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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C327-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-13
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C251-02
filingDate 2011-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eaec901516ff704116b85df050d8e6bb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b49151d6bc9b876c3f509a99f4833555
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dfad7c17786421826bd28f8300b89898
publicationDate 2014-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8680155-B2
titleOfInvention Synthesis and antitumor activity of novel bis(benzylidene-benzenamine)disulfides
abstract Novel synthetic bis(benzylidene-benzenamine)disulfides and the preparation method are disclosed in the present invention. These compounds are afforded with the oxidizing reagent at low temperature and short time period via intra-molecular coupling reaction. In vitro experiments have been revealed that bis-disulfides are cytotoxic to cancer cells, especially human breast cancer cells MCF-7. Additionally, bis-disulfides arrest the cell cycle at sub-G1 phase and increase p38 phosphorylation to result in apoptosis. Bis-disulfides also inhibit growth of murine melanoma B16 cells but have no cytotoxicity to human fibroblasts. Bis-disulfides also can reduce murine melanoma size in the mouse model. The prepared compounds of the invention would be applicable in anticancer and anti-tumor therapies.
priorityDate 2011-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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