Supuran CT - Search Results

1

Discovery of new sulfonamide-tethered 2-aryl-4-anilinoquinazolines as the first-in-class dual carbonic anhydrase and EGFR inhibitors.

Eldehna WM, Elsayed ZM, Ammara A, El Hassab MA, Almahli H, Fares M, Nocentini A, Supuran CT, Abou-Seri SM. Eldehna WM, et al. Among authors: supuran ct. Int J Biol Macromol. 2024 Nov;279(Pt 2):135010. doi: 10.1016/j.ijbiomac.2024.135010. Epub 2024 Aug 26. Int J Biol Macromol. 2024. PMID: 39197616

2

Isatin-pyrazole benzenesulfonamide hybrids potently inhibit tumor-associated carbonic anhydrase isoforms IX and XII.

Ibrahim HS, Abou-Seri SM, Tanc M, Elaasser MM, Abdel-Aziz HA, Supuran CT. Ibrahim HS, et al. Among authors: supuran ct. Eur J Med Chem. 2015 Oct 20;103:583-93. doi: 10.1016/j.ejmech.2015.09.021. Epub 2015 Sep 16. Eur J Med Chem. 2015. PMID: 26408817

3

Click-tailed coumarins with potent and selective inhibitory action against the tumor-associated carbonic anhydrases IX and XII.

Nocentini A, Carta F, Ceruso M, Bartolucci G, Supuran CT. Nocentini A, et al. Among authors: supuran ct. Bioorg Med Chem. 2015 Nov 1;23(21):6955-66. doi: 10.1016/j.bmc.2015.09.041. Epub 2015 Sep 28. Bioorg Med Chem. 2015. PMID: 26432607

4

7-Aryl-triazolyl-substituted sulfocoumarins are potent, selective inhibitors of the tumor-associated carbonic anhydrase IX and XII.

Nocentini A, Ceruso M, Carta F, Supuran CT. Nocentini A, et al. Among authors: supuran ct. J Enzyme Inhib Med Chem. 2016 Dec;31(6):1226-33. doi: 10.3109/14756366.2015.1115401. Epub 2015 Dec 18. J Enzyme Inhib Med Chem. 2016. PMID: 26681367 Free article.

5

Development of certain new 2-substituted-quinazolin-4-yl-aminobenzenesulfonamide as potential antitumor agents.

Alafeefy AM, Ahmad R, Abdulla M, Eldehna WM, Al-Tamimi AM, Abdel-Aziz HA, Al-Obaid O, Carta F, Al-Kahtani AA, Supuran CT. Alafeefy AM, et al. Among authors: supuran ct. Eur J Med Chem. 2016 Feb 15;109:247-53. doi: 10.1016/j.ejmech.2016.01.001. Epub 2016 Jan 6. Eur J Med Chem. 2016. PMID: 26774930

6

Amido/ureidosubstituted benzenesulfonamides-isatin conjugates as low nanomolar/subnanomolar inhibitors of the tumor-associated carbonic anhydrase isoform XII.

Eldehna WM, Fares M, Ceruso M, Ghabbour HA, Abou-Seri SM, Abdel-Aziz HA, Abou El Ella DA, Supuran CT. Eldehna WM, et al. Among authors: supuran ct. Eur J Med Chem. 2016 Mar 3;110:259-66. doi: 10.1016/j.ejmech.2016.01.030. Epub 2016 Jan 20. Eur J Med Chem. 2016. PMID: 26840366

7

N-Nitrosulfonamides: A new chemotype for carbonic anhydrase inhibition.

Nocentini A, Vullo D, Bartolucci G, Supuran CT. Nocentini A, et al. Among authors: supuran ct. Bioorg Med Chem. 2016 Aug 15;24(16):3612-7. doi: 10.1016/j.bmc.2016.05.072. Epub 2016 May 30. Bioorg Med Chem. 2016. PMID: 27290692

8

Intramolecular oxidative deselenization of acylselenoureas: a facile synthesis of benzoxazole amides and carbonic anhydrase inhibitors.

Angeli A, Peat TS, Bartolucci G, Nocentini A, Supuran CT, Carta F. Angeli A, et al. Among authors: supuran ct. Org Biomol Chem. 2016 Dec 28;14(48):11353-11356. doi: 10.1039/c6ob02299e. Epub 2016 Nov 28. Org Biomol Chem. 2016. PMID: 27892589

9

Benzenesulfonamides Incorporating Flexible Triazole Moieties Are Highly Effective Carbonic Anhydrase Inhibitors: Synthesis and Kinetic, Crystallographic, Computational, and Intraocular Pressure Lowering Investigations.

Nocentini A, Ferraroni M, Carta F, Ceruso M, Gratteri P, Lanzi C, Masini E, Supuran CT. Nocentini A, et al. Among authors: supuran ct. J Med Chem. 2016 Dec 8;59(23):10692-10704. doi: 10.1021/acs.jmedchem.6b01389. Epub 2016 Nov 21. J Med Chem. 2016. PMID: 27933963

10

Dithiocarbamates effectively inhibit the β-carbonic anhydrase from the dandruff-producing fungus Malassezia globosa.

Vullo D, Del Prete S, Nocentini A, Osman SM, AlOthman Z, Capasso C, Bozdag M, Carta F, Gratteri P, Supuran CT. Vullo D, et al. Among authors: supuran ct. Bioorg Med Chem. 2017 Feb 1;25(3):1260-1265. doi: 10.1016/j.bmc.2016.12.040. Epub 2016 Dec 27. Bioorg Med Chem. 2017. PMID: 28057408

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