|
GB1219606A
(en)
|
1968-07-15 |
1971-01-20 |
Rech S Et D Applic Scient Soge |
Quinuclidinol derivatives and preparation thereof
|
|
GB1528382A
(en)
|
1974-12-26 |
1978-10-11 |
Teijin Ltd |
Cyclopentene diols and acyl esters thereof and processes for their preparation
|
|
FR2459240A1
(fr)
|
1979-06-21 |
1981-01-09 |
Cm Ind |
Aminopiperidines anorexigenes, procede pour leur preparation, intermediaires dans ledit procede et medicaments qui les contiennent
|
|
EP0147716A3
(fr)
|
1983-12-24 |
1987-10-28 |
ANT Nachrichtentechnik GmbH |
Procédé et dispositif pour la transmission chiffrable d'une suite de signaux binaires d'information avec contrôle d'authenticité
|
|
JPS6235216A
(ja)
|
1985-08-09 |
1987-02-16 |
Noritoshi Nakabachi |
不均質物質層の層厚非破壊測定方法および装置
|
|
US4738954A
(en)
|
1985-11-06 |
1988-04-19 |
Warner-Lambert Company |
Novel N6 -substituted-5'-oxidized adenosine analogs
|
|
US4873360A
(en)
|
1986-07-10 |
1989-10-10 |
Board Of Governors Of Wayne State University |
Process for the preparation of cyclopentanoids and novel intermediates produced thereby
|
|
US4954504A
(en)
|
1986-11-14 |
1990-09-04 |
Ciba-Geigy Corporation |
N9 -cyclopentyl-substituted adenine derivatives having adenosine-2 receptor stimulating activity
|
|
EP0267878A1
(fr)
|
1986-11-14 |
1988-05-18 |
Ciba-Geigy Ag |
Dérivés de l'adénine N9-substitués par le groupement cyclopentyle
|
|
JP2586897B2
(ja)
|
1987-03-09 |
1997-03-05 |
富士薬品工業株式会社 |
光学活性なシス−シクロペンテン−3,5−ジオ−ルモノエステルの製造法
|
|
US4916224A
(en)
*
|
1988-01-20 |
1990-04-10 |
Regents Of The University Of Minnesota |
Dideoxycarbocyclic nucleosides
|
|
ATE84302T1
(de)
|
1988-10-20 |
1993-01-15 |
Ciba Geigy Ag |
Sulfamoylphenylharnstoffe.
|
|
GB8923590D0
(en)
|
1989-10-19 |
1989-12-06 |
Pfizer Ltd |
Antimuscarinic bronchodilators
|
|
ATE147074T1
(de)
|
1990-09-25 |
1997-01-15 |
Rhone Poulenc Rorer Int |
Verbindungen welche antihypertensive und antiischemische eigenschaften besitzen
|
|
PT100441A
(pt)
|
1991-05-02 |
1993-09-30 |
Smithkline Beecham Corp |
Pirrolidinonas, seu processo de preparacao, composicoes farmaceuticas que as contem e uso
|
|
US5451700A
(en)
|
1991-06-11 |
1995-09-19 |
Ciba-Geigy Corporation |
Amidino compounds, their manufacture and methods of treatment
|
|
WO1993018007A1
(fr)
|
1992-03-13 |
1993-09-16 |
Tokyo Tanabe Company Limited |
Nouveau derive de carbostyrile
|
|
AU3924993A
(en)
|
1992-04-02 |
1993-11-08 |
Smithkline Beecham Corporation |
Compounds useful for treating inflammatory diseases and inhibiting production of tumor necrosis factor
|
|
JP3192424B2
(ja)
|
1992-04-02 |
2001-07-30 |
スミスクライン・ビーチャム・コーポレイション |
アレルギーまたは炎症疾患の治療用化合物
|
|
NZ251092A
(en)
|
1992-04-02 |
1996-12-20 |
Smithkline Beecham Corp |
4-cyano-cyclohexane derivatives; medicaments; used in treating asthma
|
|
IT1254915B
(it)
|
1992-04-24 |
1995-10-11 |
Gloria Cristalli |
Derivati di adenosina ad attivita' a2 agonista
|
|
US5688774A
(en)
|
1993-07-13 |
1997-11-18 |
The United States Of America As Represented By The Department Of Health And Human Services |
A3 adenosine receptor agonists
|
|
US5691188A
(en)
*
|
1994-02-14 |
1997-11-25 |
American Cyanamid Company |
Transformed yeast cells expressing heterologous G-protein coupled receptor
|
|
GB9414193D0
(en)
|
1994-07-14 |
1994-08-31 |
Glaxo Group Ltd |
Compounds
|
|
US6143749A
(en)
*
|
1995-06-07 |
2000-11-07 |
Abbott Laboratories |
Heterocyclic substituted cyclopentane compounds
|
|
AU722894B2
(en)
|
1996-01-02 |
2000-08-10 |
Aventis Pharmaceuticals Inc. |
Process for preparing 2,4-dihydroxypyridine and 2,4-dihydroxy-3-nitropyridine
|
|
US6376472B1
(en)
|
1996-07-08 |
2002-04-23 |
Aventis Pharmaceuticals, Inc. |
Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties
|
|
GB9622386D0
(en)
|
1996-10-28 |
1997-01-08 |
Sandoz Ltd |
Organic compounds
|
|
AU750322B2
(en)
|
1997-05-09 |
2002-07-18 |
Trustees Of The University Of Pennsylvania, The |
Methods and compositions for reducing ischemic injury of the heart by administering adenosine receptor agonists and antagonists
|
|
US6166037A
(en)
|
1997-08-28 |
2000-12-26 |
Merck & Co., Inc. |
Pyrrolidine and piperidine modulators of chemokine receptor activity
|
|
AU9281298A
(en)
|
1997-10-01 |
1999-04-23 |
Kyowa Hakko Kogyo Co. Ltd. |
Benzodioxole derivatives
|
|
YU44900A
(sh)
*
|
1998-01-31 |
2003-01-31 |
Glaxo Group Limited |
Derivati 2-(purin-9-il)tetrahidrofuran-3,4-diola
|
|
US6541669B1
(en)
|
1998-06-08 |
2003-04-01 |
Theravance, Inc. |
β2-adrenergic receptor agonists
|
|
FR2780057B1
(fr)
|
1998-06-18 |
2002-09-13 |
Sanofi Sa |
Phenoxypropanolamines, procede pour leur preparation et compositions pharmaceutiques les contenant
|
|
GB9813535D0
(en)
|
1998-06-23 |
1998-08-19 |
Glaxo Group Ltd |
Chemical compounds
|
|
GB9813540D0
(en)
|
1998-06-23 |
1998-08-19 |
Glaxo Group Ltd |
Chemical compounds
|
|
JP3933870B2
(ja)
|
1998-06-23 |
2007-06-20 |
グラクソ グループ リミテッド |
2−(プリン−9−イル)−テトラヒドロフラン−3,4−ジオール誘導体
|
|
GB9813554D0
(en)
|
1998-06-23 |
1998-08-19 |
Glaxo Group Ltd |
Chemical compounds
|
|
EP1098923B1
(fr)
|
1998-06-30 |
2004-11-17 |
Dow Global Technologies Inc. |
Polymeres et leur procede de production
|
|
WO2000023457A1
(fr)
|
1998-10-16 |
2000-04-27 |
Pfizer Limited |
Derives d'adenine
|
|
BR9917000A
(pt)
|
1998-12-31 |
2001-12-11 |
Aventis Pharm Prod Inc |
Processo para preparar derivados dedesaza-adenosina n6-substituìda
|
|
US7427606B2
(en)
|
1999-02-01 |
2008-09-23 |
University Of Virginia Patent Foundation |
Method to reduce inflammatory response in transplanted tissue
|
|
GB9913083D0
(en)
|
1999-06-04 |
1999-08-04 |
Novartis Ag |
Organic compounds
|
|
WO2000066558A1
(fr)
|
1999-05-04 |
2000-11-09 |
Schering Corporation |
Derives de piperazine faisant office d'antagonistes ccr5
|
|
SK286968B6
(sk)
|
1999-05-04 |
2009-08-06 |
Schering Corporation |
Piperidín-piperidinyl ako CCR5 antagonista, farmaceutický prostriedok s jeho obsahom a jeho použitie
|
|
RU2258071C2
(ru)
*
|
1999-05-24 |
2005-08-10 |
Юниверсити Оф Вирджиния Пэйтент Фаундейшн |
Производные 2-алкиниладенозина для борьбы с воспалительной реакцией
|
|
US6683115B2
(en)
|
1999-06-02 |
2004-01-27 |
Theravance, Inc. |
β2-adrenergic receptor agonists
|
|
US6322771B1
(en)
|
1999-06-18 |
2001-11-27 |
University Of Virginia Patent Foundation |
Induction of pharmacological stress with adenosine receptor agonists
|
|
US6214807B1
(en)
*
|
1999-06-22 |
2001-04-10 |
Cv Therapeutics, Inc. |
C-pyrazole 2A A receptor agonists
|
|
US6403567B1
(en)
*
|
1999-06-22 |
2002-06-11 |
Cv Therapeutics, Inc. |
N-pyrazole A2A adenosine receptor agonists
|
|
ES2165768B1
(es)
|
1999-07-14 |
2003-04-01 |
Almirall Prodesfarma Sa |
Nuevos derivados de quinuclidina y composiciones farmaceuticas que los contienen.
|
|
SK287231B6
(sk)
|
1999-08-21 |
2010-04-07 |
Nycomed Gmbh |
Liečivo zahŕňajúce PDE inhibítor a agonistu beta2 adrenoreceptora
|
|
GB9924361D0
(en)
*
|
1999-10-14 |
1999-12-15 |
Pfizer Ltd |
Purine derivatives
|
|
US6586413B2
(en)
|
1999-11-05 |
2003-07-01 |
The United States Of America As Represented By The Department Of Health And Human Services |
Methods and compositions for reducing ischemic injury of the heart by administering adenosine receptor agonists and antagonists
|
|
OA11558A
(en)
|
1999-12-08 |
2004-06-03 |
Advanced Medicine Inc |
Beta 2-adrenergic receptor agonists.
|
|
GB0003960D0
(en)
*
|
2000-02-18 |
2000-04-12 |
Pfizer Ltd |
Purine derivatives
|
|
KR20020093083A
(ko)
|
2000-04-27 |
2002-12-12 |
베링거 잉겔하임 파르마 카게 |
신규한 완효성 베타모사체, 이의 제조방법 및 약제로서의이의 용도
|
|
TWI227240B
(en)
|
2000-06-06 |
2005-02-01 |
Pfizer |
2-aminocarbonyl-9H-purine derivatives
|
|
GB0015727D0
(en)
*
|
2000-06-27 |
2000-08-16 |
Pfizer Ltd |
Purine derivatives
|
|
AU2001266100B9
(en)
|
2000-06-27 |
2005-10-06 |
Laboratorios S.A.L.V.A.T., S.A. |
Carbamates derived from arylalkylamines
|
|
GB0015876D0
(en)
|
2000-06-28 |
2000-08-23 |
Novartis Ag |
Organic compounds
|
|
DE10038639A1
(de)
|
2000-07-28 |
2002-02-21 |
Schering Ag |
Nichtsteroidale Entzündungshemmer
|
|
PT2348032E
(pt)
|
2000-08-05 |
2015-10-14 |
Glaxo Group Ltd |
Éster s-fluorometílico do ácido 6.alfa.,9.alfa.-difluoro- 17.alfa.-'(2-furanilcarboxil)oxi]-11.beta.-hidroxi-16.alfa.- metil-3-oxo-androsta-1,4-dieno-17-carbotióico como um agente anti-inflamatório
|
|
GB0022695D0
(en)
|
2000-09-15 |
2000-11-01 |
Pfizer Ltd |
Purine Derivatives
|
|
GB0028383D0
(en)
|
2000-11-21 |
2001-01-03 |
Novartis Ag |
Organic compounds
|
|
PL362989A1
(en)
|
2000-12-22 |
2004-11-15 |
Almirall Prodesfarma Ag |
Quinuclidine carbamate derivatives and their use as m3 antagonists
|
|
EE05404B1
(et)
|
2000-12-28 |
2011-04-15 |
Almirall Prodesfarma Ag |
Kinuklidiini derivaat, selle saamine ja kasutamine ravimi valmistamiseks, mis on ette nhtud respiratoorsete, kuseelundite v?i mao-soolte haiguste ravimiseks, ning seda sisaldav ravimkompositsioon
|
|
DE60203702T2
(de)
|
2001-01-16 |
2006-03-02 |
Can-Fite Biopharma Ltd. |
Verwendung eines adenosin-a3-rezeptor-agonisten zur hemmung der virenreplikation
|
|
GB0103630D0
(en)
|
2001-02-14 |
2001-03-28 |
Glaxo Group Ltd |
Chemical compounds
|
|
GB2372741A
(en)
|
2001-03-03 |
2002-09-04 |
Univ Leiden |
C2,8-Disubstituted adenosine derivatives and their different uses
|
|
JP2004526720A
(ja)
|
2001-03-08 |
2004-09-02 |
グラクソ グループ リミテッド |
βアドレナリン受容体のアゴニスト
|
|
US20040162422A1
(en)
|
2001-03-20 |
2004-08-19 |
Adrian Hall |
Chemical compounds
|
|
EP1370521B1
(fr)
|
2001-03-22 |
2007-12-19 |
Glaxo Group Limited |
Derives formanilides utilises en tant qu'agonistes de l'adrenorecepteur beta2
|
|
JP2002283758A
(ja)
|
2001-03-28 |
2002-10-03 |
Fuji Photo Film Co Ltd |
平版印刷版用原版
|
|
CA2445839A1
(fr)
|
2001-04-30 |
2002-11-07 |
Glaxo Group Limited |
Derives anti-inflammatoires d'androstane 17.beta.-carbothioate ester avec un groupe cyclique en position 17.alpha
|
|
EP1258247A1
(fr)
|
2001-05-14 |
2002-11-20 |
Aventis Pharma Deutschland GmbH |
Analogues d'adénosine pour le traitement de le diabete et de la resistance à l' insuline
|
|
EP1395604B1
(fr)
|
2001-06-12 |
2008-06-25 |
Glaxo Group Limited |
17 alpha esters heterocycliques anti-inflammatoires de derives de 17 beta carbothioate androstane
|
|
DK2327767T3
(en)
|
2001-06-21 |
2015-07-27 |
Basf Enzymes Llc |
nitrilases
|
|
AU2002326026B2
(en)
|
2001-09-14 |
2005-04-28 |
Glaxo Group Limited |
Phenethanolamine derivatives for treatment of respiratory diseases
|
|
NZ556354A
(en)
|
2001-10-01 |
2008-10-31 |
Univ Virginia |
2-Propynyl adenosine analogs having A2A agonist activity and compositions thereof
|
|
WO2003033495A1
(fr)
|
2001-10-17 |
2003-04-24 |
Ucb, S.A. |
Derives de quinuclidine, leurs procedes de preparation, et leurs utilisations en tant qu'inhibiteurs de recepteur muscarinique m2 et/ou m3
|
|
GB0125259D0
(en)
|
2001-10-20 |
2001-12-12 |
Glaxo Group Ltd |
Novel compounds
|
|
MY130622A
(en)
|
2001-11-05 |
2007-07-31 |
Novartis Ag |
Naphthyridine derivatives, their preparation and their use as phosphodiesterase isoenzyme 4 (pde4) inhibitors
|
|
TWI249515B
(en)
|
2001-11-13 |
2006-02-21 |
Theravance Inc |
Aryl aniline beta2 adrenergic receptor agonists
|
|
US6653323B2
(en)
|
2001-11-13 |
2003-11-25 |
Theravance, Inc. |
Aryl aniline β2 adrenergic receptor agonists
|
|
AU2002356759A1
(en)
|
2001-12-01 |
2003-06-17 |
Glaxo Group Limited |
17.alpha. -cyclic esters of 16-methylpregnan-3,20-dione as anti-inflammatory agents
|
|
RS52522B
(sr)
|
2001-12-20 |
2013-04-30 |
Chiesi Farmaceutici S.P.A. |
Derivati 1-alkil-1-azoniabiciklo/2.2.2./oktan karbamata i njihova upotreba kao antagonista muskarinskih receptora
|
|
WO2003072592A1
(fr)
|
2002-01-15 |
2003-09-04 |
Glaxo Group Limited |
17 alpha esters cycloalkyle/cycloalcenyle d'alkyle ou haloalkyle-androst-4-en-3-on-11 beta, 17 alpha-diol 17 beta-carboxylates comme agents anti-inflammatoires
|
|
AU2003201693A1
(en)
|
2002-01-21 |
2003-09-02 |
Glaxo Group Limited |
Non-aromatic 17.alpha.-esters of androstane-17.beta.-carboxylate esters as anti-inflammatory agents
|
|
US7414036B2
(en)
|
2002-01-25 |
2008-08-19 |
Muscagen Limited |
Compounds useful as A3 adenosine receptor agonists
|
|
GB0202216D0
(en)
|
2002-01-31 |
2002-03-20 |
Glaxo Group Ltd |
Novel compounds
|
|
GB0204719D0
(en)
|
2002-02-28 |
2002-04-17 |
Glaxo Group Ltd |
Medicinal compounds
|
|
AU2003230700A1
(en)
|
2002-03-26 |
2003-10-13 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof
|
|
PL373043A1
(en)
|
2002-03-26 |
2005-08-08 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof
|
|
JP2006515829A
(ja)
|
2002-04-10 |
2006-06-08 |
ユニバーシティ オブ バージニア パテント ファウンデーション |
炎症性疾病の処置のための、a2aアデノシン受容体アゴニストの使用
|
|
US7282591B2
(en)
|
2002-04-11 |
2007-10-16 |
Merck & Co., Inc. |
1h-benzo{f}indazol-5-yl derivatives as selective glucocorticoid receptor modulators
|
|
ES2206021B1
(es)
|
2002-04-16 |
2005-08-01 |
Almirall Prodesfarma, S.A. |
Nuevos derivados de pirrolidinio.
|
|
AU2003223702A1
(en)
|
2002-04-23 |
2003-11-10 |
Vddi Pharmaceuticals |
Inhibition of platelet aggregation
|
|
ES2298511T3
(es)
|
2002-04-25 |
2008-05-16 |
Glaxo Group Limited |
Derivados de fenetanolamina.
|
|
US6747043B2
(en)
|
2002-05-28 |
2004-06-08 |
Theravance, Inc. |
Alkoxy aryl β2 adrenergic receptor agonists
|
|
ES2201907B1
(es)
|
2002-05-29 |
2005-06-01 |
Almirall Prodesfarma, S.A. |
Nuevos derivados de indolilpiperidina como potentes agentes antihistaminicos y antialergicos.
|
|
US7186864B2
(en)
|
2002-05-29 |
2007-03-06 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof
|
|
DE10224888A1
(de)
|
2002-06-05 |
2003-12-24 |
Merck Patent Gmbh |
Pyridazinderivate
|
|
US7074806B2
(en)
|
2002-06-06 |
2006-07-11 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof
|
|
DE10225574A1
(de)
|
2002-06-10 |
2003-12-18 |
Merck Patent Gmbh |
Aryloxime
|
|
DE10227269A1
(de)
|
2002-06-19 |
2004-01-08 |
Merck Patent Gmbh |
Thiazolderivate
|
|
EP1517895B1
(fr)
|
2002-06-25 |
2007-03-14 |
Merck Frosst Canada Ltd. |
Inhibiteurs de pde4 8-(biaryle)quinolines
|
|
ES2204295B1
(es)
|
2002-07-02 |
2005-08-01 |
Almirall Prodesfarma, S.A. |
Nuevos derivados de quinuclidina-amida.
|
|
WO2004005258A1
(fr)
|
2002-07-02 |
2004-01-15 |
Merck Frosst Canada & Co. |
Ethane pyridone a substitution diaryle, inhibiteurs d'enzyme pde4
|
|
WO2004005229A1
(fr)
|
2002-07-08 |
2004-01-15 |
Pfizer Products Inc. |
Modulateurs du recepteur glucocorticoide
|
|
GB0217225D0
(en)
|
2002-07-25 |
2002-09-04 |
Glaxo Group Ltd |
Medicinal compounds
|
|
AR040962A1
(es)
|
2002-08-09 |
2005-04-27 |
Novartis Ag |
Compuestos derivados de tiazol 1,3-2-ona, composicion farmaceutica y proceso de preparacion del compuesto
|
|
WO2004018450A1
(fr)
|
2002-08-10 |
2004-03-04 |
Altana Pharma Ag |
Derives de n-oxyde de piperidine
|
|
AU2003255376A1
(en)
|
2002-08-10 |
2004-03-11 |
Altana Pharma Ag |
Piperidine-derivatives as pde4 inhibitors
|
|
US20060167001A1
(en)
|
2002-08-10 |
2006-07-27 |
Sterk Jan G |
Pyridazinone-derivatives as pde4 inhibitors
|
|
CN1671695A
(zh)
|
2002-08-10 |
2005-09-21 |
奥坦纳医药公司 |
用作pde4抑制剂的吡咯烷二酮取代的哌啶-2,3-二氮杂萘酮化合物
|
|
RS20050116A
(sr)
|
2002-08-17 |
2007-11-15 |
Altana Pharma Ag., |
Novi fenantridini
|
|
RS20050117A
(sr)
|
2002-08-17 |
2007-06-04 |
Altana Pharma Ag., |
Novi benzonaftiridini
|
|
SE0202483D0
(sv)
|
2002-08-21 |
2002-08-21 |
Astrazeneca Ab |
Chemical compounds
|
|
EP1532113B1
(fr)
|
2002-08-21 |
2008-08-06 |
Boehringer Ingelheim Pharmaceuticals Inc. |
Composes mimetiques de glucocorticoide, leurs procedes de fabrication, compositions pharmaceutiques, et leurs utilisations
|
|
CN1688544A
(zh)
|
2002-08-23 |
2005-10-26 |
兰贝克赛实验室有限公司 |
作为蕈毒碱受体拮抗剂的含氟代和磺酰氨基的3,6-二取代的氮杂双环(3.1.0)己烷衍生物
|
|
JP4587295B2
(ja)
|
2002-08-29 |
2010-11-24 |
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 |
Pde4インヒビターとしての3−ヒドロキシ−6−フェニルフェナントリジン
|
|
CA2496580A1
(fr)
|
2002-08-29 |
2004-03-11 |
Boehringer Ingelheim Pharmaceuticals, Inc. |
Derives de -3 (sulfonamidoethyl) -indole destines a etre utilises comme agents mimetiques glucocorticoides dans le traitement des maladies inflammatoires, allergiques et proliferatives
|
|
DE60310576T2
(de)
|
2002-08-29 |
2007-10-31 |
Altana Pharma Ag |
2-hydroxy-6-phenylphenanthridine als pde-4-hemmer
|
|
GB0220730D0
(en)
|
2002-09-06 |
2002-10-16 |
Glaxo Group Ltd |
Medicinal compounds
|
|
KR20050057408A
(ko)
|
2002-09-18 |
2005-06-16 |
오노 야꾸힝 고교 가부시키가이샤 |
트리아자스피로[5.5]운데칸 유도체 및 이를 유효 성분으로하는 약제
|
|
JP2006096662A
(ja)
|
2002-09-18 |
2006-04-13 |
Sumitomo Pharmaceut Co Ltd |
新規6−置換ウラシル誘導体及びアレルギー性疾患の治療剤
|
|
JP2004107299A
(ja)
|
2002-09-20 |
2004-04-08 |
Japan Energy Corp |
新規1−置換ウラシル誘導体及びアレルギー性疾患の治療剤
|
|
US20050245588A1
(en)
|
2002-09-20 |
2005-11-03 |
Amjad Ali |
Octahydro-2-h-naphtho[1,2-f]indole-4-carboxamide derivatives as selective glucocorticoid receptor modulators
|
|
DE10246374A1
(de)
|
2002-10-04 |
2004-04-15 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Neue Betamimetika mit verlängerter Wirkungsdauer, Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel
|
|
DE60320439T2
(de)
|
2002-10-11 |
2009-05-20 |
Pfizer Inc. |
INDOLDERIVATE ALS ß2-AGONISTEN
|
|
EP1440966A1
(fr)
|
2003-01-10 |
2004-07-28 |
Pfizer Limited |
Dérivés d'indole utilisables pour traiter des maladies
|
|
EP1554264B1
(fr)
|
2002-10-22 |
2007-08-08 |
Glaxo Group Limited |
Derives d'arylethanolamine a usage medicinal
|
|
AP2021A
(en)
|
2002-10-23 |
2009-08-03 |
Glenmark Pharmaceuticals Ltd |
Novel tricyclic compounds useful for the treatmentof inflammatory and allergic disorders: Process f or their preparation and pharmaceutical compositions containing them
|
|
CA2503588A1
(fr)
|
2002-10-28 |
2004-05-06 |
Glaxo Group Limited |
Derive de phenethanolamine utilise dans le traitement de maladies respiratoires
|
|
GB0225030D0
(en)
|
2002-10-28 |
2002-12-04 |
Glaxo Group Ltd |
Medicinal compounds
|
|
GB0225287D0
(en)
|
2002-10-30 |
2002-12-11 |
Glaxo Group Ltd |
Novel compounds
|
|
GB0225540D0
(en)
|
2002-11-01 |
2002-12-11 |
Glaxo Group Ltd |
Medicinal compounds
|
|
GB0225535D0
(en)
|
2002-11-01 |
2002-12-11 |
Glaxo Group Ltd |
Medicinal compounds
|
|
DE10253426B4
(de)
|
2002-11-15 |
2005-09-22 |
Elbion Ag |
Neue Hydroxyindole, deren Verwendung als Inhibitoren der Phosphodiesterase 4 und Verfahren zu deren Herstellung
|
|
DE10253220A1
(de)
|
2002-11-15 |
2004-05-27 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Neue Dihydroxy-Methyl-Phenyl-Derivate, Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel
|
|
DE10253282A1
(de)
|
2002-11-15 |
2004-05-27 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Neue Arzneimittel zur Behandlung von chronisch obstruktiver Lungenerkrankung
|
|
DE10261874A1
(de)
|
2002-12-20 |
2004-07-08 |
Schering Ag |
Nichtsteroidale Entzündungshemmer
|
|
CA2512987C
(fr)
|
2003-01-21 |
2011-06-14 |
Merck & Co., Inc. |
Derives cortisol de 17-carbamoyloxy utilises en tant que modulateurs selectifs des recepteurs aux glucocorticoides
|
|
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
|
|
EP1460064A1
(fr)
|
2003-03-14 |
2004-09-22 |
Pfizer Limited |
Derivés de Indole-2-carboxamide comme beta-2 agonistes
|
|
JP4767842B2
(ja)
|
2003-04-01 |
2011-09-07 |
セラヴァンス, インコーポレーテッド |
β2アドレナリン作用性レセプターアゴニスト活性およびムスカリン性レセプターアンタゴニスト活性を有するジアリールメチル化合物および関連化合物
|
|
ATE421322T1
(de)
|
2003-04-04 |
2009-02-15 |
Novartis Pharma Gmbh |
Chinolin-2-on-derivate zur behandlung von erkankungen der atemwege
|
|
US7268147B2
(en)
|
2003-05-15 |
2007-09-11 |
Pfizer Inc |
Compounds useful for the treatment of diseases
|
|
JP4616264B2
(ja)
|
2003-05-28 |
2011-01-19 |
セラヴァンス, インコーポレーテッド |
ムスカリン性レセプターアンタゴニストとしてのアザビシクロアルカン化合物
|
|
ATE384697T1
(de)
|
2003-06-04 |
2008-02-15 |
Pfizer |
2-amino-pyridin-derivate als beta-2 adrenoreceptor agonisten
|
|
GB0312832D0
(en)
|
2003-06-04 |
2003-07-09 |
Pfizer Ltd |
2-amino-pyridine derivatives useful for the treatment of diseases
|
|
US20060205671A1
(en)
|
2003-07-02 |
2006-09-14 |
Jakob Vinten-Johansen |
Compositions and methods for use of a protease inhibitor and adenosine for preventing organ ischemia and reperfusion injury
|
|
DE10332239B3
(de)
|
2003-07-16 |
2005-03-03 |
Framatome Anp Gmbh |
Zirkoniumlegierung und Bauteile für den Kern von leichtwassergekühlten Kernreaktoren
|
|
WO2005033121A2
(fr)
|
2003-10-03 |
2005-04-14 |
King Pharmaceuticals Research & Development, Inc. |
Synthese de 2-aralkyloxyadenosines, 2-alkoxyadenosines, et leurs analogues
|
|
GB0323701D0
(en)
|
2003-10-09 |
2003-11-12 |
Glaxo Group Ltd |
Formulations
|
|
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
|
|
GB0329182D0
(en)
|
2003-12-17 |
2004-01-21 |
Glaxo Group Ltd |
Chemical compounds
|
|
US7674368B2
(en)
|
2003-12-19 |
2010-03-09 |
Shell Oil Company |
Systems, methods, and catalysts for producing a crude product
|
|
DE602004006895T2
(de)
|
2003-12-29 |
2008-01-31 |
Can-Fite Biopharma Ltd. |
Verfahren zur behandlung von multipler sklerose
|
|
DE102004001413A1
(de)
|
2004-01-09 |
2005-08-18 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
3-Hydroxymethyl-4-Hydroxy-Phenyl-Derivate zur Behandlung von chronisch obstruktiver Lungenerkrankung
|
|
TW200531692A
(en)
|
2004-01-12 |
2005-10-01 |
Theravance Inc |
Aryl aniline derivatives as β2 adrenergic receptor agonists
|
|
BRPI0507041A
(pt)
|
2004-01-22 |
2007-06-12 |
Pfizer |
composto derivados de sulfonamida para o tratamento de doenças seus usos, processo para a preparação dos compostos e combinação de compostos
|
|
GEP20094781B
(en)
|
2004-01-22 |
2009-09-25 |
Pfizer |
Sulfonamide derivatives for the treatment of diseases
|
|
US7320990B2
(en)
|
2004-02-13 |
2008-01-22 |
Theravance, Inc. |
Crystalline form of a biphenyl compound
|
|
CA2552871A1
(fr)
|
2004-02-14 |
2005-08-25 |
Boehringer Ingelheim International Gmbh |
Nouveaux beta-2-agonistes a action longue duree et leur utilisation comme medicaments
|
|
MXPA06010075A
(es)
*
|
2004-03-05 |
2007-04-10 |
Cambridge Biotechnology Ltd |
Compuestos terapeuticos.
|
|
US7396825B2
(en)
|
2004-05-03 |
2008-07-08 |
University Of Virginia Patent Foundation |
Agonists of A2A adenosine receptors for treatment of diabetic nephropathy
|
|
AR049384A1
(es)
|
2004-05-24 |
2006-07-26 |
Glaxo Group Ltd |
Derivados de purina
|
|
JP4642847B2
(ja)
|
2004-07-28 |
2011-03-02 |
キャン−ファイト・バイオファーマ・リミテッド |
シェーグレン症候群を含むドライアイ疾患治療用アデノシンa3レセプターアゴニスト
|
|
US7825102B2
(en)
|
2004-07-28 |
2010-11-02 |
Can-Fite Biopharma Ltd. |
Treatment of dry eye conditions
|
|
BRPI0515030A
(pt)
|
2004-09-09 |
2008-07-01 |
Us Gov Health & Human Serv |
derivados de purina como agonistas de receptor de adenosina a3 e a1
|
|
GT200500281A
(es)
*
|
2004-10-22 |
2006-04-24 |
Novartis Ag |
Compuestos organicos.
|
|
US20080051364A1
(en)
|
2004-11-08 |
2008-02-28 |
Pninna Fishman |
Therapeutic Treatment of Accelerated Bone Resorption
|
|
GB0500785D0
(en)
|
2005-01-14 |
2005-02-23 |
Novartis Ag |
Organic compounds
|
|
US7951810B2
(en)
|
2005-02-04 |
2011-05-31 |
Millennium Pharmaceuticals, Inc. |
Substituted pyrrolo[2,3-d]pyrimidines as inhibitors of E1 activating enzymes
|
|
GB0505219D0
(en)
*
|
2005-03-14 |
2005-04-20 |
Novartis Ag |
Organic compounds
|
|
GB0514809D0
(en)
*
|
2005-07-19 |
2005-08-24 |
Glaxo Group Ltd |
Compounds
|
|
CA2622879C
(fr)
|
2005-11-30 |
2011-07-05 |
Can-Fite Biopharma Ltd. |
Utilisation de l'agoniste des recepteurs de l'adenosine a3 dans le traitement de l'osteoarthrite
|
|
WO2007089507A1
(fr)
|
2006-01-26 |
2007-08-09 |
The Government Of The United States Of America, Represented By The Secretary, Dept. Of Health And Human Services |
Modulateurs allostériques du récepteur de l’adénosine a3
|
|
DK1989206T3
(da)
|
2006-02-02 |
2012-10-08 |
Millennium Pharm Inc |
E1-aktiveringsenzymhæmmere
|
|
WO2007092936A2
(fr)
*
|
2006-02-08 |
2007-08-16 |
University Of Virginia Patent Foundation |
Procédé pour traiter des lésions gastriques
|
|
GB0607944D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
|
GB0607950D0
(en)
*
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
|
GB0607953D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
|
GB0607945D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
|
CA2649215A1
(fr)
|
2006-04-21 |
2007-11-01 |
Novartis Ag |
Composes de purine 2,6,9 trisubstitues en tant que modulateurs des recepteurs d'adenosine aza
|
|
GB0607951D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
|
GB0607948D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
|
GB0607954D0
(en)
|
2006-04-21 |
2006-05-31 |
Novartis Ag |
Organic compounds
|
|
EP1889846A1
(fr)
|
2006-07-13 |
2008-02-20 |
Novartis AG |
Dérivés de purine comme agonistes du recepteur A2a
|
|
US8008307B2
(en)
|
2006-08-08 |
2011-08-30 |
Millennium Pharmaceuticals, Inc. |
Heteroaryl compounds useful as inhibitors of E1 activating enzymes
|
|
EP1903044A1
(fr)
*
|
2006-09-14 |
2008-03-26 |
Novartis AG |
Derivés de l'adénosine en tant qu' agonistes du récepteur A2A
|
|
EP2084121A1
(fr)
|
2006-11-10 |
2009-08-05 |
Novartis AG |
Dérivés de monoacétate de cyclopentène diol
|
|
US20080312160A1
(en)
*
|
2007-04-09 |
2008-12-18 |
Guerrant Richard L |
Method of treating enteritis, intestinal damage, and diarrhea from c. difficile with an a2a adenosine receptor agonist
|
|
US20080262001A1
(en)
*
|
2007-04-23 |
2008-10-23 |
Adenosine Therapeutics, Llc |
Agonists of a2a adenosine receptors for treating recurrent tumor growth in the liver following resection
|
|
AU2008270735C1
(en)
*
|
2007-06-29 |
2014-03-06 |
Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services |
Dendrimer conjugates of agonists and antagonists of the GPCR superfamily
|
|
US20090181934A1
(en)
|
2007-10-17 |
2009-07-16 |
Novartis Ag |
Organic Compounds
|
|
KR20100068286A
(ko)
*
|
2007-10-17 |
2010-06-22 |
노파르티스 아게 |
아데노신 a1 수용체 리간드로서의 퓨린 유도체
|
|
US8183225B2
(en)
*
|
2007-11-08 |
2012-05-22 |
New York University |
Inhibition of bone resorption using medical implants containing adenosine receptor antagonists
|
|
WO2009089425A1
(fr)
*
|
2008-01-09 |
2009-07-16 |
Pgxhealth Llc |
Traitement intrathécal d'une douleur neuropathique avec des agonistes a2ar
|