Ferraroni M - Search Results

1

Mechanisms of the Antiproliferative and Antitumor Activity of Novel Telomerase-Carbonic Anhydrase Dual-Hybrid Inhibitors.

Plyasova AA, Berrino E, Khan II, Veselovsky AV, Pokrovsky VS, Angeli A, Ferraroni M, Supuran CT, Pokrovskaya MV, Alexandrova SS, Gladilina YA, Sokolov NN, Hilal A, Carta F, Zhdanov DD. Plyasova AA, et al. Among authors: ferraroni m. J Med Chem. 2021 Aug 12;64(15):11432-11444. doi: 10.1021/acs.jmedchem.1c00756. Epub 2021 Jul 20. J Med Chem. 2021. PMID: 34283610

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

Synthesis and cholinergic affinity of diastereomeric and enantiomeric isomers of 1-methyl-2-(2-methyl-1,3-dioxolan-4-yl)- pyrrolidine, 1-methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine and of Their iodomethylates.

Dei S, Bellucci C, Buccioni M, Ferraroni M, Gualtieri F, Guandalini L, Manetti D, Matucci R, Romanelli MN, Scapecchi S, Teodori E. Dei S, et al. Among authors: ferraroni m. Bioorg Med Chem. 2003 Jul 17;11(14):3153-64. doi: 10.1016/s0968-0896(03)00236-0. Bioorg Med Chem. 2003. PMID: 12818678

4

Synthesis, affinity profile, and functional activity of muscarinic antagonists with a 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine structure.

Dei S, Bellucci C, Buccioni M, Ferraroni M, Guandalini L, Manetti D, Martini E, Marucci G, Matucci R, Nesi M, Romanelli MN, Scapecchi S, Teodori E. Dei S, et al. Among authors: ferraroni m. J Med Chem. 2007 Mar 22;50(6):1409-13. doi: 10.1021/jm061374r. Epub 2007 Feb 17. J Med Chem. 2007. PMID: 17305327

5

Muscarinic antagonists with multiple stereocenters: Synthesis, affinity profile and functional activity of isomeric 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine sulfoxide derivatives.

Dei S, Bellucci C, Buccioni M, Ferraroni M, Guandalini L, Manetti D, Marucci G, Matucci R, Nesi M, Romanelli MN, Scapecchi S, Teodori E. Dei S, et al. Among authors: ferraroni m. Bioorg Med Chem. 2008 May 15;16(10):5490-500. doi: 10.1016/j.bmc.2008.04.013. Epub 2008 Apr 11. Bioorg Med Chem. 2008. PMID: 18455407

6

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

7

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

8

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

9

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

10

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

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