http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4992432-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_966a6c1f382ec9bcb5e3839dfd73e5b8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D281-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D281-06
filingDate 1990-02-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-02-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b92f9f2b4a04025f5905b206b2d734e3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d8baf8e06060c989f0d3dabc7d8a120
publicationDate 1991-02-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4992432-A
titleOfInvention 3-phenyl-thiazepinones as calcium regulating agents
abstract Compounds of the formula <IMAGE> I wherein R1 is phenyl substituted with 1 to 3 substituents selected from the group consisting of halogen and lower alkoxy; R2 is hydrogen, lower alkyl, lower alkanoyl, lower cycloalkanoyl, <IMAGE> <IMAGE> R3 and R4 are independently lower alkyl, phenyl lower alkyl or together form a piperidine or pyrrolidine ring; n is 2 ro 4; m is 1 to 2; and pharmaceutically acceptable acid addition salts thereof, with the proviso that when R1 is 4-methoxyphenyl, R2 is hydrogen and R3 and R4 are methyl; and n is 2, the compound of formula I cannot be in the (-)-cis form, are described. The compounds of formula I are active as calcium channel blockers and accordingly, are useful as agents for treating ischemia.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002115655-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6541479-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6951860-B2
priorityDate 1990-02-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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