Structurally Simple Phenanthridine Analogues Based on Nitidine and Their Antitumor Activities

A series of novel structurally simple analogues based on nitidine was designed and synthesized in search of potent anticancer agents. The antitumor activity against human cancer cell lines (HepG2, A549, NCI-H460, and CNE1) was performed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay in vitro. The results showed that some of them had good anticancer activities, especially derivatives with a [(dimethylamino)ethyl]amino side chain in the C-6 position. Planar conjugated compounds <b>15a</b>, <b>15b</b>, and <b>15c</b>, with IC₅₀ values of 1.20 &#956;M, 1.87 &#956;M, and 1.19 &#956;M against CNE1 cells, respectively, were more active than nitidine chloride. Compound <b>15b</b> and compound <b>15c</b> with IC₅₀ values of 1.19 &#956;M and 1.37 &#956;M against HepG2 cells and A549 cells demonstrated superior activities to nitidine. Besides, compound <b>5e</b> which had a phenanthridinone core displayed extraordinary cytotoxicity against all test cells, particularly against CNE1 cells with the IC₅₀ value of 1.13 &#956;M.

Abstract licence: CC BY

A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.