H., M. Hanauske-Abel,Paul Palumbo,B., M. Cracchiolo,Myung-Hee Park,Edith Wolff,Axel-Rainer Hanauske,Michael B. Mathews,Deepti Saxena,Mainul Hoque
申请号：
US10581658
公开号：
US20120095058A1
申请日:
2004.12.01
申请国别(地区):
US
年份:
2012
代理人:
摘要：
The present invention discloses compounds and pharmaceutical compositions which are highly effective at inhibiting the accumulation of spliced and unspliced viral transcripts and their utilization for viral protein synthesis at cellular ribosomes, and at inhibiting the formation of the hypusine residue in cellular eIF-5A precursor proteins, the cellular cofactors that render spliced and unspliced viral transcripts translatable at the ribosomes of infectled cells. The invention further relates to methods of using such compounds and pharmaceutical compositions therefrom for inhibiting or preventing viral protein synthesis. Such inhibition cause a dose-dependent release from the virally induced arrest of the otherwise genetically preprogrammed apoptosis of virally infected cells, and in consequence, triggers their apoptotic ablation and the eradication of the chronic infection-mediating provirus integrated into their genome.
