KR100585894B1 - C2,5'-이치환된 및 n6,c2,5'-삼치환된 아데노신 유도체및 그들의 상이한 용도 - Google Patents

C2,5'-이치환된 및 n6,c2,5'-삼치환된 아데노신 유도체및 그들의 상이한 용도 Download PDF

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KR100585894B1
KR100585894B1 KR1020037011508A KR20037011508A KR100585894B1 KR 100585894 B1 KR100585894 B1 KR 100585894B1 KR 1020037011508 A KR1020037011508 A KR 1020037011508A KR 20037011508 A KR20037011508 A KR 20037011508A KR 100585894 B1 KR100585894 B1 KR 100585894B1
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adenosine
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KR20030089512A (ko
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에리카 반틸버그
애드 이제르만
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유니버시타이트 라이덴
캔-파이트 바이오파마 리미티드
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    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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KR1020037011508A 2001-03-03 2002-03-03 C2,5'-이치환된 및 n6,c2,5'-삼치환된 아데노신 유도체및 그들의 상이한 용도 Expired - Fee Related KR100585894B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0105337.0 2001-03-03
GB0105337A GB2372742A (en) 2001-03-03 2001-03-03 C2,5'-Disubstituted and N6,C2,5'-trisubstituted adenosine derivatives and their different uses
PCT/IL2002/000160 WO2002070532A2 (en) 2001-03-03 2002-03-03 C2,5'-disubstituted and n6,c2,5'-trisubstituted adenosine derivatives and their different uses

Publications (2)

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KR20030089512A KR20030089512A (ko) 2003-11-21
KR100585894B1 true KR100585894B1 (ko) 2006-06-07

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KR1020037011508A Expired - Fee Related KR100585894B1 (ko) 2001-03-03 2002-03-03 C2,5'-이치환된 및 n6,c2,5'-삼치환된 아데노신 유도체및 그들의 상이한 용도

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US (2) US7084127B2 (https=)
EP (1) EP1368365A2 (https=)
JP (2) JP4359676B2 (https=)
KR (1) KR100585894B1 (https=)
CN (1) CN1259332C (https=)
AU (1) AU2002234851A1 (https=)
CA (1) CA2439879C (https=)
GB (1) GB2372742A (https=)
WO (1) WO2002070532A2 (https=)

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JP2005527502A (ja) * 2002-02-19 2005-09-15 シーブイ・セラピューティクス・インコーポレイテッド A1アデノシン受容体の部分的および全アゴニスト
JP2005132767A (ja) * 2003-10-30 2005-05-26 Sumitomo Chemical Co Ltd プリン化合物の製造方法
CA2550299C (en) * 2003-12-22 2010-03-30 Christopher R. Roberts Process for fluorocytidine derivatives
US20050277615A1 (en) * 2004-05-17 2005-12-15 Can-Fite Biopharma Ltd. Pharmaceutical compositions having anti-inflammatory activity
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
US20080070860A1 (en) * 2005-02-04 2008-03-20 Uti Limited Partnership Adenosine Analogs Useful as Anti-Bacterial and Anti Protozoan Agents
GB0514809D0 (en) 2005-07-19 2005-08-24 Glaxo Group Ltd Compounds
AU2009231978C1 (en) * 2008-03-31 2014-01-30 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Purine derivatives as A3 adenosine receptor- selective agonists
US8916570B2 (en) 2008-03-31 2014-12-23 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services A3 adenosine receptor agonists and antagonists
EP2331542B1 (en) * 2008-08-01 2016-07-27 The United States of America, as Represented by The Secretary, Department of Health and Human Services A3 adenosine receptor antagonists and partial agonists
US9181253B2 (en) 2008-08-01 2015-11-10 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Adenosine receptor agonists, partial agonists, and antagonists
WO2011010306A1 (en) 2009-07-21 2011-01-27 Ramot At Tel-Aviv University Ltd. A3 adenosine receptor ligands for modulation of pigmentation
SG182285A1 (en) 2010-01-11 2012-08-30 Inotek Pharmaceuticals Corp Combination, kit and method of reducing intraocular pressure
EA201290958A1 (ru) 2010-03-26 2013-04-30 Инотек Фармасьютикалз Корпорейшн Способ снижения внутриглазного давления у людей с применением n6-циклопентиладенозина (cpa), производных cpa или их пролекарств
BR112014018413A8 (pt) 2012-01-26 2017-07-11 Inotek Pharmaceuticals Corp Polimorfos anidros de nitrato de metila [(2r,3s,4r,5r)-5-(6-(ciclopentilamino)-9h-purin-9-il)-3,4-diidroxitetraidrofuran-2-il)] e processos de preparação do mesmo
WO2014068589A2 (en) * 2012-10-29 2014-05-08 Biophore India Pharmaceuticals Pvt. Ltd. Novel process for the preparation of (1-{9-[(4s, 2r, 3r, 5r)-3, 4-dihydroxy-5-(hydroxymethyl) oxolan-2-yl)-6-aminopurin-2-yl} pyrazole-4-yl)-n-methylcarboxamide
CA2903114A1 (en) 2013-03-15 2014-09-25 Inotek Pharmaceuticals Corporation Ophthalmic formulations
EP3448015B1 (en) * 2016-04-22 2021-11-24 Kowa Company, Ltd. Image capturing device provided with multiplexer

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US4357324A (en) 1981-02-24 1982-11-02 The United States Of America As Represented By The Department Of Health And Human Services Prodrug derivatives of 9β-D-arabinofuranosyl-2-fluoroadenine
US5189027A (en) * 1990-11-30 1993-02-23 Yamasa Shoyu Kabushiki Kaisha 2-substituted adenosine derivatives and pharmaceutical compositions for circulatory diseases
US5278150A (en) * 1992-04-24 1994-01-11 Whitby Research, Inc. 2-hydrazoadenosines and their utility for the treatmeat of vascular conditions
US5589467A (en) 1993-09-17 1996-12-31 Novo Nordisk A/S 2,5',N6-trisubstituted adenosine derivatives
WO1997033591A1 (en) * 1996-03-13 1997-09-18 Novo Nordisk A/S A method of treating disorders related to cytokines in mammals
GB9610031D0 (en) 1996-05-14 1996-07-17 Glaxo Group Ltd Chemical compounds
US5998423A (en) * 1996-10-08 1999-12-07 Therasys, Inc. Methods for modulating melanin production
GB9723566D0 (en) * 1997-11-08 1998-01-07 Glaxo Group Ltd Chemical compounds
YU44900A (sh) 1998-01-31 2003-01-31 Glaxo Group Limited Derivati 2-(purin-9-il)tetrahidrofuran-3,4-diola
DE69932173T2 (de) * 1998-10-16 2007-06-06 Pfizer Inc. Adeninderivate
WO2000072799A2 (en) * 1999-05-27 2000-12-07 The University Of Virginia Patent Foundation Method and compositions for treating the inflammatory response
US6605597B1 (en) * 1999-12-03 2003-08-12 Cv Therapeutics, Inc. Partial or full A1agonists-N-6 heterocyclic 5′-thio substituted adenosine derivatives
WO2001040799A2 (en) * 1999-12-03 2001-06-07 Cv Therapeutics, Inc. Method of identifying partial adenosine a1 receptor agonists and their use in the treatment of arrhythmias

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AU2002234851A1 (en) 2002-09-19
US7084127B2 (en) 2006-08-01
JP4359676B2 (ja) 2009-11-04
WO2002070532A3 (en) 2002-11-28
CA2439879A1 (en) 2002-09-12
US7189706B2 (en) 2007-03-13
GB2372742A (en) 2002-09-04
KR20030089512A (ko) 2003-11-21
US20040127452A1 (en) 2004-07-01
CN1259332C (zh) 2006-06-14
EP1368365A2 (en) 2003-12-10
WO2002070532A2 (en) 2002-09-12
JP2009167170A (ja) 2009-07-30
JP2004522794A (ja) 2004-07-29
CN1537115A (zh) 2004-10-13
CA2439879C (en) 2009-09-15
US20040132686A1 (en) 2004-07-08
GB0105337D0 (en) 2001-04-18

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