http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2008020456-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-5517
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5517
filingDate 2007-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22a770dbae89575aede4fd66e840a192
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4c7557d56d8a2ece4188110f884e53ad
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b07435a9a98aa496b637aab767d781a
publicationDate 2008-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2008020456-A2
titleOfInvention Pyrrolo[2,1-c][1,4]benzodiazepine hybrids and a process for the preparation thereof
abstract The present invention provides quinazolinone linked pyrrolo[2,1-c][1,4]benzodiazepine hybrid of general formula 5, wherein, R is alkyl or halo group selected from H, CI, F or CH3 and n=1 to 3 useful for antitumour/anticancer activity. The present invention also provides a process for the preparation of quinazolinone linked pyrrolo[2,1-c][1,4]benzodiazepine hybrid general formula 5.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2011513389-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2010058416-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2009109984-A1
priorityDate 2006-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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