AU3698295A - Amino purine-beta -d-ribofuranuronamide derivatives - Google Patents

Amino purine-beta -d-ribofuranuronamide derivatives

Info

Publication number
AU3698295A
AU3698295A AU36982/95A AU3698295A AU3698295A AU 3698295 A AU3698295 A AU 3698295A AU 36982/95 A AU36982/95 A AU 36982/95A AU 3698295 A AU3698295 A AU 3698295A AU 3698295 A AU3698295 A AU 3698295A
Authority
AU
Australia
Prior art keywords
beta
amino purine
ribofuranuronamide
derivatives
ribofuranuronamide derivatives
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
AU36982/95A
Inventor
Barry Edward Ayres
Richard Bell
George Blanch Ewan
Michael Gregson
Suzanne Elaine Keeling
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Glaxo Group Ltd
Original Assignee
Glaxo Group Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of AU3698295A publication Critical patent/AU3698295A/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • 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
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16Purine radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
AU36982/95A 1994-07-14 1995-07-14 Amino purine-beta -d-ribofuranuronamide derivatives Abandoned AU3698295A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB9414193 1994-07-14
GB9414193A GB9414193D0 (en) 1994-07-14 1994-07-14 Compounds
PCT/EP1995/002837 WO1996002553A2 (en) 1994-07-14 1995-07-14 AMINO PURINE-β-D-RIBOFURANURONAMIDE DERIVATIVES

Publications (1)

Publication Number Publication Date
AU3698295A true AU3698295A (en) 1996-02-16

Family

ID=10758311

Family Applications (1)

Application Number Title Priority Date Filing Date
AU36982/95A Abandoned AU3698295A (en) 1994-07-14 1995-07-14 Amino purine-beta -d-ribofuranuronamide derivatives

Country Status (5)

Country Link
AU (1) AU3698295A (en)
GB (1) GB9414193D0 (en)
IL (1) IL114578A0 (en)
WO (1) WO1996002553A2 (en)
ZA (1) ZA955784B (en)

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YU44900A (en) 1998-01-31 2003-01-31 Glaxo Group Limited 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives
AR017457A1 (en) * 1998-02-14 2001-09-05 Glaxo Group Ltd COMPOUNDS DERIVED FROM 2- (PURIN-9-IL) -TETRAHIDROFURAN-3,4-DIOL, PROCESSES FOR THEIR PREPARATION, COMPOSITIONS THAT CONTAIN THEM AND THEIR USE IN THERAPY FOR THE TREATMENT OF INFLAMMATORY DISEASES.
HUP0103025A3 (en) 1998-06-23 2002-04-29 Glaxo Group Ltd A2a agonist 2-(purin-9-yl)tetrahydrofuran-3,4-diol derivatives, medicaments containing the same, process for producing them and the useful intermediates
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
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US7378400B2 (en) 1999-02-01 2008-05-27 University Of Virginia Patent Foundation Method to reduce an inflammatory response from arthritis
US6232297B1 (en) 1999-02-01 2001-05-15 University Of Virginia Patent Foundation Methods and compositions for treating inflammatory response
GB9924361D0 (en) 1999-10-14 1999-12-15 Pfizer Ltd Purine derivatives
US7087589B2 (en) 2000-01-14 2006-08-08 The United States Of America As Represented By The Department Of Health And Human Services Methanocarba cycloakyl nucleoside analogues
US20010051612A1 (en) * 2000-02-23 2001-12-13 Gloria Cristalli 2-Thioether A2A receptor agonists
US6921753B2 (en) 2000-06-27 2005-07-26 Pfizer Inc Purine derivatives
AR044519A1 (en) 2003-05-02 2005-09-14 Novartis Ag DERIVATIVES OF PIRIDIN-TIAZOL AMINA AND PIRIMIDIN-TIAZOL AMINA
GB0401334D0 (en) 2004-01-21 2004-02-25 Novartis Ag Organic compounds
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AR049384A1 (en) 2004-05-24 2006-07-26 Glaxo Group Ltd PURINA DERIVATIVES
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WO2006028618A1 (en) 2004-08-02 2006-03-16 University Of Virginia Patent Foundation 2-polycyclic propynyl adenosine analogs with modified 5'-ribose groups having a2a agonist activity
WO2006023272A1 (en) 2004-08-02 2006-03-02 University Of Virginia Patent Foundation 2-polycyclic propynyl adenosine analogs having a2a agonist activity
NZ553288A (en) 2004-08-02 2010-12-24 Univ Virginia 2-propynyl adenosine analogs with modified 5'-ribose groups having A2A agonist activity
JP5011112B2 (en) 2004-09-20 2012-08-29 イノテック ファーマシューティカルズ コーポレイション Pharmaceuticals for the treatment of inflammatory diseases containing purine derivatives
GB0424284D0 (en) 2004-11-02 2004-12-01 Novartis Ag Organic compounds
GB0426164D0 (en) 2004-11-29 2004-12-29 Novartis Ag Organic compounds
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
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KR20080049113A (en) 2005-10-21 2008-06-03 노파르티스 아게 Human antibodies against il-13 and therapeutic uses
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GB0601951D0 (en) 2006-01-31 2006-03-15 Novartis Ag Organic compounds
SI2013211T1 (en) 2006-04-21 2012-07-31 Novartis Ag Purine derivatives for use as adenosin a2a receptor agonists
ATE502943T1 (en) 2006-09-29 2011-04-15 Novartis Ag PYRAZOLOPYRIMIDINES AS PI3K LIPID KINASE INHIBITORS
EP2089393A1 (en) 2006-10-30 2009-08-19 Novartis AG Heterocyclic compounds as antiinflammatory agents
WO2009006089A2 (en) * 2007-06-29 2009-01-08 Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services A2 adenosine receptor agonists
JP5584138B2 (en) 2008-01-11 2014-09-03 ノバルティス アーゲー Pyrimidines as kinase inhibitors
JP2012516345A (en) 2009-01-29 2012-07-19 ノバルティス アーゲー Substituted benzimidazoles for astrocytoma treatment
US8389526B2 (en) 2009-08-07 2013-03-05 Novartis Ag 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
AU2010283806A1 (en) 2009-08-12 2012-03-01 Novartis Ag Heterocyclic hydrazone compounds and their uses to treat cancer and inflammation
ES2709108T3 (en) 2009-08-17 2019-04-15 Intellikine Llc Heterocyclic compounds and uses thereof
AU2010284972A1 (en) 2009-08-20 2012-03-08 Novartis Ag Heterocyclic oxime compounds
EP2507241A1 (en) 2009-12-02 2012-10-10 The U.S.A. As Represented By The Secretary, Department Of Health And Human Services Methanocarba adenosine derivatives and dendrimer conjugates thereof
SI2523669T1 (en) 2010-01-11 2017-05-31 Inotek Pharmaceuticals Corporation Combination, kit and method of reducing intraocular pressure
BR112012023749A2 (en) 2010-03-26 2016-08-23 Inotek Pharmaceuticals Corp method for reducing intraocular pressure in humans using n6-cyclopentyladenosine (cpa), cpa derivatives or prodrugs thereof
WO2012034095A1 (en) 2010-09-09 2012-03-15 Irm Llc Compounds and compositions as trk inhibitors
UY33597A (en) 2010-09-09 2012-04-30 Irm Llc COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF THE TRK
EP2673277A1 (en) 2011-02-10 2013-12-18 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
WO2012116217A1 (en) 2011-02-25 2012-08-30 Irm Llc Compounds and compositions as trk inhibitors
BR112014006223A8 (en) 2011-09-15 2018-01-09 Novartis Ag 6-substituted 3- (quinolin-6-ylthio) - [1,2,4-triazol [4,3-a] pyradines, their uses, pharmaceutical compositions, and combination
JP6130391B2 (en) 2011-11-23 2017-05-17 インテリカイン, エルエルシー Enhanced treatment regimen using MTOR inhibitors
KR20140128974A (en) 2012-01-26 2014-11-06 이노텍 파마슈티컬스 코포레이션 Anhydrous polymorphs of ((2r,3s,4r,5r)-5-(6-(cyclopentylamino)-9h-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl) methyl nitrate and processes of preparation thereof
CN104245701A (en) 2012-04-03 2014-12-24 诺华有限公司 Combination products with tyrosine kinase inhibitors and their use
SG11201506882YA (en) 2013-03-15 2015-09-29 Inotek Pharmaceuticals Corp Ophthalmic formulations
EP2968340A4 (en) 2013-03-15 2016-08-10 Intellikine Llc Combination of kinase inhibitors and uses thereof
WO2015084804A1 (en) 2013-12-03 2015-06-11 Novartis Ag Combination of mdm2 inhibitor and braf inhibitor and their use
WO2016011658A1 (en) 2014-07-25 2016-01-28 Novartis Ag Combination therapy
MX2017001461A (en) 2014-07-31 2017-05-11 Novartis Ag Combination therapy.
CN109879787A (en) * 2019-01-10 2019-06-14 安徽昊帆生物有限公司 Iodo acetylthiocholine, preparation method and its application
TW202140550A (en) 2020-01-29 2021-11-01 瑞士商諾華公司 Methods of treating an inflammatory or obstructive airway disease using anti-tslp antibody

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US4738954A (en) * 1985-11-06 1988-04-19 Warner-Lambert Company Novel N6 -substituted-5'-oxidized adenosine analogs
WO1988003147A1 (en) * 1986-10-31 1988-05-05 Warner-Lambert Company Selected n6-substituted adenosines having selective a2 binding activity
EP0277917A3 (en) * 1987-02-04 1990-03-28 Ciba-Geigy Ag Certain adenosine 5'-carboxamide derivatives

Also Published As

Publication number Publication date
GB9414193D0 (en) 1994-08-31
ZA955784B (en) 1996-08-15
WO1996002553A3 (en) 1996-03-07
IL114578A0 (en) 1995-11-27
WO1996002553A2 (en) 1996-02-01

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