http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2009209520-A1

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filingDate 2007-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b20700be06b752a165ee153d05da82b6
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publicationDate 2009-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2009209520-A1
titleOfInvention 2 -oxybenzamide derivatives as parp inhibitors
abstract A compound of the formula (I): and pharmaceutically acceptable salts thereof, wherein: R 2 , R 3 , R 4 and R 5 are independently selected from the group consisting of H, C 1-7 alkoxy, amino, halo or hydroxy; Y is —CRR C2 —(CH 2 ) m —, where m is 0 or 1, R C1 is selected from H, CH 3 and CF 3 , and R C2 is selected from H and CH 3 , or R C1 and R C2′ together with the carbon atom to which they are attached form the 1,1-cyclopropylene group formula (A): R N1 and R N2 are independently selected from H and R, where R is optionally substituted C 1-10 alkyl, C 3-20 heterocyclyl and C 5-20 aryl; or R N1 and R N2 , together with the nitrogen atom to which they are attached form an optionally substituted 5-7 membered, nitrogen containing, heterocylic ring; Het is formula (ii): where Y 1 and Y 3 are independently selected from CH and N, Y 2 is selected from CX and N and X is H, Cl or F.
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Total number of triples: 2068.