WO1996002553A3 - AMINO PURINE-β-D-RIBOFURANURONAMIDE DERIVATIVES - Google Patents

AMINO PURINE-β-D-RIBOFURANURONAMIDE DERIVATIVES Download PDF

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Publication number
WO1996002553A3
WO1996002553A3 PCT/EP1995/002837 EP9502837W WO9602553A3 WO 1996002553 A3 WO1996002553 A3 WO 1996002553A3 EP 9502837 W EP9502837 W EP 9502837W WO 9602553 A3 WO9602553 A3 WO 9602553A3
Authority
WO
WIPO (PCT)
Prior art keywords
6alkyl
amino purine
oxopyrrolidin
piperidin
solvates
Prior art date
Application number
PCT/EP1995/002837
Other languages
French (fr)
Other versions
WO1996002553B1 (en
WO1996002553A2 (en
Inventor
Barry Edward Di Ayres
Michael Gregson
George Blanch Ewan
Suzanne Elaine Keeling
Richard Bell
Original Assignee
Glaxo Group Ltd
Ayres Diana Sally & Hf
Michael Gregson
George Blanch Ewan
Suzanne Elaine Keeling
Richard Bell
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, Ayres Diana Sally & Hf, Michael Gregson, George Blanch Ewan, Suzanne Elaine Keeling, Richard Bell filed Critical Glaxo Group Ltd
Priority to AU36982/95A priority Critical patent/AU3698295A/en
Publication of WO1996002553A2 publication Critical patent/WO1996002553A2/en
Publication of WO1996002553A3 publication Critical patent/WO1996002553A3/en
Publication of WO1996002553B1 publication Critical patent/WO1996002553B1/en

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

Abstract

Amino purine-β-D-ribofuranuronamide derivatives are described having general formula (I) and salts and solvates thereof, wherein: R1 is hydrogen, C¿3-8?cycloaklyl or C1-6alkyl; A represents O, S, SO, SO2, a saturated hydrocarbon moiety having from 1 to 4 carbon atoms or an unsaturated hydrocarbon moiety having from 2 to 4 carbon atoms; R?2¿ is C¿3-8?cycloalkyl, C3-8cycloalkyl C1-6alkyl, Alk1Y, -(CHR?5)¿m (Alk2)nZ or appropriately substituted C3-8cycloalkyl, C3-8cycloalkylC1-6alkyl, pyrrolidin-3-yl, 2-oxopyrrolidin-4-yl, 2-oxopyrrolidin-5-yl, piperidin-3-yl or piperidin-4-yl, and Q is oxygen or sulphur with the proviso that when A represents O, S, SO or SO2, Alk1 represents a C2-6alkylene group. Compounds of formula (I) and their salts and solvates have use in medicine as anti-inflammatory agents, particularly in the treatment of patients with inflammatory conditions who are susceptible to leukocyte-induced tissue damage.
PCT/EP1995/002837 1994-07-14 1995-07-14 AMINO PURINE-β-D-RIBOFURANURONAMIDE DERIVATIVES WO1996002553A2 (en)

Priority Applications (1)

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

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9414193.4 1994-07-14
GB9414193A GB9414193D0 (en) 1994-07-14 1994-07-14 Compounds

Publications (3)

Publication Number Publication Date
WO1996002553A2 WO1996002553A2 (en) 1996-02-01
WO1996002553A3 true WO1996002553A3 (en) 1996-03-07
WO1996002553B1 WO1996002553B1 (en) 1996-03-28

Family

ID=10758311

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1995/002837 WO1996002553A2 (en) 1994-07-14 1995-07-14 AMINO PURINE-β-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)

Families Citing this family (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW528755B (en) * 1996-12-24 2003-04-21 Glaxo Group Ltd 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives
YU44900A (en) 1998-01-31 2003-01-31 Glaxo Group Limited 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives
PE20000270A1 (en) * 1998-02-14 2000-05-20 Glaxo Group Ltd DERIVATIVES OF 2- (PURIN-9-IL) -TETRAHIDROFURAN-3,4-DIOL
AU750462B2 (en) 1998-06-23 2002-07-18 Glaxo Group Limited 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives
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
CA2336967C (en) 1998-07-10 2010-06-29 The United States Of America, Represented By The Secretary, Department Of Health And Human Services A3 adenosine receptor antagonists
US7427606B2 (en) * 1999-02-01 2008-09-23 University Of Virginia Patent Foundation Method to reduce inflammatory response in transplanted tissue
US6232297B1 (en) 1999-02-01 2001-05-15 University Of Virginia Patent Foundation Methods and compositions for treating inflammatory response
US7378400B2 (en) 1999-02-01 2008-05-27 University Of Virginia Patent Foundation Method to reduce an inflammatory response from arthritis
GB9924361D0 (en) 1999-10-14 1999-12-15 Pfizer Ltd Purine derivatives
AU3091301A (en) 2000-01-14 2001-07-24 Us Health Methanocarba cycloalkyl 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
SG176313A1 (en) 2001-10-01 2011-12-29 Univ Virginia Patent Found 2-propynyl adenosine analogs having a2a agonist activity and compositions thereof
TW200519106A (en) 2003-05-02 2005-06-16 Novartis Ag Organic compounds
GB0401334D0 (en) 2004-01-21 2004-02-25 Novartis Ag Organic compounds
GB0411056D0 (en) 2004-05-18 2004-06-23 Novartis Ag Organic compounds
AR049384A1 (en) 2004-05-24 2006-07-26 Glaxo Group Ltd PURINA DERIVATIVES
KR101167342B1 (en) 2004-05-26 2012-07-19 이노텍 파마슈티컬스 코포레이션 Purine derivatives as adenosine a1 receptor agonists and methods of use thereof
WO2006023272A1 (en) 2004-08-02 2006-03-02 University Of Virginia Patent Foundation 2-polycyclic propynyl adenosine analogs having a2a agonist activity
US7605143B2 (en) 2004-08-02 2009-10-20 University Of Virginia Patent Foundation 2-propynyl adenosine analogs with modified 5′-ribose groups having A2A agonist activity
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
AU2005286946B2 (en) 2004-09-20 2012-03-15 Inotek Pharmaceuticals Corporation Purine derivatives and methods of use thereof
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
GB0514809D0 (en) 2005-07-19 2005-08-24 Glaxo Group Ltd Compounds
EP2532679B1 (en) 2005-10-21 2017-04-12 Novartis AG Human antibodies against il13 and therapeutic uses
AU2006320578B2 (en) 2005-11-30 2013-01-31 Inotek Pharmaceuticals Corporation Purine derivatives and methods of use thereof
GB0601951D0 (en) 2006-01-31 2006-03-15 Novartis Ag Organic compounds
KR20080110925A (en) 2006-04-21 2008-12-19 노파르티스 아게 Purine derivatives for use as adenosin a2a receptor agonists
WO2008037477A1 (en) 2006-09-29 2008-04-03 Novartis Ag Pyrazolopyrimidines as p13k lipid kinase inhibitors
JP2010508315A (en) 2006-10-30 2010-03-18 ノバルティス アーゲー Heterocyclic compounds as anti-inflammatory 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
ES2442930T3 (en) 2008-01-11 2014-02-14 Novartis Ag Pyrimidines as kinase inhibitors
DK2391366T3 (en) 2009-01-29 2013-01-07 Novartis Ag Substituted benzimidazoles for the treatment of astrocytomas
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
JP5819831B2 (en) 2009-08-17 2015-11-24 インテリカイン, エルエルシー Heterocyclic compounds and their use
KR20120089463A (en) 2009-08-20 2012-08-10 노파르티스 아게 Heterocyclic oxime compounds
US8518957B2 (en) 2009-12-02 2013-08-27 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Methanocarba adenosine derivatives, pharmaceutical compositions, and method of reducing intraocular pressure
WO2011085361A1 (en) 2010-01-11 2011-07-14 Inotek Pharmaceuticals Corporation Combination, kit and method of reducing intraocular pressure
US8476247B2 (en) 2010-03-26 2013-07-02 Inotek Pharmaceuticals Corporation Method of reducing intraocular pressure in humans
US8637516B2 (en) 2010-09-09 2014-01-28 Irm Llc Compounds and compositions as TRK inhibitors
WO2012034095A1 (en) 2010-09-09 2012-03-15 Irm Llc Compounds and compositions as trk inhibitors
WO2012107500A1 (en) 2011-02-10 2012-08-16 Novartis Ag [1, 2, 4] triazolo [4, 3 -b] pyridazine compounds as inhibitors of the c-met tyrosine kinase
WO2012116237A2 (en) 2011-02-23 2012-08-30 Intellikine, Llc Heterocyclic compounds and uses thereof
BR112013021638A2 (en) 2011-02-25 2016-08-02 Irm Llc "trk inhibiting compounds, their use and compositions comprising them"
EP2755976B1 (en) 2011-09-15 2018-07-18 Novartis AG 6-substituted 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyridines as c-met tyrosine kinase inhibitors
US20130209543A1 (en) 2011-11-23 2013-08-15 Intellikine Llc Enhanced treatment regimens using mtor inhibitors
AU2013211957B2 (en) 2012-01-26 2017-08-10 Inotek Pharmaceuticals Corporation 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
CA2868202C (en) 2012-04-03 2021-08-10 Novartis Ag Combination products with tyrosine kinase inhibitors and their use
CA2903114A1 (en) 2013-03-15 2014-09-25 Inotek Pharmaceuticals Corporation Ophthalmic formulations
CA2906542A1 (en) 2013-03-15 2014-09-25 Intellikine, Llc Combination of kinase inhibitors and uses thereof
TW201605450A (en) 2013-12-03 2016-02-16 諾華公司 Combination of Mdm2 inhibitor and BRAF inhibitor and their use
WO2016011658A1 (en) 2014-07-25 2016-01-28 Novartis Ag Combination therapy
CA2954862A1 (en) 2014-07-31 2016-02-04 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

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0222330A2 (en) * 1985-11-06 1987-05-20 Warner-Lambert Company 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
EP0277917A2 (en) * 1987-02-04 1988-08-10 Ciba-Geigy Ag Certain adenosine 5'-carboxamide derivatives

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0222330A2 (en) * 1985-11-06 1987-05-20 Warner-Lambert Company 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
EP0277917A2 (en) * 1987-02-04 1988-08-10 Ciba-Geigy Ag Certain adenosine 5'-carboxamide derivatives

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
CRISTALLI G. ET AL: "2-Alkynyl Derivatives of Adenosine and Adenosine-5'-N-ethyluronamide as Selective Agonists of A2 Adenosine Receptors", JOURNAL OF MEDICINAL CHEMISTRY, vol. 35, WASHINGTON US, pages 2363 - 2368 *
CRONSTEIN B.N.: "Adenosine, an endogenous anti-inflammatory agent", JOURNAL OF APPLIED PHYSIOLOGY, vol. 76, no. 1, pages 5 - 13 *
HUTCHINSON A.J. ET AL: "2-(Arylalkylamino)adenosine-5'-uronamides: A New Class of Highly Selective Adenosine A2 Receptor Ligands", JOURNAL OF MEDICINAL CHEMISTRY, vol. 33, WASHINGTON US, pages 1919 - 1924 *
TRIVEDI B.K. AND BRUNS R.F.: "C2,N6-Disubstituted Adenosines: Synthesis and Structure-Activity Relationships", JOURNAL OF MEDICINAL CHEMISTRY, vol. 32, WASHINGTON US, pages 1667 - 1673 *
WOLLNER A ET AL: "Acting via A2 Receptors, Adenosine Inhibits the Upregulation of Mac-1 (CD11b/CD18) Expression on FMLP-stimulated Neutrophils", AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, vol. 9, pages 179 - 185 *

Also Published As

Publication number Publication date
IL114578A0 (en) 1995-11-27
WO1996002553A2 (en) 1996-02-01
ZA955784B (en) 1996-08-15
AU3698295A (en) 1996-02-16
GB9414193D0 (en) 1994-08-31

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