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 *

157 related articles for article (PubMed ID: 25291009)

  • 1. C-glycosides incorporating the 6-methoxy-2-naphthyl moiety are selective inhibitors of fungal and bacterial carbonic anhydrases.
    Riafrecha LE; Vullo D; Supuran CT; Colinas PA
    J Enzyme Inhib Med Chem; 2015; 30(5):857-61. PubMed ID: 25291009
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inhibition of β-carbonic anhydrases from Brucella suis with C-cinnamoyl glycosides incorporating the phenol moiety.
    Riafrecha LE; Vullo D; Ouahrani-Bettache S; Köhler S; Dumy P; Winum JY; Supuran CT; Colinas PA
    J Enzyme Inhib Med Chem; 2015 Dec; 30(6):1017-20. PubMed ID: 25676329
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Attachment of carbohydrates to methoxyaryl moieties leads to highly selective inhibitors of the cancer associated carbonic anhydrase isoforms IX and XII.
    Riafrecha LE; Rodríguez OM; Vullo D; Supuran CT; Colinas PA
    Bioorg Med Chem; 2014 Oct; 22(19):5308-14. PubMed ID: 25156300
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inhibition studies of bacterial, fungal and protozoan β-class carbonic anhydrases with Schiff bases incorporating sulfonamide moieties.
    Ceruso M; Carta F; Osman SM; Alothman Z; Monti SM; Supuran CT
    Bioorg Med Chem; 2015 Aug; 23(15):4181-4187. PubMed ID: 26145821
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Brucella suis carbonic anhydrases and their inhibitors: Towards alternative antibiotics?
    Köhler S; Ouahrani-Bettache S; Winum JY
    J Enzyme Inhib Med Chem; 2017 Dec; 32(1):683-687. PubMed ID: 28274160
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inhibition studies of Brucella suis β-carbonic anhydrases with a series of 4-substituted pyridine-3-sulphonamides.
    Monti SM; Meccariello A; Ceruso M; Szafrański K; Sławiński J; Supuran CT
    J Enzyme Inhib Med Chem; 2018 Dec; 33(1):255-259. PubMed ID: 29271264
    [TBL] [Abstract][Full Text] [Related]  

  • 7. N-glycosyl-N-hydroxysulfamides as potent inhibitors of Brucella suis carbonic anhydrases.
    Ombouma J; Vullo D; Köhler S; Dumy P; Supuran CT; Winum JY
    J Enzyme Inhib Med Chem; 2015 Dec; 30(6):1010-2. PubMed ID: 25792504
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Carbonic anhydrase inhibitors. Inhibition of the β-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with branched aliphatic/aromatic carboxylates and their derivatives.
    Carta F; Innocenti A; Hall RA; Mühlschlegel FA; Scozzafava A; Supuran CT
    Bioorg Med Chem Lett; 2011 Apr; 21(8):2521-6. PubMed ID: 21402476
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inhibition of beta-carbonic anhydrases from the bacterial pathogen Brucella suis with inorganic anions.
    Maresca A; Scozzafava A; Köhler S; Winum JY; Supuran CT
    J Inorg Biochem; 2012 May; 110():36-9. PubMed ID: 22459172
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Carbonic anhydrase inhibitors. Inhibition of the fungal beta-carbonic anhydrases from Candida albicans and Cryptococcus neoformans with boronic acids.
    Innocenti A; Winum JY; Hall RA; Mühlschlegel FA; Scozzafava A; Supuran CT
    Bioorg Med Chem Lett; 2009 May; 19(10):2642-5. PubMed ID: 19375309
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inhibition of α-class cytosolic human carbonic anhydrases I, II, IX and XII, and β-class fungal enzymes by carboxylic acids and their derivatives: new isoform-I selective nanomolar inhibitors.
    Sechi M; Innocenti A; Pala N; Rogolino D; Carcelli M; Scozzafava A; Supuran CT
    Bioorg Med Chem Lett; 2012 Sep; 22(18):5801-6. PubMed ID: 22901388
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Benzenesulfonamides incorporating nitrogenous bases show effective inhibition of β-carbonic anhydrases from the pathogenic fungi Cryptococcus neoformans, Candida glabrata and Malassezia globosa.
    Bua S; Osman SM; AlOthman Z; Supuran CT; Nocentini A
    Bioorg Chem; 2019 May; 86():39-43. PubMed ID: 30684862
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spirobisnaphthalenes effectively inhibit carbonic anhydrase.
    Gocer H; Aslan A; Gülçin İ; Supuran CT
    J Enzyme Inhib Med Chem; 2016; 31(3):503-7. PubMed ID: 26018418
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A new β-carbonic anhydrase from Brucella suis, its cloning, characterization, and inhibition with sulfonamides and sulfamates, leading to impaired pathogen growth.
    Joseph P; Ouahrani-Bettache S; Montero JL; Nishimori I; Minakuchi T; Vullo D; Scozzafava A; Winum JY; Köhler S; Supuran CT
    Bioorg Med Chem; 2011 Feb; 19(3):1172-8. PubMed ID: 21251841
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Discovering a new class of antifungal agents that selectively inhibits microbial carbonic anhydrases.
    Annunziato G; Giovati L; Angeli A; Pavone M; Del Prete S; Pieroni M; Capasso C; Bruno A; Conti S; Magliani W; Supuran CT; Costantino G
    J Enzyme Inhib Med Chem; 2018 Dec; 33(1):1537-1544. PubMed ID: 30284487
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inhibition of the β-carbonic anhydrases from Mycobacterium tuberculosis with C-cinnamoyl glycosides: identification of the first inhibitor with anti-mycobacterial activity.
    Buchieri MV; Riafrecha LE; Rodríguez OM; Vullo D; Morbidoni HR; Supuran CT; Colinas PA
    Bioorg Med Chem Lett; 2013 Feb; 23(3):740-3. PubMed ID: 23265903
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Carbonic anhydrase inhibitors: inhibition of the beta-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with simple anions.
    Innocenti A; Mühlschlegel FA; Hall RA; Steegborn C; Scozzafava A; Supuran CT
    Bioorg Med Chem Lett; 2008 Sep; 18(18):5066-70. PubMed ID: 18723348
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Natural product-based phenols as novel probes for mycobacterial and fungal carbonic anhydrases.
    Davis RA; Hofmann A; Osman A; Hall RA; Mühlschlegel FA; Vullo D; Innocenti A; Supuran CT; Poulsen SA
    J Med Chem; 2011 Mar; 54(6):1682-92. PubMed ID: 21332115
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Benzenesulfonamide bearing 1,2,4-triazole scaffolds as potent inhibitors of tumor associated carbonic anhydrase isoforms hCA IX and hCA XII.
    SitaRam ; Celik G; Khloya P; Vullo D; Supuran CT; Sharma PK
    Bioorg Med Chem; 2014 Mar; 22(6):1873-82. PubMed ID: 24560737
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.