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Transcript
Hepatitis C virus infects about 3 % of world’s population. Progress in molecular biology
and better knowledge of hepatitis C virus life cycle contribute to the development of
specifically targeted antiviral therapies for HCV. This new treatment also targets the internal
ribosome entry site (IRES), which is highly conserved and therefore an attractive target for
intervention. In addition, inhibition of IRES function could disable the propagation of the
virus early in the HCV life cycle. Novel therapeutics are aimed both at the HCV IRES
structure and its nucleotide sequence. Small molecules and synthetic nucleic acids, e.g.
antisense oligonucleotides and ribozymes, have been tested as potential therapeutic
substances. In this paper particular attention is paid to small molecules interacting with HCV
IRES.