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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-81
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-81
filingDate 1996-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c72063c0b7ccf109cf1d35342af33d2e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4b2c8880ec9bd65f7864aa77b2f0f0e9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9771e55f6fda3bf3610b82a6e087154e
publicationDate 1997-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5681836-A
titleOfInvention Methanesulfonate salts of antipsychotic benzofuran derivatives
abstract The methanesulfonate salt of a class of antipsychotic compounds comprising a benzo b!furan moiety and a substituted heterocyclic moiety, linked via the 3-position of the benzo b!furan moiety by a methylene group, which are antagonists of dopamine receptor subtypes within the brain, being extremely potent antagonists of the human dopamine D 4 receptor subtype and having a selective affinity for the D 4 subtype over other dopamine receptor subtypes, possess advantageous qualities in terms of their improved aqueous solubility relative to the corresponding free base and, as such, provide for greater ease of formulation and display enhanced pharmacokinetic properties, including oral absorption.
priorityDate 1995-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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