FIELD: organic chemistry, chemical technology, biochemistry, pharmacy. SUBSTANCE: invention relates to 2-(iminomethyl)amino-phenyl derivatives of the general formula (I) where A is aromatic residue of the formula (Ia) ; R1 and R2 mean independently hydrogen, halogen atom, hydroxyl-group, linear or branched C1-C6-alkyl, linear or branched C1-C6-alkoxyl; R3 is hydrogen atom, linear or branched C1-C6- alkyl or -COR4 where R4 is -C1-C6-alkyl or residue of the formula (Ib); B means linear or branched -alkyl or 5-membered heterocycle including 1-4 heteroatoms taken among O, S, N and, in part: thiophene, furan, pyrrol or thiazole where carbon atoms are unsubstituted or substituted with one or some groups taken among linear or branched C1-C6-alkyl, C1-C6-alkoxyl or halogen atom; X means -CO-C1-C6-X'-, -NH-CO-X'-, CH=, -CO- or linkage being X' means N(R3) where n = 0-6; Y means -Y'-, -Y'-NH-CO-, -CO-Y'-, -Y'-CO-, -(CH2)n-Y'-, -Y-N(R3)-, Y'-CH2-N(R3)-CO-, -Y'-O-, -Y'-O-Y' or linkage being Y' means -(CH2)n- where n = 0-6 ; Het means pyrrol, pyrrolidine, furan, thiophene, imidazole, imidazoline, oxazole, isoxazole, oxazoline, isoxazoline, thiazole, thiazoline, thiazolidine, thiazolidinone, azethidine, piperidine, imidazoli- dinedione, imidazolidinone. Compounds of the formula (I) show simultaneous activity as inhibitors of NO-synthase activity and lipid peroxidation. EFFECT: improved method of synthesis, valuable biochemical properties of compounds. 14 cl
Authors
Dates
2003-04-20—Published
1998-06-15—Filed