http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1282494-A1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-10
filingDate 1985-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c611355ea1634e793ad753ab5857c5ad
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publicationDate 1991-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1282494-A1
titleOfInvention 2-(p-tolylaminomethyleneamino)-6-phenil-3-oxazine-4 on-displaying analgetic activity
abstract The invention relates to substituted oxazines, in particular 2- (p-tolyl-aminomethylenamino) -6-phenyl-1,3-oxazine-4-one (OK), which exhibits analgesic activity and can be used in medicine. For you left. No new OK was obtained from substituted oxazine from 5-phenyp-2,3-dihydrofuran-2,3-dione and N- (p-tolyl) -n-cyanoformamidine in toluene medium by heating for 50 minutes. The precipitated OC is separated and recrystallized. Yield 70%, t, pl. 210-212 C. Testiyni shows that in analgesic activity, OK is better than amidopyrine (AI) and 2-diallyamine-6-fensh1-1,3-oxazin-4-one (FC), since the dose used is 2 times lower than the dose of AP and 1.7 times. below daza fk. Toxicity OK less toxicity AIJ. 1 tab. § (Л с 5; v X) ND
priorityDate 1985-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 28.