144 related articles for article (PubMed ID: 36576122)
1. Synthesis, characterization and docking studies of benzenesulfonamide derivatives containing 1,2,3-triazole as potential ınhibitor of carbonic anhydrase I-II enzymes.
Güngör SA; Köse M; Tümer M; Türkeş C; Beydemir Ş
J Biomol Struct Dyn; 2023 Dec; 41(20):10919-10929. PubMed ID: 36576122
[TBL] [Abstract][Full Text] [Related]
2. Discovery of novel benzenesulfonamides incorporating 1,2,3-triazole scaffold as carbonic anhydrase I, II, IX, and XII inhibitors.
Buza A; Türkeş C; Arslan M; Demir Y; Dincer B; Nixha AR; Beydemir Ş
Int J Biol Macromol; 2023 Jun; 239():124232. PubMed ID: 37001773
[TBL] [Abstract][Full Text] [Related]
3. Click chemistry-based synthesis of new benzenesulfonamide derivatives bearing triazole ring as selective carbonic anhydrase II inhibitors.
Ewies EF; Sabry E; Bekheit MS; Fouad MA; Vullo D; Supuran CT
Drug Dev Res; 2022 Sep; 83(6):1281-1291. PubMed ID: 35706360
[TBL] [Abstract][Full Text] [Related]
4. Exploration of 1,2,3-triazole linked benzenesulfonamide derivatives as isoform selective inhibitors of human carbonic anhydrase.
Kakakhan C; Türkeş C; Güleç Ö; Demir Y; Arslan M; Özkemahlı G; Beydemir Ş
Bioorg Med Chem; 2023 Jan; 77():117111. PubMed ID: 36463726
[TBL] [Abstract][Full Text] [Related]
5. Continued exploration and tail approach synthesis of benzenesulfonamides containing triazole and dual triazole moieties as carbonic anhydrase I, II, IV and IX inhibitors.
Vats L; Kumar R; Bua S; Nocentini A; Gratteri P; Supuran CT; Sharma PK
Eur J Med Chem; 2019 Dec; 183():111698. PubMed ID: 31539777
[TBL] [Abstract][Full Text] [Related]
6. Design and synthesis of novel benzenesulfonamide containing 1,2,3-triazoles as potent human carbonic anhydrase isoforms I, II, IV and IX inhibitors.
Kumar R; Vats L; Bua S; Supuran CT; Sharma PK
Eur J Med Chem; 2018 Jul; 155():545-551. PubMed ID: 29909339
[TBL] [Abstract][Full Text] [Related]
7. 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; 127():521-530. PubMed ID: 28109946
[TBL] [Abstract][Full Text] [Related]
8. Synthesis and carbonic anhydrase inhibition studies of sulfonamide based indole-1,2,3-triazole chalcone hybrids.
Singh P; Swain B; Thacker PS; Sigalapalli DK; Purnachander Yadav P; Angeli A; Supuran CT; Arifuddin M
Bioorg Chem; 2020 Jun; 99():103839. PubMed ID: 32289586
[TBL] [Abstract][Full Text] [Related]
9. Investigation of
Camadan Y; Çiçek B; Adem Ş; Çalişir Ü; Akkemik E
J Biomol Struct Dyn; 2022 Sep; 40(15):6965-6973. PubMed ID: 33645441
[TBL] [Abstract][Full Text] [Related]
10. Benzenesulfonamide bearing 1,2,4-triazole scaffolds as potent inhibitors of tumor associated carbonic anhydrase isoforms hCA IX and hCA XII.
SitaRam ; Celik G; Khloya P; Vullo D; Supuran CT; Sharma PK
Bioorg Med Chem; 2014 Mar; 22(6):1873-82. PubMed ID: 24560737
[TBL] [Abstract][Full Text] [Related]
11. Benzenesulfonamides with trisubstituted triazole motif as selective carbonic anhydrase I, II, IV, and IX inhibitors.
Sharma V; Kumar R; Angeli A; Supuran CT; Sharma PK
Arch Pharm (Weinheim); 2023 Jan; 356(1):e2200391. PubMed ID: 36316236
[TBL] [Abstract][Full Text] [Related]
12.
Korkmaz IN; Güller P; Kalın R; Öztekin A; Özdemir H
Curr Comput Aided Drug Des; 2022; 18(5):381-392. PubMed ID: 35984020
[TBL] [Abstract][Full Text] [Related]
13. Novel triazole-sulfonamide bearing pyrimidine moieties with carbonic anhydrase inhibitory action: Design, synthesis, computational and enzyme inhibition studies.
Manzoor S; Petreni A; Raza MK; Supuran CT; Hoda N
Bioorg Med Chem Lett; 2021 Sep; 48():128249. PubMed ID: 34237441
[TBL] [Abstract][Full Text] [Related]
14. Synthesis, biological and molecular dynamics investigations with a series of triazolopyrimidine/triazole-based benzenesulfonamides as novel carbonic anhydrase inhibitors.
Said MA; Eldehna WM; Nocentini A; Bonardi A; Fahim SH; Bua S; Soliman DH; Abdel-Aziz HA; Gratteri P; Abou-Seri SM; Supuran CT
Eur J Med Chem; 2020 Jan; 185():111843. PubMed ID: 31718943
[TBL] [Abstract][Full Text] [Related]
15. Novel Re(I) tricarbonyl coordination compounds based on 2-pyridyl-1,2,3-triazole derivatives bearing a 4-amino-substituted benzenesulfonamide arm: synthesis, crystal structure, computational studies and inhibitory activity against carbonic anhydrase I, II, and IX isoforms†.
Aimene Y; Eychenne R; Mallet-Ladeira S; Saffon N; Winum JY; Nocentini A; Supuran CT; Benoist E; Seridi A
J Enzyme Inhib Med Chem; 2019 Dec; 34(1):773-782. PubMed ID: 30843736
[TBL] [Abstract][Full Text] [Related]
16. Carbonic anhydrase inhibition with a series of novel benzenesulfonamide-triazole conjugates.
El-Gazzar MG; Nafie NH; Nocentini A; Ghorab MM; Heiba HI; Supuran CT
J Enzyme Inhib Med Chem; 2018 Dec; 33(1):1565-1574. PubMed ID: 30274535
[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. 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; 53(6):2401-8. PubMed ID: 20170095
[TBL] [Abstract][Full Text] [Related]
19. Synthesis of some N-aroyl-2-oxindole benzenesulfonamide conjugates with carbonic anhydrase inhibitory activity.
George RF; Bua S; Supuran CT; Awadallah FM
Bioorg Chem; 2020 Mar; 96():103635. PubMed ID: 32028060
[TBL] [Abstract][Full Text] [Related]
20. Exploration of 2-phenylquinoline-4-carboxamide linked benzene sulfonamide derivatives as isoform selective inhibitors of transmembrane human carbonic anhydrases.
Swain B; Sahoo SK; Singh P; Angeli A; Yaddanapudi VM; Supuran CT; Arifuddin M
Eur J Med Chem; 2022 Apr; 234():114247. PubMed ID: 35305463
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]