FIELD: organic chemistry, biochemistry. SUBSTANCE: invention relates to N-arylsulfonyl amino acid omega-amides of the formula (I) and/or stereoisomeric forms of the compound (I) and/or physiologically acceptable salts of the compound (I) wherein R1 means phenyl, phenyl once substituted with halogen atom, heterocycle residue taken among the following group: morpholine, pyrrolidine; R2 means hydrogen atom; R3 means -alkyl-C(O)- wherein R6 and R7 in common with nitrogen atom to which they are bound form residue if the formula (IIA) and the formula (IIe) wherein q means 0 or 1; Z means carbon atom or covalent bond; R8 means hydrogen atom or halogen atom; or R3 means -alkyl-C(O)-Y wherein Y means residue of the formula (IIc) or (IId) wherein R8 means hydrogen atom of halogen atom; R9 means hydrogen atom; or R3 means -alkyl-C(O)- wherein R9 has above given values; o means a whole number 2; R4 and R5 in common with ring amino-group form 4-7-membered ring wherein one carbon atom is substituted for -O-; A means a covalent bond; B means wherein m means 0; X means CH= CH-. Compounds of the formula (I) are inhibitors of matrix metalloproteases and can be used in medicine. EFFECT: valuable biological and medicinal properties of compounds. 4 cl, 3 tbl, 16 ex
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Authors
Dates
2004-05-10—Published
1999-10-21—Filed