Carta F - Search Results

1

Lasamide, a Potent Human Carbonic Anhydrase Inhibitor from the Market: Inhibition Profiling and Crystallographic Studies.

Baroni C, D'Agostino I, Renzi G, Kilbile JT, Tamboli Y, Ferraroni M, Carradori S, Capasso C, Carta F, Supuran CT. Baroni C, et al. Among authors: carta f. ACS Med Chem Lett. 2024 Sep 30;15(10):1749-1755. doi: 10.1021/acsmedchemlett.4c00341. eCollection 2024 Oct 10. ACS Med Chem Lett. 2024. PMID: 39411526

2

Carbonic anhydrase inhibitors: inhibition of cytosolic carbonic anhydrase isozymes II and VII with simple aromatic sulfonamides and some azo dyes.

Carta F, Pothen B, Maresca A, Tiwari M, Singh V, Supuran CT. Carta F, et al. Chem Biol Drug Des. 2009 Aug;74(2):196-202. doi: 10.1111/j.1747-0285.2009.00842.x. Epub 2009 Jun 22. Chem Biol Drug Des. 2009. PMID: 19549076

3

Carbonic anhydrase inhibitors. Inhibition of the Rv1284 and Rv3273 beta-carbonic anhydrases from Mycobacterium tuberculosis with diazenylbenzenesulfonamides.

Maresca A, Carta F, Vullo D, Scozzafava A, Supuran CT. Maresca A, et al. Among authors: carta f. Bioorg Med Chem Lett. 2009 Sep 1;19(17):4929-32. doi: 10.1016/j.bmcl.2009.07.088. Epub 2009 Jul 22. Bioorg Med Chem Lett. 2009. PMID: 19651511

4

Carbonic anhydrase inhibitors. Diazenylbenzenesulfonamides are potent and selective inhibitors of the tumor-associated isozymes IX and XII over the cytosolic isoforms I and II.

Carta F, Maresca A, Scozzafava A, Vullo D, Supuran CT. Carta F, et al. Bioorg Med Chem. 2009 Oct 15;17(20):7093-9. doi: 10.1016/j.bmc.2009.09.003. Epub 2009 Sep 6. Bioorg Med Chem. 2009. PMID: 19773173

5

Carbonic anhydrase inhibitors. Characterization and inhibition studies of the most active beta-carbonic anhydrase from Mycobacterium tuberculosis, Rv3588c.

Carta F, Maresca A, Covarrubias AS, Mowbray SL, Jones TA, Supuran CT. Carta F, et al. Bioorg Med Chem Lett. 2009 Dec 1;19(23):6649-54. doi: 10.1016/j.bmcl.2009.10.009. Epub 2009 Oct 7. Bioorg Med Chem Lett. 2009. PMID: 19846301

6

Polyamines inhibit carbonic anhydrases by anchoring to the zinc-coordinated water molecule.

Carta F, Temperini C, Innocenti A, Scozzafava A, Kaila K, Supuran CT. Carta F, et al. J Med Chem. 2010 Aug 12;53(15):5511-22. doi: 10.1021/jm1003667. J Med Chem. 2010. PMID: 20590092

7

The β-carbonic anhydrases from Mycobacterium tuberculosis as drug targets.

Nishimori I, Minakuchi T, Maresca A, Carta F, Scozzafava A, Supuran CT. Nishimori I, et al. Among authors: carta f. Curr Pharm Des. 2010;16(29):3300-9. doi: 10.2174/138161210793429814. Curr Pharm Des. 2010. PMID: 20819064 Review.

8

Inhibition of β-carbonic anhydrases with ureido-substituted benzenesulfonamides.

Pacchiano F, Carta F, Vullo D, Scozzafava A, Supuran CT. Pacchiano F, et al. Among authors: carta f. Bioorg Med Chem Lett. 2011 Jan 1;21(1):102-5. doi: 10.1016/j.bmcl.2010.11.064. Epub 2010 Nov 20. Bioorg Med Chem Lett. 2011. PMID: 21145236

9

Ureido-substituted benzenesulfonamides potently inhibit carbonic anhydrase IX and show antimetastatic activity in a model of breast cancer metastasis.

Pacchiano F, Carta F, McDonald PC, Lou Y, Vullo D, Scozzafava A, Dedhar S, Supuran CT. Pacchiano F, et al. Among authors: carta f. J Med Chem. 2011 Mar 24;54(6):1896-902. doi: 10.1021/jm101541x. Epub 2011 Mar 1. J Med Chem. 2011. PMID: 21361354

10

Carbonic anhydrase inhibitors. Inhibition of the β-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with branched aliphatic/aromatic carboxylates and their derivatives.

Carta F, Innocenti A, Hall RA, Mühlschlegel FA, Scozzafava A, Supuran CT. Carta F, et al. Bioorg Med Chem Lett. 2011 Apr 15;21(8):2521-6. doi: 10.1016/j.bmcl.2011.02.057. Epub 2011 Feb 17. Bioorg Med Chem Lett. 2011. PMID: 21402476

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