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
|
CH641470A5
(de)
|
1978-08-30 |
1984-02-29 |
Ciba Geigy Ag |
Imidgruppen enthaltende silane.
|
CH635828A5
(de)
|
1978-08-30 |
1983-04-29 |
Ciba Geigy Ag |
N-substituierte imide und bisimide.
|
US4339267A
(en)
|
1980-01-18 |
1982-07-13 |
E. I. Du Pont De Nemours And Company |
Herbicidal sulfonamides
|
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
|
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
|
US4405519A
(en)
|
1980-10-22 |
1983-09-20 |
Plastics Engineering Company |
Di-Acetylene-terminated polyimide derivatives
|
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
|
JP2723670B2
(ja)
|
1989-12-28 |
1998-03-09 |
ヘキスト・アクチェンゲゼルシャフト |
電荷制御剤としてのビスカチオンの酸アミド―および―イミド誘導体
|
EP0507824B1
(de)
|
1989-12-28 |
1994-10-19 |
Hoechst Aktiengesellschaft |
Biskationische säureamid- und -imidderivate 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
|
NZ240089A
(en)
|
1990-10-03 |
1993-04-28 |
Commw Scient Ind Res Org |
Diaminobisimide compounds and compositions comprising such compounds for curing epoxy resins
|
JPH04158084A
(ja)
|
1990-10-22 |
1992-06-01 |
Fuji Photo Film Co Ltd |
記録材料
|
JPH04179576A
(ja)
|
1990-11-14 |
1992-06-26 |
Fuji Photo Film Co Ltd |
記録材料
|
JPH04328121A
(ja)
|
1991-04-26 |
1992-11-17 |
Sumitomo Bakelite Co Ltd |
半導体封止用エポキシ樹脂組成物
|
CA2110942A1
(en)
|
1991-06-14 |
1992-12-23 |
Pharmacia & Upjohn Company Llc |
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
|
NZ252064A
(en)
|
1992-05-28 |
1995-09-26 |
Commw Scient Ind Res Org |
Bismaleimide compounds; preparation thereof, curable compositions and impregnated fibre reinforced material containing them
|
AU5619094A
(en)
|
1992-12-07 |
1994-07-04 |
Commonwealth Scientific And Industrial Research Organisation |
Bisnadimides
|
WO1994015995A1
(en)
|
1993-01-11 |
1994-07-21 |
The Trustees Of The University Of Pennsylvania |
Polycyclic aromatic compounds having nonlinear optical properties
|
AU4293193A
(en)
|
1993-04-28 |
1994-11-21 |
Du Pont Merck Pharmaceutical Company, The |
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
|
RU2139281C1
(ru)
|
1993-11-30 |
1999-10-10 |
Джи Ди Сирл энд Компани |
Пиразолилзамещенный бензолсульфонамид или его фармацевтически приемлемая соль, фармацевтическая композиция, способ лечения от воспаления или связанного с воспалением заболевания
|
US5480887A
(en)
|
1994-02-02 |
1996-01-02 |
Eli Lilly And Company |
Protease inhibitors
|
ATE198985T1
(de)
|
1994-02-02 |
2001-02-15 |
Lilly Co Eli |
Hiv-protease inhibitoren und zwischenprodukte
|
MD1861G2
(ro)
|
1994-11-14 |
2002-09-30 |
Уорнер-Ламберт Кампэни |
Derivaţi ai 6-arilpirido[2,3-d]pirimidinelor şi naftiridinelor, compoziţie farmaceutică pe baza lor, metode de tratament şi de inhibare a proliferării şi migraţiei celulei receptorului tirozinkinazei
|
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
|
WO1997047601A1
(fr)
|
1996-06-11 |
1997-12-18 |
Yoshitomi Pharmaceutical Industries, Ltd. |
Composes heterocycliques fusionnes et leurs utilisations medicinales
|
EA003188B1
(ru)
|
1996-08-06 |
2003-02-27 |
Пфайзер Инк |
Замещенные пиридо- или пиримидосодержащие 6,6- или 6,7-бициклические производные
|
WO1998006703A1
(en)
|
1996-08-14 |
1998-02-19 |
Warner-Lambert Company |
2-phenyl benzimidazole derivatives as mcp-1 antagonists
|
JP3669783B2
(ja)
|
1996-08-21 |
2005-07-13 |
三井化学株式会社 |
有機電界発光素子
|
US5994364A
(en)
|
1996-09-13 |
1999-11-30 |
Schering Corporation |
Tricyclic antitumor farnesyl protein transferase inhibitors
|
AU6908398A
(en)
|
1996-10-28 |
1998-05-22 |
Versicor Inc |
Fused 2,4-pyrimidinedione combinatorial libraries and biologically active fused 2,4-pyramidinediones
|
WO1998028281A1
(en)
|
1996-12-23 |
1998-07-02 |
Celltech Therapeutics Limited |
Fused polycyclic 2-aminopyrimidine derivatives, their preparation and their use as protein tyrosine kinase inhibitors
|
BR9807305A
(pt)
|
1997-02-05 |
2000-05-02 |
Warner Lambert Co |
Pirido [2,3-d] pirimidinas e 4-aminopirimidinas como inibidores de proliferação celular.
|
EP0973777A1
(en)
|
1997-04-11 |
2000-01-26 |
Abbott Laboratories |
Furopyridine, thienopyridine, pyrrolopyridine and related pyrimidine, pyridazine and triazine compounds useful in controlling chemical synaptic transmission
|
EA002600B1
(ru)
|
1997-05-28 |
2002-06-27 |
Авентис Фармасьютикалз Продактс Инк. |
ХИНОЛИНОВЫЕ И ХИНОКСАЛИНОВЫЕ СОЕДИНЕНИЯ, ИНГИБИРУЮЩИЕ ТИРОЗИНКИНАЗЫ ТРОМБОЦИТАРНОГО ФАКТОРА РОСТА И/ИЛИ р56
|
GB9716231D0
(en)
|
1997-07-31 |
1997-10-08 |
Amersham Int Ltd |
Base analogues
|
NZ502877A
(en)
|
1997-08-11 |
2001-11-30 |
Cor Therapeutics Inc |
Bicyclic aryl azepinone selective factor Xa inhibitors for treating thrombosis related diseases
|
NZ502704A
(en)
|
1997-08-20 |
2002-06-28 |
Warner Lambert Co |
Naphthyridinones and pharmaceuticals thereof and their use in inhibiting cellular proliferation and protein tyrosine kinase or cell cycle kinase enzymatic activity
|
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
|
EP1057812A4
(en)
|
1998-02-20 |
2001-07-25 |
Takeda Chemical Industries Ltd |
AMINOGUANIDINE HYDRAZONE DERIVATIVES, PROCESSES FOR PRODUCING SAME, AND MEDICINAL PRODUCTS BASED ON SUCH DERIVATIVES
|
EP1077946A1
(en)
|
1998-05-15 |
2001-02-28 |
Guilford Pharmaceuticals Inc. |
Fused tricyclic compounds which inhibit parp activity
|
US20040044012A1
(en)
|
1998-05-26 |
2004-03-04 |
Dobrusin Ellen Myra |
Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation
|
IL139599A0
(en)
|
1998-05-26 |
2002-02-10 |
Warner Lambert Co |
Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation
|
WO1999064400A1
(en)
|
1998-06-12 |
1999-12-16 |
Vertex Pharmaceuticals Incorporated |
INHIBITORS OF p38
|
EP1107964B8
(en)
|
1998-08-11 |
2010-04-07 |
Novartis AG |
Isoquinoline derivatives with angiogenesis inhibiting activity
|
JP2000123973A
(ja)
|
1998-10-09 |
2000-04-28 |
Canon Inc |
有機発光素子
|
HUP0104199A3
(en)
|
1998-10-23 |
2002-12-28 |
Hoffmann La Roche |
Substituted pyrimido pyrimidinone derivatives, pharmaceutical compositions containing the same, process for the preparation thereof and intermediates
|
GB9823103D0
(en)
|
1998-10-23 |
1998-12-16 |
Pfizer Ltd |
Pharmaceutically active compounds
|
US6133031A
(en)
|
1999-08-19 |
2000-10-17 |
Isis Pharmaceuticals Inc. |
Antisense inhibition of focal adhesion kinase expression
|
GB9905075D0
(en)
|
1999-03-06 |
1999-04-28 |
Zeneca Ltd |
Chemical compounds
|
DE19912638A1
(de)
|
1999-03-20 |
2000-09-21 |
Bayer Ag |
Naphthylcarbonsäureamid-substituierte Sulfonamide
|
DE19920790A1
(de)
|
1999-05-06 |
2000-11-09 |
Bayer Ag |
Bis-Sulfonamide mit anti-HCMV-Wirkung
|
PE20010306A1
(es)
|
1999-07-02 |
2001-03-29 |
Agouron Pharma |
Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa
|
JP4041624B2
(ja)
|
1999-07-21 |
2008-01-30 |
三井化学株式会社 |
有機電界発光素子
|
HU228449B1
(en)
|
1999-09-24 |
2013-03-28 |
Janssen Pharmaceutica Nv |
Antiviral compositions
|
DE19946289A1
(de)
|
1999-09-28 |
2001-03-29 |
Basf Ag |
Benzodiazepin-Derivate, deren Herstellung und Anwendung
|
HUP0203564A3
(en)
|
1999-10-21 |
2004-07-28 |
Hoffmann La Roche |
Heteroalkylamino-substituted bicyclic nitrogen heterocycles as inhibitors of p38 protein kinease, process for their preparation and pharmaceutical compositions containing them
|
TR200201058T2
(tr)
|
1999-10-21 |
2002-07-22 |
F.Hoffmann-La Roche Ag |
P38 protein kinaz inhibitörleri olarak, alkilaminoyla ornatılmış bisiklik, azotlu heterosikller
|
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
|
ES2281372T3
(es)
|
1999-12-29 |
2007-10-01 |
Wyeth |
Inhibidores de proteina-quinasa triciclicos.
|
AP2002002603A0
(en)
|
2000-01-24 |
2002-09-30 |
Warner Lambert Co |
3-aminoquinazolin-2,4-dione antibacterial agents.
|
US20040224958A1
(en)
|
2000-01-27 |
2004-11-11 |
Booth Richard John |
Pyridopyrimidinone derivatives for treatment of neurodegenerative disease
|
WO2001057038A1
(de)
|
2000-02-01 |
2001-08-09 |
Basf Aktiengesellschaft |
Heterozyklische verbindungen und deren anwendung als parp-inhibitoren
|
US20020025961A1
(en)
|
2000-02-04 |
2002-02-28 |
Scarborough Robert M. |
Platelet ADP receptor inhibitors
|
ATE295365T1
(de)
|
2000-02-09 |
2005-05-15 |
Novartis Pharma Gmbh |
Pyridinderivative als angiogenese- und/oder vegf- rezeptor-tyrosinkinase-inhibitoren
|
GB0004890D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
AU2001235804A1
(en)
|
2000-03-06 |
2001-09-17 |
Astrazeneca Ab |
Therapy
|
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
|
JP2003532728A
(ja)
|
2000-05-05 |
2003-11-05 |
コー セラピューティックス, インコーポレイテッド |
ヘテロ二環式スルホンアミドおよび血小板adpレセプターインヒビターとしてのそれらの使用
|
WO2002000655A1
(en)
|
2000-06-23 |
2002-01-03 |
Bristol-Myers Squibb Pharma Company |
1 - (heteroaryl-phenyl) - condensed pyrazol derivatives as factor xa inhibitors
|
AU2002215608B2
(en)
|
2000-06-28 |
2004-12-09 |
Smithkline Beecham P.L.C. |
Wet milling process
|
US20050009876A1
(en)
|
2000-07-31 |
2005-01-13 |
Bhagwat Shripad S. |
Indazole compounds, compositions thereof and methods of treatment therewith
|
WO2002012442A2
(en)
|
2000-08-07 |
2002-02-14 |
Neurogen Corporation |
Heterocyclic compounds as ligands of the gabaa receptor
|
HU230538B1
(hu)
|
2000-08-14 |
2016-11-28 |
Ortho Mcneil Pharmaceutical, Inc. |
Szubsztituált pirazolok és ezeket tartalmazó gyógyszerkészítmények
|
BR0114054A
(pt)
|
2000-09-06 |
2003-07-01 |
Ortho Mcneil Pharm Inc |
Método para tratar alergias usando pirazóis substituìdos
|
GB0025782D0
(en)
|
2000-10-20 |
2000-12-06 |
Pfizer Ltd |
Use of inhibitors
|
EP1217000A1
(en)
|
2000-12-23 |
2002-06-26 |
Aventis Pharma Deutschland GmbH |
Inhibitors of factor Xa and factor VIIa
|
GB0100621D0
(en)
|
2001-01-10 |
2001-02-21 |
Vernalis Res Ltd |
Chemical compounds VI
|
GB0103926D0
(en)
|
2001-02-17 |
2001-04-04 |
Astrazeneca Ab |
Chemical compounds
|
AP1699A
(en)
|
2001-03-21 |
2006-12-26 |
Warner Lambert Co |
New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors
|
US6998408B2
(en)
|
2001-03-23 |
2006-02-14 |
Bristol-Myers Squibb Pharma Company |
6-5, 6-6, or 6-7 Heterobicycles as factor Xa inhibitors
|
JP2002296731A
(ja)
|
2001-03-30 |
2002-10-09 |
Fuji Photo Film Co Ltd |
熱現像カラー画像記録材料
|
ATE449763T1
(de)
|
2001-04-16 |
2009-12-15 |
Eisai R&D Man Co Ltd |
1h-indazolverbindungen die jnk hemmen
|
DE60227794D1
(de)
|
2001-04-26 |
2008-09-04 |
Eisai R&D Man Co Ltd |
Stickstoffhaltige verbindung mit kondensiertem ring und pyrazolylgruppe als substituent und medizinische zusammensetzung davon
|
BR0209267A
(pt)
|
2001-04-30 |
2004-06-15 |
Glaxo Group Ltd |
Pirimidinas fundidas como antagonistas do fator de liberação de corticotropina (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
|
CA2446963A1
(en)
|
2001-06-19 |
2002-12-27 |
Warner-Lambert Company Llc |
Quinazolinediones as antibacterial agents
|
GB0115109D0
(en)
|
2001-06-21 |
2001-08-15 |
Aventis Pharma Ltd |
Chemical compounds
|
US20030114467A1
(en)
|
2001-06-21 |
2003-06-19 |
Shakespeare William C. |
Novel pyrazolo- and pyrrolo-pyrimidines and uses thereof
|
WO2003000690A1
(en)
|
2001-06-25 |
2003-01-03 |
Aventis Pharmaceuticals Inc. |
Synthesis of heterocyclic compounds employing microwave technology
|
WO2003009852A1
(en)
|
2001-07-24 |
2003-02-06 |
Merck & Co., Inc. |
Tyrosine kinase inhibitors
|
AU2002323787B2
(en)
|
2001-08-07 |
2008-04-24 |
Banyu Pharmaceutical Co., Ltd. |
Spiro compounds
|
NZ531378A
(en)
|
2001-09-19 |
2006-11-30 |
Aventis Pharma S |
Indolizines as kinase protein inhibitors suitable for treating solid tumours
|
ATE335490T1
(de)
|
2001-10-30 |
2006-09-15 |
Novartis Pharma Gmbh |
Staurosporin-derivate als hemmer der flt3- rezeptor-tyrosinkinase-wirkung
|
WO2003037891A1
(en)
|
2001-11-01 |
2003-05-08 |
Janssen Pharmaceutica N.V. |
Heteroaryl amines as glycogen synthase kinase 3beta inhibitors (gsk3 inhibitors)
|
CN1582284A
(zh)
|
2001-11-07 |
2005-02-16 |
霍夫曼-拉罗奇有限公司 |
氨基嘧啶类和吡啶类化合物
|
WO2003042402A2
(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
|
BRPI0307057B8
(pt)
|
2002-01-22 |
2021-05-25 |
Warner Lambert Co |
compostos 2-(piridin-2-ilamino)-pirido[2,3-d]pirimidin-7-onas
|
AU2003219953B8
(en)
|
2002-03-05 |
2008-09-25 |
Axys Pharmaceuticals, Inc. |
Cathepsin cysteine protease inhibitors
|
US6815519B2
(en)
|
2002-03-22 |
2004-11-09 |
Chung-Shan Institute Of Science & Technology |
Acidic fluorine-containing poly (siloxane amideimide) silica hybrids
|
KR100656205B1
(ko)
|
2002-04-03 |
2006-12-12 |
에프. 호프만-라 로슈 아게 |
이미다조 융합 화합물
|
DE60326950D1
(de)
|
2002-05-15 |
2009-05-14 |
Janssen Pharmaceutica Nv |
N-substituierte tricyclische 3-aminopyrazole als pdgf rezeptorenhemmer
|
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
|
MXPA04011557A
(es)
|
2002-05-23 |
2005-07-05 |
Chiron Corp |
Compuestos de quinazolinona sustituida.
|
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
|
CN1678321A
(zh)
|
2002-07-29 |
2005-10-05 |
里格尔药品股份有限公司 |
用2,4-嘧啶二胺化合物治疗或者预防自体免疫性疾病的方法
|
DE60316581T2
(de)
|
2002-08-06 |
2008-07-03 |
F. Hoffmann-La Roche Ag |
6-alkoxypyridopyrimidine als inhibitoren der p-38-map-kinase
|
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
|
US7112676B2
(en)
|
2002-11-04 |
2006-09-26 |
Hoffmann-La Roche Inc. |
Pyrimido compounds having antiproliferative activity
|
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
|
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
|
EP1565475B1
(en)
|
2002-11-18 |
2009-04-08 |
F. Hoffmann-La Roche Ag |
Diazinopyrimidines and their use as protein kinase inhibitors
|
EA200500721A1
(ru)
|
2002-11-28 |
2005-12-29 |
Шеринг Акциенгезельшафт |
Пиримидины, ингибирующие chk, pdk и акт, их получение и применение в качестве лекарственных средств
|
WO2004052291A2
(en)
|
2002-12-06 |
2004-06-24 |
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
|
US7098332B2
(en)
|
2002-12-20 |
2006-08-29 |
Hoffmann-La Roche Inc. |
5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones
|
UA80767C2
(en)
|
2002-12-20 |
2007-10-25 |
Pfizer Prod Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
CN1753912B
(zh)
|
2002-12-23 |
2011-11-02 |
惠氏公司 |
抗pd-1抗体及其用途
|
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
|
KR20050111636A
(ko)
|
2003-04-10 |
2005-11-25 |
에프. 호프만-라 로슈 아게 |
피리미도 화합물
|
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
|
CA2523015A1
(en)
|
2003-05-23 |
2004-12-29 |
Chiron Corporation |
Guanidino-substituted quinazolinone compounds as mc4-r agonists
|
DE602004025803D1
(de)
|
2003-06-06 |
2010-04-15 |
Arexis Ab |
Verwendung von kondensierten heterozyklischen verbindungen als scce-hemmern zur behandlung von hautzuständen
|
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
|
NZ544472A
(en)
|
2003-07-03 |
2009-04-30 |
Myriad Genetics Inc |
Compounds and therapeutical use thereof
|
AR045037A1
(es)
|
2003-07-10 |
2005-10-12 |
Aventis Pharma Sa |
Tetrahidro-1h-pirazolo [3,4-c] piridinas sustituidas, composiciones que las contienen y su utilizacion.
|
CN1860118A
(zh)
|
2003-07-29 |
2006-11-08 |
Irm责任有限公司 |
作为蛋白激酶抑制剂的化合物和组合物
|
US7390820B2
(en)
|
2003-08-25 |
2008-06-24 |
Amgen Inc. |
Substituted quinolinone derivatives and methods of use
|
AU2004274403A1
(en)
|
2003-09-03 |
2005-03-31 |
Aventis Pharmaceuticals Inc. |
5-aryl-Pyrazolo(4,3-d)pyrimidines, pyridines, and pyrazines and related compounds
|
EP1670802A4
(en)
|
2003-09-18 |
2010-07-07 |
Conforma Therapeutics Corp |
NOVEL HETEROCYCLIC COMPOUNDS AS INHIBITORS OF HSP90 PROTEIN
|
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
|
ES2321719T3
(es)
|
2003-10-01 |
2009-06-10 |
Xention Limited |
Derivados de tetrahidro-naftaleno y urea.
|
CN1863774B
(zh)
|
2003-10-08 |
2010-12-15 |
Irm责任有限公司 |
用作蛋白激酶抑制剂的化合物和组合物
|
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
|
WO2005047289A1
(en)
|
2003-11-17 |
2005-05-26 |
Pfizer Products Inc. |
Pyrrolopyrimidine compounds useful in treatment of cancer
|
WO2005056524A2
(en)
|
2003-12-09 |
2005-06-23 |
Euro-Celtique S.A. |
Therapeutic agents useful for treating pain
|
WO2005066162A1
(en)
|
2003-12-23 |
2005-07-21 |
Human Biomolecular Research Institute |
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
|
US20050165032A1
(en)
|
2004-01-23 |
2005-07-28 |
Norman Mark H. |
Vanilloid receptor ligands and their use in treatments
|
AP2507A
(en)
|
2004-01-23 |
2012-11-16 |
Janssen Pharmaceutica Nv |
Quinoline derivatives and use thereof as mycobacterial inhibitors.
|
US20060019952A1
(en)
|
2004-01-29 |
2006-01-26 |
Elixir Pharmaceuticals, Inc. |
Anti-viral therapeutics
|
GB0402137D0
(en)
|
2004-01-30 |
2004-03-03 |
Smithkline Beecham Corp |
Novel compounds
|
US7968557B2
(en)
|
2004-02-14 |
2011-06-28 |
Novartis Ag |
Substituted pyrrolo[2,3-2]pyrimidines as protein kinase inhibitors
|
BRPI0507852A
(pt)
|
2004-02-18 |
2007-07-10 |
Warner Lambert Co |
2-(piridin-3-ilamino)-pirido[2,3-d]pirimidin-7-onas
|
BRPI0508036A
(pt)
|
2004-02-27 |
2007-07-17 |
Hoffmann La Roche |
derivados fundidos de pirazola
|
CN1934111A
(zh)
|
2004-02-27 |
2007-03-21 |
霍夫曼-拉罗奇有限公司 |
杂芳基稠合的吡唑并衍生物
|
WO2005087765A1
(en)
|
2004-03-04 |
2005-09-22 |
Arena Pharmaceuticals, Inc. |
Ligands of follicle stimulating hormone receptor and methods of use thereof
|
EP1724264A1
(en)
|
2004-03-10 |
2006-11-22 |
Ono Pharmaceutical Co., Ltd. |
Nitriles and medicinal compositions containing the same as the active ingredient
|
JP4627528B2
(ja)
|
2004-03-29 |
2011-02-09 |
三井化学株式会社 |
新規化合物、および該化合物を用いた有機エレクトロニクス素子
|
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
|
JP2008501628A
(ja)
|
2004-06-02 |
2008-01-24 |
武田薬品工業株式会社 |
インドール誘導体およびがんの治療用途
|
PE20060426A1
(es)
|
2004-06-02 |
2006-06-28 |
Schering Corp |
DERIVADOS DE ACIDO TARTARICO COMO INHIBIDORES DE MMPs, ADAMs, TACE Y TNF-alfa
|
CA2567662C
(en)
|
2004-06-10 |
2012-11-27 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
SI2298768T1
(en)
|
2004-06-11 |
2013-01-31 |
Japan Tobacco Inc |
5-amino-2,4,7-trioxo-3,4,7,8-tetrahydro-2H-pyridoS2,3-dCpyrimidine derivatives and related compounds for the treatment of cancer
|
GB0512324D0
(en)
|
2005-06-16 |
2005-07-27 |
Novartis Ag |
Organic compounds
|
JP2006028027A
(ja)
|
2004-07-12 |
2006-02-02 |
Mitsui Chemicals Inc |
テトラカルボン酸誘導体、および該化合物を用いた電子写真感光体、電子写真装置
|
EP1789399A1
(en)
|
2004-08-31 |
2007-05-30 |
AstraZeneca AB |
Quinazolinone derivatives and their use as b-raf inhibitors
|
KR100853974B1
(ko)
|
2004-08-31 |
2008-08-25 |
에프. 호프만-라 로슈 아게 |
7-아미노-3-페닐 디히드로피리미도[4,5-d]피리미디논의아미드 유도체, 그의 제조 방법 및 약학제로서의 용도
|
EP1789416B1
(en)
|
2004-08-31 |
2009-03-11 |
F. Hoffmann-la Roche AG |
Amide derivatives of 3-phenyl dihydropyrimido[4,5-d]pyrimidinones, their manufacture and use as pharmaceutical agents
|
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
|
AU2005336092B2
(en)
|
2004-09-14 |
2010-05-27 |
Cynthia C. Bamdad |
Methods for diagnosis and treatment of cancer
|
GB0420719D0
(en)
|
2004-09-17 |
2004-10-20 |
Addex Pharmaceuticals Sa |
Novel allosteric modulators
|
WO2006038112A1
(en)
|
2004-10-01 |
2006-04-13 |
Warner-Lambert Company Llc |
Use of kinase inhibitors to promote neochondrogenesis
|
FR2876582B1
(fr)
|
2004-10-15 |
2007-01-05 |
Centre Nat Rech Scient Cnrse |
Utilisation de derives de pyrrolo-pyrazines pour la fabrication de medicaments pour le traitement de la mucoviscidose et de maladies liees a un defaut d'adressage des proteines dans les cellules
|
WO2006050162A2
(en)
|
2004-10-28 |
2006-05-11 |
Phenomix Corporation |
Imidazole derivatives
|
WO2006050076A1
(en)
|
2004-10-29 |
2006-05-11 |
Janssen Pharmaceutica, N.V. |
Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders
|
BRPI0517652A
(pt)
|
2004-11-08 |
2008-10-14 |
Baxter Healthcare Sa |
composições farmacêuticas nanoparticuladas de inibidores de tubulina, métodos para as suas preparações e respectivos usos
|
AU2005306476A1
(en)
|
2004-11-18 |
2006-05-26 |
Incyte Corporation |
Inhibitors of 11-beta hydroxyl steroid dehydrogenase type 1 and methods of using the same
|
WO2006058074A1
(en)
|
2004-11-22 |
2006-06-01 |
Vertex Pharmaceuticals Incorporated |
Pyrrolopyrazines and pyrazolopyrazines useful as inhibitors of protein kinases
|
CN101106983A
(zh)
|
2004-11-24 |
2008-01-16 |
诺瓦提斯公司 |
JAK抑制剂与至少一种Bcr-Abl、Flt-3、FAK或RAF激酶抑制剂的组合
|
MY140748A
(en)
|
2004-12-06 |
2010-01-15 |
Astrazeneca Ab |
Novel pyrrolo [3,2-d] pyrimidin-4-one derivatives and their use in therapy
|
EP1828186A1
(en)
|
2004-12-13 |
2007-09-05 |
Sunesis Pharmaceuticals, Inc. |
Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as raf kinase inhibitors
|
US20100152206A1
(en)
|
2005-01-07 |
2010-06-17 |
Ralph Mazitschek |
Bicyclic Dihydropyrimidines and Uses Thereof
|
DE102005008310A1
(de)
|
2005-02-17 |
2006-08-24 |
Schering Ag |
Verwendung von CDKII Inhibitoren zur Fertilitätskontrolle
|
MX2007010721A
(es)
|
2005-03-01 |
2007-11-13 |
Pfizer Ltd |
Nuevo uso de inhibidores de fosfodiesterasa 7 para el tratamiento de dolor neuropatico.
|
US7402596B2
(en)
|
2005-03-24 |
2008-07-22 |
Renovis, Inc. |
Bicycloheteroaryl compounds as P2X7 modulators and uses thereof
|
EP1875244B1
(en)
|
2005-03-30 |
2019-01-23 |
Minerva Biotechnologies Corporation |
Proliferation of muc1 expressing cells
|
JP2006284843A
(ja)
|
2005-03-31 |
2006-10-19 |
Mitsui Chemicals Inc |
テトラカルボン酸誘導体を用いた電子写真感光体、電子写真装置
|
US20060223993A1
(en)
|
2005-04-01 |
2006-10-05 |
Connor Daniel M |
Colorant compounds, intermediates, and compositions
|
JP2006316054A
(ja)
|
2005-04-15 |
2006-11-24 |
Tanabe Seiyaku Co Ltd |
高コンダクタンス型カルシウム感受性kチャネル開口薬
|
KR100781704B1
(ko)
|
2005-04-20 |
2007-12-03 |
에스케이케미칼주식회사 |
피리딘 유도체와 이의 제조방법, 및 이를 포함하는약제조성물
|
EP1885369B1
(en)
|
2005-05-04 |
2015-09-23 |
Evotec AG |
Fused heterocyclic compounds, and compositions and uses thereof
|
RU2406760C3
(ru)
|
2005-05-09 |
2017-11-28 |
Оно Фармасьютикал Ко., Лтд. |
Моноклональные антитела человека к белку программируемой смерти 1 (pd-1) и способы лечения рака с использованием анти-pd-1-антител самостоятельно или в комбинации с другими иммунотерапевтическими средствами
|
WO2006124731A2
(en)
|
2005-05-12 |
2006-11-23 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
RU2411242C2
(ru)
|
2005-05-13 |
2011-02-10 |
Айрм, Ллк. |
Соединения и композиции в качестве ингибиторов протеинкиназ
|
WO2006135821A2
(en)
|
2005-06-09 |
2006-12-21 |
Achille Carlisle Tisdelle |
Vehicular head and neck safety system and method
|
GB0512844D0
(en)
|
2005-06-23 |
2005-08-03 |
Novartis Ag |
Organic compounds
|
CA3018525C
(en)
|
2005-07-01 |
2023-08-01 |
E. R. Squibb & Sons, L.L.C. |
Human monoclonal antibodies to programmed death ligand 1 (pd-l1)
|
CA2615946A1
(en)
|
2005-07-22 |
2007-02-01 |
Sunesis Pharmaceuticals, Inc. |
Pyrazolo pyrimidines useful as aurora kinase inhibitors
|
US20100216798A1
(en)
|
2005-07-29 |
2010-08-26 |
Astellas Pharma Inc |
Fused heterocycles as lck inhibitors
|
ES2270715B1
(es)
|
2005-07-29 |
2008-04-01 |
Laboratorios Almirall S.A. |
Nuevos derivados de pirazina.
|
US7868018B2
(en)
|
2005-08-09 |
2011-01-11 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
US7589101B2
(en)
|
2005-08-16 |
2009-09-15 |
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
|
ES2338590T3
(es)
|
2005-09-06 |
2010-05-10 |
Glaxosmithkline Llc |
Procedimiento regioselectivo de preparacion de benzoimidazoltiofenos.
|
CN101268073B
(zh)
|
2005-09-15 |
2011-10-19 |
Aska制药株式会社 |
杂环化合物、制备方法及其用途
|
US20070116984A1
(en)
|
2005-09-21 |
2007-05-24 |
Doosan Corporation |
Spiro-compound for electroluminescent display device and electroluminescent display device comprising the same
|
US7482360B2
(en)
|
2005-09-23 |
2009-01-27 |
Schering Corporation |
Fused tetracyclic mGluR1 antagonists as therapeutic agents
|
DE102005048072A1
(de)
|
2005-09-24 |
2007-04-05 |
Bayer Cropscience Ag |
Thiazole als Fungizide
|
CA2624965A1
(en)
|
2005-10-07 |
2007-04-19 |
Exelixis, Inc. |
Pyridopyrimidinone inhibitors of pi3k.alpha.
|
US8119655B2
(en)
|
2005-10-07 |
2012-02-21 |
Takeda Pharmaceutical Company Limited |
Kinase inhibitors
|
UA116188C2
(uk)
|
2005-10-07 |
2018-02-26 |
Екселіксіс, Інк. |
Інгібітори фосфатидилінозит-3-кінази і способи їх застосування
|
WO2007061554A2
(en)
|
2005-10-21 |
2007-05-31 |
Purdue Research Foundation |
Dosage of 4-aminopyridine derivatives for treatment of central nervous system injuries
|
TW200800220A
(en)
|
2005-10-26 |
2008-01-01 |
Boehringer Ingelheim Int |
New (hetero)aryl compounds with MCH antagonistic activity and medicaments comprising these compounds
|
PL1951684T3
(pl)
|
2005-11-01 |
2017-03-31 |
Targegen, Inc. |
Biarylowe meta-pirymidynowe inhibitory kinaz
|
WO2007053498A1
(en)
|
2005-11-01 |
2007-05-10 |
Millennium Pharmaceuticals, Inc. |
Compounds useful as antagonists of ccr2
|
US8604042B2
(en)
|
2005-11-01 |
2013-12-10 |
Targegen, Inc. |
Bi-aryl meta-pyrimidine inhibitors of kinases
|
WO2007056023A2
(en)
|
2005-11-02 |
2007-05-18 |
Targegen, Inc. |
Thiazole inhibitors targeting resistant kinase mutations
|
CA2627839C
(en)
|
2005-11-02 |
2014-08-19 |
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
|
US7557213B2
(en)
|
2005-11-10 |
2009-07-07 |
Chemocentryx, Inc. |
Substituted quinolones and methods of use
|
BRPI0618354B8
(pt)
|
2005-11-10 |
2021-05-25 |
Banyu Pharma Co Ltd |
composto e seu uso, composição farmacêutica, preventivo ou remédio
|
WO2007058626A1
(en)
|
2005-11-16 |
2007-05-24 |
S*Bio Pte Ltd |
Indazole compounds
|
EP1953147A1
(en)
|
2005-11-21 |
2008-08-06 |
Japan Tobacco, Inc. |
Heterocyclic compound and medicinal application thereof
|
PE20070855A1
(es)
|
2005-12-02 |
2007-10-14 |
Bayer Pharmaceuticals Corp |
Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
|
KR20130141706A
(ko)
|
2005-12-02 |
2013-12-26 |
바이엘 헬스케어 엘엘씨 |
과다-증식성 장애 및 맥관형성과 관련된 질환의 치료에 유용한 치환된 4-아미노-피롤로트리아진 유도체
|
US8110687B2
(en)
|
2005-12-08 |
2012-02-07 |
Millennium Pharmaceuticals, Inc. |
Bicyclic compounds with kinase inhibitory activity
|
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
|
ME00011A
(me)
|
2005-12-21 |
2009-02-10 |
Novartis Ag |
Derivati pirimidinilaril uree kao fgf inhibitori
|
US7998959B2
(en)
|
2006-01-12 |
2011-08-16 |
Incyte Corporation |
Modulators of 11-β hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same
|
PE20071025A1
(es)
|
2006-01-31 |
2007-10-17 |
Mitsubishi Tanabe Pharma Corp |
Compuesto amina trisustituido
|
WO2007092879A2
(en)
|
2006-02-08 |
2007-08-16 |
Janssen Pharmaceutica, N.V. |
Substituted thiatriazaacenaphthylene-6-carbonitrile kinase inhibitors
|
ATE532784T1
(de)
|
2006-02-17 |
2011-11-15 |
Pfizer Ltd |
3-deazapurinderivate als tlr7-modulatoren
|
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
|
WO2007112347A1
(en)
|
2006-03-28 |
2007-10-04 |
Takeda Pharmaceutical Company Limited |
Dipeptidyl peptidase inhibitors
|
US8349850B2
(en)
|
2006-03-28 |
2013-01-08 |
Atir Holding S.A. |
Heterocyclic compounds and uses thereof in the treatment of sexual disorders
|
CN101460161A
(zh)
|
2006-03-29 |
2009-06-17 |
弗尔德里克斯制药股份有限公司 |
α-突触核蛋白毒性的抑制
|
JP2010505739A
(ja)
|
2006-04-06 |
2010-02-25 |
ウイスコンシン アラムニ リサーチ ファンデーション |
2−メチレン−1α,25−ジヒドロキシ−19,21−ジノルビタミンD3類縁体およびその使用
|
JP2009533426A
(ja)
|
2006-04-13 |
2009-09-17 |
アストラゼネカ・アクチエボラーグ |
チオキサンチン誘導体およびそれらのmpo阻害剤としての用途
|
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
|
ATE499374T1
(de)
|
2006-05-11 |
2011-03-15 |
Irm Llc |
Verbindungen und zusammensetzungen als proteinkinase-hemmer
|
BRPI0711628A2
(pt)
|
2006-05-15 |
2011-12-06 |
Irm Llc |
composto, composição farmacêutica, uso e processo para preparação do composto
|
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
|
CA2656825C
(en)
|
2006-06-22 |
2013-12-10 |
Prana Biotechnology Limited |
Method of treatment and agents useful for same
|
TW200817391A
(en)
|
2006-06-30 |
2008-04-16 |
Astrazeneca Ab |
Novel compounds
|
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
|
WO2008003766A2
(en)
|
2006-07-06 |
2008-01-10 |
Boehringer Ingelheim International Gmbh |
4-heter0cycl0alkylpyri(mi)dines, process for the preparation thereof and their use as medicaments
|
US8030487B2
(en)
|
2006-07-07 |
2011-10-04 |
Targegen, Inc. |
2-amino—5-substituted pyrimidine inhibitors
|
TW200811134A
(en)
|
2006-07-12 |
2008-03-01 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
WO2008012635A2
(en)
|
2006-07-26 |
2008-01-31 |
Pfizer Products Inc. |
Amine derivatives useful as anticancer agents
|
JP2010500372A
(ja)
|
2006-08-09 |
2010-01-07 |
スミスクライン ビーチャム コーポレーション |
オピオイド受容体に対するアンタゴニストまたはインバースアゴニストとしての新規化合物
|
US20100075947A1
(en)
|
2006-08-16 |
2010-03-25 |
Exelixis, Inc. |
Methods of Using PI3K and MEK Modulators
|
DE102006041382A1
(de)
|
2006-08-29 |
2008-03-20 |
Bayer Schering Pharma Ag |
Carbamoyl-Sulfoximide als Proteinkinaseinhibitoren
|
CA2661842C
(en)
|
2006-09-01 |
2017-08-22 |
Cylene Pharmaceuticals, Inc. |
Tricyclic heteroaryl compounds and their use as serine-threonine protein kinases and parp modulators
|
EP2364702A3
(en)
|
2006-09-05 |
2012-01-25 |
Emory University |
Kinase inhibitors for preventing or treating pathogen infection and method of use thereof
|
US20100160292A1
(en)
|
2006-09-11 |
2010-06-24 |
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
|
AR062928A1
(es)
|
2006-09-22 |
2008-12-17 |
Glaxo Group Ltd |
Inhibidores de la actividad quinasa utiles en el tratamiento de trastornos mediados por mecanismos de ikk2
|
JP2010504927A
(ja)
|
2006-09-28 |
2010-02-18 |
ノバルティス アーゲー |
ピラゾロ[1,5−a]ピリミジン誘導体およびそれらの治療的使用
|
US8202876B2
(en)
|
2006-10-02 |
2012-06-19 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
TW200825058A
(en)
|
2006-10-30 |
2008-06-16 |
Glaxo Group Ltd |
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
|
WO2008063583A1
(en)
|
2006-11-17 |
2008-05-29 |
Polyera Corporation |
Acene-based organic semiconductor materials and methods of preparing and using the same
|
EP2086974B1
(en)
|
2006-11-17 |
2013-07-24 |
Polyera Corporation |
Diimide-based semiconductor materials and methods of preparing and using the same
|
KR20080045536A
(ko)
|
2006-11-20 |
2008-05-23 |
에스케이케미칼주식회사 |
피리딘 화합물을 포함하는 간염 치료 및 예방 또는 간 보호효능을 갖는 약제 조성물
|
MX2009005144A
(es)
|
2006-11-22 |
2009-05-27 |
Incyte Corp |
Imidazotriazinas e imidazopirimidinas como inhibidores de cinasa.
|
MX2009006466A
(es)
|
2006-12-13 |
2009-06-26 |
Schering Corp |
Metodos de tratamiento de cancer con inhibidores del receptor del factor 1 de crecimiento similar a la insulina.
|
WO2008071455A1
(en)
|
2006-12-15 |
2008-06-19 |
Bayer Schering Pharma Aktiengesellschaft |
Bicyclic acyltryptophanols
|
WO2008074068A1
(en)
|
2006-12-20 |
2008-06-26 |
Prana Biotechnology Limited |
Substituted quinoline derivatives as antiamyloidogeneic agents
|
US7737149B2
(en)
|
2006-12-21 |
2010-06-15 |
Astrazeneca Ab |
N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]-4-(3,5-dimethylpiperazin-1-yl)benzamide and salts thereof
|
CN101679408B
(zh)
|
2006-12-22 |
2016-04-27 |
Astex治疗学有限公司 |
作为fgfr抑制剂的双环杂环化合物
|
CN101679409B
(zh)
|
2006-12-22 |
2014-11-26 |
Astex治疗学有限公司 |
双环杂环衍生化合物、其医药组合物和其用途
|
AU2007336933A1
(en)
|
2006-12-22 |
2008-07-03 |
Novartis Ag |
Heteroaryl-heteroaryl compounds as CDK inhibitors for the treatment of cancer, inflammation and viral infections
|
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
|
US7893265B2
(en)
|
2007-01-08 |
2011-02-22 |
Polyera Corporation |
Methods for preparing arene-BIS (dicarboximide)-based semiconducting materials and related intermediates for preparing same
|
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
|
JP5287253B2
(ja)
|
2007-01-12 |
2013-09-11 |
アステラス製薬株式会社 |
縮合ピリジン化合物
|
FR2911604B1
(fr)
|
2007-01-19 |
2009-04-17 |
Sanofi Aventis Sa |
Derives de n-(heteroaryl-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique
|
JP5358962B2
(ja)
|
2007-02-06 |
2013-12-04 |
住友化学株式会社 |
組成物及び該組成物を用いてなる発光素子
|
JP2008198769A
(ja)
|
2007-02-13 |
2008-08-28 |
Nippon Steel Chem Co Ltd |
有機エレクトロルミネッセント素子
|
CA2678492A1
(en)
|
2007-03-06 |
2008-09-12 |
Novartis Ag |
Bicyclic organic compounds suitable for the treatment of inflammatory or allergic conditions
|
MX2009009540A
(es)
|
2007-03-07 |
2009-09-16 |
Alantos Pharm Holding |
Inhibidores de metaloproteasa que contienen una porcion heterociclica.
|
EP3023422A1
(en)
|
2007-03-12 |
2016-05-25 |
YM BioSciences Australia Pty Ltd |
Phenyl amino pyrimidine compounds and uses thereof
|
AU2007227278B2
(en)
|
2007-03-21 |
2014-09-11 |
Epix Pharmaceuticals, Inc. |
SIP 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
|
CA2680783C
(en)
|
2007-03-23 |
2012-04-24 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
KR20080091948A
(ko)
|
2007-04-10 |
2008-10-15 |
에스케이케미칼주식회사 |
락탐형 피리딘 화합물을 포함하는 허혈성 질환의 예방 및치료용 약학조성물
|
WO2008128141A2
(en)
|
2007-04-12 |
2008-10-23 |
Advanced Technology Materials, Inc. |
Zirconium, hafnuim, 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
|
US8163752B2
(en)
|
2007-06-07 |
2012-04-24 |
Merck, Sharp & Dohme Corp. |
Tricyclic anilide heterocyclic CGRP receptor antagonists
|
US7928111B2
(en)
|
2007-06-08 |
2011-04-19 |
Senomyx, Inc. |
Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
|
US8633186B2
(en)
|
2007-06-08 |
2014-01-21 |
Senomyx Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
PL2168966T3
(pl)
|
2007-06-15 |
2017-06-30 |
Msd K.K. |
Pochodna bicykloaniliny
|
BRPI0812913B8
(pt)
|
2007-06-18 |
2021-05-25 |
Merck Sharp & Dohme |
anticorpos monoclonais ou fragmento de anticorpo para o receptor de morte programada humano pd-1, polinucleotideo, método para produzir os referidos anticorpos ou fragmentos de anticorpos, composição que os compreende e uso dos mesmos
|
PE20090506A1
(es)
|
2007-07-26 |
2009-05-28 |
Novartis Ag |
DERIVADOS DE IMIDAZO-[1,2-b]-PIRIDAZIN COMO INHIBIDORES DE ALK5 Y/O ALK4
|
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
|
EP2173354A4
(en)
|
2007-08-09 |
2011-10-05 |
Glaxosmithkline Llc |
CHINOXALIN DERIVATIVES AS PI3 KINASE INHIBITORS
|
WO2009019518A1
(en)
|
2007-08-09 |
2009-02-12 |
Astrazeneca Ab |
Pyrimidine compounds having a fgfr inhibitory effect
|
US9493419B2
(en)
|
2007-08-21 |
2016-11-15 |
The Hong Kong Polytechnic University |
Quinoline derivatives as anti-cancer agents
|
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
|
PT2200436E
(pt)
|
2007-09-04 |
2015-04-29 |
Scripps Research Inst |
Pirimidinilaminas substituídas como inibidoras da proteína quinase
|
WO2009030871A1
(en)
|
2007-09-07 |
2009-03-12 |
Vernalis R & D Ltd |
Pyrrolopyrimidine derivatives having hsp90 inhibitory activity
|
TW200920357A
(en)
|
2007-09-10 |
2009-05-16 |
Curis Inc |
HSP90 inhibitors containing a zinc binding moiety
|
JP5792955B2
(ja)
|
2007-10-01 |
2015-10-14 |
アイシス ファーマシューティカルズ, インコーポレーテッド |
線維芽細胞増殖因子受容体4発現のアンチセンスモジュレーション
|
WO2009044788A1
(ja)
|
2007-10-05 |
2009-04-09 |
Banyu Pharmaceutical Co., Ltd. |
ベンゾオキサジノン誘導体
|
WO2009047255A1
(en)
|
2007-10-09 |
2009-04-16 |
Ucb Pharma, S.A. |
Heterobicyclic compounds as histamine h4-receptor antagonists
|
WO2009049018A1
(en)
|
2007-10-10 |
2009-04-16 |
Syndax Pharmaceuticals, Inc. |
Novel compounds and methods of using them
|
US8513233B2
(en)
|
2007-10-11 |
2013-08-20 |
Shanghai Institute Of Materia Medica, Cas |
Pyrimidinyl-propionic acid derivatives and their use as PPAR agonists
|
GB0720041D0
(en)
|
2007-10-12 |
2007-11-21 |
Astex Therapeutics Ltd |
New Compounds
|
GB0720038D0
(en)
|
2007-10-12 |
2007-11-21 |
Astex Therapeutics Ltd |
New compounds
|
JP5273052B2
(ja)
|
2007-10-13 |
2013-08-28 |
コニカミノルタ株式会社 |
有機エレクトロルミネッセンス素子、表示装置及び照明装置
|
MX2010004260A
(es)
|
2007-10-16 |
2010-04-30 |
Wyeth Llc |
Compuestos de tienopirimidina y pirazolopirimidina y su uso como inhibidores de mtor cinasa y pi3 cinasa.
|
WO2009050183A2
(en)
|
2007-10-17 |
2009-04-23 |
Novartis Ag |
Imidazo [1, 2-a] pyridine derivatives useful as alk inhibitors
|
CA2703653A1
(en)
|
2007-10-25 |
2009-04-30 |
Astrazeneca Ab |
Pyridine and pyrazine derivatives -083
|
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
|
KR20100130583A
(ko)
|
2007-11-28 |
2010-12-13 |
다나-파버 캔서 인스티튜트 인크. |
Bcr-abl의 소 분자 미리스테이트 억제제 및 이의 사용 방법
|
JP2011505407A
(ja)
|
2007-12-03 |
2011-02-24 |
ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング |
過剰な又は異常な細胞増殖を特徴とする疾患を治療するためのジアミノピリジン
|
JP5537439B2
(ja)
|
2007-12-19 |
2014-07-02 |
アムジエン・インコーポレーテツド |
細胞周期阻害剤としての縮合ピリジン、ピリミジンおよびトリアジン化合物
|
CA2709784A1
(en)
|
2007-12-21 |
2009-07-09 |
University Of Rochester |
Method for altering the lifespan of eukaryotic organisms
|
US20100331333A1
(en)
|
2007-12-21 |
2010-12-30 |
Wyeth Llc |
Imidazo [1,2-B] Pyridazine Compounds
|
US8153827B2
(en)
|
2007-12-27 |
2012-04-10 |
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.
|
KR20100119777A
(ko)
|
2008-01-24 |
2010-11-10 |
알라 캠, 엘엘씨 |
치환된 사이클로알카노[e 및 d] 피라졸로 [1,5―A]피리미딘/세로토닌 5―HT6 수용체의 길항제 및 이의 제조방법 및 이의 용도
|
US8471009B2
(en)
|
2008-01-24 |
2013-06-25 |
Andrey Alexandrovich Ivashchenko |
(EN) 2-alkylamino-3-arylsulfonyl-cycloalcano [e OR d] pyrazolo [1,5-A]pyrimidines / antagonists of serotonin 5-HT6 receptors, methods for the production and the use thereof
|
CN101925606A
(zh)
|
2008-01-24 |
2010-12-22 |
Ucb医药有限公司 |
包含环丁氧基的化合物
|
CN101925301B
(zh)
|
2008-01-25 |
2014-09-17 |
高点制药有限责任公司 |
作为TNF-α合成调节剂和作为PDE4抑制剂的三环化合物
|
ES2494365T3
(es)
|
2008-01-30 |
2014-09-15 |
Genentech, Inc. |
Compuestos de pirazolopirimidina que inhiben PI3K y métodos de uso
|
WO2009099982A1
(en)
|
2008-02-04 |
2009-08-13 |
Osi Pharmaceuticals, Inc. |
2-aminopyridine kinase inhibitors
|
US20110190263A1
(en)
|
2008-02-22 |
2011-08-04 |
Irm Llc |
Compounds and compositions as modulators of gpr119 activity
|
MX2010008700A
(es)
|
2008-02-22 |
2010-08-30 |
Hoffmann La Roche |
Moduladores de beta-amiloide.
|
CA2716128A1
(en)
|
2008-02-27 |
2009-09-03 |
Vitae Pharmaceuticals, Inc. |
Inhibitors of 11.beta.-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
|
WO2009114335A2
(en)
|
2008-03-12 |
2009-09-17 |
Merck & Co., Inc. |
Pd-1 binding proteins
|
GB0804701D0
(en)
|
2008-03-13 |
2008-04-16 |
Amura Therapeutics Ltd |
Compounds
|
US8993580B2
(en)
|
2008-03-14 |
2015-03-31 |
Intellikine Llc |
Benzothiazole kinase inhibitors and methods of use
|
EP2252293B1
(en)
|
2008-03-14 |
2018-06-27 |
Intellikine, LLC |
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
|
US20100056524A1
(en)
|
2008-04-02 |
2010-03-04 |
Mciver Edward Giles |
Compound
|
US8436005B2
(en)
|
2008-04-03 |
2013-05-07 |
Abbott Laboratories |
Macrocyclic pyrimidine derivatives
|
MX2010010975A
(es)
|
2008-04-07 |
2010-11-01 |
Amgen Inc |
Amino piridinas/pirimidinas gem-disustituidas y espirociclicas como inhibidores de ciclo celular.
|
WO2009124755A1
(en)
|
2008-04-08 |
2009-10-15 |
European Molecular Biology Laboratory (Embl) |
Compounds with novel medical uses and method of identifying such compounds
|
WO2009125808A1
(ja)
|
2008-04-11 |
2009-10-15 |
第一三共株式会社 |
アミノシクロヘキシル誘導体
|
WO2009125809A1
(ja)
|
2008-04-11 |
2009-10-15 |
第一三共株式会社 |
ピペリジン誘導体
|
US20110105457A1
(en)
|
2008-04-18 |
2011-05-05 |
Shionogi & Co., Ltd. |
Heterocyclic compound having inhibitory activity on pi3k
|
WO2009131687A2
(en)
|
2008-04-22 |
2009-10-29 |
Portola Pharmaceuticals, Inc. |
Inhibitors of protein kinases
|
US7863291B2
(en)
|
2008-04-23 |
2011-01-04 |
Bristol-Myers Squibb Company |
Quinuclidine compounds as alpha-7 nicotinic acetylcholine receptor ligands
|
US8309577B2
(en)
|
2008-04-23 |
2012-11-13 |
Bristol-Myers Squibb Company |
Quinuclidine compounds as α-7 nicotinic acetylcholine receptor ligands
|
EP2280969A1
(en)
|
2008-04-29 |
2011-02-09 |
F. Hoffmann-La Roche AG |
Pyrimidinyl pyridone inhibitors of jnk.
|
RU2010148531A
(ru)
|
2008-04-29 |
2012-06-10 |
Новартис АГ (CH) |
Способы мониторинга модуляции киназной активности рецептора фактора роста фибробластов и применения указанных способов
|
AR071523A1
(es)
|
2008-04-30 |
2010-06-23 |
Merck Serono Sa |
Compuestos biciclicos fusionados, un proceso para su preparacion, el compuesto para ser utilizado como medicamento en el tratamiento y profilaxis de enfermedades, una composicion farmaceutica y un conjunto que comprende paquetes separados del compuesto y de un ingrediente activo del medicamento
|
US9315449B2
(en)
|
2008-05-15 |
2016-04-19 |
Duke University |
Substituted pyrazoles as heat shock transcription factor activators
|
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
|
MX2010013224A
(es)
|
2008-06-03 |
2010-12-21 |
Merck Sharp & Dohme |
Inhibidores de la actividad de la serina/treonina cinasa.
|
US8377332B2
(en)
|
2008-06-10 |
2013-02-19 |
Basf Se |
Transition metal complexes and use thereof in organic light emitting diodes—III
|
BRPI0909954A2
(pt)
|
2008-06-11 |
2015-11-03 |
Genentech Inc |
"diazacarbazóis e métodos de uso"
|
EP2303885B1
(en)
|
2008-06-12 |
2013-07-03 |
Merck Sharp & Dohme Corp. |
Process for producing bicycloaniline derivatives
|
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
|
GB0810902D0
(en)
|
2008-06-13 |
2008-07-23 |
Astex Therapeutics Ltd |
New compounds
|
MX2010014234A
(es)
|
2008-06-19 |
2011-03-25 |
Astrazeneca Ab |
Compuestos pirazol 436.
|
TW201004958A
(en)
|
2008-06-24 |
2010-02-01 |
Res Found Itsuu Lab |
Oxazolidinone derivatives having a fused ring
|
US8338439B2
(en)
|
2008-06-27 |
2012-12-25 |
Celgene Avilomics Research, Inc. |
2,4-disubstituted pyrimidines useful as kinase inhibitors
|
CA2729965A1
(en)
|
2008-07-14 |
2010-01-21 |
Gilead Sciences, Inc. |
Fused heterocyclyc inhibitor compounds
|
WO2010007099A1
(en)
|
2008-07-15 |
2010-01-21 |
Cellzome Limited |
2-aminoimidazo[1,2-b]pyridazine derivatives as pi3k inhibitors
|
ES2552681T3
(es)
|
2008-07-15 |
2015-12-01 |
F. Hoffmann-La Roche Ag |
Nuevas fenil-imidazopiridinas y piridazinas
|
AU2009270983A1
(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
|
AU2009270971A1
(en)
|
2008-07-16 |
2010-01-21 |
Schering Corporation |
Bicyclic Heterocycle Derivatives and use thereof as GPR119 modulators
|
WO2010009735A2
(en)
|
2008-07-23 |
2010-01-28 |
Dako Denmark A/S |
Combinatorial analysis and repair
|
WO2010017047A1
(en)
|
2008-08-05 |
2010-02-11 |
Merck & Co., Inc. |
Therapeutic compounds
|
WO2010015643A1
(en)
|
2008-08-06 |
2010-02-11 |
Novartis Ag |
New antiviral modified nucleosides
|
JP2011530596A
(ja)
|
2008-08-11 |
2011-12-22 |
プレジデント アンド フェロウズ オブ ハーバード カレッジ |
tRNA合成酵素の阻害のためのハロフジノン類似体およびそれらの使用
|
UY32049A
(es)
|
2008-08-14 |
2010-03-26 |
Takeda Pharmaceutical |
Inhibidores de cmet
|
US20110166135A1
(en)
|
2008-09-10 |
2011-07-07 |
Hiroshi Morimoto |
Aromatic nitrogen-containing 6-membered ring compounds and their use
|
CA2738252C
(en)
|
2008-09-26 |
2018-05-01 |
Dana-Farber Cancer Institute, Inc. |
Human anti-pd-1, pd-l1, and pd-l2 antibodies and uses therefor
|
WO2010038081A2
(en)
|
2008-10-03 |
2010-04-08 |
Astrazeneca Ab |
Heterocyclic derivatives and methods of use thereof
|
WO2010045371A1
(en)
|
2008-10-15 |
2010-04-22 |
Gilead Palo Alto, Inc. |
Pyrido- and pyrimido (1, 2-a) pyrimidine compounds useful as stearoyl coa desaturase inhibitors
|
US8110578B2
(en)
|
2008-10-27 |
2012-02-07 |
Signal Pharmaceuticals, Llc |
Pyrazino[2,3-b]pyrazine mTOR kinase inhibitors for oncology indications and diseases associated with the mTOR/PI3K/Akt pathway
|
WO2010049731A1
(en)
|
2008-10-29 |
2010-05-06 |
Astrazeneca Ab |
Pyrazolo- and imidazopyridinylpyrimidineamines as igf-1r tyrosine kinase inhibitors
|
US8476282B2
(en)
|
2008-11-03 |
2013-07-02 |
Intellikine 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
|
EP2362775B1
(en)
|
2008-11-20 |
2015-08-05 |
GlaxoSmithKline LLC |
Chemical compounds
|
WO2010064621A1
(ja)
|
2008-12-03 |
2010-06-10 |
コニカミノルタホールディングス株式会社 |
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
|
NZ717213A
(en)
|
2008-12-09 |
2017-10-27 |
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
|
CA2745970A1
(en)
|
2008-12-12 |
2010-06-17 |
Msd K.K. |
Dihydropyrimidopyrimidine derivative
|
JP2012511501A
(ja)
|
2008-12-12 |
2012-05-24 |
Msd株式会社 |
ジヒドロピリミドピリミジン誘導体
|
NZ593537A
(en)
|
2008-12-19 |
2013-07-26 |
Genentech Inc |
Isoquinoline derivatives and methods of use
|
PA8852901A1
(es)
|
2008-12-22 |
2010-07-27 |
Lilly Co Eli |
Inhibidores de proteina cinasa
|
US8263610B2
(en)
|
2008-12-30 |
2012-09-11 |
Arqule, Inc. |
Substituted imidazolyl-5,6-dihydrobenzo[N]isoquinoline compounds
|
US8357694B2
(en)
|
2008-12-30 |
2013-01-22 |
Arqule, Inc. |
Substituted 5,6-dihydro-6-phenylbenzo[F]isoquinolin-2-amine compounds
|
EP3828185A3
(en)
|
2009-01-06 |
2021-09-01 |
Dana Farber Cancer Institute, Inc. |
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
|
EP2387315B1
(en)
|
2009-01-16 |
2015-07-15 |
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
|
JP5844159B2
(ja)
|
2009-02-09 |
2016-01-13 |
ユニヴェルシテ デクス−マルセイユUniversite D’Aix−Marseille |
Pd−1抗体およびpd−l1抗体ならびにその使用
|
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
|
WO2010103306A1
(en)
|
2009-03-10 |
2010-09-16 |
Astrazeneca Uk Limited |
Benzimidazole derivatives and their use as antivaral agents
|
JP5615261B2
(ja)
|
2009-03-11 |
2014-10-29 |
学校法人関西学院 |
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
|
WO2010111303A2
(en)
|
2009-03-23 |
2010-09-30 |
Siemens Medical Solutions Usa, Inc. |
Imaging agents for detecting neurological disorders
|
WO2010111573A1
(en)
|
2009-03-27 |
2010-09-30 |
Abbott Laboratories |
Compounds as cannabinoid receptor ligands
|
WO2010117425A1
(en)
|
2009-03-31 |
2010-10-14 |
Biogen Idec Ma Inc. |
Certain substituted pyrimidines, pharmaceutical compositions thereof, and methods for their use
|
US8481525B2
(en)
|
2009-04-06 |
2013-07-09 |
University Of Health Network |
Kinase inhibitors and method of treating cancer with same
|
US8415378B2
(en)
|
2009-04-07 |
2013-04-09 |
Astrazeneca Ab |
Isoxazol-3(2H)-one analogs as therapeutic agents
|
GB0906470D0
(en)
|
2009-04-15 |
2009-05-20 |
Astex Therapeutics Ltd |
New compounds
|
GB0906472D0
(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.
|
US8765754B2
(en)
|
2009-04-29 |
2014-07-01 |
Locus Pharmaceuticals, Inc. |
Pyrrolotriazine compounds
|
US20100280067A1
(en)
|
2009-04-30 |
2010-11-04 |
Pakala Kumara Savithru Sarma |
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
|
WO2010151689A1
(en)
|
2009-06-25 |
2010-12-29 |
Alkermes, Inc. |
Heterocyclic compounds for the treatment of neurological and psychological disorders
|
JP5732673B2
(ja)
|
2009-06-30 |
2015-06-10 |
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
|
US20120135997A1
(en)
|
2009-07-17 |
2012-05-31 |
Shionogi & Co., Ltd. |
Pharmaceutical composition comprising a lactam or benzenesulfonamide 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
|
IN2012DN01254A
(es)
|
2009-08-05 |
2015-05-15 |
Versitech Ltd |
|
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
|
CN102574836B
(zh)
|
2009-08-07 |
2014-04-16 |
中外制药株式会社 |
氨基吡唑衍生物
|
WO2011018894A1
(en)
|
2009-08-10 |
2011-02-17 |
Raqualia Pharma Inc. |
Pyrrolopyrimidine derivatives as potassium channel modulators
|
MY162604A
(en)
|
2009-08-17 |
2017-06-30 |
Intellikine Llc |
Heterocyclic compounds and uses thereof
|
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
|
BR112012004533B1
(pt)
|
2009-09-03 |
2021-11-09 |
Bioenergenix |
Composto, composição farmacêutica, e uso do composto
|
US9340528B2
(en)
|
2009-09-04 |
2016-05-17 |
Bayer Pharma Aktiengesellschaft |
Substituted aminoquinoxalines as tyrosine threonine kinase inhibitors
|
WO2011031740A1
(en)
|
2009-09-09 |
2011-03-17 |
Achaogen, Inc. |
Antibacterial fluoroquinolone analogs
|
US9481675B2
(en)
|
2009-09-11 |
2016-11-01 |
Merck Sharp & Dohme Corp. |
Gyrase inhibitors
|
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
|
CN102666541B
(zh)
|
2009-10-22 |
2015-11-25 |
吉里德科学公司 |
用于治疗特别是病毒感染的嘌呤或脱氮嘌呤的衍生物
|
WO2011050245A1
(en)
|
2009-10-23 |
2011-04-28 |
Yangbo Feng |
Bicyclic heteroaryls as kinase inhibitors
|
MY177695A
(en)
|
2009-10-26 |
2020-09-23 |
Signal Pharm Llc |
Methods of synthesis and purification of heteroaryl compounds
|
CN102596916B
(zh)
|
2009-10-30 |
2015-06-17 |
诺瓦提斯公司 |
3-(2,6-二氯-3,5-二甲氧基-苯基)-1-{6-[4-(4-乙基-哌嗪-1-基)-苯基氨基]-嘧啶-4-基}-1-甲基-脲的n-氧化物
|
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
|
JP2013510166A
(ja)
|
2009-11-06 |
2013-03-21 |
プレキシコン インコーポレーテッド |
キナーゼ調節のための化合物、方法およびその適用
|
BR112012011287B1
(pt)
|
2009-11-13 |
2022-02-08 |
Genosco |
Compostos inibidores de cinase derivados de pirolopirimidina, sua formulação farmacêutica e seus usos
|
RU2012125070A
(ru)
|
2009-11-18 |
2013-12-27 |
Плексксикон, Инк. |
Соединения и способы модулирования киназы и показания к их применению
|
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
|
US20130017199A1
(en)
|
2009-11-24 |
2013-01-17 |
AMPLIMMUNE ,Inc. a corporation |
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
|
EP2506713A4
(en)
|
2009-12-01 |
2014-09-03 |
Abbvie Inc |
NEW TRICYCLIC COMPOUNDS
|
HUE033099T2
(en)
|
2009-12-01 |
2017-11-28 |
Abbvie Inc |
New tricyclic compounds
|
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
|
PE20121480A1
(es)
|
2009-12-17 |
2012-11-10 |
Merck Sharp & Dohme |
Aminopirimidinas como inhibidores de syk
|
US20120258940A1
(en)
|
2009-12-18 |
2012-10-11 |
Giordano Caponigro |
Method for treating haematological cancers
|
EP2516417B1
(en)
|
2009-12-22 |
2017-10-11 |
Vertex Pharmaceuticals Incorporated |
Isoindolinone inhibitors of phosphatidylinositol 3-kinase
|
FR2954315B1
(fr)
|
2009-12-23 |
2012-02-24 |
Galderma Res & Dev |
Nouveaux derives phenoliques, et leur utilisation pharmaceutique ou cosmetique
|
FR2954317B1
(fr)
|
2009-12-23 |
2012-01-27 |
Galderma Res & Dev |
Nouveaux derives phenoliques, et leur utilisation pharmaceutique ou cosmetique
|
WO2011079231A1
(en)
|
2009-12-23 |
2011-06-30 |
Gatekeeper Pharmaceutical, Inc. |
Compounds that modulate egfr activity and methods for treating or preventing conditions therewith
|
EP2519241A2
(en)
|
2009-12-28 |
2012-11-07 |
Afraxis, Inc. |
Methods for treating autism
|
AU2010343102B2
(en)
|
2009-12-29 |
2016-03-24 |
Dana-Farber Cancer Institute, Inc. |
Type II Raf kinase inhibitors
|
US8440828B2
(en)
|
2009-12-29 |
2013-05-14 |
Polyera Corporation |
Organic semiconductors and devices incorporating same
|
WO2011080755A1
(en)
|
2009-12-29 |
2011-07-07 |
Advinus Therapeutics Private Limited |
Fused nitrogen heterocyclic compounds, process of preparation and uses thereof
|
CN102892768A
(zh)
|
2009-12-30 |
2013-01-23 |
艾科尔公司 |
被取代的吡咯并氨基嘧啶化合物
|
US8329705B2
(en)
|
2009-12-30 |
2012-12-11 |
Arqule, Inc. |
Substituted triazolo-pyrazine compounds
|
WO2011082266A2
(en)
|
2009-12-30 |
2011-07-07 |
Arqule, Inc. |
Substituted heterocyclic compounds
|
CN102115026A
(zh)
|
2009-12-31 |
2011-07-06 |
清华大学 |
一维纳米结构、其制备方法及一维纳米结构作标记的方法
|
WO2011082400A2
(en)
|
2010-01-04 |
2011-07-07 |
President And Fellows Of Harvard College |
Modulators of immunoinhibitory receptor pd-1, and methods of use thereof
|
AR079975A1
(es)
|
2010-01-06 |
2012-03-07 |
British Columbia Cancer Agency |
Agentes terapeuticos derivados de bisfenol u metodos para su uso, composiciones farmaceuticas y uso de los mismos
|
CN102712640A
(zh)
|
2010-01-12 |
2012-10-03 |
弗·哈夫曼-拉罗切有限公司 |
三环杂环化合物、其组合物和应用方法
|
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
|
CA2789344A1
(en)
|
2010-02-15 |
2011-08-18 |
Jeremy Earle Wulff |
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
|
WO2011103196A1
(en)
|
2010-02-17 |
2011-08-25 |
Amgen Inc. |
Aryl carboxamide derivatives as sodium channel inhibitors for treatment of pain
|
WO2011103460A1
(en)
|
2010-02-18 |
2011-08-25 |
Medivation Technologies, Inc. |
Fused tetracyclic pyrido[4,3-b]indole and pyrido[3,4-b]ondole derivatives and methods of use
|
EP2536410B1
(en)
|
2010-02-18 |
2015-09-23 |
Merck Sharp & Dohme Corp. |
Substituted pyrimidine derivatives and their use in treating viral infections
|
US9150809B2
(en)
|
2010-02-18 |
2015-10-06 |
Ntn Corporation |
Thickener, grease, method for producing the same, and grease-packed bearing
|
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
|
CN102770981B
(zh)
|
2010-02-26 |
2015-05-13 |
新日铁住金化学株式会社 |
有机场致发光元件
|
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
|
WO2011112687A2
(en)
|
2010-03-10 |
2011-09-15 |
Kalypsys, Inc. |
Heterocyclic inhibitors of histamine receptors for the treatment of disease
|
EP2545052B1
(en)
|
2010-03-11 |
2014-11-12 |
Gilead Connecticut, Inc. |
Imidazopyridines syk inhibitors
|
EA201290919A1
(ru)
|
2010-03-16 |
2013-03-29 |
Дана-Фарбер Кэнсер Инститьют, Инк. |
Индазольные соединения и их применение
|
JP6065183B2
(ja)
|
2010-03-24 |
2017-01-25 |
アミテック セラピューティック ソリューションズ,インク. |
キナーゼ阻害に役立つ複素環式化合物
|
CN102918045A
(zh)
|
2010-03-31 |
2013-02-06 |
百时美施贵宝公司 |
作为蛋白激酶抑制剂的取代的吡咯并三嗪
|
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
|
ES2562419T3
(es)
|
2010-04-13 |
2016-03-04 |
Rigel Pharmaceuticals, Inc. |
Compuestos de 2,4-pirimidinodiamina y sus profármacos y sus usos
|
DK2558095T3
(en)
|
2010-04-16 |
2019-01-14 |
Novartis Ag |
ORGANIC RELATIONSHIP FOR USE IN TREATMENT OF DELIVERY CANCER
|
EP2560962B1
(en)
|
2010-04-22 |
2015-05-20 |
Janssen Pharmaceutica NV |
Indazole compounds useful as ketohexokinase inhibitors
|
BR112012026641A2
(pt)
|
2010-04-23 |
2016-07-12 |
Kineta Inc |
compostos antivirais
|
AR081331A1
(es)
|
2010-04-23 |
2012-08-08 |
Cytokinetics Inc |
Amino- pirimidinas composiciones de las mismas y metodos para el uso de los mismos
|
GB201007286D0
(en)
|
2010-04-30 |
2010-06-16 |
Astex Therapeutics Ltd |
New compounds
|
CN103025744A
(zh)
|
2010-04-30 |
2013-04-03 |
百时美施贵宝公司 |
作为α-7烟碱乙酰胆碱受体配体前药的氮杂二环胺N-氧化物化合物
|
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
|
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
|
CA2798831A1
(en)
|
2010-05-11 |
2011-11-17 |
Pfizer Inc. |
Morpholine compounds as mineralocorticoid receptor antagonists
|
CA2800311A1
(en)
|
2010-05-11 |
2011-11-17 |
Aveo Pharmaceuticals, Inc. |
Anti-fgfr2 antibodies
|
WO2011143430A1
(en)
|
2010-05-12 |
2011-11-17 |
Abbott Laboratories |
Indazole inhibitors of kinase
|
CA2798081C
(en)
|
2010-05-12 |
2024-02-13 |
Spectrum Pharmaceuticals, Inc. |
Lanthanum carbonate hydroxide, lanthanum oxycarbonate and methods of their manufacture and use
|
GB201008134D0
(en)
|
2010-05-14 |
2010-06-30 |
Medical Res Council Technology |
Compounds
|
WO2011147199A1
(en)
|
2010-05-28 |
2011-12-01 |
Versitech Limited |
Compounds and methods for treating viral infections
|
WO2011147198A1
(en)
|
2010-05-28 |
2011-12-01 |
Versitech Limited |
Compounds and methods for treatment of proliferative diseases
|
WO2011153553A2
(en)
|
2010-06-04 |
2011-12-08 |
The Regents Of The University Of California |
Methods and compositions for kinase inhibition
|
EA201291220A1
(ru)
|
2010-06-04 |
2013-07-30 |
Ф.Хоффманн-Ля Рош Аг |
Производные аминопиримидина в качестве модуляторов lrrk2
|
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
|
US9163087B2
(en)
|
2010-06-18 |
2015-10-20 |
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
|
CA2803446C
(en)
|
2010-07-02 |
2019-06-04 |
University Health Network |
Use of plk4 antagonists for treating pten mutant diseases
|
FR2962438B1
(fr)
|
2010-07-06 |
2012-08-17 |
Sanofi Aventis |
Derives d'indolizines, procedes de preparation et application en therapeutique
|
FR2962437B1
(fr)
|
2010-07-06 |
2012-08-17 |
Sanofi Aventis |
Derives d'imidazopyridine, leur procede de preparation et leur application en therapeutique
|
US20130109682A1
(en)
|
2010-07-06 |
2013-05-02 |
Novartis Ag |
Cyclic ether compounds useful as kinase inhibitors
|
US8962830B2
(en)
|
2010-07-09 |
2015-02-24 |
The Walter And Eliza Hall Institute Of Medical Research |
Protein kinase inhibitors and methods of treatment
|
WO2012009258A2
(en)
|
2010-07-13 |
2012-01-19 |
Edward Roberts |
Peptidomimetic galanin receptor modulators
|
WO2012008999A2
(en)
|
2010-07-14 |
2012-01-19 |
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
|
WO2012008563A1
(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
|
US8987273B2
(en)
|
2010-07-28 |
2015-03-24 |
Bayer Intellectual Property Gmbh |
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
|
JP2013539206A
(ja)
|
2010-07-30 |
2013-10-17 |
ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド |
発光材料として電界発光化合物を使用する電界発光素子
|
WO2012019093A1
(en)
|
2010-08-05 |
2012-02-09 |
Human Biomolecular Research Institute |
Synthetic compounds and methods to decrease nicotine self-administration
|
US9051280B2
(en)
|
2010-08-13 |
2015-06-09 |
AbbVie Deutschland GmbH & Co. KG |
Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy
|
US8883839B2
(en)
|
2010-08-13 |
2014-11-11 |
Abbott Laboratories |
Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy
|
EP2608669B1
(en)
|
2010-08-23 |
2016-06-22 |
Merck Sharp & Dohme Corp. |
NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
WO2012027239A1
(en)
|
2010-08-23 |
2012-03-01 |
Schering Corporation |
NOVEL PYRAZOLO[1,5-a]PYRROLO[3,2-e]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
BR112013007499A2
(pt)
|
2010-09-01 |
2016-07-12 |
Genentech Inc |
piridazinonas - métodos de criação e usos
|
CN103189369B
(zh)
|
2010-09-01 |
2016-08-24 |
吉利德康涅狄格有限公司 |
吡啶酮/吡嗪酮、其制备方法及使用方法
|
AR082799A1
(es)
|
2010-09-08 |
2013-01-09 |
Ucb Pharma Sa |
Derivados de quinolina y quinoxalina como inhibidores de quinasa
|
JP5876051B2
(ja)
|
2010-09-08 |
2016-03-02 |
グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited |
インフルエンザウィルス感染の治療に使用するためのインダゾール誘導体
|
PL2614058T3
(pl)
|
2010-09-08 |
2015-12-31 |
Glaxosmithkline Ip Dev Ltd |
Polimorfy i sole n-[5-[4-(5-{[(2r,6s)-2,6-dimetylo-4-morfolinylo]-metylo}-1,3-oksazol-2-ilo)-1h-indazol-6-ilo]-2-(metyloksy)-3-pirydynylo]metanosulfonamidu
|
TWI541243B
(zh)
|
2010-09-10 |
2016-07-11 |
拜耳知識產權公司 |
經取代咪唑并嗒
|
WO2012035996A1
(ja)
|
2010-09-14 |
2012-03-22 |
保土谷化学工業株式会社 |
電荷制御剤及びそれを用いたトナー
|
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
|
WO2012054364A2
(en)
|
2010-10-22 |
2012-04-26 |
Merck Sharp & Dohme Corp. |
Bicyclic diamines as janus kinase inhibitors
|
EP3381920B1
(en)
|
2010-10-25 |
2019-03-27 |
G1 Therapeutics, Inc. |
Cdk inhibitors
|
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
|
CA2816022C
(en)
|
2010-10-29 |
2019-09-10 |
Emory University |
Quinazoline derivatives, compositions, and uses related thereto
|
WO2012061337A1
(en)
|
2010-11-02 |
2012-05-10 |
Exelixis, Inc. |
Fgfr2 modulators
|
CA2816769A1
(en)
|
2010-11-10 |
2012-05-18 |
Gruenenthal Gmbh |
Substituted heteroaromatic carboxamide and urea derivatives as vanilloid receptor ligands
|
CN103201261A
(zh)
|
2010-11-10 |
2013-07-10 |
埃科特莱茵药品有限公司 |
用作为食欲素受体拮抗剂的内酰胺衍生物
|
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
|
EP2640715A1
(en)
|
2010-11-17 |
2013-09-25 |
Amgen Inc. |
Quinoline derivatives as pik3 inhibitors
|
RU2597609C2
(ru)
|
2010-11-18 |
2016-09-10 |
Касина Лайла Иннова Фармасьютикалз Прайвит Лимитед |
Замещенные 4-(селенофен-2(или 3)-иламино)пиримидиновые соединения и способы их применения
|
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
|
EP2651404B1
(en)
|
2010-12-14 |
2015-10-14 |
Electrophoretics Limited |
Casein kinase 1delta (ck1delta) inhibitors
|
MX2013007149A
(es)
|
2010-12-20 |
2013-10-30 |
Merck Serono Sa |
Derivados de indazoliltriazol como inhibidores de cinasas asociadas con el receptor de interleucinas-1 (irak).
|
EP2468258A1
(en)
|
2010-12-22 |
2012-06-27 |
LEK Pharmaceuticals d.d. |
Process for the preparation of a pharmaceutical composition comprising a low soluble pharmaceutically active ingredient
|
US8754114B2
(en)
|
2010-12-22 |
2014-06-17 |
Incyte Corporation |
Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
|
ES2659739T3
(es)
|
2010-12-22 |
2018-03-19 |
Leo Laboratories Limited |
3-acilatos III de ingenol y 3-carbamatos de ingenol
|
EP2655312A1
(en)
|
2010-12-22 |
2013-10-30 |
Leo Laboratories Limited |
3-acyl-ingenols ii
|
AU2011349669A1
(en)
|
2010-12-23 |
2013-07-11 |
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
|
JP5860818B2
(ja)
|
2011-01-06 |
2016-02-16 |
Jx日鉱日石エネルギー株式会社 |
イミド化合物及びその製造方法、グリース用増ちょう剤並びにグリース組成物
|
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
|
WO2012112965A1
(en)
|
2011-02-18 |
2012-08-23 |
Medivation Technologies, Inc. |
Compounds and 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
|
JP2014513930A
(ja)
|
2011-03-17 |
2014-06-19 |
ノバルティス アーゲー |
Hr陽性対象における乳がんのバイオマーカーとしてのfgfrおよびそのリガンド
|
PT2688887E
(pt)
|
2011-03-23 |
2015-07-06 |
Amgen Inc |
Inibidores duais tricíclicos fusionados de cdk 4/6 e flt3
|
ITPD20110091A1
(it)
|
2011-03-24 |
2012-09-25 |
Univ Padova |
Inibitori multitirosinchinasi utili per le patologie correlate: modelli farmacoforici, composti identificati tramite questi modelli, metodi per la loro preparazione, la loro formulazione e il loro impiego terapeutico.
|
MX351165B
(es)
|
2011-03-25 |
2017-10-04 |
Abbvie Inc |
Antagonistas de trpv1.
|
KR20140021589A
(ko)
|
2011-04-07 |
2014-02-20 |
제넨테크, 인크. |
항-fgfr4 항체 및 사용 방법
|
FR2974088A1
(fr)
|
2011-04-12 |
2012-10-19 |
Pf Medicament |
Composes pyrazolo[3,4-b]pyridines tri- et tetracycliques comme agent anticancereux
|
HUE033584T2
(hu)
|
2011-05-16 |
2017-12-28 |
Hoffmann La Roche |
FGFR1 agonisták és alkalmazási eljárások
|
EP2710004A1
(en)
|
2011-05-17 |
2014-03-26 |
Bayer Intellectual Property GmbH |
Amino-substituted imidazopyridazines as mknk1 kinase inhibitors
|
WO2012158795A1
(en)
|
2011-05-17 |
2012-11-22 |
Principia Biopharma Inc. |
Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors
|
RU2013156378A
(ru)
|
2011-05-19 |
2015-06-27 |
Новартис Аг |
4-амино-5-фтор-3-[6-(4-метилпиперазин-1-ил)-1н-бензимидазол-2-ил]-1н-хинолин-2-он для применения при лечении аденокистозной карциномы
|
US9730929B2
(en)
|
2011-06-01 |
2017-08-15 |
Bayer Intellectual Property Gmbh |
Substituted aminoimidazopyridazines
|
TW201316991A
(zh)
|
2011-06-03 |
2013-05-01 |
Millennium Pharm Inc |
Mek抑制劑與奧諾拉(aurora)a激酶選擇性抑制劑之組合
|
CN103597053B
(zh)
|
2011-06-13 |
2016-09-21 |
株式会社Lg化学 |
化合物和使用该化合物的有机电子器件
|
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
|
KR20140071361A
(ko)
|
2011-08-12 |
2014-06-11 |
에프. 호프만-라 로슈 아게 |
피라졸로[3,4-c]피리딘 화합물 및 사용 방법
|
BR112014002472A2
(pt)
|
2011-08-12 |
2017-04-11 |
Nissan Chemical Ind Ltd |
"compostos heterocíclicos tricíclicos, seu uso, agente terapêutico para reumatismo articular e medicamento"
|
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
|
US9320737B2
(en)
|
2011-09-23 |
2016-04-26 |
Bayer Intellectual Property Gmbh |
Substituted imidazopyridazines
|
US9376435B2
(en)
|
2011-09-23 |
2016-06-28 |
Jawaharlal Nehru Centre For Advanced Scientific Research |
Chromophores for the detection of volatile organic compounds
|
MX2014003889A
(es)
|
2011-09-30 |
2014-12-10 |
Kineta Inc |
Compuestos antivirales.
|
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
|
WO2013063003A1
(en)
|
2011-10-28 |
2013-05-02 |
Novartis Ag |
Method of treating gastrointestinal stromal tumors
|
RU2014120792A
(ru)
|
2011-10-28 |
2015-12-10 |
Новартис Аг |
Способ лечения стромальных опухолей желудочно-кишечного тракта
|
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
|
FR2985257B1
(fr)
|
2011-12-28 |
2014-02-14 |
Sanofi Sa |
Composes dimeres agonistes des recepteurs des fgfs (fgfrs), leur procede de preparation et leur application en therapeutique
|
FR2985258A1
(fr)
|
2011-12-28 |
2013-07-05 |
Sanofi Sa |
Composes dimeres agonistes des recepteurs des fgfs (fgfrs), leur procede de preparation et leur application en therapeutique
|
WO2013109027A1
(ko)
|
2012-01-18 |
2013-07-25 |
덕산하이메탈(주) |
화합물, 이를 이용한 유기전기소자 및 그 전자 장치
|
US10026905B2
(en)
|
2012-01-18 |
2018-07-17 |
Duk San Neolux Co., Ltd. |
Compound, organic electric element using the same, and an electronic device thereof
|
KR101623286B1
(ko)
|
2012-01-19 |
2016-05-20 |
다이호야쿠힌고교 가부시키가이샤 |
3,5-이치환 벤젠알키닐 화합물 및 그의 염
|
CN104136439B
(zh)
|
2012-02-23 |
2017-01-18 |
拜耳知识产权有限责任公司 |
取代的苯并噻吩基‑吡咯并三嗪及其用途
|
JP2013179181A
(ja)
|
2012-02-28 |
2013-09-09 |
Sumitomo Chemical Co Ltd |
有機光電変換素子
|
JP6431770B2
(ja)
|
2012-03-14 |
2018-11-28 |
ルピン・リミテッド |
Mekインヒビターとしてのヘテロシクリル化合物
|
AU2013241664B2
(en)
|
2012-03-30 |
2016-05-19 |
Novartis Ag |
FGFR inhibitor for use in the treatment of hypophosphatemic disorders
|
WO2013155506A1
(en)
|
2012-04-14 |
2013-10-17 |
Intra-Cellular Therapies, Inc. |
Novel compositions and methods
|
JP5120580B1
(ja)
|
2012-05-14 |
2013-01-16 |
Jsr株式会社 |
液晶配向剤
|
CN107115162B
(zh)
|
2012-05-20 |
2021-01-22 |
戴尔马修墨医学研究内结构和服务有限公司 |
人造二尖瓣
|
RS58514B1
(sr)
|
2012-06-13 |
2019-04-30 |
Incyte Holdings Corp |
Supstituisana triciklična jedinjenja kao inhibitori fgfr
|
IN2014DN10801A
(es)
|
2012-07-11 |
2015-09-04 |
Novartis Ag |
|
CA2878412A1
(en)
|
2012-07-11 |
2014-01-16 |
Blueprint Medicines Corporation |
Inhibitors of the fibroblast growth factor receptor
|
WO2014019186A1
(en)
|
2012-08-02 |
2014-02-06 |
Merck Sharp & Dohme Corp. |
Antidiabetic tricyclic compounds
|
JP2015525782A
(ja)
|
2012-08-02 |
2015-09-07 |
メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. |
抗糖尿病性三環式化合物
|
US9388185B2
(en)
|
2012-08-10 |
2016-07-12 |
Incyte Holdings Corporation |
Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
|
KR101985259B1
(ko)
|
2012-08-10 |
2019-06-03 |
제이에스알 가부시끼가이샤 |
액정 배향제 및 화합물
|
WO2014044846A1
(en)
|
2012-09-24 |
2014-03-27 |
Evotec (Uk) Ltd. |
3-(aryl- or heteroaryl-amino)-7-(3,5-dimethoxyphenyl)isoquinoline derivatives as fgfr inhibitors useful for the treatment of proliferative disorders or dysplasia
|
WO2014048878A1
(en)
|
2012-09-26 |
2014-04-03 |
Evotec (Uk) Ltd. |
Phenyl- or pyridyl- pyrrolo[2,3b]pyrazine derivatives useful in the treatment or prevention of proliferative disorders or dysplasia
|
WO2014062454A1
(en)
|
2012-10-15 |
2014-04-24 |
Merck Sharp & Dohme Corp. |
Compositions and methods for treating cancer
|
KR102000211B1
(ko)
|
2012-10-29 |
2019-09-30 |
삼성디스플레이 주식회사 |
유기금속 화합물 및 이를 포함한 유기 발광 소자
|
CA2892361A1
(en)
|
2012-11-28 |
2014-06-05 |
Merck Sharp & Dohme Corp. |
Use of a wee1 inhibitor for treating a cancer characterized by low pkmyt1 expression levels
|
US20140148548A1
(en)
|
2012-11-28 |
2014-05-29 |
Central Glass Company, Limited |
Fluorine-Containing Polymerizable Monomer And Polymer Compound Using Same
|
WO2014089913A1
(zh)
|
2012-12-12 |
2014-06-19 |
山东亨利医药科技有限责任公司 |
作为酪氨酸激酶抑制剂的并环化合物
|
US9266892B2
(en)
|
2012-12-19 |
2016-02-23 |
Incyte Holdings Corporation |
Fused pyrazoles as FGFR inhibitors
|
WO2014105849A1
(en)
|
2012-12-28 |
2014-07-03 |
Xoma (Us) Llc |
Antibodies specific for fgfr4 and methods of use
|
TWI629266B
(zh)
|
2012-12-28 |
2018-07-11 |
藍印藥品公司 |
纖維母細胞生長因子受體之抑制劑
|
KR102030587B1
(ko)
|
2013-01-09 |
2019-10-10 |
에스에프씨주식회사 |
두 개의 나프틸기를 포함하는 비대칭 안트라센 유도체 및 이를 포함하는 유기 발광 소자
|
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
|
JP6311093B2
(ja)
|
2013-03-07 |
2018-04-18 |
国立大学法人九州大学 |
超分子複合体、発光体、および有機化合物検出用のセンサー素子
|
WO2014138485A1
(en)
|
2013-03-08 |
2014-09-12 |
Irm Llc |
Ex vivo production of platelets from hematopoietic stem cells and the product thereof
|
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
|
BR112015021701A2
(pt)
|
2013-03-14 |
2017-07-18 |
Abbvie Deutschland |
novos compostos inibidores da fosfoestearase tipo 10a
|
CA2907243C
(en)
|
2013-03-15 |
2021-12-28 |
Celgene Avilomics Research, Inc. |
Substituted dihydropyrimidopyrimidinone compounds and pharmaceutical compositions thereof use fgfr4 inhibitor
|
TWI647220B
(zh)
|
2013-03-15 |
2019-01-11 |
美商西建卡爾有限責任公司 |
雜芳基化合物及其用途
|
EA036160B1
(ru)
|
2013-03-15 |
2020-10-08 |
Селджен Кар Ллс |
Гетероарильные соединения и их применение
|
WO2014160521A1
(en)
|
2013-03-15 |
2014-10-02 |
Blueprint Medicines Corporation |
Piperazine derivatives and their use as kit modulators
|
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
|
EP2986630B1
(en)
|
2013-04-19 |
2018-08-15 |
Covagen AG |
Novel bispecific binding molecules with antitumoral activity
|
AU2014253798C1
(en)
|
2013-04-19 |
2019-02-07 |
Incyte Holdings Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
GB201307577D0
(en)
|
2013-04-26 |
2013-06-12 |
Astex Therapeutics Ltd |
New compounds
|
WO2014182829A1
(en)
|
2013-05-09 |
2014-11-13 |
Principia Biopharma Inc. |
Quinolone derivatives as fibroblast growth factor inhibitors
|
MX2015017201A
(es)
|
2013-06-14 |
2016-04-06 |
Sanofi Sa |
Derivados de pirazolopiridina para uso en el tratamiento del cancer de vejiga.
|
KR102272606B1
(ko)
|
2013-06-28 |
2021-07-05 |
베이진 엘티디 |
Raf 키나아제 및/또는 raf 키나아제 이량체 저해제로서 융합 트리시클릭 우레아 화합물
|
WO2014206344A1
(en)
|
2013-06-28 |
2014-12-31 |
Beigene, Ltd. |
Fused tricyclic amide compounds as multiple kinase inhibitors
|
HUE049733T2
(hu)
|
2013-07-02 |
2020-10-28 |
Syngenta Participations Ag |
Növényvédõszerként aktív biciklusos vagy triciklusos heterociklusok kéntartalmú szubsztituensekkel
|
CA2917667A1
(en)
|
2013-07-09 |
2015-01-15 |
Dana-Farber Cancer Institute, Inc. |
Kinase inhibitors for the treatment of disease
|
JP6018547B2
(ja)
|
2013-07-09 |
2016-11-02 |
大成ロテック株式会社 |
舗装機械
|
SG11201600062RA
(en)
|
2013-07-11 |
2016-02-26 |
Acea Biosciences Inc |
Pyrimidine derivatives as kinase inhibitors
|
TW201605452A
(zh)
|
2013-08-28 |
2016-02-16 |
安斯泰來製藥股份有限公司 |
以嘧啶化合物作爲有效成分之醫藥組成物
|
BR112016008110B1
(pt)
|
2013-10-18 |
2019-07-02 |
Eisai R&D Management Co., Ltd. |
Composto inibidor de pirimidina fgfr4, composição farmacêutica compreendendo dito compoto e usos terapêuticos destes
|
AU2014338549B2
(en)
|
2013-10-25 |
2017-05-25 |
Novartis Ag |
Ring-fused bicyclic pyridyl derivatives as FGFR4 inhibitors
|
MX2016005297A
(es)
|
2013-10-25 |
2016-08-12 |
Blueprint Medicines Corp |
Inhibidores del receptor del factor de crecimiento de fibroblastos.
|
FR3012330B1
(fr)
|
2013-10-29 |
2015-10-23 |
Oreal |
Composition biphase comprenant un ester d'acide gras et de sucre ou un alkylpolyglucoside liquide, de hlb < 8, et un alcane ramifie en c8-c18
|
WO2015066452A2
(en)
|
2013-11-01 |
2015-05-07 |
Foundation Medicine, Inc. |
Methods of treating pediatric cancers
|
WO2015095492A1
(en)
|
2013-12-19 |
2015-06-25 |
Incyte Corporation |
Tricyclic heterocycles as bet protein inhibitors
|
US9695165B2
(en)
|
2014-01-15 |
2017-07-04 |
Blueprint Medicines Corporation |
Inhibitors of the fibroblast growth factor receptor
|
MY188447A
(en)
|
2014-08-19 |
2021-12-09 |
Shanghai Haihe Pharmaceutical Co Ltd |
Indazole compounds as fger 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
|
CN107001331A
(zh)
|
2014-09-19 |
2017-08-01 |
拜耳制药股份公司 |
作为bub1抑制剂的苄基取代的吲唑
|
US20160115164A1
(en)
|
2014-10-22 |
2016-04-28 |
Incyte Corporation |
Bicyclic heterocycles as fgfr4 inhibitors
|
US10851105B2
(en)
|
2014-10-22 |
2020-12-01 |
Incyte Corporation |
Bicyclic heterocycles as FGFR4 inhibitors
|
US9580423B2
(en)
|
2015-02-20 |
2017-02-28 |
Incyte Corporation |
Bicyclic heterocycles as FGFR4 inhibitors
|
RU2017132673A
(ru)
|
2015-02-20 |
2019-03-20 |
Орегон Хэлт Энд Сайенс Юниверсити |
Производные собетирома
|
ES2751669T3
(es)
|
2015-02-20 |
2020-04-01 |
Incyte Corp |
Heterociclos bicíclicos como inhibidores FGFR
|
MA41551A
(fr)
|
2015-02-20 |
2017-12-26 |
Incyte Corp |
Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
|
US10363220B2
(en)
|
2015-06-03 |
2019-07-30 |
Triastek, Inc. |
Compartmented pharmaceutical dosage forms
|
RU2721776C9
(ru)
|
2015-07-15 |
2020-10-22 |
Ф. Хоффманн-Ля Рош Аг |
Производные этинила как модуляторы метаботропного рецептора глутамата
|
BR112018000830B1
(pt)
|
2015-07-15 |
2022-06-21 |
Cabot Corporation |
Métodos de fabricação de um compósito de elastômero reforçado com sílica e artigo contendo o mesmo
|
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
|
AU2016293619B2
(en)
|
2015-07-15 |
2021-02-25 |
Protagonist Therapeutics, Inc. |
Peptide inhibitors of interleukin-23 receptor and their use to treat inflammatory diseases
|
UA127372C2
(uk)
|
2015-07-30 |
2023-08-02 |
Макродженікс, Інк. |
Моноспецифічне pd-1-сполучне моноклональне антитіло
|
US10392383B2
(en)
|
2015-08-03 |
2019-08-27 |
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
|
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
|
US10231956B2
(en)
|
2015-08-03 |
2019-03-19 |
Samumed, Llc |
3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
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
|
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
|
WO2017024015A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
CA2996018C
(en)
|
2015-08-20 |
2024-02-06 |
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
|
HUE060680T2
(hu)
|
2015-11-19 |
2023-04-28 |
Incyte Corp |
Heterociklusos vegyületek mint immunmodulátorok
|
WO2017106634A1
(en)
|
2015-12-17 |
2017-06-22 |
Incyte Corporation |
N-phenyl-pyridine-2-carboxamide derivatives and their use as pd-1/pd-l1 protein/protein interaction modulators
|
CR20180374A
(es)
|
2015-12-22 |
2018-10-16 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
AR108396A1
(es)
|
2016-05-06 |
2018-08-15 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
ES2905980T3
(es)
|
2016-05-26 |
2022-04-12 |
Incyte Corp |
Compuestos heterocíclicos como inmunomoduladores
|
LT3472167T
(lt)
|
2016-06-20 |
2022-11-10 |
Incyte Corporation |
Heterocikliniai junginiai kaip imunomoduliatoriai
|
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
|
US10647693B2
(en)
|
2016-08-30 |
2020-05-12 |
North & South Brother Pharmacy Investment Company Limited |
Inhibitors of influenza virus replication, application methods and uses thereof
|
US20180072718A1
(en)
|
2016-09-09 |
2018-03-15 |
Incyte Corporation |
Pyrazolopyridine compounds and uses thereof
|
RU2019107667A
(ru)
|
2016-10-05 |
2020-11-06 |
РЕКЬЮРИУМ АйПи ХОЛДИНГС, ЛЛС |
Спироциклические соединения
|
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
|
CR20190317A
(es)
|
2016-12-22 |
2019-09-13 |
Incyte Corp |
Compuestos inmunomodulares y métodos de uso
|
MA47099A
(fr)
|
2016-12-22 |
2021-05-12 |
Incyte Corp |
Composés hétéroaromatiques bicycliques utilisés en tant qu'immunomodulateurs
|
WO2018119263A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds derivatives as pd-l1 internalization inducers
|
WO2018119236A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Triazolo[1,5-a]pyridine derivatives as immunomodulators
|
US20180179179A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
EP3558985B1
(en)
|
2016-12-22 |
2022-09-07 |
Incyte Corporation |
Benzooxazole derivatives as immunomodulators
|
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
|
CA3079607A1
(en)
|
2017-10-19 |
2019-04-25 |
Effector Therapeutics, Inc. |
Benzimidazole-indole inhibitors of mnk1 and mnk2
|
WO2019105886A1
(en)
|
2017-12-02 |
2019-06-06 |
Galapagos Nv |
Novel compounds and pharmaceutical compositions thereof for the treatment of diseases
|
PT3774791T
(pt)
|
2018-03-30 |
2023-03-03 |
Incyte Corp |
Compostos heterocíclicos como imunomoduladores
|
BR112020022373A2
(pt)
|
2018-05-04 |
2021-02-02 |
Incyte Corporation |
sais de um inibidor de fgfr
|
EP3788047B1
(en)
|
2018-05-04 |
2024-09-04 |
Incyte Corporation |
Solid forms of an fgfr inhibitor and processes for preparing the same
|
SI3790877T1
(sl)
|
2018-05-11 |
2023-06-30 |
Incyte Corporation |
Tetrahidro-imidazo(4,5-c)piridinski derivati kot imunomodulatorji pd-l1
|
BR112021002614A2
(pt)
|
2018-08-14 |
2021-05-04 |
Osteoqc Inc. |
compostos pirrol-dipiridina
|
CN112654396A
(zh)
|
2018-09-07 |
2021-04-13 |
默克专利股份公司 |
5-吗啉-4-基-吡唑并[4,3-b]吡啶衍生物
|
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
|
CN113474337A
(zh)
|
2018-12-19 |
2021-10-01 |
奥瑞生物药品公司 |
作为fgfr抑制剂用于治疗癌症的7-((3,5-二甲氧基苯基)氨基)喹喔啉衍生物
|
EP3898626A1
(en)
|
2018-12-19 |
2021-10-27 |
Array Biopharma, Inc. |
Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases
|
WO2020185532A1
(en)
|
2019-03-08 |
2020-09-17 |
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
|
US20210094935A1
(en)
|
2019-10-01 |
2021-04-01 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
WO2021076602A1
(en)
|
2019-10-14 |
2021-04-22 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
US11566028B2
(en)
|
2019-10-16 |
2023-01-31 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
BR112022010664A2
(pt)
|
2019-12-04 |
2022-08-16 |
Incyte Corp |
Derivados de um inibidor de fgfr
|
CA3163875A1
(en)
|
2019-12-04 |
2021-06-10 |
Incyte Corporation |
Tricyclic heterocycles as fgfr inhibitors
|
US12012409B2
(en)
|
2020-01-15 |
2024-06-18 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
EP4323405A1
(en)
|
2021-04-12 |
2024-02-21 |
Incyte Corporation |
Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent
|