These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
297 related articles for article (PubMed ID: 31112841)
21. 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]
22. Synthesis of novel dipeptide sulfonamide conjugates with effective carbonic anhydrase I, II, IX, and XII inhibitory properties. Buğday N; Küçükbay FZ; Küçükbay H; Bua S; Bartolucci G; Leitans J; Kazaks A; Tars K; Supuran CT Bioorg Chem; 2018 Dec; 81():311-318. PubMed ID: 30176570 [TBL] [Abstract][Full Text] [Related]
23. New anthranilic acid-incorporating N-benzenesulfonamidophthalimides as potent inhibitors of carbonic anhydrases I, II, IX, and XII: Synthesis, in vitro testing, and in silico assessment. El-Azab AS; Abdel-Aziz AA; Bua S; Nocentini A; AlSaif NA; Almehizia AA; Alanazi MM; Hefnawy MM; Supuran CT Eur J Med Chem; 2019 Nov; 181():111573. PubMed ID: 31394463 [TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. 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]
27. 4-Functionalized 1,3-diarylpyrazoles bearing 6-aminosulfonylbenzothiazole moiety as potent inhibitors of carbonic anhydrase isoforms hCA I, II, IX and XII. SitaRam ; Ceruso M; Khloya P; Supuran CT; Sharma PK Bioorg Med Chem; 2014 Dec; 22(24):6945-52. PubMed ID: 25456084 [TBL] [Abstract][Full Text] [Related]
28. Design and synthesis of novel 1,3-diaryltriazene-substituted sulfonamides as potent and selective carbonic anhydrase II inhibitors. Lolak N; Akocak S; Bua S; Koca M; Supuran CT Bioorg Chem; 2018 Apr; 77():542-547. PubMed ID: 29462772 [TBL] [Abstract][Full Text] [Related]
30. A Series of Thiadiazolyl-Benzenesulfonamides Incorporating an Aromatic Tail as Isoform-Selective, Potent Carbonic Anhydrase II/XII Inhibitors. Banoglu E; Ercanlı T; Gür Maz T; Vullo D; Bonardi A; Gratteri P; Supuran CT ChemMedChem; 2022 May; 17(10):e202200056. PubMed ID: 35266325 [TBL] [Abstract][Full Text] [Related]
31. 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; 71():135-47. PubMed ID: 24291567 [TBL] [Abstract][Full Text] [Related]
32. Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating 1,2,4-triazine moieties. Garaj V; Puccetti L; Fasolis G; Winum JY; Montero JL; Scozzafava A; Vullo D; Innocenti A; Supuran CT Bioorg Med Chem Lett; 2004 Nov; 14(21):5427-33. PubMed ID: 15454239 [TBL] [Abstract][Full Text] [Related]
33. 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; 21(17):5130-8. PubMed ID: 23859774 [TBL] [Abstract][Full Text] [Related]
34. Inhibition of tumor-associated human carbonic anhydrase isozymes IX and XII by a new class of substituted-phenylacetamido aromatic sulfonamides. Akdemir A; Güzel-Akdemir O; Scozzafava A; Capasso C; Supuran CT Bioorg Med Chem; 2013 Sep; 21(17):5228-32. PubMed ID: 23842519 [TBL] [Abstract][Full Text] [Related]
35. Biological evaluation, radiosensitizing activity and structural insights of novel halogenated quinazoline-sulfonamide conjugates as selective human carbonic anhydrases IX/XII inhibitors. Ghorab MM; Soliman AM; Bua S; Supuran CT Bioorg Chem; 2021 Feb; 107():104618. PubMed ID: 33485104 [TBL] [Abstract][Full Text] [Related]
36. 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]
37. Discovery of potent anti-convulsant carbonic anhydrase inhibitors: Design, synthesis, in vitro and in vivo appraisal. Mishra CB; Kumari S; Angeli A; Bua S; Buonanno M; Monti SM; Tiwari M; Supuran CT Eur J Med Chem; 2018 Aug; 156():430-443. PubMed ID: 30015076 [TBL] [Abstract][Full Text] [Related]
38. Benzenesulfonamide bearing imidazothiadiazole and thiazolotriazole scaffolds as potent tumor associated human carbonic anhydrase IX and XII inhibitors. Kumar R; Bua S; Ram S; Del Prete S; Capasso C; Supuran CT; Sharma PK Bioorg Med Chem; 2017 Feb; 25(3):1286-1293. PubMed ID: 28065499 [TBL] [Abstract][Full Text] [Related]
39. Development of novel organometallic sulfonamides with N-ethyl or N-methyl benzenesulfonamide units as potential human carbonic anhydrase I, II, IX and XII isoforms' inhibitors: Synthesis, biological evaluation and docking studies. Gallardo M; Arancibia R; Supuran CT; Nocentini A; Villaman D; Toro PM; Muñoz-Osses M; Mascayano C J Inorg Biochem; 2024 Nov; 260():112689. PubMed ID: 39121601 [TBL] [Abstract][Full Text] [Related]
40. Carbonic anhydrase inhibitors: synthesis and inhibition of the human cytosolic isozymes I and II and transmembrane isozymes IX, XII (cancer-associated) and XIV with 4-substituted 3-pyridinesulfonamides. Brzozowski Z; Sławiński J; Saczewski F; Innocenti A; Supuran CT Eur J Med Chem; 2010 Jun; 45(6):2396-404. PubMed ID: 20202722 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]