A series of cationic anthraquinone derivatives was investigated for th
eir ability to stabilize duplex and tripler DNA. Thermal denaturation
experiments demonstrate that each of these compounds stabilizes the [p
oly(dT). poly(dA)xpoly(dT)] tripler without significantly affecting th
e [poly(dT). poly(dA)] duplex. The amount of stabilization is determin
ed by the number and placement of the cationic substituents on the ant
hraquinone skeleton. The stabilization arises primarily from higher af
finity binding of the quinones to the tripler relative to the duplex s
tructures. Phosphorescence quenching and viscometric titrations indica
te that the quinones bind to the tripler by intercalation.