http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1339022-C

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_27a71ddaaa2f5a8c228fc6cb3f3b3098
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D-
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-435
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55
filingDate 1988-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d6383d25292cc9d5696968e1e0b93d6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b4d467b93b7133bf27b44df47fc3f610
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a86564151e1f079b495d28ebae6b194d
publicationDate 1997-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1339022-C
titleOfInvention Lactam derivatives
abstract The invention relates to tricyclic lactams of the general formula (I) (I) wherein Im represents an imidazolyl group of the formula: or and R1 represents a hydrogen atom or a group selected from C1-6alkyl, C3-6alkenyl, C3-10alkynyl, C3-7cycloalkyl, C3-7cycloalkylC1-4alkyl, phenyl, phenylC1-3alkyl, phenylmethoxymethyl, phenoxyethyl, phenoxymethyl, -CO2R5, -COR5, -CONR5R6 or -SO2R5 (wherein R5 and R6, which may be the same or different, each represents a hydrogen atom, a C1-6alkyl or C3-7cycloalkyl group or a phenyl or phenylC1-4alkyl group, in which the phenyl group is optionally substituted by one or more C1-4alkyl, C1-4alkoxy or hydroxy groups or halogen atoms, with the proviso that R5 does not represent a hydrogen atom when R1 represents a group -CO2R5 or -SO2R5); one of the groups represented by R2, R3 and R4 is a hydrogen atom or a C1-6alkyl, C3-7cycloalkyl, C3-6alkenyl, phenyl or phenylC1-3alkyl group, and each of the other two groups, which may be the same or different, represents a hydrogen atom or a C1-6alkyl group; n represents 2 or 3; and physiologically acceptable salts and solvates thereof. The compounds are potent and selective antagonists of the effect of 5-HT at 5-HT3 receptors and are useful, for example, in the treatment of psychotic disorders, anxiety, and nausea and vomiting.
priorityDate 1987-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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