Inc. |
Benzothiazole kinase inhibitors and methods of use
|
WO2009114870A2
(en)
|
2008-03-14 |
2009-09-17 |
Intellikine, Inc. |
Kinase inhibitors and methods of use
|
US20090246198A1
(en)
|
2008-03-31 |
2009-10-01 |
Takeda Pharmaceutical Company Limited |
Mapk/erk kinase inhibitors and methods of use thereof
|
WO2009122180A1
(en)
|
2008-04-02 |
2009-10-08 |
Medical Research Council |
Pyrimidine derivatives capable of inhibiting one or more kinases
|
US8436005B2
(en)
|
2008-04-03 |
2013-05-07 |
Abbott Laboratories |
Macrocyclic pyrimidine derivatives
|
MX2010010975A
(es)
|
2008-04-07 |
2010-11-01 |
Amgen Inc |
Amino piridinas/pirimidinas gem-disustituidas y espirociclicas como inhibidores de ciclo celular.
|
WO2009124755A1
(en)
|
2008-04-08 |
2009-10-15 |
European Molecular Biology Laboratory (Embl) |
Compounds with novel medical uses and method of identifying such compounds
|
WO2009125808A1
(ja)
|
2008-04-11 |
2009-10-15 |
第一三共株式会社 |
アミノシクロヘキシル誘導体
|
WO2009125809A1
(ja)
|
2008-04-11 |
2009-10-15 |
第一三共株式会社 |
ピペリジン誘導体
|
EP2277881A4
(en)
|
2008-04-18 |
2011-09-07 |
Shionogi & Co |
HETEROCYCLIC COMPOUND HAVING INHIBITORY ACTIVITY ON P13K
|
EP2271631B1
(en)
|
2008-04-22 |
2018-07-04 |
Portola Pharmaceuticals, Inc. |
Inhibitors of protein kinases
|
US7863291B2
(en)
|
2008-04-23 |
2011-01-04 |
Bristol-Myers Squibb Company |
Quinuclidine compounds as alpha-7 nicotinic acetylcholine receptor ligands
|
US8309577B2
(en)
|
2008-04-23 |
2012-11-13 |
Bristol-Myers Squibb Company |
Quinuclidine compounds as α-7 nicotinic acetylcholine receptor ligands
|
JP5539963B2
(ja)
|
2008-04-29 |
2014-07-02 |
ノバルティス アーゲー |
線維芽細胞増殖因子受容体のキナーゼ活性のモジュレーションをモニタリングする方法、および該方法の使用
|
CN102015704A
(zh)
|
2008-04-29 |
2011-04-13 |
霍夫曼-拉罗奇有限公司 |
Jnk的嘧啶基吡啶酮抑制剂
|
AR071523A1
(es)
|
2008-04-30 |
2010-06-23 |
Merck Serono Sa |
Compuestos biciclicos fusionados, un proceso para su preparacion, el compuesto para ser utilizado como medicamento en el tratamiento y profilaxis de enfermedades, una composicion farmaceutica y un conjunto que comprende paquetes separados del compuesto y de un ingrediente activo del medicamento
|
US9315449B2
(en)
|
2008-05-15 |
2016-04-19 |
Duke University |
Substituted pyrazoles as heat shock transcription factor activators
|
MY155535A
(en)
|
2008-05-23 |
2015-10-30 |
Novartis Ag |
Derivatives of quinolines and quinoxalines as protien tyrosine kinase inhibitors
|
WO2009144205A1
(en)
|
2008-05-30 |
2009-12-03 |
Basf Se |
Rylene-based semiconductor materials and methods of preparation and use thereof
|
AU2009255358A1
(en)
|
2008-06-03 |
2009-12-10 |
Msd K.K. |
Inhibitors of Akt activity
|
CN102089403A
(zh)
|
2008-06-10 |
2011-06-08 |
巴斯夫欧洲公司 |
新型过渡金属配合物及其在有机发光二极管中的用途-ⅲ
|
FR2932600B1
(fr)
|
2008-06-11 |
2010-06-04 |
Areva Np |
Embout inferieur d'assemblage de combustible nucleaire
|
EP2303885B1
(en)
|
2008-06-12 |
2013-07-03 |
Merck Sharp & Dohme Corp. |
Process for producing bicycloaniline derivatives
|
GB0810902D0
(en)
|
2008-06-13 |
2008-07-23 |
Astex Therapeutics Ltd |
New compounds
|
KR20110020904A
(ko)
|
2008-06-19 |
2011-03-03 |
아스트라제네카 아베 |
피라졸 화합물 436
|
TW201004958A
(en)
|
2008-06-24 |
2010-02-01 |
Res Found Itsuu Lab |
Oxazolidinone derivatives having a fused ring
|
US8338439B2
(en)
|
2008-06-27 |
2012-12-25 |
Celgene Avilomics Research, Inc. |
2,4-disubstituted pyrimidines useful as kinase inhibitors
|
JP5640006B2
(ja)
|
2008-07-14 |
2014-12-10 |
ギリアード サイエンシーズ, インコーポレイテッド |
ヒストン脱アセチル化酵素および/またはサイクリン依存性キナーゼの縮合複素環式阻害剤
|
WO2010007099A1
(en)
|
2008-07-15 |
2010-01-21 |
Cellzome Limited |
2-aminoimidazo[1,2-b]pyridazine derivatives as pi3k inhibitors
|
CA2726460C
(en)
|
2008-07-15 |
2017-02-21 |
F. Hoffmann-La Roche Ag |
Novel phenyl-imidazopyridines and pyridazines
|
CA2730593A1
(en)
|
2008-07-16 |
2010-01-21 |
Schering Corporation |
Bicyclic heterocycle derivatives and use thereof as gpr119 modulators
|
WO2010009207A1
(en)
|
2008-07-16 |
2010-01-21 |
Schering Corporation |
Bicyclic heterocycle derivatives and their use as gpcr modulators
|
UY31982A
(es)
|
2008-07-16 |
2010-02-26 |
Boehringer Ingelheim Int |
Derivados de 1,2-dihidropiridin-3-carboxamidas n-sustituidas
|
WO2010009735A2
(en)
|
2008-07-23 |
2010-01-28 |
Dako Denmark A/S |
Combinatorial analysis and repair
|
AU2009279936A1
(en)
|
2008-08-05 |
2010-02-11 |
Banyu Pharmaceutical Co., Ltd. |
Therapeutic compounds
|
AR072906A1
(es)
|
2008-08-06 |
2010-09-29 |
Novartis Ag |
Nucleosidos modificados utiles como antivirales
|
US9284297B2
(en)
|
2008-08-11 |
2016-03-15 |
President And Fellows Of Harvard College |
Halofuginone analogs for inhibition of tRNA synthetases and uses thereof
|
UY32049A
(es)
|
2008-08-14 |
2010-03-26 |
Takeda Pharmaceutical |
Inhibidores de cmet
|
WO2010030027A1
(en)
|
2008-09-10 |
2010-03-18 |
Mitsubishi Tanabe Pharma Corporation |
Aromatic nitrogen-containing 6-membered ring compounds and their use
|
EP2342226B1
(en)
|
2008-09-26 |
2016-06-22 |
Dana-Farber Cancer Institute, Inc. |
Human anti-pd-1, pd-l1, and pd-l2 antibodies and uses thereof
|
AR073760A1
(es)
|
2008-10-03 |
2010-12-01 |
Astrazeneca Ab |
Derivados heterociclicos y metodos de uso de los mismos
|
WO2010045371A1
(en)
|
2008-10-15 |
2010-04-22 |
Gilead Palo Alto, Inc. |
Pyrido- and pyrimido (1, 2-a) pyrimidine compounds useful as stearoyl coa desaturase inhibitors
|
US8110578B2
(en)
|
2008-10-27 |
2012-02-07 |
Signal Pharmaceuticals, Llc |
Pyrazino[2,3-b]pyrazine mTOR kinase inhibitors for oncology indications and diseases associated with the mTOR/PI3K/Akt pathway
|
UY32203A
(es)
|
2008-10-29 |
2010-05-31 |
Astrazeneca Ab |
Amino pirimidinas y su uso en terapia
|
US8476431B2
(en)
|
2008-11-03 |
2013-07-02 |
Itellikine LLC |
Benzoxazole kinase inhibitors and methods of use
|
WO2010052448A2
(en)
|
2008-11-05 |
2010-05-14 |
Ucb Pharma S.A. |
Fused pyrazine derivatives as kinase inhibitors
|
WO2010059552A1
(en)
|
2008-11-18 |
2010-05-27 |
Glaxosmithkline Llc |
Prolyl hydroxylase inhibitors
|
ES2548141T3
(es)
|
2008-11-20 |
2015-10-14 |
Glaxosmithkline Llc |
Compuestos químicos
|
JP5522053B2
(ja)
|
2008-12-03 |
2014-06-18 |
コニカミノルタ株式会社 |
有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子材料、表示装置及び照明装置
|
KR101061599B1
(ko)
|
2008-12-05 |
2011-09-02 |
한국과학기술연구원 |
비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물
|
CA2746220A1
(en)
|
2008-12-08 |
2010-07-08 |
Vm Pharma Llc |
Compositions of protein receptor tyrosine kinase inhibitors
|
US8110265B2
(en)
|
2008-12-09 |
2012-02-07 |
The Coca-Cola Company |
Pet container and compositions having enhanced mechanical properties and gas barrier properties
|
CN108997498A
(zh)
|
2008-12-09 |
2018-12-14 |
霍夫曼-拉罗奇有限公司 |
抗-pd-l1抗体及它们用于增强t细胞功能的用途
|
EP2376493B1
(en)
|
2008-12-12 |
2016-10-05 |
Msd K.K. |
Dihydropyrimidopyrimidine derivative
|
JP2012511501A
(ja)
|
2008-12-12 |
2012-05-24 |
Msd株式会社 |
ジヒドロピリミドピリミジン誘導体
|
ES2544452T3
(es)
|
2008-12-19 |
2015-08-31 |
Genentech, Inc. |
Compuestos heterocíclicos y métodos de uso
|
PA8852901A1
(es)
|
2008-12-22 |
2010-07-27 |
Lilly Co Eli |
Inhibidores de proteina cinasa
|
CN102325755B
(zh)
|
2008-12-30 |
2015-07-01 |
艾科尔公司 |
取代的5,6-二氢-6-苯基苯并[f]异喹啉-2-胺化合物
|
US8263610B2
(en)
|
2008-12-30 |
2012-09-11 |
Arqule, Inc. |
Substituted imidazolyl-5,6-dihydrobenzo[N]isoquinoline compounds
|
JP5908728B2
(ja)
|
2009-01-06 |
2016-04-26 |
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 |
ピリミド−ジアゼピノンキナーゼ骨格化合物及び疾患を治療する方法
|
JOP20190231A1
(ar)
|
2009-01-15 |
2017-06-16 |
Incyte Corp |
طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به
|
US8592425B2
(en)
|
2009-01-16 |
2013-11-26 |
Merck Sharp & Dohme Corp. |
Imidazo[1,2-a]pyridines and imidazo[1,2-b]pyridazines as mark inhibitors
|
DE102009007038A1
(de)
|
2009-02-02 |
2010-08-05 |
Merck Patent Gmbh |
Metallkomplexe
|
JP2010180147A
(ja)
|
2009-02-04 |
2010-08-19 |
Mitsubishi Gas Chemical Co Inc |
シアン酸エステル化合物、およびその硬化物
|
EP3192811A1
(en)
|
2009-02-09 |
2017-07-19 |
Université d'Aix-Marseille |
Pd-1 antibodies and pd-l1 antibodies and uses thereof
|
TW201038569A
(en)
|
2009-02-16 |
2010-11-01 |
Abbott Gmbh & Co Kg |
Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy
|
TW201035102A
(en)
|
2009-03-04 |
2010-10-01 |
Gruenethal Gmbh |
Sulfonylated tetrahydroazolopyrazines and their use as medicinal products
|
US20100278835A1
(en)
|
2009-03-10 |
2010-11-04 |
Astrazeneca Uk Limited |
Novel compounds 660
|
WO2010104047A1
(ja)
|
2009-03-11 |
2010-09-16 |
国立大学法人京都大学 |
多環芳香族化合物
|
EP2408744A1
(en)
|
2009-03-18 |
2012-01-25 |
Schering Corporation |
Bicyclic compounds as inhibitors of diacylglycerol acyltransferase
|
CN103739605B
(zh)
|
2009-03-23 |
2016-08-17 |
伊莱利利公司 |
用于检测神经障碍的显像剂
|
WO2010111573A1
(en)
|
2009-03-27 |
2010-09-30 |
Abbott Laboratories |
Compounds as cannabinoid receptor ligands
|
WO2010117425A1
(en)
|
2009-03-31 |
2010-10-14 |
Biogen Idec Ma Inc. |
Certain substituted pyrimidines, pharmaceutical compositions thereof, and methods for their use
|
ES2465971T3
(es)
|
2009-04-06 |
2014-06-09 |
University Health Network |
Inhibidores de quinasa y método para tratar cáncer con los mismos
|
EA020825B1
(ru)
|
2009-04-07 |
2015-02-27 |
Эмерити Фарма Аб |
Аналоги изоксазол-3(2h)-она в качестве терапевтических агентов
|
GB0906472D0
(en)
|
2009-04-15 |
2009-05-20 |
Astex Therapeutics Ltd |
New compounds
|
GB0906470D0
(en)
|
2009-04-15 |
2009-05-20 |
Astex Therapeutics Ltd |
New compounds
|
JP5531446B2
(ja)
|
2009-04-20 |
2014-06-25 |
コニカミノルタ株式会社 |
有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子材料、表示装置および照明装置
|
ES2347630B1
(es)
|
2009-04-29 |
2011-09-08 |
Universitat Ramon Llull |
Sintesis y usos de 4-cianopentanoatos y 4-cianopentenoatos sustituidos.
|
JP5656976B2
(ja)
|
2009-04-29 |
2015-01-21 |
ローカス ファーマシューティカルズ インコーポレイテッド |
ピロロトリアジン化合物
|
WO2010127212A1
(en)
|
2009-04-30 |
2010-11-04 |
Forest Laboratories Holdings Limited |
Inhibitors of acetyl-coa carboxylase
|
AR078411A1
(es)
|
2009-05-07 |
2011-11-09 |
Lilly Co Eli |
Compuesto de vinil imidazolilo y composicion farmaceutica que lo comprende
|
JP5600891B2
(ja)
|
2009-05-15 |
2014-10-08 |
コニカミノルタ株式会社 |
有機エレクトロルミネッセンス素子、表示装置および照明装置
|
JP5604808B2
(ja)
|
2009-05-20 |
2014-10-15 |
コニカミノルタ株式会社 |
有機エレクトロルミネッセンス素子、表示装置及び照明装置
|
JP5568889B2
(ja)
|
2009-05-22 |
2014-08-13 |
コニカミノルタ株式会社 |
有機エレクトロルミネッセンス素子、表示装置、照明装置及び有機エレクトロルミネッセンス素子材料
|
JP5629980B2
(ja)
|
2009-05-22 |
2014-11-26 |
コニカミノルタ株式会社 |
有機エレクトロルミネッセンス素子、表示装置及び照明装置
|
EP2435472A1
(en)
|
2009-05-27 |
2012-04-04 |
Københavns Universitet |
Fibroblast growth factor receptor-derived peptides binding to ncam
|
JP5499519B2
(ja)
|
2009-05-27 |
2014-05-21 |
コニカミノルタ株式会社 |
有機エレクトロルミネッセンス素子、表示装置及び照明装置
|
GB0910003D0
(en)
|
2009-06-11 |
2009-07-22 |
Univ Leuven Kath |
Novel compounds for the treatment of neurodegenerative diseases
|
JP5600894B2
(ja)
|
2009-06-24 |
2014-10-08 |
コニカミノルタ株式会社 |
白色有機エレクトロルミネッセンス素子、表示装置及び照明装置
|
SMT201700430T1
(it)
|
2009-06-25 |
2018-01-11 |
Alkermes Pharma Ireland Ltd |
Composti eterociclici per il trattamento di disturbi neurologici e psicologici
|
WO2011002038A1
(ja)
|
2009-06-30 |
2011-01-06 |
日本ゼオン株式会社 |
新規なジアリールアミン化合物、並びに、老化防止剤、ポリマー組成物、ゴム架橋物、及び、その成形品、並びに、ジアリールアミン化合物の製造方法
|
JPWO2011007819A1
(ja)
|
2009-07-17 |
2012-12-27 |
塩野義製薬株式会社 |
ラクタムまたはベンゼンスルホンアミド化合物を含有する医薬
|
WO2011011597A1
(en)
|
2009-07-24 |
2011-01-27 |
Duke University |
Prochelators useful for inhibiting metal-associated toxicity
|
FR2948568B1
(fr)
|
2009-07-30 |
2012-08-24 |
Sanofi Aventis |
Formulation pharmaceutique
|
TWI468402B
(zh)
|
2009-07-31 |
2015-01-11 |
必治妥美雅史谷比公司 |
降低β-類澱粉生成之化合物
|
BR112012002331A2
(pt)
|
2009-08-05 |
2019-09-24 |
Versitech Ltd |
composição antiviral, composição farmacêutica e uso de quantidade efetiva de composição farmacêutica
|
JP2012197231A
(ja)
|
2009-08-06 |
2012-10-18 |
Oncotherapy Science Ltd |
Ttk阻害作用を有するピリジンおよびピリミジン誘導体
|
WO2011016528A1
(ja)
|
2009-08-07 |
2011-02-10 |
中外製薬株式会社 |
アミノピラゾール誘導体
|
WO2011018894A1
(en)
|
2009-08-10 |
2011-02-17 |
Raqualia Pharma Inc. |
Pyrrolopyrimidine derivatives as potassium channel modulators
|
EA026693B1
(ru)
|
2009-08-17 |
2017-05-31 |
Интелликайн ЭлЭлСи |
Производные бензоксазола и бензотиазола в качестве ингибиторов pi3-киназы
|
JP5577650B2
(ja)
|
2009-08-24 |
2014-08-27 |
コニカミノルタ株式会社 |
有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子材料、表示装置及び照明装置
|
KR101184115B1
(ko)
|
2009-08-31 |
2012-09-18 |
일동제약주식회사 |
신규 펩티드 데포르밀라제 저해제 화합물 및 그 제조방법
|
KR101650981B1
(ko)
|
2009-09-03 |
2016-08-24 |
바이오에너제닉스 |
Pask의 억제를 위한 복소환 화합물
|
CN102596932A
(zh)
|
2009-09-04 |
2012-07-18 |
拜耳医药股份有限公司 |
作为酪氨酸苏氨酸激酶抑制剂的取代氨基喹喔啉
|
WO2011031740A1
(en)
|
2009-09-09 |
2011-03-17 |
Achaogen, Inc. |
Antibacterial fluoroquinolone analogs
|
US9481675B2
(en)
|
2009-09-11 |
2016-11-01 |
Merck Sharp & Dohme Corp. |
Gyrase inhibitors
|
WO2011035376A1
(en)
|
2009-09-24 |
2011-03-31 |
Romar Engineering Pty Ltd |
A mould or mould core and a method of manufacturing a mould or mould core
|
US8426438B2
(en)
|
2009-10-01 |
2013-04-23 |
Merck Sharp & Dohme Corp. |
Heterocyclic-fused pyrazolo[4,3-c]pyridin-3-one M1 receptor positive allosteric modulators
|
US8466155B2
(en)
|
2009-10-02 |
2013-06-18 |
Boehringer Ingelheim International Gmbh |
Pyrimidines
|
GB0917571D0
(en)
|
2009-10-07 |
2009-11-25 |
Karobio Ab |
Novel estrogen receptor ligands
|
EP2308866A1
(de)
|
2009-10-09 |
2011-04-13 |
Bayer CropScience AG |
Phenylpyri(mi)dinylpyrazole und ihre Verwendung als Fungizide
|
FR2951172B1
(fr)
|
2009-10-13 |
2014-09-26 |
Pf Medicament |
Derives pyrazolopyridines en tant qu'agent anticancereux
|
US20120232062A1
(en)
|
2009-10-20 |
2012-09-13 |
Eiger Biopharmaceuticals, Inc. |
Azaindazoles to treat flaviviridae virus infection
|
KR20110043270A
(ko)
|
2009-10-21 |
2011-04-27 |
(주)씨에스엘쏠라 |
유기발광화합물 및 이를 구비한 유기발광소자
|
SI2491035T1
(sl)
|
2009-10-22 |
2017-10-30 |
Gilead Sciences, Inc. |
Derivati purina ali deazapurina uporabni za zdravljenje (med drugimi) virusnih okužb
|
WO2011050245A1
(en)
|
2009-10-23 |
2011-04-28 |
Yangbo Feng |
Bicyclic heteroaryls as kinase inhibitors
|
MY177695A
(en)
|
2009-10-26 |
2020-09-23 |
Signal Pharm Llc |
Methods of synthesis and purification of heteroaryl compounds
|
WO2011051425A1
(en)
|
2009-10-30 |
2011-05-05 |
Novartis Ag |
N-oxide of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea
|
KR20110049217A
(ko)
|
2009-11-04 |
2011-05-12 |
다우어드밴스드디스플레이머티리얼 유한회사 |
신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자
|
GB0919432D0
(en)
|
2009-11-05 |
2009-12-23 |
Glaxosmithkline Llc |
Use
|
CN102695417A
(zh)
|
2009-11-06 |
2012-09-26 |
普莱希科公司 |
用于激酶调节的化合物和方法及其适应症
|
JP5740409B2
(ja)
|
2009-11-13 |
2015-06-24 |
ジェノスコ |
キナーゼ阻害剤
|
EP2501236B1
(en)
|
2009-11-18 |
2017-03-29 |
Plexxikon Inc. |
N-[2-fluoro-3-(4-amino-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-phenyl]-4-benzenesulfonamide derivatives as Raf protein kinase modulators for the treatment of cancer
|
JP2013032290A
(ja)
|
2009-11-20 |
2013-02-14 |
Dainippon Sumitomo Pharma Co Ltd |
新規縮合ピリミジン誘導体
|
US20120232073A1
(en)
|
2009-11-23 |
2012-09-13 |
Santhosh Francis Neelamkavil |
Fused bicyclic pyrimidine derivatives and methods of use thereof
|
WO2011066342A2
(en)
|
2009-11-24 |
2011-06-03 |
Amplimmune, Inc. |
Simultaneous inhibition of pd-l1/pd-l2
|
EP2332939A1
(en)
|
2009-11-26 |
2011-06-15 |
Æterna Zentaris GmbH |
Novel Naphthyridine derivatives and the use thereof as kinase inhibitors
|
RU2012127368A
(ru)
|
2009-12-01 |
2014-01-10 |
Эбботт Лэборетриз |
Новые трициклические соединения
|
JP2011116840A
(ja)
|
2009-12-02 |
2011-06-16 |
Fujifilm Corp |
顔料微粒子分散体、これを用いた光硬化性組成物及びカラーフィルタ
|
AR079257A1
(es)
|
2009-12-07 |
2012-01-04 |
Novartis Ag |
Formas cristalinas de 3-(2,6-dicloro-3-5-dimetoxi-fenil)-1-{6-[4-(4-etil-piperazin-1-il)-fenil-amino]-pirimidin-4-il}-1-metil-urea y sales de las mismas
|
US8759366B2
(en)
|
2009-12-17 |
2014-06-24 |
Merck Sharp & Dohme Corp. |
Aminopyrimidines as SYK inhibitors
|
EP2512476A1
(en)
|
2009-12-18 |
2012-10-24 |
Novartis AG |
Method for treating haematological cancers
|
ES2842399T3
(es)
|
2009-12-22 |
2021-07-14 |
Vertex Pharma |
Inhibidores isoindolinona de fosfatidilinositol 3-quinasa
|
WO2011079231A1
(en)
|
2009-12-23 |
2011-06-30 |
Gatekeeper Pharmaceutical, Inc. |
Compounds that modulate egfr activity and methods for treating or preventing conditions therewith
|
FR2954315B1
(fr)
|
2009-12-23 |
2012-02-24 |
Galderma Res & Dev |
Nouveaux derives phenoliques, et leur utilisation pharmaceutique ou cosmetique
|
FR2954317B1
(fr)
|
2009-12-23 |
2012-01-27 |
Galderma Res & Dev |
Nouveaux derives phenoliques, et leur utilisation pharmaceutique ou cosmetique
|
US20130096115A1
(en)
|
2009-12-28 |
2013-04-18 |
Afraxis, Inc. |
Methods for treating autism
|
JP2013515785A
(ja)
|
2009-12-29 |
2013-05-09 |
ポリエラ コーポレイション |
有機半導体としてのチオン酸化芳香族ビスイミドおよびそれを組み込む装置
|
WO2011080755A1
(en)
|
2009-12-29 |
2011-07-07 |
Advinus Therapeutics Private Limited |
Fused nitrogen heterocyclic compounds, process of preparation and uses thereof
|
US9180127B2
(en)
|
2009-12-29 |
2015-11-10 |
Dana-Farber Cancer Institute, Inc. |
Type II Raf kinase inhibitors
|
US8563567B2
(en)
|
2009-12-30 |
2013-10-22 |
Arqule, Inc. |
Substituted heterocyclic compounds
|
US8329705B2
(en)
|
2009-12-30 |
2012-12-11 |
Arqule, Inc. |
Substituted triazolo-pyrazine compounds
|
EP2519525A4
(en)
|
2009-12-30 |
2013-06-12 |
Arqule Inc |
SUBSTITUTED PYRROLO-AMINOPYRIMIDINE COMPOUNDS
|
CN102115026A
(zh)
|
2009-12-31 |
2011-07-06 |
清华大学 |
一维纳米结构、其制备方法及一维纳米结构作标记的方法
|
WO2011082400A2
(en)
|
2010-01-04 |
2011-07-07 |
President And Fellows Of Harvard College |
Modulators of immunoinhibitory receptor pd-1, and methods of use thereof
|
AR079975A1
(es)
|
2010-01-06 |
2012-03-07 |
British Columbia Cancer Agency |
Agentes terapeuticos derivados de bisfenol u metodos para su uso, composiciones farmaceuticas y uso de los mismos
|
KR101483215B1
(ko)
|
2010-01-29 |
2015-01-16 |
한미약품 주식회사 |
단백질 키나아제 저해활성을 갖는 비시클릭 헤테로아릴 유도체
|
WO2011094890A1
(en)
|
2010-02-02 |
2011-08-11 |
Argusina Inc. |
Phenylalanine derivatives and their use as non-peptide glp-1 receptor modulators
|
CA2789344A1
(en)
|
2010-02-15 |
2011-08-18 |
Jeremy Earle Wulff |
Synthesis of bicyclic compounds and method for their use as therapeutic agents
|
WO2011103196A1
(en)
|
2010-02-17 |
2011-08-25 |
Amgen Inc. |
Aryl carboxamide derivatives as sodium channel inhibitors for treatment of pain
|
SA111320200B1
(ar)
|
2010-02-17 |
2014-02-16 |
ديبيوفارم اس ايه |
مركبات ثنائية الحلقة واستخداماتها كمثبطات c-src/jak مزدوجة
|
US9433621B2
(en)
|
2010-02-18 |
2016-09-06 |
Merck Sharp & Dohme Corp. |
Substituted pyridine and pyrimidine derivatives and their use in treating viral infections
|
US9193728B2
(en)
|
2010-02-18 |
2015-11-24 |
Medivation Technologies, Inc. |
Fused tetracyclic pyrido [4,3-B] indole and pyrido [3,4-B] indole derivatives and methods of use
|
DE112011100604T5
(de)
|
2010-02-18 |
2013-01-31 |
Ntn Corporation |
Verdicker, Schmierfett, Verfahren zur Herstellung derselben und fettgeschmiertes Lager
|
UY33227A
(es)
|
2010-02-19 |
2011-09-30 |
Novartis Ag |
Compuestos de pirrolopirimidina como inhibidores de la cdk4/6
|
WO2011103557A1
(en)
|
2010-02-22 |
2011-08-25 |
Advanced Cancer Therapeutics, Llc |
Small molecule inhibitors of pfkfb3 and glycolytic flux and their methods of use as anti-cancer therapeutics
|
JP5662994B2
(ja)
|
2010-02-26 |
2015-02-04 |
新日鉄住金化学株式会社 |
有機電界発光素子
|
WO2011109237A2
(en)
|
2010-03-02 |
2011-09-09 |
Emory University |
Uses of noscapine and derivatives in subjects diagnosed with fap
|
WO2011111880A1
(ko)
|
2010-03-08 |
2011-09-15 |
주식회사 메디젠텍 |
세포핵에서 세포질로의 gsk3의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 gsk3 이동에 의해 발생되는 질환의 치료 또는 예방용 약학적 조성물
|
WO2011112687A2
(en)
|
2010-03-10 |
2011-09-15 |
Kalypsys, Inc. |
Heterocyclic inhibitors of histamine receptors for the treatment of disease
|
BR112012022943A2
(pt)
|
2010-03-11 |
2018-06-05 |
Gilead Connecticut Inc |
inibidores de syk de imidazopiridnas
|
KR20130006664A
(ko)
|
2010-03-16 |
2013-01-17 |
다나-파버 캔서 인스티튜트 인크. |
인다졸 화합물 및 그의 용도
|
EP2550266B1
(en)
|
2010-03-24 |
2018-05-09 |
Amitech Therapeutics Solutions, Inc. |
Heterocyclic compounds useful for kinase inhibition
|
WO2011123493A1
(en)
|
2010-03-31 |
2011-10-06 |
Bristol-Myers Squibb Company |
Substituted pyrrolotriazines as protein kinase inhibitors
|
CN102153551B
(zh)
|
2010-04-02 |
2012-04-25 |
济南海乐医药技术开发有限公司 |
基于吲唑或氮杂吲唑的双芳基脲或硫脲类结构抗肿瘤药物
|
JP5724204B2
(ja)
|
2010-04-07 |
2015-05-27 |
コニカミノルタ株式会社 |
有機エレクトロルミネッセンス素子、表示装置、及び照明装置
|
US8618095B2
(en)
|
2010-04-13 |
2013-12-31 |
Rigel Pharmaceuticals, Inc. |
2, 4-pyrimidinediamine compounds and prodrugs thereof and their uses
|
CN102844031A
(zh)
|
2010-04-16 |
2012-12-26 |
诺华有限公司 |
用于治疗肝癌的有机化合物
|
ES2545811T3
(es)
|
2010-04-22 |
2015-09-16 |
Janssen Pharmaceutica Nv |
Compuestos de indazol útiles como inhibidores de quetohexoquinasa
|
BR112012026641A2
(pt)
|
2010-04-23 |
2016-07-12 |
Kineta Inc |
compostos antivirais
|
AR081331A1
(es)
|
2010-04-23 |
2012-08-08 |
Cytokinetics Inc |
Amino- pirimidinas composiciones de las mismas y metodos para el uso de los mismos
|
US8481555B2
(en)
|
2010-04-30 |
2013-07-09 |
Bristol-Myers Squibb Company |
Aza-bicyclic amine N-oxide compounds as alpha-7 nicotinic acetylcholine receptor ligand pro-drugs
|
GB201007286D0
(en)
|
2010-04-30 |
2010-06-16 |
Astex Therapeutics Ltd |
New compounds
|
US8759398B2
(en)
|
2010-05-03 |
2014-06-24 |
Biolink Life Sciences, Inc. |
Phosphorus binder composition for treatment of hyperphosphatemia
|
US20130137709A1
(en)
|
2010-05-05 |
2013-05-30 |
Nathanael S. Gray |
Compounds that modulate EGFR activity and methods for treating or preventing conditions therewith
|
CA2798831A1
(en)
|
2010-05-11 |
2011-11-17 |
Pfizer Inc. |
Morpholine compounds as mineralocorticoid receptor antagonists
|
TWI513694B
(zh)
|
2010-05-11 |
2015-12-21 |
Amgen Inc |
抑制間變性淋巴瘤激酶的嘧啶化合物
|
EP2569012A4
(en)
|
2010-05-11 |
2013-10-30 |
Aveo Pharmaceuticals Inc |
ANTI-FGFR2 ANTIBODY
|
JP2013526542A
(ja)
|
2010-05-12 |
2013-06-24 |
アッヴィ・インコーポレイテッド |
キナーゼのインダゾール阻害薬
|
WO2011143475A1
(en)
|
2010-05-12 |
2011-11-17 |
Spectrum Pharmaceuticals, Inc. |
Lanthanum carbonate hydroxide, lanthanum oxycarbonate and methods of their manufacture and use
|
GB201008134D0
(en)
|
2010-05-14 |
2010-06-30 |
Medical Res Council Technology |
Compounds
|
WO2011147199A1
(en)
|
2010-05-28 |
2011-12-01 |
Versitech Limited |
Compounds and methods for treating viral infections
|
WO2011147198A1
(en)
|
2010-05-28 |
2011-12-01 |
Versitech Limited |
Compounds and methods for treatment of proliferative diseases
|
EP3075730B1
(en)
|
2010-06-04 |
2018-10-24 |
Genentech, Inc. |
Aminopyrimidine derivatives as lrrk2 modulators
|
WO2011153553A2
(en)
|
2010-06-04 |
2011-12-08 |
The Regents Of The University Of California |
Methods and compositions for kinase inhibition
|
WO2011155983A1
(en)
|
2010-06-07 |
2011-12-15 |
Bikam Pharmaceuticals Inc. |
Opsin-binding ligands, compositions and methods of use
|
TW201210597A
(en)
|
2010-06-09 |
2012-03-16 |
Gilead Sciences Inc |
Inhibitors of hepatitis C virus
|
US8299117B2
(en)
|
2010-06-16 |
2012-10-30 |
Metabolex Inc. |
GPR120 receptor agonists and uses thereof
|
CA2802344C
(en)
|
2010-06-18 |
2023-06-13 |
The Brigham And Women's Hospital, Inc. |
Bi-specific antibodies against tim-3 and pd-1 for immunotherapy in chronic immune conditions
|
EP2584903B1
(en)
|
2010-06-24 |
2018-10-24 |
Merck Sharp & Dohme Corp. |
Novel heterocyclic compounds as erk inhibitors
|
US8907053B2
(en)
|
2010-06-25 |
2014-12-09 |
Aurigene Discovery Technologies Limited |
Immunosuppression modulating compounds
|
KR101486782B1
(ko)
|
2010-06-27 |
2015-01-28 |
킹 사우드 유니버시티 |
무한 중첩된 해시 체인들에 의한 1회용 패스워드 인증
|
US8933070B2
(en)
|
2010-07-02 |
2015-01-13 |
University Health Network |
Methods of targeting PTEN mutant diseases and compositions therefor
|
US20130109682A1
(en)
|
2010-07-06 |
2013-05-02 |
Novartis Ag |
Cyclic ether compounds useful as kinase inhibitors
|
FR2962438B1
(fr)
|
2010-07-06 |
2012-08-17 |
Sanofi Aventis |
Derives d'indolizines, procedes de preparation et application en therapeutique
|
FR2962437B1
(fr)
|
2010-07-06 |
2012-08-17 |
Sanofi Aventis |
Derives d'imidazopyridine, leur procede de preparation et leur application en therapeutique
|
DE102010031127A1
(de)
|
2010-07-08 |
2012-01-12 |
Endress + Hauser Flowtec Ag |
Messaufnehmer eines thermischen Durchflussmessgeräts zur Ermittlung des Durchflusses eines Mediums durch ein Messrohr und Verfahren zu dessen Herstellung
|
AU2011276955B2
(en)
|
2010-07-09 |
2014-11-06 |
The Walter And Eliza Hall Institute Of Medical Research |
Protein kinase inhibitors and methods of treatment
|
WO2012009258A2
(en)
|
2010-07-13 |
2012-01-19 |
Edward Roberts |
Peptidomimetic galanin receptor modulators
|
US20130210807A1
(en)
|
2010-07-14 |
2013-08-15 |
Nigel J Liverton |
Tricyclic Compounds as Allosteric Modulators of Metabotropic Glutamate Receptors.
|
TW201206946A
(en)
|
2010-07-15 |
2012-02-16 |
Bristol Myers Squibb Co |
Compounds for the reduction of beta-amyloid production
|
CN103003262A
(zh)
|
2010-07-16 |
2013-03-27 |
协和发酵麒麟株式会社 |
含氮芳香族杂环衍生物
|
WO2012008564A1
(ja)
|
2010-07-16 |
2012-01-19 |
協和発酵キリン株式会社 |
含窒素芳香族複素環誘導体
|
JP5926727B2
(ja)
|
2010-07-28 |
2016-05-25 |
バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH |
置換イミダゾ[1,2−b]ピリダジン
|
EP2413140A1
(en)
|
2010-07-29 |
2012-02-01 |
Sanofi |
Method for identifying a compound having an antiarrhythmic effect as well as uses relating thereto
|
JP2013539206A
(ja)
|
2010-07-30 |
2013-10-17 |
ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド |
発光材料として電界発光化合物を使用する電界発光素子
|
WO2012019093A1
(en)
|
2010-08-05 |
2012-02-09 |
Human Biomolecular Research Institute |
Synthetic compounds and methods to decrease nicotine self-administration
|
US9051280B2
(en)
|
2010-08-13 |
2015-06-09 |
AbbVie Deutschland GmbH & Co. KG |
Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy
|
US8883839B2
(en)
|
2010-08-13 |
2014-11-11 |
Abbott Laboratories |
Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy
|
EP2608669B1
(en)
|
2010-08-23 |
2016-06-22 |
Merck Sharp & Dohme Corp. |
NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
WO2012027239A1
(en)
|
2010-08-23 |
2012-03-01 |
Schering Corporation |
NOVEL PYRAZOLO[1,5-a]PYRROLO[3,2-e]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
KR101837223B1
(ko)
|
2010-09-01 |
2018-03-09 |
질레드 코네티컷 인코포레이티드 |
피리디논/피라지논, 그의 제조 방법 및 사용 방법
|
KR101864908B1
(ko)
|
2010-09-01 |
2018-06-05 |
질레드 코네티컷 인코포레이티드 |
피리다지논, 그의 제조 방법 및 사용 방법
|
AR082799A1
(es)
|
2010-09-08 |
2013-01-09 |
Ucb Pharma Sa |
Derivados de quinolina y quinoxalina como inhibidores de quinasa
|
ES2548036T3
(es)
|
2010-09-08 |
2015-10-13 |
Glaxosmithkline Intellectual Property Development Limited |
Polimorfos y sales de N-[5-[4-(5-{[(2R,6S)-2,6-dimetil-4-morfolinil]metil}-1,3-oxazol-2-il)-1H-indazol-6-il]-2-(metiloxi)-3-piridinil]metanosulfonamida
|
JP5876051B2
(ja)
|
2010-09-08 |
2016-03-02 |
グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited |
インフルエンザウィルス感染の治療に使用するためのインダゾール誘導体
|
TWI541243B
(zh)
|
2010-09-10 |
2016-07-11 |
拜耳知識產權公司 |
經取代咪唑并嗒
|
KR20130103503A
(ko)
|
2010-09-14 |
2013-09-23 |
호도가야 가가쿠 고교 가부시키가이샤 |
전하 제어제 및 그것을 사용한 토너
|
CN102399233B
(zh)
|
2010-09-15 |
2014-08-13 |
山东轩竹医药科技有限公司 |
PI3K和mTOR双重抑制剂类化合物
|
CN102399220A
(zh)
|
2010-09-15 |
2012-04-04 |
黄振华 |
三并环类PI3K和mTOR双重抑制剂
|
WO2012036233A1
(ja)
|
2010-09-17 |
2012-03-22 |
塩野義製薬株式会社 |
メラニン凝集ホルモン受容体アンタゴニスト活性を有する縮合へテロ環誘導体
|
GB201015949D0
(en)
|
2010-09-22 |
2010-11-03 |
Medical Res Council Technology |
Compounds
|
JO3062B1
(ar)
|
2010-10-05 |
2017-03-15 |
Lilly Co Eli |
R)-(e)-2-(4-(2-(5-(1-(3، 5-داي كلورو بيريدين-4-يل)إيثوكسي)-1h-إندازول-3-يل)?ينيل)-1h-بيرازول-1-يل)إيثانول بلوري
|
US8937077B2
(en)
|
2010-10-22 |
2015-01-20 |
Merck Sharp & Dohme Corp. |
Bicyclic diamines as janus kinase inhibitors
|
KR102051881B1
(ko)
|
2010-10-25 |
2019-12-04 |
쥐원 쎄라퓨틱스, 인크. |
Cdk 억제제
|
JP2012092049A
(ja)
|
2010-10-27 |
2012-05-17 |
Sumitomo Chemical Co Ltd |
有害動物防除組成物及び有害動物の防除方法
|
EP2632466A4
(en)
|
2010-10-29 |
2014-03-19 |
Univ Emory |
CHINAZOLINE DERIVATIVES, COMPOSITIONS THEREOF AND USES THEREOF
|
WO2012061337A1
(en)
|
2010-11-02 |
2012-05-10 |
Exelixis, Inc. |
Fgfr2 modulators
|
US9242970B2
(en)
|
2010-11-10 |
2016-01-26 |
Actelion Pharmaceuticals Ltd. |
Lactam derivatives useful as orexin receptor antagonists
|
US20120115903A1
(en)
|
2010-11-10 |
2012-05-10 |
Gruenenthal Gmbh |
Substituted Heteroaromatic Carboxamide and Urea Compounds as Vanilloid Receptor Ligands
|
JP2012116825A
(ja)
|
2010-11-11 |
2012-06-21 |
Ehime Univ |
アセンジイミド化合物の製造方法
|
KR101171232B1
(ko)
|
2010-11-15 |
2012-08-06 |
단국대학교 산학협력단 |
스파이로 화합물 및 이를 포함하는 유기전계 발광소자
|
WO2012065297A1
(en)
|
2010-11-16 |
2012-05-24 |
Impact Therapeutics, Inc. |
3-ARYL-6-ARYL-[1,2,4]TRIAZOLO[4,3-a]PYRIDINES AS INHIBITORS OF CELL PROLIFERATION AND THE USE THEREOF
|
WO2012068343A1
(en)
|
2010-11-17 |
2012-05-24 |
Amgen Inc. |
Quinoline derivatives as pik3 inhibitors
|
AU2011330730B2
(en)
|
2010-11-18 |
2016-02-18 |
Kasina Laila Innova Pharmaceuticals Private Limited |
Substituted 4-(selenophen-2(or 3)-ylamino)pyrimidine compounds and methods of use thereof
|
GB201020179D0
(en)
|
2010-11-29 |
2011-01-12 |
Astex Therapeutics Ltd |
New compounds
|
WO2012078777A1
(en)
|
2010-12-09 |
2012-06-14 |
Amgen Inc. |
Bicyclic compounds as pim inhibitors
|
DK2835131T3
(en)
|
2010-12-14 |
2017-12-04 |
Electrophoretics Ltd |
Casein kinase 1 delta inhibitors (CK1 delta)
|
AU2011347711B2
(en)
|
2010-12-20 |
2017-02-02 |
Merck Serono S.A. |
Indazolyl triazole derivatives as IRAK inhibitors
|
BR112013015859A2
(pt)
|
2010-12-22 |
2018-11-21 |
Leo Laboratories Ltd |
composto, uso de um composto, métodos de prevenção, tratamento, melhora ou profilaxia de distúrbios fisiológicos ou doenças, e de tratamento ou melhora de indicações cosméticas, e, composição farmacêutica
|
EP2468258A1
(en)
|
2010-12-22 |
2012-06-27 |
LEK Pharmaceuticals d.d. |
Process for the preparation of a pharmaceutical composition comprising a low soluble pharmaceutically active ingredient
|
US8754114B2
(en)
|
2010-12-22 |
2014-06-17 |
Incyte Corporation |
Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
|
JP5845283B2
(ja)
|
2010-12-22 |
2016-01-20 |
レオ・ラボラトリーズ・リミテッドLeo Laboratories Limited |
インゲノール−3−アシラートiiiおよびインゲノール−3−カルバメート
|
WO2012083866A1
(en)
|
2010-12-22 |
2012-06-28 |
The Hong Kong Polytechnic University |
Quinoline derivatives as anti-cancer agents
|
MX2013007261A
(es)
|
2010-12-23 |
2013-11-04 |
Amgen Inc |
Compuestos heterociclicos y sus usos.
|
JP5691508B2
(ja)
|
2010-12-27 |
2015-04-01 |
Jnc株式会社 |
ジイミド化合物ならびにインクジェット用インクおよびその用途
|
KR101466150B1
(ko)
|
2010-12-31 |
2014-11-27 |
제일모직 주식회사 |
유기광전소자용 화합물 및 이를 포함하는 유기광전소자
|
EP2662378B1
(en)
|
2011-01-06 |
2018-10-10 |
JX Nippon Oil & Energy Corporation |
Imide compound, method for producing same, thickening agent for grease, and grease composition
|
US8362023B2
(en)
|
2011-01-19 |
2013-01-29 |
Hoffmann-La Roche Inc. |
Pyrazolo pyrimidines
|
FR2970967B1
(fr)
|
2011-01-27 |
2013-02-15 |
Pf Medicament |
Derives de type azaindazole ou diazaindazole comme medicament
|
EP2487159A1
(en)
|
2011-02-11 |
2012-08-15 |
MSD Oss B.V. |
RorgammaT inhibitors
|
WO2012112961A1
(en)
|
2011-02-18 |
2012-08-23 |
Medivation Technologies, Inc. |
Compounds and methods of treating hypertension
|
EP2678016B1
(en)
|
2011-02-23 |
2016-08-10 |
Intellikine, LLC |
Heterocyclic compounds and uses thereof
|
TWI532742B
(zh)
|
2011-02-28 |
2016-05-11 |
艾伯維有限公司 |
激酶之三環抑制劑
|
PH12013501878A1
(en)
|
2011-03-17 |
2013-10-14 |
Novartis Ag |
Fgfr and ligands thereof as biomarkers for breast cancer in hr positive subjects
|
PT2688887E
(pt)
|
2011-03-23 |
2015-07-06 |
Amgen Inc |
Inibidores duais tricíclicos fusionados de cdk 4/6 e flt3
|
ITPD20110091A1
(it)
|
2011-03-24 |
2012-09-25 |
Univ Padova |
Inibitori multitirosinchinasi utili per le patologie correlate: modelli farmacoforici, composti identificati tramite questi modelli, metodi per la loro preparazione, la loro formulazione e il loro impiego terapeutico.
|
US8802711B2
(en)
|
2011-03-25 |
2014-08-12 |
Abbvie Inc. |
TRPV1 antagonists
|
MX342240B
(es)
|
2011-04-07 |
2016-09-21 |
Genentech Inc |
Anticuerpos anti-fgfr4 y metodos de uso.
|
FR2974088A1
(fr)
|
2011-04-12 |
2012-10-19 |
Pf Medicament |
Composes pyrazolo[3,4-b]pyridines tri- et tetracycliques comme agent anticancereux
|
EP2710035B1
(en)
|
2011-05-16 |
2017-04-12 |
F. Hoffmann-La Roche AG |
Fgfr1 agonists and methods of use
|
WO2012158795A1
(en)
|
2011-05-17 |
2012-11-22 |
Principia Biopharma Inc. |
Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors
|
US20140288069A1
(en)
|
2011-05-17 |
2014-09-25 |
Bayer Intellectual Property Gmbh |
Amino-substituted imidazopyridazines as mknk1 kinase inhibitors
|
US20150182525A1
(en)
|
2011-05-19 |
2015-07-02 |
Novartis Ag |
4-Amino-5-Fluoro-3-[6-(4-Methylpiperazin-1-YL)-1H-Benzimidazol-2-YL]-1H-Quinolin-2-one for use in the Treatment of Adenoid Cystic Carcinoma
|
WO2012163942A1
(en)
|
2011-06-01 |
2012-12-06 |
Bayer Intellectual Property Gmbh |
Substituted aminoimidazopyridazines
|
TW201316991A
(zh)
|
2011-06-03 |
2013-05-01 |
Millennium Pharm Inc |
Mek抑制劑與奧諾拉(aurora)a激酶選擇性抑制劑之組合
|
US9543524B2
(en)
|
2011-06-13 |
2017-01-10 |
Lg Chem, Ltd. |
Compounds and organic electronic device using same
|
EP2723748B1
(en)
|
2011-06-22 |
2016-10-12 |
Bayer Intellectual Property GmbH |
Heterocyclyl aminoimidazopyridazines
|
US8846656B2
(en)
|
2011-07-22 |
2014-09-30 |
Novartis Ag |
Tetrahydropyrido-pyridine and tetrahydropyrido-pyrimidine compounds and use thereof as C5a receptor modulators
|
BR112014002472A2
(pt)
|
2011-08-12 |
2017-04-11 |
Nissan Chemical Ind Ltd |
"compostos heterocíclicos tricíclicos, seu uso, agente terapêutico para reumatismo articular e medicamento"
|
WO2013024002A1
(en)
|
2011-08-12 |
2013-02-21 |
F. Hoffmann-La Roche Ag |
PYRAZOLO[3,4-c]PYRIDINE COMPOUNDS AND METHODS OF USE
|
JP2013049251A
(ja)
|
2011-08-31 |
2013-03-14 |
Fujifilm Corp |
レーザー彫刻用レリーフ印刷版原版、並びに、レリーフ印刷版及びその製版方法
|
WO2013033981A1
(zh)
|
2011-09-06 |
2013-03-14 |
江苏先声药物研究有限公司 |
一类2,7-萘啶衍生物及其制备方法和应用
|
EP2755482B1
(en)
|
2011-09-15 |
2016-06-01 |
Merck Sharp & Dohme Corp. |
Combination of mk-1775 and mk-8776 for treating cancer
|
CN103814029B
(zh)
|
2011-09-23 |
2016-10-12 |
拜耳知识产权有限责任公司 |
取代的咪唑并哒嗪
|
US9376435B2
(en)
|
2011-09-23 |
2016-06-28 |
Jawaharlal Nehru Centre For Advanced Scientific Research |
Chromophores for the detection of volatile organic compounds
|
CA2862895A1
(en)
|
2011-09-30 |
2013-04-04 |
Kineta, Inc. |
Anti-viral compounds
|
UA111382C2
(uk)
|
2011-10-10 |
2016-04-25 |
Оріон Корпорейшн |
Інгібітори протеїнкінази
|
CA2850394C
(en)
|
2011-10-12 |
2019-05-21 |
University Health Network |
Indazole compounds as kinase inhibitors and method of treating cancer with same
|
KR101897044B1
(ko)
|
2011-10-20 |
2018-10-23 |
에스에프씨 주식회사 |
유기금속 화합물 및 이를 포함하는 유기전계발광소자
|
WO2013063003A1
(en)
|
2011-10-28 |
2013-05-02 |
Novartis Ag |
Method of treating gastrointestinal stromal tumors
|
CA2853095A1
(en)
|
2011-10-28 |
2013-05-02 |
Novartis Ag |
Method of treating gastrointestinal stromal tumors
|
WO2013088191A1
(en)
|
2011-12-12 |
2013-06-20 |
Institut National De La Sante Et De La Recherche Medicale (Inserm) |
Antagonist of the fibroblast growth factor receptor 3 (fgfr3) for use in the treatment or the prevention of skeletal disorders linked with abnormal activation of fgfr3
|
WO2013088266A1
(en)
|
2011-12-13 |
2013-06-20 |
Ecolab Usa Inc. |
Concentrated warewashing compositions and methods
|
FR2985257B1
(fr)
|
2011-12-28 |
2014-02-14 |
Sanofi Sa |
Composes dimeres agonistes des recepteurs des fgfs (fgfrs), leur procede de preparation et leur application en therapeutique
|
FR2985258A1
(fr)
|
2011-12-28 |
2013-07-05 |
Sanofi Sa |
Composes dimeres agonistes des recepteurs des fgfs (fgfrs), leur procede de preparation et leur application en therapeutique
|
WO2013109027A1
(ko)
|
2012-01-18 |
2013-07-25 |
덕산하이메탈(주) |
화합물, 이를 이용한 유기전기소자 및 그 전자 장치
|
US10026905B2
(en)
|
2012-01-18 |
2018-07-17 |
Duk San Neolux Co., Ltd. |
Compound, organic electric element using the same, and an electronic device thereof
|
MX351513B
(es)
|
2012-01-19 |
2017-10-17 |
Taiho Pharmaceutical Co Ltd |
Compuesto de alquinilbenceno 3,5-disustituido y sales del mismo.
|
CN104136439B
(zh)
|
2012-02-23 |
2017-01-18 |
拜耳知识产权有限责任公司 |
取代的苯并噻吩基‑吡咯并三嗪及其用途
|
JP2013179181A
(ja)
|
2012-02-28 |
2013-09-09 |
Sumitomo Chemical Co Ltd |
有機光電変換素子
|
PE20141974A1
(es)
|
2012-03-14 |
2014-12-12 |
Lupin Ltd |
Compuestos de heterociclilo
|
KR102126092B1
(ko)
|
2012-03-30 |
2020-06-24 |
노파르티스 아게 |
저인산혈증성 장애의 치료에 사용하기 위한 fgfr 억제제
|
JP5120580B1
(ja)
|
2012-05-14 |
2013-01-16 |
Jsr株式会社 |
液晶配向剤
|
US10292816B2
(en)
|
2012-05-20 |
2019-05-21 |
Tel Hashomer Medical Research Infrastructure And Services Ltd. |
Prosthetic mitral valve
|
DK3176170T3
(en)
|
2012-06-13 |
2019-01-28 |
Incyte Holdings Corp |
SUBSTITUTED TRICYCLIC RELATIONS AS FGFR INHIBITORS
|
CA2878251A1
(en)
|
2012-07-11 |
2014-01-16 |
Novartis Ag |
Method of treating gastrointestinal stromal tumors
|
RU2019102203A
(ru)
|
2012-07-11 |
2019-03-05 |
Блюпринт Медсинс Корпорейшн |
Ингибиторы рецептора фактора роста фибробластов
|
WO2014019186A1
(en)
|
2012-08-02 |
2014-02-06 |
Merck Sharp & Dohme Corp. |
Antidiabetic tricyclic compounds
|
JP2015525782A
(ja)
|
2012-08-02 |
2015-09-07 |
メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. |
抗糖尿病性三環式化合物
|
US9388185B2
(en)
|
2012-08-10 |
2016-07-12 |
Incyte Holdings Corporation |
Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
|
KR101985259B1
(ko)
|
2012-08-10 |
2019-06-03 |
제이에스알 가부시끼가이샤 |
액정 배향제 및 화합물
|
WO2014044846A1
(en)
|
2012-09-24 |
2014-03-27 |
Evotec (Uk) Ltd. |
3-(aryl- or heteroaryl-amino)-7-(3,5-dimethoxyphenyl)isoquinoline derivatives as fgfr inhibitors useful for the treatment of proliferative disorders or dysplasia
|
WO2014048878A1
(en)
|
2012-09-26 |
2014-04-03 |
Evotec (Uk) Ltd. |
Phenyl- or pyridyl- pyrrolo[2,3b]pyrazine derivatives useful in the treatment or prevention of proliferative disorders or dysplasia
|
WO2014062454A1
(en)
|
2012-10-15 |
2014-04-24 |
Merck Sharp & Dohme Corp. |
Compositions and methods for treating cancer
|
KR102000211B1
(ko)
|
2012-10-29 |
2019-09-30 |
삼성디스플레이 주식회사 |
유기금속 화합물 및 이를 포함한 유기 발광 소자
|
US20140148548A1
(en)
|
2012-11-28 |
2014-05-29 |
Central Glass Company, Limited |
Fluorine-Containing Polymerizable Monomer And Polymer Compound Using Same
|
CA2892361A1
(en)
|
2012-11-28 |
2014-06-05 |
Merck Sharp & Dohme Corp. |
Use of a wee1 inhibitor for treating a cancer characterized by low pkmyt1 expression levels
|
WO2014089913A1
(zh)
|
2012-12-12 |
2014-06-19 |
山东亨利医药科技有限责任公司 |
作为酪氨酸激酶抑制剂的并环化合物
|
US9266892B2
(en)
|
2012-12-19 |
2016-02-23 |
Incyte Holdings Corporation |
Fused pyrazoles as FGFR inhibitors
|
WO2014105849A1
(en)
|
2012-12-28 |
2014-07-03 |
Xoma (Us) Llc |
Antibodies specific for fgfr4 and methods of use
|
TWI629266B
(zh)
|
2012-12-28 |
2018-07-11 |
藍印藥品公司 |
纖維母細胞生長因子受體之抑制劑
|
KR102030587B1
(ko)
|
2013-01-09 |
2019-10-10 |
에스에프씨주식회사 |
두 개의 나프틸기를 포함하는 비대칭 안트라센 유도체 및 이를 포함하는 유기 발광 소자
|
EP2945623B1
(en)
|
2013-01-15 |
2018-09-05 |
Suzhou Kintor Pharmaceuticals, Inc. |
Hedgehog pathway signaling inhibitors and therapeutic applications thereof
|
CN103694236B
(zh)
|
2013-01-15 |
2017-05-31 |
苏州开拓药业股份有限公司 |
一种嘧啶骨架具有刺猬通路拮抗剂活性的抗肿瘤化合物
|
KR101456626B1
(ko)
|
2013-02-01 |
2014-11-03 |
대영이앤비 주식회사 |
냉장고 부압 방지 장치
|
JP6311093B2
(ja)
|
2013-03-07 |
2018-04-18 |
国立大学法人九州大学 |
超分子複合体、発光体、および有機化合物検出用のセンサー素子
|
WO2014138485A1
(en)
|
2013-03-08 |
2014-09-12 |
Irm Llc |
Ex vivo production of platelets from hematopoietic stem cells and the product thereof
|
US9498532B2
(en)
|
2013-03-13 |
2016-11-22 |
Novartis Ag |
Antibody drug conjugates
|
US9771327B2
(en)
|
2013-03-13 |
2017-09-26 |
Flatley Discovery Lab, Llc |
Compounds and methods for the treatment of cystic fibrosis
|
MX2015012008A
(es)
|
2013-03-14 |
2016-04-15 |
Abbvie Deutschland |
Compuestos inhibidores novedosos de fosfodiesterasa tipo 10a.
|
EP2970231A1
(en)
|
2013-03-15 |
2016-01-20 |
Blueprint Medicines Corporation |
Piperazine derivatives and their use as kit modulators
|
UA120248C2
(uk)
|
2013-03-15 |
2019-11-11 |
Селджен Кар Ллс |
Гетероарильні сполуки та їх застосування
|
MX374558B
(es)
|
2013-03-15 |
2025-03-06 |
Sanofi Sa |
Compuestos de heteroarilo y sus usos.
|
AR095464A1
(es)
|
2013-03-15 |
2015-10-21 |
Celgene Avilomics Res Inc |
Compuestos de heteroarilo y usos de los mismos
|
TWI628176B
(zh)
|
2013-04-04 |
2018-07-01 |
奧利安公司 |
蛋白質激酶抑制劑
|
KR101573611B1
(ko)
|
2013-04-17 |
2015-12-01 |
주식회사 엘지화학 |
플러렌 유도체, 이를 이용한 유기 태양 전지 및 이의 제조 방법
|
WO2014170063A1
(en)
|
2013-04-19 |
2014-10-23 |
Covagen Ag |
Novel bispecific binding molecules with antitumoral activity
|
CA3130452C
(en)
|
2013-04-19 |
2023-10-31 |
Incyte Holdings Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
GB201307577D0
(en)
|
2013-04-26 |
2013-06-12 |
Astex Therapeutics Ltd |
New compounds
|
WO2014182829A1
(en)
|
2013-05-09 |
2014-11-13 |
Principia Biopharma Inc. |
Quinolone derivatives as fibroblast growth factor inhibitors
|
WO2014198942A1
(en)
|
2013-06-14 |
2014-12-18 |
Sanofi |
Pyrazolopyridine derivatives for use in the treatment of bladder cancer
|
US9670231B2
(en)
|
2013-06-28 |
2017-06-06 |
Beigene, Ltd. |
Fused tricyclic amide compounds as multiple kinase inhibitors
|
SG11201600147TA
(en)
|
2013-06-28 |
2016-02-26 |
Beigene Ltd |
Fused tricyclic urea compounds as raf kinase and/or raf kinase dimer inhibitors
|
RU2016103149A
(ru)
|
2013-07-02 |
2017-08-07 |
Зингента Партисипейшнс Аг |
Пестицидно-активные би-или трициклические гетероциклы с серосодержащими заместителями
|
WO2015006492A1
(en)
|
2013-07-09 |
2015-01-15 |
Dana-Farber Cancer Institute, Inc. |
Kinase inhibitors for the treatment of disease
|
JP6018547B2
(ja)
|
2013-07-09 |
2016-11-02 |
大成ロテック株式会社 |
舗装機械
|
AU2014287016B2
(en)
|
2013-07-11 |
2018-11-01 |
Acea Biosciences Inc. |
Pyrimidine derivatives as kinase inhibitors
|
AR097455A1
(es)
|
2013-08-28 |
2016-03-16 |
Astellas Pharma Inc |
Composición farmacéutica que contiene compuesto de pirimidina como un ingrediente activo
|
DK3057943T3
(en)
|
2013-10-18 |
2018-07-30 |
Eisai R&D Man Co Ltd |
PYRIMIDINE-FGFR4 INHIBITORS
|
EA028819B1
(ru)
|
2013-10-25 |
2018-01-31 |
Новартис Аг |
Производные бициклического пиридила с конденсированными кольцами в качестве ингибиторов fgfr4
|
ES2924111T3
(es)
|
2013-10-25 |
2022-10-04 |
Blueprint Medicines Corp |
Inhibidores del receptor del factor de crecimiento de fibroblastos
|
FR3012330B1
(fr)
|
2013-10-29 |
2015-10-23 |
Oreal |
Composition biphase comprenant un ester d'acide gras et de sucre ou un alkylpolyglucoside liquide, de hlb < 8, et un alcane ramifie en c8-c18
|
WO2015066452A2
(en)
|
2013-11-01 |
2015-05-07 |
Foundation Medicine, Inc. |
Methods of treating pediatric cancers
|
WO2015108992A1
(en)
|
2014-01-15 |
2015-07-23 |
Blueprint Medicines Corporation |
Heterobicyclic compounds and their use as fgfr4 receptor inhibitors
|
CN105524048B
(zh)
|
2014-08-19 |
2019-11-12 |
上海海和药物研究开发有限公司 |
作为fgfr激酶抑制剂的吲唑类化合物及其制备和应用
|
CN104262330B
(zh)
|
2014-08-27 |
2016-09-14 |
广东东阳光药业有限公司 |
一种脲取代联苯类化合物及其组合物及用途
|
MX2017003664A
(es)
|
2014-09-19 |
2017-07-13 |
Bayer Pharma AG |
Indazoles sustituidos con benzilo como inhibidores de bub1.
|
WO2016064960A1
(en)
|
2014-10-22 |
2016-04-28 |
Incyte Corporation |
Bicyclic heterocycles as fgfr4 inhibitors
|
US10851105B2
(en)
|
2014-10-22 |
2020-12-01 |
Incyte Corporation |
Bicyclic heterocycles as FGFR4 inhibitors
|
MX373169B
(es)
|
2015-02-20 |
2020-04-24 |
Incyte Holdings Corp |
Heterociclos bicíclicos como inhibidores de receptores del factor de crecimiento fibroblástico (fgfr).
|
MX2017010638A
(es)
|
2015-02-20 |
2018-05-07 |
Univ Oregon Health & Science |
Derivados de sobetiroma.
|
MA41551A
(fr)
|
2015-02-20 |
2017-12-26 |
Incyte Corp |
Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
|
US9580423B2
(en)
|
2015-02-20 |
2017-02-28 |
Incyte Corporation |
Bicyclic heterocycles as FGFR4 inhibitors
|
WO2016192680A1
(en)
|
2015-06-03 |
2016-12-08 |
Triastek, Inc. |
Dosage forms and use thereof
|
SG10201912066SA
(en)
|
2015-07-15 |
2020-02-27 |
Protagonist Therapeutics Inc |
Peptide inhibitors of interleukin-23 receptor and their use to treat inflammatory diseases
|
MY189596A
(en)
|
2015-07-15 |
2022-02-18 |
Immatics Biotechnologies Gmbh |
A novel peptides for use in immunotherapy against epithelial ovarian cancer and other cancers
|
DE112016003168B4
(de)
|
2015-07-15 |
2024-08-08 |
Cabot Corporation |
Verfahren zum herstellen eines silica-elastomerkomposits, und dieses enthaltende produkte
|
CN107580598B
(zh)
|
2015-07-15 |
2020-11-13 |
豪夫迈·罗氏有限公司 |
作为代谢型谷氨酸受体调节剂的乙炔基衍生物
|
CR20220194A
(es)
|
2015-07-30 |
2022-06-16 |
Macrogenics Inc |
Moléculas de unión a pd-1 y métodos de uso de las mismas
|
WO2017023972A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
US10519169B2
(en)
|
2015-08-03 |
2019-12-31 |
Samumed, Llc |
3-(1H-pyrrolo[2,3-C]pyridin-2-yl)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
US10188634B2
(en)
|
2015-08-03 |
2019-01-29 |
Samumed, Llc |
3-(3H-imidazo[4,5-C]pyridin-2-yl)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
WO2017023989A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(1h-benzo[d]imidazol-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
US10231956B2
(en)
|
2015-08-03 |
2019-03-19 |
Samumed, Llc |
3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
WO2017024004A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(1h-pyrrolo[2,3-b]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
US10329309B2
(en)
|
2015-08-03 |
2019-06-25 |
Samumed, Llc |
3-(3H-imidazo[4,5-B]pyridin-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
WO2017028314A1
(en)
|
2015-08-20 |
2017-02-23 |
Changzhou Jiekai Pharmatech Co., Ltd. |
Pyrazolo fused heterocyclic compounds as erk inhibitors
|
WO2017058915A1
(en)
|
2015-09-28 |
2017-04-06 |
Araxes Pharma Llc |
Inhibitors of kras g12c mutant proteins
|
ES2928164T3
(es)
|
2015-10-19 |
2022-11-15 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
EP3365335B1
(en)
|
2015-10-23 |
2024-02-14 |
Array Biopharma, Inc. |
2-aryl- and 2-heteroaryl-substituted 2-pyridazin-3(2h)-one compounds as inhibitors of fgfr tyrosine kinases
|
CA3005727A1
(en)
|
2015-11-19 |
2017-05-26 |
Incyte Corporation |
Substituted 2-methylbiphenyl-3-yl heterocyclic compounds and pharmaceutical compositions thereof useful as immunomodulators
|
MA44075A
(fr)
|
2015-12-17 |
2021-05-19 |
Incyte Corp |
Dérivés de n-phényl-pyridine-2-carboxamide et leur utilisation en tant que modulateurs des interactions protéine/protéine pd-1/pd-l1
|
SMT202000694T1
(it)
|
2015-12-22 |
2021-03-15 |
Incyte Corp |
Composti eterociclici come immunomodulatori
|
AR108396A1
(es)
|
2016-05-06 |
2018-08-15 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
US20170342060A1
(en)
|
2016-05-26 |
2017-11-30 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
EP4137489A1
(en)
|
2016-06-20 |
2023-02-22 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
US10138248B2
(en)
|
2016-06-24 |
2018-11-27 |
Incyte Corporation |
Substituted imidazo[2,1-f][1,2,4]triazines, substituted imidazo[1,2-a]pyridines, substituted imidazo[1,2-b]pyridazines and substituted imidazo[1,2-a]pyrazines as PI3K-γ inhibitors
|
MA45669A
(fr)
|
2016-07-14 |
2019-05-22 |
Incyte Corp |
Composés hétérocycliques utilisés comme immunomodulateurs
|
MA46045A
(fr)
|
2016-08-29 |
2021-04-28 |
Incyte Corp |
Composés hétérocycliques utilisés comme immunomodulateurs
|
WO2018041091A1
(en)
|
2016-08-30 |
2018-03-08 |
Sunshine Lake Pharma Co., Ltd. |
Inhibitors of influenza virus replication, application methods and uses thereof
|
WO2018049214A1
(en)
|
2016-09-09 |
2018-03-15 |
Incyte Corporation |
Pyrazolopyridine derivatives as hpk1 modulators and uses thereof for the treatment of cancer
|
KR20190075931A
(ko)
|
2016-10-05 |
2019-07-01 |
제노 로얄티즈 앤 마일스톤즈, 엘엘씨 |
스피로 고리 화합물
|
KR101755556B1
(ko)
|
2016-11-18 |
2017-07-07 |
주식회사 케마스 |
육산화사비소의 결정다형을 포함하는 뇌암 예방 또는 치료용 약학 조성물 및 이의 제조방법
|
KR101834366B1
(ko)
|
2016-11-21 |
2018-03-05 |
주식회사 케마스 |
육산화사비소의 결정다형을 포함하는 유방암 예방 또는 치료용 약학 조성물 및 이의 제조방법
|
KR101844049B1
(ko)
|
2016-12-05 |
2018-03-30 |
주식회사 케마스 |
육산화사비소의 결정다형을 포함하는 간암 예방 또는 치료용 약학 조성물
|
KR101844050B1
(ko)
|
2016-12-09 |
2018-05-14 |
주식회사 케마스 |
육산화사비소의 결정다형을 포함하는 암 예방 또는 치료용 약학 조성물
|
EP3558989B1
(en)
|
2016-12-22 |
2021-04-14 |
Incyte Corporation |
Triazolo[1,5-a]pyridine derivatives as immunomodulators
|
US20180177784A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
US20180179202A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
MA47120A
(fr)
|
2016-12-22 |
2021-04-28 |
Incyte Corp |
Dérivés pyridine utilisés en tant qu'immunomodulateurs
|
LT3558990T
(lt)
|
2016-12-22 |
2022-12-27 |
Incyte Corporation |
Tetrahidroimidazo[4,5-c]piridino dariniai kaip pd-l1 internalizavimo induktoriai
|
MX391981B
(es)
|
2016-12-22 |
2025-03-21 |
Incyte Corp |
Derivados de benzooxazol como inmunomoduladores.
|
AR111960A1
(es)
|
2017-05-26 |
2019-09-04 |
Incyte Corp |
Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
|
WO2018234354A1
(en)
|
2017-06-20 |
2018-12-27 |
Grünenthal GmbH |
NOVEL SUBSTITUTED 3-INDOLE AND 3-INDAZOLE COMPOUNDS AS PHOSPHODIESTERASE INHIBITORS
|
US11242334B2
(en)
|
2017-08-22 |
2022-02-08 |
Js Innopharm (Shanghai) Ltd. |
Heterocyclic compounds as kinase inhibitors, compositions comprising the heterocyclic compound, and methods of use thereof
|
US10793551B2
(en)
|
2017-10-19 |
2020-10-06 |
Effector Therapeutics Inc. |
Benzimidazole-indole inhibitors of Mnk1 and Mnk2
|
JP7326276B2
(ja)
|
2017-12-02 |
2023-08-15 |
ガラパゴス・ナムローゼ・フェンノートシャップ |
新規化合物及び疾患の治療のためのその医薬組成物
|
CN112135824B
(zh)
|
2018-03-30 |
2024-11-05 |
因赛特公司 |
作为免疫调节剂的杂环化合物
|
AU2019262579B2
(en)
|
2018-05-04 |
2024-09-12 |
Incyte Corporation |
Salts of an FGFR inhibitor
|
CN112867716B
(zh)
|
2018-05-04 |
2024-09-13 |
因赛特公司 |
Fgfr抑制剂的固体形式和其制备方法
|
SG11202011165TA
(en)
|
2018-05-11 |
2020-12-30 |
Incyte Corp |
Tetrahydro-imidazo[4,5-c]pyridine derivatives as pd-l1 immunomodulators
|
WO2020037004A1
(en)
|
2018-08-14 |
2020-02-20 |
Osteoqc Inc. |
Pyrrolo - dipyridine compounds
|
IL281212B2
(en)
|
2018-09-07 |
2023-12-01 |
Merck Patent Gmbh |
The history of 5-morpholine-4-yl-pyrazolo[[4,3-Bpyridine and their use
|
WO2020081898A1
(en)
|
2018-10-20 |
2020-04-23 |
The Johns Hopkins University |
Non-invasive urinary biomarkers for the detection of urothelial carcinoma of the bladder
|
JP2022515198A
(ja)
|
2018-12-19 |
2022-02-17 |
アレイ バイオファーマ インコーポレイテッド |
FGFRチロシンキナーゼの阻害剤としての置換ピラゾロ[1,5-a]ピリジン化合物
|
EP3898615A1
(en)
|
2018-12-19 |
2021-10-27 |
Array Biopharma, Inc. |
7-((3,5-dimethoxyphenyl)amino)quinoxaline derivatives as fgfr inhibitors for treating cancer
|
US11628162B2
(en)
|
2019-03-08 |
2023-04-18 |
Incyte Corporation |
Methods of treating cancer with an FGFR inhibitor
|
WO2021007269A1
(en)
|
2019-07-09 |
2021-01-14 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
US12122767B2
(en)
|
2019-10-01 |
2024-10-22 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
PH12022550892A1
(en)
|
2019-10-14 |
2023-05-03 |
Incyte Corp |
Bicyclic heterocycles as fgfr inhibitors
|
US11566028B2
(en)
|
2019-10-16 |
2023-01-31 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
CA3162010A1
(en)
|
2019-12-04 |
2021-06-10 |
Incyte Corporation |
Derivatives of an fgfr inhibitor
|
CA3163875A1
(en)
|
2019-12-04 |
2021-06-10 |
Incyte Corporation |
Tricyclic heterocycles as fgfr inhibitors
|
WO2021146424A1
(en)
|
2020-01-15 |
2021-07-22 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
JP2024513575A
(ja)
|
2021-04-12 |
2024-03-26 |
インサイト・コーポレイション |
Fgfr阻害剤及びネクチン-4標的化剤を含む併用療法
|