M. Camplo et al., Synthesis and biological evaluation of polyaminated 2 ',3 '-dideoxy-3 '-thiacytidine prodrugs, NUCLEOS NUC, 18(4-5), 1999, pp. 879-880
The syntheses and biological evaluation of polyaminated 2',3'-dideoxy-3'-th
iacytidine have been performed. A new lead was found to increase the in vit
ro antiviral potency (syncitia formation on MT-4 cell line) of two order ma
gnitude greater than the parent nucleoside drug. Moreover, the in vitro act
ivity on HIV macrophages was found to be more than 3 log greater than the a
ctivity of the parent drug 1.