http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1441733-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-506
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-675
filingDate 2002-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_776061c26879d66aba182c0295a854f9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fdf205068ac1c618b3c89c3309f36da7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b1154abd889228253d6eb3f4972169d3
publicationDate 2004-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1441733-A1
titleOfInvention Pharmaceutical compositions for the treatment of leukemia comprising dioxolane nucleosides analogs
abstract The present invention provides a novel method for treating leukemia in a host that has been previously treated with a BrcAbl tyrosine kinase inhibitor comprising administering to the host a therapeutically effective amount of a compound having the formula I: wherein B is cytosine or 5-fluorocytosine and R is selected from H, monophosphate, diphosphate, triphosphate, carbonyl substituted with. a C1-5 alkyl, C1-5 alkenyl, C1-5 alkynyl, C5-10 aryl, and and wherein each. Rc is independently selected from the group comprising H, C1-5, alkyl, C1-5 alkenyl, C1-5.alkynyl an hydroxy protecting group
priorityDate 2001-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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