Cosimo Gianluca Fortuna

Summary

Affiliation: University of Catania
Country: Italy

Publications

  1. ncbi 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. ncbi 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
  3. ncbi 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
  4. ncbi 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

Collaborators

Detail Information

Publications4

  1. ncbi 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...
  2. ncbi 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...
  3. ncbi 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...
  4. ncbi 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
    ....