FIELD: organic chemistry, biochemistry. SUBSTANCE: invention describes substituted 6- and 7-aminotetrahydroisoquinoline carboxylic acids of the formula (I) and/or their R- isomeric form, and/or their physiologically tolerated salts wherein R1 is phenyl monosubstituted with (C1-C6)-alkyl-O-, halogen atom; -OR14 wherein R14 is (C1-C6)-alkyl; R2 is HO(H)N- or R7-O- wherein R7 is hydrogen atom or (C1-C6)-alkyl; R3 and R4 are similar or different and mean hydrogen atom, R8-(CO)-, wherein R8 is R7-O-C(O)-(CH2)n; R7-N(H)-(R9)-C(H)-wherein R9 means specific radical of proteinogenic 2-amino acid alanine, R10-O-C(O)-N(H)-(R9)-C(H)-wherein R10 is (C1-C6)-alkyl or benzyl; R3 and R4 in common with nitrogen atom form nitro radical; A is covalent bond; B is (CH2)m, wherein m = 0; x is CH=CH-. Compounds are inhibitors of matrix metallo- proteinases. EFFECT: valuable biochemical properties of compounds. 2 cl, 1 dwg, 2 tbl, 11 ex
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Authors
Dates
2003-09-20—Published
1998-05-12—Filed