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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00
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filingDate 1977-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1979-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a990e0b1659e2b3532ca92aca6ed1c7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e6cce3e4af81a1e51af4e530e70409b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_87c18d8023457912ee69f1f1902edaea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47ce47223b27bfb76b237dc27cb6e14c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6cb3729b65365bcb045a0eea5415c2ad
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4c6d9cb351db55f0fbd55c53d0f25a1b
publicationDate 1979-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4179463-A
titleOfInvention 2-Amino-cyclopent-1-ene-1-dithiocarboxylic acids
abstract 2-Amino-cyclopent-1-ene-1-dithiocarboxylic acid derivatives of the formula, <IMAGE> (I) wherein R is C2-4 alkenyl, or C1-6 alkyl group having optionally a C1-4 alkoxy, hydroxy, carboxy and/or amino substituent, with the proviso that if R is an unsubstituted alkyl group, this group contains at least 5 carbon atoms, are prepared by reacting 2-amino-cyclopent-1-ene-1-dithiocarboxylic acid or a salt thereof with an amine of the formula, R-NH2 (II) wherein R is as defined above. The new compounds of the invention exert dopamine- beta -hydroxylase inhibiting effects.
priorityDate 1976-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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