FIELD: chemistry.
SUBSTANCE: invention relates to the field of organic chemistry, specifically to a heterocyclic compound of formula (I) or to a pharmaceutically acceptable salt thereof, where R is group r is 0; each of R1a, R1b, R1c, R1d and R1e independently represents hydrogen; R3 represents -O-; R4 is a direct bond; R7 is hydrogen; R9 is absent; each of R10 and R11 is independently selected from the group consisting of hydrogen and phenyl, substituted with 1–3 substituents selected from NO2, OH, OCH3 and chlorine; R16 is cyano; R17 is independently selected from the group consisting of phenyl substituted with one or two substituents selected from NO2, C(O)OH and S(O2)CH3, and pyridyl, substituted C(O)OH, and C(O)R10, NR10R11; w is 1. Invention also relates to a pharmaceutical composition based on a compound of formula (I) and a method for treating a disease or disorder that can be alleviated by inhibiting the activity of leukotriene-A4-hydrolase.
EFFECT: obtaining novel heterocyclic compounds possessing useful biological properties.
17 cl, 2 tbl, 3 ex
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Authors
Dates
2019-01-24—Published
2014-03-14—Filed