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Ether lipid-ester prodrugs of acyclic nucleoside phosphonates: activity against adenovirus replication in vitro
Caroll B Hartline1, Kortney M Gustin, William B Wan
1University of Alabama School of Medicine, Birmingham, Alabama 35233, USA.
Abstract:
The acyclic nucleoside phosphonate cidofovir (CDV) and its closely related analogue (S)-9-(3-hydroxy-2-phosphonylmethoxypropyl)-adenine ([S]-HPMPA) have been reported to have activity against many adenovirus (AdV) serotypes. A new series of orally active ether lipid-ester prodrugs of CDV and of (S)-HPMPA that have slight differences in the structure of their lipid esters were evaluated, in tissue-culture cells, for activity against 5 AdV serotypes. The results indicated that, against several AdV serotypes, the most active compounds were 15-2500-fold more active than the unmodified parent compounds and should be evaluated further for their potential to treat AdV infections in humans.
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