Discovery of New Ligand with Quinoline Scaffold as Potent Allosteric Inhibitor of HIV-1 and Its Copper Complexes as a Powerful Catalyst for the Synthesis of Chiral Benzimidazole Derivatives, and in Silico Anti-HIV-1 Studies

Abstract

In this paper, the novel Schi1 base ligand containing quinoline moiety and its novel copper chelate complexes were successfully prepared. ,e catalytic activity of the (nal complex in the organic reaction such as synthesis of chiral benzimidazoles and anti- HIV-1 activity of Schi1 base ligand and the products of this reaction were investigated. In addition, green chemistry reactions using microwaves, powerful catalyst synthesis, green recovery and reusability, and separation of products with economic, safe, and clean methods (green chemistry) are among the advantages of this protocol. ,e potency of these compounds as anti-HIV-1 agents was investigated using molecular docking into integrase (IN) enzyme with code 1QS4 and the GROMACS software for molecular dynamics simulation. ,e (nal steps were evaluated in case of RMSD, RMSF, and Rg. ,e results revealed that the compound VII exhibit a good binding a>nity to integrase (g = −10.99 kcal/mol) during 100 ns simulation time, and the analysis of RMSD suggested that compound VII was stable in the binding site of integrase.