http://rdf.ncbi.nlm.nih.gov/pubchem/patent/NZ-588001-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2ca2e4410855da087e11bf3eea8933fa
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04
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/A61K31-502
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
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filingDate 2009-04-01^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d6272343fe195d6395c3ab42126d0915
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b3e02da9e775de810d16dc614cdcc242
publicationDate 2012-06-29^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-588001-A
titleOfInvention Disubstituted phthalazine hedgehog pathway antagonists
abstract Di-substituted phthalazines of structural formula depicted herein and pharmaceutically acceptable salts thereof are disclosed, wherein R1 is hydrogen, fluoro, cyano, trifluoromethyl, methoxy, or trifluoromethoxy; R2 is hydrogen or methyl; and R3, R4, R5, R6 and R7 are independently hydrogen, chloro, fluoro, cyano, trifluoromethyl or trifluoromethoxy, provided that at least two of R3, R4, R5, R6 and R7 are hydrogen. These compounds are useful as hedgehog antagonists and are suitable for treating cancer selected from the group consisting medulloblastoma, basal cell carcinoma, esophagus cancer, gastric cancer, pancreatic cancer, biliary tract cancer, prostate cancer, breast cancer, small-cell lung cancer, non-small cell lung cancer, B-cell lymphoma, multiple myeloma, ovarian cancer, colorectal cancer, liver cancer, kidney cancer, and melanoma.
priorityDate 2008-04-29^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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