Abstract
Two new spiro-acridines were synthesized by introducing cyano-N-acylhydrazone between the acridine and phenyl rings followed by spontaneous cyclization. The final compounds (E)-1⿲-(benzylideneamino)-5⿲-oxo-1⿲,5⿲-dihydro-10H-spiro[acridine-9,2⿲-pyrrole]-4⿲-carbonitrile (AMTAC-01) and (E)-1⿲-((4-methoxybenzylidene)amino)-5⿲-oxo-1⿲,5⿲-dihydro-10H-spiro[acridine-9,2⿲-pyrrole]-4⿲-carbonitrile (AMTAC-02) were evaluated for their interactions with calf thymus DNA, antiproliferative and human topoisomerase I and IIα inhibitory activities. Both compounds presented ability to bind DNA. The binding constant determined by UV⿿vis spectroscopy was found to be 104M⿿1. Antiproliferative assay demonstrated that AMTAC-01 and AMTAC-02 were most active against prostate and melanoma tumor cell lines, respectively. The compound did not present Topo I inhibitory activity. However, both derivatives displayed topoisomerase IIα inhibitory activity comparable to amsacrine, and AMTAC-02 was more potent than AMTAC-01 with methoxy substituent group on phenyl ring. This study demonstrates that the new derivatives are promising molecules with topoisomerase IIα inhibitory and antiproliferative activities.
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