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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

725 related items for PubMed ID: 20889345

  • 41. Novel indolin-2-one-based sulfonamides as carbonic anhydrase inhibitors: Synthesis, in vitro biological evaluation against carbonic anhydrases isoforms I, II, IV and VII and molecular docking studies.
    Eldehna WM, Al-Ansary GH, Bua S, Nocentini A, Gratteri P, Altoukhy A, Ghabbour H, Ahmed HY, Supuran CT.
    Eur J Med Chem; 2017 Feb 15; 127():521-530. PubMed ID: 28109946
    [Abstract] [Full Text] [Related]

  • 42. Anticonvulsant 4-aminobenzenesulfonamide derivatives with branched-alkylamide moieties: X-ray crystallography and inhibition studies of human carbonic anhydrase isoforms I, II, VII, and XIV.
    Hen N, Bialer M, Yagen B, Maresca A, Aggarwal M, Robbins AH, McKenna R, Scozzafava A, Supuran CT.
    J Med Chem; 2011 Jun 09; 54(11):3977-81. PubMed ID: 21506569
    [Abstract] [Full Text] [Related]

  • 43. Synthesis of a new series of N⁴-substituted 4-(2-aminoethyl)benzenesulfonamides and their inhibitory effect on human carbonic anhydrase cytosolic isozymes I and II and transmembrane tumor-associated isozymes IX and XII.
    Sławiński J, Brzozowski Z, Żołnowska B, Szafrański K, Pogorzelska A, Vullo D, Supuran CT.
    Eur J Med Chem; 2014 Sep 12; 84():59-67. PubMed ID: 25016228
    [Abstract] [Full Text] [Related]

  • 44. Development of novel organometallic sulfonamides with N-ethyl or N-methyl benzenesulfonamide units as potential human carbonic anhydrase I, II, IX and XII isoforms' inhibitors: Synthesis, biological evaluation and docking studies.
    Gallardo M, Arancibia R, Supuran CT, Nocentini A, Villaman D, Toro PM, Muñoz-Osses M, Mascayano C.
    J Inorg Biochem; 2024 Nov 12; 260():112689. PubMed ID: 39121601
    [Abstract] [Full Text] [Related]

  • 45. Inhibition of human carbonic anhydrase isozymes I, II and VI with a series of bisphenol, methoxy and bromophenol compounds.
    Balaydin HT, Durdaği S, Ekinci D, Sentürk M, Göksu S, Menzek A.
    J Enzyme Inhib Med Chem; 2012 Aug 12; 27(4):467-75. PubMed ID: 21815772
    [Abstract] [Full Text] [Related]

  • 46. Synthesis and biological evaluation of novel aromatic and heterocyclic bis-sulfonamide Schiff bases as carbonic anhydrase I, II, VII and IX inhibitors.
    Akocak S, Lolak N, Nocentini A, Karakoc G, Tufan A, Supuran CT.
    Bioorg Med Chem; 2017 Jun 15; 25(12):3093-3097. PubMed ID: 28400084
    [Abstract] [Full Text] [Related]

  • 47.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 48. Conformational variability of different sulfonamide inhibitors with thienyl-acetamido moieties attributes to differential binding in the active site of cytosolic human carbonic anhydrase isoforms.
    Biswas S, Aggarwal M, Güzel Ö, Scozzafava A, McKenna R, Supuran CT.
    Bioorg Med Chem; 2011 Jun 15; 19(12):3732-8. PubMed ID: 21620713
    [Abstract] [Full Text] [Related]

  • 49.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 50. Synthesis of 4-(2-substituted hydrazinyl)benzenesulfonamides and their carbonic anhydrase inhibitory effects.
    Gul HI, Kucukoglu K, Yamali C, Bilginer S, Yuca H, Ozturk I, Taslimi P, Gulcin I, Supuran CT.
    J Enzyme Inhib Med Chem; 2016 Aug 15; 31(4):568-73. PubMed ID: 26044365
    [Abstract] [Full Text] [Related]

  • 51. Discovery of potent anti-convulsant carbonic anhydrase inhibitors: Design, synthesis, in vitro and in vivo appraisal.
    Mishra CB, Kumari S, Angeli A, Bua S, Buonanno M, Monti SM, Tiwari M, Supuran CT.
    Eur J Med Chem; 2018 Aug 05; 156():430-443. PubMed ID: 30015076
    [Abstract] [Full Text] [Related]

  • 52. Intrinsic thermodynamics of sulfonamide inhibitor binding to human carbonic anhydrases I and II.
    Morkūnaitė V, Gylytė J, Zubrienė A, Baranauskienė L, Kišonaitė M, Michailovienė V, Juozapaitienė V, Todd MJ, Matulis D.
    J Enzyme Inhib Med Chem; 2015 Apr 05; 30(2):204-11. PubMed ID: 24758348
    [Abstract] [Full Text] [Related]

  • 53. Synthesis of novel acridine bis-sulfonamides with effective inhibitory activity against the carbonic anhydrase isoforms I, II, IX and XII.
    Esirden İ, Ulus R, Aday B, Tanç M, Supuran CT, Kaya M.
    Bioorg Med Chem; 2015 Oct 15; 23(20):6573-80. PubMed ID: 26422787
    [Abstract] [Full Text] [Related]

  • 54. Benzenesulfonamides with benzimidazole moieties as inhibitors of carbonic anhydrases I, II, VII, XII and XIII.
    Zubrienė A, Čapkauskaitė E, Gylytė J, Kišonaitė M, Tumkevičius S, Matulis D.
    J Enzyme Inhib Med Chem; 2014 Feb 15; 29(1):124-31. PubMed ID: 23356363
    [Abstract] [Full Text] [Related]

  • 55. A class of sulfonamides as carbonic anhydrase I and II inhibitors.
    Gokcen T, Gulcin I, Ozturk T, Goren AC.
    J Enzyme Inhib Med Chem; 2016 Feb 15; 31(sup2):180-188. PubMed ID: 27353698
    [Abstract] [Full Text] [Related]

  • 56. Carbonic anhydrase inhibitors. X-ray crystal studies of the carbonic anhydrase II-trithiocarbonate adduct--an inhibitor mimicking the sulfonamide and urea binding to the enzyme.
    Temperini C, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2010 Jan 15; 20(2):474-8. PubMed ID: 20005709
    [Abstract] [Full Text] [Related]

  • 57. Synthesis and investigation of inhibition effect of fluorinated sulfonamide derivatives on carbonic anhydrase.
    Benfodda Z, Guillen F, Romestand B, Dahmani A, Blancou H.
    Eur J Med Chem; 2010 Mar 15; 45(3):1225-9. PubMed ID: 20036446
    [Abstract] [Full Text] [Related]

  • 58. Carbonic anhydrase inhibitors: inhibition of human cytosolic isozyme II and mitochondrial isozyme V with a series of benzene sulfonamide derivatives.
    Innocenti A, Antel J, Wurl M, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2004 Nov 15; 14(22):5703-7. PubMed ID: 15482952
    [Abstract] [Full Text] [Related]

  • 59. In vitro inhibition of salicylic acid derivatives on human cytosolic carbonic anhydrase isozymes I and II.
    Bayram E, Senturk M, Kufrevioglu OI, Supuran CT.
    Bioorg Med Chem; 2008 Oct 15; 16(20):9101-5. PubMed ID: 18819808
    [Abstract] [Full Text] [Related]

  • 60. Synthesis of isoxazole-containing sulfonamides with potent carbonic anhydrase II and VII inhibitory properties.
    Altug C, Güneş H, Nocentini A, Monti SM, Buonanno M, Supuran CT.
    Bioorg Med Chem; 2017 Feb 15; 25(4):1456-1464. PubMed ID: 28111158
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 37.