Mazzei M - Search Results

1

Synthesis and biological evaluation of novel heterocyclic ionone-like derivatives as anti-inflammatory agents.

Balbi A, Anzaldi M, Mazzei M, Miele M, Bertolotto M, Ottonello L, Dallegri F. Balbi A, et al. Among authors: mazzei m. Bioorg Med Chem. 2006 Aug 1;14(15):5152-60. doi: 10.1016/j.bmc.2006.04.007. Epub 2006 May 8. Bioorg Med Chem. 2006. PMID: 16682209

2

Activity of Mannich bases of 7-hydroxycoumarin against Flaviviridae.

Mazzei M, Nieddu E, Miele M, Balbi A, Ferrone M, Fermeglia M, Mazzei MT, Pricl S, La Colla P, Marongiu F, Ibba C, Loddo R. Mazzei M, et al. Among authors: mazzei mt. Bioorg Med Chem. 2008 Mar 1;16(5):2591-605. doi: 10.1016/j.bmc.2007.11.045. Epub 2007 Nov 22. Bioorg Med Chem. 2008. PMID: 18054491

3

Synthesis and biological evaluation of novel pyrazole derivatives with anticancer activity.

Balbi A, Anzaldi M, Macciò C, Aiello C, Mazzei M, Gangemi R, Castagnola P, Miele M, Rosano C, Viale M. Balbi A, et al. Among authors: mazzei m. Eur J Med Chem. 2011 Nov;46(11):5293-309. doi: 10.1016/j.ejmech.2011.08.014. Epub 2011 Aug 31. Eur J Med Chem. 2011. PMID: 21920636

4

Synthesis and hybridization properties of the conjugates of oligonucleotides and stabilization agents. Part 3.

Sottofattori E, Anzaldi M, Mazzei M, Miele M, Balbi A, Pyshnyi DS, Zakharova OD, Abramova TV. Sottofattori E, et al. Among authors: mazzei m. Bioorg Med Chem. 2005 Mar 1;13(5):1515-22. doi: 10.1016/j.bmc.2004.12.030. Bioorg Med Chem. 2005. PMID: 15698767

5

Antiproliferative and proapoptotic activities of a new class of pyrazole derivatives in HL-60 cells.

Anzaldi M, Macciò C, Mazzei M, Bertolotto M, Ottonello L, Dallegri F, Balbi A. Anzaldi M, et al. Among authors: mazzei m. Chem Biodivers. 2009 Oct;6(10):1674-87. doi: 10.1002/cbdv.200800354. Chem Biodivers. 2009. PMID: 19842131

6

Unsymmetrical methylene derivatives of indoles as antiproliferative agents.

Mazzei M, Miele M, Nieddu E, Barbieri F, Bruzzo C, Alama A. Mazzei M, et al. Eur J Med Chem. 2001 Nov-Dec;36(11-12):915-23. Eur J Med Chem. 2001. PMID: 11755234

7

The search for a common structural moiety among selected pharmacological correctors of the mutant CFTR chloride channel.

Nieddu E, Pollarolo B, Mazzei MT, Anzaldi M, Schenone S, Pedemonte N, Pesce E, Galietta LJ, Mazzei M. Nieddu E, et al. Among authors: mazzei mt, mazzei m. Future Med Chem. 2014;6(17):1857-68. doi: 10.4155/fmc.14.118. Future Med Chem. 2014. PMID: 25495980

8

Synthesis and hybridization properties of the conjugates of oligonucleotides and stabilization agents--II.

Balbi A, Sottofattori E, Grandi T, Mazzei M, Pyshnyi DS, Lokhov SG, Lebedev AV. Balbi A, et al. Among authors: mazzei m. Bioorg Med Chem. 1997 Oct;5(10):1903-10. doi: 10.1016/s0968-0896(97)00127-2. Bioorg Med Chem. 1997. PMID: 9370034

9

[Derivatives of pyrimidine 1,2-condensate. IV. Synthesis and pharmacological properties of the N,N-disubstituted 4-amino-2H-pyrido(1,2-a)pyrimidin- 2-ones and 2-amino-4H-pyrido(1,2-a)pyrmidin-4-ones].

Di Braccio M, Roma G, Mazzei M, Balbi A, Schiantarelli P, Cadel S, Bongrani S. Di Braccio M, et al. Among authors: mazzei m. Farmaco Sci. 1988 Sep;43(9):705-23. Farmaco Sci. 1988. PMID: 3229496 Italian.

10

Asymmetric 4-aryl-1,4-dihydropyridines potentiate mutant cystic fibrosis transmembrane conductance regulator (CFTR).

Giampieri M, Vanthuyne N, Nieddu E, Mazzei MT, Anzaldi M, Pedemonte N, Galietta LJ, Roussel C, Mazzei M. Giampieri M, et al. Among authors: mazzei mt, mazzei m. ChemMedChem. 2012 Oct;7(10):1799-807. doi: 10.1002/cmdc.201200311. Epub 2012 Aug 27. ChemMedChem. 2012. PMID: 22927224

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