http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2065388-A1

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filingDate 2007-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bd185c73e23b0e072eed818039e85121
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a8deb5aff42a1826cab291529dd4ccc9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5ddb5ed037f093a30eadd6090fae829
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_830d52d0ff177df1d7a788f1fa8b680b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81715413d1266a6097576180ad9fbcf7
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publicationDate 2009-06-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2065388-A1
titleOfInvention Pyrazolopyrimidine derivative
abstract Problem to be Solved n To provide a novel compound inhibiting the effect of HSP90, in particular a novel compound inhibiting the function of HSP90 as a chaperone protein and having antitumor activity. n Solution n The present invention provides a pyrazolopyrimidine compound represented by the formula (1) having various substituents which inhibits the ATPase activity of HSP90 and which has antitumor activity, an HSP90 inhibitor comprising the compound represented by the formula (1), a medicament comprising the compound represented by the formula (1), an anticancer agent comprising the compound represented by the formula (1), a pharmaceutical composition comprising the compound represented by the formula (1) and a method for treating cancer using the compound represented by the formula (1).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2520966-C2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2810945-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2610259-A4
priorityDate 2006-09-19-04:00^^<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: 2953.