FIELD: medicine. SUBSTANCE: present invention describes compounds of general formula I wherein Ar1 is phenyl, naphthyl, quinolyl, isoquinolyl optionally substituted with chlorine, fluorine, alkyl, alkoxy or dialkylamino; Ar2 is phenyl optionally substituted by chlorine, fluorine, alkyl or alkoxy, or thienyl; R1 and R2 are H or alkyl; is hydrogen or R2 and form double bond or R1 has no values, then N is attached to Ar2; R3 and R4 are alkyl or form with N to which they are attached, pyrrolidine, piperidine or hexahydroazepine; Z1 is C1-12 alkylene optionally interrupted by C5-7-cycloalkyl or phenyl; Q1 is H, methyl, amino, hydroxy, dialkylamino, guanidino, alkyl guanidino, pyridyl, indolyl, alkyl-4-piperazinyl, aminoalkyl-N-alkylamino, alkoxycarbonylamino, carbamoyl, phenyl optionally substituted by alkoxy, or pyridyl, imidazolyl, indolyl or pyrrolidinyl; Q2 and Q3 is H or alkil, or Q2 and Q3 form together C2-3-alkylene as pure enantiomers or mixtures thereof, and also pharmaceutically acceptable acid salts thereof. Compounds of formula I and pharmaceutically acceptable salts thereof are capable of being fixed on biological neuropeptide receptors Y (NPY), peptide from 36 amino acids having wide spectrum of physiological activity, more particularly with respect to central nervous system or cardiovascular system. EFFECT: improved properties of title compounds. 8 cl, 83 ex, 1 tbl
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