http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4560786-A

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filingDate 1982-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1985-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a7f309e46f1dd9fe6033fc7eb6f5675
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publicationDate 1985-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4560786-A
titleOfInvention Δ8,9 -Prostaglandin derivatives, their preparation and use as medicinal agents
abstract Δ 8 ,9 -Prostane derivatives of Formula I ##STR1## wherein R 1 is CH 2 OH or ##STR2## wherein R 2 is hydrogen, alkyl, cycloalkyl, aryl, or a heterocyclic residue; or R 1 is ##STR3## wherein R 3 is an acid residue or R 2 ; A is --CH 2 --CH 2 -- or cis--CH═CH; n B is --CH 2 --CH 2 --, trans--CH═CH-- or --C.tbd.C-- n W is a free or functionally modified hydroxymethylene group or free or functionally modified ##STR4## wherein the OH--group can be in the α-- or β-- position; D and E jointly are a direct bond or n D is straight chain or branched alkylene or alkenylene of 1-10 carbon atoms which can optionally be substituted by fluorine atoms, and E is oxygen, sulfur, a direct bond, --C.tbd.C-- or --CR 6 ═CR 7 --, wherein R 6 and R 7 differ from each other and each is hydrogen, chlorine or alkyl; n R 4 is free or functionally modified hydroxy and n R 5 is an optionally substituted aliphatic group, cycloalkyl, optionally substituted aryl, or a heterocyclic group, and when R 2 is hydrogen, physiologically compatible salts thereof with bases, n have valuable pharmacological properties, e.g. luteolytic and abortifacient activities.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6303658-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004122102-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5023273-A
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priorityDate 1981-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 385.