Synthesis, structure–activity relationship, and biological evaluation of quinolines for development of anticancer agents

Abstract

AbstractTetrahydro‐β‐carbolines (THβCs) are a kind of natural alkaloids with multiple pharmaceutical activities. Herein, a focused compound library derived from THβCs was synthesized and their anticancer activities were studied in several cancer cell lines. Among them, three compounds showed considerable anticancer activities with low micromolar to submicromolar IC50 values. The abilities to induce apoptosis and alter mitochondrial membrane potential levels, which are comparable to those of the commercial anticancer drug adriamycin, were confirmed by one representative compound (21) on the B16/F10 cell line. Our preliminary structure–activity relationship studies indicated that alkylamines with suitable lengths are very important for potency improvement.