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filingDate 2005-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2008-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2008514603-A
titleOfInvention 4- (Heteroaryl-methyl and substituted heteroaryl-methyl) -imidazol-2-thiones as α2 adrenergic agonists
abstract Formula 1: [Wherein the symbols are as defined in the description] Is a α 2 adrenergic receptor agonist. Some of the compounds of the present invention are specific or selective for α 2B and / or α 2C adrenergic receptors over α 2A adrenergic receptors. In addition, some of the compounds of the invention have no or minimal cardiovascular and / or sedative effects. The compounds of formula 1 are useful as therapeutic agents for mammals, including humans, for the treatment of diseases and / or relief of symptoms in response to treatment with α 2 adrenergic receptor agonists. Compounds of formula 1 that do not have significant cardiovascular and / or sedative effects are useful for treating pain and other conditions with minimal side effects.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012517433-A
priorityDate 2004-09-24-04:00^^<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: 452.