http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3027607-A1

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filingDate 2014-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9c142236cdc757db4aa6c5fbf2ffd2c4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d0122060d119d5049e5a3951b0c0254
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1cb60c619178651a256f403738bb497d
publicationDate 2016-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-3027607-A1
titleOfInvention Substituted heteroaryl compounds and methods of use thereof
abstract Provided herein are novel heteroaryl compounds, pharmaceutically acceptable salts and pharmaceutical formulations thereof for selectively inhibiting serotonin reuptake and/or acting as 5-HT 1A receptor agonists. Also provided herein are pharmaceutical compositions comprising the heteroaryl compounds and methods of using the pharmaceutical compositions in treating central nervous system (CNS) dysfunction in a mammal, especially a human being.
priorityDate 2013-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4158
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID311231111
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10220528
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394001
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID292652
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226405609
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3821
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226397462
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID60854
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226644035
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4184
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID90646799
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Total number of triples: 536.