cycloSal-d4TMP pronucleotides structural variations, mechanistic insights and antiviral activity

Chris Meiera¹, Jürgen Renzea, Christian Ducho

¹Institute of Organic Chemistry, University of Hamburg, Martin-Luther-King-Platz 6, Hamburg, D-20146, Germany. chris.meier@chemie.uni-hamburg.de

|August 14, 2002

Abstract:

Pronucleotides represent a promising alternative to improve the biological activity of nucleoside analogues against different viral diseases. The basic idea is to achieve nucleotide delivery into cells, bypassing limitations with intracellular formation of nucleotides from their nucleoside precursors. The cycloSal-concept is one of several pronucleotide systems reported so far. For the nucleoside analogue d4T, the cycloSal-approach improved antiviral potency. The basic idea, chemistry, different structural modifications and their effects on the antiviral potency of the cycloSal-d4TMP triesters have been discussed in this review.

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Abstract:

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