265 related articles for article (PubMed ID: 28569564)
1. Inhibition of the α-carbonic anhydrase from Vibrio cholerae with amides and sulfonamides incorporating imidazole moieties.
De Vita D; Angeli A; Pandolfi F; Bortolami M; Costi R; Di Santo R; Suffredini E; Ceruso M; Del Prete S; Capasso C; Scipione L; Supuran CT
J Enzyme Inhib Med Chem; 2017 Dec; 32(1):798-804. PubMed ID: 28569564
[TBL] [Abstract][Full Text] [Related]
2. Quinazoline-sulfonamides with potent inhibitory activity against the α-carbonic anhydrase from Vibrio cholerae.
Alafeefy AM; Ceruso M; Al-Tamimi AM; Del Prete S; Capasso C; Supuran CT
Bioorg Med Chem; 2014 Oct; 22(19):5133-40. PubMed ID: 25194929
[TBL] [Abstract][Full Text] [Related]
3. Synthesis and carbonic anhydrase inhibitory activities of new thienyl-substituted pyrazoline benzenesulfonamides.
Mete E; Comez B; Inci Gul H; Gulcin I; Supuran CT
J Enzyme Inhib Med Chem; 2016; 31(sup2):1-5. PubMed ID: 27435177
[TBL] [Abstract][Full Text] [Related]
4. Synthesis and carbonic anhydrase I, II, VII, and IX inhibition studies with a series of benzo[d]thiazole-5- and 6-sulfonamides.
Abdoli M; Angeli A; Bozdag M; Carta F; Kakanejadifard A; Saeidian H; Supuran CT
J Enzyme Inhib Med Chem; 2017 Dec; 32(1):1071-1078. PubMed ID: 28753093
[TBL] [Abstract][Full Text] [Related]
5. 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; 31(sup2):180-188. PubMed ID: 27353698
[TBL] [Abstract][Full Text] [Related]
6. Novel sulphonamides incorporating triazene moieties show powerful carbonic anhydrase I and II inhibitory properties.
Bilginer S; Gonder B; Gul HI; Kaya R; Gulcin I; Anil B; Supuran CT
J Enzyme Inhib Med Chem; 2020 Dec; 35(1):325-329. PubMed ID: 31813300
[TBL] [Abstract][Full Text] [Related]
7. 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; 26(4):1337-41. PubMed ID: 26804228
[TBL] [Abstract][Full Text] [Related]
8. 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; 23(20):6573-80. PubMed ID: 26422787
[TBL] [Abstract][Full Text] [Related]
9. Synthesis and carbonic anhydrase inhibitory properties of novel chalcone substituted benzenesulfonamides.
Arslan T; Türkoğlu EA; Şentürk M; Supuran CT
Bioorg Med Chem Lett; 2016 Dec; 26(24):5867-5870. PubMed ID: 27884694
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 25068730
[TBL] [Abstract][Full Text] [Related]
11. 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; 21(17):5168-74. PubMed ID: 23867389
[TBL] [Abstract][Full Text] [Related]
12. Sulfonamides incorporating 1,3,5-triazine moieties selectively and potently inhibit carbonic anhydrase transmembrane isoforms IX, XII and XIV over cytosolic isoforms I and II: Solution and X-ray crystallographic studies.
Carta F; Garaj V; Maresca A; Wagner J; Avvaru BS; Robbins AH; Scozzafava A; McKenna R; Supuran CT
Bioorg Med Chem; 2011 May; 19(10):3105-19. PubMed ID: 21515057
[TBL] [Abstract][Full Text] [Related]
13. Comparison of the sulfonamide inhibition profiles of the α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
Del Prete S; Vullo D; De Luca V; Carginale V; Osman SM; AlOthman Z; Supuran CT; Capasso C
Bioorg Med Chem Lett; 2016 Apr; 26(8):1941-6. PubMed ID: 26972117
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 15499997
[TBL] [Abstract][Full Text] [Related]
15. Synthesis of novel acyl selenoureido benzensulfonamides as carbonic anhydrase I, II, VII and IX inhibitors.
Angeli A; Carta F; Bartolucci G; Supuran CT
Bioorg Med Chem; 2017 Jul; 25(13):3567-3573. PubMed ID: 28522267
[TBL] [Abstract][Full Text] [Related]
16. Selenides bearing benzenesulfonamide show potent inhibition activity against carbonic anhydrases from pathogenic bacteria Vibrio cholerae and Burkholderia pseudomallei.
Angeli A; Abbas G; Del Prete S; Capasso C; Supuran CT
Bioorg Chem; 2018 Sep; 79():319-322. PubMed ID: 29803078
[TBL] [Abstract][Full Text] [Related]
17. Synthesis of novel 4-functionalized 1,5-diaryl-1,2,3-triazoles containing benzenesulfonamide moiety as carbonic anhydrase I, II, IV and IX inhibitors.
Vats L; Sharma V; Angeli A; Kumar R; Supuran CT; Sharma PK
Eur J Med Chem; 2018 Apr; 150():678-686. PubMed ID: 29571155
[TBL] [Abstract][Full Text] [Related]
18. 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; 101():334-47. PubMed ID: 26160114
[TBL] [Abstract][Full Text] [Related]
19. Synthesis and human/bacterial carbonic anhydrase inhibition with a series of sulfonamides incorporating phthalimido moieties.
Mohamed MA; Abdel-Aziz AA; Sakr HM; El-Azab AS; Bua S; Supuran CT
Bioorg Med Chem; 2017 Apr; 25(8):2524-2529. PubMed ID: 28318894
[TBL] [Abstract][Full Text] [Related]
20. Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
Del Prete S; Vullo D; De Luca V; Carginale V; Ferraroni M; Osman SM; AlOthman Z; Supuran CT; Capasso C
Bioorg Med Chem; 2016 Mar; 24(5):1115-20. PubMed ID: 26850377
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
