FIELD: medicine; pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (I), or a pharmaceutically acceptable salt thereof
,
where ring A is 4–7 membered heterocycloalkyl ring, containing one ring nitrogen atom, or 7–9-member bicyclic heterocycloalkyl ring containing one ring nitrogen atom; Z is O, NR3, S or SO2; R1 is H, C1-6alkyl, C1-6hydroxyalkyl, C(O)C1-6alkyl, C0-3alkylene-C3-10cycloalkyl or C0-3alkylene-C2-5heterocycloalkyl containing 1 or 2 heteroatoms selected from O, S, N and N (C1-4alkyl); R2 denotes H, F, Cl or CH3; R3 is H, C1-6alkyl, C1-6haloalkyl, C0-3alkylene-C3-7cycloalkyl, C(O)C1-6alkyl or C(O)C0-3alkylene-C3-7cycloalkyl; and R4 is H or C1-3alkyl, as well as a pharmaceutical composition, a method of treating and methods of inhibiting histone deacetylase ("HDAC") enzymes (e.g., HDAC1, HDAC2 and HDAC3) using compounds of formula (1).
EFFECT: disclosed are histone deacetylase inhibitors.
98 cl, 2 tbl
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Authors
Dates
2020-05-12—Published
2016-07-01—Filed