http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-102163494-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D498-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-395
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D498-16
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-395
filingDate 2018-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2020-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-102163494-B1
titleOfInvention heteroaromatic macrocyclic derivatives as protein kinase inhibitors
abstract The present invention provides a 2,7-substituted cyano[3,2- d ]pyrimidine cyclized compound having protein kinase inhibitory activity, a pharmaceutically acceptable salt thereof, and abnormal cells containing the compound as an active ingredient. It relates to a pharmaceutical composition for the prevention, alleviation or treatment of diseases caused by growth, and the novel 2,7-substituted cyano[3,2- d ]pyrimidine cyclized compound of the present invention is used for growth factor signaling Since it exhibits an excellent inhibitory effect on various protein kinases involved, it is useful as a prevention, alleviation or therapeutic agent for abnormal cell growth diseases caused by these protein kinases.
priorityDate 2018-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID147746
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419475039

Total number of triples: 649.