
Molecular docking guided structure based design of symmetrical N,Nâ²-disubstituted urea/thiourea as HIV-1 gp120-CD4 binding inhibitors
Keywords: پیوندهای بین مولکولی; HIV-1 gp120; Symmetrical N,Nâ²-disubtituted urea; Symmetrical N,Nâ²-disubtituted thiourea; Molecular docking; Induced fit docking (IFD); Enzyme-linked immunosorbent assay (ELISA);