A series of DNA-binding potential antitumor agents, (omega -aminoalkyl)-4-acridinecarboxamides, has been prepared either by reduction:of the corresponding (omega -aminoalkyl)-9-oxo-9,10-dihydro-4-acridinecarboxamides with aluminum amalgam or by aminolysis of the corresponding (omega -aminoalkyl)-1-chloro -4-acridinecarboxamides with the suitable amine. The noncovalent DNA-binding properties of these compounds have been examined using a fluorometric technique. In vitro cytotoxic potencies of these derivatives toward six tumor cell lines, including human colon adenocarcinoma (HT29) and human ovarian-carcinoma (A2780-sensitive, A2780cisR cisplatin-resistant, CH1-sensitive, CH1cisR cisplatin-resistant, and SKOV-3) cells, are described and compared to that of reference drugs.:One highly DNA affinic analogue (3a) has been identified with a; useful broad spectrum of cytotoxic activity in the 4-7 nM range (mean IC50 of 6 nM).