FIELD: organic chemistry, biochemistry, pharmacy. SUBSTANCE: invention describes derivatives of hydroxamic and carboxylic acid with MMP-inhibiting activity represented by the formula (I) where m = 0-1; X means SO2; Y means OH or NHOH; R1 means optionally substituted C1-6-alkyl or piperidinyl; R2 means hydrogen atom or C1-6-alkyl; or CR1R2 means optionally substituted cycloalkyl, piperidinyl or tetrahydropyranyl; each B is similar or different and means hydrogen atom, C1-6-alkylnaphthyl, C1-6- alkylphenyl, C1-6-alkyl, cycloalkyl that is condensed optionally with benzene, C1-6-alkylcycloalkyl, phenyl, furanyl, thiophenyl, pyrrolyl that are optionally condensed with benzene, C1-6-alkylbenzofuranyl, C1-6- alkylbenzothiophenyl, C1-6-alkylindolyl where any of these groups is substituted optionally, or B-N-B is piperidinyl substituted with =NOR4; or when neither R1 nor R2 is not hydrogen atom then B-N-B means piperazinyl, piperidinyl, pyrrolidinyl optionally condensed with benzene and optionally substituted; R4 means hydrogen atom, C1-6-alkyl, phenyl, C1-6-alkylphenol, pyridyl, pyrazinyl optionally substituted, and its salts, solvates, hydrates, protected amino, carboxy or protected derivatives of hydroxamic acid and pharmaceutical composition eliciting MMP-inhibiting activity. Described compounds can be used for treatment of prevention of state associated with activity of matrix metalloproteinases. EFFECT: valuable medicinal and biochemical properties of compounds. 13 cl
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Authors
Dates
2003-08-20—Published
1998-11-12—Filed