These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

524 related articles for article (PubMed ID: 22607219)

  • 1. Multiple binding modes of inhibitors to carbonic anhydrases: how to design specific drugs targeting 15 different isoforms?
    Alterio V; Di Fiore A; D'Ambrosio K; Supuran CT; De Simone G
    Chem Rev; 2012 Aug; 112(8):4421-68. PubMed ID: 22607219
    [No Abstract]   [Full Text] [Related]  

  • 2. Salicylaldoxime derivatives as new leads for the development of carbonic anhydrase inhibitors.
    Tuccinardi T; Bertini S; Granchi C; Ortore G; Macchia M; Minutolo F; Martinelli A; Supuran CT
    Bioorg Med Chem; 2013 Mar; 21(6):1511-5. PubMed ID: 23018095
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Homology modeling and receptor-based 3D-QSAR study of carbonic anhydrase IX.
    Tuccinardi T; Ortore G; Rossello A; Supuran CT; Martinelli A
    J Chem Inf Model; 2007; 47(6):2253-62. PubMed ID: 17949069
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Saccharin inhibits carbonic anhydrases: possible explanation for its unpleasant metallic aftertaste.
    Köhler K; Hillebrecht A; Schulze Wischeler J; Innocenti A; Heine A; Supuran CT; Klebe G
    Angew Chem Int Ed Engl; 2007; 46(40):7697-9. PubMed ID: 17705204
    [No Abstract]   [Full Text] [Related]  

  • 5. Carbonic anhydrase inhibitors. Sulfonamide diuretics revisited--old leads for new applications?
    Temperini C; Cecchi A; Scozzafava A; Supuran CT
    Org Biomol Chem; 2008 Jul; 6(14):2499-506. PubMed ID: 18600270
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hydroxamate represents a versatile zinc binding group for the development of new carbonic anhydrase inhibitors.
    Di Fiore A; Maresca A; Supuran CT; De Simone G
    Chem Commun (Camb); 2012 Sep; 48(70):8838-40. PubMed ID: 22836518
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X-ray crystallography-promoted drug design of carbonic anhydrase inhibitors.
    Ivanova J; Leitans J; Tanc M; Kazaks A; Zalubovskis R; Supuran CT; Tars K
    Chem Commun (Camb); 2015 Apr; 51(33):7108-11. PubMed ID: 25813715
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Indanesulfonamides as carbonic anhydrase inhibitors. Toward structure-based design of selective inhibitors of the tumor-associated isozyme CA IX.
    Thiry A; Ledecq M; Cecchi A; Dogné JM; Wouters J; Supuran CT; Masereel B
    J Med Chem; 2006 May; 49(9):2743-9. PubMed ID: 16640335
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Discovering isozyme-selective inhibitor scaffolds of human carbonic anhydrases using structural alignment and de novo drug design approaches.
    Xiang F; Xiang J; Fang Y; Zhang M; Li M
    Chem Biol Drug Des; 2014 Feb; 83(2):247-58. PubMed ID: 24112770
    [TBL] [Abstract][Full Text] [Related]  

  • 10. S-glycosyl primary sulfonamides--a new structural class for selective inhibition of cancer-associated carbonic anhydrases.
    Lopez M; Paul B; Hofmann A; Morizzi J; Wu QK; Charman SA; Innocenti A; Vullo D; Supuran CT; Poulsen SA
    J Med Chem; 2009 Oct; 52(20):6421-32. PubMed ID: 19827837
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The design of new carbonic anhydrase inhibitors.
    Mansoor UF; Zhang XR; Blackburn GM
    EXS; 2000; (90):437-59. PubMed ID: 11268529
    [No Abstract]   [Full Text] [Related]  

  • 12. Probing the surface of human carbonic anhydrase for clues towards the design of isoform specific inhibitors.
    Pinard MA; Mahon B; McKenna R
    Biomed Res Int; 2015; 2015():453543. PubMed ID: 25811028
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthesis of C-cinnamoyl glycosides and their inhibitory activity against mammalian carbonic anhydrases.
    Riafrecha LE; Rodríguez OM; Vullo D; Supuran CT; Colinas PA
    Bioorg Med Chem; 2013 Mar; 21(6):1489-94. PubMed ID: 23010455
    [TBL] [Abstract][Full Text] [Related]  

  • 14. (In)organic anions as carbonic anhydrase inhibitors.
    De Simone G; Supuran CT
    J Inorg Biochem; 2012 Jun; 111():117-29. PubMed ID: 22192857
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Carbonic anhydrase inhibitors: inhibition studies of a coral secretory isoform with inorganic anions.
    Bertucci A; Innocenti A; Zoccola D; Scozzafava A; Allemand D; Tambutté S; Supuran CT
    Bioorg Med Chem Lett; 2009 Feb; 19(3):650-3. PubMed ID: 19121582
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dithiocarbamates: a new class of carbonic anhydrase inhibitors. Crystallographic and kinetic investigations.
    Carta F; Aggarwal M; Maresca A; Scozzafava A; McKenna R; Supuran CT
    Chem Commun (Camb); 2012 Feb; 48(13):1868-70. PubMed ID: 22218610
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: new pharmacological opportunities due to related binding site recognition.
    Weber A; Casini A; Heine A; Kuhn D; Supuran CT; Scozzafava A; Klebe G
    J Med Chem; 2004 Jan; 47(3):550-7. PubMed ID: 14736236
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inhibition and catalysis of carbonic anhydrase. Recent crystallographic analyses.
    Liljas A; Håkansson K; Jonsson BH; Xue Y
    Eur J Biochem; 1994 Jan; 219(1-2):1-10. PubMed ID: 8306976
    [No Abstract]   [Full Text] [Related]  

  • 19. Crystal structure of human carbonic anhydrase XIII and its complex with the inhibitor acetazolamide.
    Di Fiore A; Monti SM; Hilvo M; Parkkila S; Romano V; Scaloni A; Pedone C; Scozzafava A; Supuran CT; De Simone G
    Proteins; 2009 Jan; 74(1):164-75. PubMed ID: 18618712
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Structural basis for the interaction between carbonic anhydrase and 1,2,3,4-tetrahydroisoquinolin-2-ylsulfonamides.
    Mader P; Brynda J; Gitto R; Agnello S; Pachl P; Supuran CT; Chimirri A; Řezáčová P
    J Med Chem; 2011 Apr; 54(7):2522-6. PubMed ID: 21395315
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 27.