Combinatorial chemistry is playing an increasingly prominent role in the pr
ocess of drug discovery. A nucleic acid-based (NAB (TM)) scaffold can be en
gineered to create functional group and topological diversity in a library.
Described herein is the parallel solid-phase synthesis of combinatorial li
braries of nucleoside phosphoramidates. and the first evaluation of antivir
al activity against hepatitis B virus (HBV). (C) 2001 Elsevier Science Ltd.
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