Design, synthesis, and antitumor evaluation of novel acenaphtho[1,2- b]pyrrole-carboxylic acid esters with amino chain substitution

Abstract

8-Oxo-8 H-acenaphtho[1,2- b]pyrrole-9-carboxylic acid esters and derivatives were prepared and evaluated for cytotoxicity against A549 and P388 cell lines. Based on a novel chromophore precursor 8-oxo-8 H-acenaphtho[1,2- b]pyrrol-9-carbonitrile 1, the very insoluble 1 was converted to more soluble esters 5 and a series of 3-amino derivatives from 5 were obtained by mild S NAr H reaction between 5 and various amines. The biological evaluation indicated that methyl esters 5a are the most cytotoxic with IC 50 values of 0.45 and 0.80 μM (against A549 and P388, respectively) among the parent esters 5a– 5f, but 3-amino derivatives 4b and 4c of 5f with bromine showed the highest activity (with IC 50 values of 0.019–0.60 μM) among the 3-amino derivatives.