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Parallel one-pot synthesis and structure-activity relationship study of symmetric formimidoester disulfides as a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors.
Cesarini S, Spallarossa A, Ranise A, Schenone S, Bruno O, La Colla P, Casula L, Collu G, Sanna G, Loddo R. Cesarini S, et al. Among authors: collu g. Bioorg Med Chem. 2008 Jun 15;16(12):6353-63. doi: 10.1016/j.bmc.2008.05.010. Epub 2008 May 7. Bioorg Med Chem. 2008. PMID: 18502646
Antiviral and cytotoxic activities of aminoarylazo compounds and aryltriazene derivatives.
Tonelli M, Vazzana I, Tasso B, Boido V, Sparatore F, Fermeglia M, Paneni MS, Posocco P, Pricl S, La Colla P, Ibba C, Secci B, Collu G, Loddo R. Tonelli M, et al. Among authors: collu g. Bioorg Med Chem. 2009 Jul 1;17(13):4425-40. doi: 10.1016/j.bmc.2009.05.020. Epub 2009 May 15. Bioorg Med Chem. 2009. PMID: 19482481 Free PMC article.
A combined in silico/in vitro approach unveils common molecular requirements for efficient BVDV RdRp binding of linear aromatic N-polycyclic systems.
Carta A, Briguglio I, Piras S, Corona P, Ibba R, Laurini E, Fermeglia M, Pricl S, Desideri N, Atzori EM, La Colla P, Collu G, Delogu I, Loddo R. Carta A, et al. Among authors: collu g. Eur J Med Chem. 2016 Jul 19;117:321-34. doi: 10.1016/j.ejmech.2016.03.080. Epub 2016 Apr 8. Eur J Med Chem. 2016. PMID: 27161176
Structure-based design, parallel synthesis, structure-activity relationship, and molecular modeling studies of thiocarbamates, new potent non-nucleoside HIV-1 reverse transcriptase inhibitor isosteres of phenethylthiazolylthiourea derivatives.
Ranise A, Spallarossa A, Cesarini S, Bondavalli F, Schenone S, Bruno O, Menozzi G, Fossa P, Mosti L, La Colla M, Sanna G, Murreddu M, Collu G, Busonera B, Marongiu ME, Pani A, La Colla P, Loddo R. Ranise A, et al. Among authors: collu g. J Med Chem. 2005 Jun 2;48(11):3858-73. doi: 10.1021/jm049252r. J Med Chem. 2005. PMID: 15916438
60 results