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filingDate 2004-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fb954caae11d655f496cb0a3fcc8ea0
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publicationDate 2006-05-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20060056978-A
titleOfInvention Oligonucleotide Analogues and Methods for Treating Flavivirus Infections
abstract Methods of inhibiting the replication of flaviviruses in mammalian cells, and oligonucleotide compounds for use in the methods are described. Oligonucleotide analogues (i) have a nuclease resistant backbone, (ii) can be ingested by cells, (iii) contain 8-40 nucleotide bases, and (iv) SEQ ID NOS: 1-4 Have at least 8 base sequences complementary to the virus positive strand RNA genomic region comprising at least a portion. Exposure to the analogs of cells infected with flaviviruses is effective within the cells, the analogs are heteroduplex structures composed of viral ssRNAs and oligonucleotides, have a dissociation temperature (Tm) of at least 45 ° C., virus 5 ′ and Characterized by having base pairs broken between the 3 'cyclized sequences.
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