DE3751524T2
(de)
|
1986-07-28 |
1996-06-13 |
American Cyanamid Co |
5(und/oder6) Substituierte 2-(2-Imidazolin-2-yl)nicotinsäuren, Ester und Salze, verwendbar als herbizide Mittel und Zwischenverbindungen für die Herstellung dieser Nikotinsäuren, Ester und Salze.
|
FR2624698A1
(fr)
|
1987-12-18 |
1989-06-23 |
Bernard Lyon I Universite Clau |
Derives heterocycliques de n-carbamoyl-, n-thiocarbamoyl- ou n-amidino-aminomalonyl ou aminosuccinyl amides utiles comme agents edulcorants
|
JPH04503672A
(ja)
|
1989-02-27 |
1992-07-02 |
イー・アイ・デュポン・ドゥ・ヌムール・アンド・カンパニー |
放射線増感剤としての新規なナフタレンスルホンアミド
|
US5776963A
(en)
|
1989-05-19 |
1998-07-07 |
Hoechst Marion Roussel, Inc. |
3-(heteroaryl)-1- (2,3-dihydro-1h-isoindol-2-yl)alkyl!pyrrolidines and 3-(heteroaryl)-1- (2,3-dihydro-1h-indol-1-yl)alkyl!pyrrolidines and related compounds and their therapeutic untility
|
GB8927872D0
(en)
|
1989-12-08 |
1990-02-14 |
Beecham Group Plc |
Pharmaceuticals
|
JP2807577B2
(ja)
|
1990-06-15 |
1998-10-08 |
エーザイ株式会社 |
環状アミド誘導体
|
DE4121214A1
(de)
|
1991-06-27 |
1993-01-14 |
Bayer Ag |
7-azaisoindolinyl-chinolon- und -naphthyridoncarbonsaeure-derivate
|
EP0520573A1
(en)
|
1991-06-27 |
1992-12-30 |
Glaxo Inc. |
Cyclic imide derivatives
|
US5378620A
(en)
|
1991-08-30 |
1995-01-03 |
Beckman Instruments, Inc. |
Streptolysin O derivatives
|
US5272158A
(en)
|
1991-10-29 |
1993-12-21 |
Merck & Co., Inc. |
Fibrinogen receptor antagonists
|
US5416099A
(en)
|
1991-10-29 |
1995-05-16 |
Merck & Co., Inc. |
Fibrinogen receptor antagonists
|
US5389631A
(en)
|
1991-10-29 |
1995-02-14 |
Merck & Co., Inc. |
Fibrinogen receptor antagonists
|
US5238950A
(en)
|
1991-12-17 |
1993-08-24 |
Schering Corporation |
Inhibitors of platelet-derived growth factor
|
US5364869A
(en)
|
1992-03-09 |
1994-11-15 |
Abbott Laboratories |
Heterocycle-substituted benzyaminopyridine angiotensin II receptor antagonists
|
US5326760A
(en)
|
1992-06-29 |
1994-07-05 |
Glaxo, Inc. |
Aminobutanoic acid compounds having metalloprotease inhibiting properties
|
JPH06236056A
(ja)
|
1993-02-10 |
1994-08-23 |
Fuji Xerox Co Ltd |
電子写真感光体
|
JP3760474B2
(ja)
|
1993-04-22 |
2006-03-29 |
ダイキン工業株式会社 |
電気エネルギーを発生させる方法、装置およびそれに用いるn−f結合を有する化合物
|
CA2134192A1
(en)
|
1993-11-12 |
1995-05-13 |
Michael L. Denney |
5, 6-bicyclic glycoprotein iib/iiia antagonists
|
DE4343922A1
(de)
|
1993-12-22 |
1995-06-29 |
Basf Ag |
Pyridin-2,3-dicarbonsäureimide, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
|
KR970007419B1
(ko)
|
1993-12-30 |
1997-05-08 |
한솔제지 주식회사 |
승화형 열전사 기록용 색소
|
FR2725946A1
(fr)
|
1994-10-24 |
1996-04-26 |
Lohr Ind |
Cale a rapporter sur un plan porteur presentant des perforations
|
US5719144A
(en)
|
1995-02-22 |
1998-02-17 |
Merck & Co., Inc. |
Fibrinogen receptor antagonists
|
US5770590A
(en)
|
1995-03-24 |
1998-06-23 |
Takeda Chemical Industries, Ltd. |
Cyclic compounds, their prudiction and use
|
ES2194937T3
(es)
|
1995-03-24 |
2003-12-01 |
Takeda Chemical Industries Ltd |
Compuestos ciclicos, su produccion y uso como antagonistas de los receptores de taquiquinina.
|
DE19608791A1
(de)
|
1996-03-07 |
1997-09-11 |
Hoechst Ag |
Verfahren zur Herstellung von fluorierten Aromaten und fluorierten stickstoffhaltigen Heteroaromaten
|
DE19702282C2
(de)
|
1997-01-23 |
1998-11-19 |
Hoechst Ag |
Katalysator für Halex-Reaktionen
|
US6177443B1
(en)
|
1997-03-07 |
2001-01-23 |
Novo Nordisk A/S |
4,5,6,7-tetrahydro-thieno[3, 2-C]pyridine derivatives, their preparation and use
|
WO1998040385A1
(en)
|
1997-03-07 |
1998-09-17 |
Novo Nordisk A/S |
4,5,6,7-TETRAHYDRO-THIENO[3,2-c]PYRIDINE DERIVATIVES, THEIR PREPARATION AND USE
|
KR19980074060A
(ko)
|
1997-03-21 |
1998-11-05 |
김윤배 |
신규한 치환된 3,4-디알콕시페닐 유도체
|
JPH1143489A
(ja)
|
1997-05-30 |
1999-02-16 |
Takeda Chem Ind Ltd |
ヘテロ環化合物、その製造法および剤
|
JPH11143489A
(ja)
|
1997-11-10 |
1999-05-28 |
Sony Corp |
音声操作機能付き電子機器、電子機器における音声操作方法、及び音声操作機能付き電子機器を備える自動車
|
US20020132817A1
(en)
|
1998-03-19 |
2002-09-19 |
Hideaki Natsugari |
Heterocyclic compounds, their production and use
|
WO1999047132A2
(en)
|
1998-03-19 |
1999-09-23 |
Takeda Chemical Industries, Ltd. |
Heterocyclic compounds, their production and use as tachykinin receptor antagonists
|
FR2778662B1
(fr)
|
1998-05-12 |
2000-06-16 |
Adir |
Nouveaux composes cycliques substitues, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
|
JP2000007661A
(ja)
|
1998-06-23 |
2000-01-11 |
Nippon Nohyaku Co Ltd |
複素環ジカルボン酸ジアミド誘導体及びその中間体並びに除草剤
|
US6444617B1
(en)
|
1998-07-28 |
2002-09-03 |
Nihon Nohyaku Co., Ltd. |
Fused-heterocycle dicarboxylic acid diamide derivatives or salts thereof, herbicide and usage thereof
|
EP1145714A4
(en)
|
1998-11-27 |
2004-12-15 |
Takeda Chemical Industries Ltd |
DRUGS
|
WO2000067754A1
(en)
|
1999-05-12 |
2000-11-16 |
Nitromed, Inc. |
Nitrosated and nitrosylated potassium channel activators, compositions and methods of use
|
SK822002A3
(en)
|
1999-07-21 |
2002-09-10 |
Astrazeneca Ab |
New compounds
|
KR100466730B1
(ko)
|
1999-08-02 |
2005-01-24 |
에프. 호프만-라 로슈 아게 |
신규한 선택적 레티노이드 작용물질
|
US6512117B1
(en)
|
1999-11-09 |
2003-01-28 |
Abbott Laboratories |
Hydromorphone and hydrocodone compositions and methods for their synthesis
|
CN1623984A
(zh)
|
1999-12-27 |
2005-06-08 |
日本烟草产业株式会社 |
稠环化合物及其药物用途
|
US6770666B2
(en)
|
1999-12-27 |
2004-08-03 |
Japan Tobacco Inc. |
Fused-ring compounds and use thereof as drugs
|
WO2001051128A1
(en)
|
2000-01-12 |
2001-07-19 |
Merck & Co., Inc. |
Inhibitors of prenyl-protein transferase
|
CN1366518A
(zh)
|
2000-04-25 |
2002-08-28 |
三星电子株式会社 |
作为基质金属蛋白酶抑制剂的联苯基丁酸衍生物
|
CN1293034C
(zh)
|
2000-05-02 |
2007-01-03 |
霍夫曼-拉罗奇有限公司 |
新的γ选择性视黄酸类
|
CA2408156A1
(en)
|
2000-05-05 |
2001-11-15 |
Millennium Pharmaceuticals, Inc. |
Heterobicyclic sulfonamides and their use as platelet adp receptor inhibitors
|
US6552015B2
(en)
|
2000-08-03 |
2003-04-22 |
Pfizer Inc. |
Azabicycloalkane derivatives and therapeutic uses thereof
|
WO2002024650A2
(en)
|
2000-09-19 |
2002-03-28 |
Centre National De La Recherche Scientifique (Cnrs) |
Pyridinone and pyridinethione derivatives having hiv inhibiting properties
|
US6884782B2
(en)
|
2000-11-08 |
2005-04-26 |
Amgen Inc. |
STAT modulators
|
TWI236474B
(en)
|
2001-04-03 |
2005-07-21 |
Telik Inc |
Antagonists of MCP-1 function and methods of use thereof
|
WO2002081447A1
(en)
|
2001-04-06 |
2002-10-17 |
Daewoong Pharmaceutical Co., Ltd. |
3-cyclopentyloxy-4-methoxyphenyl-isothiazolinone derivatives and the use thereof
|
WO2002081443A1
(en)
|
2001-04-09 |
2002-10-17 |
Chiron Corporation |
Novel guanidino compounds
|
WO2002088092A1
(fr)
|
2001-04-19 |
2002-11-07 |
Eisai Co., Ltd. |
Derive de 2-imino-imidazole (2)
|
WO2003008421A1
(fr)
|
2001-07-16 |
2003-01-30 |
Shionogi & Co., Ltd. |
Procede de preparation de derives amidine
|
WO2003029254A1
(fr)
|
2001-09-28 |
2003-04-10 |
Takeda Chemical Industries, Ltd. |
Procede de preparation de composes tricycliques
|
JP2003171380A
(ja)
|
2001-09-28 |
2003-06-20 |
Takeda Chem Ind Ltd |
三環性化合物の製造法
|
CZ2004408A3
(cs)
|
2001-10-02 |
2005-03-16 |
Pharmacia & Upjohn Company |
Azabicyklicky substituované kondenzované heteroarylsloučeniny
|
DE10207037A1
(de)
|
2002-02-20 |
2003-08-28 |
Bayer Cropscience Gmbh |
2-Amino-4-bicyclyamino-6H-1,3.5-triazine, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren
|
US7189851B2
(en)
|
2002-03-06 |
2007-03-13 |
Smithkline Beecham Corporation |
Condensed heterocyclic compounds as calcitonin agonists
|
WO2003104216A1
(en)
|
2002-06-10 |
2003-12-18 |
Acadia Pharmaceuticals Inc. |
Urotensin ii receptor modulators
|
WO2004014365A1
(en)
|
2002-08-13 |
2004-02-19 |
Warner-Lambert Company Llc |
Phthalimide derivatives as matrix metalloproteinase inhibitors
|
CA2504929C
(en)
|
2002-11-05 |
2014-07-22 |
Charles Allerson |
Compositions comprising alternating 2'-modified nucleosides for use in gene modulation
|
JP2004203791A
(ja)
|
2002-12-25 |
2004-07-22 |
Dai Ichi Seiyaku Co Ltd |
芳香族化合物
|
CN1212674C
(zh)
|
2003-01-08 |
2005-07-27 |
东南大学 |
横向缓冲p型金属氧化物半导体管
|
TW200503994A
(en)
|
2003-01-24 |
2005-02-01 |
Novartis Ag |
Organic compounds
|
GB0308025D0
(en)
|
2003-04-07 |
2003-05-14 |
Glaxo Group Ltd |
Compounds
|
JP4728962B2
(ja)
|
2003-05-19 |
2011-07-20 |
アイアールエム・リミテッド・ライアビリティ・カンパニー |
免疫抑制化合物および組成物
|
TW200505442A
(en)
|
2003-05-19 |
2005-02-16 |
Genomics Inst Of The Novartis Res Foundation |
Immunosuppressant compounds and compositions
|
MY150088A
(en)
|
2003-05-19 |
2013-11-29 |
Irm Llc |
Immunosuppressant compounds and compositions
|
CN1791395B
(zh)
|
2003-05-19 |
2012-09-26 |
Irm责任有限公司 |
免疫抑制剂化合物及组合物
|
EP1628661A2
(en)
|
2003-06-05 |
2006-03-01 |
Vertex Pharmaceuticals Incorporated |
Modulators of vr1 receptor
|
CN1566099A
(zh)
|
2003-06-13 |
2005-01-19 |
中国科学院上海药物研究所 |
异喹啉-1,3,4-三酮类化合物、制备方法及其用途
|
EP1660454A1
(en)
|
2003-07-07 |
2006-05-31 |
Vernalis (R&D) Limited |
Azacyclic compounds as inhibitors of sensory neurone specific channels
|
FR2857966A1
(fr)
|
2003-07-24 |
2005-01-28 |
Aventis Pharma Sa |
Produits aryl-heteroaromatiques, compositions les contenant et utilisation
|
MXPA06001320A
(es)
|
2003-08-01 |
2006-05-04 |
Pfizer Prod Inc |
Compuestos heteroarilo de 6 miembros para el tratamiento de trastornos neurodegenerativos.
|
EP1675858A2
(en)
|
2003-09-03 |
2006-07-05 |
Neurogen Corporation |
5-aryl-pyrazolo [4,3-d] pyrimidines, pyridines, and pyrazines and related compounds
|
AP2006003559A0
(en)
|
2003-09-05 |
2006-04-30 |
Neurogen Corp Ventis Pharmaceuticals Inc |
Heteroaryl fused pyridines, pyrazines and pyrimidines as CRF 1 receptor ligands
|
US20070088163A1
(en)
|
2003-09-12 |
2007-04-19 |
Kemia, Inc. |
Modulators of calcitonin and amylin activity
|
US20050182061A1
(en)
|
2003-10-02 |
2005-08-18 |
Jeremy Green |
Phthalimide compounds useful as protein kinase inhibitors
|
PL1689233T3
(pl)
|
2003-11-19 |
2012-11-30 |
Array Biopharma Inc |
Bicykliczne inhibitory MEK
|
US7732616B2
(en)
|
2003-11-19 |
2010-06-08 |
Array Biopharma Inc. |
Dihydropyridine and dihydropyridazine derivatives as inhibitors of MEK and methods of use thereof
|
WO2005060958A1
(en)
|
2003-12-19 |
2005-07-07 |
Kalypsys, Inc. |
(5- (2-phenyl)-thiazol-5-ylmethoxy)-indol-1-yl) -acetic acid derivatives and related compounds as modulators of the human ppar-delta receptor for the treatment of metabolic disorders such as type 2 diabetes
|
BRPI0418092A
(pt)
|
2003-12-23 |
2007-04-17 |
Pfizer Prod Inc |
combinação terapêutica para melhora cognitiva e transtornos psicóticos
|
WO2005100334A1
(en)
|
2004-04-14 |
2005-10-27 |
Pfizer Products Inc. |
Dipeptidyl peptidase-iv inhibitors
|
EA012452B1
(ru)
|
2004-09-22 |
2009-10-30 |
Янссен Фармацевтика Н.В. |
Ингибиторы взаимодействия между mdm2 и р53
|
US20060128710A1
(en)
|
2004-12-09 |
2006-06-15 |
Chih-Hung Lee |
Antagonists to the vanilloid receptor subtype 1 (VR1) and uses thereof
|
WO2006065842A2
(en)
|
2004-12-13 |
2006-06-22 |
Synta Pharmaceuticals Corp. |
5,6,7,8-tetrahydroquinolines and related compounds and uses thereof
|
WO2006074428A2
(en)
|
2005-01-07 |
2006-07-13 |
Emory University |
Cxcr4 antagonists for the treatment of medical disorders
|
NZ556434A
(en)
|
2005-02-07 |
2010-05-28 |
Hoffmann La Roche |
Heterocyclic substituted phenyl methanones as inhibitors of the glycine transporter 1
|
GB0504556D0
(en)
|
2005-03-04 |
2005-04-13 |
Pfizer Ltd |
Novel pharmaceuticals
|
DK2332909T3
(da)
|
2005-04-13 |
2014-11-10 |
Astex Therapeutics Ltd |
Hydroxybenzamidderivater og deres anvendelse som inhibitorer af hsp90
|
WO2007050124A1
(en)
|
2005-05-19 |
2007-05-03 |
Xenon Pharmaceuticals Inc. |
Fused piperidine derivatives and their uses as therapeutic agents
|
WO2007007054A1
(en)
|
2005-07-08 |
2007-01-18 |
Cancer Research Technology Limited |
Phthalamides, succinimides and related compounds and their use as pharmaceuticals
|
US20080255186A1
(en)
|
2005-09-29 |
2008-10-16 |
Siegfried Benjamin Christensen |
Pyrazolo[3,4-B]Pyridine Compound, and Its Use as a Pde4 Inhibitor
|
NZ568292A
(en)
|
2005-11-10 |
2011-08-26 |
Msd Kk |
Spiro[cyclohexane-1,1'-(3'H)-4'-azaisobenzofuran]-4-carboxamide derivatives
|
AR059036A1
(es)
|
2006-01-17 |
2008-03-12 |
Schering Corp |
Compuestos para el tratamiento de trastornos inflamatorios
|
AU2007218053B2
(en)
|
2006-02-15 |
2010-05-27 |
Merck Sharp & Dohme Corp. |
Aminotetrahydropyrans as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes
|
WO2007101224A2
(en)
|
2006-02-27 |
2007-09-07 |
The Board Of Trustees Of The Leland Stanford Junior University |
Inhibitors of the unfolded protein response and methods for their use
|
WO2007107545A1
(en)
|
2006-03-22 |
2007-09-27 |
Janssen Pharmaceutica N.V. |
Cyclic-alkylaminederivatives as inhibitors of the interaction between mdm2 and p53
|
US7977351B2
(en)
|
2006-03-22 |
2011-07-12 |
Allergan, Inc. |
Heteroaryl dihydroindolones as kinase inhibitors
|
US7700616B2
(en)
|
2006-05-08 |
2010-04-20 |
Molecular Neuroimaging, Llc. |
Compounds and amyloid probes thereof for therapeutic and imaging uses
|
KR101422456B1
(ko)
|
2006-05-16 |
2014-07-23 |
베링거 인겔하임 인터내셔날 게엠베하 |
치환된 프롤린아미드, 이의 제조방법 및 약물로서의 이의 용도
|
CN1869036A
(zh)
|
2006-06-30 |
2006-11-29 |
中国药科大学 |
7-取代-3-氯吡咯并[3,4-b]吡啶化合物
|
US9102622B2
(en)
|
2006-07-28 |
2015-08-11 |
University Of Connecticut |
Fatty acid amide hydrolase inhibitors
|
US8389739B1
(en)
|
2006-10-05 |
2013-03-05 |
Orphagen Pharmaceuticals |
Modulators of retinoid-related orphan receptor gamma
|
JP5410285B2
(ja)
|
2006-10-12 |
2014-02-05 |
アステックス、セラピューティックス、リミテッド |
医薬化合物
|
JP5528807B2
(ja)
|
2006-10-12 |
2014-06-25 |
アステックス、セラピューティックス、リミテッド |
複合薬剤
|
JP5518478B2
(ja)
|
2006-10-12 |
2014-06-11 |
アステックス、セラピューティックス、リミテッド |
医薬化合物
|
EP2073802A1
(en)
|
2006-10-12 |
2009-07-01 |
Astex Therapeutics Limited |
Pharmaceutical combinations
|
JP5528806B2
(ja)
|
2006-10-12 |
2014-06-25 |
アステックス、セラピューティックス、リミテッド |
複合薬剤
|
PE20080888A1
(es)
|
2006-10-18 |
2008-08-26 |
Novartis Ag |
COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE LA ACIL-TRANSFERASA DE ACIL-CoA-DIACIL-GLICEROL 1 (DGAT1)
|
BRPI0720023A2
(pt)
|
2006-12-11 |
2018-09-04 |
Novartis Ag |
método para prevenir ou tratar isquemia do miocárdio por inibição da enzima dgat1 com um inibidor de dgat1
|
WO2008083070A1
(en)
|
2006-12-29 |
2008-07-10 |
Neurogen Corporation |
Crf1 receptor ligands comprising fused bicyclic heteroaryl moieties
|
CA2679563A1
(en)
|
2007-01-08 |
2008-07-17 |
Phenomix Corporation |
Macrocyclic hepatitis c protease inhibitors
|
WO2009004496A2
(en)
|
2007-04-13 |
2009-01-08 |
University Of Manitoba |
Bisanthrapyrazoles as anti-cancer agents
|
US20110189167A1
(en)
|
2007-04-20 |
2011-08-04 |
Flynn Daniel L |
Methods and Compositions for the Treatment of Myeloproliferative Diseases and other Proliferative Diseases
|
US20100129933A1
(en)
|
2007-04-26 |
2010-05-27 |
Forschungszentrum Karlsruhe Gmbh |
Method for detecting the binding between mdm2 and the proteasome
|
TW200902533A
(en)
|
2007-05-02 |
2009-01-16 |
Boehringer Ingelheim Int |
Carboxylic acid amides, manufacturing and use thereof as medicaments
|
WO2008135524A2
(en)
|
2007-05-02 |
2008-11-13 |
Boehringer Ingelheim International Gmbh |
Substituted anthranilamides and analogues, manufacturing and use thereof as medicaments
|
US7994245B2
(en)
|
2007-05-10 |
2011-08-09 |
Constar International L.L.C. |
Oxygen scavenging molecules, articles containing same, and methods of their use
|
TW200902499A
(en)
|
2007-05-15 |
2009-01-16 |
Astrazeneca Ab |
New compounds
|
GB0710844D0
(en)
|
2007-06-06 |
2007-07-18 |
Lectus Therapeutics Ltd |
Potassium ion channel modulators & uses thereof
|
DE102007034620A1
(de)
|
2007-07-25 |
2009-01-29 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Neue B1-Antagonisten
|
WO2009026248A2
(en)
|
2007-08-17 |
2009-02-26 |
The Government Of The United States, As Represented By The Secretary Of Health And Human Services, National Institutes Of Health, Office Of Technology Transfer |
Hydrazide, amide, phthalimide and phthalhydrazide analogs as inhibitors of retroviral integrase
|
CA2976793A1
(en)
|
2007-09-17 |
2009-03-26 |
Abbvie Ireland Unlimited Company |
Uracil or thymine derivative for treating hepatitis c
|
US20090076275A1
(en)
|
2007-09-19 |
2009-03-19 |
David Robert Bolin |
Diacylglycerol acyltransferase inhibitors
|
EP2203058A4
(en)
|
2007-10-16 |
2011-08-31 |
Univ Northeastern |
METHODS AND COMPOUNDS FOR MODULATING CANNABINOID ACTIVITY
|
EA201000620A1
(ru)
|
2007-10-18 |
2010-12-30 |
Новартис Аг |
Ингибиторы csf-1r, предназначенные для лечения рака и заболеваний костей
|
AU2008328951B2
(en)
|
2007-11-29 |
2012-12-13 |
F. Hoffmann-La Roche Ag |
Preparation of dihydropyrrol derivatives as intermediates
|
WO2009073788A1
(en)
|
2007-12-07 |
2009-06-11 |
Firestone Leigh H |
Compositions and methods for treating menopausal females
|
FR2926554B1
(fr)
|
2008-01-22 |
2010-03-12 |
Sanofi Aventis |
Derives de carboxamides azabicycliques, leur preparation et leur application en therapeutique
|
CN101225070B
(zh)
|
2008-01-31 |
2010-04-14 |
上海交通大学 |
用于抗肿瘤的药物
|
ES2400322T3
(es)
|
2008-02-05 |
2013-04-09 |
Sanofi |
Derivados de SF5 como inhibidores de PAR-1, su preparación y utilización como medicamento
|
WO2009112445A1
(en)
|
2008-03-10 |
2009-09-17 |
Novartis Ag |
Method of increasing cellular phosphatidyl choline by dgat1 inhibition
|
GB0804702D0
(en)
|
2008-03-13 |
2008-04-16 |
Amura Therapeutics Ltd |
Compounds
|
GB0804701D0
(en)
|
2008-03-13 |
2008-04-16 |
Amura Therapeutics Ltd |
Compounds
|
WO2009124755A1
(en)
|
2008-04-08 |
2009-10-15 |
European Molecular Biology Laboratory (Embl) |
Compounds with novel medical uses and method of identifying such compounds
|
US8309577B2
(en)
|
2008-04-23 |
2012-11-13 |
Bristol-Myers Squibb Company |
Quinuclidine compounds as α-7 nicotinic acetylcholine receptor ligands
|
US7863291B2
(en)
|
2008-04-23 |
2011-01-04 |
Bristol-Myers Squibb Company |
Quinuclidine compounds as alpha-7 nicotinic acetylcholine receptor ligands
|
GB0809776D0
(en)
|
2008-05-29 |
2008-07-09 |
Amura Therapeutics Ltd |
Compounds
|
AU2009266953A1
(en)
|
2008-07-01 |
2010-01-07 |
Genentech, Inc. |
Isoindolone derivatives as MEK kinase inhibitors and methods of use
|
ES2612731T3
(es)
|
2008-08-19 |
2017-05-18 |
Janssen Pharmaceutica Nv |
Antagonistas de receptores al frío de mentol
|
CA2741400A1
(en)
|
2008-09-16 |
2010-03-25 |
Merck & Co., Inc. |
Sulfonamide derivative metabotropic glutamate r4 ligands
|
WO2010056195A1
(en)
|
2008-11-14 |
2010-05-20 |
Astrazeneca Ab |
New compounds 575
|
WO2010056194A1
(en)
|
2008-11-14 |
2010-05-20 |
Astrazeneca Ab |
5h-pyrrolo [ 3, 4-b] pyridin derivatives and their use
|
CN101455661B
(zh)
|
2008-11-19 |
2012-10-10 |
中国科学院上海有机化学研究所 |
3-取代苯酞及其类似物的用途
|
CA2746220A1
(en)
|
2008-12-08 |
2010-07-08 |
Vm Pharma Llc |
Compositions of protein receptor tyrosine kinase inhibitors
|
PL2391608T3
(pl)
|
2009-01-28 |
2013-08-30 |
Bayer Ip Gmbh |
Pochodne N-cykloalkilo-N-bicyklometyleno-karboksyamidów jako środki grzybobójcze
|
WO2011078143A1
(ja)
|
2009-12-22 |
2011-06-30 |
塩野義製薬株式会社 |
ピリミジン誘導体およびそれらを含有する医薬組成物
|
JP2013517326A
(ja)
|
2010-01-19 |
2013-05-16 |
リサーチ・トライアングル・インスティチュート |
κオピオイド受容体結合リガンド
|
US20130045992A1
(en)
|
2010-01-28 |
2013-02-21 |
President And Fellows Of Harvard College |
Compositions and Methods for Enhancing Proteasome Activity
|
EP2368886A1
(en)
|
2010-03-01 |
2011-09-28 |
Phenex Pharmaceuticals AG |
Novel compounds for modulation of orphan nuclear receptor RAR-related orphan receptor-gamma (ROR gamma, NR1F3) activity and for the treatment of chronic inflammatory and autoimmune desease
|
CN102241621A
(zh)
|
2010-05-11 |
2011-11-16 |
江苏恒瑞医药股份有限公司 |
5,5-双取代-2-亚氨基吡咯烷类衍生物、其制备方法及其在医药上的应用
|
EP2571876B1
(en)
|
2010-05-21 |
2016-09-07 |
Merck Sharp & Dohme Corp. |
Substituted seven-membered heterocyclic compounds as dipeptidyl peptidase-iv inhibitors for the treatment of diabetes
|
US8299117B2
(en)
|
2010-06-16 |
2012-10-30 |
Metabolex Inc. |
GPR120 receptor agonists and uses thereof
|
JP5746334B2
(ja)
|
2010-06-16 |
2015-07-08 |
シマベイ セラピューティクス, インコーポレーテッド |
Gpr120受容体作動薬及びその使用
|
WO2012027965A1
(en)
|
2010-09-01 |
2012-03-08 |
Glaxo Group Limited |
Novel compounds
|
WO2012028100A1
(en)
|
2010-09-01 |
2012-03-08 |
Glaxo Group Limited |
Novel compounds
|
KR20130114119A
(ko)
|
2010-09-03 |
2013-10-16 |
포르마 티엠, 엘엘씨. |
Nampt의 억제를 위한 신규 화합물 및 조성물
|
MX336726B
(es)
|
2010-09-27 |
2016-01-27 |
Abbott Gmbh & Co Kg |
Compuestos heterociclicos y su uso como inhibidores de la glucogeno sintasa quinasa-3.
|
JP2013253019A
(ja)
|
2010-09-28 |
2013-12-19 |
Kowa Co |
新規なピペリジン誘導体及びこれを含有する医薬
|
WO2012064744A2
(en)
|
2010-11-08 |
2012-05-18 |
Lycera Corporation |
Tetrahydroquinoline and related bicyclic compounds for inhibition of rorϒ activity and the treatment of disease
|
US20120115903A1
(en)
|
2010-11-10 |
2012-05-10 |
Gruenenthal Gmbh |
Substituted Heteroaromatic Carboxamide and Urea Compounds as Vanilloid Receptor Ligands
|
WO2012100732A1
(en)
|
2011-01-24 |
2012-08-02 |
Glaxo Group Limited |
Retinoid-related orphan receptor gamma modulators, composition containing them and uses thereof
|
WO2012100734A1
(en)
|
2011-01-24 |
2012-08-02 |
Glaxo Group Limited |
Compounds useful as retinoid-related orphan receptor gamma modulators
|
EP2487159A1
(en)
|
2011-02-11 |
2012-08-15 |
MSD Oss B.V. |
RorgammaT inhibitors
|
CN102180780A
(zh)
|
2011-03-07 |
2011-09-14 |
中国科学技术大学 |
茚酮类衍生物及其作为淀粉样蛋白沉积物和神经纤维缠结的显像剂和聚集抑制剂的用途
|
US9090568B2
(en)
|
2011-03-14 |
2015-07-28 |
Impact Therapeutics, Inc. |
Quinazolinediones and their use
|
US8802711B2
(en)
|
2011-03-25 |
2014-08-12 |
Abbvie Inc. |
TRPV1 antagonists
|
US9469667B2
(en)
|
2011-04-04 |
2016-10-18 |
Merck Patent Gmbh |
Metal complexes
|
EP2511263A1
(en)
|
2011-04-14 |
2012-10-17 |
Phenex Pharmaceuticals AG |
Pyrrolo sulfonamide compounds for modulation of orphan nuclear receptor RAR-related orphan receptor-gamma (RORgamma, NR1F3) activity and for the treatment of chronic inflammatory and autoimmune diseases
|
AU2012248223B2
(en)
|
2011-04-28 |
2017-03-02 |
Japan Tobacco Inc. |
Amide compound and pharmaceutical application therefor
|
US9938269B2
(en)
|
2011-06-30 |
2018-04-10 |
Abbvie Inc. |
Inhibitor compounds of phosphodiesterase type 10A
|
WO2013019626A1
(en)
|
2011-07-29 |
2013-02-07 |
Tempero Pharmaceuticals, Inc. |
Compounds and methods
|
US9156837B2
(en)
|
2011-07-29 |
2015-10-13 |
Takeda Pharmaceutical Company Limited |
Heterocyclic compound
|
US20140256740A1
(en)
|
2011-07-29 |
2014-09-11 |
Tempero Pharmaceuticals, Inc. |
Compounds and methods
|
US20140155419A1
(en)
|
2011-07-29 |
2014-06-05 |
Erkan Baloglu |
Compounds and methods
|
EP2736330A4
(en)
*
|
2011-07-29 |
2015-05-27 |
Tempero Pharmaceuticals Inc |
COMPOUNDS AND METHODS
|
WO2013029338A1
(en)
|
2011-09-01 |
2013-03-07 |
Glaxo Group Limited |
Novel compounds
|
US9120776B2
(en)
|
2011-09-22 |
2015-09-01 |
Takeda Pharmaceutical Company Limited |
Condensed heterocyclic compound
|
GB201116641D0
(en)
|
2011-09-27 |
2011-11-09 |
Glaxo Group Ltd |
Novel compounds
|
US20140256767A1
(en)
|
2011-10-31 |
2014-09-11 |
The Broad Institute, Inc. |
Direct inhibitors of keap1-nrf2 interaction as antioxidant inflammation modulators
|
WO2013064231A1
(en)
|
2011-10-31 |
2013-05-10 |
Phenex Pharmaceuticals Ag |
SEVEN-MEMBERED SULFONAMIDES AS MODULATORS OF RAR-RELATED ORPHAN RECEPTOR-GAMMA (RORγ, NR1F3)
|
WO2013079223A1
(en)
|
2011-12-02 |
2013-06-06 |
Phenex Pharmaceuticals Ag |
Pyrrolo carboxamides as modulators of orphan nuclear receptor rar-related orphan receptor-gamma (rorϒ, nr1f3) activity and for the treatment of chronic inflammatory and autoimmune diseases
|
US8741892B2
(en)
|
2011-12-05 |
2014-06-03 |
Boehringer Ingelheim International Gmbh |
Compounds
|
US8642774B2
(en)
|
2011-12-08 |
2014-02-04 |
Boehringer Ingelheim International Gmbh |
Compounds
|
US8796467B2
(en)
|
2011-12-13 |
2014-08-05 |
Boehringer Ingelheim International Gmbh |
Compounds
|
WO2013092460A1
(en)
|
2011-12-20 |
2013-06-27 |
Syngenta Participations Ag |
Cyclic bisoxime microbicides
|
AU2012358978B2
(en)
|
2011-12-21 |
2017-10-05 |
Allergan, Inc. |
Compounds acting at multiple prostaglandin receptors giving a general anti-inflammatory response
|
US9216988B2
(en)
|
2011-12-22 |
2015-12-22 |
Genentech, Inc. |
Benzyl sulfonamide derivatives as RORc modulators
|
US20130190356A1
(en)
|
2011-12-22 |
2013-07-25 |
Genentech, Inc. |
Benzyl sulfonamide derivatives as rorc modulators
|
WO2013100027A1
(ja)
|
2011-12-28 |
2013-07-04 |
武田薬品工業株式会社 |
複素環化合物
|
US9321750B2
(en)
|
2012-04-20 |
2016-04-26 |
Innov17 Llc |
ROR modulators and their uses
|
MX2014012989A
(es)
|
2012-04-27 |
2015-01-22 |
Glaxo Group Ltd |
Compuestos novedosos.
|
GB201207406D0
(en)
|
2012-04-27 |
2012-06-13 |
Glaxo Group Ltd |
Novel compounds
|
US9708268B2
(en)
|
2012-04-30 |
2017-07-18 |
Innov17 Llc |
ROR modulators and their uses
|
JP6236068B2
(ja)
|
2012-05-08 |
2017-11-22 |
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. |
RORγ活性を阻害し疾患を治療するためのテトラヒドロナフチリジンおよび関連二環式化合物
|
EP2846794B1
(en)
|
2012-05-08 |
2017-11-01 |
Merck Sharp & Dohme Corp. |
BICYCLIC SULFONE COMPOUNDS FOR INHIBITION OF RORgamma ACTIVITY AND THE TREATMENT OF DISEASE
|
US9394315B2
(en)
|
2012-05-08 |
2016-07-19 |
Lycera Corporation |
Tetrahydro[1,8]naphthyridine sulfonamide and related compounds for use as agonists of RORγ and the treatment of disease
|
JP6225178B2
(ja)
|
2012-05-31 |
2017-11-01 |
フェネックス ファーマシューティカルス アーゲー |
オーファン核内受容体RORγの調整剤としてのカルボキサミドまたはスルホンアミド置換されたチアゾールおよび関連する誘導体
|
WO2014008214A1
(en)
|
2012-07-02 |
2014-01-09 |
Biogen Idec Ma Inc. |
Biaryl-containing compounds as inverse agonists of ror-gamma receptors
|
TW201408652A
(zh)
|
2012-07-11 |
2014-03-01 |
Hoffmann La Roche |
作爲RORc調節劑之芳基磺內醯胺衍生物
|
WO2014028669A1
(en)
|
2012-08-15 |
2014-02-20 |
Biogen Idec Ma Inc. |
Novel compounds for modulation of ror-gamma activity
|
WO2014026329A1
(en)
|
2012-08-15 |
2014-02-20 |
Merck Sharp & Dohme Corp. |
N-alkylated indole and indazole compounds as rorgammat inhibitors and uses thereof
|
WO2014026327A1
(en)
|
2012-08-15 |
2014-02-20 |
Merck Sharp & Dohme Corp. |
4-heteroaryl substituted benzoic acid compounds as rorgammat inhibitors and uses thereof
|
WO2014026330A1
(en)
|
2012-08-15 |
2014-02-20 |
Merck Sharp & Dohme Corp. |
3-AMINOCYCLOALKYL COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF
|
WO2014026328A1
(en)
|
2012-08-15 |
2014-02-20 |
Merck Sharp & Dohme Corp. |
3-cyclohexenyl substituted indole and indazole compounds as rorgammat inhibitors and uses thereof
|
WO2014062938A1
(en)
|
2012-10-19 |
2014-04-24 |
Bristol-Myers Squibb Company |
Rory modulators
|
TW201427959A
(zh)
|
2012-12-06 |
2014-07-16 |
Glaxo Group Ltd |
新穎化合物
|
WO2013171729A2
(en)
|
2013-01-08 |
2013-11-21 |
Glenmark Pharmaceuticals S.A. |
Aryl and heteroaryl amide compounds as rorgamat modulator
|
CA2938311C
(en)
|
2014-02-03 |
2023-03-07 |
Vitae Pharmaceuticals, Inc. |
Dihydropyrrolopyridine inhibitors of ror-gamma
|
JP6564029B2
(ja)
|
2014-10-14 |
2019-08-21 |
ヴァイティー ファーマシューティカルズ,エルエルシー |
Ror−ガンマのジヒドロピロロピリジン阻害剤
|
US9663515B2
(en)
*
|
2014-11-05 |
2017-05-30 |
Vitae Pharmaceuticals, Inc. |
Dihydropyrrolopyridine inhibitors of ROR-gamma
|
US9481674B1
(en)
*
|
2016-06-10 |
2016-11-01 |
Vitae Pharmaceuticals, Inc. |
Dihydropyrrolopyridine inhibitors of ROR-gamma
|