http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0098794-A1

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filingDate 1983-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3166ac2742ed8d27971a1a42e170bacb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9272d10cf463bd847a26b467681b6cda
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a3dea168bfcd34fbeb4959a76284b88
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_acb8180877b4292618c0c09f52eae538
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_43f2cd06124280737d8a8949d07026f7
publicationDate 1984-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0098794-A1
titleOfInvention Carbacyclines, process for their preparation and their use as medicines
abstract The invention relates to carbacyclin derivatives of the general formula I <IMAGE> wherein R1 is OR2, where R2 is hydrogen, alkyl, cycloalkyl, aryl, -CH2 -? - aryl or a heterocyclic radical, or R1 is NHR3 with R3 in the meaning of an acid radical or the radical R2 A a -CH2-CH2-, trans -CH = CH- or -C ^ C group, W a free or functionally modified hydroxymethylene group or a free or functionally modified <IMAGE> group, the OH group can be α- or β-permanent, D the group <IMAGE> is a straight-chain saturated alkylene group with 1-5 C atoms, a branched saturated or a straight-chain or branched unsaturated alkylene group with 2-5 C atoms, which, if appropriate can be substituted by fluorine atoms, n can denote the number 1, 2 or 3, E represents a direct bond, a -C ^ C group or a - CR6 = CR7 group, where R6 is hydrogen or
priorityDate 1982-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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