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Inhibition of human cytomegalovirus replication by benzimidazole nucleosides involves three distinct mechanisms
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Phosphorylation of β-D-ribosylbenzimidazoles is not required for activity against human cytomegalovirus
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Recent strategies in the development of new human cytomegalovirus inhibitors
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From 1-acyl-β-lactam human cytomegalovirus protease inhibitors to 1-benzyloxycarbonyl-azetidines with improved antiviral activity. A straightforward approach to convert covalent to noncovalent inhibitors
Gerona-Navarro, G.; Pérez de Vega, M. J.; García- López, M. T.; Andrei, G.; Snoeck, R.; De Clercq, E.; Balzarini, J.; González-Muñiz, R. From 1-acyl-β-lactam human cytomegalovirus protease inhibitors to 1-benzyloxycarbonyl-azetidines with improved antiviral activity. A straightforward approach to convert covalent to noncovalent inhibitors. J. Med. Chem. 2005, 48, 2612-2621.
Influence of 6- or 8-substitution on the antiviral activity of 3-phenethylthiomethylimidazo[1,2-a]pyridine against human cytomegalovirus (HCMV) and varicella zoster virus (VZV)
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