http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110372579-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-50
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-50
filingDate 2019-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a7677766c10256d4429ec6683abef490
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_725f7b9c771413c7095260624868ff31
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_588556b563cb1b55607939702c8bf1eb
publicationDate 2019-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110372579-A
titleOfInvention A kind of 1-aryl-3-(6-arylpyridin-2-yl)-propenone and its preparation method and application
abstract The present invention relates to a kind of 1-aryl-3-(6-arylpyridine-2-yl)-propenone, and the molecular structure of the compound is shown in the following general formula: In the general formula, R 1 is hydrogen or methoxy base, R 2 is hydrogen or methoxy, R 3 is hydrogen or methoxy, Ar is phenyl, 4-methoxyphenyl, 3,4-dimethoxyphenyl, 3,5-dimethyl oxyphenyl or 3,4,5-trimethoxyphenyl. The compound can be obtained by aldehyde-ketone condensation reaction between 6-arylpyridine-2-carbaldehyde and substituted acetophenone. The 1-aryl-3-(6-arylpyridin-2-yl)-propenone of the present invention shows good antitumor activity on human intestinal cancer cells, human lung cancer cells and human glioma cells.
priorityDate 2019-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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