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Journal Abstract Search

146 related items for PubMed ID: 20118557

  • 1. Timolol activates the enzyme activities of human carbonic anhydrase I and II.
    Sugimoto A, Ikeda H, Tsukamoto H, Kihira K, Ishioka M, Hirose J, Hata T, Fujioka H, Ono Y.
    Biol Pharm Bull; 2010; 33(2):301-6. PubMed ID: 20118557
    [Abstract] [Full Text] [Related]

  • 2. The mechanisms by which latanoprost free acid inhibits human carbonic anhydrase I and II.
    Sugimoto A, Ikeda H, Tsukamoto H, Kihira K, Takeda C, Hirose J, Hata T, Baba E, Ono Y.
    Biol Pharm Bull; 2008 May; 31(5):796-801. PubMed ID: 18451496
    [Abstract] [Full Text] [Related]

  • 3. Synthesis and biological evaluation of histamine Schiff bases as carbonic anhydrase I, II, IV, VII, and IX activators.
    Akocak S, Lolak N, Vullo D, Durgun M, Supuran CT.
    J Enzyme Inhib Med Chem; 2017 Dec; 32(1):1305-1312. PubMed ID: 29072105
    [Abstract] [Full Text] [Related]

  • 4. Carbonic anhydrase inhibitors. Inhibition of the cytosolic and tumor-associated carbonic anhydrase isozymes I, II, and IX with a series of 1,3,4-thiadiazole- and 1,2,4-triazole-thiols.
    Almajan GL, Innocenti A, Puccetti L, Manole G, Barbuceanu S, Saramet I, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2005 May 02; 15(9):2347-52. PubMed ID: 15837323
    [Abstract] [Full Text] [Related]

  • 5. In vitro inhibition effect and structure-activity relationships of some saccharin derivatives on erythrocyte carbonic anhydrase I and II.
    Sonmez F, Bilen C, Sumersan S, Gencer N, Isik S, Arslan O, Kucukislamoglu M.
    J Enzyme Inhib Med Chem; 2014 Feb 02; 29(1):118-23. PubMed ID: 23339426
    [Abstract] [Full Text] [Related]

  • 6. Chemical rescue in catalysis by human carbonic anhydrases II and III.
    An H, Tu C, Duda D, Montanez-Clemente I, Math K, Laipis PJ, McKenna R, Silverman DN.
    Biochemistry; 2002 Mar 05; 41(9):3235-42. PubMed ID: 11863462
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Carbonic anhydrase inhibitors: novel sulfonamides incorporating 1,3,5-triazine moieties as inhibitors of the cytosolic and tumour-associated carbonic anhydrase isozymes I, II and IX.
    Garaj V, Puccetti L, Fasolis G, Winum JY, Montero JL, Scozzafava A, Vullo D, Innocenti A, Supuran CT.
    Bioorg Med Chem Lett; 2005 Jun 15; 15(12):3102-8. PubMed ID: 15905091
    [Abstract] [Full Text] [Related]

  • 9. Effects of dopaminergic compounds on carbonic anhydrase isozymes I, II, and VI.
    Sentürk M, Ekinci D, Göksu S, Supuran CT.
    J Enzyme Inhib Med Chem; 2012 Jun 15; 27(3):365-9. PubMed ID: 21699374
    [Abstract] [Full Text] [Related]

  • 10. Structural and kinetic characterization of active-site histidine as a proton shuttle in catalysis by human carbonic anhydrase II.
    Fisher Z, Hernandez Prada JA, Tu C, Duda D, Yoshioka C, An H, Govindasamy L, Silverman DN, McKenna R.
    Biochemistry; 2005 Feb 01; 44(4):1097-105. PubMed ID: 15667203
    [Abstract] [Full Text] [Related]

  • 11. Mutation of Phe91 to Asn in human carbonic anhydrase I unexpectedly enhanced both catalytic activity and affinity for sulfonamide inhibitors.
    Kockar F, Maresca A, Aydin M, Işik S, Turkoglu S, Sinan S, Arslan O, Güler OO, Turan Y, Supuran CT.
    Bioorg Med Chem; 2010 Aug 01; 18(15):5498-503. PubMed ID: 20624682
    [Abstract] [Full Text] [Related]

  • 12. Carbonic anhydrase I and II activation with mono- and dihalogenated histamine derivatives.
    Saada MC, Vullo D, Montero JL, Scozzafava A, Winum JY, Supuran CT.
    Bioorg Med Chem Lett; 2011 Aug 15; 21(16):4884-7. PubMed ID: 21742491
    [Abstract] [Full Text] [Related]

  • 13. Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, IX, and XII with N-hydroxysulfamides--a new zinc-binding function in the design of inhibitors.
    Winum JY, Innocenti A, Nasr J, Montero JL, Scozzafava A, Vullo D, Supuran CT.
    Bioorg Med Chem Lett; 2005 May 02; 15(9):2353-8. PubMed ID: 15837324
    [Abstract] [Full Text] [Related]

  • 14. The effects of some bromophenols on human carbonic anhydrase isoenzymes.
    Taslimi P, Gülçin İ, Öztaşkın N, Çetinkaya Y, Göksu S, Alwasel SH, Supuran CT.
    J Enzyme Inhib Med Chem; 2016 Aug 02; 31(4):603-7. PubMed ID: 26133541
    [Abstract] [Full Text] [Related]

  • 15. Synthesis, carbonic anhydrase I and II inhibition studies of the 1,3,5-trisubstituted-pyrazolines.
    Gul HI, Mete E, Taslimi P, Gulcin I, Supuran CT.
    J Enzyme Inhib Med Chem; 2017 Dec 02; 32(1):189-192. PubMed ID: 27774818
    [Abstract] [Full Text] [Related]

  • 16. Carbonic anhydrase activators: activation of human isozymes I, II and IX with phenylsulfonylhydrazido l-histidine derivatives.
    Abdo MR, Vullo D, Saada MC, Montero JL, Scozzafava A, Winum JY, Supuran CT.
    Bioorg Med Chem Lett; 2009 May 01; 19(9):2440-3. PubMed ID: 19345095
    [Abstract] [Full Text] [Related]

  • 17. Carbonic anhydrase inhibitors. Synthesis, and molecular structure of novel series N-substituted N'-(2-arylmethylthio-4-chloro-5-methylbenzenesulfonyl)guanidines and their inhibition of human cytosolic isozymes I and II and the transmembrane tumor-associated isozymes IX and XII.
    Żołnowska B, Sławiński J, Pogorzelska A, Chojnacki J, Vullo D, Supuran CT.
    Eur J Med Chem; 2014 Jan 01; 71():135-47. PubMed ID: 24291567
    [Abstract] [Full Text] [Related]

  • 18. Synthesis and characterisation of two novel proton transfer compounds and their inhibition studies on carbonic anhydrase isoenzymes.
    Yenikaya C, Sari M, Bülbül M, Ilkimen H, Cinar B, Büyükgüngör O.
    J Enzyme Inhib Med Chem; 2011 Feb 01; 26(1):104-14. PubMed ID: 20860527
    [Abstract] [Full Text] [Related]

  • 19. Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isoforms I and II and transmembrane, tumor-associated isoforms IX and XII with boronic acids.
    Winum JY, Innocenti A, Scozzafava A, Montero JL, Supuran CT.
    Bioorg Med Chem; 2009 May 15; 17(10):3649-52. PubMed ID: 19375921
    [Abstract] [Full Text] [Related]

  • 20. 5-Substituted-(1,2,3-triazol-4-yl)thiophene-2-sulfonamides strongly inhibit human carbonic anhydrases I, II, IX and XII: solution and X-ray crystallographic studies.
    Leitans J, Sprudza A, Tanc M, Vozny I, Zalubovskis R, Tars K, Supuran CT.
    Bioorg Med Chem; 2013 Sep 01; 21(17):5130-8. PubMed ID: 23859774
    [Abstract] [Full Text] [Related]

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