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.
336 related articles for article (PubMed ID: 32203788)
61. Sulfonamide-incorporated bis(α-aminophosphonates) as promising carbonic anhydrase inhibitors: Design, synthesis, biological evaluation, and X-ray crystallographic studies. Sobati M; Abdoli M; Angeli A; Bonardi A; Ferraroni M; Supuran CT; Žalubovskis R Arch Pharm (Weinheim); 2024 Jul; 357(7):e2400038. PubMed ID: 38498884 [TBL] [Abstract][Full Text] [Related]
62. Exploring structure-activity relationship of S-substituted 2-mercaptoquinazolin-4(3H)-one including 4-ethylbenzenesulfonamides as human carbonic anhydrase inhibitors. El-Azab AS; Abdel-Aziz AA; Ahmed HEA; Bua S; Nocentini A; AlSaif NA; Obaidullah AJ; Hefnawy MM; Supuran CT J Enzyme Inhib Med Chem; 2020 Dec; 35(1):598-609. PubMed ID: 32009479 [TBL] [Abstract][Full Text] [Related]
63. New series of sulfonamides containing amino acid moiety act as effective and selective inhibitors of tumor-associated carbonic anhydrase XII. Ceruso M; Bragagni M; AlOthman Z; Osman SM; Supuran CT J Enzyme Inhib Med Chem; 2015 Jun; 30(3):430-4. PubMed ID: 25089707 [TBL] [Abstract][Full Text] [Related]
64. Synthesis and biological evaluation of novel 8-substituted quinoline-2-carboxamides as carbonic anhydrase inhibitors. Thacker PS; Shaikh P; Angeli A; Arifuddin M; Supuran CT J Enzyme Inhib Med Chem; 2019 Dec; 34(1):1172-1177. PubMed ID: 31218888 [TBL] [Abstract][Full Text] [Related]
65. Synthesis, molecular modelling and QSAR study of new Said MF; George RF; Petreni A; Supuran CT; Mohamed NM J Enzyme Inhib Med Chem; 2022 Dec; 37(1):701-717. PubMed ID: 35168458 [TBL] [Abstract][Full Text] [Related]
66. 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]
67. Synthesis and biological evaluation of some coumarin hybrids as selective carbonic anhydrase IX and XII inhibitors. Thacker PS; Sridhar Goud N; Argulwar OS; Soman J; Angeli A; Alvala M; Arifuddin M; Supuran CT Bioorg Chem; 2020 Nov; 104():104272. PubMed ID: 32961467 [TBL] [Abstract][Full Text] [Related]
68. Synthesis and exploration of 2-morpholino-4-phenylthiazol-5-yl acrylamide derivatives for their effects against carbonic anhydrase I, II, IX and XII isoforms as a non-sulfonamide class of inhibitors. Swain B; Singh Digwal C; Angeli A; Alvala M; Singh P; Supuran CT; Arifuddin M Bioorg Med Chem; 2019 Nov; 27(21):115090. PubMed ID: 31515058 [TBL] [Abstract][Full Text] [Related]
69. Synthesis of isoxazole-containing sulfonamides with potent carbonic anhydrase II and VII inhibitory properties. Altug C; Güneş H; Nocentini A; Monti SM; Buonanno M; Supuran CT Bioorg Med Chem; 2017 Feb; 25(4):1456-1464. PubMed ID: 28111158 [TBL] [Abstract][Full Text] [Related]
70. Syntesis of thio- and seleno-acetamides bearing benzenesulfonamide as potent inhibitors of human carbonic anhydrase II and XII. Tanini D; Capperucci A; Scopelliti M; Milaneschi A; Angeli A; Supuran CT Bioorg Chem; 2019 Aug; 89():102984. PubMed ID: 31112841 [TBL] [Abstract][Full Text] [Related]
71. Carbonic anhydrase inhibitors: novel sulfonamides incorporating 1,3,5-triazine moieties as inhibitors of the cytosolic and tumour-associated carbonic anhydrase isozymes I, II and IX. Garaj V; Puccetti L; Fasolis G; Winum JY; Montero JL; Scozzafava A; Vullo D; Innocenti A; Supuran CT Bioorg Med Chem Lett; 2005 Jun; 15(12):3102-8. PubMed ID: 15905091 [TBL] [Abstract][Full Text] [Related]
72. Carbonic anhydrase inhibitors: synthesis and inhibition of the human carbonic anhydrase isoforms I, II, VII, IX and XII with benzene sulfonamides incorporating 4,5,6,7-tetrabromophthalimide moiety. Sethi KK; Vullo D; Verma SM; Tanç M; Carta F; Supuran CT Bioorg Med Chem; 2013 Oct; 21(19):5973-82. PubMed ID: 23965175 [TBL] [Abstract][Full Text] [Related]
73. Appliance of the piperidinyl-hydrazidoureido linker to benzenesulfonamide compounds: Synthesis, in vitro and in silico evaluation of potent carbonic anhydrase II, IX and XII inhibitors. Moi D; Nocentini A; Deplano A; Osman SM; AlOthman ZA; Piras V; Balboni G; Supuran CT; Onnis V Bioorg Chem; 2020 May; 98():103728. PubMed ID: 32182519 [TBL] [Abstract][Full Text] [Related]
74. 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]
75. New anticancer drug candidates sulfonamides as selective hCA IX or hCA XII inhibitors. Gul HI; Yamali C; Sakagami H; Angeli A; Leitans J; Kazaks A; Tars K; Ozgun DO; Supuran CT Bioorg Chem; 2018 Apr; 77():411-419. PubMed ID: 29427856 [TBL] [Abstract][Full Text] [Related]
76. Inhibition Studies on Carbonic Anhydrase Isoforms I, II, IX, and XII with a Series of Sulfaguanidines. Abdoli M; De Luca V; Capasso C; Supuran CT; Žalubovskis R ChemMedChem; 2023 Mar; 18(6):e202200658. PubMed ID: 36691902 [TBL] [Abstract][Full Text] [Related]
77. Discovery of novel aminosaccharide-based sulfonamide derivatives as potential carbonic anhydrase II inhibitors. Wang X; Feng YL; Zhao XY; An R; Cao C; Guo MB; Zhang R; Wang YX; Hou Z; Guo C Bioorg Med Chem Lett; 2021 Dec; 53():128420. PubMed ID: 34728369 [TBL] [Abstract][Full Text] [Related]
78. Novel synthesized SLC-0111 thiazole and thiadiazole analogues: Determination of their carbonic anhydrase inhibitory activity and molecular modeling studies. Abo-Ashour MF; Eldehna WM; Nocentini A; Ibrahim HS; Bua S; Abdel-Aziz HA; Abou-Seri SM; Supuran CT Bioorg Chem; 2019 Jun; 87():794-802. PubMed ID: 30978604 [TBL] [Abstract][Full Text] [Related]