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228 related items for PubMed ID: 24758348
1. 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; 30(2):204-11. PubMed ID: 24758348 [Abstract] [Full Text] [Related]
2. Intrinsic thermodynamics of trifluoromethanesulfonamide and ethoxzolamide binding to human carbonic anhydrase VII. Pilipuitytė V, Matulis D. J Mol Recognit; 2015 Mar; 28(3):166-72. PubMed ID: 25652363 [Abstract] [Full Text] [Related]
3. Characterization of human carbonic anhydrase XII stability and inhibitor binding. Jogaitė V, Zubrienė A, Michailovienė V, Gylytė J, Morkūnaitė V, Matulis D. Bioorg Med Chem; 2013 Mar 15; 21(6):1431-6. PubMed ID: 23159038 [Abstract] [Full Text] [Related]
4. Thermodynamic, kinetic, and structural parameterization of human carbonic anhydrase interactions toward enhanced inhibitor design. Linkuvienė V, Zubrienė A, Manakova E, Petrauskas V, Baranauskienė L, Zakšauskas A, Smirnov A, Gražulis S, Ladbury JE, Matulis D. Q Rev Biophys; 2018 Jan 15; 51():e10. PubMed ID: 30912486 [Abstract] [Full Text] [Related]
5. Synthesis and evaluation of N-heteroarylsubstituted triazolosulfonamides as carbonic anhydrase inhibitors. Balci A, Arslan M, Nixha AR, Bilen C, Ergun A, Gençer N. J Enzyme Inhib Med Chem; 2015 Jun 15; 30(3):377-82. PubMed ID: 25068730 [Abstract] [Full Text] [Related]
6. 4-[N-(substituted 4-pyrimidinyl)amino]benzenesulfonamides as inhibitors of carbonic anhydrase isozymes I, II, VII, and XIII. Sūdžius J, Baranauskienė L, Golovenko D, Matulienė J, Michailovienė V, Torresan J, Jachno J, Sukackaitė R, Manakova E, Gražulis S, Tumkevičius S, Matulis D. Bioorg Med Chem; 2010 Nov 01; 18(21):7413-21. PubMed ID: 20889345 [Abstract] [Full Text] [Related]
7. Intrinsic thermodynamics of inhibitor binding to human carbonic anhydrase IX. Linkuvienė V, Matulienė J, Juozapaitienė V, Michailovienė V, Jachno J, Matulis D. Biochim Biophys Acta; 2016 Apr 01; 1860(4):708-18. PubMed ID: 26794023 [Abstract] [Full Text] [Related]
8. Synthesis of new sulfonamide inhibitors of carbonic anhydrase. Arslan O, Cakir U, Ugraş HI. Biochemistry (Mosc); 2002 Sep 01; 67(9):1055-7. PubMed ID: 12387722 [Abstract] [Full Text] [Related]
9. Probing the 'bipolar' nature of the carbonic anhydrase active site: aromatic sulfonamides containing 1,3-oxazol-5-yl moiety as picomolar inhibitors of cytosolic CA I and CA II isoforms. Krasavin M, Korsakov M, Dorogov M, Tuccinardi T, Dedeoglu N, Supuran CT. Eur J Med Chem; 2015 Aug 28; 101():334-47. PubMed ID: 26160114 [Abstract] [Full Text] [Related]
10. Synthesis and carbonic anhydrase isoenzymes I and II inhibitory effects of novel benzylamine derivatives. Çetinkaya Y, Göçer H, Göksu S, Gülçin İ. J Enzyme Inhib Med Chem; 2014 Apr 28; 29(2):168-74. PubMed ID: 23391138 [Abstract] [Full Text] [Related]
11. Synthesis, characterization and in vitro inhibition of metal complexes of pyrazole based sulfonamide on human erythrocyte carbonic anhydrase isozymes I and II. Büyükkıdan N, Büyükkıdan B, Bülbül M, Kasımoğulları R, Mert S. J Enzyme Inhib Med Chem; 2017 Dec 28; 32(1):208-213. PubMed ID: 28114829 [Abstract] [Full Text] [Related]
12. Benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulfonamides as inhibitors of carbonic anhydrase. Dudutiene V, Baranauskiene L, Matulis D. Bioorg Med Chem Lett; 2007 Jun 15; 17(12):3335-8. PubMed ID: 17442568 [Abstract] [Full Text] [Related]
13. Indapamide-like benzenesulfonamides as inhibitors of carbonic anhydrases I, II, VII, and XIII. Čapkauskaitė E, Baranauskienė L, Golovenko D, Manakova E, Gražulis S, Tumkevičius S, Matulis D. Bioorg Med Chem; 2010 Nov 01; 18(21):7357-64. PubMed ID: 20926301 [Abstract] [Full Text] [Related]
14. N-Acylsulfonamides strongly inhibit human carbonic anhydrase isoenzymes I and II. Yıldırım A, Atmaca U, Keskin A, Topal M, Çelik M, Gülçin İ, Supuran CT. Bioorg Med Chem; 2015 May 15; 23(10):2598-605. PubMed ID: 25863492 [Abstract] [Full Text] [Related]
15. Synthesis and characterization of novel dioxoacridine sulfonamide derivatives as new carbonic anhydrase inhibitors. Kaya M, Basar E, Cakir E, Tunca E, Bülbül M. J Enzyme Inhib Med Chem; 2012 Aug 15; 27(4):509-14. PubMed ID: 21846203 [Abstract] [Full Text] [Related]
16. Pyridazinone substituted benzenesulfonamides as potent carbonic anhydrase inhibitors. Yaseen R, Ekinci D, Senturk M, Hameed AD, Ovais S, Rathore P, Samim M, Javed K, Supuran CT. Bioorg Med Chem Lett; 2016 Feb 15; 26(4):1337-41. PubMed ID: 26804228 [Abstract] [Full Text] [Related]
17. Carbonic anhydrase inhibitors: Design, synthesis, kinetic, docking and molecular dynamics analysis of novel glycine and phenylalanine sulfonamide derivatives. Fidan İ, Salmas RE, Arslan M, Şentürk M, Durdagi S, Ekinci D, Şentürk E, Coşgun S, Supuran CT. Bioorg Med Chem; 2015 Dec 01; 23(23):7353-8. PubMed ID: 26534780 [Abstract] [Full Text] [Related]
18. Carbonic anhydrase inhibitory properties of novel benzylsulfamides using molecular modeling and experimental studies. Göksu S, Naderi A, Akbaba Y, Kalın P, Akıncıoğlu A, Gülçin İ, Durdagi S, Salmas RE. Bioorg Chem; 2014 Oct 01; 56():75-82. PubMed ID: 25159522 [Abstract] [Full Text] [Related]
19. 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 Oct 01; 31(sup2):180-188. PubMed ID: 27353698 [Abstract] [Full Text] [Related]
20. New 4-[(3-cyclohexyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzene-1-sulfonamides, synthesis and inhibitory activity toward carbonic anhydrase I, II, IX, XII. Meleddu R, Maccioni E, Distinto S, Bianco G, Melis C, Alcaro S, Cottiglia F, Ceruso M, Supuran CT. Bioorg Med Chem Lett; 2015 Aug 15; 25(16):3281-4. PubMed ID: 26073006 [Abstract] [Full Text] [Related] Page: [Next] [New Search]