Cosimo Gianluca Fortuna

Summary

Affiliation: University of Catania
Country: Italy

Publications

  1. doi request reprint New linezolid-like 1,2,4-oxadiazoles active against Gram-positive multiresistant pathogens
    Cosimo G Fortuna
    Dipartimento di Scienze Chimiche, Universita degli Studi di Catania, Viale Andrea Doria 6, I 95125 Catania, Italy
    Eur J Med Chem 65:533-45. 2013
  2. doi request reprint Design, synthesis and in vitro antitumour activity of new heteroaryl ethylenes
    Cosimo G Fortuna
    Dipartimento di Scienze Chimiche, Universita degli Studi di Catania, Viale A Doria 6 95125, Catania, Italy
    Eur J Med Chem 47:221-7. 2012
  3. doi request reprint Design and synthesis of trans 2-(furan-2-yl)vinyl heteroaromatic iodides with antitumour activity
    Cosimo Gianluca Fortuna
    Dipartimento di Scienze Chimiche, Universita di Catania, Viale A Doria, 6, 95125 Catania, Italy
    Bioorg Med Chem 16:4150-9. 2008
  4. doi request reprint Design, synthesis and biological evaluation of trans 2-(thiophen-2-yl)vinyl heteroaromatic iodides
    Cosimo G Fortuna
    Dipartimento di Scienze Chimiche, Universita di Catania, Viale A Doria, Catania, Italy
    Bioorg Med Chem 18:4516-23. 2010
  5. doi request reprint Synthesis and NLO properties of new trans 2-(thiophen-2-yl)vinyl heteroaromatic iodides
    Cosimo Gianluca Fortuna
    Dipartimento di Scienze Chimiche, Universita di Catania, Viale A Doria, 6, 95125, Catania, Italy
    Org Biomol Chem 9:1608-13. 2011

Detail Information

Publications5

  1. doi request reprint New linezolid-like 1,2,4-oxadiazoles active against Gram-positive multiresistant pathogens
    Cosimo G Fortuna
    Dipartimento di Scienze Chimiche, Universita degli Studi di Catania, Viale Andrea Doria 6, I 95125 Catania, Italy
    Eur J Med Chem 65:533-45. 2013
    ....
  2. doi request reprint Design, synthesis and in vitro antitumour activity of new heteroaryl ethylenes
    Cosimo G Fortuna
    Dipartimento di Scienze Chimiche, Universita degli Studi di Catania, Viale A Doria 6 95125, Catania, Italy
    Eur J Med Chem 47:221-7. 2012
    ..2-{(E)-2-[5'-(Dibutylamino)-2,2'-bithien-5-yl]vinyl}-1-methylquinolinium iodide exhibited in vitro antiproliferative activity two orders of magnitude higher than that of the most active compound previously synthesized in our laboratory...
  3. doi request reprint Design and synthesis of trans 2-(furan-2-yl)vinyl heteroaromatic iodides with antitumour activity
    Cosimo Gianluca Fortuna
    Dipartimento di Scienze Chimiche, Universita di Catania, Viale A Doria, 6, 95125 Catania, Italy
    Bioorg Med Chem 16:4150-9. 2008
    ..The synthesis and in vitro antitumour tests on a breast carcinoma cell line (MCF7) confirmed VOLSURF predicted activity values...
  4. doi request reprint Design, synthesis and biological evaluation of trans 2-(thiophen-2-yl)vinyl heteroaromatic iodides
    Cosimo G Fortuna
    Dipartimento di Scienze Chimiche, Universita di Catania, Viale A Doria, Catania, Italy
    Bioorg Med Chem 18:4516-23. 2010
    ..An Almond model, derived to have an overall structural insight on the above compounds, supported the validity of Volsurf and provided guidelines for the synthesis of new compounds...
  5. doi request reprint Synthesis and NLO properties of new trans 2-(thiophen-2-yl)vinyl heteroaromatic iodides
    Cosimo Gianluca Fortuna
    Dipartimento di Scienze Chimiche, Universita di Catania, Viale A Doria, 6, 95125, Catania, Italy
    Org Biomol Chem 9:1608-13. 2011
    ....