http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0432899-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ef2e9f5ce8630d9b282043b8d060caff
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P27-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P27-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P27-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P27-06
filingDate 1990-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_70ea7781a66493541cb1ac3fa51bd1b5
publicationDate 1991-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0432899-A1
titleOfInvention Novel pharmaceutical epinephrine-pilocarpine derivatives
abstract The present invention relates to new racemic and optically active compounds containing a first moiety derived from a pilocarpine compound in which the furanone ring of pilocarpine is replaced by a hetero-ring containing a secondary nitrogen hetero­atom, and a second moiety derived from an epinephrine compound or a β-adrenergic blocking compound, linked at the secondary nitrogen atom of the furanone-replacing hetero-ring of the pilocarpine compound and at the hydroxyl group of the epinephrine compound or of the β-adrenergic blocking compound, via a carbonyl linker, and pharmaceutically acceptable acid addition salts thereof. n The new compounds of the present invention are potent ocular hypotensives exhibiting minimal deleterious pupillary effects.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5484780-A
priorityDate 1989-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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