5-Amino-2,9-dimethyl-1,10-phenanthroline-oligonucleotide conjugates have be
en synthesized. A 2'-O-methyl octaribonucleotide carrying a 2'-aminoethoxym
ethyl linker in a central position was produced. Reaction of the aminoneocu
proine phenyl carbamate with the fully deprotected oligonucleotide in aqueo
us solution gave virtually quantitative conversion into the conjugate. Prel
iminary cleavage studies in presence of zinc ions show nuclease activity to
wards RNA targets.