EP0710109B1
(en)
*
|
1993-06-18 |
2004-09-15 |
Smithkline Beecham Corporation |
Method for identifying a PDE IV inhibitor
|
GB9312853D0
(en)
|
1993-06-22 |
1993-08-04 |
Euro Celtique Sa |
Chemical compounds
|
AU7375194A
(en)
*
|
1993-07-30 |
1995-02-28 |
Smithkline Beecham Corporation |
3-cyano-3-(3,4-disubstituted)phenylcyclohexyl-1-carboxylates
|
US6013827A
(en)
*
|
1994-03-11 |
2000-01-11 |
Smithkline Beecham Corporation |
Compounds
|
GB9404706D0
(en)
*
|
1994-03-11 |
1994-04-27 |
Smithkline Beecham Corp |
Compounds
|
US5998428A
(en)
*
|
1995-05-31 |
1999-12-07 |
Smithkline Beecham Corporation |
Compounds and methods for treating PDE IV-related diseases
|
US20060019963A1
(en)
*
|
1994-06-17 |
2006-01-26 |
Smithkline Beecham Corporation |
Compounds
|
US5922751A
(en)
|
1994-06-24 |
1999-07-13 |
Euro-Celtique, S.A. |
Aryl pyrazole compound for inhibiting phosphodiesterase IV and methods of using same
|
US5591776A
(en)
*
|
1994-06-24 |
1997-01-07 |
Euro-Celtique, S.A. |
Pheynl or benzyl-substituted rolipram-based compounds for and method of inhibiting phosphodiesterase IV
|
EP0799181A4
(en)
*
|
1994-12-23 |
1998-03-25 |
Smithkline Beecham Corp |
DIMERES 3.3- (DISUBSTITUTED) CYCLOHEXANE-1-CARBOXYLATE AND RELATED COMPOUNDS
|
EP0796096A4
(en)
*
|
1994-12-23 |
1998-04-29 |
Smithkline Beecham Corp |
4,4- (DISUBSTITUTED) CYCLOHEXAN-1-CARBOXYLATE MONOMERS AND RELATED COMPOUNDS
|
EP0799182A4
(en)
*
|
1994-12-23 |
1998-03-25 |
Smithkline Beecham Corp |
DIMERES 3.3- (DISUBSTITUTED) CYCLOHEXAN-1-OL AND RELATED COMPOUNDS
|
WO1996019994A1
(en)
*
|
1994-12-23 |
1996-07-04 |
Smithkline Beecham Corporation |
3,3-(disubstituted)cyclohexan-1-carboxylate monomers and related compounds
|
WO1996020163A1
(en)
*
|
1994-12-23 |
1996-07-04 |
Smithkline Beecham Corporation |
4,4-(disubstituted)cyclohexan-1-carboxylate dimers and related compounds
|
CA2221351A1
(en)
*
|
1995-05-18 |
1996-11-21 |
Byk Gulden Lomberg Chemische Fabrik Gmbh |
Cyclohexyl dihydrobenzofuranes
|
US5902824A
(en)
*
|
1995-05-18 |
1999-05-11 |
Byk Gulden Lomberg Chemische Fabrik Gmbh |
Phenyldihydrobenzofuranes
|
US6166041A
(en)
|
1995-10-11 |
2000-12-26 |
Euro-Celtique, S.A. |
2-heteroaryl and 2-heterocyclic benzoxazoles as PDE IV inhibitors for the treatment of asthma
|
US5891883A
(en)
*
|
1995-12-21 |
1999-04-06 |
Smithkline Beecham Corporation |
4,4-(disubstituted)cyclohexan-1-ols monomers and related compounds
|
US6075016A
(en)
|
1996-04-10 |
2000-06-13 |
Euro-Celtique S.A. |
6,5-fused aromatic ring systems having enhanced phosphodiesterase IV inhibitory activity
|
AP1147A
(en)
*
|
1996-05-03 |
2003-02-25 |
Pfizer |
Substituted indazole derivatives and related compounds.
|
AU3102697A
(en)
|
1996-06-19 |
1998-01-07 |
Rhone-Poulenc Rorer Limited |
Substituted azabicylic compounds and their use as inhibitors of the production of tnf and cyclic amp phosphodiesterase
|
CZ423398A3
(cs)
*
|
1996-06-25 |
1999-12-15 |
Pfizer Inc. |
Deriváty indazolu, farmaceutické kompozice na jejich bázi a způsoby léčení
|
SI0941221T1
(en)
*
|
1996-11-20 |
2003-10-31 |
Altana Pharma Ag |
Substituted dihydrobenzofurans as pde inhibitors
|
SI1023279T1
(en)
*
|
1997-02-12 |
2003-12-31 |
Smithkline Beecham Corporation |
Compounds and method for preparing substituted 4-phenyl-4-cyanocyclohexanoic acids
|
UY24882A1
(es)
|
1997-02-12 |
2001-08-27 |
Smithkline Beecham Corp |
Ácidos 4-fenil-4-ciano-ciclohexanoicos sustituidos
|
EP1524268B1
(en)
*
|
1997-02-12 |
2007-01-17 |
Smithkline Beecham Corporation |
Compounds and method for preparing sustituted 4-phenyl-4-cyanocyclohexanoic acids
|
UA67753C2
(uk)
*
|
1997-10-10 |
2004-07-15 |
Смітклайн Бічам Корпорейшн |
Спосіб отримання заміщених 4-феніл-4-ціанциклогексанових кислот
|
CA2317548A1
(en)
*
|
1998-01-07 |
1999-07-15 |
Theodore Torphy |
Method for treating multiple sclerosis
|
UY25338A1
(es)
|
1998-01-07 |
2001-08-27 |
Smithkline Beecham Corp |
Método para tratar copd
|
US6118017A
(en)
*
|
1998-04-14 |
2000-09-12 |
Smithkline Beecham Corporation |
Substituted-(3-cyclopentyloxy-4-methoxyphenyl)-3-phenylcyanocyclobutan-1-one
|
US6395273B1
(en)
|
1998-06-10 |
2002-05-28 |
Promega Corporation |
Prevention and treatment of inflammatory bowel disease
|
US7811990B2
(en)
*
|
1998-09-25 |
2010-10-12 |
Sciaticon Ab |
Soluble cytokine receptors TNF-α blocking antibodies for treating spinal disorders mediated by nucleus pulposus
|
US7906481B2
(en)
*
|
1998-09-25 |
2011-03-15 |
Sciaticon Ab |
Specific TNF-A inhibitors for treating spinal disorders mediated by nucleous pulposus
|
US7115557B2
(en)
*
|
1998-09-25 |
2006-10-03 |
Sciaticon Ab |
Use of certain drugs for treating nerve root injury
|
SE9803710L
(sv)
*
|
1998-09-25 |
2000-03-26 |
A & Science Invest Ab |
Användning av vissa substanser för behandling av nervrotsskador
|
WO2000020391A1
(fr)
|
1998-10-06 |
2000-04-13 |
Dainippon Pharmaceutical Co., Ltd. |
Derives pyridine disubstitues en position 2,3, procede de preparation associe, compositions de medicament contenant ces derives, et intermediaires servant dans cette preparation
|
MY121142A
(en)
*
|
1999-02-23 |
2005-12-30 |
Smithkline Beecham Corp |
Controlled release formulation for treating copd
|
US6419934B1
(en)
*
|
1999-02-24 |
2002-07-16 |
Edward L. Tobinick |
TNF modulators for treating neurological disorders associated with viral infection
|
AR035987A1
(es)
*
|
1999-03-01 |
2004-08-04 |
Smithkline Beecham Corp |
Uso de un compuesto inhibidor de la pde 4 para la manufactura de un medicamento y el medicamento para tratar asma inducida por ejercicio
|
DZ3019A1
(fr)
*
|
1999-03-01 |
2005-05-20 |
Smithkline Beecham Corp |
Utilisation d'un inhibiteur de pde4 dans la préparation d'un médicament contre la copd.
|
CA2373607A1
(en)
*
|
1999-05-14 |
2000-11-23 |
Bristol-Myers Squibb Pharma Research Labs, Inc. |
Cyclic amine derivatives and their uses
|
AR024076A1
(es)
*
|
1999-05-25 |
2002-09-04 |
Smithkline Beecham Corp |
Sales de cis-[4-ciano-4-(3-ciclopentiloxi-4-metoxifenil) ciclohexan-1-carboxilato]
|
US6296840B1
(en)
*
|
1999-08-06 |
2001-10-02 |
Rodan & Fields, Llc |
Masque
|
US20040220424A1
(en)
*
|
1999-08-06 |
2004-11-04 |
Smithkline Beecham Corporation |
Process for preparing acids via alpha-chloroepoxy esters
|
UY26268A1
(es)
*
|
1999-08-06 |
2001-01-31 |
Smithkline Beecham Corp |
Procedimiento para preparar acidos a traves de alfa-cloroep xi- esteres ley 17164 art 127
|
US6740765B1
(en)
*
|
1999-08-06 |
2004-05-25 |
Smithkline Beecham Corporation |
Method for preparing cyclohexane carboxylic acids
|
HU229439B1
(hu)
|
1999-08-21 |
2013-12-30 |
Takeda Gmbh |
Roflumilast és salmeterol szinergetikus kombinációja
|
UY26333A1
(es)
*
|
1999-09-15 |
2001-07-31 |
Smithkline Beecham Corp |
Procedimiento e intermedios para preparar ácidos (4-ciano sustituido)- ciclohexanoicos
|
AR029788A1
(es)
*
|
2000-01-12 |
2003-07-16 |
Smithkline Beecham Corp |
Procedimiento para reducir acidos ciclohexeno carboxilicos alfa,beta-insaturados, procedimiento para preparar acidos 4-nitrilo-4-aril-ciclohexanoicos, procedimiento para preparar acidos ciclohexeno carboxilicos alfa,beta-insaturados, y procedimientos para preparar intermediarios
|
US20030050497A1
(en)
*
|
2002-07-11 |
2003-03-13 |
Webb Kevin Scott |
Process and intermediates for preparing a cyclohexylnitrile
|
EA200200791A1
(ru)
*
|
2000-01-26 |
2002-12-26 |
Смитклайн Бичам Корпорейшн |
Моногидрат цис-литий 4-циано-4-[3-(циклопентилокси)-4-метоксифенил]циклогексанкарбоксилата
|
KR20020073577A
(ko)
*
|
2000-02-08 |
2002-09-27 |
스미스클라인 비참 코포레이션 |
염증 질환의 치료 방법 및 조성물
|
JP2004502643A
(ja)
*
|
2000-02-16 |
2004-01-29 |
ユニバーシティ・オブ・ネブラスカ・メディカル・センター |
線維症性疾患の治療法および治療用組成物
|
EP1265861A2
(en)
*
|
2000-03-16 |
2002-12-18 |
Inflazyme Pharmaceuticals, Ltd. |
Benzylated pde4 inhibitors
|
GB0011802D0
(en)
*
|
2000-05-16 |
2000-07-05 |
Smithkline Beecham |
Method for enhancing cognitive function
|
US20040005995A1
(en)
*
|
2001-07-26 |
2004-01-08 |
Edelson Jeffrey D |
Method for reducing exacerbations associated with copd
|
BRPI0113042B8
(pt)
|
2000-08-05 |
2021-05-25 |
Glaxo Group Ltd |
composto da fórmula ou um seu solvato fisiologicamente aceitável, uso do mesmo, composição farmacêutica, formulação farmacêutica, método para o tratamento de um indivíduo humano ou animal com uma condição inflamatória e/ou alérgica, e, processo para preparar um composto ou um seu solvato
|
US20040224316A1
(en)
|
2000-08-10 |
2004-11-11 |
Tully Timothy P. |
Augmented cognitive training
|
EE200300361A
(et)
*
|
2001-01-31 |
2003-12-15 |
Pfizer Products Inc. |
PDE4 isosüümide inhibiitoritena kasutatavad eetriderivaadid
|
US7250518B2
(en)
*
|
2001-01-31 |
2007-07-31 |
Pfizer Inc. |
Nicotinamide acids, amides, and their mimetics active as inhibitors of PDE4 isozymes
|
EA200300622A1
(ru)
*
|
2001-01-31 |
2003-12-25 |
Пфайзер Продактс Инк. |
Производные амидов тиазолил-, оксазолил, пирролил- и имидазолилкислот, полезные в качестве ингибиторов изоферментов pde4
|
EA200300621A1
(ru)
|
2001-01-31 |
2003-12-25 |
Пфайзер Продактс Инк. |
Биарильные производные никотинамида, полезные в качестве ингибиторов изоферментов pde4
|
GB0103630D0
(en)
*
|
2001-02-14 |
2001-03-28 |
Glaxo Group Ltd |
Chemical compounds
|
DE60224172T2
(de)
*
|
2001-03-22 |
2008-12-04 |
Glaxo Group Ltd., Greenford |
Formanilid-derivative als beta2-adrenorezeptor-agonisten
|
JP4446661B2
(ja)
|
2001-04-30 |
2010-04-07 |
グラクソ グループ リミテッド |
抗炎症性の、17α位に環状エステル基を有するアンドロスタンの17β−カルボチオ酸エステル誘導体
|
MXPA03010679A
(es)
*
|
2001-05-23 |
2004-03-02 |
Tanabe Seiyaku Co |
Una composicion para acelerar la cicatrizacion de fractura osea.
|
ES2427930T3
(es)
*
|
2001-05-23 |
2013-11-04 |
Mitsubishi Tanabe Pharma Corporation |
Composición terapéutica para el tratamiento regenerativo de enfermedades de los cartílagos
|
PT2042168E
(pt)
|
2001-09-14 |
2014-01-03 |
Glaxo Group Ltd |
Formulação de inalação compreendendo derivados de fenetanolamina para o tratamento de doenças respiratórias
|
GB0217199D0
(en)
*
|
2002-07-25 |
2002-09-04 |
Glaxo Group Ltd |
Medicament dispenser
|
GB0201677D0
(en)
|
2002-01-25 |
2002-03-13 |
Glaxo Group Ltd |
Medicament dispenser
|
JP4625637B2
(ja)
|
2002-02-22 |
2011-02-02 |
シャイア エルエルシー |
活性物質送達系及び活性物質を保護し投与する方法
|
GB0204719D0
(en)
*
|
2002-02-28 |
2002-04-17 |
Glaxo Group Ltd |
Medicinal compounds
|
ATE381535T1
(de)
*
|
2002-04-25 |
2008-01-15 |
Glaxo Group Ltd |
Phenethanolaminderivate
|
US20030013905A1
(en)
*
|
2002-06-10 |
2003-01-16 |
Huang Guishu Kris |
Salts of cis-4-cyano-4[3(cyclopentyloxy)-4-methoxyphenyl]cyclohexane-1-carboxylic acid
|
GB0217225D0
(en)
|
2002-07-25 |
2002-09-04 |
Glaxo Group Ltd |
Medicinal compounds
|
GB0217196D0
(en)
*
|
2002-07-25 |
2002-09-04 |
Glaxo Group Ltd |
Medicament dispenser
|
GB0217198D0
(en)
*
|
2002-07-25 |
2002-09-04 |
Glaxo Group Ltd |
Medicament dispenser
|
EP1554264B1
(en)
*
|
2002-10-22 |
2007-08-08 |
Glaxo Group Limited |
Medicinal arylethanolamine compounds
|
KR20050057681A
(ko)
|
2002-10-28 |
2005-06-16 |
글락소 그룹 리미티드 |
호흡기 질환의 치료에 유용한 페네탄올아민 유도체
|
EP1592419A1
(en)
*
|
2002-11-22 |
2005-11-09 |
Merck Frosst Canada & Co. |
Use of phosphodiesterase-4 inhibitors as enhancers of cognition
|
US7772188B2
(en)
|
2003-01-28 |
2010-08-10 |
Ironwood Pharmaceuticals, Inc. |
Methods and compositions for the treatment of gastrointestinal disorders
|
GB0303396D0
(en)
*
|
2003-02-14 |
2003-03-19 |
Glaxo Group Ltd |
Medicinal compounds
|
JP2006522151A
(ja)
|
2003-04-01 |
2006-09-28 |
アプライド リサーチ システムズ エーアールエス ホールディング ナームロゼ フェンノートシャップ |
不妊症におけるホスホジエステラーゼ阻害剤
|
WO2005002626A2
(en)
*
|
2003-04-25 |
2005-01-13 |
Gilead Sciences, Inc. |
Therapeutic phosphonate compounds
|
WO2004098578A2
(en)
*
|
2003-05-12 |
2004-11-18 |
Altana Pharma Ag |
Composition comprising a pde4 inhibitor and a tnf-alfa antagonist selected from infliximab, adalimumab, cdp870 and cdp517
|
WO2004098606A1
(en)
*
|
2003-05-12 |
2004-11-18 |
Altana Pharma Ag |
Composition comprising a pde4 inhibitor and shuil-1r ii
|
AU2004242777B2
(en)
|
2003-05-30 |
2011-05-12 |
Ranbaxy Laboratories Limited |
Substituted pyrrole derivatives and their use as HMG-Co inhibitors
|
GB0316290D0
(en)
|
2003-07-11 |
2003-08-13 |
Glaxo Group Ltd |
Novel compounds
|
DE10331798B4
(de)
*
|
2003-07-14 |
2012-06-21 |
Giesecke & Devrient Gmbh |
Sicherheitselement, Wertgegenstand, Transfermaterial und Herstellungsverfahren
|
GB0317374D0
(en)
|
2003-07-24 |
2003-08-27 |
Glaxo Group Ltd |
Medicament dispenser
|
US20090274676A1
(en)
*
|
2003-07-31 |
2009-11-05 |
Robinson Cynthia B |
Combination of dehydroepiandrosterone or dehydroepiandrosterone-sulfate with a pde-4 inhibitor for treatment of asthma or chronic obstructive pulmonary disease
|
US20050026883A1
(en)
*
|
2003-07-31 |
2005-02-03 |
Robinson Cynthia B. |
Combination of dehydroepiandrosterone or dehydroepiandrosterone-sulfate with a PDE-4 inhibitor for treatment of asthma or chronic obstructive pulmonary disease
|
US20050085430A1
(en)
*
|
2003-07-31 |
2005-04-21 |
Robinson Cynthia B. |
Combination of dehydroepiandrosterone or dehydroepiandrosterone-sulfate with a PDE-4 inhibitor for treatment of asthma or chronic obstructive pulmonary disease
|
GB0324654D0
(en)
*
|
2003-10-22 |
2003-11-26 |
Glaxo Group Ltd |
Medicinal compounds
|
GB0324886D0
(en)
*
|
2003-10-24 |
2003-11-26 |
Glaxo Group Ltd |
Medicinal compounds
|
GB0401334D0
(en)
|
2004-01-21 |
2004-02-25 |
Novartis Ag |
Organic compounds
|
EP1730104A1
(en)
*
|
2004-04-02 |
2006-12-13 |
Glaxo Group Limited |
Chemical process and new crystalline form
|
GB0411056D0
(en)
|
2004-05-18 |
2004-06-23 |
Novartis Ag |
Organic compounds
|
AR049384A1
(es)
|
2004-05-24 |
2006-07-26 |
Glaxo Group Ltd |
Derivados de purina
|
TWI307630B
(en)
|
2004-07-01 |
2009-03-21 |
Glaxo Group Ltd |
Immunoglobulins
|
GB0418045D0
(en)
|
2004-08-12 |
2004-09-15 |
Glaxo Group Ltd |
Compounds
|
KR101061850B1
(ko)
|
2004-09-08 |
2011-09-02 |
삼성전자주식회사 |
박막 트랜지스터 표시판 및 그 제조방법
|
GT200500281A
(es)
|
2004-10-22 |
2006-04-24 |
Novartis Ag |
Compuestos organicos.
|
GB0424284D0
(en)
|
2004-11-02 |
2004-12-01 |
Novartis Ag |
Organic compounds
|
GB0426164D0
(en)
|
2004-11-29 |
2004-12-29 |
Novartis Ag |
Organic compounds
|
US20090124588A1
(en)
*
|
2005-01-10 |
2009-05-14 |
Glaxo Group Limited |
Androstane 17-Alpha-Carbonate for Use in the Treatment of Inflammatory and Allergic Conditions
|
US7579335B2
(en)
*
|
2005-01-10 |
2009-08-25 |
Glaxo Group Limited |
Androstane 17α-carbonate derivatives for use in the treatment of allergic and inflammatory conditions
|
EP1846374A1
(en)
*
|
2005-01-11 |
2007-10-24 |
Glaxo Group Limited |
Cinnamate salts of a beta-2 adrenergic agonist
|
TWI389690B
(zh)
|
2005-03-25 |
2013-03-21 |
Glaxo Group Ltd |
新穎化合物(一)
|
GB0507577D0
(en)
|
2005-04-14 |
2005-05-18 |
Novartis Ag |
Organic compounds
|
GB0510390D0
(en)
|
2005-05-20 |
2005-06-29 |
Novartis Ag |
Organic compounds
|
GB0514809D0
(en)
|
2005-07-19 |
2005-08-24 |
Glaxo Group Ltd |
Compounds
|
JP5006330B2
(ja)
|
2005-10-21 |
2012-08-22 |
ノバルティス アーゲー |
Il13に対するヒト抗体および治療的使用
|
BRPI0618379A2
(pt)
|
2005-11-08 |
2011-08-30 |
Ranbaxy Lab Ltd |
processo para preparação do hemi-sal de cálcio do ácido (3r,5r) -7-[2-(4-fluorofenil)-5-isopropil-3-fenil-4-[(4-hidroxime tilfenilamino) carbonil]-pirrol-1-il] -3, 5-diidroxi heptanóico
|
AR058109A1
(es)
|
2005-12-20 |
2008-01-23 |
Glaxo Group Ltd |
Acido 3 - (4 - {[4 -(4 -{[3 - (3, 3 - dimetil - 1 - piperidinil)propil]oxi}fenil) - 1 - piperidinil]carbonil} - 1 - naftalenil)propanoico como antagonistas de los receptotres de histamina h1/h3, composiciones farmaceuticas que los contienen y su uso en la preparacion de medicamentos para el tratamie
|
GB0526244D0
(en)
|
2005-12-22 |
2006-02-01 |
Novartis Ag |
Organic compounds
|
AU2007205114B2
(en)
|
2006-01-06 |
2012-11-08 |
Sunovion Pharmaceuticals Inc. |
Cycloalkylamines as monoamine reuptake inhibitors
|
GB0601951D0
(en)
|
2006-01-31 |
2006-03-15 |
Novartis Ag |
Organic compounds
|
BRPI0710240A2
(pt)
|
2006-04-20 |
2011-08-09 |
Glaxo Group Ltd |
composto, uso de um composto, método para o tratamento de um paciente humano ou animal com uma condição ou doença, composição farmacêutica, combinação, e, processo para a preparação de um composto
|
JP5373599B2
(ja)
|
2006-04-21 |
2013-12-18 |
ノバルティス アーゲー |
アデノシンa2a受容体アゴニストとして使用するためのプリン誘導体
|
SG172602A1
(en)
|
2006-05-19 |
2011-07-28 |
Helicon Therapeutics Inc |
Phosphodiesterase 4 inhibitors for cognitive and motor rehabilitation
|
GB0611587D0
(en)
|
2006-06-12 |
2006-07-19 |
Glaxo Group Ltd |
Novel compounds
|
PE20080943A1
(es)
|
2006-06-23 |
2008-09-27 |
Smithkline Beecham Corp |
Sal toluenosulfonato de 4-{[6-cloro-3-({[(2-cloro-3-fluorofenil)amino]carbonil}amino)-2-hidroxifenil]sulfonil}-1-piperazinacarboxilato de 1,1-dimetiletilo como antagonista del receptor de il-8
|
CN102764440A
(zh)
|
2006-07-05 |
2012-11-07 |
奈科明有限责任公司 |
用于治疗炎症性肺部疾病的HMG-CoA还原酶抑制剂与磷酸二酯酶4抑制剂的组合
|
US20080019970A1
(en)
*
|
2006-07-07 |
2008-01-24 |
Gorman James R |
Methods for preventing, postponing or improving the outcome of spinal device and fusion procedures
|
BRPI0717564A2
(pt)
|
2006-09-29 |
2013-10-22 |
Novartis Ag |
Pirazolopirimidinas como inibidores de pi3k lipídeo cinase
|
RU2009120389A
(ru)
|
2006-10-30 |
2010-12-10 |
Новартис АГ (CH) |
Гетероциклические соединения в качестве противовоспалительных агентов
|
EP2125841A1
(en)
*
|
2006-12-13 |
2009-12-02 |
Gilead Sciences, Inc. |
Monophosphates as mutual prodrugs of anti-inflammatory signal transduction modulators (aistm's) and beta-agonists for the treatment of pulmonary inflammation and bronchoconstriction
|
ATE493174T1
(de)
|
2007-01-10 |
2011-01-15 |
Irm Llc |
Verbindungen und zusammensetzungen als kanal- aktivierende proteasehemmer
|
AR065804A1
(es)
|
2007-03-23 |
2009-07-01 |
Smithkline Beecham Corp |
Compuesto de indol carboxamida, composicion farmaceutica que lo comprende y uso de dicho compuesto para preparar un medicamento
|
US20090182035A1
(en)
*
|
2007-04-11 |
2009-07-16 |
Alcon Research, Ltd. |
Use of a combination of olopatadine and cilomilast to treat non-infectious rhinitis and allergic conjunctivitis
|
AU2008240279A1
(en)
*
|
2007-04-11 |
2008-10-23 |
Alcon Research, Ltd. |
Use of an inhibitor of TNFa plus an antihistamine to treat allergic rhinitis and allergic conjunctivitis
|
CA2685546A1
(en)
|
2007-05-07 |
2008-11-13 |
Novartis Ag |
Organic compounds
|
US8969514B2
(en)
|
2007-06-04 |
2015-03-03 |
Synergy Pharmaceuticals, Inc. |
Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases
|
CN103601792B
(zh)
|
2007-06-04 |
2016-06-29 |
协同医药品公司 |
有效用于胃肠功能紊乱、炎症、癌症和其他疾病治疗的鸟苷酸环化酶激动剂
|
DK2164825T3
(da)
|
2007-06-05 |
2014-07-14 |
Sanofi Sa |
Di(hetero)arylcyclohexanderivater, deres fremstilling, deres anvendelse og terapeutiske præparater, der omfatter disse
|
US7943658B2
(en)
*
|
2007-07-23 |
2011-05-17 |
Bristol-Myers Squibb Company |
Indole indane amide compounds useful as CB2 agonists and method
|
TW200920369A
(en)
*
|
2007-10-26 |
2009-05-16 |
Amira Pharmaceuticals Inc |
5-lipoxygenase activating protein (flap) inhibitor
|
ES2654395T3
(es)
|
2007-12-10 |
2018-02-13 |
Novartis Ag |
Análogos de amilorida espirocíclicos como bloqueantes de ENaC
|
WO2009087224A1
(en)
|
2008-01-11 |
2009-07-16 |
Novartis Ag |
Pyrimidines as kinase inhibitors
|
MX2010012814A
(es)
|
2008-05-23 |
2010-12-20 |
Amira Pharmaceuticals Inc |
Inhibidor de proteina activadora de 5-lipoxigenasa.
|
CA2726917C
(en)
|
2008-06-04 |
2018-06-26 |
Synergy Pharmaceuticals Inc. |
Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders
|
WO2009147190A1
(en)
|
2008-06-05 |
2009-12-10 |
Glaxo Group Limited |
Novel compounds
|
WO2009147187A1
(en)
|
2008-06-05 |
2009-12-10 |
Glaxo Group Limited |
4-carboxamide indazole derivatives useful as inhibitors of p13-kinases
|
US8236808B2
(en)
|
2008-06-10 |
2012-08-07 |
Novartis Ag |
Pyrazine derivatives as ENAC blockers
|
EP2321341B1
(en)
|
2008-07-16 |
2017-02-22 |
Synergy Pharmaceuticals Inc. |
Agonists of guanylate cyclase useful for the treatment of gastrointestinal, inflammation, cancer and other disorders
|
WO2010088335A1
(en)
|
2009-01-29 |
2010-08-05 |
Novartis Ag |
Substituted benzimidazoles for the treatment of astrocytomas
|
WO2010094643A1
(en)
|
2009-02-17 |
2010-08-26 |
Glaxo Group Limited |
Quinoline derivatives and their uses for rhinitis and urticaria
|
WO2010102958A1
(en)
|
2009-03-09 |
2010-09-16 |
Glaxo Group Limited |
4-oxadiazol-2 -yl- indazoles as inhibitors of p13 kinases
|
US8354539B2
(en)
|
2009-03-10 |
2013-01-15 |
Glaxo Group Limited |
Indole derivatives as IKK2 inhibitors
|
US20120058984A1
(en)
|
2009-03-17 |
2012-03-08 |
Catherine Mary Alder |
Pyrimidine derivatives used as itk inhibitors
|
JP2012520686A
(ja)
|
2009-03-19 |
2012-09-10 |
メルク・シャープ・エンド・ドーム・コーポレイション |
低分子干渉核酸(siNA)を用いたシグナル伝達性転写因子6(STAT6)遺伝子発現のRNA干渉媒介性阻害
|
WO2010107952A2
(en)
|
2009-03-19 |
2010-09-23 |
Merck Sharp & Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF CONNECTIVE TISSUE GROWTH FACTOR (CTGF) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
|
JP2012520685A
(ja)
|
2009-03-19 |
2012-09-10 |
メルク・シャープ・エンド・ドーム・コーポレイション |
低分子干渉核酸(siNA)を用いたGATA結合タンパク質3(GATA3)遺伝子発現のRNA干渉媒介性阻害
|
KR20110137799A
(ko)
|
2009-03-19 |
2011-12-23 |
머크 샤프 앤드 돔 코포레이션 |
짧은 간섭 핵산 (siNA) 서열 목록을 사용한 BTB 및 CNC 상동체 1, 염기성 류신 지퍼 전사 인자 1 (BACH1) 유전자 발현의 RNA 간섭 매개 억제
|
US20120004281A1
(en)
|
2009-03-27 |
2012-01-05 |
Merck Sharp & Dohme Corp |
RNA Interference Mediated Inhibition of the Nerve Growth Factor Beta Chain (NGFB) Gene Expression Using Short Interfering Nucleic Acid (siNA)
|
WO2010111464A1
(en)
|
2009-03-27 |
2010-09-30 |
Merck Sharp & Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF APOPTOSIS SIGNAL-REGULATING KINASE 1 (ASK1) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
|
WO2010111490A2
(en)
|
2009-03-27 |
2010-09-30 |
Merck Sharp & Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF THE THYMIC STROMAL LYMPHOPOIETIN (TSLP) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
|
JP2012521763A
(ja)
|
2009-03-27 |
2012-09-20 |
メルク・シャープ・エンド・ドーム・コーポレイション |
低分子干渉核酸(siNA)を用いたシグナル伝達性転写因子1(STAT1)遺伝子発現のRNA干渉媒介性阻害
|
SG174581A1
(en)
|
2009-03-27 |
2011-10-28 |
Merck Sharp & Dohme |
RNA INTERFERENCE MEDIATED INHIBITION OF THE INTERCELLULAR ADHESION MOLECULE 1 (ICAM-1)GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
|
JP2012524754A
(ja)
|
2009-04-24 |
2012-10-18 |
グラクソ グループ リミテッド |
Cracチャネル阻害剤としてのピラゾールおよびトリアゾ−ルカルボキサミド
|
US8399436B2
(en)
|
2009-04-24 |
2013-03-19 |
Glaxo Group Limited |
N-pyrazolyl carboxamides as CRAC channel inhibitors
|
WO2010125082A1
(en)
|
2009-04-30 |
2010-11-04 |
Glaxo Group Limited |
Oxazole substituted indazoles as pi3-kinase inhibitors
|
US8389526B2
(en)
|
2009-08-07 |
2013-03-05 |
Novartis Ag |
3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
|
JP5781510B2
(ja)
|
2009-08-12 |
2015-09-24 |
ノバルティス アーゲー |
ヘテロ環式ヒドラゾン化合物および癌および炎症の処置のためのそれらの使用
|
CN105078978A
(zh)
|
2009-08-17 |
2015-11-25 |
因特利凯公司 |
杂环化合物及其用途
|
JP5775871B2
(ja)
|
2009-08-20 |
2015-09-09 |
ノバルティス アーゲー |
ヘテロ環式オキシム化合物
|
JP5721722B2
(ja)
*
|
2009-10-01 |
2015-05-20 |
アルコン リサーチ, リミテッド |
オロパタジン組成物およびその使用
|
AU2010310449A1
(en)
|
2009-10-22 |
2012-05-03 |
Vertex Pharmaceuticals Incorporated |
Compositions for treatment of cystic fibrosis and other chronic diseases
|
JP2013512878A
(ja)
|
2009-12-03 |
2013-04-18 |
グラクソ グループ リミテッド |
新規化合物
|
US20120238571A1
(en)
|
2009-12-03 |
2012-09-20 |
Glaxo Group Limited |
Indazole derivatives as pi 3-kinase
|
JP2013512879A
(ja)
|
2009-12-03 |
2013-04-18 |
グラクソ グループ リミテッド |
Pi3キナーゼの阻害剤としてのベンズピラゾール誘導体
|
EP2512438B1
(en)
|
2009-12-16 |
2017-01-25 |
3M Innovative Properties Company |
Formulations and methods for controlling mdi particle size delivery
|
WO2011110575A1
(en)
|
2010-03-11 |
2011-09-15 |
Glaxo Group Limited |
Derivatives of 2-[2-(benzo- or pyrido-) thiazolylamino]-6-aminopyridine, useful in the treatment of respiratoric, allergic or inflammatory diseases
|
US8247436B2
(en)
|
2010-03-19 |
2012-08-21 |
Novartis Ag |
Pyridine and pyrazine derivative for the treatment of CF
|
GB201007203D0
(en)
|
2010-04-29 |
2010-06-16 |
Glaxo Group Ltd |
Novel compounds
|
SI2614058T1
(sl)
|
2010-09-08 |
2015-10-30 |
Glaxosmithkline Intellectual Property Development Limited |
Polimorfi in soli N-(5-(4-(5-(((2R,6S)-2,6-dimetil-4-morfolinil)metil)-1,3-oksazol-2-il)- 1H-indazol-6-il)-2-(metiloksi)-3-piridinil)metansulfonamida
|
EP2613781B1
(en)
|
2010-09-08 |
2016-08-24 |
GlaxoSmithKline Intellectual Property Development Limited |
Indazole derivatives for use in the treatment of influenza virus infection
|
WO2012034095A1
(en)
|
2010-09-09 |
2012-03-15 |
Irm Llc |
Compounds and compositions as trk inhibitors
|
US8637516B2
(en)
|
2010-09-09 |
2014-01-28 |
Irm Llc |
Compounds and compositions as TRK inhibitors
|
US9616097B2
(en)
|
2010-09-15 |
2017-04-11 |
Synergy Pharmaceuticals, Inc. |
Formulations of guanylate cyclase C agonists and methods of use
|
US8372845B2
(en)
|
2010-09-17 |
2013-02-12 |
Novartis Ag |
Pyrazine derivatives as enac blockers
|
WO2012035055A1
(en)
|
2010-09-17 |
2012-03-22 |
Glaxo Group Limited |
Novel compounds
|
ES2532213T3
(es)
|
2010-10-21 |
2015-03-25 |
Glaxo Group Limited |
Compuestos de pirazol que actúan contra afecciones alérgicas, inmunitarias e inflamatorias
|
EP2630127A1
(en)
|
2010-10-21 |
2013-08-28 |
Glaxo Group Limited |
Pyrazole compounds acting against allergic, inflammatory and immune disorders
|
GB201018124D0
(en)
|
2010-10-27 |
2010-12-08 |
Glaxo Group Ltd |
Polymorphs and salts
|
US20130324526A1
(en)
|
2011-02-10 |
2013-12-05 |
Novartis Ag |
[1,2,4] triazolo [4,3-b] pyridazine compounds as inhibitors of the c-met tyrosine kinase
|
US9127000B2
(en)
|
2011-02-23 |
2015-09-08 |
Intellikine, LLC. |
Heterocyclic compounds and uses thereof
|
CA2828219A1
(en)
|
2011-02-25 |
2012-08-30 |
Irm Llc |
Pyrazolo [1,5-a] pyridines as trk inhibitors
|
CN108676076A
(zh)
|
2011-03-01 |
2018-10-19 |
辛纳吉制药公司 |
制备鸟苷酸环化酶c激动剂的方法
|
GB201104153D0
(en)
|
2011-03-11 |
2011-04-27 |
Glaxo Group Ltd |
Novel compounds
|
JP2014507458A
(ja)
|
2011-03-11 |
2014-03-27 |
グラクソ グループ リミテッド |
Sykインヒビターとしてのピリド[3,4−B]ピラジン誘導体
|
UY34305A
(es)
|
2011-09-01 |
2013-04-30 |
Novartis Ag |
Derivados de heterociclos bicíclicos para el tratamiento de la hipertensión arterial pulmonar
|
AU2012310168B2
(en)
|
2011-09-15 |
2015-07-16 |
Novartis Ag |
6 - substituted 3 - (quinolin- 6 - ylthio) - [1,2,4] triazolo [4, 3 -a] pyradines as tyrosine kinase
|
WO2013038378A1
(en)
|
2011-09-16 |
2013-03-21 |
Novartis Ag |
Pyridine amide derivatives
|
WO2013038373A1
(en)
|
2011-09-16 |
2013-03-21 |
Novartis Ag |
Pyridine amide derivatives
|
WO2013038381A1
(en)
|
2011-09-16 |
2013-03-21 |
Novartis Ag |
Pyridine/pyrazine amide derivatives
|
ES2558457T3
(es)
|
2011-09-16 |
2016-02-04 |
Novartis Ag |
Compuestos heterocíclicos para el tratamiento de fibrosis quística
|
ES2882807T3
(es)
|
2011-09-16 |
2021-12-02 |
Novartis Ag |
Heterociclil carboxamidas N-sustituidas
|
CN104363914A
(zh)
|
2011-11-23 |
2015-02-18 |
因特利凯有限责任公司 |
使用mTOR抑制剂的增强的治疗方案
|
WO2013084182A1
(en)
|
2011-12-08 |
2013-06-13 |
Glenmark Pharmaceuticals S.A. |
Pharmaceutical composition that includes a pde4 enzyme inhibitor and an analgesic agent
|
US8809340B2
(en)
|
2012-03-19 |
2014-08-19 |
Novartis Ag |
Crystalline form
|
WO2013149581A1
(en)
|
2012-04-03 |
2013-10-10 |
Novartis Ag |
Combination products with tyrosine kinase inhibitors and their use
|
HK1218629A1
(zh)
|
2013-02-25 |
2017-03-03 |
Bausch Health Ireland Limited |
用於结肠清洁的鸟苷酸环化酶受体激动剂
|
US9073921B2
(en)
|
2013-03-01 |
2015-07-07 |
Novartis Ag |
Salt forms of bicyclic heterocyclic derivatives
|
US9486494B2
(en)
|
2013-03-15 |
2016-11-08 |
Synergy Pharmaceuticals, Inc. |
Compositions useful for the treatment of gastrointestinal disorders
|
CA2905438A1
(en)
|
2013-03-15 |
2014-09-25 |
Synergy Pharmaceuticals Inc. |
Agonists of guanylate cyclase and their uses
|
CN105246482A
(zh)
|
2013-03-15 |
2016-01-13 |
因特利凯有限责任公司 |
激酶抑制剂的组合及其用途
|
SI3004138T1
(sl)
|
2013-06-05 |
2024-07-31 |
Bausch Health Ireland Limited |
Ultra čisti agonisti gvanilat ciklaze C, postopek za njihovo pripravo in uporabo
|
MX375926B
(es)
|
2013-08-09 |
2025-03-07 |
Ardelyx Inc |
Compuestos y metodos para inhibir el transporte de fosfato.
|
MX2016003457A
(es)
|
2013-09-22 |
2017-05-25 |
Calitor Sciences Llc |
Compuestos aminopirimidina sustituidos y metodos de uso.
|
EP3057588A1
(en)
|
2013-10-17 |
2016-08-24 |
GlaxoSmithKline Intellectual Property Development Limited |
Pi3k inhibitor for treatment of respiratory disease
|
US20160256466A1
(en)
|
2013-10-17 |
2016-09-08 |
Glaxosmithkline Intellectual Property Development Limited |
Pi3k inhibitor for treatment of respiratory disease
|
WO2015084804A1
(en)
|
2013-12-03 |
2015-06-11 |
Novartis Ag |
Combination of mdm2 inhibitor and braf inhibitor and their use
|
JP6517319B2
(ja)
|
2014-03-28 |
2019-05-22 |
キャリター・サイエンシーズ・リミテッド・ライアビリティ・カンパニーCalitor Sciences, Llc |
置換されたヘテロアリール化合物および使用方法
|
AU2014391608A1
(en)
|
2014-04-24 |
2016-10-27 |
Novartis Ag |
Amino pyrazine derivatives as phosphatidylinositol 3-kinase inhibitors
|
EP3134396B1
(en)
|
2014-04-24 |
2019-09-18 |
Novartis AG |
Amino pyridine derivatives as phosphatidylinositol 3-kinase inhibitors
|
PT3134395T
(pt)
|
2014-04-24 |
2018-04-16 |
Novartis Ag |
Derivados de pirazina como inibidores de fosfatidilinositol 3-quinase
|
CR20160529A
(es)
|
2014-05-12 |
2017-01-02 |
Glaxosmithkline Intellectual Property (No 2) Ltd |
Composiciones farmacéuticas para tratar enfermedades infecciosas
|
WO2016011658A1
(en)
|
2014-07-25 |
2016-01-28 |
Novartis Ag |
Combination therapy
|
US10195208B2
(en)
|
2014-07-31 |
2019-02-05 |
Novartis Ag |
Combination therapy
|
EP3347097B1
(en)
|
2015-09-11 |
2021-02-24 |
Sunshine Lake Pharma Co., Ltd. |
Substituted aminopyrimidine derivatives as modulators of the kinases jak, flt3 and aurora
|
EP3165224A1
(en)
|
2015-11-09 |
2017-05-10 |
Albert-Ludwigs-Universität Freiburg |
Use of pde4 inhibitors for the prophylaxis and/or therapy of dyslipoproteinaemia and related disorders
|
WO2017089347A1
(en)
|
2015-11-25 |
2017-06-01 |
Inserm (Institut National De La Sante Et De La Recherche Medicale) |
Methods and pharmaceutical compositions for the treatment of braf inhibitor resistant melanomas
|
GB201602527D0
(en)
|
2016-02-12 |
2016-03-30 |
Glaxosmithkline Ip Dev Ltd |
Chemical compounds
|
US20190161480A1
(en)
|
2016-08-08 |
2019-05-30 |
Glaxosmithkline Intellectual Property Development Limited |
Chemical Compounds
|
US20190307975A1
(en)
|
2016-11-21 |
2019-10-10 |
Lupin Inc. |
Medicament dispenser
|
GB201706102D0
(en)
|
2017-04-18 |
2017-05-31 |
Glaxosmithkline Ip Dev Ltd |
Chemical compounds
|
GB201712081D0
(en)
|
2017-07-27 |
2017-09-13 |
Glaxosmithkline Ip Dev Ltd |
Chemical compounds
|
JP7254076B2
(ja)
|
2017-11-19 |
2023-04-07 |
サンシャイン・レイク・ファーマ・カンパニー・リミテッド |
置換ヘテロアリール化合物及び使用方法
|
EP3740468A4
(en)
|
2018-01-20 |
2021-10-06 |
Sunshine Lake Pharma Co., Ltd. |
SUBSTITUTED AMINOPYRIMIDINE COMPOUNDS AND METHODS OF USE
|
US20210085897A1
(en)
|
2018-04-06 |
2021-03-25 |
Lupin Inc. |
Medicament dispenser
|
EP3778544A4
(en)
*
|
2018-04-11 |
2021-06-09 |
Mitsubishi Gas Chemical Company, Inc. |
PROCESS FOR THE PREPARATION OF 1,4-CYCLOHEXANEDICARBONIC ACID DERIVATIVE, 1,4-DICYANOCYCLOHEXANE AND 1,4-BIS (AMINOMETHYL) CYCLOHEXANE
|
WO2020058823A1
(en)
|
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