http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-94028194-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4015
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-02
filingDate 1994-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_963251a7950b7d83ab120a030af646af
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9ad7019df45d10fe9ba0e8fad6411c3d
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publicationDate 1996-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-94028194-A
titleOfInvention 4-acetyl-5-n-iodophenyl-1-carboxymethyl-3-hydroxy-2,5-dihydropyrrole-2- -on possessing analgetic activity
abstract 4-acetyl-5-p-iodophenyl-1-carboxymethyl-3-hydroxy-2,5-β-dihydropyrrol-2-one formula can be used in medicine as an analgesic. It is prepared by reacting methyl ester of acetylpyruvic acid, glycol and p-iodobenzaldehyde at room temperature according to the scheme CHCOCHCOCOOCH + NHCHCOOH + Yield 71%. T286 - 288 ° C (with decomposition). Found,%: C 41.80; H 3.00; N, 3.45; J 31.60. CHNOJ. Calculated,%: C 41.87; H 3.01; N 3.49; J 31.65. The analgesic activity of compound 35.4 exceeds that of the analog compound and the orthophene standard by 2 times. The toxicity of the compound is 2500 mg / kg, which is 2 times less than the toxicity of the analogue and 6.6 times less than the toxicity of orthophene.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2485100-C1
priorityDate 1994-07-27-04:00^^<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: 25.