Design, Synthesis and Evaluations of New 10‐Triazolyl‐1‐methoxygenipin Analogues for Their Cytotoxicity to Cancer Cells

Abstract

AbstractGenipin 1, derived from geniposide present in the fruit of Gardenia jasminoides Ellis has been reported to show diverse pharmacological activity. In this work, a new series of genipin‐triazole analogues was designed and synthesized yielding high yields from naturally genipin and their cytotoxicity evaluated against six cancer cell lines. Twenty‐seven analogues were obtained using a convenient four‐step reaction methods. Six analogues showed higher cytotoxic activity than the original genipin and benzylether‐triazolegenipin 5 j exhibited the strongest activity against P‐388 and A‐549 cancer cell lines with IC50 values of 2.54 and 4.53 μM. The structure‐activity relationships (SARs) study indicated that the introduction of dibenzyl ether, substituted silyl and long chain aliphatic‐triazoles at C‐10 position of genipin were most effective in improving cytotoxicity. Molecular docking results provided the information for further modification of genipin scaffold for development as cytotoxic agent.