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filingDate 1994-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_01107c4d258a81f4b0b34148d214a87d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6c49bdc8d4d2a03e29b598ecd40569c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81dc102f9b440969c2e6452140061954
publicationDate 1999-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2139290-C1
titleOfInvention DERIVATIVES OF 3-β-ALKENYLPENAM AND THEIR PHARMACEUTICALLY COMPATIBLE SALTS
abstract FIELD: organic chemistry, antibiotics. SUBSTANCE: invention relates to new derivatives of 3-β-alkenylpenam of the general formula (I): β where one of and R 1 means R 2 , -CN, -COR 4 , halogen atom, -CH= -CH 2 R 5 or Q and other means hydrogen atom and either lower alkyl or both in common mean CHR 6 -lactam ring; γ means hydrogen atom, lower alkyl, arylalkyl, allyl or a radical splitting in vivo; R 3 means hydrogen atom, lower alkyl, lower alkoxy-, benzyl-oxy-, amino-, lower alkylamino-group or lower alkyl-lower alkoxyamino-group; R 4 means hydroxyl group, R 5 or five- or six-membered N-, S- and/or O-containing heteroaromatic ring bound through nitrogen atom; -OCONHR 7 ,-OCONH 2 means -CN or -CHO; R 6 means R 7 ; Q means five- or six-membered N-, S- and/or O-containing heteroaromatic ring and n = 0, 1 or 2, and pharmaceutically compatible salts of these compounds. These compounds show an inhibitory effect on -COCH 2 Cl-lactamase activity. Under definite conditions they can be used in combination with β-lactam antibiotic for prophylaxis and control of pathogens of diseases producing β-lactamase. EFFECT: new compounds indicated above, valuable pharmacological properties. 17 cl, 3 tbl, 27 ex
priorityDate 1993-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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