http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102260297-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_653c418e41edbb4e1ce8bc5e53e70cec
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H7-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7016
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-706
filingDate 2011-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a073107591080df9160557c5396a3f1f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad147d4a95a9cd32b7e4870fa7d11103
publicationDate 2013-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102260297-B
titleOfInvention Trehalose amide derivative as well as preparation method thereof and application thereof
abstract The invention relates to a trehalose amide derivative as well as a preparation method thereof and an application thereof, wherein 6,6'-di(2-hydroxy benzamido)-6,6'-didesoxy-alpha, alpha-D-trehalose shows more superior activity against invasion of colon cancer 26-L5 cells than a natural product Brartemicin; IC50 is 0.20 micrograms per milliliter (0.33 microns); and the 6,6'-di(2-hydroxy benzamido)-6,6'-didesoxy-alpha, alpha-D-trehalose shows no cytotoxicity while the IC 50 is 10 micrograms per milliliter, shows antitumor invasion activity with high selectivity and is used for preparing drugs for preventing and treating invasion and transfer of colon cancers and the like.
priorityDate 2011-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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