Ferraroni M - Search Results

1

Exploring the Polypharmacological Potential of PCI-27483: A Selective Inhibitor of Carbonic Anhydrases IX and XII.

D'Agostino I, Bonardi A, Ferraroni M, Gratteri P, Angeli A, Supuran CT. D'Agostino I, et al. Among authors: ferraroni m. ACS Med Chem Lett. 2024 Oct 21;15(11):2042-2045. doi: 10.1021/acsmedchemlett.4c00443. eCollection 2024 Nov 14. ACS Med Chem Lett. 2024. PMID: 39563799

2

Crystal structure of a zinc-activated variant of human carbonic anhydrase I, CA I Michigan 1: evidence for a second zinc binding site involving arginine coordination.

Ferraroni M, Tilli S, Briganti F, Chegwidden WR, Supuran CT, Wiebauer KE, Tashian RE, Scozzafava A. Ferraroni M, et al. Biochemistry. 2002 May 21;41(20):6237-44. doi: 10.1021/bi0120446. Biochemistry. 2002. PMID: 12009884

3

X-Ray diffraction analyses of the natural isoquinoline alkaloids Berberine and Sanguinarine complexed with double helix DNA d(CGTACG).

Ferraroni M, Bazzicalupi C, Bilia AR, Gratteri P. Ferraroni M, et al. Chem Commun (Camb). 2011 May 7;47(17):4917-9. doi: 10.1039/c1cc10971e. Epub 2011 Mar 22. Chem Commun (Camb). 2011. PMID: 21431128

4

The crystal structure of human telomeric DNA complexed with berberine: an interesting case of stacked ligand to G-tetrad ratio higher than 1:1.

Bazzicalupi C, Ferraroni M, Bilia AR, Scheggi F, Gratteri P. Bazzicalupi C, et al. Among authors: ferraroni m. Nucleic Acids Res. 2013 Jan 7;41(1):632-8. doi: 10.1093/nar/gks1001. Epub 2012 Oct 26. Nucleic Acids Res. 2013. PMID: 23104378 Free PMC article.

5

Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: solution and X-ray crystallographic studies.

Bozdag M, Ferraroni M, Nuti E, Vullo D, Rossello A, Carta F, Scozzafava A, Supuran CT. Bozdag M, et al. Among authors: ferraroni m. Bioorg Med Chem. 2014 Jan 1;22(1):334-40. doi: 10.1016/j.bmc.2013.11.016. Epub 2013 Nov 18. Bioorg Med Chem. 2014. PMID: 24300919

6

Structural insights on carbonic anhydrase inhibitory action, isoform selectivity, and potency of sulfonamides and coumarins incorporating arylsulfonylureido groups.

Bozdag M, Ferraroni M, Carta F, Vullo D, Lucarini L, Orlandini E, Rossello A, Nuti E, Scozzafava A, Masini E, Supuran CT. Bozdag M, et al. Among authors: ferraroni m. J Med Chem. 2014 Nov 13;57(21):9152-67. doi: 10.1021/jm501314c. Epub 2014 Oct 17. J Med Chem. 2014. PMID: 25310626

7

Crystal structure and kinetic studies of a tetrameric type II β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.

Ferraroni M, Del Prete S, Vullo D, Capasso C, Supuran CT. Ferraroni M, et al. Acta Crystallogr D Biol Crystallogr. 2015 Dec 1;71(Pt 12):2449-56. doi: 10.1107/S1399004715018635. Epub 2015 Nov 26. Acta Crystallogr D Biol Crystallogr. 2015. PMID: 26627652

8

Fluorescent sulfonamide carbonic anhydrase inhibitors incorporating 1,2,3-triazole moieties: Kinetic and X-ray crystallographic studies.

Carta F, Ferraroni M, Scozzafava A, Supuran CT. Carta F, et al. Among authors: ferraroni m. Bioorg Med Chem. 2016 Jan 15;24(2):104-12. doi: 10.1016/j.bmc.2015.11.031. Epub 2015 Nov 25. Bioorg Med Chem. 2016. PMID: 26682703

9

Thioxocoumarins Show an Alternative Carbonic Anhydrase Inhibition Mechanism Compared to Coumarins.

Ferraroni M, Carta F, Scozzafava A, Supuran CT. Ferraroni M, et al. J Med Chem. 2016 Jan 14;59(1):462-73. doi: 10.1021/acs.jmedchem.5b01720. Epub 2015 Dec 29. J Med Chem. 2016. PMID: 26688270

10

4-Arylbenzenesulfonamides as Human Carbonic Anhydrase Inhibitors (hCAIs): Synthesis by Pd Nanocatalyst-Mediated Suzuki-Miyaura Reaction, Enzyme Inhibition, and X-ray Crystallographic Studies.

Cornelio B, Laronze-Cochard M, Ceruso M, Ferraroni M, Rance GA, Carta F, Khlobystov AN, Fontana A, Supuran CT, Sapi J. Cornelio B, et al. Among authors: ferraroni m. J Med Chem. 2016 Jan 28;59(2):721-32. doi: 10.1021/acs.jmedchem.5b01771. Epub 2016 Jan 15. J Med Chem. 2016. PMID: 26741028

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