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filingDate 2004-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2007-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2007533611-A
titleOfInvention Pyrimidothiophene compound
abstract Formula (I): [Where: R 2 has the formula-(Ar 1 ) m- (Alk 1 ) p- (Z) r- (Alk 2 ) s -Q, where Ar 1 is an optionally substituted aryl or heteroaryl group And Alk 1 and Alk 2 are optionally substituted divalent C 1 -C 3 alkylene or C 2 -C 3 alkenylene groups, and m, p, r and s are independently 0 or 1 and Z is -O-, -S-,-(C = O)-,-(C = S)-, -SO 2- , -C (= O) O-, -C (= O) NR A- , -C (= S) NR A- , -SO 2 NR A- , -NR A C (= O)-, -NR A SO 2 -or -NR A- (where R A is hydrogen Or is a C 1 -C 6 alkyl), and Q is hydrogen or an optionally substituted carbocyclic or heterocyclic group); R 3 is hydrogen, an optional substituent, or an optionally substituted (C 1 -C 6 ) alkyl, aryl or heteroaryl group; and R 4 is a carboxyester, carboxyamide or sulfonamido group] These compounds are inhibitors of HSP90 in vitro or in vivo and are particularly useful for the treatment of cancer.
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12394686
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397310
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID396245
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID84124
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID397191
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP14602
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458395703
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID89394
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394281
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID431904250
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424538828

Total number of triples: 362.