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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f2d3599fb8f8f479dba95ca9bb504884
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-27
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-165
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-325
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-08
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-165
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-08
filingDate 2006-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22c9f4eeffe9d820dcb3ae1c2553fb24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc4d77bac04fc4691539e678463707a5
publicationDate 2008-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20080028485-A
titleOfInvention How to treat epilepsy outbreaks
abstract The present invention comprises administering to a subject in need thereof a therapeutically effective amount of a compound selected from the group consisting of formula (I) and formula (II), or a pharmaceutically acceptable salt or ester thereof To prevent, treat, reverse, inhibit or inhibit development:n n n n n n n n Wherein phenyl is substituted with 1 to 5 halogen atoms wherein X is selected from the group consisting of fluorine, chlorine, bromine and iodine; R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are independently selected from the group consisting of hydrogen and C 1 -C 4 alkyl; Wherein C 1 -C 4 alkyl is optionally substituted with phenyl, wherein phenyl is independently selected from the group consisting of halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, amino, nitro and cyano Optionally substituted).
priorityDate 2005-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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