Design, synthesis and in vitro evaluation of L-amino acid esters prodrugs of acyclic nucleoside phos

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A series of novel L-amino acid esters prodrugs of acyclic nucleoside phosphonates was synthesized and their anti-HBV activity was evaluated in HepG2 2.2.15 cells. Compound 1d exhibited more potent anti-HBV activity and lower cytotoxicity than those of adefovir dipivoxil with EC50 and CC50 values of 0.207 μmol/L and 2530 μmol/L, respectively.(C) 2007 Yu She Yang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
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