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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-453
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K45-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-453
filingDate 2001-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_04dc1321dc1bc30f31db83d405c39744
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a1919f989d03fdf7e61a461e5b153440
publicationDate 2001-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2001051635-A1
titleOfInvention Flavopiridol methods and compositions for HIV therapy
abstract Disclosed is the unexpected discovery that flavopiridol binds tightly to the transcription elongation factor, P-TEFb and dramatically inhibits its activity. As P-TEFb is required for HIV propagation and replication, this invention provides new methods, compositions and kits for the effective treatment of HIV infections and AIDS using flavopiridol, both alone and combination with other therapies.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006204975-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7364842-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006171923-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004104587-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004254094-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004104587-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2012104039-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2010096831-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006062733-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010332029-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006188898-A1
priorityDate 2000-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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