http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1342421-A3

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-00
filingDate 1984-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1987-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1011f715d444fc1f0fbc6249d98db96b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ffb63ba5ce3b7f514b29d6636de9628
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd232b1e2f40c3ddeac074f33bec396d
publicationDate 1987-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1342421-A3
titleOfInvention Method of producing derivatives of purine
abstract The invention relates to purine derivatives, in particular compounds of the general formula I -NHcH H, NC NC-NCHj -OCH R, -CH, jR2, where R ,, Rj is hydroxyl, or R ,, Rj is a benzoyloxy group having antiviral activity that allows you to use them in medicine. New compounds 1 were obtained to reveal the pharmacological properties of purine derivatives. They are synthesized from 2-amino-6-chloro-9 (2-benzoyloxy-1-benzosh10 Xymethyl ethoxy) methyl 3-9H-purine, which is subjected to catalytic hydrogenation if necessary, the resulting product is subjected to hydrolysis. Studies I show that they have a higher antiviral activity against herpes viruses than adiclovir, and they are classified as low-toxic compounds. Oj
priorityDate 1982-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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