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filingDate 1991-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e61480aca97c2a4daea522072aa31f8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10292d786dc5c931600d64c5eb16da98
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_58805ae07275869223b359d75c51ac45
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8acc5d0a6cf2ce783a69e49d6fa20e26
publicationDate 1993-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-419091-A3
titleOfInvention Propenoetheroximes, process of their preparation and pharmaceutical compositions in which said oximes are comprised
abstract The present invention relates to novel propenone oxime ethers, a process for their preparation and the pharmaceutical compositions containing them. …<??>The propenone oxime ethers according to the invention correspond to the formula: …<IMAGE>… in which… Ar and Ar' independently represent an unsubstituted, monosubstituted or polysubstituted phenyl group, a 9-anthryl or naphthyl radical or a pyridyl, thienyl or furyl group,… R1 and R2 independently denote a hydrogen atom, a C1-C4-alkyl group or, together with the nitrogen atom to which they are bonded, a pyrrolidinyl-1, piperidino, morpholino or piperazinyl-1 group,… n = 2 or 3 and… M = H, Cl, Br or a C1-C6-alkyl group. …<??>The invention also relates to the salts of the compounds of formula (I). …<??>These compounds have anti-platelet aggregation properties and are 5HT2 receptor antagonists.
priorityDate 1988-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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