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Items: 1 to 20 of 130

1.

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;30(3):377-82. doi: 10.3109/14756366.2014.940933. Epub 2014 Jul 28.

PMID:
25068730
2.

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;27(4):509-14. doi: 10.3109/14756366.2011.599029. Epub 2011 Aug 16.

PMID:
21846203
3.

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;29(2):168-74. doi: 10.3109/14756366.2012.763163. Epub 2013 Feb 7.

PMID:
23391138
4.

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;56:75-82. doi: 10.1016/j.bioorg.2014.07.009. Epub 2014 Aug 1.

PMID:
25159522
5.

Synthesis of new sulfonamide inhibitors of carbonic anhydrase.

Arslan O, Cakir U, Ugraş HI.

Biochemistry (Mosc). 2002 Sep;67(9):1055-7.

PMID:
12387722
6.

In vitro inhibition effects of some new sulfonamide inhibitors on human carbonic anhydrase I and II.

Cakir U, Uğraş HI, Ozensoy O, Sinan S, Arslan O.

J Enzyme Inhib Med Chem. 2004 Jun;19(3):257-61.

PMID:
15499997
7.

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. doi: 10.1016/j.bmc.2015.09.022. Epub 2015 Sep 15.

PMID:
26422787
8.

Synthesis of 3,4-dihydroxypyrrolidine-2,5-dione and 3,5-dihydroxybenzoic acid derivatives and evaluation of the carbonic anhydrase I and II inhibition.

Arslan M, Şentürk M, Fidan İ, Talaz O, Ekinci D, Coşgun S, Supuran CT.

J Enzyme Inhib Med Chem. 2015 Dec;30(6):896-900. doi: 10.3109/14756366.2014.983917. Epub 2015 Mar 6.

PMID:
25744511
9.

Effects of new 5-amino-1,3,4-thiadiazole-2-sulfonamide derivatives on human carbonic anhydrase isozymes.

Kasimoğullari R, Bülbül M, Günhan H, Güleryüz H.

Bioorg Med Chem. 2009 May 1;17(9):3295-301. doi: 10.1016/j.bmc.2009.03.048. Epub 2009 Mar 28.

PMID:
19362844
10.

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. doi: 10.1016/j.bmc.2014.12.054. Epub 2015 Mar 20.

PMID:
25863492
11.

Facile synthesis and characterization of novel pyrazole-sulfonamides and their inhibition effects on human carbonic anhydrase isoenzymes.

Balseven H, Mustafa İşgör M, Mert S, Alım Z, Beydemir S, Ok S, Kasımoğulları R.

Bioorg Med Chem. 2013 Jan 1;21(1):21-7. doi: 10.1016/j.bmc.2012.11.012. Epub 2012 Nov 27.

PMID:
23218470
12.

Identification of 3,4-Dihydroisoquinoline-2(1H)-sulfonamides as potent carbonic anhydrase inhibitors: synthesis, biological evaluation, and enzyme--ligand X-ray studies.

Gitto R, Agnello S, Ferro S, De Luca L, Vullo D, Brynda J, Mader P, Supuran CT, Chimirri A.

J Med Chem. 2010 Mar 25;53(6):2401-8. doi: 10.1021/jm9014026.

PMID:
20170095
13.

Carbonic anhydrase inhibitors: Synthesis and inhibition of the cytosolic mammalian carbonic anhydrase isoforms I, II and VII with benzene sulfonamides incorporating 4,5,6,7-tetrachlorophthalimide moiety.

Sethi KK, Verma SM, Tanç M, Carta F, Supuran CT.

Bioorg Med Chem. 2013 Sep 1;21(17):5168-74. doi: 10.1016/j.bmc.2013.06.035. Epub 2013 Jun 26.

PMID:
23867389
14.

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;27(3):365-9. doi: 10.3109/14756366.2011.591290. Epub 2011 Jun 23.

PMID:
21699374
15.

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. doi: 10.1016/j.ejmech.2015.06.022. Epub 2015 Jun 25.

PMID:
26160114
16.

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. doi: 10.1016/j.bmcl.2015.05.076. Epub 2015 May 30.

PMID:
26073006
17.
18.

In Vitro inhibition of human carbonic anhydrase I and II isozymes with natural phenolic compounds.

Sentürk M, Gülçin I, Beydemir S, Küfrevioğlu Oİ, Supuran CT.

Chem Biol Drug Des. 2011 Jun;77(6):494-9. doi: 10.1111/j.1747-0285.2011.01104.x. Epub 2011 Mar 25.

PMID:
21332948
19.

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;27(4):467-75. doi: 10.3109/14756366.2011.596836. Epub 2011 Aug 4.

PMID:
21815772
20.

Novel sulphamides and sulphonamides incorporating the tetralin scaffold as carbonic anhydrase and acetylcholine esterase inhibitors.

Akıncıoğlu A, Topal M, Gülçin I, Göksu S.

Arch Pharm (Weinheim). 2014 Jan;347(1):68-76. doi: 10.1002/ardp.201300273. Epub 2013 Nov 18.

PMID:
24243403
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