Cecchetti V - Search Results

1

Engagement of Nuclear Coactivator 7 by 3-Hydroxyanthranilic Acid Enhances Activation of Aryl Hydrocarbon Receptor in Immunoregulatory Dendritic Cells.

Gargaro M, Vacca C, Massari S, Scalisi G, Manni G, Mondanelli G, Mazza EMC, Bicciato S, Pallotta MT, Orabona C, Belladonna ML, Volpi C, Bianchi R, Matino D, Iacono A, Panfili E, Proietti E, Iamandii IM, Cecchetti V, Puccetti P, Tabarrini O, Fallarino F, Grohmann U. Gargaro M, et al. Among authors: cecchetti v. Front Immunol. 2019 Aug 20;10:1973. doi: 10.3389/fimmu.2019.01973. eCollection 2019. Front Immunol. 2019. PMID: 31481962 Free PMC article.

2

Functionalized sulfonyl anthranilic acid derivatives inhibit replication of all the four dengue serotypes.

Felicetti T, Gwee CP, Burali MS, Chan KWK, Alonso S, Pismataro MC, Sabatini S, Barreca ML, Cecchetti V, Vasudevan SG, Manfroni G. Felicetti T, et al. Among authors: cecchetti v. Eur J Med Chem. 2023 Apr 5;252:115283. doi: 10.1016/j.ejmech.2023.115283. Epub 2023 Mar 16. Eur J Med Chem. 2023. PMID: 36965228 Free article.

3

7-(Disubstituted thiazolyl)-3,5-dihydroxy-6-heptenoic/heptanoic acid derivatives as HMG-CoA reductase inhibitors.

Cecchetti V, Fravolini A, Pagella PG, Tabarrini O, Temperini A. Cecchetti V, et al. Bioorg Med Chem. 1994 Aug;2(8):799-806. doi: 10.1016/s0968-0896(00)82180-x. Bioorg Med Chem. 1994. PMID: 7894974

4

Quinolinecarboxylic acids. 3. Synthesis and antibacterial evaluation of 2-substituted-7-oxo-2,3-dihydro-7H-pyrido[1,2,3-de] [1,4]benzothiazine-6-carboxylic acids related to rufloxacin.

Cecchetti V, Fravolini A, Pagella PG, Savino A, Tabarrini O. Cecchetti V, et al. J Med Chem. 1993 Oct 29;36(22):3449-54. doi: 10.1021/jm00074a028. J Med Chem. 1993. PMID: 8230136

5

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

Cecchetti V, Fravolini A, Lorenzini MC, Tabarrini O, Terni P, Xin T. Cecchetti V, et al. J Med Chem. 1996 Jan 19;39(2):436-45. doi: 10.1021/jm950558v. J Med Chem. 1996. PMID: 8558512

6

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

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

7

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. Among authors: cecchetti v. J Med Chem. 2008 Sep 11;51(17):5454-8. doi: 10.1021/jm701585h. Epub 2008 Aug 19. J Med Chem. 2008. PMID: 18710207

8

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: cecchetti v. 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

9

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: cecchetti v. J Med Chem. 2009 May 28;52(10):3354-65. doi: 10.1021/jm801608u. J Med Chem. 2009. PMID: 19388645

10

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: cecchetti v. J Med Chem. 2010 Jan 28;53(2):641-8. doi: 10.1021/jm901211d. J Med Chem. 2010. PMID: 19958026

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