http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007254446-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_37caa7c14ee6a6f4a1ae73318957b0ba
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-99
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-062
filingDate 2006-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d8a02fa6b84151771599d275652a219
publicationDate 2007-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2007254446-A
titleOfInvention Novel dipeptides, L-leucyl-L-tryptophan and prolyl endopeptidase inhibitors
abstract [Objective] To extract a protein from seaweed and microalgae extract and to provide a novel peptide having prolyl endopeptidase inhibitory activity from this protein. [Composition] After extracting dry powder of seaweed (Wakame, Okinawa Mozuku, Arame, Kombu, Hijiki, Honda Walla, Akamok, Nori, etc.) and microalgae (Chlorella, Spirulina) with weak alkaline aqueous solution, ethanol fractionation to obtain seaweed And obtaining a microalgal protein. Further, the novel seaweed and microalgae peptides obtained by cleaving into peptide chains and then isolated and purified by reverse phase HPLC are L-leucyl-L-tryptophan, have prolyl endopeptidase inhibitory activity, and are Has an anti-amnesic effect in the body and extremely low toxicity. [Selection figure] None
priorityDate 2006-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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