http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3441387-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-13
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5377
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filingDate 2017-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d39355800097d7d7782249ad6500c621
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8019f419d4a173f3d190226d5256d2e9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_065e70b54804df640730a94f5643a00d
publicationDate 2019-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-3441387-A1
titleOfInvention Pi3k inhibitor, and pharmaceutically acceptable salt, polycrystalline form, and application thereof
abstract The present invention relates to a PI3K inhibitor, and a pharmaceutically acceptable salt, polycrystalline form, and application thereof. The invention specifically provides a polycrystalline form of 4-chloro-5-(6-(1-(methylsulfonyl)cyclopropyl)-2-morpholinopyrimidin-4-yl)pyridin-2-amine, a pharmaceutically acceptable salt thereof, or a polycrystalline form of the salt. The invention further discloses a pharmaceutical composition comprising the inhibitor and an application of the pharmaceutical composition.
priorityDate 2016-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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