Sbardella G - Search Results

1

The emerging role of lysine methyltransferase SETD8 in human diseases.

Milite C, Feoli A, Viviano M, Rescigno D, Cianciulli A, Balzano AL, Mai A, Castellano S, Sbardella G. Milite C, et al. Among authors: sbardella g. Clin Epigenetics. 2016 Sep 22;8:102. doi: 10.1186/s13148-016-0268-4. eCollection 2016. Clin Epigenetics. 2016. PMID: 27688818 Free PMC article. Review.

2

Synthesis and anti-HIV-1 activity of thio analogues of dihydroalkoxybenzyloxopyrimidines.

Mai A, Artico M, Sbardella G, Massa S, Loi AG, Tramontano E, Scano P, La Colla P. Mai A, et al. Among authors: sbardella g. J Med Chem. 1995 Aug 18;38(17):3258-63. doi: 10.1021/jm00017a010. J Med Chem. 1995. PMID: 7650679

3

Dihydro(alkylthio)(naphthylmethyl)oxopyrimidines: novel non-nucleoside reverse transcriptase inhibitors of the S-DABO series.

Mai A, Artico M, Sbardella G, Quartarone S, Massa S, Loi AG, De Montis A, Scintu F, Putzolu M, La Colla P. Mai A, et al. Among authors: sbardella g. J Med Chem. 1997 May 9;40(10):1447-54. doi: 10.1021/jm960802y. J Med Chem. 1997. PMID: 9154967

4

N-[4-(1,1'-biphenyl)methyl]-4-(4-thiomorpholinylmethyl) benzenamines as non-oxazolidinone analogues of antimycobacterial U-100480.

Artico M, Mai A, Sbardella G, Massa S, Lampis G, Deidda D, Pompei R. Artico M, et al. Among authors: sbardella g. Bioorg Med Chem Lett. 1998 Jun 16;8(12):1493-8. doi: 10.1016/s0960-894x(98)00248-0. Bioorg Med Chem Lett. 1998. PMID: 9873376

5

5-Alkyl-2-(alkylthio)-6-(2,6-dihalophenylmethyl)-3, 4-dihydropyrimidin-4(3H)-ones: novel potent and selective dihydro-alkoxy-benzyl-oxopyrimidine derivatives.

Mai A, Artico M, Sbardella G, Massa S, Novellino E, Greco G, Loi AG, Tramontano E, Marongiu ME, La Colla P. Mai A, et al. Among authors: sbardella g. J Med Chem. 1999 Feb 25;42(4):619-27. doi: 10.1021/jm980260f. J Med Chem. 1999. PMID: 10052969

6

Nitroquinolones with broad-spectrum antimycobacterial activity in vitro.

Artico M, Mai A, Sbardella G, Massa S, Musiu C, Lostia S, Demontis F, La Colla P. Artico M, et al. Among authors: sbardella g. Bioorg Med Chem Lett. 1999 Jun 21;9(12):1651-6. doi: 10.1016/s0960-894x(99)00251-6. Bioorg Med Chem Lett. 1999. PMID: 10397494

7

Chiral resolution and molecular modeling investigation of rac-2-cyclopentylthio-6-[1-(2,6-difluorophenyl)ethyl]-3,4-dihydro-5-methylpyrimidin-4(3H)-one (MC-1047), a potent anti-HIV-1 reverse transcriptase agent of the DABO class.

Quaglia M, Mai A, Sbardella G, Artico M, Ragno R, Massa S, del Piano D, Setzu G, Doratiotto S, Cotichini V. Quaglia M, et al. Among authors: sbardella g. Chirality. 2001 Feb;13(2):75-80. doi: 10.1002/1520-636X(2001)13:2<75::AID-CHIR1001>3.0.CO;2-W. Chirality. 2001. PMID: 11170249

8

3-(4-aroyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides, a new class of synthetic histone deacetylase inhibitors.

Massa S, Mai A, Sbardella G, Esposito M, Ragno R, Loidl P, Brosch G. Massa S, et al. Among authors: sbardella g. J Med Chem. 2001 Jun 21;44(13):2069-72. doi: 10.1021/jm015515v. J Med Chem. 2001. PMID: 11405644

9

Structure-activity relationship studies on new DABOS: effect of substitutions at pyrimidine C-5 and C-6 positions on anti-HIV-1 activity.

Sbardella G, Mai A, Artico M, Chimenti P, Massa S, Loddo R, Marongiu ME, La Collat P, Pani A. Sbardella G, et al. Antivir Chem Chemother. 2001 Jan;12(1):37-50. doi: 10.1177/095632020101200102. Antivir Chem Chemother. 2001. PMID: 11437321 Free article.

10

3-(1H-Pyrrol-1-yl)-2-oxazolidinones as reversible, highly potent, and selective inhibitors of monoamine oxidase type A.

Mai A, Artico M, Esposito M, Sbardella G, Massa S, Befani O, Turini P, Giovannini V, Mondovì B. Mai A, et al. Among authors: sbardella g. J Med Chem. 2002 Mar 14;45(6):1180-3. doi: 10.1021/jm015578d. J Med Chem. 2002. PMID: 11881986

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