FIELD: organic chemistry, chemical technology, pharmacy. SUBSTANCE: invention describes cinnamic acid substituted guanidides of the formula (1) where R(3) means -Xa-Уб-Ln-U where X means O, S; "a" = 0 or 1; Y means alkylene with 1, 2, 3, 4, 5, 6, 7 or 8 C-atoms; T where T means alkylene with 1, 2, 3, 4, 5, 6, 7 or 8 C-atoms in alkylene moiety; T means phenylene; "n" = 0; U means NR(24), R(25) or pyridyl being R(24) and R(25) means alkyl with 1, 2, 3, 4, 5, 6, 7 or 8C-atoms; R(1), R(2), R(4) and R(5) mean H, F, Cl, Br, J, CN, -Op-(CH2)s-CqF2q+1 where "p" = 0; "q" = 1, 2, 3, 4, 5, 6, 7 or 8; "s" = 0; R(6) and R(7) mean independently each of other hydrogen atom, F, Cl, Br, J, alkyl with 1, 2, 3, 4, 5, 6, 7 or 8 C-atoms, and their pharmaceutically acceptable salts also. Novel compounds are inhibitors of cellular sodium-protonic exchange. Invention describes also a method of synthesis of compounds of the formula (1) and a pharmaceutical composition eliciting an inhibitory activity with respect to Na+/H+-exchange and comprising a compound of the formula (1) as an active substance. EFFECT: improved method of synthesis, valuable medicinal properties. 6 cl, 1 tbl, 12 ex
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Authors
Dates
2002-10-10—Published
1996-07-25—Filed