FIELD: organic chemistry, pharmacy. SUBSTANCE: invention describes a new heterocyclic compound of the formula (I): A1-X-(CH2)n-O-A2-A3-YR2 or its tautomeric form and/or pharmaceutically acceptable salt and/or pharmaceutically acceptable solvate where A1 means benzoxazolyl or pyridyl; A2 means benzene ring optionally substituted with C1-6-alkyl or C1-6-alkoxy-group; A3 means a fragment of the formula -(CH2)m-CH(OR′)- or -(CH2)m-1-CH=C(OR′)- where R1 means C1-6-alkyl optionally substituted with up to three substituents taken from the group including halogen atom, C1-6-alkoxy- and carboxyl-group; or R1 means naphthyl or phenyl optionally substituted with up to three substituents taken from the group including halogen atom, C1-6-alkyl and C1-6-alkoxy-group or R′ means phenyl-C1-6-alkyl and m = 1-5; R2 means amino-group or OR3 where R3 means hydrogen atom or C1-6-alkyl or when Y means a bond; R2 means triazolyl, tetrazolyl or oxadiazolyl; X means NR where R means C1-6-alkyl; Y means CO or CS or a bond at condition that Y means a bond only if R2 means triazolyl, tetrazolyl or oxadiazolyl; and n = 2-6. New compounds show good activity with respect to blood glucose decrease and therefore they can be used for treatment and/or prophylaxis of hyperglycaemia and especially for treatment of patients with diabetes mellitus of type-2 and also for treatment and prophylaxis of cardiovascular diseases, in part, atherosclerosis. Invention describes pharmaceutical compositions based on compounds of the formula (I) that can be used in medicine. EFFECT: enhanced antidiabetic effectiveness of compound synthesized. 15 cl, 1 tbl, 78 ex
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