FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to compounds presented by formula (IV) or to their pharmaceutically acceptable salts: , wherein: R140 specified in a group consisting of: H and halo; xa and xb mean the numbers each of which is independently specified in 0, 1 and 2; R150 and R160 are independently specified in a group consisting of H, halo, -CN, -CF3, -OCF3, -C1-C6alkyl, -C1-C6alkoxyl, -O-C2-C6alkyl-O-R53, -OR53, -C0-C6alkyl-S(O)0-2-R53, -C0-C6alkyl-C(O)NR50R51, -C0-C6alkyl-heterocyclyl wherein heterocyclyl is monocyclic and contains 6 atoms, and one or two atoms are independently specified in O and N; R50 and R51 and R53 are independently specified in a group consisting of -C1-C6alkyl.
EFFECT: developing a pharmaceutical composition, a method for histone deacetylase inhibition and a method of treating a polyglutamate disease wherein the polyglutamate disease is Huntington's disease.
8 cl, 332 ex, 10 tbl, 91 dwg
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Authors
Dates
2012-08-27—Published
2007-10-26—Filed