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This study focuses on the design, synthesis, and evaluation of 4-aminoquinoline hybrid compounds as potential inhibitors of the kinesin spindle protein (Eg5), which is crucial in cell division and a target for cancer therapy. The research identifies several compounds with promising inhibitory activity, particularly compounds 4 and 6c, which exhibited low IC50 values in assays. Molecular dynamics simulations and docking studies were conducted to assess the interactions of these compounds with Eg5, suggesting

Author

tselvanj7

Language

EN