|
US6548490B1
(en)
*
|
1997-10-28 |
2003-04-15 |
Vivus, Inc. |
Transmucosal administration of phosphodiesterase inhibitors for the treatment of erectile dysfunction
|
|
US6403597B1
(en)
|
1997-10-28 |
2002-06-11 |
Vivus, Inc. |
Administration of phosphodiesterase inhibitors for the treatment of premature ejaculation
|
|
WO2001019818A1
(en)
*
|
1999-09-14 |
2001-03-22 |
Byk Gulden Lomberg Chemische Fabrik Gmbh |
Phthalazinone derivatives as pd3/4 inhibitors
|
|
HUP0203487A2
(hu)
|
1999-10-25 |
2003-02-28 |
Byk Gulden Lomberg Chemische Fabrik Gmbh |
Tetrahidrotiopirán-ftalazinon-származékok, mint PDE4-inhibitorok és ezeket tartalmazó gyógyszerkészítmények
|
|
EP1228046B1
(de)
|
1999-10-25 |
2007-09-26 |
Nycomed GmbH |
Phthalazinon-derivate als pde 4 hemmer
|
|
EP2067784A3
(de)
|
2000-08-05 |
2012-08-22 |
Glaxo Group Limited |
17.beta.-Carbothioat-17.alpha.-Arylcarbonyloxyloxy-Androstan-Derivate als entzündungshemmende Mittel
|
|
GB0103630D0
(en)
|
2001-02-14 |
2001-03-28 |
Glaxo Group Ltd |
Chemical compounds
|
|
HRP20030636B1
(en)
|
2001-02-15 |
2012-05-31 |
Nycomed Gmbh |
Phthalayinone-piperidino-derivatives as pde4 inhibitors
|
|
WO2002076933A1
(en)
|
2001-03-22 |
2002-10-03 |
Glaxo Group Limited |
Formailide derivatives as beta2-adrenoreceptor agonists
|
|
JP4021329B2
(ja)
*
|
2001-04-25 |
2007-12-12 |
ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング |
ピペラジノ誘導体およびpde4阻害剤としてのその使用
|
|
EE200300514A
(et)
*
|
2001-04-25 |
2004-02-16 |
Altana Pharma Ag |
Ftalasinoonid, nende kasutamine hingamisteede haigusnähte leevendavate ravimite valmistamiseks ningneid sisaldavad ravimid
|
|
WO2002088167A1
(en)
|
2001-04-30 |
2002-11-07 |
Glaxo Group Limited |
Anti-inflammatory 17.beta.-carbothioate ester derivatives of androstane with a cyclic ester group in position 17.alpha
|
|
WO2003008396A1
(en)
*
|
2001-07-16 |
2003-01-30 |
Nikken Chemicals Co., Ltd. |
Optically active oxazine derivative
|
|
US20030073711A1
(en)
*
|
2001-08-23 |
2003-04-17 |
Whitehead Clark M. |
Methods for treatment of scleroderma
|
|
US6479493B1
(en)
|
2001-08-23 |
2002-11-12 |
Cell Pathways, Inc. |
Methods for treatment of type I diabetes
|
|
ATE417606T1
(de)
|
2001-09-14 |
2009-01-15 |
Glaxo Group Ltd |
Phenethanolamin-derivate zur behandlung von erkrankungen der atemwege
|
|
GB0201677D0
(en)
|
2002-01-25 |
2002-03-13 |
Glaxo Group Ltd |
Medicament dispenser
|
|
ATE381535T1
(de)
|
2002-04-25 |
2008-01-15 |
Glaxo Group Ltd |
Phenethanolaminderivate
|
|
GB0217225D0
(en)
|
2002-07-25 |
2002-09-04 |
Glaxo Group Ltd |
Medicinal compounds
|
|
CA2494650A1
(en)
*
|
2002-08-10 |
2004-03-04 |
Altana Pharma Ag |
Pyridazinone-derivatives as pde4 inhibitors
|
|
HRP20050197A2
(en)
*
|
2002-08-10 |
2006-06-30 |
Altana Pharma Ag |
Piperidine-n-oxide-derivatives
|
|
WO2004018449A1
(en)
*
|
2002-08-10 |
2004-03-04 |
Altana Pharma Ag |
Piperidine-derivatives as pde4 inhibitors
|
|
JP2005538140A
(ja)
*
|
2002-08-10 |
2005-12-15 |
アルタナ ファルマ アクチエンゲゼルシャフト |
Pde4インヒビターとしてのピペリジン−ピリダゾン及びフタラゾン
|
|
US7442839B2
(en)
|
2002-10-28 |
2008-10-28 |
Glaxo Group Limited |
Phenethanolamine derivative for the treatment of respiratory diseases
|
|
PE20040950A1
(es)
|
2003-02-14 |
2005-01-01 |
Theravance Inc |
DERIVADOS DE BIFENILO COMO AGONISTAS DE LOS RECEPTORES ADRENERGICOS ß2 Y COMO ANTAGONISTAS DE LOS RECEPTORES MUSCARINICOS
|
|
GB0303396D0
(en)
|
2003-02-14 |
2003-03-19 |
Glaxo Group Ltd |
Medicinal compounds
|
|
GB0316290D0
(en)
|
2003-07-11 |
2003-08-13 |
Glaxo Group Ltd |
Novel compounds
|
|
GB0317374D0
(en)
|
2003-07-24 |
2003-08-27 |
Glaxo Group Ltd |
Medicament dispenser
|
|
GB0329182D0
(en)
|
2003-12-17 |
2004-01-21 |
Glaxo Group Ltd |
Chemical compounds
|
|
AU2005210042B2
(en)
*
|
2004-02-04 |
2011-04-21 |
Takeda Gmbh |
2-(piperidin-4-yl) -4, 5-dihydro-2H-pyridazin-3-one derivatives as PDE4 inhibitors
|
|
US20080227790A1
(en)
*
|
2004-02-04 |
2008-09-18 |
Altana Pharma Ag |
Pyridazinone Derivatives and their Use as Pde4 Inhibitors
|
|
TWI341836B
(en)
|
2004-03-11 |
2011-05-11 |
Theravance Inc |
Biphenyl compounds useful as muscarinic receptor antagonists
|
|
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
|
|
WO2006023460A2
(en)
|
2004-08-16 |
2006-03-02 |
Theravance, Inc. |
COMPOUNDS HAVING β2 ADRENERGIC RECEPTOR AGONIST AND MUSCARINIC RECEPTOR ANTAGONIST ACTIVITY
|
|
EP1841780B1
(de)
|
2005-01-10 |
2011-07-27 |
Glaxo Group Limited |
Androstan-17-alpha-carbonat-derivate zur verwendung bei der behandlung allergischer und entzündlicher zustände
|
|
PE20061351A1
(es)
|
2005-03-25 |
2007-01-14 |
Glaxo Group Ltd |
COMPUESTOS 8H-PIRIDO[2,3-d]PIRIMIDIN-7-ONA 2,4,8-TRISUSTITUIDOS COMO INHIBIDORES DE LA QUINASA CSBP/RK/p38
|
|
GB0514809D0
(en)
|
2005-07-19 |
2005-08-24 |
Glaxo Group Ltd |
Compounds
|
|
PE20071068A1
(es)
|
2005-12-20 |
2007-12-13 |
Glaxo Group Ltd |
Acido 3-(4-{[4-(4-{[3-(3,3-dimetil-1-piperidinil)propil]oxi}fenil)-1-piperidinil]carbonil}-1-naftalenil)propanoico o propenoico, sales de los mismos, como antagonistas de los receptores h1 y h3
|
|
KR20090003349A
(ko)
|
2006-04-20 |
2009-01-09 |
글락소 그룹 리미티드 |
화합물
|
|
GB0611587D0
(en)
|
2006-06-12 |
2006-07-19 |
Glaxo Group Ltd |
Novel compounds
|
|
MX2009000884A
(es)
|
2006-07-25 |
2009-06-05 |
Cephalon Inc |
Derivados de piridizinona.
|
|
WO2008111631A1
(ja)
*
|
2007-03-14 |
2008-09-18 |
Nippon Shinyaku Co., Ltd. |
α-メチルベンジルアミン塩の製法
|
|
PE20081889A1
(es)
|
2007-03-23 |
2009-03-05 |
Smithkline Beecham Corp |
Indol carboxamidas como inhibidores de ikk2
|
|
US7943658B2
(en)
|
2007-07-23 |
2011-05-17 |
Bristol-Myers Squibb Company |
Indole indane amide compounds useful as CB2 agonists and method
|
|
CN102137858B
(zh)
|
2008-05-23 |
2014-07-23 |
潘米拉制药有限责任公司 |
5-脂氧合酶-活化蛋白抑制剂
|
|
JP5502858B2
(ja)
|
2008-06-05 |
2014-05-28 |
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有用な4−カルボキサミドインダゾール誘導体
|
|
EP2297142B1
(de)
|
2008-06-24 |
2015-10-14 |
F. Hoffmann-La Roche AG |
Neue substituierte pyridin-2-one und pyridazin-3-one
|
|
CA2728683C
(en)
|
2008-07-02 |
2017-05-02 |
F.Hoffmann-La Roche Ag |
Novel phenylpyrazinones as kinase inhibitors
|
|
WO2010094643A1
(en)
|
2009-02-17 |
2010-08-26 |
Glaxo Group Limited |
Quinoline derivatives and their uses for rhinitis and urticaria
|
|
EP2406255B1
(de)
|
2009-03-09 |
2015-04-29 |
Glaxo Group Limited |
4-oxadiazol-2-ylindazole als inhibitoren von pi3-kinasen
|
|
WO2010102968A1
(en)
|
2009-03-10 |
2010-09-16 |
Glaxo Group Limited |
Indole derivatives as ikk2 inhibitors
|
|
WO2010106016A1
(en)
|
2009-03-17 |
2010-09-23 |
Glaxo Group Limited |
Pyrimidine derivatives used as itk inhibitors
|
|
WO2010107958A1
(en)
|
2009-03-19 |
2010-09-23 |
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)
|
|
JP2012520683A
(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)を用いた結合組織増殖因子(CTGF)遺伝子発現のRNA干渉媒介性阻害
|
|
CA2755773A1
(en)
|
2009-03-19 |
2010-09-23 |
Merck Sharp & Dohme Corp. |
Rna interference mediated inhibition of btb and cnc homology 1, basic leucine zipper transcription factor 1 (bach 1) gene expression using short interfering nucleic acid (sina)
|
|
WO2010107957A2
(en)
|
2009-03-19 |
2010-09-23 |
Merck Sharp & Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF GATA BINDING PROTEIN 3 (GATA3) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
|
|
US20120010272A1
(en)
|
2009-03-27 |
2012-01-12 |
Merck Sharp & Dohme Corp. |
RNA Interference Mediated Inhibition of Apoptosis Signal-Regulating Kinase 1 (ASK1) Gene Expression Using Short Interfering Nucleic Acid (siNA)
|
|
WO2010111471A2
(en)
|
2009-03-27 |
2010-09-30 |
Merck Sharp & Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 1 (STAT1) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
|
|
WO2010111468A2
(en)
|
2009-03-27 |
2010-09-30 |
Merck Sharp & Dohme Corp. |
RNA INTERFERENCE MEDIATED INHIBITION OF THE NERVE GROWTH FACTOR BETA CHAIN (NGFß) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (SINA)
|
|
EP2411520A2
(de)
|
2009-03-27 |
2012-02-01 |
Merck Sharp&Dohme Corp. |
Rna-interferenz-vermittelte hemmung der genexpression von tslp (thymic stromal lymphopoietin) unter verwendung von sina (short interfering nucleic acid)
|
|
MX2011010072A
(es)
|
2009-03-27 |
2011-10-06 |
Merck Sharp & Dohme |
Inhibicion mediada por interferencia de acido ribonucleico de la expresion del gen de la molecula de adhesion intercelular 1 usando acido nucleico corto de interferencia.
|
|
JP2012524755A
(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n−ピラゾリルカルボキサミド
|
|
EP2421834A1
(de)
|
2009-04-24 |
2012-02-29 |
Glaxo Group Limited |
Pyrazol- und triazolcarbonsäureamide als inhibitoren des crac-kanals
|
|
AR076435A1
(es)
|
2009-04-30 |
2011-06-08 |
Glaxo Group Ltd |
Compuestos de indazoles sustituidos, composiciones farmaceuticas que los contienen y procesos de obtencion de los mismos
|
|
SI2453894T1
(sl)
|
2009-07-15 |
2016-02-29 |
Theravance Biopharma R&D Ip, Llc |
Kristalinična oblika proste baze bifenilne spojine
|
|
WO2011067365A1
(en)
|
2009-12-03 |
2011-06-09 |
Glaxo Group Limited |
Benzpyrazole derivatives as inhibitors of p13 kinases
|
|
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
|
|
JP2013512880A
(ja)
|
2009-12-03 |
2013-04-18 |
グラクソ グループ リミテッド |
Pi3−キナーゼ阻害剤としてのインダゾール誘導体
|
|
EP2512438B1
(de)
|
2009-12-16 |
2017-01-25 |
3M Innovative Properties Company |
Formulierungen und verfahren zur steuerung der mdi-partikelgrössenfreisetzung
|
|
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
|
|
GB201007203D0
(en)
|
2010-04-29 |
2010-06-16 |
Glaxo Group Ltd |
Novel compounds
|
|
RS54286B1
(sr)
|
2010-09-08 |
2016-02-29 |
Glaxosmithkline Intellectual Property Development Limited |
Polimorfi i 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
|
|
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
|
|
WO2012035055A1
(en)
|
2010-09-17 |
2012-03-22 |
Glaxo Group Limited |
Novel compounds
|
|
WO2012052459A1
(en)
|
2010-10-21 |
2012-04-26 |
Glaxo Group Limited |
Pyrazole compounds acting against allergic, inflammatory and immune disorders
|
|
EP2630126B1
(de)
|
2010-10-21 |
2015-01-07 |
Glaxo Group Limited |
Pyrazolverbindungen gegen allergie-, immun- und entzündungserkrankungen
|
|
GB201018124D0
(en)
|
2010-10-27 |
2010-12-08 |
Glaxo Group Ltd |
Polymorphs and salts
|
|
EP2683716A1
(de)
|
2011-03-11 |
2014-01-15 |
Glaxo Group Limited |
Pyrido[3,4-b]pyrazinderivate als syk-hemmer
|
|
GB201104153D0
(en)
|
2011-03-11 |
2011-04-27 |
Glaxo Group Ltd |
Novel compounds
|
|
EP2721030B1
(de)
*
|
2011-06-17 |
2015-12-16 |
Takeda GmbH |
Neuartige phthalazinon-pyrrolopyrimidincarboxamidderivate
|
|
EP2804603A1
(de)
|
2012-01-10 |
2014-11-26 |
President and Fellows of Harvard College |
Betazellen-replikation für promoterverbindungen und verwendungsverfahren dafür
|
|
CN105307655B
(zh)
|
2013-03-13 |
2019-05-03 |
弗拉特利发现实验室有限责任公司 |
哒嗪酮化合物及其用于制备治疗囊肿状纤维化的药物的应用
|
|
US20140275102A1
(en)
*
|
2013-03-14 |
2014-09-18 |
Cephalon, Inc. |
Solid State Forms of 6-[4-[3-((R)-2-Methylpyrrolidine-1-yl)-propoxy]phenyl] 2H-pyridazine-3-one Hydrochloride
|
|
JP2016537327A
(ja)
|
2013-10-17 |
2016-12-01 |
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 |
呼吸器疾患の治療のためのpi3k阻害剤
|
|
RU2016112266A
(ru)
|
2013-10-17 |
2017-11-20 |
Глаксосмитклайн Интеллекчуал Проперти Дивелопмент Лимитед |
Ингибитор PI3K для лечения респираторного заболевания
|
|
WO2015173701A2
(en)
|
2014-05-12 |
2015-11-19 |
Glaxosmithkline Intellectual Property (No. 2) Limited |
Pharmaceutical compositions for treating infectious diseases
|
|
CN106573898B
(zh)
|
2014-08-14 |
2018-11-09 |
豪夫迈·罗氏有限公司 |
治疗和预防乙型肝炎病毒感染的新的哒嗪酮和三嗪酮
|
|
CN104478809B
(zh)
*
|
2014-11-14 |
2016-08-17 |
成都新恒创药业有限公司 |
一种左西孟旦杂质及其制备和检测方法
|
|
GB201602527D0
(en)
|
2016-02-12 |
2016-03-30 |
Glaxosmithkline Ip Dev Ltd |
Chemical compounds
|
|
JP2019524792A
(ja)
|
2016-08-08 |
2019-09-05 |
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 |
化合物
|
|
WO2018094392A1
(en)
|
2016-11-21 |
2018-05-24 |
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
|
|
WO2019195711A1
(en)
|
2018-04-06 |
2019-10-10 |
Lupin Inc. |
Medicament dispenser
|
|
WO2020058823A1
(en)
|
2018-09-17 |
2020-03-26 |
Lupin, Inc. |
Dose indicator assembly for a medicament dispenser
|
|
EP4126139A1
(de)
|
2020-03-25 |
2023-02-08 |
Lupin Inc. |
Mehrträger-medikamentenspender
|
|
CN116210004A
(zh)
|
2020-07-23 |
2023-06-02 |
鲁平股份有限公司 |
用于药剂分配器的剂量计数器组件
|