http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-I750403-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-519
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
filingDate 2018-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b4240ae3b7ec59690ec54024046a455c
publicationDate 2021-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-I750403-B
titleOfInvention Fibroblast growth factor receptor inhibitors, pharmaceutical preparations containing them, and uses thereof
abstract The invention belongs to the technical field of medicine, and particularly relates to an irreversible inhibitor of fibroblast growth factor receptor (FGFR) represented by formula I, a pharmaceutically acceptable salt and a stereoisomer thereof. The present invention also relates to pharmaceutical formulations, pharmaceutical compositions and uses of these compounds. R 1 , R 2 , R 3 , R 4 , m, X, warhead 1 , warhead 2 are as defined in the specification. The compounds of the present invention have efficient and highly selective inhibitory effects on fibroblast growth factor receptors, and can be applied to the treatment of related diseases mediated by abnormal FGF/FGFR, especially the treatment of cancer diseases.
priorityDate 2017-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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