FIELD: chemistry; pharmacology.
SUBSTANCE: there are disclosed compounds composed as to formula 
, where n and m stand for integer 1 to 3; z stands for integer 0 to 1; R is chosen from hydrogen, hydroxy or alkoxy; R2 stands for hydrogen; R3 and R4 are independently chosen from the group consisting of hydrogen, halogen; R5 is chosen from the group consisting of halogen, alkyl; R6 represents alkyl; E is chosen from the group specified in item 1 of formula of invention, A is chosen from N and C(R11), X is chosen from C, a stands for double bond and b stands for single bond; and Y is chosen from N(R1) provided when Y stands for N(R1), X stands for C, where R1 is chosen from C3-C6-cyclolkyl, phenyl; provided if A stands for C(R11), X stands for C, and Y stands for N(R1), then R11 and R1 can be bonded thus forming morpholinyl.
EFFECT: compounds possess antibacterial activity and are suitable as antibacterial means for treating bacterial infections in humans and animals.
13 cl, 10 tbl
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| COMPOUND, PHARMACEUTICAL COMPOSITION | 1999 |
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| ALKYLSUPHINYL-SUBSTITUTED THIAZOLIDE COMPOUNDS | 2011 |
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| NOVEL AROMATIC FLUOROGLYCOSIDE DERIVATIVES, MEDICATIONS, CONTAINING SAID COMPOUNDS AND THEIR APPLICATION | 2003 |
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| SULFUR-CONTAINING PHOSPHONIC ACIDS OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS OR ESTERS AND PHARMACEUTICAL COMPOSITION BASED ON SAID | 1993 |
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| LIGANDS FOR MELANOCORTIN RECEPTORS | 2001 |
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