Fattorusso C - Search Results

1

Manadoperoxides A-D from the Indonesian sponge Plakortis cfr. simplex. Further insights on the structure-activity relationships of simple 1,2-dioxane antimalarials.

Fattorusso C, Persico M, Calcinai B, Cerrano C, Parapini S, Taramelli D, Novellino E, Romano A, Scala F, Fattorusso E, Taglialatela-Scafati O. Fattorusso C, et al. Among authors: fattorusso e. J Nat Prod. 2010 Jun 25;73(6):1138-45. doi: 10.1021/np100196b. J Nat Prod. 2010. PMID: 20521782

2

Shape-dependent effects in a series of aromatic nitro compounds acting as mutagenic agents on S. typhimurium TA98.

Caliendo G, Fattorusso C, Greco G, Novellino E, Perissutti E, Santagada V. Caliendo G, et al. Among authors: fattorusso c. SAR QSAR Environ Res. 1995;4(1):21-7. doi: 10.1080/10629369508234011. SAR QSAR Environ Res. 1995. PMID: 8765901

3

Specific targeting of acetylcholinesterase and butyrylcholinesterase recognition sites. Rational design of novel, selective, and highly potent cholinesterase inhibitors.

Savini L, Gaeta A, Fattorusso C, Catalanotti B, Campiani G, Chiasserini L, Pellerano C, Novellino E, McKissic D, Saxena A. Savini L, et al. Among authors: fattorusso c. J Med Chem. 2003 Jan 2;46(1):1-4. doi: 10.1021/jm0255668. J Med Chem. 2003. PMID: 12502352

4

Neuronal high-affinity sodium-dependent glutamate transporters (EAATs): targets for the development of novel therapeutics against neurodegenerative diseases.

Campiani G, Fattorusso C, De Angelis M, Catalanotti B, Butini S, Fattorusso R, Fiorini I, Nacci V, Novellino E. Campiani G, et al. Among authors: fattorusso c, fattorusso r. Curr Pharm Des. 2003;9(8):599-625. doi: 10.2174/1381612033391261. Curr Pharm Des. 2003. PMID: 12570795 Review.

5

Simplakidine A, a unique pyridinium alkaloid from the Caribbean sponge plakortis simplex.

Campagnuolo C, Fattorusso C, Fattorusso E, Ianaro A, Pisano B, Taglialatela-Scafati O. Campagnuolo C, et al. Among authors: fattorusso c, fattorusso e. Org Lett. 2003 Mar 6;5(5):673-6. doi: 10.1021/ol027437r. Org Lett. 2003. PMID: 12605487

6

Development of molecular probes for the identification of extra interaction sites in the mid-gorge and peripheral sites of butyrylcholinesterase (BuChE). Rational design of novel, selective, and highly potent BuChE inhibitors.

Campiani G, Fattorusso C, Butini S, Gaeta A, Agnusdei M, Gemma S, Persico M, Catalanotti B, Savini L, Nacci V, Novellino E, Holloway HW, Greig NH, Belinskaya T, Fedorko JM, Saxena A. Campiani G, et al. Among authors: fattorusso c. J Med Chem. 2005 Mar 24;48(6):1919-29. doi: 10.1021/jm049510k. J Med Chem. 2005. PMID: 15771436

7

Specific targeting of hepatitis C virus NS3 RNA helicase. Discovery of the potent and selective competitive nucleotide-mimicking inhibitor QU663.

Maga G, Gemma S, Fattorusso C, Locatelli GA, Butini S, Persico M, Kukreja G, Romano MP, Chiasserini L, Savini L, Novellino E, Nacci V, Spadari S, Campiani G. Maga G, et al. Among authors: fattorusso c. Biochemistry. 2005 Jul 19;44(28):9637-44. doi: 10.1021/bi047437u. Biochemistry. 2005. PMID: 16008349

8

Specific targeting highly conserved residues in the HIV-1 reverse transcriptase primer grip region. Design, synthesis, and biological evaluation of novel, potent, and broad spectrum NNRTIs with antiviral activity.

Fattorusso C, Gemma S, Butini S, Huleatt P, Catalanotti B, Persico M, De Angelis M, Fiorini I, Nacci V, Ramunno A, Rodriquez M, Greco G, Novellino E, Bergamini A, Marini S, Coletta M, Maga G, Spadari S, Campiani G. Fattorusso C, et al. J Med Chem. 2005 Nov 17;48(23):7153-65. doi: 10.1021/jm050257d. J Med Chem. 2005. PMID: 16279773

9

Discovery of huperzine A-tacrine hybrids as potent inhibitors of human cholinesterases targeting their midgorge recognition sites.

Gemma S, Gabellieri E, Huleatt P, Fattorusso C, Borriello M, Catalanotti B, Butini S, De Angelis M, Novellino E, Nacci V, Belinskaya T, Saxena A, Campiani G. Gemma S, et al. Among authors: fattorusso c. J Med Chem. 2006 Jun 1;49(11):3421-5. doi: 10.1021/jm060257t. J Med Chem. 2006. PMID: 16722663

10

Synthesis of N1-arylidene-N2-quinolyl- and N2-acrydinylhydrazones as potent antimalarial agents active against CQ-resistant P. falciparum strains.

Gemma S, Kukreja G, Fattorusso C, Persico M, Romano MP, Altarelli M, Savini L, Campiani G, Fattorusso E, Basilico N, Taramelli D, Yardley V, Butini S. Gemma S, et al. Among authors: fattorusso c, fattorusso e. Bioorg Med Chem Lett. 2006 Oct 15;16(20):5384-8. doi: 10.1016/j.bmcl.2006.07.060. Epub 2006 Aug 4. Bioorg Med Chem Lett. 2006. PMID: 16890433

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