http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007000043-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-437
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 2006-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9c6c43b61ba1d530ed1fd0070459104
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d5a1159b9450bfc9bb56682f41593e75
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c32b0c835902085ac97bacfb2c66568b
publicationDate 2007-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2007000043-A2
titleOfInvention Pyrazolo[3,4-b]pyridin-2-yl]-benzoic acid derivatives as hiv integrase inhibitors
abstract The present invention provides compounds of formula (I) wherein Cx represents -CHO, -CH=N-OR3, -CH=N-NR3R4, -CH=N-R5 or -CH(OR3)2; m and n can be present up to four times and the other R radicals can vary from a hydrogen atom to different alkyl groups, halogen, rings or more. These compounds are used in pharmaceutical compositions for the treatment or prevention of AIDS or HIV infection, or for reducing HIV replication.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2017222921-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2011503119-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8461180-B2
priorityDate 2005-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 597.