Herein, azadipeptidomimetic molecules were designed and synthesized using a quinoline‐histidine‐amino acid sequence with terminal amino acid modification. In‐silico studies were carried out to evaluate the compound's HIV protease‐1 inhibition temperament. In‐vitro anti‐proliferative possessions of the test compounds were studied by executing a series of experiments, namely DNA binding, bovine serum albumin (BSA) binding capability, and cytotoxicity assay on MCF‐7 cells. The molecule 5j exhibited remarkable results in all experiments; it has an excellent DNA binding constant (3.76 × 105), higher serum albumin unbound concentration of 5.96%, and a significant antiproliferative effect on MCF‐7 cells with IC50 value 0.31 nM.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.