|
WO1995000139A1
(fr)
*
|
1993-06-18 |
1995-01-05 |
Smithkline Beecham Corporation |
Composes
|
|
GB9312853D0
(en)
|
1993-06-22 |
1993-08-04 |
Euro Celtique Sa |
Chemical compounds
|
|
EP0714293A4
(fr)
*
|
1993-07-30 |
1999-04-07 |
Smithkline Beecham Corp |
3-cyano-(3,4-disubstitues)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
|
|
US20060019963A1
(en)
*
|
1994-06-17 |
2006-01-26 |
Smithkline Beecham Corporation |
Compounds
|
|
US5998428A
(en)
*
|
1995-05-31 |
1999-12-07 |
Smithkline Beecham Corporation |
Compounds and methods for treating PDE IV-related diseases
|
|
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
|
|
US5723681A
(en)
*
|
1994-12-23 |
1998-03-03 |
Smithkline Beecham Corporation |
3,3-(disubstituted)cyclohexan-1-01 dimers and related compounds
|
|
EP0796097A4
(fr)
*
|
1994-12-23 |
1998-03-25 |
Smithkline Beecham Corp |
Monomeres 3,3-(disubstitues) cyclohexan-1-carboxylate et composes correspondants
|
|
EP0799187A4
(fr)
*
|
1994-12-23 |
1998-03-25 |
Smithkline Beecham Corp |
Dimeres 4,4-(disubstitue)cyclohexane-1-carboxylate et composes apparentes
|
|
WO1996019990A1
(fr)
*
|
1994-12-23 |
1996-07-04 |
Smithkline Beecham Corporation |
Monomeres 4,4-(disubstitues)cyclohexan-1-carboxylate et composes correspondants
|
|
WO1996020156A1
(fr)
*
|
1994-12-23 |
1996-07-04 |
Smithkline Beecham Corporation |
Dimeres 3,3-(disubstitues)cyclohexane-1-carboxylate et leurs composes apparentes
|
|
ES2191754T3
(es)
*
|
1995-05-18 |
2003-09-16 |
Altana Pharma Ag |
Fenil-dihidrobenzofuranos.
|
|
ES2189871T3
(es)
*
|
1995-05-18 |
2003-07-16 |
Altana Pharma Ag |
Ciclohexil-dihidro-benzofuranos.
|
|
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
|
|
AP2001002304A0
(en)
*
|
1996-05-03 |
2001-12-31 |
Pfizer |
Substituted indazole derivatives and related compounds
|
|
CA2258728C
(fr)
|
1996-06-19 |
2011-09-27 |
Rhone Poulenc Rorer Limited |
Composes azabicycliques substitues et leur utilisation en tant qu'inhibiteurs de la production de tnf et de la photodiesterase cyclique d'amp
|
|
ES2201299T3
(es)
*
|
1996-06-25 |
2004-03-16 |
Pfizer Inc. |
Derivados sustituidos de indazol y su uso como inhibidores de fosfodiesterasa (pde) de tipo iv y factor de necrosis tumoral (tnf)`.
|
|
US6054475A
(en)
*
|
1996-11-20 |
2000-04-25 |
Byk Gulden Lomberg Chemische Fabrik Gmbh |
Substituted dihydrobenzofuran-based phosphodiesterase 4 inhibitors useful for treating airway disorders
|
|
EP1524268B1
(fr)
*
|
1997-02-12 |
2007-01-17 |
Smithkline Beecham Corporation |
Composés et procédé de préparation d'acides 4-phényle-4-cyanocyclohexanoiques substitués
|
|
EP1295869B1
(fr)
*
|
1997-02-12 |
2005-07-27 |
SmithKline Beecham Corporation |
Composés et procédé de préparation d'acides 4-phényl-4-cyanocyclohéxanoiques substitués
|
|
AR012550A1
(es)
*
|
1997-02-12 |
2000-11-08 |
Smithkline Beecham Corp |
Metodo para preparar acidos 4-fenil-4-ciano-ciclohexanoicos sustituidos y compuestos intermediarios
|
|
UA67753C2
(uk)
*
|
1997-10-10 |
2004-07-15 |
Смітклайн Бічам Корпорейшн |
Спосіб отримання заміщених 4-феніл-4-ціанциклогексанових кислот
|
|
UY25338A1
(es)
*
|
1998-01-07 |
2001-08-27 |
Smithkline Beecham Corp |
Método para tratar copd
|
|
EP1043994A4
(fr)
*
|
1998-01-07 |
2002-09-11 |
Smithkline Beecham Corp |
Methode de traitement de la sclerose en plaques
|
|
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
|
|
SE9803710L
(sv)
*
|
1998-09-25 |
2000-03-26 |
A & Science Invest Ab |
Användning av vissa substanser för behandling av nervrotsskador
|
|
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
|
|
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
|
|
ID27509A
(id)
|
1998-10-06 |
2001-04-12 |
Dainippon Pharmaceutical Co |
Turunan piridin tersubstitusi-2,3 proses pembuatannya, komposisi farmasi yang mengandung senyawa tersebut, dan senyawa-antaranya
|
|
AR028986A1
(es)
*
|
1999-02-23 |
2003-06-04 |
Smithkline Beecham Corp |
USO DE UN INHIBIDOR DE PDE4 EN LA FABRICACIoN DE UNA PREPARACIoN DE LIBERACIoN CONTROLADA; FORMULACION DE LIBERACION CONTROLADA PARA EL TRATAMIENTO DE COPD, UN PROCEDIMIENTO PARA SU PREPARACIoN Y COMPOSICIoN FARMACÉUTICA
|
|
US6419934B1
(en)
*
|
1999-02-24 |
2002-07-16 |
Edward L. Tobinick |
TNF modulators for treating neurological disorders associated with viral infection
|
|
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.
|
|
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
|
|
AU5011300A
(en)
*
|
1999-05-14 |
2000-12-05 |
Combichem, 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]
|
|
US20040220424A1
(en)
*
|
1999-08-06 |
2004-11-04 |
Smithkline Beecham Corporation |
Process for preparing acids via alpha-chloroepoxy esters
|
|
US6296840B1
(en)
*
|
1999-08-06 |
2001-10-02 |
Rodan & Fields, Llc |
Masque
|
|
US6740765B1
(en)
*
|
1999-08-06 |
2004-05-25 |
Smithkline Beecham Corporation |
Method for preparing cyclohexane carboxylic acids
|
|
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
|
|
AU777012B2
(en)
*
|
1999-08-21 |
2004-09-30 |
Takeda Gmbh |
Synergistic combination of PDE inhibitors and beta 2 adrenoceptor agonist
|
|
UY26333A1
(es)
*
|
1999-09-15 |
2001-07-31 |
Smithkline Beecham Corp |
Procedimiento e intermedios para preparar ácidos (4-ciano sustituido)- ciclohexanoicos
|
|
US20030050497A1
(en)
*
|
2002-07-11 |
2003-03-13 |
Webb Kevin Scott |
Process and intermediates for preparing a cyclohexylnitrile
|
|
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
|
|
DZ3285A1
(fr)
*
|
2000-01-26 |
2001-08-02 |
Smithkline Beecham Corp |
Monohydrate cis-lithium-4-cyano-4-(3-(cyclopentyloxy)-4methoxyphenyl) cyclohexanecarboxylate
|
|
JP2003522142A
(ja)
*
|
2000-02-08 |
2003-07-22 |
スミスクライン・ビーチャム・コーポレイション |
炎症性疾患の治療法および治療用組成物
|
|
EP1261331A4
(fr)
*
|
2000-02-16 |
2005-01-05 |
Univ Nebraska Medical Ct |
Procede et compositions permettant de traiter les maladies fibrosantes
|
|
US6555572B2
(en)
|
2000-03-16 |
2003-04-29 |
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
|
|
KR100889426B1
(ko)
|
2000-08-05 |
2009-03-23 |
글락소 그룹 리미티드 |
항염증제로서의 6.알파.,9.알파.-디플루오로-17.알파.-'(2-푸라닐카르복실)옥시-11.베타.-히드록시-16.알파.-메틸-3-옥소-안드로스트-1,4-디엔-17-카르보티오산 s-플루오로메틸 에스테르
|
|
US20040224316A1
(en)
|
2000-08-10 |
2004-11-11 |
Tully Timothy P. |
Augmented cognitive training
|
|
NZ526531A
(en)
|
2001-01-31 |
2005-02-25 |
Pfizer Prod Inc |
Ether derivatives useful as inhibitors of phosphodiesterase type IV (PDE4) isozymes
|
|
EE200300360A
(et)
|
2001-01-31 |
2003-12-15 |
Pfizer Products Inc. |
PDE4 isosüümide inhibiitoritena kasutatavad nikotiinamiidi biarüülderivaadid
|
|
US7250518B2
(en)
*
|
2001-01-31 |
2007-07-31 |
Pfizer Inc. |
Nicotinamide acids, amides, and their mimetics active as inhibitors of PDE4 isozymes
|
|
CA2436551A1
(fr)
*
|
2001-01-31 |
2002-08-08 |
Pfizer Products Inc. |
Derives amide acide de thiazolyle, oxazolyle, pyrrolyle et imidazolyle utilises en tant qu'inhibiteurs des isozymes pde4
|
|
GB0103630D0
(en)
*
|
2001-02-14 |
2001-03-28 |
Glaxo Group Ltd |
Chemical compounds
|
|
ATE381537T1
(de)
*
|
2001-03-22 |
2008-01-15 |
Glaxo Group Ltd |
Formanilid-derivative als beta2-adrenorezeptor- agonisten
|
|
AU2002253342B2
(en)
|
2001-04-30 |
2007-01-04 |
Glaxo Group Limited |
Novel anti-inflammatory androstane derivatives
|
|
US20040180900A1
(en)
*
|
2001-05-23 |
2004-09-16 |
Masaharu Takigawa |
Therapeutic composition for repairing chondropathy
|
|
KR20040007596A
(ko)
*
|
2001-05-23 |
2004-01-24 |
다나베 세이야꾸 가부시키가이샤 |
골절 치료 촉진용 조성물
|
|
AU2002326026B2
(en)
*
|
2001-09-14 |
2005-04-28 |
Glaxo Group Limited |
Phenethanolamine derivatives for treatment of respiratory diseases
|
|
GB0201677D0
(en)
|
2002-01-25 |
2002-03-13 |
Glaxo Group Ltd |
Medicament dispenser
|
|
GB0217199D0
(en)
*
|
2002-07-25 |
2002-09-04 |
Glaxo Group Ltd |
Medicament dispenser
|
|
CA2477088A1
(fr)
|
2002-02-22 |
2003-10-02 |
New River Pharmaceuticals Inc. |
Systemes de distribution d'agents actifs et methodes de protection et d'administration d'agents actifs
|
|
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
|
|
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
|
|
GB0217225D0
(en)
|
2002-07-25 |
2002-09-04 |
Glaxo Group Ltd |
Medicinal compounds
|
|
JP2006506373A
(ja)
*
|
2002-10-22 |
2006-02-23 |
グラクソ グループ リミテッド |
医薬アリールエタノールアミン化合物
|
|
AU2003286143A1
(en)
|
2002-10-28 |
2004-05-13 |
Glaxo Group Limited |
Phenethanolamine derivative for the treatment of respiratory diseases
|
|
US20060040981A1
(en)
*
|
2002-11-22 |
2006-02-23 |
Daniel Dube |
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
(fr)
*
|
2003-04-25 |
2005-01-13 |
Gilead Sciences, Inc. |
Composes de phosphonate therapeutiques
|
|
WO2004098606A1
(fr)
*
|
2003-05-12 |
2004-11-18 |
Altana Pharma Ag |
Composition comprenant un inhibiteur de la pde4 et shuil-1r ii
|
|
WO2004098578A2
(fr)
*
|
2003-05-12 |
2004-11-18 |
Altana Pharma Ag |
Composition comprenant un inhibiteur de la pde4 et un antagoniste du tnf?
|
|
CN1812983A
(zh)
|
2003-05-30 |
2006-08-02 |
兰贝克赛实验室有限公司 |
取代的吡咯衍生物及其作为hmg-co抑制剂的用途
|
|
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
|
|
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
|
|
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
|
|
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
|
|
AU2005227733A1
(en)
*
|
2004-04-02 |
2005-10-13 |
Glaxo Group Limited |
Chemical process and new crystalline form
|
|
GB0411056D0
(en)
|
2004-05-18 |
2004-06-23 |
Novartis Ag |
Organic compounds
|
|
PE20060272A1
(es)
|
2004-05-24 |
2006-05-22 |
Glaxo Group Ltd |
(2r,3r,4s,5r,2'r,3'r,4's,5's)-2,2'-{trans-1,4-ciclohexanodiilbis-[imino(2-{[2-(1-metil-1h-imidazol-4-il)etil]amino}-9h-purin-6,9-diil)]}bis[5-(2-etil-2h-tetrazol-5-il)tetrahidro-3,4-furanodiol] como agonista a2a
|
|
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
|
|
WO2006072599A2
(fr)
*
|
2005-01-10 |
2006-07-13 |
Glaxo Group Limited |
Nouveaux composes
|
|
EP1846374A1
(fr)
*
|
2005-01-11 |
2007-10-24 |
Glaxo Group Limited |
Sels de cinnamate d'un agoniste beta-2-adrenergique
|
|
UY29440A1
(es)
|
2005-03-25 |
2006-10-02 |
Glaxo Group Ltd |
Nuevos compuestos
|
|
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
|
|
MY144906A
(en)
|
2005-10-21 |
2011-11-30 |
Novartis Ag |
Human antibodies against il13 and therapeutic uses
|
|
SG166829A1
(en)
|
2005-11-08 |
2010-12-29 |
Ranbaxy Lab Ltd |
Process for (3r, 5r)-7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4- [(4-hydroxy methyl phenyl amino) carbonyl]-pyrrol-1-yl]-3, 5-dihydroxy-heptanoic acid hemi calcium salt
|
|
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
|
|
MX2008013411A
(es)
|
2006-04-20 |
2008-11-04 |
Glaxo Group Ltd |
Nuevos compuestos.
|
|
RU2457209C2
(ru)
|
2006-04-21 |
2012-07-27 |
Новартис Аг |
Производные пурина, предназначенные для применения в качестве агонистов аденозинового рецептора а2а
|
|
MX2008014713A
(es)
|
2006-05-19 |
2009-04-17 |
Helicon Therapeutics Inc |
Inhibidores de fosfodiesterasa 4 para rehabilitacion cognitiva y motora.
|
|
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
|
|
ES2378281T3
(es)
|
2006-07-05 |
2012-04-10 |
Nycomed Gmbh |
Combinación de atorvastatina con un inhibidor de fosfodiesterasa 4 para el tratamiento de neumopatías inflamatorias
|
|
WO2008006117A2
(fr)
*
|
2006-07-07 |
2008-01-10 |
Bioassets Development Corporation |
Procédé permettant d'éviter ou de différer des interventions de mise en place de dispositifs vertébraux ou de fusion vertébrale ou d'obtenir de meilleurs résultats suite à ces types d'interventions
|
|
MX2009003185A
(es)
|
2006-09-29 |
2009-04-03 |
Novartis Ag |
Pirazolopirimidinas como inhibidores de lipido cinasa pi3k.
|
|
AU2007315234A1
(en)
|
2006-10-30 |
2008-05-08 |
Novartis Ag |
Heterocyclic compounds as antiinflammatory agents
|
|
EP2125841A1
(fr)
*
|
2006-12-13 |
2009-12-02 |
Gilead Sciences, Inc. |
Monophosphates utilisés comme promédicaments mutuels de modulateurs de la transduction du signal anti-inflammatoires et de beta-agonistes dans le traitement de l'inflammaton pulmonaire et de la bronchoconstriction
|
|
HRP20110201T1
(hr)
|
2007-01-10 |
2011-08-31 |
Irm Llc |
Spojevi i sastavi kao inhibitori proteaze kanalizirane aktivacije
|
|
PE20081889A1
(es)
|
2007-03-23 |
2009-03-05 |
Smithkline Beecham Corp |
Indol carboxamidas como inhibidores de ikk2
|
|
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
|
|
JP2010523695A
(ja)
*
|
2007-04-11 |
2010-07-15 |
アルコン リサーチ, リミテッド |
アレルギー性鼻炎およびアレルギー性結膜炎を処置するためのTNFαのインヒビターおよび抗ヒスタミン薬の使用
|
|
DE602008005140D1
(de)
|
2007-05-07 |
2011-04-07 |
Novartis Ag |
Organische verbindungen
|
|
WO2008151257A2
(fr)
|
2007-06-04 |
2008-12-11 |
Synergy Pharmaceuticals Inc. |
Agonistes de guanylase cyclase utiles pour le traitement de troubles gastro-intestinaux, d'inflammation, de cancer et d'autres troubles
|
|
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
|
|
KR101608702B1
(ko)
|
2007-06-05 |
2016-04-04 |
사노피 |
디(헤테로)아릴사이클로헥산 유도체, 이들의 제조방법, 이들의 용도 및 이들을 포함하는 약제학적 조성물
|
|
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
|
|
AR069637A1
(es)
|
2007-12-10 |
2010-02-10 |
Novartis Ag |
Derivados de pirazinas
|
|
CN101910153B
(zh)
|
2008-01-11 |
2014-01-22 |
诺华股份有限公司 |
作为激酶抑制剂的嘧啶类
|
|
MX2010012814A
(es)
|
2008-05-23 |
2010-12-20 |
Amira Pharmaceuticals Inc |
Inhibidor de proteina activadora de 5-lipoxigenasa.
|
|
WO2009149279A2
(fr)
|
2008-06-04 |
2009-12-10 |
Synergy Pharmaceuticals Inc. |
Agonistes de guanylate cyclase utile dans le traitement de troubles gastro-intestinaux, d'une inflammation, d'un cancer et d'autres troubles
|
|
WO2009147190A1
(fr)
|
2008-06-05 |
2009-12-10 |
Glaxo Group Limited |
Nouveaux composés
|
|
WO2009147187A1
(fr)
|
2008-06-05 |
2009-12-10 |
Glaxo Group Limited |
Dérivés de 4-carboxamide indazole utiles en tant qu'inhibiteurs de p13 kinases
|
|
WO2009150137A2
(fr)
|
2008-06-10 |
2009-12-17 |
Novartis Ag |
Composés organiques
|
|
CA2730603C
(fr)
|
2008-07-16 |
2019-09-24 |
Synergy Pharmaceuticals Inc. |
Agonistes de la guanylate cyclase utiles dans le traitement des affections gastro-intestinales, de l'inflammation gastro-intestinale, du cancer gastro-intestinal et d'autres affections
|
|
PT2391366E
(pt)
|
2009-01-29 |
2013-02-05 |
Novartis Ag |
Benzimidazoles substituídos para o tratamento de astrocitomas
|
|
WO2010094643A1
(fr)
|
2009-02-17 |
2010-08-26 |
Glaxo Group Limited |
Dérivés de quinoline et applications associées dans la rhinite et l'urticaire
|
|
WO2010102958A1
(fr)
|
2009-03-09 |
2010-09-16 |
Glaxo Group Limited |
4-oxadiazol-2-yl-indazoles en tant qu'inhibiteurs des 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
|
|
WO2010107952A2
(fr)
|
2009-03-19 |
2010-09-23 |
Merck Sharp & Dohme Corp. |
Inhibition médiée par arn interférence de l'expression génique de facteur de croissance de tissu conjonctif (ctgf) en utilisant un acide nucléique interférant court (ansi)
|
|
US20120035247A1
(en)
|
2009-03-19 |
2012-02-09 |
Merck Sharp & Dohme Corp. |
RNA Interference Mediated Inhibition of Signal Transducer and Activator of Transcription 6 (STAT6) Gene Expression Using Short Interfering Nucleic Acid (siNA)
|
|
US20120016010A1
(en)
|
2009-03-19 |
2012-01-19 |
Merck Sharp & Dohme Corp |
RNA Interference Mediated Inhibition of BTB and CNC Homology 1, Basic Leucine Zipper Transcription Factor 1 (BACH1) Gene Expression Using Short Interfering Nucleic Acid (siNA)
|
|
US20120029054A1
(en)
|
2009-03-19 |
2012-02-02 |
Merck Sharp & Dohme Corp. |
RNA Interference Mediated Inhibition of GATA Binding Protein 3 (GATA3) Gene Expression Using Short Intefering Nucleic Acid (siNA)
|
|
EP2411019A2
(fr)
|
2009-03-27 |
2012-02-01 |
Merck Sharp&Dohme Corp. |
Inhibition par interférence arn de l'expression du gène du signal transducteur et activateur de la transcription 1 (stat1) au moyen d'un acide nucléique interférent court (ansi)
|
|
WO2010111468A2
(fr)
|
2009-03-27 |
2010-09-30 |
Merck Sharp & Dohme Corp. |
INHIBITION PAR INTERFÉRENCE ARN DE L'EXPRESSION DU GÈNE DE LA CHAÎNE BÊTA DU FACTEUR DE CROISSANCE DES NERFS (NGFß) AU MOYEN D'UN ACIDE NUCLÉIQUE INTERFÉRENT COURT (ANSI)
|
|
KR20110138223A
(ko)
|
2009-03-27 |
2011-12-26 |
머크 샤프 앤드 돔 코포레이션 |
짧은 간섭 핵산 (siNA)을 사용한 세포간 부착 분자 1 (ICAM-1) 유전자 발현의 RNA 간섭 매개 억제
|
|
WO2010111464A1
(fr)
|
2009-03-27 |
2010-09-30 |
Merck Sharp & Dohme Corp. |
Inhibition par interférence arn de l'expression du gène kinase 1 de régulation du signal d'apoptose (ask1) au moyen d'un acide nucléique interférent court (ansi)
|
|
US20120022143A1
(en)
|
2009-03-27 |
2012-01-26 |
Merck Sharp & Dohme Corp |
RNA Interference Mediated Inhibition of the Thymic Stromal Lymphopoietin (TSLP) Gene Expression Using Short Interfering Nucliec 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
|
|
AR076373A1
(es)
|
2009-04-24 |
2011-06-08 |
Glaxo Group Ltd |
N-pirazolil carboxamidas como inhibidores de canales de calcio
|
|
PL2899191T3
(pl)
|
2009-04-30 |
2018-01-31 |
Glaxo Group Ltd |
Indazole podstawione oksazolem jako inhibitory kinazy PI3
|
|
US8389526B2
(en)
|
2009-08-07 |
2013-03-05 |
Novartis Ag |
3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
|
|
BR112012003262A8
(pt)
|
2009-08-12 |
2016-05-17 |
Novartis Ag |
compostos de hidrazona heterocíclica e seus usos para tratar câncer e inflamação
|
|
PE20121148A1
(es)
|
2009-08-17 |
2012-09-07 |
Intellikine Llc |
Compuestos heterociclicos y usos de los mismos
|
|
BR112012008061A2
(pt)
|
2009-08-20 |
2016-03-01 |
Novartis Ag |
compostos de oxima heterocíclica
|
|
CA2773483A1
(fr)
*
|
2009-10-01 |
2011-04-07 |
Alcon Research, Ltd. |
Compositions d'olopatadine et leurs utilisations
|
|
JP2013508414A
(ja)
|
2009-10-22 |
2013-03-07 |
バーテックス ファーマシューティカルズ インコーポレイテッド |
嚢胞性線維症および他の慢性疾患の治療のための組成物
|
|
WO2011067365A1
(fr)
|
2009-12-03 |
2011-06-09 |
Glaxo Group Limited |
Dérivés de benzpyrazole comme inhibiteurs des pi3 kinases
|
|
EP2507231A1
(fr)
|
2009-12-03 |
2012-10-10 |
Glaxo Group Limited |
Dérivés d'indazole comme inhibiteurs des pi3-kinases
|
|
US20120238559A1
(en)
|
2009-12-03 |
2012-09-20 |
Glaxo Group Limited |
Novel compounds
|
|
EP2512438B1
(fr)
|
2009-12-16 |
2017-01-25 |
3M Innovative Properties Company |
Formulations et procédés pour le réglage de l'administration de particules d'une certaine taille dans un aérosol-doseur
|
|
WO2011110575A1
(fr)
|
2010-03-11 |
2011-09-15 |
Glaxo Group Limited |
Dérivés de 2-[2-(benzo- ou pyrido-)thiazolylamino]-6- aminopyridine, utiles dans le traitement de maladies respiratoires, allergiques ou inflammatoires
|
|
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
|
|
US9326987B2
(en)
|
2010-09-08 |
2016-05-03 |
Glaxo Group Limited |
Indazole derivatives for use in the treatment of influenza virus infection
|
|
HUE026059T2
(en)
|
2010-09-08 |
2016-05-30 |
Glaxosmithkline Ip Dev Ltd |
N- [5- [4- (5 - {[(2R, 6S) -2,6-dimethyl-4-morpholinyl] methyl} -1,3-oxazol-2-yl) -1H-indazol-6-yl ] Polymorphs and salts of 2 - (methyloxy) -3-pyridinyl] methanesulfonamide
|
|
WO2012034095A1
(fr)
|
2010-09-09 |
2012-03-15 |
Irm Llc |
Composés et compositions comme inhibiteurs de trk
|
|
UY33597A
(es)
|
2010-09-09 |
2012-04-30 |
Irm Llc |
Compuestos y composiciones como inhibidores de la trk
|
|
US9616097B2
(en)
|
2010-09-15 |
2017-04-11 |
Synergy Pharmaceuticals, Inc. |
Formulations of guanylate cyclase C agonists and methods of use
|
|
WO2012035055A1
(fr)
|
2010-09-17 |
2012-03-22 |
Glaxo Group Limited |
Nouveaux composés
|
|
US8372845B2
(en)
|
2010-09-17 |
2013-02-12 |
Novartis Ag |
Pyrazine derivatives as enac blockers
|
|
US9149462B2
(en)
|
2010-10-21 |
2015-10-06 |
Glaxo Group Limited |
Pyrazole compounds acting against allergic, inflammatory and immune disorders
|
|
WO2012052458A1
(fr)
|
2010-10-21 |
2012-04-26 |
Glaxo Group Limited |
Composés pyrazole agissant contre des états allergiques, immunitaires et inflammatoires
|
|
GB201018124D0
(en)
|
2010-10-27 |
2010-12-08 |
Glaxo Group Ltd |
Polymorphs and salts
|
|
EP2673277A1
(fr)
|
2011-02-10 |
2013-12-18 |
Novartis AG |
Composés de [1, 2, 4]triazolo [4, 3 -b]pyridazine en tant qu'inhibiteurs de la tyrosine kinase c-met
|
|
JP5808826B2
(ja)
|
2011-02-23 |
2015-11-10 |
インテリカイン, エルエルシー |
複素環化合物およびその使用
|
|
BR112013021638A2
(pt)
|
2011-02-25 |
2016-08-02 |
Irm Llc |
"compostos inibidores de trk, seu uso e composições que os compreendem"
|
|
KR102034748B1
(ko)
|
2011-03-01 |
2019-10-21 |
시너지 파마슈티컬즈 인코포레이티드 |
구아닐레이트 사이클라제 c 작용제의 제조 방법
|
|
EP2683716A1
(fr)
|
2011-03-11 |
2014-01-15 |
Glaxo Group Limited |
Dérivés pyrido[3,4-b]pyrazine en tant qu'inhibiteurs de syk
|
|
GB201104153D0
(en)
|
2011-03-11 |
2011-04-27 |
Glaxo Group Ltd |
Novel compounds
|
|
UY34305A
(es)
|
2011-09-01 |
2013-04-30 |
Novartis Ag |
Derivados de heterociclos bicíclicos para el tratamiento de la hipertensión arterial pulmonar
|
|
EP2755976B1
(fr)
|
2011-09-15 |
2018-07-18 |
Novartis AG |
3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyradines substituées en position 6 à activité tyrosine kinase
|
|
CN103946221B
(zh)
|
2011-09-16 |
2016-08-03 |
诺华股份有限公司 |
用于治疗囊性纤维化的杂环化合物
|
|
WO2013038378A1
(fr)
|
2011-09-16 |
2013-03-21 |
Novartis Ag |
Dérivés pyridinamides
|
|
ES2882807T3
(es)
|
2011-09-16 |
2021-12-02 |
Novartis Ag |
Heterociclil carboxamidas N-sustituidas
|
|
WO2013038373A1
(fr)
|
2011-09-16 |
2013-03-21 |
Novartis Ag |
Dérivés pyrimidinamides
|
|
WO2013038381A1
(fr)
|
2011-09-16 |
2013-03-21 |
Novartis Ag |
Dérivés d'amide pyridine/pyrazine
|
|
US20130209543A1
(en)
|
2011-11-23 |
2013-08-15 |
Intellikine Llc |
Enhanced treatment regimens using mtor inhibitors
|
|
WO2013084182A1
(fr)
|
2011-12-08 |
2013-06-13 |
Glenmark Pharmaceuticals S.A. |
Composition pharmaceutique comprenant un inhibiteur de l'enzyme pde4 et un agent analgésique
|
|
US8809340B2
(en)
|
2012-03-19 |
2014-08-19 |
Novartis Ag |
Crystalline form
|
|
JP2015512425A
(ja)
|
2012-04-03 |
2015-04-27 |
ノバルティス アーゲー |
チロシンキナーゼ阻害剤との組合せ製品及びそれらの使用
|
|
US9545446B2
(en)
|
2013-02-25 |
2017-01-17 |
Synergy Pharmaceuticals, Inc. |
Agonists of guanylate cyclase and their uses
|
|
US9073921B2
(en)
|
2013-03-01 |
2015-07-07 |
Novartis Ag |
Salt forms of bicyclic heterocyclic derivatives
|
|
EP2970384A1
(fr)
|
2013-03-15 |
2016-01-20 |
Synergy Pharmaceuticals Inc. |
Agonistes de la guanylate cyclase et leurs utilisations
|
|
WO2014151147A1
(fr)
|
2013-03-15 |
2014-09-25 |
Intellikine, Llc |
Combinaison d'inhibiteurs de kinase et ses utilisations
|
|
WO2014151200A2
(fr)
|
2013-03-15 |
2014-09-25 |
Synergy Pharmaceuticals Inc. |
Compositions utiles pour le traitement de troubles gastro-intestinaux
|
|
AU2014274812B2
(en)
|
2013-06-05 |
2018-09-27 |
Bausch Health Ireland Limited |
Ultra-pure agonists of guanylate cyclase C, method of making and using same
|
|
WO2015021358A2
(fr)
|
2013-08-09 |
2015-02-12 |
Dominique Charmot |
Composés et procédés d'inhibition du transport de phosphate
|
|
JP6494634B2
(ja)
|
2013-09-22 |
2019-04-03 |
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 |
置換されているアミノピリミジン化合物および使用方法
|
|
WO2015055691A1
(fr)
|
2013-10-17 |
2015-04-23 |
Glaxosmithkline Intellectual Property Development Limited |
Inhibiteur de pi3k pour le traitement d'une maladie respiratoire
|
|
CA2923995A1
(fr)
|
2013-10-17 |
2015-04-23 |
Glaxosmithkline Intellectual Property Development Limited |
Inhibiteur de pi3k pour le traitement d'une maladie respiratoire
|
|
WO2015084804A1
(fr)
|
2013-12-03 |
2015-06-11 |
Novartis Ag |
Combinaison d'un inhibiteur de mdm2 et d'un inhibiteur de braf, et leur utilisation
|
|
EP3312164B1
(fr)
|
2014-03-28 |
2020-12-09 |
Calitor Sciences, LLC |
Composés d'hétéroaryle substitués et procédés d'utilisation
|
|
CN106458979B
(zh)
|
2014-04-24 |
2020-03-27 |
诺华股份有限公司 |
作为磷脂酰肌醇3-激酶抑制剂的氨基吡嗪衍生物
|
|
BR112016023967A2
(pt)
|
2014-04-24 |
2017-08-15 |
Novartis Ag |
derivados de pirazina como inibidores de fosfatidilinositol 3-cinase
|
|
EP3134396B1
(fr)
|
2014-04-24 |
2019-09-18 |
Novartis AG |
Dérivés aminés de pyridine utilisables en tant qu'inhibiteurs de la phosphatidylinositol 3-kinase
|
|
TW201625247A
(zh)
|
2014-05-12 |
2016-07-16 |
葛蘭素史密斯克藍智慧財產權有限公司 |
用於治療傳染性疾病之醫藥組合物
|
|
WO2016011658A1
(fr)
|
2014-07-25 |
2016-01-28 |
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|
|
AU2015294889B2
(en)
|
2014-07-31 |
2018-03-15 |
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|
|
JP2018527362A
(ja)
|
2015-09-11 |
2018-09-20 |
サンシャイン・レイク・ファーマ・カンパニー・リミテッドSunshine Lake Pharma Co.,Ltd. |
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|
|
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(fr)
|
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|
|
WO2017089347A1
(fr)
|
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2017-06-01 |
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|
|
GB201602527D0
(en)
|
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2016-03-30 |
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|
|
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(fr)
|
2016-08-08 |
2019-06-19 |
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|
|
US20190307975A1
(en)
|
2016-11-21 |
2019-10-10 |
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|
|
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(en)
|
2017-04-18 |
2017-05-31 |
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|
|
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(en)
|
2017-07-27 |
2017-09-13 |
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|
|
US10683297B2
(en)
|
2017-11-19 |
2020-06-16 |
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|
|
US10751339B2
(en)
|
2018-01-20 |
2020-08-25 |
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|
|
US20210085897A1
(en)
|
2018-04-06 |
2021-03-25 |
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|
|
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(fr)
*
|
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2021-06-09 |
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|
|
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(fr)
|
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|
|
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(zh)
|
2019-05-21 |
2022-04-12 |
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|
|
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(en)
|
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2024-01-18 |
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|
|
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(es)
|
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2022-03-14 |
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|
|
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(pt)
|
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|
|
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(fr)
|
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|
|
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(en)
|
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|