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filingDate 1993-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1707f2d0c4ec87cf8acde85c2b0108a4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5440077bdb28739c055c5a2242d9a800
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f5f87cec8215a612f8833258a375b97
publicationDate 1999-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2125986-C1
titleOfInvention 7-(substituted)-9-(substituted-glycyl)-amido-6-demethyl-6- -deoxytetracyclines, intermediate compounds, methods of their synthesis, method of treatment and composition
abstract FIELD: organic chemistry, antibiotics. SUBSTANCE: invention relates to 6-demethyl-6-deoxytetracyclines of the formula (I) where R - halogen or NR 1 R 2 when R 1 - hydrogen, R 2 - methyl, ethyl, n-propyl; or when R 1 - methyl or ethyl, R 2 - methyl, ethyl, n-propyl, n-butyl; R 3 - hydrogen, C 4-8 -alkyl; R 4 - hydrogen, methyl ethyl; W - hydroxylamino-group, C 7-12 -alkyl-monosubstituted amino-group or R 3 and W taken together mean -(CH 2 ) n (R 5 )N-; n = 3; R 5 - trifluoroacetyl, or their pharmaceutically acceptable salts or metal complexes. Compounds of the formula (I) show antibiotic activity with respect to broad spectrum of organisms including that showing resistance to tetracyclines and they are useful as antibiotic agents. EFFECT: improved method of synthesis, enhanced effectiveness of compounds. 11 cl, 4 tbl, 27 ex
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2464261-C2
priorityDate 1992-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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