FIELD: chemistry.
SUBSTANCE: invention relates to a compound of formula (I) or its pharmaceutically acceptable salt thereof, wherein R1 represents radical of formula (IA), (IB), or (IC), wherein R4b is C1-C6 alkyl, C3-C6 cyclo alkyl, phenyl, which is optionally substituted 1-2 substitutes selected from halogen, hydroxy or O-benzyl; or radical of formula (IIa) or (IIb), wherein n equals 1 or 2; and R3 and R4 are independently h or C1-C6 alkyl; R3b is optionally substituted C1-C-6 alkyl, wherein substitute is selected from (C1-C6) alkoxy; y represents-O-; A is a cyclo-alkylene radical, having 5, 6 or 7 atoms of ring condensed with phenyl ring; R2 represents radical of formula (IIIa), (IIIb), (IIIc), wherein q is equal to 0, 1, 2 or 3; R7 is -CH3; R8 is -CH3 or C2H5 and each presence R6 is independently H, C1-C6 alkyl. Invention also relates to pharmaceutical composition inhibiting activity of MAP-kinase p38 containing effective amount of compound of formula I, together with one or more pharmaceutically acceptable carriers.
EFFECT: technical result is compound for use in treating disease or condition, which has positive result of MAP-kinase p38 inhibiting.
11 cl, 2 tbl, 22 ex
(I)
(IA) (IB) (IC)
(IIa) (IIb)
(IIIa) (IIIb) (IIIc)
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Authors
Dates
2016-06-10—Published
2011-06-09—Filed