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 <i>in Silico</i> Anti-HIV-1 Studies

<div>Graph of RMSF changes of alpha carbon integrase according to residue in connection with compound VII at 100 ns and 300 K. RMSF of integrase is in orange, and in the presence of compound VII, it is in red.</div>

Bioinorganic Chemistry and Applications

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Figure 9

Figure 9: 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 <i>in Silico</i> Anti-HIV-1 Studies 

Figure 9 | 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 