http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11242354-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04
filingDate 2020-03-20^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-02-08^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36cc6548f7c81daeefa0bd20c610b4d5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_24b1beb3237986b6e5bbab0d42ef5692
publicationDate 2022-02-08^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-11242354-B2
titleOfInvention 4-sulfur substituted podophyllotoxin derivative and preparation method therefor and use thereof
abstract Disclosed are a 4-sulfur substituted podophyllotoxin derivative and a synthetic method therefor and the use thereof. In the present invention, introducing heteroaromatic compounds with rigidity, such as 4-trifluoromethylpyridin-2-thiol, 4-trifluoromethyl-2-mercaptopyrimidine, and para-fluorothiophenol, respectively as substituent groups to position 4 of C ring of a podophyllotoxin or 4 demethylepipodophyllotoxin, obtaining a podophyllotoxin derivative as shown in formula (V) with a significantly improved antitumour activity and reduced toxic side effects. Experiments of in vitro tumour cell activity inhibition indicate that the antitumour activity of the compound as shown in formula (V) of the present invention is significantly improved compared to that of the podophyllotoxin or 4 demethylepipodophyllotoxin.
priorityDate 2017-09-22^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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