Aryl furano pyrimidines: The most potent and selective anti-VZV agents reported to date
Author:
Publisher
Elsevier BV
Subject
Virology,Pharmacology
Reference27 articles.
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3. Lack of susceptibility of the highly potent inhibitors of varicella-zoster virus, bicyclic nucleoside analogues (BCNAs), to the catabolic action of thymidine phosphorylase and dihydropyrimidine dehydrogenase;Balzarini;Mol. Pharmacol.,2002
4. Chemotherapy of varicella-zoster virus by a novel class of highly specific anti-VZV bicyclic pyrimidine nucleosides;Balzarini;Biochim. Biophys. Acta,2002
5. Non-nucleoside structures retain full anti-HCMV potency of the dideoxy furanopyrimidine family;Bidet;Antivir. Chem. Chemother.,2004
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