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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-12
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-495
filingDate 1997-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c0b572d50017076e67225e02d5fbbc84
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c344d8e3fc0800667200821b40cbff83
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publicationDate 2000-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20000016320-A
titleOfInvention Imidazole-substituted quinoxalinedione derivatives_
abstract The present invention is directed to a pharmaceutical composition useful as a glutamate receptor antagonist comprising an imidazole-substituted quinoxalindioone derivative of formula (I) or a pharmaceutically acceptable salt thereof, and the compound or salt thereof and a pharmaceutically acceptable carrier: It is about.n n n Formula In n n n n n n n In the above formula,n n n A is a group represented by the formula (CH 2 ) m or a group represented by the formula Ph- (CH 2 ) p , wherein Ph is a phenyl group,n n n X is an oxygen atom or a group represented by the formula NR 4 ,n n n R 1 is a hydrogen atom, a hydroxyl group or a triazolyl group (where X may be a bond when R 1 is a triazolyl group),n n n R 2 is a hydrogen atom, a nitro group, a halogen-lower alkyl group, a cyano group, an amino group, a mono- or di-lower alkylamino group or a halogen atom,n n n R 3 and R 4 are the same as or different from each other, and are each a hydrogen atom or a lower alkyl group,n n n n is 0, 1 or 2,n n n m is an integer from 2 to 6,n n n p is an integer of 1-6.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-102137358-B1
priorityDate 1996-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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