FIELD: organic chemistry, biochemistry. SUBSTANCE: invention relates to benzopyrane and benzocondensed compounds of the formula (I) and its pharmaceutically acceptable salts where A' is O or CH2; R3, R4 - H or hydroxy-group; R5 is -(CH2)nCHX9X10, -(CH2)nX10, -CH(OH)X10; n = 0 or 1; X9 - H or phenyl; X10 - H, alkyl, phenyl possibly substituted with R6 and R7 each of the latter - H or alkyl; R1 is cis- or trans-(CH2)m-CX3X4X5 and substituted six-membered aromatic ring where m = 0 and X3 and X4 taken together with carbon atom to which they are bound form C4-7-cycloalkyl; X5 - carboxy-group; R2 - H. Synthesized compounds are antagonists of leukotriene B4. EFFECT: improved method of synthesis and inhibition. 13 cl, 1 tbl, 16 ex
             
         
            
              
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