http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H10130215-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C229-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A23L33-175
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A23L1-305
filingDate 1996-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d73f694543b73aad24d363601d8f7f83
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4ec3ca49ab5287cf5cc29abbd3d49609
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publicationDate 1998-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H10130215-A
titleOfInvention β-hydroxyaspartic acid derivative
abstract PROBLEM TO BE SOLVED: To provide a blocker for glutamate transporter [Solution] Synthetic development based on inhibition of glutamate uptake in Xenopus oocytes injected with bovine glutamate transporter gene (BGLAST) Then, the following formula (1) is used. (Wherein, R is an aromatic acyl group which may be substituted on a ring, a linear or branched lower aliphatic acyl group, an aryl group which may be substituted on a ring, Or an aralkyl group or a linear or branched lower alkyl group which may be substituted.) And a salt thereof. [Effect] The compound of the present invention is useful as a glutamate transporter blocker for elucidating the function of the glutamate transporter and also for treating various neurodegenerative diseases.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2005504016-A
priorityDate 1996-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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