Befani O - Search Results

1

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: befani o. J Med Chem. 2002 Mar 14;45(6):1180-3. doi: 10.1021/jm015578d. J Med Chem. 2002. PMID: 11881986

2

Inhibition of amine oxidases activity by 1-acetyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives.

Manna F, Chimenti F, Bolasco A, Secci D, Bizzarri B, Befani O, Turini P, Mondovi B, Alcaro S, Tafi A. Manna F, et al. Among authors: befani o. Bioorg Med Chem Lett. 2002 Dec 16;12(24):3629-33. doi: 10.1016/s0960-894x(02)00699-6. Bioorg Med Chem Lett. 2002. PMID: 12443791

3

Simple, potent, and selective pyrrole inhibitors of monoamine oxidase types A and B.

Silvestri R, La Regina G, De Martino G, Artico M, Befani O, Palumbo M, Agostinelli E, Turini P. Silvestri R, et al. Among authors: befani o. J Med Chem. 2003 Mar 13;46(6):917-20. doi: 10.1021/jm0256124. J Med Chem. 2003. PMID: 12620068

4

Synthesis and selective inhibitory activity of 1-acetyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives against monoamine oxidase.

Chimenti F, Bolasco A, Manna F, Secci D, Chimenti P, Befani O, Turini P, Giovannini V, Mondovì B, Cirilli R, La Torre F. Chimenti F, et al. Among authors: befani o. J Med Chem. 2004 Apr 8;47(8):2071-4. doi: 10.1021/jm031042b. J Med Chem. 2004. PMID: 15056004

5

Inhibition of monoamine oxidases by coumarin-3-acyl derivatives: biological activity and computational study.

Chimenti F, Secci D, Bolasco A, Chimenti P, Granese A, Befani O, Turini P, Alcaro S, Ortuso F. Chimenti F, et al. Among authors: befani o. Bioorg Med Chem Lett. 2004 Jul 16;14(14):3697-703. doi: 10.1016/j.bmcl.2004.05.010. Bioorg Med Chem Lett. 2004. PMID: 15203146

6

Design, synthesis, and biological activities of pyrrolylethanoneamine derivatives, a novel class of monoamine oxidases inhibitors.

Di Santo R, Costi R, Roux A, Artico M, Befani O, Meninno T, Agostinelli E, Palmegiani P, Turini P, Cirilli R, Ferretti R, Gallinella B, La Torre F. Di Santo R, et al. Among authors: befani o. J Med Chem. 2005 Jun 30;48(13):4220-3. doi: 10.1021/jm050172c. J Med Chem. 2005. PMID: 15974574

7

Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)- pyrazole derivatives.

Chimenti F, Maccioni E, Secci D, Bolasco A, Chimenti P, Granese A, Befani O, Turini P, Alcaro S, Ortuso F, Cirilli R, La Torre F, Cardia MC, Distinto S. Chimenti F, et al. Among authors: befani o. J Med Chem. 2005 Nov 17;48(23):7113-22. doi: 10.1021/jm040903t. J Med Chem. 2005. PMID: 16279769

8

Synthesis, biological evaluation and 3D-QSAR of 1,3,5-trisubstituted-4,5-dihydro-(1H)-pyrazole derivatives as potent and highly selective monoamine oxidase A inhibitors.

Chimenti F, Bolasco A, Manna F, Secci D, Chimenti P, Granese A, Befani O, Turini P, Cirilli R, La Torre F, Alcaro S, Ortuso F, Langer T. Chimenti F, et al. Among authors: befani o. Curr Med Chem. 2006;13(12):1411-28. doi: 10.2174/092986706776872907. Curr Med Chem. 2006. PMID: 16719786 Review.

9

Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of N,N'-bis[2-oxo-2H-benzopyran]-3-carboxamides.

Chimenti F, Secci D, Bolasco A, Chimenti P, Granese A, Carradori S, Befani O, Turini P, Alcaro S, Ortuso F. Chimenti F, et al. Among authors: befani o. Bioorg Med Chem Lett. 2006 Aug 1;16(15):4135-40. doi: 10.1016/j.bmcl.2006.04.026. Epub 2006 Jun 12. Bioorg Med Chem Lett. 2006. PMID: 16759860

10

Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivatives.

Chimenti F, Maccioni E, Secci D, Bolasco A, Chimenti P, Granese A, Befani O, Turini P, Alcaro S, Ortuso F, Cardia MC, Distinto S. Chimenti F, et al. Among authors: befani o. J Med Chem. 2007 Feb 22;50(4):707-12. doi: 10.1021/jm060869d. Epub 2007 Jan 25. J Med Chem. 2007. PMID: 17253676

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