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Journal Abstract Search

237 related items for PubMed ID: 16503144

  • 1. The purines: potent and versatile small molecule inhibitors and modulators of key biological targets.
    Legraverend M, Grierson DS.
    Bioorg Med Chem; 2006 Jun 15; 14(12):3987-4006. PubMed ID: 16503144
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  • 2. Synthesis and application of functionally diverse 2,6,9-trisubstituted purine libraries as CDK inhibitors.
    Chang YT, Gray NS, Rosania GR, Sutherlin DP, Kwon S, Norman TC, Sarohia R, Leost M, Meijer L, Schultz PG.
    Chem Biol; 1999 Jun 15; 6(6):361-75. PubMed ID: 10375538
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  • 5. Identification of purine inhibitors of phosphodiesterase 7 (PDE7).
    Pitts WJ, Vaccaro W, Huynh T, Leftheris K, Roberge JY, Barbosa J, Guo J, Brown B, Watson A, Donaldson K, Starling GC, Kiener PA, Poss MA, Dodd JH, Barrish JC.
    Bioorg Med Chem Lett; 2004 Jun 07; 14(11):2955-8. PubMed ID: 15125967
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  • 9. 8-azapurine nucleus: a versatile scaffold for different targets.
    Giorgi I, Scartoni V.
    Mini Rev Med Chem; 2009 Oct 07; 9(12):1367-78. PubMed ID: 19939217
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  • 10. Assessing the chemical diversity of an hsp90 database.
    Audisio D, Messaoudi S, Ijjaali I, Dubus E, Petitet F, Peyrat JF, Brion JD, Alami M.
    Eur J Med Chem; 2010 May 07; 45(5):2000-9. PubMed ID: 20170986
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  • 11. Protein kinase inhibitors--potential chemotherapeutic agents.
    Shugar D.
    Acta Biochim Pol; 1995 May 07; 42(4):405-18. PubMed ID: 8852331
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  • 13. 1,3,5-Triazine-based analogues of purine: from isosteres to privileged scaffolds in medicinal chemistry.
    Lim FP, Dolzhenko AV.
    Eur J Med Chem; 2014 Oct 06; 85():371-90. PubMed ID: 25105925
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  • 14. Synthesis and full characterisation of 6-chloro-2-iodopurine, a template for the functionalisation of purines.
    Taddei D, Kilian P, Slawin AM, Derek Woollins J.
    Org Biomol Chem; 2004 Mar 07; 2(5):665-70. PubMed ID: 14985806
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  • 15. Dedifferentiation of lineage-committed cells by a small molecule.
    Chen S, Zhang Q, Wu X, Schultz PG, Ding S.
    J Am Chem Soc; 2004 Jan 21; 126(2):410-1. PubMed ID: 14719906
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  • 16. SAR of carbon-linked, 2-substituted purines: synthesis and characterization of AP23451 as a novel bone-targeted inhibitor of Src tyrosine kinase with in vivo anti-resorptive activity.
    Shakespeare WC, Wang Y, Bohacek R, Keenan T, Sundaramoorthi R, Metcalf C, Dilauro A, Roeloffzen S, Liu S, Saltmarsh J, Paramanathan G, Dalgarno D, Narula S, Pradeepan S, van Schravendijk MR, Keats J, Ram M, Liou S, Adams S, Wardwell S, Bogus J, Iuliucci J, Weigele M, Xing L, Boyce B, Sawyer TK.
    Chem Biol Drug Des; 2008 Feb 21; 71(2):97-105. PubMed ID: 18179464
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  • 20. Structure-based design, synthesis, and antimicrobial activity of purine derived SAH/MTA nucleosidase inhibitors.
    Tedder ME, Nie Z, Margosiak S, Chu S, Feher VA, Almassy R, Appelt K, Yager KM.
    Bioorg Med Chem Lett; 2004 Jun 21; 14(12):3165-8. PubMed ID: 15149667
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