Flaviviridae are an important family of viruses, responsible for widely spread diseases such as dengue and West Nile fever and hepatitis C. Despite the severity of the related diseases, no effective antiviral treatments for infection are available. Following our discovery of adenosine-hindered analogs as potent antiflaviviridae agents, we have continued our investigation on guanosine and inosine derivs., which were evaluated for activity against BVDV, YFV, DENV, and WNV viruses in cell-based assays. The present study allowed us to identify some newer features that led to improve the antiviral potency (down to the microM range) and to selectively inhibit BVDV and YFV viruses. The mol. modeling results were consistent with the hypothesis that test analogs act as RNA-dependent RNA polymerase (RdRp) inhibitors by interacting with a surface allosteric binding pocket
Hindered nucleoside analogs as antiflaviviridae agents
MANFREDINI, Stefano;ANGUSTI, Angela;VERONESE, Augusto;DURINI, Elisa;VERTUANI, Silvia;NALIN, Federico;SOLAROLI, Nicola;MURA M;
2004
Abstract
Flaviviridae are an important family of viruses, responsible for widely spread diseases such as dengue and West Nile fever and hepatitis C. Despite the severity of the related diseases, no effective antiviral treatments for infection are available. Following our discovery of adenosine-hindered analogs as potent antiflaviviridae agents, we have continued our investigation on guanosine and inosine derivs., which were evaluated for activity against BVDV, YFV, DENV, and WNV viruses in cell-based assays. The present study allowed us to identify some newer features that led to improve the antiviral potency (down to the microM range) and to selectively inhibit BVDV and YFV viruses. The mol. modeling results were consistent with the hypothesis that test analogs act as RNA-dependent RNA polymerase (RdRp) inhibitors by interacting with a surface allosteric binding pocketI documenti in SFERA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.