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filingDate 1986-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07343a04eeb9923ac73324c25a09d3b1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_38bf13ecdbdc0dea599f8ad50d9ba9a1
publicationDate 1986-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0197752-A2
titleOfInvention Pharmaceutical compositions
abstract Compounds of formula (II)wherein R, and R<sub>2</sub> are each separately selected from hydrogen, alkyl, alkenyl and alkynyl groups having up to a maximum of four carbon atoms and being unsubstituted, and alkyl, alkenyl and alkynyl groups having up to a maximum of three carbon atoms and being substituted by one, or in the case of fluoro by one or more, substituents but with the proviso that when R, is hydrogen then R<sub>2</sub> is hydrogen or methyl, or R, and R<sub>2</sub> together constitute an ethylene bridging group, and R<sub>3</sub> is a group which under physiological conditions undergoes elimination with the formation of a 3,5-dioxopiperazinyl ring, with the further proviso that the compound is in the meso or erythro configuration when each of R, and R<sub>2</sub> is the same or different unsubstituted or substituted alkyl, alkenyl or alkynyl group, and salts thereof with a physiologically acceptable inorganic or organic acid, are of value as prodrugs, particularly in the therapy of cancer and psoriasis.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9200951-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-612119-B2
priorityDate 1985-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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