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filingDate 2004-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_28a36a0c51bc8e2a22e87ea7e889a154
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_132afef981c13cec26595c99016a1f05
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b442fd3d673debca056bdf624b6f16cd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a459ea044436e0f1f5ac906bac9df8aa
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a0f196da47cf96fc300712286c23b77c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e795395a71fe92819976630107c2c4f7
publicationDate 2004-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2004266774-A1
titleOfInvention Amide compounds
abstract The present invention is a compound and pharmaceutical composition comprising a compound of formula (I): n n n where R 1 is an N-containing heterocyclic group selected from an imidazolyl, a triazolyl, a pyridyl, a pyridazinyl, a pyrimidinyl and a pyrazinyl group, each of which may be substituted with one or more lower alkyl groups, R 2 is a hydrogen atom or a lower alkyl group, and R 3 is a phenyl group substituted with thienyl or halophenyl; a thienyl group substituted with thienyl, phenyl or halophenyl; a pyrrolyl group substituted with phenyl; a thiazolyl group substituted with phenyl; an indolyl group substituted with lower alkyl and/or halo(lower)alkyl; a fluorenyl group; or a carbazolyl group which is unsubstituted or substituted with a fluorine atom. The compound of formula (I) includes pharmaceutically acceptable salts. The compound of formula (I) and salts thereof have 5 -HT antagonism activity.
priorityDate 1999-10-01-04:00^^<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: 884.