Sabatini S - Search Results

1

Sustainable, three-component, one-pot procedure to obtain active anti-flavivirus agents.

Felicetti T, Burali MS, Gwee CP, Ki Chan KW, Alonso S, Massari S, Sabatini S, Tabarrini O, Barreca ML, Cecchetti V, Vasudevan SG, Manfroni G. Felicetti T, et al. Among authors: sabatini s. Eur J Med Chem. 2021 Jan 15;210:112992. doi: 10.1016/j.ejmech.2020.112992. Epub 2020 Nov 4. Eur J Med Chem. 2021. PMID: 33208235

2

Design and synthesis of modified quinolones as antitumoral acridones.

Tabarrini O, Cecchetti V, Fravolini A, Nocentini G, Barzi A, Sabatini S, Miao H, Sissi C. Tabarrini O, et al. Among authors: sabatini s. J Med Chem. 1999 Jun 17;42(12):2136-44. doi: 10.1021/jm980324m. J Med Chem. 1999. PMID: 10377219

3

Studies on 6-aminoquinolones: synthesis and antibacterial evaluation of 6-amino-8-ethyl- and 6-amino-8-methoxyquinolones.

Cecchetti V, Tabarrini O, Sabatini S, Miao H, Filipponi E, Fravolini A. Cecchetti V, et al. Among authors: sabatini s. Bioorg Med Chem. 1999 Nov;7(11):2465-71. doi: 10.1016/s0968-0896(99)00207-2. Bioorg Med Chem. 1999. PMID: 10632056

4

Highly potent 1,4-benzothiazine derivatives as K(ATP)-channel openers.

Cecchetti V, Calderone V, Tabarrini O, Sabatini S, Filipponi E, Testai L, Spogli R, Martinotti E, Fravolini A. Cecchetti V, et al. Among authors: sabatini s. J Med Chem. 2003 Aug 14;46(17):3670-9. doi: 10.1021/jm030791q. J Med Chem. 2003. PMID: 12904071

5

Structure modifications of 6-aminoquinolones with potent anti-HIV activity.

Tabarrini O, Stevens M, Cecchetti V, Sabatini S, Dell'Uomo M, Manfroni G, Palumbo M, Pannecouque C, De Clercq E, Fravolini A. Tabarrini O, et al. Among authors: sabatini s. J Med Chem. 2004 Oct 21;47(22):5567-78. doi: 10.1021/jm049721p. J Med Chem. 2004. PMID: 15481992

6

Binding studies and GRIND/ALMOND-based 3D QSAR analysis of benzothiazine type K(ATP)-channel openers.

Carosati E, Lemoine H, Spogli R, Grittner D, Mannhold R, Tabarrini O, Sabatini S, Cecchetti V. Carosati E, et al. Among authors: sabatini s. Bioorg Med Chem. 2005 Oct 1;13(19):5581-91. doi: 10.1016/j.bmc.2005.06.010. Bioorg Med Chem. 2005. PMID: 16002299

7

Synthesis and anti-BVDV activity of acridones as new potential antiviral agents.

Tabarrini O, Manfroni G, Fravolini A, Cecchetti V, Sabatini S, De Clercq E, Rozenski J, Canard B, Dutartre H, Paeshuyse J, Neyts J. Tabarrini O, et al. Among authors: sabatini s. J Med Chem. 2006 Apr 20;49(8):2621-7. doi: 10.1021/jm051250z. J Med Chem. 2006. PMID: 16610805

8

From cromakalim to different structural classes of K(ATP) channel openers.

Cecchetti V, Tabarrini O, Sabatini S. Cecchetti V, et al. Among authors: sabatini s. Curr Top Med Chem. 2006;6(10):1049-68. doi: 10.2174/156802606777323683. Curr Top Med Chem. 2006. PMID: 16787279 Review.

9

From phenothiazine to 3-phenyl-1,4-benzothiazine derivatives as inhibitors of the Staphylococcus aureus NorA multidrug efflux pump.

Sabatini S, Kaatz GW, Rossolini GM, Brandini D, Fravolini A. Sabatini S, et al. J Med Chem. 2008 Jul 24;51(14):4321-30. doi: 10.1021/jm701623q. Epub 2008 Jun 25. J Med Chem. 2008. PMID: 18578473

10

Novel 1,4-benzothiazine derivatives as large conductance Ca2+-activated potassium channel openers.

Calderone V, Spogli R, Martelli A, Manfroni G, Testai L, Sabatini S, Tabarrini O, Cecchetti V. Calderone V, et al. Among authors: sabatini s. J Med Chem. 2008 Aug 28;51(16):5085-92. doi: 10.1021/jm701605f. Epub 2008 Aug 5. J Med Chem. 2008. PMID: 18680269

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