Please use this identifier to cite or link to this item:
Title: A Versatile and Practical Synthesis toward the Development of Novel HIV-1 Integrase Inhibitors
Authors: Rinaldi, Marta
Tintori, Cristina
Franchi, Luigi
Vignaroli, Giulia
A., Innitzer
S., Massa
J. A., Esté
E., Gonzalo
F., Christ
Z., Debyser
Botta, Maurizio 
Keywords: antiviral agents; HIV; inhibitors; integrase
Issue Date: 2011
Project: None 
As a continuation of our previous work, which resulted in the identification of a new hit compound as an HIV-1 integrase inhibitor, three novel series of salicylic acid derivatives were synthesized using three versatile and practical synthetic strategies and were assayed for their capacity to inhibit the catalytic activity of HIV-1 integrase. Biological evaluations revealed that some of the synthesized compounds possess good inhibitory potency in enzymatic assays and are able to inhibit viral replication in MT-4 cells at low micromolar concentrations. Finally, docking studies were conducted to analyze the binding mode of the synthesized compounds within the DNA binding site of integrase in order to refine their structure-activity relationships.
ISSN: 1860-7187
DOI: 10.1002/cmdc.201000510
Appears in Collections:Publications

Show full item record

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.