FIELD: organic chemistry, medicine, pharmacy. SUBSTANCE: invention describes piperazine compound of the general formula (I) α or its pharmaceutically acceptable salt where and R1 are similar or different and each mean hydrogen atom, halogen atom, lower alkyl, amino-group, amino-group substituted with monosubstituted lower acyl, nitro-group; R2 are similar or different and each means hydrogen atom, halogen atom, lower alkyl, lower alkoxy-group, nitro-group, hydroxy- -group, amino-group mono- or disubstituted with group taken among group including lower alkyl or lower acyl; R3, R4, R5 and R6 are similar or different and each means hydrogen atom, acyl; R7 and R8 are similar or different and each means hydrogen atom or lower alkyl; Y means formula: R9 where and R10 mean hydrogen atom; R11 and R12 are similar or different and each means hydrogen atom or lower alkyl; or R13 and R12 form in common alkylene; R13 and R14 mean hydrogen atom; m is a whole number 0-2; n is a whole number 0-2 and R15; cycle A means phenyl, pyrimidinyl, thiazolyl, pyridyl, pyrazolyl or imidazolyl. Invention describes also inhibitor of production of TNF-0≤m+n≤2 and/or promoter of production of IL-10 containing compound of the formula (I) or its pharmaceutically acceptable salt as an active component and agent used for prophylaxis and treatment of diseases induced by anomalous production of TNF-α, diseases mediated by TNF-α or diseases that can be treated with IL-10 and comprising compound of the formula (I) or its pharmaceutically acceptable salt as an active component. EFFECT: valuable medicinal properties of compounds. 22 cl, 2 tbl
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Authors
Dates
2003-02-27—Published
1998-10-13—Filed