DE280853C
(es)
|
|
|
|
|
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
|
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
|
JPS522706Y2
(es)
|
1974-07-31 |
1977-01-21 |
|
|
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
|
JPS6336665U
(es)
|
1986-08-27 |
1988-03-09 |
|
|
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
|
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
|
CA2072560A1
(en)
|
1989-12-28 |
1991-06-29 |
Hans-Tobias Macholdt |
Biscationic acid amide and acid imide derivatives as charge controllers
|
WO1991009835A1
(de)
|
1989-12-28 |
1991-07-11 |
Hoechst Aktiengesellschaft |
Biskationische säureamid- und -imidderivative und verfahren zu ihrer herstellung
|
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
|
EP0552197B1
(en)
|
1990-10-03 |
1999-01-13 |
Commonwealth Scientific And Industrial Research Organisation |
Epoxy resins based on diaminobisimide compounds
|
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
|
WO1992022552A1
(en)
|
1991-06-14 |
1992-12-23 |
The Upjohn Company |
IMIDAZO[1,5-a]QUINOXALINES
|
DE4119767A1
(de)
|
1991-06-15 |
1992-12-17 |
Dresden Arzneimittel |
Verfahren zur herstellung von (pyrimid-2-yl-thio- bzw. seleno)-essigsaeurederivaten
|
JP3120127B2
(ja)
|
1991-10-24 |
2000-12-25 |
松下電工株式会社 |
複合型火災感知器
|
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
|
JPH07506836A
(ja)
|
1992-05-28 |
1995-07-27 |
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 |
ビスマレイミド化合物
|
CA2150566A1
(en)
|
1992-12-07 |
1994-06-23 |
Jonathan Howard Hodgkin |
Bisnadimides
|
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
|
JPH06336665A
(ja)
|
1993-05-27 |
1994-12-06 |
Kobe Steel Ltd |
耐黒変性に優れた溶融Zn−Al合金めっき鋼板の製 造方法
|
US5536725A
(en)
|
1993-08-25 |
1996-07-16 |
Fmc Corporation |
Insecticidal substituted-2,4-diamino-5,6,7,8-tetrahydroquinazolines
|
ATE212985T1
(de)
|
1993-11-30 |
2002-02-15 |
Searle & Co |
Tricyclische,substituierte pyrazolyl- benzolsulfonamide und ihre verwendung als cyclooxygenase ii inhibitoren
|
PT746320E
(pt)
|
1994-02-02 |
2001-05-31 |
Lilly Co Eli |
Intermediarios e inibidores da protease de hiv
|
US5480887A
(en)
|
1994-02-02 |
1996-01-02 |
Eli Lilly And Company |
Protease inhibitors
|
RU2191188C2
(ru)
|
1994-11-14 |
2002-10-20 |
Варнер-Ламберт Компани |
Производные 6-арилпиридо[2,3-d]-пиримидины и -нафтиридины, фармацевтическая композиция, обладающая ингибирующим действием клеточной пролиферации, вызываемой протеиновой тирозинкиназой, и способ ингибирования клеточной пролиферации
|
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
|
US6492520B1
(en)
|
1996-08-06 |
2002-12-10 |
Pfizer Inc |
Substituted pyrido-or pyrimido-containing 6,6- or 6,7-bicyclic derivatives
|
US6184235B1
(en)
|
1996-08-14 |
2001-02-06 |
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
|
KR20000070751A
(ko)
|
1997-02-05 |
2000-11-25 |
로즈 암스트롱, 크리스틴 에이. 트러트웨인 |
세포 증식 억제제로서의 피리도[2,3-d]피리미딘 및 4-아미노피리미딘
|
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
|
ATE286886T1
(de)
|
1997-05-28 |
2005-01-15 |
Aventis Pharma Inc |
Chinolin- und chinoxalin-verbindungen die den von blutplättchen abstammmenden wachstumsfaktor und/oder pdgf- und p56lck-tyrosin-kinase hemmen
|
GB9716231D0
(en)
|
1997-07-31 |
1997-10-08 |
Amersham Int Ltd |
Base analogues
|
CA2300478A1
(en)
|
1997-08-11 |
1999-02-18 |
Cor Therapeutics, Inc. |
Selective factor xa inhibitors
|
ATE286053T1
(de)
|
1997-08-20 |
2005-01-15 |
Warner Lambert Co |
Naphthyridinone zur hemmung der durch protein- tyrosin-kinase und zellzyklus kinase hervorgerufenen zellvermehrung
|
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
|
CA2316944A1
(en)
|
1998-02-20 |
1999-08-26 |
Mitsuru Shiraishi |
Aminoguanidinehydrazone derivative, production and use thereof
|
JP2002515490A
(ja)
|
1998-05-15 |
2002-05-28 |
ギルフォード ファーマシューティカルズ インコーポレイテッド |
Parp活性を抑制する縮合三環化合物
|
IL139599A0
(en)
|
1998-05-26 |
2002-02-10 |
Warner Lambert Co |
Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation
|
US20040044012A1
(en)
|
1998-05-26 |
2004-03-04 |
Dobrusin Ellen Myra |
Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation
|
EP1086085A1
(en)
|
1998-06-12 |
2001-03-28 |
Vertex Pharmaceuticals Incorporated |
INHIBITORS OF p38
|
CA2339961C
(en)
|
1998-08-11 |
2009-01-20 |
Novartis Ag |
Isoquinoline derivatives with angiogenesis inhibiting activity
|
JP2000123973A
(ja)
|
1998-10-09 |
2000-04-28 |
Canon Inc |
有機発光素子
|
GB9823103D0
(en)
|
1998-10-23 |
1998-12-16 |
Pfizer Ltd |
Pharmaceutically active compounds
|
PL347432A1
(en)
|
1998-10-23 |
2002-04-08 |
Hoffmann La Roche |
Bicyclic nitrogen heterocycles
|
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
|
CA2384188C
(en)
|
1999-09-24 |
2008-06-17 |
Janssen Pharmaceutica N.V. |
Antiviral compositions
|
DE19946289A1
(de)
|
1999-09-28 |
2001-03-29 |
Basf Ag |
Benzodiazepin-Derivate, deren Herstellung und Anwendung
|
KR100537241B1
(ko)
|
1999-10-21 |
2005-12-19 |
에프. 호프만-라 로슈 아게 |
P38 단백질 키나제의 억제제로서의 알킬아미노 치환된이중고리 질소 헤테로고리 화합물
|
AU776250B2
(en)
|
1999-10-21 |
2004-09-02 |
F. Hoffmann-La Roche Ag |
Heteroalkylamino-substituted bicyclic nitrogen heterocycles as inhibitors of P38 protein kinase
|
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
|
DE60033316T2
(de)
|
1999-12-29 |
2007-11-22 |
Wyeth |
Tricyclische proteinkinasehemmer
|
ATE398110T1
(de)
|
2000-01-24 |
2008-07-15 |
Warner Lambert Co |
3-aminochinazolin-2,4-dione als antibakterielle mittel
|
AU1808601A
(en)
|
2000-01-27 |
2001-08-07 |
Warner-Lambert Company |
Pyridopyrimidinone derivatives for treatment of neurodegenerative disease
|
ATE372337T1
(de)
|
2000-02-01 |
2007-09-15 |
Abbott Gmbh & Co Kg |
Heterozyklische verbindungen und deren anwendung als parp-inhibitoren
|
EP1257550B1
(en)
|
2000-02-04 |
2005-11-16 |
Portola Pharmaceuticals, Inc. |
Platelet adp receptor inhibitors
|
EP1254138B1
(en)
|
2000-02-09 |
2005-05-11 |
Novartis AG |
Pyridine derivatives inhibiting angiogenesis and/or vegf receptor tyrosine kinase
|
GB0004890D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
DE60112268T2
(de)
|
2000-03-06 |
2006-05-24 |
Astrazeneca Ab |
Verwendung von quinazolinderivate als inhibitoren der angiogenese
|
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
|
DE10012549A1
(de)
|
2000-03-15 |
2001-09-20 |
Bayer Ag |
Arzneimittel gegen virale Erkrankungen
|
AU2001259190B2
(en)
|
2000-04-28 |
2007-01-25 |
Acadia Pharmaceuticals, Inc. |
Muscarinic agonists
|
WO2001085722A1
(en)
|
2000-05-05 |
2001-11-15 |
Cor Therapeutics, 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
|
CN1321628C
(zh)
|
2000-06-28 |
2007-06-20 |
史密斯克莱·比奇曼公司 |
湿磨方法
|
US20050009876A1
(en)
|
2000-07-31 |
2005-01-13 |
Bhagwat Shripad S. |
Indazole compounds, compositions thereof and methods of treatment therewith
|
CN1468241A
(zh)
|
2000-08-07 |
2004-01-14 |
|
作为gabaa受体配体的杂环化合物
|
MXPA03001422A
(es)
|
2000-08-14 |
2004-01-26 |
Johnson & Johnson |
Pirazoles substituidos.
|
JP2004531456A
(ja)
|
2000-09-06 |
2004-10-14 |
オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド |
置換ピラゾールを用いてアレルギーを治療する方法
|
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
|
US6982274B2
(en)
|
2001-04-16 |
2006-01-03 |
Eisai Co., Ltd. |
1H-indazole compound
|
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
|
IL158062A0
(en)
|
2001-04-30 |
2004-03-28 |
Glaxo Group Ltd |
Fused 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
|
AU2002302894A1
(en)
|
2001-06-19 |
2003-01-02 |
Warner-Lambert Company Llc |
Quinazolinediones as antibacterial agents
|
AU2002315389A1
(en)
|
2001-06-21 |
2003-01-08 |
Ariad Pharmaceuticals, Inc. |
Novel pyrazolo-and pyrrolo-pyrimidines and uses thereof
|
GB0115109D0
(en)
|
2001-06-21 |
2001-08-15 |
Aventis Pharma Ltd |
Chemical compounds
|
WO2003000690A1
(en)
|
2001-06-25 |
2003-01-03 |
Aventis Pharmaceuticals Inc. |
Synthesis of heterocyclic compounds employing microwave technology
|
WO2003009852A1
(en)
|
2001-07-24 |
2003-02-06 |
Merck & Co., Inc. |
Tyrosine kinase inhibitors
|
ATE427935T1
(de)
|
2001-08-07 |
2009-04-15 |
Banyu Pharma Co Ltd |
Spiro isobenzofurane als neuropeptid y rezeptor antagonisten
|
WO2003024967A2
(en)
|
2001-09-19 |
2003-03-27 |
Aventis Pharma S.A. |
Indolizines as kinase protein inhibitors
|
ATE335490T1
(de)
|
2001-10-30 |
2006-09-15 |
Novartis Pharma Gmbh |
Staurosporin-derivate als hemmer der flt3- rezeptor-tyrosinkinase-wirkung
|
MXPA04004178A
(es)
|
2001-11-01 |
2004-09-06 |
Janssen Pharmaceutica Nv |
Heteroarilaminas como inhibidores de glucogeno cintasa cinasa 3beta.
|
MXPA04004166A
(es)
|
2001-11-07 |
2004-07-08 |
Hoffmann La Roche |
Aminopirimidinas y piridinas.
|
CA2466279A1
(en)
|
2001-11-13 |
2003-05-22 |
Dana-Farber Cancer Institute, Inc. |
Agents that modulate immune cell activation and methods of use thereof
|
GB0129476D0
(en)
|
2001-12-10 |
2002-01-30 |
Syngenta Participations Ag |
Organic compounds
|
KR20060111716A
(ko)
|
2002-01-22 |
2006-10-27 |
워너-램버트 캄파니 엘엘씨 |
2-(피리딘-2-일아미노)-피리도[2,3-d]피리미딘-7-온
|
JP4201716B2
(ja)
|
2002-03-05 |
2008-12-24 |
メルク フロスト カナダ リミテツド |
カテプシンシステインプロテアーゼ阻害剤
|
US6815519B2
(en)
|
2002-03-22 |
2004-11-09 |
Chung-Shan Institute Of Science & Technology |
Acidic fluorine-containing poly (siloxane amideimide) silica hybrids
|
AU2003215675B2
(en)
|
2002-04-03 |
2007-07-12 |
F. Hoffmann-La Roche Ag |
Imidazo fused compounds
|
KR20040106554A
(ko)
|
2002-05-15 |
2004-12-17 |
얀센 파마슈티카 엔.브이. |
Pdfg 수용체 저해제로서의 n-치환된 트리사이클릭3-아미노피라졸
|
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
|
WO2003099818A1
(en)
|
2002-05-23 |
2003-12-04 |
Chiron Corporation |
Substituted quinazolinone compounds
|
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
|
US7196090B2
(en)
|
2002-07-25 |
2007-03-27 |
Warner-Lambert Company |
Kinase inhibitors
|
IL166241A
(en)
|
2002-07-29 |
2011-12-29 |
Rigel Pharmaceuticals Inc |
2,4-pyrimidinediamine compounds for use in the treatment of autoimmune diseases
|
JP4252534B2
(ja)
|
2002-08-06 |
2009-04-08 |
エフ.ホフマン−ラ ロシュ アーゲー |
p−38MAPキナーゼインヒビターとしての6−アルコキシ−ピリド−ピリミジン類
|
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
|
US7112676B2
(en)
|
2002-11-04 |
2006-09-26 |
Hoffmann-La Roche Inc. |
Pyrimido compounds having antiproliferative activity
|
AU2003291310A1
(en)
|
2002-11-06 |
2004-06-03 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds and use thereof
|
TWI335913B
(en)
|
2002-11-15 |
2011-01-11 |
Vertex Pharma |
Diaminotriazoles useful as inhibitors of protein kinases
|
CN100357293C
(zh)
|
2002-11-18 |
2007-12-26 |
霍夫曼-拉罗奇有限公司 |
二嗪并嘧啶类
|
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
|
US7759336B2
(en)
|
2002-12-10 |
2010-07-20 |
Ono Pharmaceutical Co., Ltd. |
Nitrogen-containing heterocyclic compounds and medicinal use thereof
|
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
|
BR0316880A
(pt)
|
2002-12-23 |
2005-10-25 |
Wyeth Corp |
Anticorpos contra pd-1 e usos dos mesmos
|
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
|
CA2512646A1
(en)
|
2003-01-17 |
2004-08-05 |
Warner-Lambert Company Llc |
2-aminopyridine substituted heterocycles as inhibitors of cellular proliferation
|
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
|
US7687625B2
(en)
|
2003-03-25 |
2010-03-30 |
Takeda Pharmaceutical Company Limited |
Dipeptidyl peptidase inhibitors
|
GB0308208D0
(en)
|
2003-04-09 |
2003-05-14 |
Glaxo Group Ltd |
Chemical compounds
|
AU2004228155A1
(en)
|
2003-04-10 |
2004-10-21 |
F.Hoffman-La Roche Ag |
Pyrimido compounds
|
EP1622910A1
(en)
|
2003-05-05 |
2006-02-08 |
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
|
AU2004249120B2
(en)
|
2003-05-23 |
2008-07-24 |
Glaxosmithkline |
Guanidino-substituted quinazolinone compounds as MC4-R agonists
|
KR101099409B1
(ko)
|
2003-06-06 |
2011-12-27 |
아렉시스 악티에볼라그 |
피부 상태 또는 암 치료를 위한 scce 저해제로서의융합된 헤테로사이클 화합물의 용도
|
IL156495A0
(en)
|
2003-06-17 |
2004-01-04 |
Prochon Biotech Ltd |
Use of fgfr3 antagonists for treating t cell mediated diseases
|
EP1637523A4
(en)
|
2003-06-18 |
2009-01-07 |
Ube Industries |
PROCESS FOR PRODUCING A PYRIMIDIN-4-ONE COMPOUND
|
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
|
JP5129957B2
(ja)
|
2003-07-03 |
2013-01-30 |
ミリアド ジェネティクス, インコーポレイテッド |
カスパーゼの活性化因子およびアポトーシスの誘発因子としての4−アリールアミノ−キナゾリン
|
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.
|
US7371750B2
(en)
|
2003-07-29 |
2008-05-13 |
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
|
JP2007505933A
(ja)
|
2003-09-18 |
2007-03-15 |
コンフォーマ・セラピューティクス・コーポレイション |
Hsp90インヒビターとしての新規なヘテロ環化合物
|
DE602004021611D1
(de)
|
2003-09-19 |
2009-07-30 |
Gilead Sciences Inc |
Azachinolinolphosphonatverbindungen als integraseinhibitoren
|
PE20050952A1
(es)
|
2003-09-24 |
2005-12-19 |
Novartis Ag |
Derivados de isoquinolina como inhibidores de b-raf
|
US7615557B2
(en)
|
2003-10-01 |
2009-11-10 |
Xention Limited |
Tetrahydro-naphthalene and urea derivatives
|
CA2542105C
(en)
|
2003-10-08 |
2011-08-02 |
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
|
MXPA06005578A
(es)
|
2003-11-17 |
2006-08-11 |
Pfizer Prod Inc |
Compuestos de pirrolopirimidina utiles en el tratamiento del 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
|
AU2005206562A1
(en)
|
2004-01-23 |
2005-08-04 |
Amgen Inc. |
Vanilloid receptor ligands and their use in treatments
|
DE602005016890D1
(de)
|
2004-01-23 |
2009-11-12 |
Janssen Pharmaceutica Nv |
Chinolinderivate und ihre verwendung als mycobakterielle inhibitoren
|
EP1715855A4
(en)
|
2004-01-29 |
2010-06-16 |
Elixir Pharmaceuticals Inc |
ANTIVIRAL DRUGS
|
GB0402137D0
(en)
|
2004-01-30 |
2004-03-03 |
Smithkline Beecham Corp |
Novel compounds
|
BRPI0507668A
(pt)
|
2004-02-14 |
2007-07-17 |
Irm Llc |
compostos e composições como inibidores de proteìna cinase
|
EP1718645A1
(en)
|
2004-02-18 |
2006-11-08 |
Warner-Lambert Company LLC |
2-(pyridin-3-ylamino)-pyrido 2,3-d pyrimidin-7-ones
|
KR100843526B1
(ko)
|
2004-02-27 |
2008-07-03 |
에프. 호프만-라 로슈 아게 |
피라졸의 접합 유도체
|
KR100844864B1
(ko)
|
2004-02-27 |
2008-07-09 |
에프. 호프만-라 로슈 아게 |
헤테로아릴-융합 피라졸로 유도체
|
US20080004263A1
(en)
|
2004-03-04 |
2008-01-03 |
Santora Vincent J |
Ligands of Follicle Stimulating Hormone Receptor and Methods of Use Thereof
|
JPWO2005085210A1
(ja)
|
2004-03-10 |
2008-01-17 |
小野薬品工業株式会社 |
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
|
CN1938321B
(zh)
|
2004-03-29 |
2010-05-05 |
三井化学株式会社 |
新型化合物及使用该化合物的有机电子元件
|
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
|
BRPI0511512A
(pt)
|
2004-05-27 |
2007-12-26 |
Pfizer Prod Inc |
derivados pirrolpirimidina úteis no tratamento do cáncer
|
US20070254877A1
(en)
|
2004-06-02 |
2007-11-01 |
Takada Pharmaceutical Company Limited |
Indole Derivative and Use for Treatment of Cancer
|
PE20060426A1
(es)
|
2004-06-02 |
2006-06-28 |
Schering Corp |
DERIVADOS DE ACIDO TARTARICO COMO INHIBIDORES DE MMPs, ADAMs, TACE Y TNF-alfa
|
CN1960988B
(zh)
|
2004-06-10 |
2012-01-25 |
Irm责任有限公司 |
作为蛋白激酶抑制剂的化合物和组合物
|
EP1894932A1
(en)
|
2004-06-11 |
2008-03-05 |
Japan Tobacco, Inc. |
5-amino-2,4,7-trioxo-3,4,7,8-tetrahydro-2H-pyrido[2,3-d]pyrimidine 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
|
RU2007111757A
(ru)
|
2004-08-31 |
2008-10-10 |
Ф.Хоффманн-Ля Рош Аг (Ch) |
Амидные производные 3-фенилдигидропиримидо [4,5-d] пиримидинонов, их получение и использованиев качестве фармацевтических агентов
|
JP2008511599A
(ja)
|
2004-08-31 |
2008-04-17 |
アストラゼネカ アクチボラグ |
キナゾリノン誘導体およびB−Raf阻害薬としてのそれらの使用
|
BRPI0514750A
(pt)
|
2004-08-31 |
2008-06-24 |
Hoffmann La Roche |
derivados amida de 7-amino-3-fenil-diidropirimido[4, 5-d]pirimidinonas, sua fabricação e uso como inibidores de proteìna cinase
|
DE102004042667A1
(de)
|
2004-09-01 |
2006-03-30 |
Ewald Dörken Ag |
Mehrschichtige Gebäudewand
|
TWI370147B
(en)
|
2004-09-10 |
2012-08-11 |
Ube Industries |
Modified polyimide resin and curable resin composition
|
EP1811844A4
(en)
|
2004-09-14 |
2009-12-02 |
Minerva Biotechnologies Corp |
METHOD FOR THE 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
|
WO2006050162A2
(en)
|
2004-10-28 |
2006-05-11 |
Phenomix Corporation |
Imidazole derivatives
|
US7855205B2
(en)
|
2004-10-29 |
2010-12-21 |
Janssen Pharmaceutica Nv |
Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders
|
EP1809279B1
(en)
|
2004-11-08 |
2013-05-29 |
Baxter International Inc. |
Particulate compositions of tubulin inhibitor
|
KR20070097441A
(ko)
|
2004-11-18 |
2007-10-04 |
인사이트 산 디에고 인코포레이티드 |
11-β 하이드록실 스테로이드 데하이드로게나제 유형 1의억제제 및 이를 사용하는 방법
|
JP2008520738A
(ja)
|
2004-11-22 |
2008-06-19 |
バーテックス ファーマシューティカルズ インコーポレイテッド |
プロテインキナーゼの阻害剤として有用なピロロピラジンおよびピラゾロピラジン
|
RU2007123675A
(ru)
|
2004-11-24 |
2008-12-27 |
Новартис АГ (CH) |
Комбинации ингибиторов jak
|
MY140748A
(en)
|
2004-12-06 |
2010-01-15 |
Astrazeneca Ab |
Novel pyrrolo [3,2-d] pyrimidin-4-one derivatives and their use in therapy
|
WO2006065703A1
(en)
|
2004-12-13 |
2006-06-22 |
Sunesis Pharmaceuticals, Inc. |
Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as raf kinase inhibitors
|
WO2006074293A2
(en)
|
2005-01-07 |
2006-07-13 |
President And Fellows Of Harvard College |
Bicyclic dihydropyrimidines as eg5 inhibitors
|
DE102005008310A1
(de)
|
2005-02-17 |
2006-08-24 |
Schering Ag |
Verwendung von CDKII Inhibitoren zur Fertilitätskontrolle
|
RU2007132865A
(ru)
|
2005-03-01 |
2009-03-10 |
Пфайзер Лимитед (GB) |
Применение ингибиторов pde7 для лечения невропатической боли
|
US7297700B2
(en)
|
2005-03-24 |
2007-11-20 |
Renovis, Inc. |
Bicycloheteroaryl compounds as P2X7 modulators and uses thereof
|
CA2610292C
(en)
|
2005-03-30 |
2015-06-02 |
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
|
MX2007013595A
(es)
|
2005-05-04 |
2008-01-24 |
Renovis Inc |
Compuestos heterociclicos fusionados y composiciones y usos de estos.
|
EP3530736A3
(en)
|
2005-05-09 |
2019-11-06 |
ONO Pharmaceutical Co., Ltd. |
Human monoclonal antibodies to programmed death 1 (pd-1) and methods for treating cancer using anti-pd-1 antibodies alone or in combination with other immunotherapeutics
|
WO2006124731A2
(en)
|
2005-05-12 |
2006-11-23 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
PL1891066T3
(pl)
|
2005-05-13 |
2011-05-31 |
Irm Llc |
Związki i kompozycje jako inhibitory kinazy białkowej
|
US20060279115A1
(en)
|
2005-06-09 |
2006-12-14 |
Ash Tisdelle |
Vehicular head and neck safety system and method
|
GB0512844D0
(en)
|
2005-06-23 |
2005-08-03 |
Novartis Ag |
Organic compounds
|
SG163554A1
(en)
|
2005-07-01 |
2010-08-30 |
Medarex Inc |
Human monoclonal antibodies to programmed death ligand 1 (pd-l1)
|
EP1915377A1
(en)
|
2005-07-22 |
2008-04-30 |
Sunesis Pharmaceuticals, Inc. |
Pyrazolo pyrimidines useful as aurora kinase inhibitors
|
ES2270715B1
(es)
|
2005-07-29 |
2008-04-01 |
Laboratorios Almirall S.A. |
Nuevos derivados de pirazina.
|
US20100216798A1
(en)
|
2005-07-29 |
2010-08-26 |
Astellas Pharma Inc |
Fused heterocycles as lck inhibitors
|
BRPI0614804A2
(pt)
|
2005-08-09 |
2011-04-12 |
Irm Llc |
compostos e composições como inibidores de proteìna cinase
|
AU2006279536A1
(en)
|
2005-08-16 |
2007-02-22 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
JP2009506004A
(ja)
|
2005-08-25 |
2009-02-12 |
エフ.ホフマン−ラ ロシュ アーゲー |
p38MAPキナーゼ阻害剤としての縮合ピラゾール
|
US7678917B2
(en)
|
2005-09-01 |
2010-03-16 |
Hoffman-La Roche Inc. |
Factor Xa inhibitors
|
ATE453634T1
(de)
|
2005-09-06 |
2010-01-15 |
Smithkline Beecham Corp |
Regioselektives verfahren zur zubereitung von benzimidazol-thiophenen
|
US8193356B2
(en)
|
2005-09-15 |
2012-06-05 |
Aska Pharmaceutical Co., Ltd. |
Heterocycle compound, and production process and application thereof
|
US20070116984A1
(en)
|
2005-09-21 |
2007-05-24 |
Doosan Corporation |
Spiro-compound for electroluminescent display device and electroluminescent display device comprising the same
|
MX2008004024A
(es)
|
2005-09-23 |
2009-02-27 |
Schering Corp |
Antagonistas de receptor de glutamato metabotropico-1 tetraciclicos fusionados como agentes terapeuticos.
|
DE102005048072A1
(de)
|
2005-09-24 |
2007-04-05 |
Bayer Cropscience Ag |
Thiazole als Fungizide
|
US8119655B2
(en)
|
2005-10-07 |
2012-02-21 |
Takeda Pharmaceutical Company Limited |
Kinase inhibitors
|
EP1931645B1
(en)
|
2005-10-07 |
2014-07-16 |
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
|
US20070111981A1
(en)
|
2005-10-26 |
2007-05-17 |
Roth Gerald J |
New (hetero)aryl compounds with MCH antagonistic activity and medicaments comprising these compounds
|
US8604042B2
(en)
|
2005-11-01 |
2013-12-10 |
Targegen, Inc. |
Bi-aryl meta-pyrimidine inhibitors of kinases
|
MX362412B
(es)
|
2005-11-01 |
2019-01-15 |
Targegen Inc |
Inhibidores de biaril meta-pirimidina de cinasas.
|
WO2007053498A1
(en)
|
2005-11-01 |
2007-05-10 |
Millennium Pharmaceuticals, Inc. |
Compounds useful as antagonists of ccr2
|
WO2007056170A2
(en)
|
2005-11-02 |
2007-05-18 |
Bayer Healthcare Ag |
Pyrrolo[2,1-f] [1,2,4] triazin-4-ylamines igf-1r kinase inhibitors for the treatment of cancer and other hyperproliferative diseases
|
US20070149508A1
(en)
|
2005-11-02 |
2007-06-28 |
Targegen, Inc. |
Six membered heteroaromatic inhibitors targeting resistant kinase mutations
|
AU2006315514B2
(en)
|
2005-11-10 |
2012-03-01 |
Chemocentryx, Inc. |
Substituted quinolones and methods of use
|
RU2428423C2
(ru)
|
2005-11-10 |
2011-09-10 |
Баниу Фармасьютикал Ко., Лтд. |
Азазамещенные спиропроизводные
|
WO2007058626A1
(en)
|
2005-11-16 |
2007-05-24 |
S*Bio Pte Ltd |
Indazole compounds
|
WO2007058392A1
(ja)
|
2005-11-21 |
2007-05-24 |
Japan Tobacco Inc. |
ヘテロ環化合物およびその医薬用途
|
CA2631741C
(en)
|
2005-12-02 |
2014-01-28 |
Bayer Healthcare Llc |
Substituted 4-amino-pyrrolotriazine derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis
|
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
|
WO2007120339A1
(en)
|
2005-12-19 |
2007-10-25 |
Genentech, Inc. |
Pyrimidine kinase inhibitors
|
CN101336237B
(zh)
|
2005-12-21 |
2015-09-30 |
诺华股份有限公司 |
作为fgf抑制剂的嘧啶基芳基脲衍生物
|
WO2007084314A2
(en)
|
2006-01-12 |
2007-07-26 |
Incyte Corporation |
MODULATORS OF 11-ß HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME
|
UY30118A1
(es)
|
2006-01-31 |
2007-06-29 |
Tanabe Seiyaku Co |
Compueto amina trisustituido
|
US7427625B2
(en)
|
2006-02-08 |
2008-09-23 |
Janssen Pharmaceutica, N.V. |
Substituted thiatriazaacenaphthylene-6-carbonitrile kinase inhibitors
|
CA2640672A1
(en)
|
2006-02-17 |
2007-08-23 |
Pfizer Limited |
3 -deazapurine derivatives as tlr7 modulators
|
EP2233472B1
(en)
|
2006-03-28 |
2014-01-15 |
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
|
WO2008117269A2
(en)
|
2007-03-28 |
2008-10-02 |
Atir Holding S.A. |
Heterotri cyciii c compounds as serotonergic and/or dopaminergic agents and uses thereof
|
BRPI0709699A2
(pt)
|
2006-03-29 |
2011-07-26 |
Foldrx Pharmaceuticals Inc |
inibiÇço da toxidez da alfa-sinucleina
|
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
|
CN101472926A
(zh)
|
2006-04-13 |
2009-07-01 |
阿斯利康(瑞典)有限公司 |
硫代黄嘌呤衍生物以及它们作为髓过氧化物酶抑制剂的用途
|
GB0608386D0
(en)
|
2006-04-27 |
2006-06-07 |
Senexis Ltd |
Compounds
|
EP2024342A2
(en)
|
2006-05-01 |
2009-02-18 |
Pfizer Products Incorporated |
Substituted 2-amino-fused heterocyclic compounds
|
ES2361782T3
(es)
|
2006-05-11 |
2011-06-22 |
Irm Llc |
Compuesto y composiciones como inhibidores de proteína quinasa.
|
US20090312321A1
(en)
|
2006-05-15 |
2009-12-17 |
Irm Llc |
Compositions and methods for fgf receptor kinases inhibitors
|
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
|
DK2044026T3
(da)
|
2006-06-22 |
2014-06-30 |
Prana Biotechnology Ltd |
Fremgangsmde til behandling af cerebral glioma tumor
|
JP2009541480A
(ja)
|
2006-06-30 |
2009-11-26 |
アストラゼネカ アクチボラグ |
癌の治療において有用なピリミジン誘導体
|
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
|
CA2654670A1
(en)
|
2006-07-06 |
2008-01-10 |
Boehringer Ingelheim International Gmbh |
New compounds
|
WO2008008234A1
(en)
|
2006-07-07 |
2008-01-17 |
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
|
EP2049481A2
(en)
|
2006-08-09 |
2009-04-22 |
SmithKline Beecham Corporation |
Novel compounds as antagonists or inverse agonists for opioid receptors
|
JP2010500994A
(ja)
|
2006-08-16 |
2010-01-14 |
エグゼリクシス, インコーポレイテッド |
Pi3kおよびmekモジュレーターを使用する方法
|
DE102006041382A1
(de)
|
2006-08-29 |
2008-03-20 |
Bayer Schering Pharma Ag |
Carbamoyl-Sulfoximide als Proteinkinaseinhibitoren
|
DK2061765T3
(en)
|
2006-09-01 |
2015-01-26 |
Senhwa Biosciences Inc |
Serine-threonine protein kinase AND PARP-MODULATOR
|
JP5600004B2
(ja)
|
2006-09-05 |
2014-10-01 |
エモリー ユニバーシティー |
感染の予防または治療のためのチロシンキナーゼ阻害剤
|
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
|
WO2008034859A1
(en)
|
2006-09-21 |
2008-03-27 |
Boehringer Ingelheim International Gmbh |
Glucopyranosyl-substituted difluorobenzyl-benzene derivatives, medicaments containing such compounds, their use and process for their manufacture
|
WO2008034860A1
(en)
|
2006-09-22 |
2008-03-27 |
Glaxo Group Limited |
Pyrrolo[2, 3-b]pyridin-4-yl-benzenesulfonamide compounds as ikk2 inhibitors
|
US20100029636A1
(en)
|
2006-09-28 |
2010-02-04 |
Peter Buehlmayer |
Lck inhibitors
|
CN101522661A
(zh)
|
2006-10-02 |
2009-09-02 |
Irm责任有限公司 |
作为蛋白激酶抑制剂的化合物和组合物
|
US20100009956A1
(en)
|
2006-10-30 |
2010-01-14 |
Glaxo Group Limited , a corporation |
Novel substituted pyrimidines as cysteine protease inhibitors
|
US7858645B2
(en)
|
2006-11-01 |
2010-12-28 |
Hoffmann-La Roche Inc. |
Indazole derivatives
|
CN101600714B
(zh)
|
2006-11-10 |
2013-08-21 |
百时美施贵宝公司 |
吡咯并吡啶激酶抑制剂
|
US7892454B2
(en)
|
2006-11-17 |
2011-02-22 |
Polyera Corporation |
Acene-based organic semiconductor materials and methods of preparing and using the same
|
US7902363B2
(en)
|
2006-11-17 |
2011-03-08 |
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
|
DK3034075T3
(en)
|
2006-11-22 |
2018-10-22 |
Incyte Holdings Corp |
IMIDAZOTRIAZINES AND IMIDAZOPYRIMIDINES AS KINASEI INHIBITORS
|
NZ578329A
(en)
|
2006-12-13 |
2012-05-25 |
Schering Corp |
Igf1r inhibitors for treating cancer
|
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
|
MX2009006536A
(es)
|
2006-12-22 |
2009-06-26 |
Novartis Ag |
Compuestos de heteroaril-heteroarilo como inhibidores de cdk para el tratamiento de cancer, inflamacion e infecciones virales.
|
EP2114941B1
(en)
|
2006-12-22 |
2015-03-25 |
Astex Therapeutics Limited |
Bicyclic heterocyclic compounds as fgfr inhibitors
|
AU2007337895C1
(en)
|
2006-12-22 |
2014-07-31 |
Astex Therapeutics Limited |
Tricyclic amine derivatives as protein tyrosine kinase inhibitors
|
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
|
JP2010515684A
(ja)
|
2007-01-08 |
2010-05-13 |
ポリエラ コーポレイション |
アレーン−ビス(ジカルボキシイミド)系半導体材料、およびそれを調製するための関連する中間体を調製する方法
|
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
|
CA2674589A1
(en)
|
2007-01-12 |
2008-07-24 |
Biocryst Pharmaceuticals, Inc. |
Antiviral nucleoside analogs
|
MX2009007426A
(es)
|
2007-01-12 |
2009-07-17 |
Astellas Pharma Inc |
Compuesto de piridina condensado.
|
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
|
MX2009009492A
(es)
|
2007-03-06 |
2009-09-15 |
Novartis Ag |
Compuestos organicos biciclicos adecuados para el tratamiento de condiciones inflamatorias o alergicas.
|
JP2010520292A
(ja)
|
2007-03-07 |
2010-06-10 |
アラントス・フアーマシユーテイカルズ・ホールデイング・インコーポレイテツド |
複素環式部分を含有するメタロプロテアーゼ阻害剤
|
RU2498983C2
(ru)
|
2007-03-12 |
2013-11-20 |
Юм Биосайнсес Аустралия Пти Лтд |
Соединения фениламинопиримидина и их применения
|
CA2679980A1
(en)
|
2007-03-21 |
2007-09-27 |
Epix Pharmaceuticals, Inc. |
S1p receptor modulating compounds and use thereof
|
US20080234262A1
(en)
|
2007-03-21 |
2008-09-25 |
Wyeth |
Pyrazolopyrimidine analogs and their use as mtor kinase and pi3 kinase inhibitors
|
WO2008118454A2
(en)
|
2007-03-23 |
2008-10-02 |
Amgen Inc. |
Derivatives of quinoline or benzopyrazine and their uses for the treatment of (inter alia) inflammatory diseases, autoimmune diseases or various kinds of cancer
|
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
|
EP2148870A1
(en)
|
2007-04-20 |
2010-02-03 |
Schering Corporation |
Pyrimidinone derivatives and methods of use thereof
|
EP1985612A1
(en)
|
2007-04-26 |
2008-10-29 |
Bayer Schering Pharma Aktiengesellschaft |
Arymethylen substituted N-Acyl-gamma-aminoalcohols
|
EP1990342A1
(en)
|
2007-05-10 |
2008-11-12 |
AEterna Zentaris GmbH |
Pyridopyrazine Derivatives, Process of Manufacturing and Uses thereof
|
TW200902008A
(en)
|
2007-05-10 |
2009-01-16 |
Smithkline Beecham Corp |
Quinoxaline derivatives as PI3 kinase inhibitors
|
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
|
AU2008259776A1
(en)
|
2007-06-03 |
2008-12-11 |
Vanderbilt University |
Benzamide mGluR5 positive allosteric modulators and methods of making and using same
|
CA2689444A1
(en)
|
2007-06-07 |
2008-12-18 |
Merck Sharp & Dohme Corp. |
Tricyclic anilide heterocyclic cgrp receptor antagonists
|
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
|
LT2168966T
(lt)
|
2007-06-15 |
2017-01-10 |
Msd K.K. |
Bicikloanilino darinys
|
US8354509B2
(en)
|
2007-06-18 |
2013-01-15 |
Msd Oss B.V. |
Antibodies to human programmed death receptor PD-1
|
CN101765442B
(zh)
|
2007-07-26 |
2014-09-17 |
诺华股份有限公司 |
有机化合物
|
EP2018859A1
(en)
|
2007-07-26 |
2009-01-28 |
Bayer Schering Pharma Aktiengesellschaft |
Arylmethylene substituted N-acyl-beta-amino alcohols
|
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
|
WO2009029625A1
(en)
|
2007-08-27 |
2009-03-05 |
Kalypsys, Inc. |
4- [heterocyclyl-methyl] -8-fluoro-quinolin-2-ones useful as nitric oxide synthase inhibitors
|
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
|
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
|
NZ584827A
(en)
|
2007-10-01 |
2012-10-26 |
Isis Pharmaceuticals Inc |
Antisense modulation of fibroblast growth factor receptor 4 expression
|
ES2549084T3
(es)
|
2007-10-05 |
2015-10-22 |
Msd K.K. |
Derivados de benzoxazinona
|
EP2209775A1
(en)
|
2007-10-09 |
2010-07-28 |
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
|
WO2009046606A1
(en)
|
2007-10-11 |
2009-04-16 |
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
|
WO2009047993A1
(ja)
|
2007-10-13 |
2009-04-16 |
Konica Minolta Holdings, Inc. |
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
|
KR20100083170A
(ko)
|
2007-10-16 |
2010-07-21 |
와이어쓰 엘엘씨 |
티에노피리미딘 및 피라졸로피리미딘 화합물 및 이의 mTOR 키나제 및 PI3 키나제 억제제로서의 용도
|
CA2703037A1
(en)
|
2007-10-17 |
2009-04-23 |
Novartis Ag |
Organic compounds
|
WO2009053737A2
(en)
|
2007-10-25 |
2009-04-30 |
Astrazeneca Ab |
Pyridine and pyrazine derivatives useful in the treatment of cell proliferative disorders
|
RU2007139634A
(ru)
|
2007-10-25 |
2009-04-27 |
Сергей Олегович Бачурин (RU) |
Новые тиазол-, триазол- или оксадиазол-содержащие тетрациклические соединения
|
WO2009056886A1
(en)
|
2007-11-01 |
2009-05-07 |
Astrazeneca Ab |
Pyrimidine derivatives and their use as modulators of fgfr activity
|
US8921336B2
(en)
|
2007-11-28 |
2014-12-30 |
Dana-Farber Cancer Institute, Inc. |
Small molecule myristate inhibitors of BCR-ABL and methods of use
|
WO2009071535A1
(en)
|
2007-12-03 |
2009-06-11 |
Boehringer Ingelheim International Gmbh |
Diaminopyridines for the treatment of diseases which are characterised by excessive or anomal cell proliferation
|
CA2709202C
(en)
|
2007-12-19 |
2013-04-23 |
Amgen Inc. |
Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors
|
JP2011507902A
(ja)
|
2007-12-21 |
2011-03-10 |
ワイス・エルエルシー |
肝臓X受容体のモジュレーターとしてのイミダゾ[1,2−b]ピリダジン化合物
|
AU2008345225A1
(en)
|
2007-12-21 |
2009-07-09 |
University Of Rochester |
Method for altering the lifespan of eukaryotic organisms
|
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.
|
EA017805B1
(ru)
|
2008-01-24 |
2013-03-29 |
Андрей Александрович ИВАЩЕНКО |
2-АЛКИЛАМИНО-3-АРИЛСУЛЬФОНИЛЦИКЛОАЛКАНО[e ИЛИ d]ПИРАЗОЛО[1,5-a]ПИРИМИДИНЫ - АНТАГОНИСТЫ СЕРОТОНИНОВЫХ 5-НТРЕЦЕПТОРОВ, СПОСОБЫ ИХ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ
|
EA017818B1
(ru)
|
2008-01-24 |
2013-03-29 |
Андрей Александрович ИВАЩЕНКО |
ЗАМЕЩЕННЫЕ ЦИКЛОАЛКАНО[e ИЛИ d]ПИРАЗОЛО[1,5-a]ПИРИМИДИНЫ - АНТАГОНИСТЫ СЕРОТОНИНОВЫХ 5-НТРЕЦЕПТОРОВ, СПОСОБЫ ИХ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ
|
US20100292188A1
(en)
|
2008-01-24 |
2010-11-18 |
Ucb Pharma S.A. |
Compounds Comprising A Cyclobutoxy Group
|
NZ586695A
(en)
|
2008-01-25 |
2011-12-22 |
High Point Pharmaceuticals Llc |
TRICYCLIC COMPOUNDS AS MODULATORS OF TNF-alpha SYNTHESIS AND AS PDE4 INHIBITORS
|
EP2252616B1
(en)
|
2008-01-30 |
2014-07-23 |
Genentech, Inc. |
Pyrazolopyrimidine pi3k inhibitor compounds and methods of use
|
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
|
MX2010009205A
(es)
|
2008-02-22 |
2010-11-10 |
Irm Llc |
Compuestos y composiciones como moduladores de la actividad de gpr119.
|
CA2713716A1
(en)
|
2008-02-22 |
2009-08-27 |
F. Hoffmann-La Roche Ag |
Modulators for amyloid beta
|
WO2009108332A1
(en)
|
2008-02-27 |
2009-09-03 |
Vitae Pharmaceuticals, Inc. |
INHIBITORS OF 11β -HYDROXYSTEROID DEHYDROGENASE TYPE 1
|
WO2009108827A1
(en)
|
2008-02-29 |
2009-09-03 |
Wyeth |
Fused tricyclic pyrazolo[1, 5-a]pyrimidines, methods for preparation and uses thereof
|
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
|
JP5547099B2
(ja)
|
2008-03-14 |
2014-07-09 |
インテリカイン, エルエルシー |
キナーゼ阻害剤および使用方法
|
US8993580B2
(en)
|
2008-03-14 |
2015-03-31 |
Intellikine Llc |
Benzothiazole 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
|
ATE531372T1
(de)
|
2008-04-07 |
2011-11-15 |
Amgen Inc |
Gem-disubstituierte und spirocyclische aminopyridine/pyrimidine als zellcyclus- inhibitoren
|
WO2009124755A1
(en)
|
2008-04-08 |
2009-10-15 |
European Molecular Biology Laboratory (Embl) |
Compounds with novel medical uses and method of identifying such compounds
|
WO2009125809A1
(ja)
|
2008-04-11 |
2009-10-15 |
第一三共株式会社 |
ピペリジン誘導体
|
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
|
JPWO2009128520A1
(ja)
|
2008-04-18 |
2011-08-04 |
塩野義製薬株式会社 |
Pi3k阻害活性を有する複素環化合物
|
CN103224497A
(zh)
|
2008-04-22 |
2013-07-31 |
波托拉医药品公司 |
蛋白激酶抑制剂
|
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
|
WO2009132980A1
(en)
|
2008-04-29 |
2009-11-05 |
F. Hoffmann-La Roche Ag |
Pyrimidinyl pyridone inhibitors of jnk.
|
WO2009133127A1
(en)
|
2008-04-30 |
2009-11-05 |
Merck Serono S.A. |
Fused bicyclic compounds and use thereof as pi3k inhibitors
|
US9315449B2
(en)
|
2008-05-15 |
2016-04-19 |
Duke University |
Substituted pyrazoles as heat shock transcription factor activators
|
GEP20125502B
(en)
|
2008-05-23 |
2012-04-25 |
Novartis Ag |
Derivatives of quinolines and quinoxalines as protein tyrosine kinase inhibitors
|
WO2009144205A1
(en)
|
2008-05-30 |
2009-12-03 |
Basf Se |
Rylene-based semiconductor materials and methods of preparation and use thereof
|
EP2303269B1
(en)
|
2008-06-03 |
2014-07-30 |
Merck Sharp & Dohme Corp. |
Inhibitors of akt activity
|
AU2009255329A1
(en)
|
2008-06-03 |
2009-12-10 |
Msd K.K. |
Inhibitors of Akt activity
|
KR101656793B1
(ko)
|
2008-06-10 |
2016-09-12 |
유디씨 아일랜드 리미티드 |
신규한 전이 금속 착물 및 이의 유기 발광 다이오드에서의 용도 - ⅲ
|
AR072092A1
(es)
|
2008-06-11 |
2010-08-04 |
Genentech Inc |
Diazacarbazoles y metodos de uso
|
AR072084A1
(es)
|
2008-06-12 |
2010-08-04 |
Sanofi Aventis |
Derivados de azacarbolinas, su preparacion y su utilizacion terapeutica como inhibidores de las quinasas pim
|
ES2430053T3
(es)
|
2008-06-12 |
2013-11-18 |
Merck Sharp & Dohme Corp. |
Procedimiento para producir derivados de bicicloanilina
|
GB0810902D0
(en)
|
2008-06-13 |
2008-07-23 |
Astex Therapeutics Ltd |
New compounds
|
EP2328872A1
(en)
|
2008-06-19 |
2011-06-08 |
AstraZeneca AB |
Pyrazole compounds 436
|
US8575337B2
(en)
|
2008-06-24 |
2013-11-05 |
Research Foundation Itsuu Laboratory |
Oxazolidinone derivative having fused ring
|
US8338439B2
(en)
|
2008-06-27 |
2012-12-25 |
Celgene Avilomics Research, Inc. |
2,4-disubstituted pyrimidines useful as kinase inhibitors
|
EP2303881A2
(en)
|
2008-07-14 |
2011-04-06 |
Gilead Sciences, Inc. |
Fused heterocyclyc inhibitors of histone deacetylase and/or cyclin-dependent kinases
|
WO2010006947A1
(en)
|
2008-07-15 |
2010-01-21 |
F. Hoffmann-La Roche Ag |
Novel phenyl-imidazopyridines and pyridazines
|
WO2010007099A1
(en)
|
2008-07-15 |
2010-01-21 |
Cellzome Limited |
2-aminoimidazo[1,2-b]pyridazine derivatives as pi3k inhibitors
|
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
|
MX2011000664A
(es)
|
2008-07-16 |
2011-02-24 |
Schering Corp |
Derivados biciclicos heterociclicos y uso de los mismos como moduladores de gpr119.
|
WO2010009735A2
(en)
|
2008-07-23 |
2010-01-28 |
Dako Denmark A/S |
Combinatorial analysis and repair
|
US8455477B2
(en)
|
2008-08-05 |
2013-06-04 |
Merck Sharp & Dohme Corp. |
Therapeutic compounds
|
WO2010015643A1
(en)
|
2008-08-06 |
2010-02-11 |
Novartis Ag |
New antiviral modified nucleosides
|
WO2010019210A2
(en)
|
2008-08-11 |
2010-02-18 |
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
|
JP2012501962A
(ja)
|
2008-09-10 |
2012-01-26 |
田辺三菱製薬株式会社 |
芳香族含窒素六員環化合物及びその使用
|
SI2342226T1
(sl)
|
2008-09-26 |
2016-11-30 |
Dana-Farber Cancer Institute Inc. |
Humana protitelesa proti PD-1, PD-L1 in PD-L2 in njihove uporabe
|
UY32158A
(es)
|
2008-10-03 |
2010-04-30 |
Astrazeneca Ab |
Derivados heterociclicos y metodos de uso de los mismos
|
US20100267748A1
(en)
|
2008-10-15 |
2010-10-21 |
Gilead Palo Alto, Inc. |
HETEROCYCLIC 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
|
TW201022262A
(en)
|
2008-10-29 |
2010-06-16 |
Astrazeneca Ab |
Novel compounds 515
|
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
|
AR074199A1
(es)
|
2008-11-20 |
2010-12-29 |
Glaxosmithkline Llc |
Compuesto de 6-(4-pirimidinil)-1h-indazol, composiciones farmaceuticas que lo comprenden y su uso para preparar un medicamento util para el tratamiento o disminucion de la gravedad del cancer.
|
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
|
RU2016116516A
(ru)
|
2008-12-08 |
2018-12-07 |
Мандифарма Интернэшнл Корпорейшн Лимитед |
Композиции ингибиторов тирозинкиназных рецепторов белков
|
SG172059A1
(en)
|
2008-12-09 |
2011-07-28 |
Genentech Inc |
Anti-pd-l1 antibodies and their use to enhance t-cell function
|
US8110265B2
(en)
|
2008-12-09 |
2012-02-07 |
The Coca-Cola Company |
Pet container and compositions having enhanced mechanical properties and gas barrier properties
|
WO2010067888A1
(en)
|
2008-12-12 |
2010-06-17 |
Banyu Pharmaceutical Co.,Ltd. |
Dihydropyrimidopyrimidine derivatives
|
US8507505B2
(en)
|
2008-12-12 |
2013-08-13 |
Msd K.K. |
Dihydropyrazolopyrimidinone derivative
|
EP2373163B1
(en)
|
2008-12-19 |
2015-06-10 |
Genentech, Inc. |
Heterocyclic compounds and methods of use
|
PA8852901A1
(es)
|
2008-12-22 |
2010-07-27 |
Lilly Co Eli |
Inhibidores de proteina cinasa
|
CA2748276A1
(en)
|
2008-12-30 |
2010-07-08 |
Arqule, Inc. |
Substituted pyrazolo [3, 4-b] pyridine compounds
|
MX2011006959A
(es)
|
2008-12-30 |
2011-12-06 |
Arqule Inc |
Compuestos substituidos de 5,6-dihidro-6-fenilbenzo [f] isoquinolina-2-amina.
|
CA2748181C
(en)
|
2009-01-06 |
2019-07-16 |
Nathanael S. Gray |
Pyrimido-diazepinone kinase scaffold compounds and methods of treating disorders
|
JOP20190230A1
(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
|
CA2755251A1
(en)
|
2009-03-18 |
2010-09-23 |
Schering Corporation |
Bicyclic compounds as inhibitors of diacylglycerol acyltransferase
|
US8491869B2
(en)
|
2009-03-23 |
2013-07-23 |
Eli Lilly And Company |
Imaging agents for detecting neurological disorders
|
ES2540119T3
(es)
|
2009-03-27 |
2015-07-08 |
Abbvie Inc. |
Compuestos como ligandos de receptores cannabinoides
|
TW201102391A
(en)
|
2009-03-31 |
2011-01-16 |
Biogen Idec Inc |
Certain substituted pyrimidines, pharmaceutical compositions thereof, and methods for their use
|
US8481525B2
(en)
|
2009-04-06 |
2013-07-09 |
University Of Health Network |
Kinase inhibitors and method of treating cancer with same
|
JP5711723B2
(ja)
|
2009-04-07 |
2015-05-07 |
エメリティ・ファーマ・アクチボラグ |
治療剤としてのイソオキサゾール−3(2h)−オン類似体
|
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.
|
EP2424368B1
(en)
|
2009-04-29 |
2014-12-31 |
Locus Pharmaceuticals, Inc. |
Pyrrolotriazine compounds
|
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
|
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
|
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
|
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
|
WO2010136031A1
(en)
|
2009-05-27 |
2010-12-02 |
Københavns Universitet |
Fibroblast growth factor receptor-derived peptides binding to ncam
|
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
|
NZ597107A
(en)
|
2009-06-25 |
2013-12-20 |
Alkermes Pharma Ireland Ltd |
Heterocyclic compounds for the treatment of neurological and psychological disorders
|
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
|
EP2455370A1
(en)
|
2009-07-17 |
2012-05-23 |
Shionogi&Co., Ltd. |
Pharmaceutical product containing lactam or benzene sulfonamide compound
|
US8680077B2
(en)
|
2009-07-24 |
2014-03-25 |
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
|
AU2010281265A1
(en)
|
2009-08-05 |
2012-03-22 |
Versitech Limited |
Antiviral compounds and methods of making and using thereof
|
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
|
CA2770195C
(en)
|
2009-08-07 |
2015-10-13 |
Chugai Seiyaku Kabushiki Kaisha |
Aminopyrazole derivative
|
WO2011018894A1
(en)
|
2009-08-10 |
2011-02-17 |
Raqualia Pharma Inc. |
Pyrrolopyrimidine derivatives as potassium channel modulators
|
KR101721280B1
(ko)
|
2009-08-17 |
2017-03-29 |
인텔리카인, 엘엘씨 |
헤테로사이클릭 화합물 및 이의 용도
|
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
|
NZ598294A
(en)
|
2009-09-03 |
2013-07-26 |
Bioenergenix |
Heterocyclic compounds for the inhibition of pask
|
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
|
EP2475666A2
(en)
|
2009-09-11 |
2012-07-18 |
Trius Therapeutics, Inc. |
Gyrase inhibitors
|
WO2011041143A1
(en)
|
2009-10-01 |
2011-04-07 |
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
|
CN102666537A
(zh)
|
2009-10-20 |
2012-09-12 |
艾格尔生物制药股份有限公司 |
治疗黄病毒科病毒感染的氮杂吲唑
|
KR20110043270A
(ko)
|
2009-10-21 |
2011-04-27 |
(주)씨에스엘쏠라 |
유기발광화합물 및 이를 구비한 유기발광소자
|
JP5694345B2
(ja)
|
2009-10-22 |
2015-04-01 |
ギリアード サイエンシーズ, インコーポレイテッド |
Toll様受容体の調節因子
|
WO2011050245A1
(en)
|
2009-10-23 |
2011-04-28 |
Yangbo Feng |
Bicyclic heteroaryls as kinase inhibitors
|
CN102686225A
(zh)
|
2009-10-26 |
2012-09-19 |
西格诺药品有限公司 |
杂芳基化合物的合成和纯化方法
|
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
|
CA2780190C
(en)
|
2009-11-06 |
2020-05-05 |
Plexxikon, Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
JP5740409B2
(ja)
|
2009-11-13 |
2015-06-24 |
ジェノスコ |
キナーゼ阻害剤
|
WO2011063159A1
(en)
|
2009-11-18 |
2011-05-26 |
Plexxikon, Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
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
|
EP2504010A4
(en)
|
2009-11-23 |
2013-04-17 |
Merck Sharp & Dohme |
Fused Bicyclic Pyrimidine Derivatives and Methods of Use Therefor
|
EP2504028A4
(en)
|
2009-11-24 |
2014-04-09 |
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
|
MY167076A
(en)
|
2009-12-01 |
2018-08-10 |
Abbvie Inc |
Novel tricyclic compounds
|
JP2013512282A
(ja)
|
2009-12-01 |
2013-04-11 |
アボット・ラボラトリーズ |
新規三環式化合物
|
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
|
US20110183938A1
(en)
|
2009-12-16 |
2011-07-28 |
Genentech, Inc. |
1,7-diazacarbazoles and methods of use
|
ES2609040T3
(es)
|
2009-12-17 |
2017-04-18 |
Merck Sharp & Dohme Corp. |
Aminopirimidinas como inhibidores de Syk
|
WO2011075620A1
(en)
|
2009-12-18 |
2011-06-23 |
Novartis Ag |
Method for treating haematological cancers
|
SG10201502073PA
(en)
|
2009-12-22 |
2015-05-28 |
Vertex Pharma |
Isoindolinone inhibitors of phosphatidylinositol 3-kinase
|
WO2011079231A1
(en)
|
2009-12-23 |
2011-06-30 |
Gatekeeper Pharmaceutical, Inc. |
Compounds that modulate egfr activity and methods for treating or preventing conditions therewith
|
FR2954317B1
(fr)
|
2009-12-23 |
2012-01-27 |
Galderma Res & Dev |
Nouveaux derives phenoliques, et leur utilisation pharmaceutique ou cosmetique
|
FR2954315B1
(fr)
|
2009-12-23 |
2012-02-24 |
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
|
EP2519517B1
(en)
|
2009-12-29 |
2015-03-25 |
Dana-Farber Cancer Institute, Inc. |
Type ii raf kinase inhibitors
|
CN102933581A
(zh)
|
2009-12-29 |
2013-02-13 |
破立纪元有限公司 |
作为有机半导体的硫代硫酸芳香二酰亚胺以及使用它们的器件
|
WO2011080755A1
(en)
|
2009-12-29 |
2011-07-07 |
Advinus Therapeutics Private Limited |
Fused nitrogen heterocyclic compounds, process of preparation and uses thereof
|
WO2011082266A2
(en)
|
2009-12-30 |
2011-07-07 |
Arqule, Inc. |
Substituted heterocyclic compounds
|
JP2013516420A
(ja)
|
2009-12-30 |
2013-05-13 |
アークル インコーポレイテッド |
置換されたピロロ−アミノピリミジン化合物
|
US8329705B2
(en)
|
2009-12-30 |
2012-12-11 |
Arqule, Inc. |
Substituted triazolo-pyrazine 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
|
WO2011082488A1
(en)
|
2010-01-06 |
2011-07-14 |
British Columbia Cancer Agency Branch |
Bisphenol derivative therapeutics and methods for their use
|
JP2013517220A
(ja)
|
2010-01-12 |
2013-05-16 |
エフ.ホフマン−ラ ロシュ アーゲー |
三環式複素環式化合物、その組成物、及び使用の方法
|
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
|
WO2011097717A1
(en)
|
2010-02-15 |
2011-08-18 |
University Of Victoria Innovation And Development Corporation |
Synthesis of bicyclic compounds and method for their use as therapeutic agents
|
SA111320200B1
(ar)
|
2010-02-17 |
2014-02-16 |
ديبيوفارم اس ايه |
مركبات ثنائية الحلقة واستخداماتها كمثبطات c-src/jak مزدوجة
|
US9334269B2
(en)
|
2010-02-17 |
2016-05-10 |
Amgen Inc. |
Carboxamides as inhibitors of voltage-gated sodium channels
|
EP2536410B1
(en)
|
2010-02-18 |
2015-09-23 |
Merck Sharp & Dohme Corp. |
Substituted 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
|
CN103740434B
(zh)
|
2010-02-18 |
2016-02-03 |
Ntn株式会社 |
增稠剂、润滑脂及它们的制造方法以及润滑脂封入轴承
|
UY33227A
(es)
|
2010-02-19 |
2011-09-30 |
Novartis Ag |
Compuestos de pirrolopirimidina como inhibidores de la cdk4/6
|
US9403769B2
(en)
|
2010-02-22 |
2016-08-02 |
Advanced Cancer Therapeutics, Llc |
Small molecule inhibitors of PFKFB3 and glycolytic flux and their methods of use as anti-cancer therapeutics
|
EP2541635B1
(en)
|
2010-02-26 |
2018-12-12 |
Nippon Steel & Sumikin Chemical Co., Ltd. |
Organic electroluminescent element
|
US20130045203A1
(en)
|
2010-03-02 |
2013-02-21 |
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
|
US20110237599A1
(en)
|
2010-03-10 |
2011-09-29 |
Kalypsys, Inc. |
Heterocyclic inhibitors of histamine receptors for the treatment of disease
|
PT2545052E
(pt)
|
2010-03-11 |
2015-02-18 |
Gilead Connecticut Inc |
Inibidores da syk à base de imidazopiridinas
|
US8987275B2
(en)
|
2010-03-16 |
2015-03-24 |
Dana-Farber Cancer Institute, Inc. |
Indazole compounds and their uses
|
RU2018100142A
(ru)
|
2010-03-24 |
2019-02-20 |
Амитек Терапетикс Солюшинс, Инк. |
Гетероциклические соединения, эффективные для ингибирования киназы
|
EP2552922A1
(en)
|
2010-03-31 |
2013-02-06 |
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
|
WO2011128403A1
(en)
|
2010-04-16 |
2011-10-20 |
Novartis Ag |
Organic compound for use in the treatment of liver cancer
|
AU2011242711C1
(en)
|
2010-04-22 |
2016-04-21 |
Janssen Pharmaceutica Nv |
Indazole compounds useful as ketohexokinase inhibitors
|
AR081331A1
(es)
|
2010-04-23 |
2012-08-08 |
Cytokinetics Inc |
Amino- pirimidinas composiciones de las mismas y metodos para el uso de los mismos
|
AU2011242683A1
(en)
|
2010-04-23 |
2012-12-13 |
Kineta, Inc. |
Anti-viral compounds
|
JP2013525457A
(ja)
|
2010-04-30 |
2013-06-20 |
ブリストル−マイヤーズ スクイブ カンパニー |
アルファ−7ニコチン性アセチルコリン受容体リガンドプロドラッグとしてのアザ−二環式アミンn−オキシド化合物
|
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
|
WO2011141848A1
(en)
|
2010-05-11 |
2011-11-17 |
Pfizer Inc. |
Morpholine compounds as mineralocorticoid receptor antagonists
|
EP2569012A4
(en)
|
2010-05-11 |
2013-10-30 |
Aveo Pharmaceuticals Inc |
ANTI-FGFR2 ANTIBODY
|
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
|
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
|
MX350075B
(es)
|
2010-05-12 |
2017-08-25 |
Spectrum Pharmaceuticals Inc |
Hidroxido de carbonato de lantano, oxicarbonato de lantano y metodos para su fabricacion y uso.
|
GB201008134D0
(en)
|
2010-05-14 |
2010-06-30 |
Medical Res Council Technology |
Compounds
|
WO2011147198A1
(en)
|
2010-05-28 |
2011-12-01 |
Versitech Limited |
Compounds and methods for treatment of proliferative diseases
|
WO2011147199A1
(en)
|
2010-05-28 |
2011-12-01 |
Versitech Limited |
Compounds and methods for treating viral infections
|
CN103038230B
(zh)
|
2010-06-04 |
2016-05-25 |
霍夫曼-拉罗奇有限公司 |
作为lrrk2调节剂的氨基嘧啶衍生物
|
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
|
WO2011159877A2
(en)
|
2010-06-18 |
2011-12-22 |
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
|
EP2588110B1
(en)
|
2010-07-02 |
2018-10-17 |
University Health Network |
Methods of targeting pten mutant diseases and compositions therefor
|
FR2962438B1
(fr)
|
2010-07-06 |
2012-08-17 |
Sanofi Aventis |
Derives d'indolizines, procedes de preparation et application en therapeutique
|
EP2590968A1
(en)
|
2010-07-06 |
2013-05-15 |
Novartis AG |
Cyclic ether compounds useful as kinase inhibitors
|
FR2962437B1
(fr)
|
2010-07-06 |
2012-08-17 |
Sanofi Aventis |
Derives d'imidazopyridine, leur procede de preparation et leur application en therapeutique
|
JP5810157B2
(ja)
|
2010-07-09 |
2015-11-11 |
ザ・ウォルター・アンド・エリザ・ホール・インスティテュート・オブ・メディカル・リサーチ |
プロテインキナーゼ阻害剤および処置の方法
|
WO2012009258A2
(en)
|
2010-07-13 |
2012-01-19 |
Edward Roberts |
Peptidomimetic galanin receptor modulators
|
EP2595996A2
(en)
|
2010-07-14 |
2013-05-29 |
Merck Sharp & Dohme Corp. |
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
|
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
|
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
|
WO2012013713A2
(en)
|
2010-07-28 |
2012-02-02 |
Bayer Pharma Aktiengesellschaft |
Substituted imidazo[1,2-b]pyridazines
|
EP2413140A1
(en)
|
2010-07-29 |
2012-02-01 |
Sanofi |
Method for identifying a compound having an antiarrhythmic effect as well as uses relating thereto
|
EP2857395A1
(en)
|
2010-07-30 |
2015-04-08 |
Rohm And Haas Electronic Materials Korea Ltd. |
Organic electroluminescent device employing organic light emitting compound as light emitting material
|
US8906943B2
(en)
|
2010-08-05 |
2014-12-09 |
John R. Cashman |
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
|
WO2012027239A1
(en)
|
2010-08-23 |
2012-03-01 |
Schering Corporation |
NOVEL PYRAZOLO[1,5-a]PYRROLO[3,2-e]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
EP2608669B1
(en)
|
2010-08-23 |
2016-06-22 |
Merck Sharp & Dohme Corp. |
NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
ES2561277T3
(es)
|
2010-09-01 |
2016-02-25 |
Gilead Connecticut, Inc. |
Piridinonas/pirazinonas, procedimiento de preparación y procedimiento de utilización de las mismas
|
EP2611798B1
(en)
|
2010-09-01 |
2015-04-08 |
Gilead Connecticut, Inc. |
Pyridazinones, method of making, and method of use thereof
|
AR082799A1
(es)
|
2010-09-08 |
2013-01-09 |
Ucb Pharma Sa |
Derivados de quinolina y quinoxalina como inhibidores de quinasa
|
WO2012032065A1
(en)
|
2010-09-08 |
2012-03-15 |
Glaxo Group Limited |
Indazole derivatives for use in the treatment of influenza virus infection
|
SI2614058T1
(sl)
|
2010-09-08 |
2015-10-30 |
Glaxosmithkline Intellectual Property Development Limited |
Polimorfi in soli N-(5-(4-(5-(((2R,6S)-2,6-dimetil-4-morfolinil)metil)-1,3-oksazol-2-il)- 1H-indazol-6-il)-2-(metiloksi)-3-piridinil)metansulfonamida
|
TWI541243B
(zh)
|
2010-09-10 |
2016-07-11 |
拜耳知識產權公司 |
經取代咪唑并嗒
|
EP2618219A4
(en)
|
2010-09-14 |
2015-03-18 |
Hodogaya Chemical Co Ltd |
LOAD CONTROLLER AND TONER THEREOF
|
CN102399220A
(zh)
|
2010-09-15 |
2012-04-04 |
黄振华 |
三并环类PI3K和mTOR双重抑制剂
|
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
|
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
|
EP2629777B1
(en)
|
2010-10-22 |
2018-12-19 |
Merck Sharp & Dohme Corp. |
Bicyclic diamines as janus kinase inhibitors
|
CN104045654A
(zh)
|
2010-10-25 |
2014-09-17 |
G1治疗公司 |
Cdk抑制剂
|
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
|
JP5847830B2
(ja)
|
2010-11-10 |
2016-01-27 |
アクテリオン ファーマシューティカルズ リミテッドActelion Pharmaceuticals Ltd |
オレキシン受容体拮抗薬として有用なラクタム誘導体
|
BR112013010768A2
(pt)
|
2010-11-10 |
2016-07-12 |
Gruenenthal Gmbh |
derivados de ureia e carboxamida substituídos por heteroaromáticos como ligantes dos receptores vaniloides
|
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
|
CA2816144A1
(en)
|
2010-11-17 |
2012-05-24 |
Amgen Inc. |
Quinoline derivatives as pik3 inhibitors
|
WO2012066578A2
(en)
|
2010-11-18 |
2012-05-24 |
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
|
EP2649065A1
(en)
|
2010-12-09 |
2013-10-16 |
Amgen Inc. |
Bicyclic compounds as pim inhibitors
|
ES2553610T3
(es)
|
2010-12-14 |
2015-12-10 |
Electrophoretics Limited |
Inhibidores de la caseína cinasa 1 delta (CK1delta)
|
EA023544B1
(ru)
|
2010-12-20 |
2016-06-30 |
Мерк Сероно С.А. |
Производные индазолилтриазола
|
CA2822312A1
(en)
|
2010-12-22 |
2012-06-28 |
Gunnar Grue-Sorensen |
3-acyl-ingenols ii
|
WO2012088266A2
(en)
|
2010-12-22 |
2012-06-28 |
Incyte Corporation |
Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3
|
CN103402977B
(zh)
|
2010-12-22 |
2016-01-20 |
利奥实验室有限公司 |
巨大戟二萜醇-3-酰化物iii和巨大戟二萜醇-3-氨基甲酸酯
|
CN102603628B
(zh)
|
2010-12-22 |
2016-08-17 |
香港理工大学 |
作为抗癌试剂的喹啉衍生物
|
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
|
WO2012087784A1
(en)
|
2010-12-23 |
2012-06-28 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
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
|
US9434747B2
(en)
|
2011-02-18 |
2016-09-06 |
Medivation Technologies, Inc. |
Methods of treating diabetes
|
US9127000B2
(en)
|
2011-02-23 |
2015-09-08 |
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
|
US20130345234A1
(en)
|
2011-03-17 |
2013-12-26 |
Humphrey Athelstan Roy Gardner |
Fgfr and ligands thereof as biomarkers for breast cancer in hr positive subjects
|
EP2937349B1
(en)
|
2011-03-23 |
2016-12-28 |
Amgen Inc. |
Fused tricyclic dual inhibitors of cdk 4/6 and 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.
|
CA2831146C
(en)
|
2011-03-25 |
2019-06-04 |
Abbvie Inc. |
Trpv1 antagonists
|
JP2014516511A
(ja)
|
2011-04-07 |
2014-07-17 |
ジェネンテック, インコーポレイテッド |
抗fgfr4抗体及び使用方法
|
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
|
US9376438B2
(en)
|
2011-05-17 |
2016-06-28 |
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
|
SG194445A1
(en)
|
2011-05-19 |
2013-12-30 |
Novartis Ag |
Method for treating adenoid cystic carcinoma
|
JP6073868B2
(ja)
|
2011-06-01 |
2017-02-01 |
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 |
置換アミノイミダゾピリダジン
|
AR086656A1
(es)
|
2011-06-03 |
2014-01-15 |
Millennium Pharm Inc |
Combinacion de inhibidores de mek e inhibidores selectivos de la quinasa aurora a
|
KR101412437B1
(ko)
|
2011-06-13 |
2014-06-26 |
주식회사 엘지화학 |
신규한 화합물 및 이를 이용한 유기 전자 소자
|
WO2012175591A1
(en)
|
2011-06-22 |
2012-12-27 |
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
|
MX355852B
(es)
|
2011-08-12 |
2018-05-02 |
Hoffmann La Roche |
Compuestos de pirazolo [3,4-c] piridina y métodos de uso.
|
MY166970A
(en)
|
2011-08-12 |
2018-07-26 |
Nissan Chemical Ind Ltd |
Subtituted pyrrolo [2,3-h][1,6]naphthyridines and compositions thereof as jak inhibitors
|
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
|
US9345705B2
(en)
|
2011-09-15 |
2016-05-24 |
Merck Sharp & Dohme Corp. |
Compositions and methods 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
|
AU2012315988A1
(en)
|
2011-09-30 |
2014-04-10 |
Kineta, Inc. |
Anti-viral compounds
|
UA111382C2
(uk)
|
2011-10-10 |
2016-04-25 |
Оріон Корпорейшн |
Інгібітори протеїнкінази
|
US9580390B2
(en)
|
2011-10-12 |
2017-02-28 |
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
|
WO2013063000A1
(en)
|
2011-10-28 |
2013-05-02 |
Novartis Ag |
Method of treating gastrointestinal stromal tumors
|
WO2013063003A1
(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
|
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
|
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
|
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
|
WO2013109027A1
(ko)
|
2012-01-18 |
2013-07-25 |
덕산하이메탈(주) |
화합물, 이를 이용한 유기전기소자 및 그 전자 장치
|
EP2657233B1
(en)
|
2012-01-19 |
2014-08-27 |
Taiho Pharmaceutical Co., Ltd. |
3,5-disubstituted alkynylbenzene compound and salt thereof
|
WO2013124316A1
(en)
|
2012-02-23 |
2013-08-29 |
Bayer Intellectual Property Gmbh |
Substituted benzothienyl-pyrrolotriazines and uses thereof
|
JP2013179181A
(ja)
|
2012-02-28 |
2013-09-09 |
Sumitomo Chemical Co Ltd |
有機光電変換素子
|
PE20141973A1
(es)
|
2012-03-14 |
2014-12-12 |
Lupin Ltd |
Compuestos de heterociclilo como inhibidores de mek
|
RU2643326C2
(ru)
|
2012-03-30 |
2018-01-31 |
Новартис Аг |
Ингибитор рецептора фрф для применения в лечении гипофосфатемических заболеваний
|
KR20140146192A
(ko)
|
2012-04-14 |
2014-12-24 |
인트라-셀룰라 써래피스, 인코퍼레이티드. |
유기 화합물
|
JP5120580B1
(ja)
|
2012-05-14 |
2013-01-16 |
Jsr株式会社 |
液晶配向剤
|
JP6219377B2
(ja)
|
2012-05-20 |
2017-10-25 |
テル ハショマー メディカル リサーチ インフラストラクチャー アンド サーヴィシーズ リミテッド |
人工僧帽弁
|
HUE042374T2
(hu)
|
2012-06-13 |
2019-06-28 |
Incyte Holdings Corp |
Szubsztituált triciklusos vegyületek mint FGFR inhibitorok
|
CN104540809B
(zh)
|
2012-07-11 |
2018-12-11 |
蓝印药品公司 |
成纤维细胞生长因子受体的抑制剂
|
BR112015000349A2
(pt)
|
2012-07-11 |
2017-06-27 |
Novartis Ag |
método de tratamento de tumores estromais gastrointestinais
|
WO2014019186A1
(en)
|
2012-08-02 |
2014-02-06 |
Merck Sharp & Dohme Corp. |
Antidiabetic tricyclic compounds
|
EP2880028B1
(en)
|
2012-08-02 |
2020-09-30 |
Merck Sharp & Dohme Corp. |
Antidiabetic tricyclic compounds
|
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
|
EP2925888B1
(en)
|
2012-11-28 |
2017-10-25 |
Merck Sharp & Dohme Corp. |
Compositions and methods for treating cancer
|
US20140148548A1
(en)
|
2012-11-28 |
2014-05-29 |
Central Glass Company, Limited |
Fluorine-Containing Polymerizable Monomer And Polymer Compound Using Same
|
CN104968664A
(zh)
|
2012-12-12 |
2015-10-07 |
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
|
WO2014113191A1
(en)
|
2013-01-15 |
2014-07-24 |
Xiaohu Zhang |
Hedgehog pathway signaling inhibitors and therapeutic applications thereof
|
CN103588771B
(zh)
|
2013-01-15 |
2016-01-27 |
苏州云轩医药科技有限公司 |
具有刺猬通路拮抗剂活性的嘧啶类抗肿瘤化合物
|
KR101456626B1
(ko)
|
2013-02-01 |
2014-11-03 |
대영이앤비 주식회사 |
냉장고 부압 방지 장치
|
WO2014136972A1
(ja)
|
2013-03-07 |
2014-09-12 |
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
|
US20140371238A1
(en)
|
2013-03-13 |
2014-12-18 |
Flatley Discovery Lab |
Compounds and methods for the treatment of cystic fibrosis
|
US9498532B2
(en)
|
2013-03-13 |
2016-11-22 |
Novartis Ag |
Antibody drug conjugates
|
EP2970258B1
(en)
|
2013-03-14 |
2018-04-18 |
AbbVie Deutschland GmbH & Co KG |
Novel inhibitor compounds of phosphodiesterase type 10a
|
MY181020A
(en)
|
2013-03-15 |
2020-12-16 |
Sanofi Sa |
Heteroaryl compounds and uses thereof
|
AR095464A1
(es)
|
2013-03-15 |
2015-10-21 |
Celgene Avilomics Res Inc |
Compuestos de heteroarilo y usos de los mismos
|
WO2014160521A1
(en)
|
2013-03-15 |
2014-10-02 |
Blueprint Medicines Corporation |
Piperazine derivatives and their use as kit modulators
|
US9663524B2
(en)
|
2013-03-15 |
2017-05-30 |
Celgene Car Llc |
Substituted pyrido[2,3-d]pyrimidines as protein kinase inhibitors
|
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
|
BR112015026143A2
(pt)
|
2013-04-19 |
2017-10-17 |
Covagen Ag |
moléculas ligante biespecífica e de ácido nucleico, vetor, célula hospedeira ou hospedeiro não humano, e, composição farmacêutica
|
CA2909207C
(en)
|
2013-04-19 |
2021-11-02 |
Incyte 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
|
CA2915321A1
(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
|
BR112015032539B1
(pt)
|
2013-06-28 |
2022-07-12 |
Beigene, Ltd |
Compostos ureia tricíclicos fundidos como inibidores de raf cinase e/ou dímero de raf cinase e composição farmacêutica compreendendo os referidos compostos
|
MX2015017821A
(es)
|
2013-07-02 |
2016-04-15 |
Syngenta Participations Ag |
Heterociclos bi-o triciclicos activos como plaguicidas con sustituyentes que contienen azufre.
|
JP6018547B2
(ja)
|
2013-07-09 |
2016-11-02 |
大成ロテック株式会社 |
舗装機械
|
EP3019491A4
(en)
|
2013-07-09 |
2016-12-21 |
Dana Farber Cancer Inst Inc |
KINASE INHIBITORS FOR THE TREATMENT OF DISEASE
|
DK3019496T3
(da)
|
2013-07-11 |
2019-12-09 |
Acea Therapeutics Inc |
Pyrimidinderivater som kinaseinhibitorer
|
AR097455A1
(es)
|
2013-08-28 |
2016-03-16 |
Astellas Pharma Inc |
Composición farmacéutica que contiene compuesto de pirimidina como un ingrediente activo
|
WO2015057938A1
(en)
|
2013-10-18 |
2015-04-23 |
Eisai R&D Management Co., Ltd. |
Pyrimidine fgfr4 inhibitors
|
ES2682493T3
(es)
|
2013-10-25 |
2018-09-20 |
Novartis Ag |
Compuestos derivados de piridilo bicíclicos fusionados a anillo como inhibidores de FGFR4
|
CN110028491B
(zh)
|
2013-10-25 |
2022-02-11 |
缆图药品公司 |
纤维母细胞生长因子受体抑制剂
|
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
|
US9309246B2
(en)
|
2013-12-19 |
2016-04-12 |
Incyte Corporation |
Tricyclic heterocycles as BET protein inhibitors
|
WO2015108992A1
(en)
|
2014-01-15 |
2015-07-23 |
Blueprint Medicines Corporation |
Heterobicyclic compounds and their use as fgfr4 receptor inhibitors
|
US10562900B2
(en)
|
2014-08-19 |
2020-02-18 |
Shanghai Haihe Pharmaceutical Co., Ltd. |
Indazole compounds as FGFR kinase inhibitor, preparation and use thereof
|
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
|
CU20170029A7
(es)
|
2014-09-19 |
2017-08-08 |
Bayer Pharma AG |
Indazoles sustituidos con bencilo en calidad de inhibidores de bub1, útiles para el tratamiento o profilaxis de una enfermedad hiperproliferativa y/o un trastorno que responde a la inducción de la muerte celular, un procedimiento para la preparación de estos compuestos, y compuestos intermediarios
|
US10851105B2
(en)
|
2014-10-22 |
2020-12-01 |
Incyte Corporation |
Bicyclic heterocycles as FGFR4 inhibitors
|
WO2016064960A1
(en)
|
2014-10-22 |
2016-04-28 |
Incyte Corporation |
Bicyclic heterocycles as fgfr4 inhibitors
|
MA41551A
(fr)
|
2015-02-20 |
2017-12-26 |
Incyte Corp |
Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
|
WO2016134294A1
(en)
|
2015-02-20 |
2016-08-25 |
Incyte Corporation |
Bicyclic heterocycles as fgfr4 inhibitors
|
PE20180021A1
(es)
|
2015-02-20 |
2018-01-09 |
Univ Oregon Health & Science |
Derivados de sobetiroma
|
AU2016219822B2
(en)
|
2015-02-20 |
2020-07-09 |
Incyte Holdings Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
WO2016192680A1
(en)
|
2015-06-03 |
2016-12-08 |
Triastek, Inc. |
Dosage forms and use thereof
|
UA123772C2
(uk)
|
2015-07-15 |
2021-06-02 |
Протагоніст Терепьютікс, Інк. |
Пептидний інгібітор рецептора інтерлейкіну-23 та спосіб лікування запального захворювання кишечнику (ibd)
|
WO2017009275A1
(en)
|
2015-07-15 |
2017-01-19 |
F. Hoffmann-La Roche Ag |
Ethynyl derivatives as metabotropic glutamate receptor modulators
|
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
|
IT201600073305A1
(it)
|
2015-07-15 |
2018-01-13 |
Cabot Corp |
Composito di elastomero rinforzato con silice e prodotti che lo contengono.
|
MD3328419T2
(ro)
|
2015-07-30 |
2022-01-31 |
Macrogenics Inc |
Molecule de legare la PD-1 şi procedee de utilizare a acestora
|
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
|
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
|
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
|
WO2017024025A1
(en)
|
2015-08-03 |
2017-02-09 |
Sunil Kumar Kc |
3-(1h-pyrrolo[2,3-c]pyridin-2-yl)-1h-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
|
US10195185B2
(en)
|
2015-08-03 |
2019-02-05 |
Samumed, Llc |
3-(1H-imidazo[4,5-C]pyridin-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
WO2017024003A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc |
3-(1h-pyrrolo[3,2-c]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
|
WO2017070089A1
(en)
|
2015-10-19 |
2017-04-27 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
CA3002560A1
(en)
|
2015-10-23 |
2017-04-27 |
Array Biopharma, Inc. |
2-aryl- and 2-heteroaryl-substituted 2-pyridazin-3(2h)-one compounds as inhibitors of fgfr tyrosine kinases
|
HRP20221035T1
(hr)
|
2015-11-19 |
2022-11-11 |
Incyte Corporation |
Heterociklički spojevi kao imunomodulatori
|
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
|
TWI767896B
(zh)
|
2015-12-22 |
2022-06-21 |
美商英塞特公司 |
作為免疫調節劑之雜環化合物
|
MA44860A
(fr)
|
2016-05-06 |
2019-03-13 |
Incyte Holdings Corp |
Composés hétérocycliques utilisés comme immunomodulateurs
|
ES2905980T3
(es)
|
2016-05-26 |
2022-04-12 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
US20170362253A1
(en)
|
2016-06-20 |
2017-12-21 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
TW201803871A
(zh)
|
2016-06-24 |
2018-02-01 |
英塞特公司 |
作為PI3K-γ抑制劑之雜環化合物
|
US20180016260A1
(en)
|
2016-07-14 |
2018-01-18 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
EP3504198B1
(en)
|
2016-08-29 |
2023-01-25 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
CN109641868B
(zh)
|
2016-08-30 |
2021-12-03 |
广东东阳光药业有限公司 |
流感病毒复制抑制剂及其使用方法和用途
|
WO2018049214A1
(en)
|
2016-09-09 |
2018-03-15 |
Incyte Corporation |
Pyrazolopyridine derivatives as hpk1 modulators and uses thereof for the treatment of cancer
|
US10934304B2
(en)
|
2016-10-05 |
2021-03-02 |
Recurium Ip Holdings, Llc |
Spirocyclic compounds
|
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
|
US20180179179A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
ES2874756T3
(es)
|
2016-12-22 |
2021-11-05 |
Incyte Corp |
Derivados de triazolo[1,5-A]piridina como inmunomoduladores
|
SG10202106743QA
(en)
|
2016-12-22 |
2021-08-30 |
Incyte Corp |
Tetrahydro imidazo[4,5-c]pyridine derivatives as pd-l1 internalization inducers
|
UA126394C2
(uk)
|
2016-12-22 |
2022-09-28 |
Інсайт Корпорейшн |
Похідні бензоксазолу як імуномодулятори
|
US20180177784A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
ES2918974T3
(es)
|
2016-12-22 |
2022-07-21 |
Incyte Corp |
Compuestos heteroaromaticos biciclicos 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
|
CN111032656B
(zh)
|
2017-08-22 |
2022-12-02 |
捷思英达医药技术(上海)有限公司 |
杂环化合物激酶抑制剂及其药物组合物和应用
|
US10793551B2
(en)
|
2017-10-19 |
2020-10-06 |
Effector Therapeutics Inc. |
Benzimidazole-indole inhibitors of Mnk1 and Mnk2
|
ES2908283T3
(es)
|
2017-12-02 |
2022-04-28 |
Galapagos Nv |
Nuevos compuestos y composiciones farmacéuticas de los mismos para el tratamiento de enfermedades
|
IL313101A
(en)
|
2018-03-30 |
2024-07-01 |
Incyte Corp |
Heterocyclic compounds as immunomodulators
|
SG11202010882XA
(en)
|
2018-05-04 |
2020-11-27 |
Incyte Corp |
Salts of an fgfr inhibitor
|
PT3788047T
(pt)
|
2018-05-04 |
2024-10-22 |
Incyte Corp |
Formas sólidas de um inibidor de fgfr e processos para a sua preparação
|
WO2019217821A1
(en)
|
2018-05-11 |
2019-11-14 |
Incyte Corporation |
Tetrahydro-imidazo[4,5-c]pyridine derivatives as pd-l1 immunomodulators
|
JP2022504011A
(ja)
|
2018-08-14 |
2022-01-13 |
オステオーク インコーポレイティド |
ピロロ-ジピリジン化合物
|
WO2020049017A1
(en)
|
2018-09-07 |
2020-03-12 |
Merck Patent Gmbh |
5-morpholin-4-yl-pyrazolo[4,3-b]pyridine derivatives
|
US20210355547A1
(en)
|
2018-10-20 |
2021-11-18 |
The Johns Hopkins University |
Non-invasive urinary biomarkers for the detection of urothelial carcinoma of the bladder
|
US20220041579A1
(en)
|
2018-12-19 |
2022-02-10 |
Array Biopharma Inc. |
Substituted quinoxaline compounds as inhibitors of fgfr tyrosine kinases
|
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
|
US11628162B2
(en)
|
2019-03-08 |
2023-04-18 |
Incyte Corporation |
Methods of treating cancer with an FGFR inhibitor
|
US11591329B2
(en)
|
2019-07-09 |
2023-02-28 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
WO2021067374A1
(en)
|
2019-10-01 |
2021-04-08 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
PE20221085A1
(es)
|
2019-10-14 |
2022-07-05 |
Incyte Corp |
Heterociclos biciclicos como inhibidores de fgfr
|
US11566028B2
(en)
|
2019-10-16 |
2023-01-31 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
EP4069696A1
(en)
|
2019-12-04 |
2022-10-12 |
Incyte Corporation |
Tricyclic heterocycles as fgfr inhibitors
|
JP2023505257A
(ja)
|
2019-12-04 |
2023-02-08 |
インサイト・コーポレイション |
Fgfr阻害剤の誘導体
|
WO2021146424A1
(en)
|
2020-01-15 |
2021-07-22 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
CA3215903A1
(en)
|
2021-04-12 |
2022-10-20 |
Incyte Corporation |
Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent
|