http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9307881-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-70
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-70
filingDate 1992-10-16^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_95ebf9e09350b2830f8fa81c8bc85e0f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6c0f7b633c55785889d7c9f4384418e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_762c51369003c937e14ac66976e3bbfa
publicationDate 1993-04-29^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9307881-A1
titleOfInvention Inhibition of viruses by the administration of homopolyribonucleotides and/or duplex polymers
abstract A series of polyribonucleotides containing methyl and/or sulphur substitutions such as poly(1-methyl-6-thioinosinic acid) also [poly(m1s6I)], poly(1-methyl-6-thioguanylic) acid [poly(m1s6G)], and poly(6-thioguanylic acid) complexed with polycytidylic acid [poly(s6G)-poly(C)] are useful in treating human cells infected with AIDS viruses or viral opportunistic pathogens by inhibiting the virus from developing or spreading to unaffected cells. Poly(m1s6I), poly(m1s6G), and poly(s6G)-poly(C) may be administered orally, parenterally or transdermally per se or in the form of a pharmaceutically acceptable salt. As regarding the AIDS virus, these agents function in one or more ways as inhibitors of the viral reverse transcriptase necessary for viral replication, and/or also block the formation of syncytia (giant cells) which are characteristic of HIV infection and facilitate the transmission of the virus to uninfected cells.
priorityDate 1991-10-16^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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