New 3 '-, 5 '-, 5-bromo-2 '-deoxyuridine (3a-g) and 3 '-, 5 '- thymidine (4
a-i) analogues with amino acid and peptide residues were synthesized and ev
aluated for antiviral activity. The influence of long peptide chains, essen
tial amino acids and the effect of this structural modification on the anti
viral activity has been also reported.
Three 5-bromo-2 '-deoxyuridine derivatives containing glycyl-, glycyl-glycy
l- and glycyl-glycyl-glycyl- residues (3a, 3b, 3c) showed a strong activity
against the herpes virus PsRV and a moderate one vs. HSV-1.
The corresponding thymidine analogues were considerably less effective, and
only compounds 4d and 4h showed a borderline effect against PsRV.