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filingDate 2015-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_12b81cdd77ebc0f59f51c47516224285
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c82989464dadd1c9891273ca119baee
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f4d24dd42feb3bbea2a549b4ef87aad6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_098080770f0e546851da875a68f51137
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0aecadbd73ddeb4df3a2b0cb52bab582
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publicationDate 2016-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2015252640-A1
titleOfInvention A novel KCNQ potassium channel agonist, the preparation method therefor and use thereof
abstract The present invention provides a compound with a structure represented by general formula I or a pharmaceutically acceptable salt thereof, a preparation method for the compound or the salt, and a use of the compound or the pharmaceutically acceptable salt thereof in the preparation of medicaments for treating nervous system diseases, such as epilepsy, convulsion, neuropathic pain, acute ischemic stroke or neurodegenerative diseases. Compared with Retigabine, the compound of the present invention has better brain tissue absorption. Moreover, the compound provided by the present invention not only has greatly improved efficacy, but also has far fewer neurological side effects than Retigabine, and therefore has a wider safe window.
priorityDate 2014-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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