http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2003181479-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-64
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D271-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-54
filingDate 2002-11-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4ea9b2df9e8790d76137519558b4a7f1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_772d4bd3ecd008c730bfe49686040423
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4557cb80e388ad7e0e29a06359f96763
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_04241c57d772e7827009024da27ea5eb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9212a766731a607788117a4df874ad3e
publicationDate 2003-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2003181479-A1
titleOfInvention Substituted imidazoles
abstract The present invention relates to novel substituted imidazoles, to the use of these compounds as medicaments, to pharmaceutical compositions comprising the compounds, and to a method of treatment employing these compounds and compositions. The present compounds show a high and selective binding affinity to the histamine H3 receptor indicating a histamine H3 receptor antagonistic or agonistic activity. As a result, the compounds are useful for the treatment of disorders related to the histamine H3 receptor. More particularly, the present compounds possess a histamine H3 receptor agonistic activity and are accordingly useful in the treatment of disorders in which a histamine H3 receptor activation is beneficial.
priorityDate 2001-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 1096.