A wide range of compounds capable of hydrolyzing RNA under mild condit
ions are considered. Their effectiveness can be enhanced by coupling t
hem to molecules affine to nucleic acids, such as intercalators and po
lycations. Attachment of reactive groups to oligonucleotides complemen
tary to segments of the target RNA not only allows the neighboring eff
ect to be employed but also hydrolytically active groups to be directe
d to the desired RNA sites. As hydrolytically active groups, the most
widespread are metallocomplexes, oligopeptides, amines, and organic co
nstructs containing reactive groups that usually are constituents of t
he active centers of nucleases: imidazole, guanidinium, carboxyl, and
amino groups. Design of compounds capable of effective catalytic cleav
age of RNA under physiological conditions may enable one to develop co
njugates of anti-sense oligonucleotides used in molecular-biological a
nd biomedical studies.