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publicationDate 2018-11-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2017219032-B2
titleOfInvention Novel tetrahydropyridopyrimidine compound or salt thereof
abstract A method of treating a disease selected from the group consisting of ovarian cancer, bladder cancer, uterine cancer, pancreatic cancer, and hepatocellular cancer, comprising administering an effective amount of a tetrahydropyridopyrimidine compound represented by the following formula (I) or a pharmaceutically acceptable salt thereof to a subject in need thereof: N'--N N' x (1) wherein, in the formula, X represents a halogen atom or a halogeno-C1 _3 alkyl group; R represents a C6_14 aryl group which is substituted with R' and may be substituted simultaneously with R 2, or a 5- or 6 membered heteroaryl group which is substituted with R' and may be substituted simultaneously with R2 ; R represents a hydrogen atom, a phenyl group, a hydroxy-C1 alkyl group, a hydroxy-C3 7 cycloalkyl group, a Ci-6 alkoxy group which may be substituted with Ra, a C3-7 cycloalkylaminosulfonyl group, a 3- to 7-membered monocyclic heterocycloalkylsulfonyl group, a halogeno-C1 _3 alkoxycarbonylamino group, a halogeno-C1 _3 alkylcarbonylamino group, a 3- to 7-membered monocyclic heterocycloalkanecarbonyl group substituted with a hydroxy-Ci 6 alkyl group, or -(CH 2)n C(=0)-NHRf; R2 represents a hydrogen atom, a halogen atom, or a halogeno Ci_3 alkyl group; Ra represents a Ci-6 alkylpyrazolyl group, a triazolyl group, a tetrazolyl group, or a Ci-6 alkylsulfonylpiperazinyl group; Rf represents a halogeno-C 1 _3 alkyl group, a hydroxy-C1 - alkyl group, a hydroxy-C3_7 cycloalkyl group, a hydroxy-C 3_7 cycloalkyl-C1 _6 alkyl group, or a CI_ alkyl group substituted with Rfa; Rfa represents a C1-6 alkylpyrazolyl group, a halogeno-C1 _3 alkylthiazolyl group, an oxadiazolyl group, or a halogeno-C1 _3 alkyloxadiazolyl group; and n represents an integer of from 0 to 3.
priorityDate 2014-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID118545189
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5881
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409771284
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP15122
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419567129
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID433029658
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID118545187
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID433029906
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID433029702
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69268791
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419645220
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424908444
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457280508
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID118545188
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID433029642
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID118545184
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15182658
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID433029845
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID433029648
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419644274
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID118545186
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67972
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID433029629
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ6RX08
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24614
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID118545199
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414866485
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ5HJP2
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID433029633
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12582612

Total number of triples: 630.