Tabarrini O - Search Results

1

4-(Phenoxy) and 4-(benzyloxy)benzamides as potent and selective inhibitors of mono-ADP-ribosyltransferase PARP10/ARTD10.

Murthy S, Desantis J, Verheugd P, Maksimainen MM, Venkannagari H, Massari S, Ashok Y, Obaji E, Nkizinkinko Y, Lüscher B, Tabarrini O, Lehtiö L. Murthy S, et al. Among authors: tabarrini o. Eur J Med Chem. 2018 Aug 5;156:93-102. doi: 10.1016/j.ejmech.2018.06.047. Epub 2018 Jun 20. Eur J Med Chem. 2018. PMID: 30006177

2

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. J Med Chem. 2004 Oct 21;47(22):5567-78. doi: 10.1021/jm049721p. J Med Chem. 2004. PMID: 15481992

3

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. J Med Chem. 2006 Apr 20;49(8):2621-7. doi: 10.1021/jm051250z. J Med Chem. 2006. PMID: 16610805

4

Structure-activity relationship study on anti-HIV 6-desfluoroquinolones.

Tabarrini O, Massari S, Daelemans D, Stevens M, Manfroni G, Sabatini S, Balzarini J, Cecchetti V, Pannecouque C, Fravolini A. Tabarrini O, et al. J Med Chem. 2008 Sep 11;51(17):5454-8. doi: 10.1021/jm701585h. Epub 2008 Aug 19. J Med Chem. 2008. PMID: 18710207

5

Studies on anti-HIV quinolones: new insights on the C-6 position.

Massari S, Daelemans D, Manfroni G, Sabatini S, Tabarrini O, Pannecouque C, Cecchetti V. Massari S, et al. Among authors: tabarrini o. Bioorg Med Chem. 2009 Jan 15;17(2):667-74. doi: 10.1016/j.bmc.2008.11.056. Epub 2008 Dec 3. Bioorg Med Chem. 2009. PMID: 19091580

6

2-Phenylquinolones as inhibitors of the HIV-1 Tat-TAR interaction.

Gatto B, Tabarrini O, Massari S, Giaretta G, Sabatini S, Del Vecchio C, Parolin C, Fravolini A, Palumbo M, Cecchetti V. Gatto B, et al. Among authors: tabarrini o. ChemMedChem. 2009 Jun;4(6):935-8. doi: 10.1002/cmdc.200800437. ChemMedChem. 2009. PMID: 19283692

7

Inhibition of subgenomic hepatitis C virus RNA replication by acridone derivatives: identification of an NS3 helicase inhibitor.

Manfroni G, Paeshuyse J, Massari S, Zanoli S, Gatto B, Maga G, Tabarrini O, Cecchetti V, Fravolini A, Neyts J. Manfroni G, et al. Among authors: tabarrini o. J Med Chem. 2009 May 28;52(10):3354-65. doi: 10.1021/jm801608u. J Med Chem. 2009. PMID: 19388645

8

A 1,8-naphthyridone derivative targets the HIV-1 Tat-mediated transcription and potently inhibits the HIV-1 replication.

Massari S, Daelemans D, Barreca ML, Knezevich A, Sabatini S, Cecchetti V, Marcello A, Pannecouque C, Tabarrini O. Massari S, et al. Among authors: tabarrini o. J Med Chem. 2010 Jan 28;53(2):641-8. doi: 10.1021/jm901211d. J Med Chem. 2010. PMID: 19958026

9

Studies of anti-HIV transcription inhibitor quinolones: identification of potent N1-vinyl derivatives.

Tabarrini O, Massari S, Daelemans D, Meschini F, Manfroni G, Bottega L, Gatto B, Palumbo M, Pannecouque C, Cecchetti V. Tabarrini O, et al. ChemMedChem. 2010 Nov 8;5(11):1880-92. doi: 10.1002/cmdc.201000267. ChemMedChem. 2010. PMID: 20928882

10

6-desfluoroquinolones as HIV-1 Tat-mediated transcription inhibitors.

Tabarrini O, Massari S, Cecchetti V. Tabarrini O, et al. Future Med Chem. 2010 Jul;2(7):1161-80. doi: 10.4155/fmc.10.208. Future Med Chem. 2010. PMID: 21426162 Review.

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