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filingDate 1996-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4ed15b055dc0c9193b6b3e1e8178ec1d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ac259f3d9575c8a5e582cacbb273fcb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1b824b051bd9dcce3135b022bacfc288
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a2d7218dfee081620ec77a61273e84d7
publicationDate 2007-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2227533-C
titleOfInvention Improved therapeutic agents
abstract This invention relates to now nucleoside derivatives of formula (I); wherein R1 and R2 are independently selected from hydrogen, elaidoyl, oleoyl, stearoyl, eicosenoyl (cis or trans) and eicosanoyl, with the provisos that R1 and R2 cannot both be hydrogen, oleoyl or stearoyl, R1 cannot be hydrogen when R2 is oleoyl or stearoyl, and R2 cannot be hydrogen when R1 is elaidoyl, oleoyl or stearoyl. Further, the invention relates to the use of the nucleoside derivatives of formula (I) wehrein R1 and R2 are independently selected from hydrogen, and C18- and C20-saturated and mono-unsaturated acyl groups, with the provisos that R1 and R2 cannot both be hydrogen, in the manufacture of a pharmaceutical preparation for the treatment of tumours.
priorityDate 1995-07-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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