tetano
Editor, Senior Moderator
J Med Chem. 2015 Apr 9. [Epub ahead of print]
[h=1]A Broad Anti-influenza Hybrid Small Molecule that Potently Disrupts the Polymerase Acidic Protein-Basic Protein 1 (PA-PB1) Subunits Interaction.[/h] Massari S, Nannetti G, Desantis J, Muratore G, Sabatini S, Manfroni G, Mercorelli B, Cecchetti V, Pal? G, Cruciani G, Loregian A, Goracci L, Tabarrini O.
[h=3]Abstract[/h] In continuing our efforts to identify small molecules able to disrupt PA-PB1 subunits interaction of influenza virus (Flu) RNA-dependent RNA polymerase, this paper was devoted to the optimization of a dihydrotriazolopyrimidine derivative, previously identified through a SBDD. The structure modifications performed around the bicyclic core led to the identification of compounds endowed with both the ability to disrupt PA-PB1 subunits interaction and anti-Flu activity with no cytotoxicity. Very interesting results were obtained with the hybrid molecules 36 and 37, designed by merging some peculiar structural features known to impart PA-PB1 interaction inhibition, with compound 36 that emerged as the most potent PA-PB1 interaction inhibitor (IC[SUB]50[/SUB] of 1.1 ?M) among all the small molecules reported so far. Calculations showed a very favored H-bonding between the 2-amidic carbonyl of 36 and Q408, which seems to justify its potent ability to interfere with the polymerase subunits interaction.
PMID: 25856229 [PubMed - as supplied by publisher]
[h=1]A Broad Anti-influenza Hybrid Small Molecule that Potently Disrupts the Polymerase Acidic Protein-Basic Protein 1 (PA-PB1) Subunits Interaction.[/h] Massari S, Nannetti G, Desantis J, Muratore G, Sabatini S, Manfroni G, Mercorelli B, Cecchetti V, Pal? G, Cruciani G, Loregian A, Goracci L, Tabarrini O.
[h=3]Abstract[/h] In continuing our efforts to identify small molecules able to disrupt PA-PB1 subunits interaction of influenza virus (Flu) RNA-dependent RNA polymerase, this paper was devoted to the optimization of a dihydrotriazolopyrimidine derivative, previously identified through a SBDD. The structure modifications performed around the bicyclic core led to the identification of compounds endowed with both the ability to disrupt PA-PB1 subunits interaction and anti-Flu activity with no cytotoxicity. Very interesting results were obtained with the hybrid molecules 36 and 37, designed by merging some peculiar structural features known to impart PA-PB1 interaction inhibition, with compound 36 that emerged as the most potent PA-PB1 interaction inhibitor (IC[SUB]50[/SUB] of 1.1 ?M) among all the small molecules reported so far. Calculations showed a very favored H-bonding between the 2-amidic carbonyl of 36 and Q408, which seems to justify its potent ability to interfere with the polymerase subunits interaction.
PMID: 25856229 [PubMed - as supplied by publisher]