Serendipity and VZV drug discovery
Author:
Publisher
Elsevier BV
Subject
Drug Discovery,Molecular Medicine
Reference33 articles.
1. Potent and selective inhibition of varicella-zoster virus (VZV) by nucleoside analogues with an unusual bicyclic base;McGuigan;J. Med. Chem.,1999
2. Nucleic acid related compounds. 39. Efficient conversion of 5-iodo to 5-alkynyl and derived 5-substituted uracil bases and nucleosides;Robins;J. Org. Chem.,1983
3. Palladium-catalyzed coupling of terminal alkynes with 5-(trifluoromethanesulfonyloxy)pyrimidine nucleosides;Crisp;J. Org. Chem.,1993
4. Highly potent and selective inhibition of varicella-zoster virus by bicyclic furo pyrimidine nucleosides bearing an aryl side chain;McGuigan;J. Med. Chem.,2000
5. Bicyclic nucleoside inhibitors of varicella-zoster virus (VZV): the effect of a terminal halogen substitution in the side-chain;Brancale;Bioorg. Med. Chem. Lett.,2000
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