FIELD: organic chemistry, medicine. SUBSTANCE: invention relates to compound of thiazolidine of pyridine type and its salt of the formula (I) where X1 is S; X2 is S or O; Y is -CR6R7; R6 and R7 - hydrogen atom, or R7 together with R4 forms a bond; Z is C1-10-alkyl, substituted silyl-group; or -A-B where A is bivalent C1-6-saturated or C2-6-unsaturated hydrocarbon group possibly substituted with 3 hydroxyl-groups (not above), oxo- and C1-7-alkyls, and B means a radical of the formulas: (a) , (b) , (c) , (d) , (e) , (f) , (g) , (h) , (i) , (j) , (k) , (l) and (m) . Each Ra and Rb - hydrogen atom, alkyl, halogen, phenyl, α--naphthyl, β--naphthyl, furyl, and Rc - hydrogen atom or C1-7-alkyl; R1, R2 and R3 each means hydrogen; n = 0. Compounds of the formula (I) or their pharmaceutically acceptable salts can be used for prophylaxis or treatment of diabetes mellitus in mammalian. Also, compounds (I) show antiglycation activity and useful for diabetic complications treatment. EFFECT: improved method of synthesis, enhanced effectiveness of compounds. 9 cl, 28 tbl, 15 ex
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Authors
Dates
1999-01-20—Published
1995-03-27—Filed