Design, Synthesis, Antitumor Activity and NMR‐Based Metabolomics of Novel Amino Substituted Tetracyclic Imidazo4,5‐bPyridine Derivatives

Newly prepared tetracyclic imidazo4,5-bpyridine derivatives were synthesized to study their antiproliferative activity against human cancer cells. Additionally, the structure-activity was studied to confirm the impact of the N atom position in pyridine nuclei as well as the chosen amino side chains on antiproliferative activity. Targeted amino substituted regioisomers were prepared by using uncatalyzed amination from corresponding chloro substituted precursors. The most active compounds 6 a, 8 and 10 showed improved activity in comparison to standard drug etoposide with IC