Saccomanni G - Search Results

1

Synthesis and In Vitro Characterization of Selective Cannabinoid CB2 Receptor Agonists: Biological Evaluation against Neuroblastoma Cancer Cells.

Gado F, Ferrisi R, Di Somma S, Napolitano F, Mohamed KA, Stevenson LA, Rapposelli S, Saccomanni G, Portella G, Pertwee RG, Laprairie RB, Malfitano AM, Manera C. Gado F, et al. Among authors: saccomanni g. Molecules. 2022 May 7;27(9):3019. doi: 10.3390/molecules27093019. Molecules. 2022. PMID: 35566369 Free PMC article.

2

Synthesis and evaluation of antimycobacterial activity of 4-phenyl-1,8-naphthyridine derivatives.

Ferrarini PL, Manera C, Mori C, Badawneh M, Saccomanni G. Ferrarini PL, et al. Among authors: saccomanni g. Farmaco. 1998 Dec 30;53(12):741-6. doi: 10.1016/s0014-827x(98)00094-9. Farmaco. 1998. PMID: 10230055

3

Synthesis of variously substituted 1,8-naphthyridine derivatives and evaluation of their antimycobacterial activity.

Badawneh M, Manera C, Mori C, Saccomanni G, Ferrarini PL. Badawneh M, et al. Among authors: saccomanni g. Farmaco. 2002 Aug;57(8):631-9. doi: 10.1016/s0014-827x(02)01235-1. Farmaco. 2002. PMID: 12361230

4

4-[6-(Dansylamino)hexylamino]-7-methyl-2-phenyl-1,8-naphthyridine as a new potential fluorescent probe for studying A1-adenosine receptor.

Macchia M, Bertini S, Di Bussolo V, Manera C, Martini C, Minutolo F, Mori C, Saccomanni G, Tuscano D, Ferrarini PL. Macchia M, et al. Among authors: saccomanni g. Farmaco. 2002 Oct;57(10):783-6. doi: 10.1016/s0014-827x(02)01275-2. Farmaco. 2002. PMID: 12420873

5

Synthesis and beta-blocking activity of (R,S)-(E)-oximeethers of 2,3-dihydro-1,8-naphthyridine and 2,3-dihydrothiopyrano[2,3-b]pyridine: identification of beta 3-antagonists.

Saccomanni G, Badawneh M, Adinolfi B, Calderone V, Cavallini T, Ferrarini PL, Greco R, Manera C, Testai L. Saccomanni G, et al. Bioorg Med Chem. 2003 Nov 17;11(23):4921-31. doi: 10.1016/j.bmc.2003.09.017. Bioorg Med Chem. 2003. PMID: 14604653

6

Synthesis and biological evaluation of 1,8-naphthyridin-4(1H)-on-3-carboxamide derivatives as new ligands of cannabinoid receptors.

Ferrarini PL, Calderone V, Cavallini T, Manera C, Saccomanni G, Pani L, Ruiu S, Gessa GL. Ferrarini PL, et al. Among authors: saccomanni g. Bioorg Med Chem. 2004 Apr 15;12(8):1921-33. doi: 10.1016/j.bmc.2004.01.035. Bioorg Med Chem. 2004. PMID: 15051060

7

1,8-Naphthyridin-4-one derivatives as new ligands of A2A adenosine receptors.

Manera C, Betti L, Cavallini T, Giannaccini G, Martinelli A, Ortore G, Saccomanni G, Trincavelli L, Tuccinardi T, Ferrarini PL. Manera C, et al. Among authors: saccomanni g. Bioorg Med Chem Lett. 2005 Oct 15;15(20):4604-10. doi: 10.1016/j.bmcl.2005.06.064. Bioorg Med Chem Lett. 2005. PMID: 16099648

8

Adenosine receptor modelling. A1/A2a selectivity.

Tuccinardi T, Ortore G, Manera C, Saccomanni G, Martinelli A. Tuccinardi T, et al. Among authors: saccomanni g. Eur J Med Chem. 2006 Mar;41(3):321-9. doi: 10.1016/j.ejmech.2005.09.011. Epub 2006 Jan 19. Eur J Med Chem. 2006. PMID: 16427161

9

Cannabinoid CB2/CB1 selectivity. Receptor modeling and automated docking analysis.

Tuccinardi T, Ferrarini PL, Manera C, Ortore G, Saccomanni G, Martinelli A. Tuccinardi T, et al. Among authors: saccomanni g. J Med Chem. 2006 Feb 9;49(3):984-94. doi: 10.1021/jm050875u. J Med Chem. 2006. PMID: 16451064

10

Design, synthesis, and biological evaluation of new 1,8-naphthyridin-4(1H)-on-3-carboxamide and quinolin-4(1H)-on-3-carboxamide derivatives as CB2 selective agonists.

Manera C, Benetti V, Castelli MP, Cavallini T, Lazzarotti S, Pibiri F, Saccomanni G, Tuccinardi T, Vannacci A, Martinelli A, Ferrarini PL. Manera C, et al. Among authors: saccomanni g. J Med Chem. 2006 Oct 5;49(20):5947-57. doi: 10.1021/jm0603466. J Med Chem. 2006. PMID: 17004710

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