Nuti E - Search Results

1

Development of Thioaryl-Based Matrix Metalloproteinase-12 Inhibitors with Alternative Zinc-Binding Groups: Synthesis, Potentiometric, NMR, and Crystallographic Studies.

Nuti E, Cuffaro D, Bernardini E, Camodeca C, Panelli L, Chaves S, Ciccone L, Tepshi L, Vera L, Orlandini E, Nencetti S, Stura EA, Santos MA, Dive V, Rossello A. Nuti E, et al. J Med Chem. 2018 May 24;61(10):4421-4435. doi: 10.1021/acs.jmedchem.8b00096. Epub 2018 May 16. J Med Chem. 2018. PMID: 29727184

2

New N-arylsulfonyl-N-alkoxyaminoacetohydroxamic acids as selective inhibitors of gelatinase A (MMP-2).

Rossello A, Nuti E, Orlandini E, Carelli P, Rapposelli S, Macchia M, Minutolo F, Carbonaro L, Albini A, Benelli R, Cercignani G, Murphy G, Balsamo A. Rossello A, et al. Among authors: nuti e. Bioorg Med Chem. 2004 May 1;12(9):2441-50. doi: 10.1016/j.bmc.2004.01.047. Bioorg Med Chem. 2004. PMID: 15080939

3

Synthesis and antimicrobial activity of new 7 beta-(benzo[a]dihydrocarbazolyloxyacetyl)-substituted cephalosporins.

Rossello A, Orlandini E, Nuti E, Rapposelli S, Macchia M, Di Modugno E, Balsamo A. Rossello A, et al. Among authors: nuti e. Farmaco. 2004 Sep;59(9):691-6. doi: 10.1016/j.farmac.2004.05.001. Farmaco. 2004. PMID: 15337434

4

N-i-Propoxy-N-biphenylsulfonylaminobutylhydroxamic acids as potent and selective inhibitors of MMP-2 and MT1-MMP.

Rossello A, Nuti E, Carelli P, Orlandini E, Macchia M, Nencetti S, Zandomeneghi M, Balzano F, Uccello Barretta G, Albini A, Benelli R, Cercignani G, Murphy G, Balsamo A. Rossello A, et al. Among authors: nuti e. Bioorg Med Chem Lett. 2005 Mar 1;15(5):1321-6. doi: 10.1016/j.bmcl.2005.01.024. Bioorg Med Chem Lett. 2005. PMID: 15713379

5

A new development of matrix metalloproteinase inhibitors: twin hydroxamic acids as potent inhibitors of MMPs.

Rossello A, Nuti E, Catalani MP, Carelli P, Orlandini E, Rapposelli S, Tuccinardi T, Atkinson SJ, Murphy G, Balsamo A. Rossello A, et al. Among authors: nuti e. Bioorg Med Chem Lett. 2005 May 2;15(9):2311-4. doi: 10.1016/j.bmcl.2005.03.002. Bioorg Med Chem Lett. 2005. PMID: 15837315

6

Amber force field implementation, molecular modelling study, synthesis and MMP-1/MMP-2 inhibition profile of (R)- and (S)-N-hydroxy-2-(N-isopropoxybiphenyl-4-ylsulfonamido)-3-methylbutanamides.

Tuccinardi T, Martinelli A, Nuti E, Carelli P, Balzano F, Uccello-Barretta G, Murphy G, Rossello A. Tuccinardi T, et al. Among authors: nuti e. Bioorg Med Chem. 2006 Jun 15;14(12):4260-76. doi: 10.1016/j.bmc.2006.01.056. Epub 2006 Feb 17. Bioorg Med Chem. 2006. PMID: 16483784

7

alpha-Biphenylsulfonylamino 2-methylpropyl phosphonates: enantioselective synthesis and selective inhibition of MMPs.

Biasone A, Tortorella P, Campestre C, Agamennone M, Preziuso S, Chiappini M, Nuti E, Carelli P, Rossello A, Mazza F, Gallina C. Biasone A, et al. Among authors: nuti e. Bioorg Med Chem. 2007 Jan 15;15(2):791-9. doi: 10.1016/j.bmc.2006.10.047. Epub 2006 Oct 25. Bioorg Med Chem. 2007. PMID: 17088065

8

Methotrexate gamma-hydroxamate derivatives as potential dual target antitumor drugs.

Santos MA, Enyedy EA, Nuti E, Rossello A, Krupenko NI, Krupenko SA. Santos MA, et al. Among authors: nuti e. Bioorg Med Chem. 2007 Feb 1;15(3):1266-74. doi: 10.1016/j.bmc.2006.11.017. Epub 2006 Nov 14. Bioorg Med Chem. 2007. PMID: 17127067

9

Carbonic anhydrase and matrix metalloproteinase inhibitors. Inhibition of human tumor-associated isozymes IX and cytosolic isozyme I and II with sulfonylated hydroxamates.

Nuti E, Orlandini E, Nencetti S, Rossello A, Innocenti A, Scozzafava A, Supuran CT. Nuti E, et al. Bioorg Med Chem. 2007 Mar 15;15(6):2298-311. doi: 10.1016/j.bmc.2007.01.023. Epub 2007 Jan 19. Bioorg Med Chem. 2007. PMID: 17276072

10

Analysis of human carbonic anhydrase II: docking reliability and receptor-based 3D-QSAR study.

Tuccinardi T, Nuti E, Ortore G, Supuran CT, Rossello A, Martinelli A. Tuccinardi T, et al. Among authors: nuti e. J Chem Inf Model. 2007 Mar-Apr;47(2):515-25. doi: 10.1021/ci600469w. Epub 2007 Feb 13. J Chem Inf Model. 2007. PMID: 17295464

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