http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2017005954-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-165
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-165
filingDate 2016-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f871cc14694baab1e512b6f4602956d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_21004ed3cb667b903f29323dcd690aed
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publicationDate 2017-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2017005954-A1
titleOfInvention Melatonin analogues for treating cancer
abstract The present invention demonstrates that the compound N-[2-(7-methoxynaphthalen-1-yl) ethyl] acetamide (agomelatine) inhibits the growth of colon cancer cell lines in vitro as well as in vivo , suggesting the oncostatic/cytotoxic role of this compound. The lines having wild-type p53 demonstrated higher levels of inhibition than those having mutant p53. The effect of the compound depends on the state, mutated or unmutated, of p53, although, unlike melatonin or 5-fluorouracil, the compound is also able to inhibit growth when p53 is mutated, thereby increasing the number of treatable patients.
priorityDate 2015-07-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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