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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_faf522b8b83eded745c73018576219ba
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 2006-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9874737e2d7af0f2ddfa1bee23dfe23
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_efc90a6b22cc4096de93c961e82d9e5d
publicationDate 2008-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2008013496-A
titleOfInvention Rhizo GM3 oligomer
abstract The present invention provides an oligomer of lyso GM3 and analogs thereof having an activity of inhibiting phosphorylation of EGFR (epidermal growth factor receptor) and useful as an anticancer agent. (2S, 3R, 4E) -2-Amino-3-O-benzoyl-4-octadecenyl 4-O- (2,4-di-O-acetyl-3-O- (1-methyl-4) , 7,8,9-tetra-O-acetyl-α-sialyl) 6-O-benzoyl-β-D-galactopyranosyl) -3-O-acetyl-2,6-di-O-benzoyl-β -D-glucopyranoside and a condensed compound of glutamic acid dimer to tetramer having an amino group at the C-terminus. [Selection figure] None
priorityDate 2006-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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