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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-519
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-551
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
filingDate 2020-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-111454264-B
titleOfInvention Luotonin A series compound and preparation method and application thereof
abstract The invention relates to the technical field of pharmaceutical chemistry, and discloses a Luotonin A series compound and a preparation method and application thereof. Luotonin A series compound shown as formula (I) and pharmaceutically acceptable salt thereof, wherein R is 1 Is H or halogen; r 2 Is ethylenediamine, ethylenediamine substituted by C1-C6 alkyl, piperazinyl substituted by C1-C6 alkyl, morpholinyl substituted by C1-C6 alkyl, homopiperazinyl or homopiperazinyl substituted by C1-C6 alkyl; x is C or N. The Luotonin A series compound provided by the invention has a stable structure, is easy to synthesize and prepare, can be used as a novel topoisomerase I inhibitor, and has strong antiproliferative activity on liver cancer, lung cancer, breast cancer and cervical cancer cell strains. 。
priorityDate 2020-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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