FIELD: organic chemistry, biochemistry. SUBSTANCE: invention describes a new heterocyclic derivative of the general formula (I) or its pharmaceutically acceptable salts where Ar1 means imidazolyl, pyrazolyl, 1,2,3- -triazolyl, 1,2,4-triazolyl that bound with X1 by the ring nitrogen atom and can be optionally substituted with one or two C1-4-alkyls; X1 means a direct bond or C1-4-alkylene; Ar2 means phenylene optionally substituted with one or two halogen atom; X2 means -A-X- or -X-A- where A means a direct bond or C1-4-alkylene and X means hydroxy- or thio-group; Ar3 means phenylene optionally substituted with one or two substituents taken among halogen atom or cyano-group; R1 and R2 in common form the group of the formula -D1-Z-D2- that in common with carbon atom to which it bound forms a ring having 3-8 atoms where D1 and D2 mean C1-4-alkylene and Z means a direct bond, hydroxy-group or vinylene; D1 and D2 can be substituted with C1-3-alkyl and Y means CONR3R4,CN,C(R3)=N-OR4,COOR3 or COR3 where R3 and R4 each means H or C1-4-alkyl. Compounds of the formula (I) inhibit activity of enzyme 5-lipoxygenase and can be used for treatment or relief of inflammatory diseases, allergy and cardiovascular diseases in mammals. Invention describes also a pharmaceutical composition on the base of compounds of the formula (I) and a method of inhibition of activity of 5-lipoxygenase. EFFECT: valuable pharmacological and biochemical properties of compounds. 12 cl, 44 ex
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Authors
Dates
1999-09-10—Published
1995-05-29—Filed