FIELD: chemistry.
SUBSTANCE: invention relates to the compound represented by formula I, its optical isomer, or its pharmaceutically acceptable salt. In formula I, X represents a heterocyclic alkyl selected from the group consisting of
and ,
where each Z and W are independently CH or N, at that, at least one of Z and W is N, each a, b, c and d are independently 1, 2 or 3, each R3, R4, R5 and R6 independently represent -H or -C1-C4-alkyl; Y is C or N; each A and B independently represent -C1-C4 alkyl, -C6-C10 aryl, -C3-C12 N-containing heteroaryl, where -C6-C10 aryl can be independently unsubstituted or one or more hydrogen atoms therein can be substituted with -CF3 or halogen; Q is C = O or SO2; R1 represents -H or -C1-C4 alkyl; R2 represents -H, -OH, halogen or absent; n is equal to 1, 2, 3 or 4. Invention also relates to the pharmaceutical composition, to the histone deacetylase mediated disease treatment method, and to the said compound use for the histone deacetylase mediated disease treatment medicine manufacturing.
.
EFFECT: disclosed is the compound with inhibitory activity against histone deacetylase (HDAC).
8 cl, 1 dwg, 4 tbl, 27 ex
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