http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2017114765-A

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filingDate 2014-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_60025d0d05b449856dc35ea3800fb98a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_769821268042bba1507879eed383728d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b85eac0de5db3728d57681c960cce8b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_23f8af84e7bc3a2325806a39619a75c5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f086c91fe699f5d9b066066c5e102d3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f5b5e43e70b3e02959291d02929a06a2
publicationDate 2017-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2017114765-A
titleOfInvention Heteroaryl compounds substituted with triazolyl
abstract The present invention provides a compound having an excellent prolyl hydroxylase (PHD) 2 inhibitory action. A heteroaryl compound substituted with a triazolyl represented by the formula (I) or a pharmaceutically acceptable salt thereof. (R1 is H or optionally substituted C1-3 alkyl; X is formula CR2 or N; R3 is H, halogen atom, C1-3 alkyl, or C1-3 alkoxy; Y is formula -CONR41-W1-, formula -CONR42-W2-CO-, formula -CH2NHCO-, formula -CH2OCH2-, or formula -NHCOCH2-; ring A is optionally substituted C3-8 cycloalkyl, optionally substituted C3-8 cycloalkenyl, substituted Aryl optionally substituted, saturated heterocyclyl optionally substituted, or heteroaryl optionally substituted) None
priorityDate 2014-04-25-04:00^^<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: 479.