http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2349416-T3

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-04
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filingDate 2005-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-01-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad2bfa26a9cc2eb36335a9578931fee5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_431c9ff55a94f1af6d744aeb78fe9eb4
publicationDate 2011-01-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2349416-T3
titleOfInvention TIENOPIRIDINES AS ALLOSTERIC POTENTIALS OF THE M4 MUSCARINIC RECEIVER.
abstract A compound of Formula I: ** (See formula) ** m is 1 or 2; n is 0, 1 or 2; X is a bond, -O-, -SOp-, -C (O) -, -NR2-, -C (O) -NR2-or -NR2-C (O) -; p is 0, 1 or 2; R1 is hydrogen, hydroxyl, C1-C4 alkyl, phenyl, pyridyl, pyrrolidinyl, piperazinyl, morpholino, thiazolyl, imidazolyl or 1,3-dioxalanyl; whose phenyl, piperazinyl or thiazolyl group may be optionally substituted with a substituent selected from the group consisting of halo or C1-C2 alkyl; where n cannot be 0 when p is 0, or when X is -O-, -NR2 or -NR2-C (O) -; R2 is hydrogen or C1-C2 alkyl; whose C1-C2 alkyl may be optionally substituted with a hydroxyl; or a pharmaceutically acceptable salt thereof.
priorityDate 2004-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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